<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0">
    <channel>
        <title>Pediatric Cardiology via MedWorm.com</title>
        <description>MedWorm.com provides a medical RSS filtering service. Over 6000 RSS medical sources are combined and output via different filters. This feed contains the latest items from the 'Pediatric Cardiology' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Pediatric+Cardiology&t=Pediatric+Cardiology&s=Search&f=source]]></link>
        <lastBuildDate>Wed, 08 Feb 2012 09:32:58 +0100</lastBuildDate>
        <item>
            <title>Portal Venous Gas: A Clinical Finding in Obstructed Infracardiac Total Anomalous Pulmonary Venous Connection</title>
            <link>http://www.medworm.com/index.php?rid=5666982&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj8534789q5j043l3%2F</link>
            <description>We report a case of obstructive total anomalous pulmonary venous connection (TAPVC) which presented in a way
 that has not previously been described. An infant with mixed type obstructive TAPVC was found to have pulmonary interstitial
 emphysema and portal venous gas on a scout radiograph obtained prior to computed tomography scan. The presence of portal venous
 gas indicated a connection between the pulmonary venous system and the portal venous system infradiaphragmatically.
 
 
	Content Type Journal ArticleCategory Images in Pediatric CardiologyPages 1-3DOI 10.1007/s00246-012-0195-xAuthors
		Hoyoung Chung, Pediatric Residency Program, Phoenix Children’s Hospital, Phoenix, AZ 85016, USALawrence D. Lilien, Division of Neonatology, St. Joseph’s Hospital and Medical Center, Neonatology A...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666982</comments>
            <pubDate>Fri, 03 Feb 2012 17:51:35 +0100</pubDate>
            <guid isPermaLink="false">5666982</guid>        </item>
        <item>
            <title>Improved Closure of Patent Ductus Arteriosus With High Doses of Ibuprofen</title>
            <link>http://www.medworm.com/index.php?rid=5666983&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr10286w847n40466%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The patent ductus arteriosus (PDA) is associated with various complications of prematurity. Cyclooxygenase-inhibitors are
 the first-line intervention for closure of the PDA. However, the rates of PDA closure still are unsatisfactory. Therefore,
 an individual trial was performed by changing the strategy for treating neonates with ibuprofen to induce the closure of PDA.
 In a retrospective study, patients receiving 20, 10, and 10&amp;nbsp;mg/kg bodyweight ibuprofen (group 1) were compared by chart review
 with those receiving 10, 5, 5&amp;nbsp;mg/kg (group 2). The rate of PDA closure, the incidence of side effects related to the use of
 ibuprofen, and the need for surgical intervention for closure of the PDA were analyzed. A higher rate of closure after three
 doses in group 1 ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666983</comments>
            <pubDate>Fri, 03 Feb 2012 17:51:34 +0100</pubDate>
            <guid isPermaLink="false">5666983</guid>        </item>
        <item>
            <title>The Role of Shox2 in SAN Development and Function</title>
            <link>http://www.medworm.com/index.php?rid=5666984&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9753355222533280%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Embryonic development is a tightly regulated process, and many families of genes functions to provide a regulatory genetic
 network to achieve such a program. The homeobox genes are an extensive family that encodes transcription factors with a characteristic
 60-amino acid homeodomain. Mutations in these genes or in the encoded proteins might result in structural malformations, physiological
 defects, and even embryonic death. Mutations in the short-stature homeobox gene (SHOX) is associated with idiopathic short stature in humans, as observed in patients with Turner syndrome and/or Leri-Weill dyschondrosteosis.
 A closely related human homolog, SHOX2, has not been linked to any syndrome or defect so far. In mice, a SHOX ortholog gene is not present in the genome; howev...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666984</comments>
            <pubDate>Fri, 03 Feb 2012 17:51:33 +0100</pubDate>
            <guid isPermaLink="false">5666984</guid>        </item>
        <item>
            <title>The Molecular Autopsy: Should the Evaluation Continue After the Funeral?</title>
            <link>http://www.medworm.com/index.php?rid=5666985&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg66312kvm15132g5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Sudden cardiac death (SCD) is one of the most common causes of death in developed countries, with most SCDs involving the
 elderly, and structural heart disease evident at autopsy. Each year, however, thousands of sudden deaths involving individuals
 younger than 35&amp;nbsp;years of age remain unexplained after a comprehensive medicolegal investigation that includes an autopsy.
 In fact, several epidemiologic studies have estimated that at least 3% and up to 53% of sudden deaths involving previously
 healthy children, adolescents, and young adults show no morphologic abnormalities identifiable at autopsy. Cardiac channelopathies
 associated with structurally normal hearts such as long QT syndrome (LQTS), catecholaminergic polymorphic ventricular tachycardia
 (CPVT), and Br...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666985</comments>
            <pubDate>Fri, 03 Feb 2012 17:51:30 +0100</pubDate>
            <guid isPermaLink="false">5666985</guid>        </item>
        <item>
            <title>Automated External Defibrillators and Secondary Prevention of Sudden Cardiac Death Among Children and Adolescents</title>
            <link>http://www.medworm.com/index.php?rid=5666986&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv23437783m387684%2F</link>
            <description>This report discusses
 the outcomes for patients with out-of-hospital cardiac arrest (OHCA) and describes public access defibrillation programs in
 general and those directed at children and adolescents. In addition, the relatively new concept of cardiopulmonary resuscitation
 (CPR)–automated external defibrillator (AED) programs directed at schools is discussed. Although limited data are available,
 some of the preliminary data suggest improved OHCA outcomes associated with CPR-AED programs implemented in schools. These
 early data provide hope for the future potential reduction in the incidence of sudden cardiac deaths in the school setting,
 not only among children and adolescents, but also among adults.
 
 
	Content Type Journal ArticleCategory Review ArticlePages 1-5DOI 10.1007/s002...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5666986</comments>
            <pubDate>Thu, 02 Feb 2012 18:15:58 +0100</pubDate>
            <guid isPermaLink="false">5666986</guid>        </item>
        <item>
            <title>Review of Inhaled Nitric Oxide in the Pediatric Cardiac Surgery Setting</title>
            <link>http://www.medworm.com/index.php?rid=5659529&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw5x554153267p892%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Surgical intervention for congenital heart disease (CHD) can be complicated by pulmonary hypertension (PH), which increases
 morbidity, mortality, and medical burden. Consequently, postoperative management of PH is an important clinical consideration
 to improve outcomes. Inhaled nitric oxide (iNO) is a widely accepted standard of care for PH and has been studied in the context
 of cardiac surgery for CHD. However, large randomized, double-blind, placebo-controlled, multicenter clinical trials in pediatric
 patients are limited. This review will provide an overview of the clinical studies in this setting and will discuss general
 treatment considerations to facilitate a better understanding of the clinical use of iNO for PH after pediatric cardiac surgery.
 
 
	Content ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659529</comments>
            <pubDate>Wed, 01 Feb 2012 17:13:49 +0100</pubDate>
            <guid isPermaLink="false">5659529</guid>        </item>
        <item>
            <title>Primary Cardiac Leiomyoma of the Ventricular Septum: A Rare Form of Pediatric Intracardiac Tumor</title>
            <link>http://www.medworm.com/index.php?rid=5659528&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fmnvk6248q58u91vv%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A case of ventricular septal tumor diagnosed in 7-month-old boy is reported. An echocardiogram was performed for investigation
 of a heart murmur in an otherwise healthy infant. He remained asymptomatic, and the tumor had a very slow growth. When the
 boy was 9&amp;nbsp;years old, partial surgical excision was performed for right ventricular outflow tract obstruction. Histology showed
 a primary cardiac leiomyoma. To the authors’ knowledge, a primary cardiac leiomyoma of the ventricular septum has not been
 reported previously.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-012-0161-7Authors
		Isabel S. Melo, Serviço de Cardiologia Pediátrica, Hospital de Santa Cruz, Centro Hospitalar de Lisboa Ocidental, Av. Prof. Reinaldo dos Santos, ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659528</comments>
            <pubDate>Wed, 01 Feb 2012 17:13:49 +0100</pubDate>
            <guid isPermaLink="false">5659528</guid>        </item>
        <item>
            <title>Attention-Deficit/Hyperactivity Disorder, Stimulant Therapy, and the Patient with Congenital Heart Disease: Evidence and Reason</title>
            <link>http://www.medworm.com/index.php?rid=5659527&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Few3385ur5876345r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Attention-deficit/hyperactivity disorder (ADHD) is the most common neurobehavioral disorder of childhood, and congenital heart
 disease (CHD) is the most common form of birth defect. Children with CHD are at increased risk for neurodevelopmental disorders
 such as ADHD. Stimulant medications, specifically methylphenidates and amphetamines, are frequently prescribed and effective
 in reducing the symptoms of ADHD. Despite their efficacy and long history of use, the safety of these medications has recently
 come into question due to isolated reports describing sudden unexplained death of children undergoing treatment. This review
 summarizes the current literature on the cardiovascular risks associated with the use of pharmacologic therapy for ADHD, with
 an emphasis on p...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659527</comments>
            <pubDate>Wed, 01 Feb 2012 17:13:49 +0100</pubDate>
            <guid isPermaLink="false">5659527</guid>        </item>
        <item>
            <title>Prevalence and Spectrum Diseases Predisposing to Sudden Cardiac Death: Are They the Same for Both the Athlete and the Nonathlete?</title>
            <link>http://www.medworm.com/index.php?rid=5659531&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg526818447218661%2F</link>
            <description>This report highlights the prevalence
 and spectrum of SCD-predisposing diseases and how they are affected by athletic participation. In addition, disease-specific
 guidelines for sports participation are addressed.
 
 
	Content Type Journal ArticleCategory Review ArticlePages 1-8DOI 10.1007/s00246-012-0159-1Authors
		Anjan S. Batra, Division of Pediatric Cardiology, Children’s Hospital of Orange County, University of California at Irvine, 455 S Main Street, Orange, CA 92868, USASeshadri Balaji, Division of Cardiology, Oregon Health and Science University, Portland, OR, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659531</comments>
            <pubDate>Tue, 31 Jan 2012 16:45:46 +0100</pubDate>
            <guid isPermaLink="false">5659531</guid>        </item>
        <item>
            <title>Pulmonary Vein Atresia with Severe Contralateral Pulmonary Vein Stenosis in a Child</title>
            <link>http://www.medworm.com/index.php?rid=5659530&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg270243273142328%2F</link>
            <description>We present an infant who died due to unilateral right-sided pulmonary vein atresia in conjunction with severe contralateral
 pulmonary vein stenosis who was diagnosed with the assistance of cardiac computed tomography scanning.
 
 
	Content Type Journal ArticleCategory Images in Pediatric CardiologyPages 1-3DOI 10.1007/s00246-012-0178-yAuthors
		Jeffrey E. Vergales, Division of Pediatric Cardiology, Department of Pediatrics, University of Virginia Health System, Charlottesville, VA, USAShawn C. West, Division of Pediatric Cardiology, Department of Pediatrics, University of Virginia Health System, Charlottesville, VA, USAAndrew W. Hoyer, Division of Pediatric Cardiology, Department of Pediatrics, University of Virginia Health System, Charlottesville, VA, USA
	

	
		Journal Pediatric Cardiol...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659530</comments>
            <pubDate>Tue, 31 Jan 2012 16:45:46 +0100</pubDate>
            <guid isPermaLink="false">5659530</guid>        </item>
        <item>
            <title>Congenital Left Ventricular Diverticulum Diagnosed by Echocardiography</title>
            <link>http://www.medworm.com/index.php?rid=5659533&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhv70451h65846130%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Congenital left ventricular diverticulum is a rare cardiac malformation. The incidence of left ventricular diverticulum is
 reported to be 0.05% of all congenital heart malformations. This case series comprised three infants with the diagnosis of
 congenital left ventricular diverticulum determined by echocardiography. In addition, two of the three babies also were detected
 to have other cardiac disease. Echocardiography is a useful tool for diagnosing congenital left ventricular diverticulum.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-012-0153-7Authors
		Hui Yang, Department of Ultrasound, West China Second University Hospital, West China Medical School, Sichuan Univeisity, 20 ren min nan lu san duan, Chengdu, 610041 ChinaQi Zhu, ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659533</comments>
            <pubDate>Tue, 31 Jan 2012 07:04:43 +0100</pubDate>
            <guid isPermaLink="false">5659533</guid>        </item>
        <item>
            <title>Angina Pectoris with Troponin Increase in Arrhythmogenic Right Ventricle Dysplasia: Case Article and Review of the Literature</title>
            <link>http://www.medworm.com/index.php?rid=5659532&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2182t820q7668t47%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 16-year-old Hispanic girl with arrhythmogenic right-ventricle dysplasia (ARVD) presented with angina pectoris and troponin
 increase on three occasions. There was a family history of sudden cardiac death in a cousin. Her mother was diagnosed with
 ARVD. The patient herself had a history of nonsustained ventricular tachycardia but did not meet diagnostic criteria for ARVD.
 Cardiac workup, including serial transthoracic echocardiograms and a coronary angiogram, showed a structurally normal heart
 without coronary artery stenosis. Results of cardiac magnetic resonance imaging were questionable, but endomyocardial biopsy
 did not show evidence of viral myocarditis by polymerase chain reaction. Genetic testing confirmed ARVD.
 
 
	Content Type Journal ArticleCategory Case...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659532</comments>
            <pubDate>Tue, 31 Jan 2012 07:04:43 +0100</pubDate>
            <guid isPermaLink="false">5659532</guid>        </item>
        <item>
            <title>Implantable Cardioverter-Defibrillators and the Young Athlete: Can the Two Coexist?</title>
            <link>http://www.medworm.com/index.php?rid=5659534&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq2711tjh876548jq%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Since the incorporation of implantable cardioverter-defibrillators (ICDs) into the management of life-threatening arrhythmias
 in the 1980s, tremendous advances in device and lead technology have allowed the implantation of ICD systems in younger and
 smaller patients. The majority of these young patients with “electrical” cardiac disease and a significant number of those
 with other indications for ICD placement have near normal to normal cardiac function, which has resulted in a large population
 of young ICD patients with minimal to no symptoms. This population has pushed the boundaries of published guidelines on activity
 restrictions for the disease state and the presence of an ICD, creating a dilemma for the patient, the family, and the health
 care team with ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5659534</comments>
            <pubDate>Tue, 31 Jan 2012 07:04:41 +0100</pubDate>
            <guid isPermaLink="false">5659534</guid>        </item>
        <item>
            <title>Access to Pediatric Cardiac Care After Health Care Reform in China</title>
            <link>http://www.medworm.com/index.php?rid=5647505&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk40076633m512018%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00246-012-0177-zAuthors
		Xuefei Wang, Department of Administration, Children’s Hospital, Zhejiang University School of Medicine, Hangzhou, 310003 ChinaWeize Xu, Department of Cardiothoracic Surgery, Children’s Hospital, Zhejiang University School of Medicine, 57 Zhugan Xiang, Hangzhou, 310003 ChinaQiang Shu, Department of Cardiothoracic Surgery, Children’s Hospital, Zhejiang University School of Medicine, 57 Zhugan Xiang, Hangzhou, 310003 China
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647505</comments>
            <pubDate>Sat, 28 Jan 2012 16:52:01 +0100</pubDate>
            <guid isPermaLink="false">5647505</guid>        </item>
        <item>
            <title>Ellis-van Creveld Syndrome and Congenital Heart Defects: Presentation of an Additional 32 Cases</title>
            <link>http://www.medworm.com/index.php?rid=5647506&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5n6227tt203851th%2F</link>
            <description>Content Type Journal ArticleCategory EditorialPages 1-2DOI 10.1007/s00246-012-0155-5Authors
		Matthew J. O’Connor, University of Arkansas for Medical Sciences, Arkansas Children’s Hospital, Little Rock, AR 72202, USAR. Thomas Collins, University of Arkansas for Medical Sciences, Arkansas Children’s Hospital, Little Rock, AR 72202, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5647506</comments>
            <pubDate>Fri, 27 Jan 2012 17:56:46 +0100</pubDate>
            <guid isPermaLink="false">5647506</guid>        </item>
        <item>
            <title>Functional Echocardiographic Assessment of Myocardial Performance in Anemic Premature Infants: A Pilot Study</title>
            <link>http://www.medworm.com/index.php?rid=5638314&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa4l3l886821x4640%2F</link>
            <description>In this study, 32 anemic premature
 infants had serial echocardiographic assessment of left ventricular (LV) systolic performance, LV preload, and afterload immediately
 before, within 48&amp;nbsp;h, and up to 120&amp;nbsp;h after the transfusion of pRBCs. Pretransfusional evaluations also were compared with
 similar assessments of 71 nonanemic inpatient premature infants analogous for sex, gestational age at birth, and postnatal
 age. Left ventricular systolic performance was estimated from fractional shortening, LV output, and LV myocardial performance
 index (LVMPI). The LV preload was estimated from the LV end-diastolic dimension and the ratio of left atrium-to-aortic root
 dimension (LA/Ao ratio). The LV afterload was estimated from end-systolic wall stress. The LVMPI was found to decrease wi...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5638314</comments>
            <pubDate>Tue, 24 Jan 2012 18:09:39 +0100</pubDate>
            <guid isPermaLink="false">5638314</guid>        </item>
        <item>
            <title>From Other Journals</title>
            <link>http://www.medworm.com/index.php?rid=5619893&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh66x335m54621830%2F</link>
            <description>Content Type Journal ArticleCategory From Other JournalsPages 1-3DOI 10.1007/s00246-012-0156-4Authors
		Sanjiv Gandhi, 1507 W. Harrison Street, Chicago, IL 60607, USAOmar M. Khalid, 1507 W. Harrison Street, Chicago, IL 60607, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5619893</comments>
            <pubDate>Wed, 18 Jan 2012 06:52:07 +0100</pubDate>
            <guid isPermaLink="false">5619893</guid>        </item>
        <item>
            <title>Upcoming Events in Pediatric Cardiology</title>
            <link>http://www.medworm.com/index.php?rid=5619892&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2458042818206667%2F</link>
            <description>Content Type Journal ArticleCategory Upcoming EventsPages 1-1DOI 10.1007/s00246-012-0157-3

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5619892</comments>
            <pubDate>Wed, 18 Jan 2012 06:52:07 +0100</pubDate>
            <guid isPermaLink="false">5619892</guid>        </item>
        <item>
            <title>Outcome of Biventricular Repair in Infants With Multiple Left Heart Obstructive Lesions</title>
            <link>http://www.medworm.com/index.php?rid=5494788&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg6k2m141w232n01g%2F</link>
            <description>This study sought to assess the mortality and morbidity of patients
 with LHL after biventricular repair and to determine the growth of the left-sided cardiac structures. Retrospective analysis
 of 39 consecutive infants with LHL who underwent biventricular repair was performed. The median age at surgery was 7&amp;nbsp;days
 (range 1–225&amp;nbsp;days), and the median follow-up period was 34&amp;nbsp;months (range 1–177&amp;nbsp;months). Between diagnosis and the end of the
 follow-up period, the size of the aortic annulus (z-score −4.1&amp;nbsp;±&amp;nbsp;2.8 vs. −0.1&amp;nbsp;±&amp;nbsp;2.7) and the LV (LV end-diastolic diameter z-score −1.7&amp;nbsp;±&amp;nbsp;2.8 vs. 0.21&amp;nbsp;±&amp;nbsp;1.7) normalized. During the follow-up period, 23 patients required 39 reinterventions (62%) consisting
 of redo surgery for 21 pa...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5494788</comments>
            <pubDate>Sat, 10 Dec 2011 16:56:13 +0100</pubDate>
            <guid isPermaLink="false">5494788</guid>        </item>
        <item>
            <title>From Other Journals</title>
            <link>http://www.medworm.com/index.php?rid=5486643&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F28l337rg84733635%2F</link>
            <description>Content Type Journal ArticleCategory From Other JournalsPages 1-3DOI 10.1007/s00246-011-0151-1Authors
		Sanjiv Gandhi, 1507 W. Harrison Street, Chicago, IL 60607, USAOmar M. Khalid, 1507 W. Harrison Street, Chicago, IL 60607, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486643</comments>
            <pubDate>Wed, 07 Dec 2011 16:44:26 +0100</pubDate>
            <guid isPermaLink="false">5486643</guid>        </item>
        <item>
            <title>Upcoming Events in Pediatric Cardiology</title>
            <link>http://www.medworm.com/index.php?rid=5486644&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv58765050h423t4w%2F</link>
            <description>Content Type Journal ArticleCategory Upcoming EventsPages 1-1DOI 10.1007/s00246-011-0152-0

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5486644</comments>
            <pubDate>Tue, 06 Dec 2011 17:04:29 +0100</pubDate>
            <guid isPermaLink="false">5486644</guid>        </item>
        <item>
            <title>Lost Unilateral Capillary Perfusion During Nonpulsatile Pulmonary Circulation: Successful Recovery by Oral Sildenafil</title>
            <link>http://www.medworm.com/index.php?rid=5457243&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F571600011p182344%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Good status of pulmonary perfusion is essential for a successful outcome after the Fontan procedure. Increased pulmonary pressure
 and vascular resistance, small size of the pulmonary arteries, and significant branch stenoses reflect some of the main problems
 causing failing Fontan circulation. Here we report a child who underwent a staged Fontan procedure with subsequent subtotal
 loss of the left-sided pulmonary perfusion, although branch stenosis was successfully treated by stent implantation. Oral
 sildenafil caused restoration of the capillary vascular bed, improved left-sided lung perfusion, and resulted in significant
 clinical benefit.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-5DOI 10.1007/s00246-011-0136-0Authors
		Levent Celik, Department f...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5457243</comments>
            <pubDate>Sat, 26 Nov 2011 16:46:33 +0100</pubDate>
            <guid isPermaLink="false">5457243</guid>        </item>
        <item>
            <title>Ischemic Stroke Caused by Paradoxical Embolism After an Unsuccessful Transcatheter Atrial Septal Defect Closure Procedure: A Word of Caution</title>
            <link>http://www.medworm.com/index.php?rid=5457244&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc6687m6287078222%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Transcatheter device closure of atrial septal defect (ASD) has become a well-accepted alternative to surgical repair. Serious
 complications of transcatheter ASD closure are rare, but when they occur, devastating consequences may result. Herein, we
 present the case of a 4-year-old girl who had an ischemic stroke caused by a presumptive paradoxical embolism after an unsuccessful
 transcatheter ASD procedure and in whom subsequent venous color Doppler showed deep venous thrombosis (DVT) of the right lower
 extremity. The risk factors that predisposed to paradoxical cerebral embolism and DVT in this patient are discussed, and the
 literature is reviewed.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-4DOI 10.1007/s00246-011-0150-2Authors
		Zhen-fei Fang, Dep...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5457244</comments>
            <pubDate>Sat, 26 Nov 2011 16:46:31 +0100</pubDate>
            <guid isPermaLink="false">5457244</guid>        </item>
        <item>
            <title>Cor Triatriatum With Partial Anomalous Pulmonary Venous Return: A Rare Case of Parallel Obstruction and Successful Staged Treatment</title>
            <link>http://www.medworm.com/index.php?rid=5449662&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4463t7416300774p%2F</link>
            <description>We present a case of such rare anatomy with multilevel obstruction that presented
 in infancy as cardiogenic shock. The patient underwent staged treatment with extracorporeal membrane oxygenation stabilization,
 catheter-based balloon dilatation of the cor triatriatum and atrial septostomy, followed by definitive surgical repair, with
 excellent result.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-011-0148-9Authors
		Ofer Schiller, Division of Cardiology, Children’s National Medical Center, Washington, DC 20010, USAKristin M. Burns, Division of Cardiology, Children’s National Medical Center, Washington, DC 20010, USAPranava Sinha, Department of Cardiovascular Surgery, Children’s National Medical Center, Washington, DC 20010, USASusan D. Cummings, D...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449662</comments>
            <pubDate>Thu, 24 Nov 2011 17:45:08 +0100</pubDate>
            <guid isPermaLink="false">5449662</guid>        </item>
        <item>
            <title>Feasibility of Improving the Motor Development of Toddlers With Congenital Heart Defects Using a Home-Based Intervention</title>
            <link>http://www.medworm.com/index.php?rid=5449663&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk208u583r4t46001%2F</link>
            <description>This study investigated the feasibility of administering motor assessments, delivering rehabilitation via parent-led activities,
 and enhancing motor function in children with complex congenital heart defects. Gross and fine motor development were evaluated
 in 20 toddlers ages 12 to 26&amp;nbsp;months after either a superior cavopulmonary connection (SCPC) procedure or an arterial switch
 operation (ASO) using the Peabody developmental scale, version 2 (PDMS-2). Feasibility of assessment and program delivery
 were examined using open-ended interviews with parents. The ASO group scored consistently higher than the SCPC group in every
 subscore of the PDMS-2 (ASO gross motor quotient, 96.78&amp;nbsp;±&amp;nbsp;7.396 vs SCPC gross motor quotient, 77.56&amp;nbsp;±&amp;nbsp;7.715 [P&amp;nbsp;&amp;lt;&amp;nbsp;0.001]; ASO f...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5449663</comments>
            <pubDate>Thu, 24 Nov 2011 17:45:06 +0100</pubDate>
            <guid isPermaLink="false">5449663</guid>        </item>
        <item>
            <title>Update on the Amplatzer Duct Occluder: A 10-Year Experience in Asia</title>
            <link>http://www.medworm.com/index.php?rid=5440582&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk6607n2534045207%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Few data exist regarding the efficacy and safety of the Amplatzer ductal occluder (ADO) type 1 device in the Asian region.
 This retrospective study, conducted between August 2001 and April 2011, attempted device placement for 231 patients (165 females
 and 66 males) with a median age of 7.4&amp;nbsp;years (range, 3&amp;nbsp;months to 64&amp;nbsp;years) and an average weight of 19.4&amp;nbsp;kg (range, 4.1–81.0&amp;nbsp;kg).
 Among the patients in this study, 66 (28.6%) had pulmonary hypertension, ten (4.3%) had trisomy 21, and eight (3.5%) had other
 congenital cardiac anomalies. The mean narrowest patent ductus arteriosus (PDA) diameter was 4.2&amp;nbsp;mm (range, 1.3–10&amp;nbsp;mm), and
 the ampulla size was 9.6&amp;nbsp;mm (range, 4–20&amp;nbsp;mm). Successful implantation was achieved for 229 ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5440582</comments>
            <pubDate>Mon, 21 Nov 2011 17:53:35 +0100</pubDate>
            <guid isPermaLink="false">5440582</guid>        </item>
        <item>
            <title>Assessment of Risk Factors for Korean Children with Kawasaki Disease</title>
            <link>http://www.medworm.com/index.php?rid=5440583&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj511434125664771%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Kawasaki disease (KD) is the most common cause of acquired heart disease in children. Intravenous immunoglobulin (IVIG) is
 the standard therapy for KD, but more than 10% of KD patients do not respond to IVIG and are at high risk for the development
 of coronary artery lesions (CALs). To identify clinical and genetic risk factors associated with CAL development and IVIG
 nonresponsiveness, this study analyzed the clinical data for 478 Korean KD patients. Multivariate logistic regression analysis
 showed that incomplete KD, IVIG nonresponse, fever duration of 7&amp;nbsp;days or longer, and the CC/AC genotypes of the rs7604693
 single nucleotide polymorphism (SNP) in the PELI1 gene were significantly associated with the development of CALs, with odds ratios (ORs) ranging from...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5440583</comments>
            <pubDate>Mon, 21 Nov 2011 17:53:34 +0100</pubDate>
            <guid isPermaLink="false">5440583</guid>        </item>
        <item>
            <title>A Novel GATA4 Loss-of-Function Mutation Associated With Congenital Ventricular Septal Defect</title>
            <link>http://www.medworm.com/index.php?rid=5440584&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj87007550573k8h7%2F</link>
            <description>In this study, the entire coding region of GATA4, a gene encoding a zinc finger transcription factor essential for normal cardiac morphogenesis, was sequenced in 160 unrelated
 patients with VSD. The available relatives of the index patient harboring the identified mutation and 200 unrelated control
 individuals were subsequently genotyped. The disease-causing potential of a sequence alteration was evaluated by MutationTaster,
 and the functional effect of the mutation was characterized using a luciferase reporter assay system. As a result, a novel
 heterozygous GATA4 variation, p.R43W, was identified in a proband with VSD, that was absent in control subjects. Genetic analysis
 of the family members of the variation carrier showed that the substitution co-segregated with VSD. The p.R43W va...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5440584</comments>
            <pubDate>Sat, 19 Nov 2011 16:54:34 +0100</pubDate>
            <guid isPermaLink="false">5440584</guid>        </item>
        <item>
            <title>Outcomes of Infants Undergoing Superior Cavopulmonary Connection in the Presence of Ventricular Dysfunction</title>
            <link>http://www.medworm.com/index.php?rid=5431570&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr456314482515251%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Outcomes in patients with ventricular dysfunction undergoing superior cavopulmonary connection (SCPC) are not well known.
 We reviewed records of patients undergoing SCPC at our center from December 2005 to October 2009 and studied those whose pre-SCPC
 echocardiograms demonstrated at least moderate systemic ventricular dysfunction. Of the 213 patients undergoing SCPC, 19 (9%)
 met inclusion criteria. Diagnoses were hypoplastic left heart syndrome (n&amp;nbsp;=&amp;nbsp;18) and rightward unbalanced atrioventricular canal with pulmonary stenosis (n&amp;nbsp;=&amp;nbsp;1). In those surviving &amp;gt;2&amp;nbsp;months after SCPC, ventricular function was assessed by echocardiography 4.9 (range 3.5 to 9.7)
 months after SCPC and was improved in ten of 17 (59%), unchanged in six of 17 (35%), and wo...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5431570</comments>
            <pubDate>Fri, 18 Nov 2011 17:29:29 +0100</pubDate>
            <guid isPermaLink="false">5431570</guid>        </item>
        <item>
            <title>Use of Troponin as a Screen for Chest Pain in the Pediatric Emergency Department</title>
            <link>http://www.medworm.com/index.php?rid=5421831&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb87jl9r336287472%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Troponin levels are commonly employed in the assessment of adults presenting with chest pain or concern for coronary ischemia.
 However, the utility of troponin measurements in children is not well defined. The purpose of this study was to review the
 use and clinical yield of serum troponin assay in a large pediatric emergency department (ED). We identified all patients&amp;nbsp;&amp;lt;22&amp;nbsp;years
 of age, not previously known to have cardiac disease, who presented with chest pain and whose troponin levels were evaluated
 in our pediatric ED during a 7-year period. Test results were correlated to patient factors, such as chief complaint, cardiac
 history, diagnostic workup, and discharge diagnoses. Of the 212 study patients who presented with chest pain, troponin levels
 we...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5421831</comments>
            <pubDate>Wed, 16 Nov 2011 16:48:05 +0100</pubDate>
            <guid isPermaLink="false">5421831</guid>        </item>
        <item>
            <title>Environmental Factors and Rheumatic Heart Disease in Fiji</title>
            <link>http://www.medworm.com/index.php?rid=5386017&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx10363161374w528%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Rheumatic heart disease (RHD) is an important cause of cardiac morbidity and mortality globally, particularly in the Pacific
 region. Susceptibility to RHD is thought to be due to genetic factors that are influenced by environmental factors, such as
 crowding and poverty. However, there are few data relating to these environmental factors in the Pacific region. We conducted
 a case-control study of 80 cases of RHD with age- and sex-matched controls in Fiji using a questionnaire to investigate associations
 of RHD with a number of environmental factors. There was a trend toward increased risk of RHD in association with poor-quality
 housing and lower socioeconomic status, but only one factor, maternal unemployment, reached statistical significance (OR 2.6,
 95% confidenc...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5386017</comments>
            <pubDate>Sat, 05 Nov 2011 17:08:47 +0100</pubDate>
            <guid isPermaLink="false">5386017</guid>        </item>
        <item>
            <title>Age- and Chamber-Specific Differences in Oxidative Stress After Ischemic Injury</title>
            <link>http://www.medworm.com/index.php?rid=5386019&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fml006413410r6114%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Each year, tens of thousands of children undergo cardiopulmonary bypass (CPB) to correct congenital heart defects. Although
 necessary for surgery, CPB involves stopping the heart and exposing it to ischemic conditions. On reoxygenation, the heart
 can experience effects similar to that of acute myocardial infarction. Although much is known about adult injury, little is
 known about the effects of global ischemia on newborn ventricles. We studied newborn (2 to 4&amp;nbsp;days old) and adult (&amp;gt;8&amp;nbsp;weeks
 old) rabbit hearts subjected to ischemia–reperfusion (30&amp;nbsp;min of ischemia and 60&amp;nbsp;min of reperfusion). Our data demonstrated
 chamber- and age-specific changes in oxidative stress. During ischemia, hydrogen peroxide (H2O2) increased in both right-ventricular ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5386019</comments>
            <pubDate>Sat, 05 Nov 2011 17:08:45 +0100</pubDate>
            <guid isPermaLink="false">5386019</guid>        </item>
        <item>
            <title>Improvement and Defervescence of Persistent Fever After One Course of Intravenous Immunoglobulin in a Patient With Bacterial Infective Endocarditis</title>
            <link>http://www.medworm.com/index.php?rid=5386018&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw801280537156vm1%2F</link>
            <description>Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-011-0138-yAuthors
		Musaab Ramsi, Floating Hospital for Children, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USARashed Durgham, Floating Hospital for Children, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USAMichael de Moor, Floating Hospital for Children, Tufts Medical Center, Tufts University School of Medicine, Boston, MA, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5386018</comments>
            <pubDate>Sat, 05 Nov 2011 17:08:45 +0100</pubDate>
            <guid isPermaLink="false">5386018</guid>        </item>
        <item>
            <title>From Other Journals</title>
            <link>http://www.medworm.com/index.php?rid=5360198&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk7865v0h5333h573%2F</link>
            <description>Content Type Journal ArticleCategory From Other JournalsPages 1-2DOI 10.1007/s00246-011-0140-4Authors
		Sanjiv Gandhi, 1507 W. Harrison Street, Chicago, IL 60607, USAOmar M. Khalid, 1507 W. Harrison Street, Chicago, IL 60607, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5360198</comments>
            <pubDate>Fri, 28 Oct 2011 17:16:11 +0100</pubDate>
            <guid isPermaLink="false">5360198</guid>        </item>
        <item>
            <title>Upcoming Events in Pediatric Cardiology</title>
            <link>http://www.medworm.com/index.php?rid=5360199&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft32w16775m820405%2F</link>
            <description>Content Type Journal ArticleCategory Upcoming EventsPages 1-1DOI 10.1007/s00246-011-0141-3

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5360199</comments>
            <pubDate>Fri, 28 Oct 2011 17:16:09 +0100</pubDate>
            <guid isPermaLink="false">5360199</guid>        </item>
        <item>
            <title>Comparison of Long-Term Clinical Outcomes and Costs Between Video-Assisted Thoracoscopic Surgery and Transcatheter Amplatzer Occlusion of the Patent Ductus Arteriosus</title>
            <link>http://www.medworm.com/index.php?rid=5360200&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa3nl353371k22x54%2F</link>
            <description>This study enrolled 294 patients with isolated patent ductus arteriosus
 (PDA) from April 2002 to April 2007, and 290 of these patients were followed up until April 2010. Of the 294 patients, 196
 underwent VATS and 98 accepted TAO for PDA closure. The two groups were similar in terms of demographics and preoperative
 clinical characteristics. No cardiac deaths occurred in either group. All the patients in the VATS group had successful PDA
 closure, and 94 patients (94/98, 95.9%) in the TAO group had successful PDA occlusion. The incidence of acute procedure-related
 complications recorded was 1.5% in the VATS group compared with 10.2% in TAO group (P&amp;nbsp;&amp;lt;&amp;nbsp;0.05). The cost per patient was $1,309.40&amp;nbsp;±&amp;nbsp;$312.20 in the VATS group and $3,415.80&amp;nbsp;±&amp;nbsp;$637.30 in the TA...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5360200</comments>
            <pubDate>Fri, 28 Oct 2011 17:16:08 +0100</pubDate>
            <guid isPermaLink="false">5360200</guid>        </item>
        <item>
            <title>Various Modalities for Evaluation of a Fused Heart in Conjoined Twins</title>
            <link>http://www.medworm.com/index.php?rid=5323823&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffu3g5t7368278030%2F</link>
            <description>We report a series of 20 sets of thoracopagus conjoined twins as well as the results of a PubMed
 database literature review literature from 1982 to 2009. Twenty sets of fused-heart thoracopagus conjoined twins were evaluated
 by echocardiography, cardiac catheterization, magnetic resonance image (MRI), and three-dimensional computed tomography angiography
 (3D-CTA). Imaging results were compared to findings at surgery or autopsy. All sets of conjoined twins underwent postnatal
 echocardiography; 11 sets (55%) underwent cardiac catheterization; 4 sets (20%) underwent MRI; and 1 set (5%) underwent 3D-CTA.
 All intracardiac anatomy (ICA) was identified by echocardiography. Cardiac catheterization, MRI, and 3D-CTA were able to identify
 extracardiac vascular structures as well as the ICA. 3D-...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5323823</comments>
            <pubDate>Sat, 15 Oct 2011 05:52:28 +0100</pubDate>
            <guid isPermaLink="false">5323823</guid>        </item>
        <item>
            <title>Transseptal Catheter Decompression of the Left Ventricle During Extracorporeal Membrane Oxygenation</title>
            <link>http://www.medworm.com/index.php?rid=5314214&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl0122242j2mn8305%2F</link>
            <description>We present the case of a 13-year-old girl who presented with cardiogenic shock. VA-ECMO was initiated,
 but after 6&amp;nbsp;days, severe left-ventricular distension resulted in decreased VA-ECMO flows. With guidance by bedside transesophageal
 echocardiography, a percutaneous atrial transseptal cannula was placed and connected to the venous circuit, thus decompressing
 the left ventricle. The patient improved, was weaned from VA-ECMO 5&amp;nbsp;days later, and was discharged from the hospital. Bedside
 transseptal catheter insertion is an effective method of left-ventricular decompression.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-011-0113-7Authors
		Michael F. Swartz, Department of Surgery, Strong Memorial Hospital, University of Rochester, Rochester, NY 14...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5314214</comments>
            <pubDate>Sat, 08 Oct 2011 15:44:39 +0100</pubDate>
            <guid isPermaLink="false">5314214</guid>        </item>
        <item>
            <title>Hypoplastic Left Heart Syndrome, Restrictive Patent Foramen Ovale, and Pulmonary Valve Stenosis: An Unusual Combination</title>
            <link>http://www.medworm.com/index.php?rid=5314215&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F4wt8526u07667051%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;An infant presented with a rare combination of hypoplastic left heart syndrome, restricted patent foramen ovale, and moderately
 dysplastic pulmonary valve. In preparation for heart transplantation, bilateral pulmonary artery banding was performed to
 protect the pulmonary vasculature.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-011-0119-1Authors
		Sanjeev Aggarwal, Department of Pediatrics, Children’s Hospital of Michigan, 3901 Beaubien Boulevard, Detroit, MI 48201, USARalph E. Delius, Department of Cardiovascular Surgery, Children’s Hospital of Michigan, 3901 Beaubien Boulevard, Detroit, MI 48201, USAHenry L. Walters, Department of Cardiovascular Surgery, Children’s Hospital of Michigan, 3901 Beaubien Boulevard, Detroit, MI 4...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5314215</comments>
            <pubDate>Sat, 08 Oct 2011 15:44:38 +0100</pubDate>
            <guid isPermaLink="false">5314215</guid>        </item>
        <item>
            <title>Heart Rate Variability in Children With Fontan Circulation: Lateral Tunnel and Extracardiac Conduit</title>
            <link>http://www.medworm.com/index.php?rid=5304256&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu35450u42t716h42%2F</link>
            <description>This study aimed to investigate HRV in a cohort of children with univentricular
 hearts, focusing on the relation between HRV and surgical procedure. For 112 children with Fontan circulation, HRV was analyzed
 using power spectral analysis. Spectral power was determined in three regions: very-low-frequency (VLF), low-frequency (LF),
 and high-frequency (HF) regions. Patients were compared with 66 healthy controls subject. Patients with LT were compared with
 patients who had EC. The children with Fontan circulation showed a significantly reduced HRV including total power (P&amp;nbsp;&amp;lt;&amp;nbsp;0.0001), VLF (P&amp;nbsp;&amp;lt;&amp;nbsp;0.0001), LF (P&amp;nbsp;&amp;lt;&amp;nbsp;0.0001), and HF (P&amp;nbsp;=&amp;nbsp;0.001) compared with the control subjects. The LT and EC patients did not differ significantly. Reduced HRV was ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5304256</comments>
            <pubDate>Fri, 07 Oct 2011 15:59:49 +0100</pubDate>
            <guid isPermaLink="false">5304256</guid>        </item>
        <item>
            <title>Right Ventricle Myocardial Perfusion Scintigraphy: Feasibility and Expected Values in Children</title>
            <link>http://www.medworm.com/index.php?rid=5296812&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Frp6154232r751823%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Stress myocardial perfusion scintigraphy imaging (SMPSI) has important applications for evaluating coronary disease and ventricular
 function. Studies consistently focus on the left ventricle (LV), with no normal right ventricle (RV) data available. This
 study sought to evaluate the feasibility of RV perfusion with technetium (Tc-99m) sestamibi using a low radiotracer dose for
 children free of coronary artery (CA) anomalies and to determine its normal pattern. Patients with a history of Kawasaki disease
 who showed no coronary complications on selective angiography or no LV perfusion defects on SMPSI were studied at rest and
 during an exercise challenge. The RV uptake counts were compared with those for different segments of the LV, and multiple
 ratios of the uptake...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296812</comments>
            <pubDate>Tue, 04 Oct 2011 05:52:45 +0100</pubDate>
            <guid isPermaLink="false">5296812</guid>        </item>
        <item>
            <title>Usefulness of Doppler Derived End Diastolic Flow Gradient Across the Patent Ductus Arteriosus in Selecting Coils for Ductal Occlusion</title>
            <link>http://www.medworm.com/index.php?rid=5296813&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F11h3n74642244703%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Transcatheter closure of patent ductus arteriosus (PDA) with coils is accepted as an alternative to surgical ligation. We
 evaluated whether flow gradient across PDA, obtained by Doppler echocardiography, can aid in selecting coils for percutaneous
 ductal occlusion. 79 consecutive patients with PDA, who underwent successful percutaneous coil occlusion were retrospectively
 reviewed. Patients with other structural heart disease and pulmonary hypertension with right-to-left shunt were excluded.
 Echocardiogram and cardiac catheterization were done in all patients. Gianturco (Occluding Spring Emboli; Cook, Bloomington,
 IN) non-detachable coils of 0.038 and 0.052-inch core sizes were used for ductal occlusion. Trough diastolic gradient was
 correlated with the size and th...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296813</comments>
            <pubDate>Tue, 04 Oct 2011 05:52:44 +0100</pubDate>
            <guid isPermaLink="false">5296813</guid>        </item>
        <item>
            <title>Heterogeneity of Ventricular Repolarization in Newborns With Severe Aortic Coarctation</title>
            <link>http://www.medworm.com/index.php?rid=5296814&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fqq51044u1238632j%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Sudden death is a possible occurrence for newborns younger than 1&amp;nbsp;year with severe aortic coarctation (CoA) before surgical
 correction. Basic research and animal experiments have shown electrophysiologic changes during mechanical ventricular pressure
 overload. The current study aimed to evaluate the effect of severe CoA on the heterogeneity of ventricular repolarization
 by examining corrected QT and JT interval dispersion (respectively, QTc-D and JTc-D) and electrocardiographic parameters of
 spatial heterogeneity of ventricular repolarization in newborns with no associated congenital cardiac malformations. The study
 enrolled 30 isolated severe CoA neonates (age, 45&amp;nbsp;±&amp;nbsp;15&amp;nbsp;days; 17 males) with normal size and wall thickness of the left ventricle
 ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296814</comments>
            <pubDate>Tue, 04 Oct 2011 05:52:43 +0100</pubDate>
            <guid isPermaLink="false">5296814</guid>        </item>
        <item>
            <title>Atypical Partial Anomalous Pulmonary Venous Drainage of the Left Upper Pulmonary Vein Through a Compressed Vertical Vein Between the Aorta and the Pulmonary Artery</title>
            <link>http://www.medworm.com/index.php?rid=5296815&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy67836458j685685%2F</link>
            <description>Content Type Journal ArticleCategory Images in Pediatric CardiologyPages 1-2DOI 10.1007/s00246-011-0134-2Authors
		Habiba Mizouni, Department of Radiology, La Rabta University Hospital, Jebbari, 1007 Tunis, TunisiaMonia Attia, Department of Radiology, La Rabta University Hospital, Jebbari, 1007 Tunis, TunisiaJalel Zaidi, Department of Cardiovascular Surgery, La Rabta University Hospital, Jebbari, 1007 Tunis, TunisiaEmna Menif, Department of Radiology, La Rabta University Hospital, Jebbari, 1007 Tunis, Tunisia
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5296815</comments>
            <pubDate>Tue, 04 Oct 2011 05:52:42 +0100</pubDate>
            <guid isPermaLink="false">5296815</guid>        </item>
        <item>
            <title>Plasmin Generation and Fibrinolysis in Pediatric Patients Undergoing Cardiopulmonary Bypass Surgery</title>
            <link>http://www.medworm.com/index.php?rid=5285353&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fw25423k0316nt064%2F</link>
            <description>This study establishes the foundation for future studies in this area, particularly those focusing on clinical
 outcomes after CPB surgery.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-6DOI 10.1007/s00246-011-0122-6Authors
		Vera Ignjatovic, Murdoch Childrens Research Institute, Flemington Road, Parkville, VIC 3052, AustraliaAparajith Chandramouli, Department of Clinical Haematology, Royal Children’s Hospital, Melbourne, AustraliaJenny Than, Department of Clinical Haematology, Royal Children’s Hospital, Melbourne, AustraliaRobyn Summerhayes, Murdoch Childrens Research Institute, Flemington Road, Parkville, VIC 3052, AustraliaFiona Newall, Murdoch Childrens Research Institute, Flemington Road, Parkville, VIC 3052, AustraliaSteve Horton, Department of Cardiac Surgery...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285353</comments>
            <pubDate>Sun, 02 Oct 2011 05:50:11 +0100</pubDate>
            <guid isPermaLink="false">5285353</guid>        </item>
        <item>
            <title>Changes in Hemodynamic Parameters and Cerebral Saturation During Supraventricular Tachycardia</title>
            <link>http://www.medworm.com/index.php?rid=5285354&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fc42n23u50347g1n4%2F</link>
            <description>This study aimed first to determine the hemodynamic
 changes associated with electrophysiology testing for SVT and second to determine whether the hemodynamic changes are associated
 with similar changes in the cerebral saturation as determined by NIRS. The study enrolled 30 patients 5–20&amp;nbsp;years of age with
 a history of SVT who underwent an EPS. The demographic data included age, gender, weight, height, and type of SVT. Hemodynamic
 data (invasive blood pressure and heart rate), NIRS, bispectral index (BIS), end-tidal carbon dioxide, and pulse oximetry
 were collected before and during three episodes of induced SVT. The linear correlation coefficient (r) was measured to calculate the relationship of the changes in systolic blood pressure (SBP), diastolic blood pressure (DBP),
 and m...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285354</comments>
            <pubDate>Sun, 02 Oct 2011 05:46:08 +0100</pubDate>
            <guid isPermaLink="false">5285354</guid>        </item>
        <item>
            <title>Epidemiologic Survey of Kawasaki Disease in Jilin from 1999 Through 2008</title>
            <link>http://www.medworm.com/index.php?rid=5285355&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2166964450k31320%2F</link>
            <description>In conclusion, incidences of KD increased in Jilin Province. Age and gender distribution shared
 similarities with previous reports, and the seasonal distribution was different. Age and lower serum albumin were the most
 important risk factors of coronary arterial lesions (CAL) in KD. In addition, patients treated with steroids also had a possible
 heightened risk of contracting CAL.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00246-011-0121-7Authors
		Xiaomei Zhang, Department of Pediatrics, The First Hospital of Jilin University, 71 Xin Min Street, Changchun, 130021 Jilin, ChinaZhen Zhang, Department of Pediatrics, The First Hospital of Jilin University, 71 Xin Min Street, Changchun, 130021 Jilin, ChinaShicheng Liu, Department of Pediatrics, The First ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285355</comments>
            <pubDate>Sat, 01 Oct 2011 06:46:41 +0100</pubDate>
            <guid isPermaLink="false">5285355</guid>        </item>
        <item>
            <title>Multiple External Electrical Cardioversions for Refractory Neonatal Atrial Flutter</title>
            <link>http://www.medworm.com/index.php?rid=5285356&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq111v46054228k42%2F</link>
            <description>This report describes a case of atrial flutter in a fetal/neonatal patient who did not respond to adenosine, a propafenone
 bolus, and three electrical external cardioversions. A fourth direct current cardioversion after propafenone premedication
 resolved the atrial flutter. The arrhythmia did not recur with propafenone therapy during a 12-month follow-up period.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-011-0131-5Authors
		Simone Gulletta, Department of Cardiology, San Raffaele University Hospital, Milan, ItalyRosanna Rovelli, Department of Pediatrics, San Raffaele University Hospital, Milan, ItalyRossana Fiori, Department of Anesthesia and Intensive Care, San Raffaele University Hospital, Milan, ItalyPaolo Della Bella, Department of Cardiology, San...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285356</comments>
            <pubDate>Sat, 01 Oct 2011 06:46:40 +0100</pubDate>
            <guid isPermaLink="false">5285356</guid>        </item>
        <item>
            <title>Transcatheter Closure of Ruptured Sinus of Valsalva Aneurysm Into the Left Ventricle: A Retrograde Approach</title>
            <link>http://www.medworm.com/index.php?rid=5285358&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg683w76884w78w8p%2F</link>
            <description>This report presents a rare case of a patient with treated infective endocarditis who had a patent ductus arteriosus (PDA),
 a coronary cameral fistula, and a ruptured ASOV (RASOV) into the left ventricle (LV). Successful transcatheter closure of
 the ruptured ASOV and the other two lesions was performed using three Amplatzer duct occluders (AGA Medical Corporation, Golden
 Valley, MN, USA).
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-4DOI 10.1007/s00246-011-0127-1Authors
		Anurakti Srivastava, Department of Pediatric Cardiology, Apollo Health City, Jubilee Hills, Hyderabad, IndiaAnil Sivadasan Radha, Department of Pediatric Cardiology, Apollo Health City, Jubilee Hills, Hyderabad, India
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285358</comments>
            <pubDate>Fri, 30 Sep 2011 06:29:07 +0100</pubDate>
            <guid isPermaLink="false">5285358</guid>        </item>
        <item>
            <title>Short- and Mid-Term Outcomes of Total Correction of Taussig–Bing Anomaly</title>
            <link>http://www.medworm.com/index.php?rid=5285357&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F10514418m76w4qjv%2F</link>
            <description>This study evaluates
 our experience and outcomes of total correction of DORV-TB anomaly at King Abdulaziz Cardiac Center. We conducted a retrospective
 study for all cases of TB anomaly repaired between June 2001 and April 2009. Patients were divided into two groups: Group
 A included patients repaired with arterial switch operation, and group (B) included patients repaired with Rastelli procedure.
 Thirteen patients with TB anomaly underwent total correction. There were 5 male (38%) and 8 female (62%) patients. Mean age
 and weight at surgery were 6.8&amp;nbsp;±&amp;nbsp;6&amp;nbsp;weeks and 3.6&amp;nbsp;±&amp;nbsp;0.7&amp;nbsp;kg, respectively. Of the 13 patients, 9 (69%) were in group A, and
 4 (31%) were in group B. Aortic arch abnormalities were present in 9 patients (69%); abnormal coronary artery patter...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285357</comments>
            <pubDate>Fri, 30 Sep 2011 06:29:07 +0100</pubDate>
            <guid isPermaLink="false">5285357</guid>        </item>
        <item>
            <title>Conjoined Hearts in Thoracopagus Twins</title>
            <link>http://www.medworm.com/index.php?rid=5285360&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F03872r527qu140tq%2F</link>
            <description>This study aimed to identify the anatomic and pathologic structural cardiac abnormalities in conjoined twins and to focus
 on those that have prevented the successful separation of conjoined hearts. A retrospective review was undertaken to examine
 consecutive cases of thoracopagus conjoined twins with conjoined hearts evaluated at The Children’s Hospital of Philadelphia
 from 1 January 1980 through 6 October 2008. The records included autopsy and surgical findings as well as clinical reports.
 The study group included nine sets of conjoined twins with a mean gestational age at birth of 33.8&amp;nbsp;±&amp;nbsp;5.5&amp;nbsp;weeks. Three twin
 pairs were stillborn. Five twin pairs died afterward. One pair died of cardiopulmonary failure. The median age at death was
 22&amp;nbsp;days (range, 0–345&amp;nbsp...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285360</comments>
            <pubDate>Fri, 30 Sep 2011 06:29:06 +0100</pubDate>
            <guid isPermaLink="false">5285360</guid>        </item>
        <item>
            <title>Influence of Fetal Diagnosis on the Clinical Presentation of a Vascular Ring</title>
            <link>http://www.medworm.com/index.php?rid=5285359&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8nq6u457k5707182%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A fetus had a diagnosis of a vascular ring formed by a right aortic arch with an aberrant left subclavian artery. The infant
 experienced isolated dysphagia and vomiting 3&amp;nbsp;months after birth. Magnetic resonance imaging (MRI) confirmed the vascular
 ring and demonstrated profound, isolated esophageal dilation with normal airways. The severity of postnatal symptoms due to
 a vascular ring is difficult to determine in utero. Expectant management of the lesion is necessary, and use of MRI as the
 imaging method allows for both confirmation of the diagnosis and evaluation of the airway and esophagus while avoiding radiation.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-011-0129-zAuthors
		Laura J. Olivieri, Division of Cardiology, W3-...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285359</comments>
            <pubDate>Fri, 30 Sep 2011 06:29:06 +0100</pubDate>
            <guid isPermaLink="false">5285359</guid>        </item>
        <item>
            <title>The Cause of B-Type Natriuretic Peptide Elevation and the Dose-Dependent Effect of Angiotensin-Converting Enzyme Inhibitor on Patients Late After Tetralogy of Fallot Repair</title>
            <link>http://www.medworm.com/index.php?rid=5285361&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ffk14357k464278n4%2F</link>
            <description>In conclusion, elevation of BNP in patients after TOF repair could reflect volume and pressure load in the RV end-diastolic
 phase, and ACE-I may reduce BNP levels in a dose-dependent manner.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-8DOI 10.1007/s00246-011-0135-1Authors
		Takuo Furukawa, Department of Pediatrics, Hokkaido University Hospital, Kita 14, Nishi 5, Kita-ku, Sapporo City, Hokkaido 060-8648, JapanTomoaki Murakami, Department of Pediatrics and Adult Congenital Heart Disease, Chiba Cardiovascular Center, Ichihara City, Chiba, JapanMichihiko Ueno, Department of Pediatrics, Hokkaido University Hospital, Kita 14, Nishi 5, Kita-ku, Sapporo City, Hokkaido 060-8648, JapanAtsuhito Takeda, Department of Pediatrics, Hokkaido University Hospital, Kita 14, Nishi 5, Ki...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285361</comments>
            <pubDate>Fri, 30 Sep 2011 06:29:05 +0100</pubDate>
            <guid isPermaLink="false">5285361</guid>        </item>
        <item>
            <title>Regionalization in Neonatal Congenital Heart Surgery: The Impact of Distance on Outcome After Discharge</title>
            <link>http://www.medworm.com/index.php?rid=5285362&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff467nv0k2513uj36%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Studies have shown improved perioperative outcomes after neonatal heart surgery at centers with greater surgical volumes.
 The impact of increasing distance from such centers on outcome after discharge has not yet been reported. Chart review and
 cross-sectional survey were performed on children discharged or transferred after undergoing neonatal congenital heart surgery
 as neonates (&amp;lt;30&amp;nbsp;days of age) from January 2005 to June 2006. The association of distance from center with mortality and adverse
 events was analyzed by univariate and multivariate regression and stratified by the Risk Adjustment for Congenital Heart Surgery-1
 for complexity. Among 217 patients, those living further from the surgical center were smaller and older at surgery and more
 likely to...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5285362</comments>
            <pubDate>Thu, 29 Sep 2011 06:06:38 +0100</pubDate>
            <guid isPermaLink="false">5285362</guid>        </item>
        <item>
            <title>Association Between Left Atrial Size and Measures of Adiposity Among Normal Adolescent Boys</title>
            <link>http://www.medworm.com/index.php?rid=5273496&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl35h1277t7703m42%2F</link>
            <description>This study aimed
 to determine the association between LA size and (1) different components of the metabolic syndrome (body mass index [BMI],
 waist circumference [WC], insulin levels, lipid levels, and blood pressure), and (2) left ventricular (LV) diameters and diastolic
 function. Data were collected cross-sectionally from 142 healthy adolescent boys age 16.8&amp;nbsp;±&amp;nbsp;2.0&amp;nbsp;years in 2009. Measurements
 of BMI, WC, blood pressure, lipid profile, and insulin were performed. Mode M, two-dimensional Doppler echocardiography was
 performed. Measurements of LA area, LV end diastolic diameter (EDD), end systolic diameter (ESD), posterior wall, interventricular
 septum (IVS), and shortening fraction were performed. Tisular Doppler of the diastolic mitral annular E wave (DTE) and A wave
 ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273496</comments>
            <pubDate>Wed, 28 Sep 2011 05:52:50 +0100</pubDate>
            <guid isPermaLink="false">5273496</guid>        </item>
        <item>
            <title>Right Ventricular Outpouching Associated With a Ventricular Septal Defect: Case Report</title>
            <link>http://www.medworm.com/index.php?rid=5273497&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1rvm4r8104487611%2F</link>
            <description>Content Type Journal ArticleCategory Images in Pediatric CardiologyPages 1-2DOI 10.1007/s00246-011-0059-9Authors
		Patricia Martínez Olorón, Department of Pediatric Cardiology, Virgen del Camino Hospital, Pamploma, SpainCarlos Romero Ibarra, Department of Pediatric Cardiology, Virgen del Camino Hospital, Pamploma, SpainJose Miguel Galdeano Miranda, Department of Pediatric Cardiology, Cruces Hospital, Pamploma, Spain
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5273497</comments>
            <pubDate>Tue, 27 Sep 2011 05:48:19 +0100</pubDate>
            <guid isPermaLink="false">5273497</guid>        </item>
        <item>
            <title>Predictors of Chronic Valvular Disease in Patients With Rheumatic Carditis</title>
            <link>http://www.medworm.com/index.php?rid=5260410&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg528377113r071q7%2F</link>
            <description>This study investigated the predictors of chronic valvular disease in children with rheumatic carditis. The short- to mid-term
 follow-up records of 88 patients (mean age, 10.68&amp;nbsp;±&amp;nbsp;2.5&amp;nbsp;years) with chronic rheumatic heart disease were reviewed. The mean
 follow-up period was 2.95&amp;nbsp;±&amp;nbsp;1.4&amp;nbsp;years. Valvular involvement completely improved for 24 of the patients (27%) during the follow-up
 period. The multivariate logistic regression analysis found initial left ventricular dilation to be a significant independent
 risk factor associated with the persistence of either valvular involvement or mitral regurgitation. Furthermore, persistence
 of mitral regurgitation was found to be strongly correlated with cardiac murmur at admission. No significant correlation was
 detec...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260410</comments>
            <pubDate>Sat, 24 Sep 2011 05:43:59 +0100</pubDate>
            <guid isPermaLink="false">5260410</guid>        </item>
        <item>
            <title>Critical Ebstein Anomaly in a Fetus Successfully Managed by Elective Preterm Delivery and Surgical Intervention Without Delay After Birth</title>
            <link>http://www.medworm.com/index.php?rid=5260411&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F02620646t6g7838t%2F</link>
            <description>This report describes a case of Ebstein anomaly in a fetus with cardiomegaly, severe tricuspid regurgitation, pulmonary regurgitation,
 and retrograde ductal flow that showed a marked increase in the size of the right atrium with advancing gestational age. Elective
 preterm delivery was performed at 35 weeks gestation. The prostaglandin E1 infusion resulted in more pronounced systemic hypotension
 and acidosis secondary to circular shunt across the patent ductus arteriosus as well as pulmonary regurgitation and tricuspid
 regurgitation. Emergency surgical intervention consisting of main pulmonary artery ligation, ductus arteriosus ligation, central
 shunt creation, and plication of the right atrium without cardiopulmonary bypass was performed 4 h after birth. At the age
 of 16 days, the St...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260411</comments>
            <pubDate>Sat, 24 Sep 2011 05:43:58 +0100</pubDate>
            <guid isPermaLink="false">5260411</guid>        </item>
        <item>
            <title>Fontan Operation, Vasopressin and Septic Shock: A Case Report on the Usual Treatment in a Peculiar Setting</title>
            <link>http://www.medworm.com/index.php?rid=5260413&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F771033815t27128p%2F</link>
            <description>Content Type Journal ArticleCategory Letter to the EditorPages 1-2DOI 10.1007/s00246-011-0104-8Authors
		Vincenzo Vitale, Department of Pediatric Cardiology and Cardiac Surgery, Intensive Care Unit, Bambino Gesù Children’s Hospital, Piazza S. Onofrio 4, 00165 Rome, ItalyZaccaria Ricci, Department of Pediatric Cardiology and Cardiac Surgery, Intensive Care Unit, Bambino Gesù Children’s Hospital, Piazza S. Onofrio 4, 00165 Rome, ItalyIsabella Favia, Department of Pediatric Cardiology and Cardiac Surgery, Intensive Care Unit, Bambino Gesù Children’s Hospital, Piazza S. Onofrio 4, 00165 Rome, ItalyTiziana Fragasso, Department of Pediatric Cardiology and Cardiac Surgery, Intensive Care Unit, Bambino Gesù Children’s Hospital, Piazza S. Onofrio 4, 00165 Rome, ItalyPaola Cogo, Depart...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260413</comments>
            <pubDate>Thu, 22 Sep 2011 06:37:34 +0100</pubDate>
            <guid isPermaLink="false">5260413</guid>        </item>
        <item>
            <title>Absence of the Right Pulmonary Artery Associated With a Partial Anomalous Pulmonary Venous Connection</title>
            <link>http://www.medworm.com/index.php?rid=5260412&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ff8568175l1406468%2F</link>
            <description>This report describes the case of a missing right pulmonary artery associated
 with anomalous left pulmonary venous connection not previously described in the medical literature.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-011-0110-xAuthors
		Köksal Binnetoğlu, Department of Pediatric Cardiology, Kocaeli University, Faculty of Medicine, Kocaeli, TurkeyCanan Ayabakan, Department of Pediatric Cardiology, Baskent University, Istanbul Research and Teaching Hospital, Oymaci Sokak No: 7, Altunizade/Istanbul, TurkeyÖzlem Sarisoy, Department of Pediatric Cardiology, Baskent University, Istanbul Research and Teaching Hospital, Oymaci Sokak No: 7, Altunizade/Istanbul, TurkeyKürşad Tokel, Department of Pediatric Cardiology, Baskent University, Istanbul Resear...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5260412</comments>
            <pubDate>Thu, 22 Sep 2011 06:37:34 +0100</pubDate>
            <guid isPermaLink="false">5260412</guid>        </item>
        <item>
            <title>Vertically Oriented Intramural Right Coronary Artery in Complete Transposition of the Great Arteries: Prospective Recognition and Surgical Implications</title>
            <link>http://www.medworm.com/index.php?rid=5236998&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fa52k58516752j604%2F</link>
            <description>This report describes a rare case of complete transposition of the great arteries (TGA) with an intramural right coronary
 artery arising well above the sinotubular junction. Additionally in this case, the left circumflex artery arose anomalously
 as a branch from the right coronary. Identification of this anatomic anomaly was made by transthoracic echocardiography before
 surgery. The patient underwent a successful arterial switch operation on day 6 of life. Due to the preoperative diagnosis
 of the unusual right intramural coronary artery, the coronary transfer technique during the arterial switch was altered, allowing
 preservation of the right coronary artery.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-4DOI 10.1007/s00246-011-0108-4Authors
		Jennifer A. Johnson, Divis...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5236998</comments>
            <pubDate>Sat, 17 Sep 2011 17:07:00 +0100</pubDate>
            <guid isPermaLink="false">5236998</guid>        </item>
        <item>
            <title>John Locke, “Rhickets” and the Cardiopulmonary Circulation</title>
            <link>http://www.medworm.com/index.php?rid=5236997&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj63m231805542377%2F</link>
            <description>Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00246-011-0100-zAuthors
		A. N. Williams, Virtual Academic Unit, CDC, Northampton General Hospital, Northampton, UK
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5236997</comments>
            <pubDate>Sat, 17 Sep 2011 17:07:00 +0100</pubDate>
            <guid isPermaLink="false">5236997</guid>        </item>
        <item>
            <title>Incidence and Risk Factors for Venous Thromboembolism in Critically Ill Children With Cardiac Disease</title>
            <link>http://www.medworm.com/index.php?rid=5236999&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F56022525m5068288%2F</link>
            <description>In this study, we investigated the incidence
 and risk factors of VTE in critically ill children with cardiac disease, who were prospectively followed-up for VTE after
 admission to a tertiary care pediatric intensive care unit (PICU). Risk factors were compared between VTE cases and (1) patients
 in the cohort who did not develop VTE and (2) the next three cardiac patients sequentially admitted to the PICU (case control).
 Forty-one cases of VTE were identified from 1070 admissions (3.8%). Thirty-seven percent of VTE cases were central venous
 catheter (CVC)–associated, and 56% of cases were intracardiac. Sixty-six percent of patients were receiving anticoagulation
 at the time of VTE diagnosis. Increased VTE incidence was associated with unscheduled PICU admission, age &amp;lt;6&amp;nbsp;month...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5236999</comments>
            <pubDate>Sat, 17 Sep 2011 05:45:07 +0100</pubDate>
            <guid isPermaLink="false">5236999</guid>        </item>
        <item>
            <title>Differences in Healthy Lifestyles Between Prehypertensive and Normotensive Children and Adolescents in Northern China</title>
            <link>http://www.medworm.com/index.php?rid=5225174&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft73428004n752726%2F</link>
            <description>Conclusion&amp;nbsp;&amp;nbsp;Among children and adolescents, poor prehypertensive status was associated with a low likelihood of healthy lifestyles. Evaluation
 of multiple healthy lifestyles as a whole should receive more attention for better prevention and control of high blood pressure.
 
 
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-7DOI 10.1007/s00246-011-0112-8Authors
		Xiaofan Guo, Department of Cardiology, The First Affiliated Hospital of China Medical University, 155 Nanjing North Street, Heping District, Shenyang 110001, People’s Republic of ChinaXingang Zhang, Department of Cardiology, The First Affiliated Hospital of China Medical University, 155 Nanjing North Street, Heping District, Shenyang 110001, People’s Republic of ChinaYang Li, Department of Cardiolog...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225174</comments>
            <pubDate>Wed, 14 Sep 2011 05:52:47 +0100</pubDate>
            <guid isPermaLink="false">5225174</guid>        </item>
        <item>
            <title>Vitamin D Deficiency and Arterial Wall Stiffness in Children With Chronic Kidney Disease</title>
            <link>http://www.medworm.com/index.php?rid=5225175&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg1562x7209761506%2F</link>
            <description>This study explored the relationship between
 various parameters of calcium–phosphorus metabolism including 25-hydroxy vitamin D and arterial wall stiffness in pediatric
 patients with CKD. This study investigated a cohort of 43 children with CKD who had no history of underlying congenital or
 structural cardiac disease. The Augmentation Index (AI), a measure of peripheral arterial reflective properties using radial
 artery tonometry, was used as an indirect measure of central aortic stiffness. Serum biochemical markers of calcium–phosphorus
 metabolism were simultaneously measured. Univariate testing showed that AI correlated with worsening kidney function. Serum
 25-hydroxy vitamin D levels were low and correlated negatively with AI (r&amp;nbsp;=&amp;nbsp;−0.39; p&amp;nbsp;&amp;lt;&amp;nbsp;0.05). Mul...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225175</comments>
            <pubDate>Tue, 13 Sep 2011 05:49:32 +0100</pubDate>
            <guid isPermaLink="false">5225175</guid>        </item>
        <item>
            <title>Chronic Constrictive Pericarditis: Unique Cause of Heart Failure in a Child With Tetralogy of Fallot</title>
            <link>http://www.medworm.com/index.php?rid=5225176&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F42r27000470m4383%2F</link>
            <description>This report presents a case of tetralogy of Fallot who presented with heart failure at
 young age of 18 months. This is the first description of coexisting tubercular chronic constrictive pericarditis and tetralogy
 of Fallot. This case is reported for its unique association of two relatively uncommon clinical entities. The logistic dictum
 of Hickam in similar circumstances is discussed.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-3DOI 10.1007/s00246-011-0095-5Authors
		Saurabh Kumar Gupta, Department of Cardiology, All India Institute of Medical Sciences, Room 29, 7th Floor, New Delhi, 110029 IndiaAnita Saxena, Department of Cardiology, All India Institute of Medical Sciences, Room 29, 7th Floor, New Delhi, 110029 IndiaSachin Talwar, Department of Cardiothoracic and Vasc...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225176</comments>
            <pubDate>Mon, 12 Sep 2011 15:50:48 +0100</pubDate>
            <guid isPermaLink="false">5225176</guid>        </item>
        <item>
            <title>Early Outcomes and Prognostic Factors for Left Atrioventricular Valve Reoperation After Primary Atrioventricular Septal Defect Repair</title>
            <link>http://www.medworm.com/index.php?rid=5225177&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp308p8n6410j029w%2F</link>
            <description>This study aimed to identify early outcomes of and prognostic factors for left atrioventricular valve (LAVV) reoperation after
 primary atrioventricular septal defect (AVSD) repair. A retrospective cohort study was performed using the Pediatric Cardiac
 Care Consortium database, which included 370 patients with previously repaired AVSDs who subsequently underwent LAVV reoperation
 between 1982 and 2007. Of these patients, 243 underwent LAVV repair, and 127 underwent LAVV replacement. Median time to first
 reoperation after primary repair was 0.67&amp;nbsp;years in the repair subgroup and 0.18&amp;nbsp;years in the replacement subgroup. Thirty-day
 survival was significantly poorer in the replacement subgroup compared with the repair subgroup (P&amp;nbsp;=&amp;nbsp;0.0002). In multivariable analysis, indep...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225177</comments>
            <pubDate>Sat, 10 Sep 2011 15:41:33 +0100</pubDate>
            <guid isPermaLink="false">5225177</guid>        </item>
        <item>
            <title>Noncompaction Cardiomyopathy in Children With Congenital Heart Disease: Evaluation Using Cardiovascular Magnetic Resonance Imaging</title>
            <link>http://www.medworm.com/index.php?rid=5225178&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe81v47535m665117%2F</link>
            <description>This study aimed to assess the impact of NCM on the cardiovascular physiology of children with coexisting CHDs
 evaluated by cardiovascular magnetic resonance imaging. A case-control study was performed with 12 children (6 patients with
 combined NCM and CHD and 6 control subjects with isolated CHD). The mean left ventricular end-diastolic and end-systolic volume
 indices were significantly higher in the CHD patients presenting with NCM than in the CHD patients with no NCM (P&amp;nbsp;=&amp;nbsp;0.028). However, no differences were observed for right ventricular end-diastolic and end-systolic volume indices, biventricular
 ejection fractions, stroke volumes and indices, left ventricular wall thickness, left ventricular fractional shortening, cardiac
 output, or cardiac index. This study suggests t...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225178</comments>
            <pubDate>Sat, 10 Sep 2011 15:41:29 +0100</pubDate>
            <guid isPermaLink="false">5225178</guid>        </item>
        <item>
            <title>Recurrent Congestive Heart Failure in a Child Due to Probable Myocarditis</title>
            <link>http://www.medworm.com/index.php?rid=5225180&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5kn3145587559r2j%2F</link>
            <description>This report describes the case of an 8-year-old girl who had three clinically identical episodes of CHF, beginning at the
 age of 5&amp;nbsp;years, with each episode preceded by a viral prodrome. The clinical features and the echocardiography and electrocardiogram
 findings were most supportive of myocarditis. Symptoms and investigations completely normalized between episodes. The third
 episode, associated with influenza A (strain H1N1) infection, led to cardiac arrest and death on day&amp;nbsp;2 after admission. Autopsy
 showed mild cardiomegaly with microscopic foci of myocardial fibrosis and extensive contraction band necrosis. This report
 is the first to describe recurrent CHF due to probable myocarditis in a pediatric patient.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-6DO...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225180</comments>
            <pubDate>Sat, 10 Sep 2011 15:41:28 +0100</pubDate>
            <guid isPermaLink="false">5225180</guid>        </item>
        <item>
            <title>Intermediate-Term Effects of Intracardiac Communications Created Noninvasively by Therapeutic Ultrasound (Histotripsy) in a Porcine Model</title>
            <link>http://www.medworm.com/index.php?rid=5225179&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm2283x1776267gmq%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The authors have demonstrated that histotripsy (pulsed cavitational ultrasound) can create atrial septal defects and ventricular
 septal defects (VSDs) in an open-chest canine model transcutaneously through the intact chest of neonatal pigs. To assess
 the potential untoward effects of these applications, the clinical, systemic, and pathologic effects of histotripsy-induced
 intracardiac communications were analyzed. Six neonatal pigs received noninvasive ultrasound therapy to their ventricular
 septa, then were allowed to survive 1&amp;nbsp;month for evaluation of intermediate-term effects. The results were compared with those
 of six previous animals killed immediately and three others killed 2–3&amp;nbsp;days after the procedure. Brain magnetic resonance
 imaging (MRI) and...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225179</comments>
            <pubDate>Sat, 10 Sep 2011 15:41:28 +0100</pubDate>
            <guid isPermaLink="false">5225179</guid>        </item>
        <item>
            <title>Challenges in Echocardiographic Assessment of Mitral Regurgitation in Children After Repair of Atrioventricular Septal Defect</title>
            <link>http://www.medworm.com/index.php?rid=5225182&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp64x3x06j266k113%2F</link>
            <description>In conclusion, echocardiographic assessment of MR
 severity after AVSD remains challenging. Among the quantitative methods used in this trial, i-VCW and i-VCA performed the best but offered little advantage compared with qualitative MR grade. The utility of regurgitant volume
 and fraction was severely limited by poor interobserver agreement and frequently negative values.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-10DOI 10.1007/s00246-011-0107-5Authors
		Ashwin Prakash, Department of Cardiology, Children’s Hospital Boston, 300 Longwood Avenue, Boston, MA 02115, USARonald V. Lacro, Department of Cardiology, Children’s Hospital Boston, 300 Longwood Avenue, Boston, MA 02115, USALynn A. Sleeper, New England Research Institutes, Watertown, MA, USAL. LuAnn Minich, Uni...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225182</comments>
            <pubDate>Sat, 10 Sep 2011 06:02:16 +0100</pubDate>
            <guid isPermaLink="false">5225182</guid>        </item>
        <item>
            <title>Dexmedetomidine: Applications for the Pediatric Patient With Congenital Heart Disease</title>
            <link>http://www.medworm.com/index.php?rid=5225181&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy567434x88716n55%2F</link>
            <description>This study aimed to provide a general description of the cardiovascular and hemodynamic effects of dexmedetomidine and an
 evidence-based review of the literature regarding its use in infants and children with congenital heart disease (CHD). A computerized
 bibliographic search of the literature on dexmedetomidine use in infants and children with CHD was performed. The cardiovascular
 effects of dexmedetomidine have been well studied in animal and adult human models. Adverse cardiovascular effects include
 occasional episodes of bradycardia, with rare reports of sinus pause or cardiac arrest. Both hypotension and hypertension
 also have been reported. The latter is related to peripheral α2B agonism leading to vasoconstriction. No adverse effects on the pulmonary vasculature have been note...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225181</comments>
            <pubDate>Sat, 10 Sep 2011 06:02:16 +0100</pubDate>
            <guid isPermaLink="false">5225181</guid>        </item>
        <item>
            <title>Chiari’s Network as a Cause of Fetal and Neonatal Pathology</title>
            <link>http://www.medworm.com/index.php?rid=5225183&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe7747m0760l242u0%2F</link>
            <description>This report describes
 a case with the novel finding of prenatal compromise due to redundant Chiari’s network and an uncommon case with significant
 postnatal symptoms. In both cases, the symptoms (fetal hydrops and postnatal cyanosis) resolved spontaneously. The variety
 of cardiovascular pathologies described in the literature is believed to be associated with persistence of a Chiari network.
 Knowledge about this not always harmless structure is important for perinatologists, pediatricians, and pediatric cardiologists
 alike. The clinical importance of this rare pathology is that prenatal counseling may anticipate a generally positive outcome
 and that surgical intervention generally should be avoided.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-4DOI 10.1007/s00246-01...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5225183</comments>
            <pubDate>Sat, 10 Sep 2011 06:02:14 +0100</pubDate>
            <guid isPermaLink="false">5225183</guid>        </item>
        <item>
            <title>Assessment of Coronary Flow Reserve in the Coronary Sinus by Cine 3T-Magnetic Resonance Imaging in Young Adults after Surgery for Tetralogy of Fallot</title>
            <link>http://www.medworm.com/index.php?rid=5208319&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F258427v4vj84706g%2F</link>
            <description>This study aimed to evaluate CFR by assessing blood flow in the coronary sinus and systemic endothelial function measured
 by FMD of the brachial artery in an open prospective study of 10 control subjects and 10 patients (ages, 15–25&amp;nbsp;years) who
 have undergone surgical TOF repair. Reduced ventricular function, impaired exercise capacity, and ventricular arrhythmia have
 been proposed as risk factors for sudden cardiac death after surgical repair of TOF. Some of this may be related to impaired
 myocardial perfusion. A 3.0T GE Signa Excite scanner was used to achieve phase-contrast, velocity-encoding cine magnetic resonance
 imaging in the coronary sinus before and during infusion with adenosine (0.14&amp;nbsp;mg/kg/min). FMD was measured in the brachial
 artery before arterial occlusion ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208319</comments>
            <pubDate>Thu, 08 Sep 2011 06:06:13 +0100</pubDate>
            <guid isPermaLink="false">5208319</guid>        </item>
        <item>
            <title>Independent Risk Factors for Cardiac Operations in Adults With Congenital Heart Disease: A Retrospective Study of 543 Operations for 500 Patients</title>
            <link>http://www.medworm.com/index.php?rid=5208318&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fahhv813504236w02%2F</link>
            <description>This study aimed to identify clinical, morphologic, and hemodynamic
 risk factors for an adverse outcome. This study retrospectively analyzed a cohort of 500 patients (ages &amp;gt;16&amp;nbsp;years) who underwent
 543 operations between January 2004 and December 2008 at a single center. The composite end point of an adverse outcome was
 in-hospital death, a prolonged intensive care exceeding 4&amp;nbsp;days, or both. The composite end point was reached by 253 of the
 patients (50.6%). Of the 500 patients, 13 (2.6%) died within 30&amp;nbsp;days after the operation. After logistic regression analysis,
 the following eight items remained significant: male gender (P&amp;nbsp;=&amp;nbsp;0.003; odds ratio [OR] 1.8; 95% confidence interval [CI] 1.2–2.6), cyanosis (P&amp;nbsp;&amp;gt;&amp;nbsp;0.006; OR 3.7; 95% CI 1.5–9.4), fu...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208318</comments>
            <pubDate>Thu, 08 Sep 2011 06:06:13 +0100</pubDate>
            <guid isPermaLink="false">5208318</guid>        </item>
        <item>
            <title>P-Wave Dispersion in Children With Acute Rheumatic Fever</title>
            <link>http://www.medworm.com/index.php?rid=5208320&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp6lp307uu6u74500%2F</link>
            <description>In conclusion, the P-wave dispersion was higher in the children with acute rheumatic fever than in the healthy control subjects.
 
 
	Content Type Journal ArticleCategory Original ArticlePages 1-5DOI 10.1007/s00246-011-0096-4Authors
		Celebi Kocaoglu, Department of Pediatrics, Konya Training and Research Hospital, 42080 Konya, TurkeyAhmet Sert, Department of Pediatric Cardiology, Konya Training and Research Hospital, 42080 Konya, TurkeyEbru Aypar, Department of Pediatric Cardiology, Konya Training and Research Hospital, 42080 Konya, TurkeyBulent Oran, Department of Pediatric Cardiology, Selcuk University Hospital, Konya, TurkeyDursun Odabas, Department of Pediatric Cardiology, Konya Training and Research Hospital, 42080 Konya, TurkeyDerya Arslan, Department of Pediatric Cardiology, Selcuk ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208320</comments>
            <pubDate>Tue, 06 Sep 2011 15:50:45 +0100</pubDate>
            <guid isPermaLink="false">5208320</guid>        </item>
        <item>
            <title>Ascending Aortic Aneurysm</title>
            <link>http://www.medworm.com/index.php?rid=5208321&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu75u688158170474%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 14-year-old boy presented with an unusual bulging chest noted to be increasing slowly over the last few years. He had no
 other complaints. Cardiac echocardiography and cardiac magnetic resonance imaging (MRI) showed aneurysmal dilation of the
 ascending aorta with moderate aortic valve insufficiency and moderate pericardial effusion. The boy underwent reconstruction
 of his ascending aorta in the form of a Bentall procedure using a 25-mm Carbomedic valve conduit.
 
 
	Content Type Journal ArticleCategory Images in Pediatric CardiologyPages 1-3DOI 10.1007/s00246-011-0103-9Authors
		Mohammed S. AlHabdan, Section of Pediatric Cardiology, King Faisal Heart Institute, King Faisal Specialist Hospital and Research Center, P.O. Box 3354, Riyadh, Saudi ArabiaAbdullah A. AlSeh...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208321</comments>
            <pubDate>Tue, 06 Sep 2011 05:47:47 +0100</pubDate>
            <guid isPermaLink="false">5208321</guid>        </item>
        <item>
            <title>Left Ventricle Pseudoaneurysm After Aortic Valvuloplasty</title>
            <link>http://www.medworm.com/index.php?rid=5208322&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh01j02u87227h56v%2F</link>
            <description>This report describes an infant with acquired left ventricular
 aneurysm after percutaneous aortic balloon valvuloplasty for critical aortic stenosis. The potential risk factors for myocardial
 injury during cardiac catheterization and potential complications are discussed.
 
 
	Content Type Journal ArticleCategory Case ReportPages 1-4DOI 10.1007/s00246-011-0102-xAuthors
		Abdullah AlHuzaimi, Division of Cardiology, Faculty of Medicine, British Columbia Children’s Hospital, University of British Columbia, Room 1F22, 4480 Oak Street, Vancouver, BC V6H 3V4, CanadaMartin Hosking, Division of Cardiology, Faculty of Medicine, British Columbia Children’s Hospital, University of British Columbia, Room 1F22, 4480 Oak Street, Vancouver, BC V6H 3V4, CanadaDerek Human, Division of Cardiology, Fac...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208322</comments>
            <pubDate>Mon, 05 Sep 2011 16:16:39 +0100</pubDate>
            <guid isPermaLink="false">5208322</guid>        </item>
        <item>
            <title>Restrictive Physiology is Associated With Poor Outcomes in Children With Hypertrophic Cardiomyopathy</title>
            <link>http://www.medworm.com/index.php?rid=5208323&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fj0020860rr7v88gu%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pediatric patients with hypertrophic cardiomyopathy (HCM) and restrictive physiology (RP) with poor outcomes have been identified,
 but data on their course are limited. Our goal was to delineate the clinical features and course of children with HCM and
 RP. An institutional review of 119 patients identified between 1985 and 2010 with the diagnosis of HCM was performed. The
 diagnosis of RP was based on &amp;gt;1 echocardiogram along with at least one of the following: left atrial enlargement without evidence
 of left ventricle dilation, E/E′ ratio&amp;nbsp;≥&amp;nbsp;10, and E/A ratio&amp;nbsp;≥&amp;nbsp;3. Outcomes analysis was performed using Cox or Poisson regression
 when appropriate. RP was present in 50 (42%) patients. In patients without RP, 10-year freedom-from-death or abor...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208323</comments>
            <pubDate>Sun, 04 Sep 2011 10:55:08 +0100</pubDate>
            <guid isPermaLink="false">5208323</guid>        </item>
        <item>
            <title>Cryo-Balloon Angioplasty for Pulmonary Vein Stenosis in Pediatric Patients</title>
            <link>http://www.medworm.com/index.php?rid=5208326&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F9l35685762n741l3%2F</link>
            <description>This study sought to determine the safety and effectiveness of cryo-balloon angioplasty (CbA) for pulmonary vein stenosis
 (PVS) in pediatric patients. Current therapy options for PVS are less than satisfactory due to recurrent progressive restenosis
 and neointimal proliferation. Catheterization database, hospital records, imaging studies, and pathologic specimens were reviewed
 for procedural-related and outcomes data in all patients who underwent pulmonary vein (PV) CbA using the Boston Scientific
 PolarCath Peripheral Dilation System between August 2006 and June 2009. Thirteen patients (19 PVs; median age 13&amp;nbsp;months [range
 3.5&amp;nbsp;months to 18.5&amp;nbsp;years] and weight 7.9&amp;nbsp;kg [range 3.8 to 47.7]) underwent CbA. Mean PVS diameter after CbA increased from
 2.19 (±0.6) to 3.77 ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208326</comments>
            <pubDate>Sun, 04 Sep 2011 10:55:07 +0100</pubDate>
            <guid isPermaLink="false">5208326</guid>        </item>
        <item>
            <title>Near Infrared Spectroscopy Describes Physiologic Payback Associated With Excess Postexercise Oxygen Consumption in Healthy Controls and Children With Complex Congenital Heart Disease</title>
            <link>http://www.medworm.com/index.php?rid=5208325&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh41t6ku3wvr22m03%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Exercise creates a physiologic burden with recovery from such effort crucial to adaptation. Excess postexercise oxygen consumption
 (EPOC) refers to the body’s increased metabolic need after work. This investigation was designed to determine the role of
 near infrared spectroscopy (NIRS) in the description of exercise recovery in healthy controls (NL) and children with congenital
 heart disease (CHD). Subjects were recruited with exercise testing performed to exhaustion. Exercise time (EXT), heart rate
 (HR), and oxygen consumption (VO2) were measured. Four-site NIRS (brain, kidney, deltoid, and vastus lateralis) were measured during exercise and into recovery
 to establish trends. Fifty individuals were recruited for each group (NL&amp;nbsp;=&amp;nbsp;26 boys and 24 girls; C...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208325</comments>
            <pubDate>Sun, 04 Sep 2011 10:55:07 +0100</pubDate>
            <guid isPermaLink="false">5208325</guid>        </item>
        <item>
            <title>Multiple Risk Factors Before Pediatric Cardiac Transplantation Are Associated With Increased Graft Loss</title>
            <link>http://www.medworm.com/index.php?rid=5208324&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F210322nj36011348%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Identification of heart transplant recipients at highest risk for a poor outcome could lead to improved posttransplantation
 survival. A chart review of primary heart transplantations from 1993 to 2006 was performed. Analysis was performed to evaluate
 the risk of graft loss for those with a transplantation age less than 1&amp;nbsp;year, congenital heart disease (CHD), elevated pulmonary
 vascular resistance (index&amp;nbsp;&amp;gt;&amp;nbsp;6), positive panel reactive antibody or crossmatch, liver or renal dysfunction, mechanical ventilation,
 or mechanical circulatory support (MCS). Primary transplantation was performed for 189 patients. Among these patients, 37%
 had CHD, 23% had mechanical ventilation, and 6% had renal dysfunction. Overall graft survival was 82% at 1&amp;nbsp;year and ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208324</comments>
            <pubDate>Sun, 04 Sep 2011 10:55:07 +0100</pubDate>
            <guid isPermaLink="false">5208324</guid>        </item>
        <item>
            <title>Upcoming Events in Pediatric Cardiology</title>
            <link>http://www.medworm.com/index.php?rid=5208327&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq0368321327035r4%2F</link>
            <description>Content Type Journal ArticleCategory Upcoming EventsPages 1-1DOI 10.1007/s00246-011-0090-x

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5208327</comments>
            <pubDate>Sun, 04 Sep 2011 10:55:06 +0100</pubDate>
            <guid isPermaLink="false">5208327</guid>        </item>
        <item>
            <title>Prevalence of Obesity Among Patients With Congenital and Acquired Heart Disease</title>
            <link>http://www.medworm.com/index.php?rid=5196204&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F85m8p0458876ml3p%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Overweight and obesity rates have risen dramatically in the United States, with subsequent detrimental comorbidity risks.
 The rates for obesity among children with congenital and acquired heart disease have rarely been reported. A retrospective
 cross-sectional study was conducted to determine the prevalence of overweight and obesity in children with heart disease and
 to identify subgroups at increased risk. A total of 795 cases were identified from a chart review of patients presenting to
 an urban center’s Pediatric Cardiology Program between 1 January and 31 December 2006. A body mass index (BMI) at the 85th
 percentile or higher was defined as overweight, and a BMI at the 95th percentile or higher was defined as obese. Subjects
 with comorbidities affecting body...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5196204</comments>
            <pubDate>Sat, 03 Sep 2011 06:40:02 +0100</pubDate>
            <guid isPermaLink="false">5196204</guid>        </item>
        <item>
            <title>From Other Journals</title>
            <link>http://www.medworm.com/index.php?rid=5196205&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F20127lt17379h197%2F</link>
            <description>Content Type Journal ArticleCategory From Other JournalsPages 1-3DOI 10.1007/s00246-011-0089-3Authors
		Sanjiv Gandhi, 1507 W. Harrison Street, Chicago, IL 60607, USAOmar M. Khalid, 1507 W. Harrison Street, Chicago, IL 60607, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5196205</comments>
            <pubDate>Thu, 01 Sep 2011 06:12:46 +0100</pubDate>
            <guid isPermaLink="false">5196205</guid>        </item>
        <item>
            <title>Call for a Sudden Cardiac Death Registry: Should Reporting of Sudden Cardiac Death be Mandatory?</title>
            <link>http://www.medworm.com/index.php?rid=5161392&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe412124255112202%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;There is currently no central mandatory pediatric sudden cardiac arrest (SCA) registry in the United States. Perhaps the time
 is right to actively endorse and develop a pediatric SCD registry, in collaboration with other agencies, advocacy groups,
 and organizations. This registry, if well constructed, thorough, and validated, would serve not only important SCD epidemiologic
 purposes but also provide the seed bed for closer collaboration with medical examiners and coroners and enhance critical cascade
 testing for identification of genotypically and/or phenotypically affected family members.
 
 
	Content Type Journal ArticleCategory Review ArticlePages 1-3DOI 10.1007/s00246-011-0085-7Authors
		Robert M. Campbell, Department of Pediatrics, Children’s Healthcare of At...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161392</comments>
            <pubDate>Mon, 22 Aug 2011 16:00:36 +0100</pubDate>
            <guid isPermaLink="false">5161392</guid>        </item>
        <item>
            <title>Antenatal Calcium Channel Blocker Exposure and Subsequent Patent Ductus Arteriosus in Extremely Low-Birth-Weight Infants</title>
            <link>http://www.medworm.com/index.php?rid=5161393&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fd48r28t5j2j54167%2F</link>
            <description>This study aimed to assess whether tocolytic fetal exposure to antenatal calcium channel blockers (aCCB) increases the risk
 for hemodynamically significant patent ductus arterioses (hsPDA) in extremely low-birth-weight (ELBW) infants. This case-control
 study investigated ELBW infants (&amp;lt;1,000&amp;nbsp;g) without cardiac defects in a level 3 neonatal intensive care unit who had survived
 at least 7&amp;nbsp;days. Nifedipine was the only aCCB used for this study population. The measurements included the history of aCCB
 exposure, selected maternal data, hsPDA diagnosis, gestational age at birth, birth weight, mode of delivery, sex, maternal
 race, location of birth, Apgar scores, and selected neonatal morbidities. The end point of the study was hsPDA, defined as
 an echocardiographically confirm...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161393</comments>
            <pubDate>Mon, 22 Aug 2011 16:00:35 +0100</pubDate>
            <guid isPermaLink="false">5161393</guid>        </item>
        <item>
            <title>Echocardiographic Detection of Coronary Air Embolism as the Cause of Cardiac Arrest in a Neonate With Transposition of the Great Arteries</title>
            <link>http://www.medworm.com/index.php?rid=5161394&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F71k3515p086x1547%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A hemodynamically stable neonate with transposition of the great arteries suddenly went into cardiac arrest during preparation
 for transport to the operating room. Emergency echocardiography during cardiac massage detected coronary air embolism as the
 presumed cause of arrest. After about 15&amp;nbsp;minutes of resuscitation, it was possible to establish return of spontaneous circulation.
 Since the most likely source of air was the neonate’s peripheral venous line, we have introduced inline microfilters for all
 neonates and all patients with right-to-left shunt lesions and did not encounter proven air embolism thereafter.
 
 
	Content Type Journal ArticleCategory Images in Pediatric CardiologyPages 1-2DOI 10.1007/s00246-011-0088-4Authors
		Michael Weidenbach, Departme...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161394</comments>
            <pubDate>Sat, 20 Aug 2011 15:52:22 +0100</pubDate>
            <guid isPermaLink="false">5161394</guid>        </item>
        <item>
            <title>Tetralogy of Fallot With Inverted Great Arteries S, D, I: Case Report, Literature Review, and Discussion of Embryology</title>
            <link>http://www.medworm.com/index.php?rid=5161395&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb504u70148088532%2F</link>
            <description>Discussion of Embryology
	Content Type Journal ArticleCategory Case ReportPages 1-5DOI 10.1007/s00246-011-0071-0Authors
		Lowell H. Frank, Division of Cardiology, Children’s National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010, USAT. K. Susheel Kumar, Division of Cardiovascular Surgery, University of Michigan, Cardiovascular Center Floor 3 Reception C, 1500 E Medical Center Dr SPC 5864, Ann Arbor, MI 48109, USARichard A. Jonas, Division of Cardiovascular Surgery, Children’s National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010, USAMary T. Donofrio, Division of Cardiology, Children’s National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161395</comments>
            <pubDate>Thu, 18 Aug 2011 05:48:18 +0100</pubDate>
            <guid isPermaLink="false">5161395</guid>        </item>
        <item>
            <title>Postoperative Outcome for Hyperglycemic Pediatric Cardiac Surgery Patients</title>
            <link>http://www.medworm.com/index.php?rid=5161396&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Ft6v1726517g667xk%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;This prospective cohort study aimed to determine the morbidity and mortality among hyperglycemic pediatric patients after
 cardiac surgery. The study was conducted in a pediatric intensive care unit (PICU) for cardiac surgery patients at a university-affiliated,
 referral, heart hospital. A total of 379 postcardiac surgery pediatric patients participated in the study. No interventions
 were performed. Measurements of blood glucose level together with other clinical and laboratory data were collected on postoperative
 days 1, 2, 3, and 7. Mean blood glucose level exceeding 126 mg/dl was considered hyperglycemia, and a level exceeding 200
 mg/dl determined severe hyperglycemia. These measurements were analyzed for association with major complications and death.
 Hyperglyc...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5161396</comments>
            <pubDate>Thu, 18 Aug 2011 05:48:17 +0100</pubDate>
            <guid isPermaLink="false">5161396</guid>        </item>
        <item>
            <title>Improvement of Cardiac Geometry and Function After Cardiac Resynchronization Therapy for Relapsed Deterioration of Pediatric Dilated Cardiomyopathy Due to a Noncompacted Left Ventricle and Cardiac Dyssynchrony</title>
            <link>http://www.medworm.com/index.php?rid=5131905&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F5m4524xu51812304%2F</link>
            <description>We report a pediatric case of successful cardiac resynchronization therapy (CRT) for acute relapsed deterioration of dilated
 cardiomyopathy with cardiac dyssynchrony due to a noncompacted left ventricle (LV). A 20-month-old female developed severe
 congestive heart failure, which was classified as New York Heart Association class IV. She failed to thrive despite intravenous
 inotropic support. Her LV function and dimension improved markedly after CRT. The beneficial effect of CRT in this patient
 has remained for more than 3&amp;nbsp;years.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s00246-011-0086-6Authors
		Tomoyasu Sasaki, Department of Cardiovascular Surgery, Osaka Medical College Hospital, Daigakutyou 2-7, Takatsuki, Osaka, JapanShintaro Nemoto, Department of Cardiovascular Su...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131905</comments>
            <pubDate>Sat, 13 Aug 2011 06:12:55 +0100</pubDate>
            <guid isPermaLink="false">5131905</guid>        </item>
        <item>
            <title>Mitral Regurgitation due to Chordae Tendineae Rupture in an Infant with Aortic Coarctation</title>
            <link>http://www.medworm.com/index.php?rid=5131906&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl41064481vt14463%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 2-month-old male suddenly developed mitral regurgitation aggravation while waiting for surgical repair of aortic coarctation.
 There were no signs of infection or history of trauma. Emergency surgery was performed, during which rupture of chordae tendineae
 of the A2 portion of the anterior mitral leaflet was confirmed. At last follow-up, 11&amp;nbsp;months postsurgery, the patient was
 in an acceptable state, with continuing moderate mitral valve regurgitation. This case demonstrates an unusual but dangerous
 natural course of aortic coarctation and suggests an additional basis of urgent repair of aortic coarctation.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0087-5Authors
		Myung-Mi Kim, Division of Pediatric Cardiology, College of Medicine, Univer...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131906</comments>
            <pubDate>Sat, 13 Aug 2011 06:12:54 +0100</pubDate>
            <guid isPermaLink="false">5131906</guid>        </item>
        <item>
            <title>Improving Outcomes from Out-of-Hospital Cardiac Arrest in Young Children and Adolescents</title>
            <link>http://www.medworm.com/index.php?rid=5131907&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu5h27326hh8655j5%2F</link>
            <description>This article will review the epidemiology of OHCA, the 2010 CPR guidelines, and developments in public access
 defibrillation for children.
 
 
	Content Type Journal ArticlePages 1-10DOI 10.1007/s00246-011-0084-8Authors
		Dianne L. Atkins, Carver College of Medicine, University of Iowa Children’s Hospital, Iowa City, IA 52242, USAStuart Berger, Children’s Hospital of Wisconsin, Medical College of Wisconsin, Milwaukee, WI 53226, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131907</comments>
            <pubDate>Sat, 13 Aug 2011 06:12:53 +0100</pubDate>
            <guid isPermaLink="false">5131907</guid>        </item>
        <item>
            <title>Acute Myocardial Infarction in a Teenager Due to Adderall XR</title>
            <link>http://www.medworm.com/index.php?rid=5131908&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk1m702274gu47406%2F</link>
            <description>We present
 a case of a 15-year-old male who suffered a myocardial infarction after starting Adderall XR. Patient was otherwise in good
 health with no previous cardiac abnormalities. Cardiac catheterization was normal, and etiology was presumed to be secondary
 to acute vasospasm. The patient improved with cessation of medication. Physicians need to carefully screen patients for cardiac
 abnormalities prior to starting amphetamine-based medications.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0083-9Authors
		Angela L. Sylvester, Department of Family Practice, Hinsdale Hospital, Hinsdale, IL, USABrojendra Agarwala, Pediatric Cardiology Comer Children’s Hospital, University of Chicago, Chicago, IL 60637-1470, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-197...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5131908</comments>
            <pubDate>Sat, 13 Aug 2011 06:12:52 +0100</pubDate>
            <guid isPermaLink="false">5131908</guid>        </item>
        <item>
            <title>Left Main Coronary Artery Atresia: The Role of Computed Tomographic Coronary Angiography</title>
            <link>http://www.medworm.com/index.php?rid=5126176&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fdlr20614935pw17p%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0081-yAuthors
		B. Srinivas, Nizam’s Institute of Medical Sciences, Hyderabad, IndiaS. P. Suryawanshi, Nizam’s Institute of Medical Sciences, Hyderabad, IndiaRao D. Seshagiri, Nizam’s Institute of Medical Sciences, Hyderabad, India
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5126176</comments>
            <pubDate>Mon, 08 Aug 2011 19:55:09 +0100</pubDate>
            <guid isPermaLink="false">5126176</guid>        </item>
        <item>
            <title>A Case of Cor Triatriatum With an Abnormal P Wave: The Pacemaker Action From the Specialized Tissue in the Abnormal Septum</title>
            <link>http://www.medworm.com/index.php?rid=5119821&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fgj44622246512x07%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A boy presented with an abnormal P wave shown on an electrocardiogram (ECG) checkup at school. An echocardiogram and contrast-enhanced
 computed tomography (CT) showed cor triatriatum with a slit-like opening between the accessory chamber and the left atrium
 located along the interatrial septum. The boy underwent open heart surgery for excision of the anomalous membrane, and a postoperative
 ECG showed normal P waves. The excised tissue was examined immnunohistopathologically using antihyperpolarization-activated
 cyclic nucleotide-gated potassium channel 4 (HCN4) antibody and other staining. The authors confirmed the existence of cells
 positive to HCN4, indicating that they were sinoatrial node cells or at least cells with electrical automaticity.
 
 
	Content Type J...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5119821</comments>
            <pubDate>Sun, 07 Aug 2011 05:48:40 +0100</pubDate>
            <guid isPermaLink="false">5119821</guid>        </item>
        <item>
            <title>Cardiac-Related Varicella Mortality in Childhood: A Literature Review With Clinical Experience</title>
            <link>http://www.medworm.com/index.php?rid=5119822&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F043v435k286484p5%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Among unvaccinated populations, primary varicella zoster virus (VZV) infection results in a minor childhood illness for the
 majority of individuals. Mortality is rare, and fatalities associated with cardiac complications are exceptional. In a population
 where routine VZV vaccination is not practised, we report a death in a previously healthy child secondary to VZV myocarditis.
 A literature review of cardiac-related VZV mortality in childhood is included. This identified a further 13 cases where death
 was associated with or attributable to, direct involvement of the myocardium or conducting system with what is frequently
 considered a benign childhood illness.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0076-8Authors
		Michael J. O’Grady, Acade...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5119822</comments>
            <pubDate>Sun, 07 Aug 2011 05:48:39 +0100</pubDate>
            <guid isPermaLink="false">5119822</guid>        </item>
        <item>
            <title>Partial Anomalous Pulmonary Venous Return: Transcatheter Repair</title>
            <link>http://www.medworm.com/index.php?rid=5109196&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx38854q263233444%2F</link>
            <description>This report describes a case of partial anomalous pulmonary venous return in a young white girl for whom transcatheter intervention
 successfully replaced surgical correction. This intervention was feasible because the left lung had dual pulmonary venous
 drainage.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0075-9Authors
		George Kasarala, Division of Cardiology, Department of Pediatrics, Cardinal Glennon Children’s Medical Center, Saint Louis University School of Medicine, 1465 S. Grand Boulevard, St. Louis, MO 63104, USAAndrew Fiore, Department of Surgery, Cardiothoracic, Saint Louis University School of Medicine, 1465 S. Grand Boulevard, St. Louis, MO 63104, USAKenneth Schowengerdt, Division of Cardiology, Department of Pediatrics, Cardinal Glennon Children’s M...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5109196</comments>
            <pubDate>Sat, 06 Aug 2011 05:47:18 +0100</pubDate>
            <guid isPermaLink="false">5109196</guid>        </item>
        <item>
            <title>Occlusion of Pulmonary Arteriovenous Malformations Using the Amplatzer Vascular Plug/Duct Occluder for a Family With Hereditary Hemorrhagic Telangiectasia</title>
            <link>http://www.medworm.com/index.php?rid=5109197&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn4q2656402h07812%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0073-yAuthors
		Min Jung Cho, Department of Pediatrics, Pusan National University Hospital, Ami-dong, Seo-gu, Busan, 602-739 Republic of KoreaJi Ae Park, Department of Pediatrics, Pusan National University Children’s Hospital, Beomeu-li, Mulgum-eup, Yangsan, Keungsangnam-do, 626-770 Republic of KoreaHyoung Doo Lee, Department of Pediatrics, Pusan National University Children’s Hospital, Beomeu-li, Mulgum-eup, Yangsan, Keungsangnam-do, 626-770 Republic of Korea
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5109197</comments>
            <pubDate>Sat, 06 Aug 2011 05:47:17 +0100</pubDate>
            <guid isPermaLink="false">5109197</guid>        </item>
        <item>
            <title>Clinical Significance of Thrombosis in an Intracardiac Blind Pouch After a Fontan Operation</title>
            <link>http://www.medworm.com/index.php?rid=5109198&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fjv71tm6274412711%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The univentricular heart after the Fontan operation may have a blind pouch formed by the pulmonary stump or rudimentary ventricle
 according to the anatomy before surgery. Thrombosis in an intracardiac blind pouch of patients with a univentricular heart
 is a hazardous complication. Because only a few reports have described this complication, the authors evaluated the clinical
 significance of thrombosis in an intracardiac blind pouch of a univentricular heart. They performed a retrospective review
 of medical records from August 1986 to December 2007. Four patients were confirmed as having thrombosis in a pulmonary artery
 stump and one patient as having thrombosis in a rudimentary ventricle shown by cardiac computed tomography (CT). This represents
 1.85% (5/271) of p...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5109198</comments>
            <pubDate>Fri, 05 Aug 2011 05:54:00 +0100</pubDate>
            <guid isPermaLink="false">5109198</guid>        </item>
        <item>
            <title>Intrapericardial and Retrocardial Implantation of Implantable Cardioverter-Defibrillator Lead in a Child with Type 3 Long QT Syndrome</title>
            <link>http://www.medworm.com/index.php?rid=5109199&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh4581861t2x44178%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;A 6-year-old girl with type 3 long QT syndrome was safely and successfully implanted with an implantable cardioverter-defibrillator
 (ICD) system. Prior to implantation, she had experienced uncontrollable life-threatening arrhythmia in spite of high-dose
 administration of mexiletine. An ICD coil lead for transvenous use was placed in the intrapericardial and retrocardial space
 and was connected to a generator placed in front of the posterior sheath of the right abdominal rectal muscle. Administration
 of a beta-blocker in addition to atrial pacing almost completely eliminated the patient’s life-threatening arrhythmia attacks.
 Intrapericardial and retrocardial implantation of ICD coil leads might be useful for children.
 
 
	Content Type Journal ArticlePages 1-5DOI ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5109199</comments>
            <pubDate>Fri, 05 Aug 2011 05:53:58 +0100</pubDate>
            <guid isPermaLink="false">5109199</guid>        </item>
        <item>
            <title>Echocardiographic Detection of Early Myocardial Calcification in Acute Neonatal Myocarditis Due to Coxsackie Virus Type B</title>
            <link>http://www.medworm.com/index.php?rid=5109200&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fh776822r78456053%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0080-zAuthors
		Alessandra Benettoni, Institute for Maternal and Child Health—IRCCS Burlo Garofolo, Trieste, ItalyEmanuela Berton, Institute for Maternal and Child Health—IRCCS Burlo Garofolo, Trieste, Italy
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5109200</comments>
            <pubDate>Thu, 04 Aug 2011 15:41:36 +0100</pubDate>
            <guid isPermaLink="false">5109200</guid>        </item>
        <item>
            <title>Novel Electrocardiogram Manifestations of a Tension Pneumothorax</title>
            <link>http://www.medworm.com/index.php?rid=5103796&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8x7j52720010r250%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0067-9Authors
		Rajesh Punn, Division of Pediatric Cardiology, Stanford University, Lucile Packard Children’s Hospital, 750 Welch Road, Suite # 305, Palo Alto, CA 94304, USAStephen P. Seslar, Division of Cardiology, Electrophysiology, and Pacing, Seattle Children’s Hospital and Regional Medical Center, University of Washington, Washington, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5103796</comments>
            <pubDate>Tue, 02 Aug 2011 15:53:19 +0100</pubDate>
            <guid isPermaLink="false">5103796</guid>        </item>
        <item>
            <title>Radiation Exposure in Children During the Current Era of Pediatric Cardiac Intervention</title>
            <link>http://www.medworm.com/index.php?rid=5103797&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fp87nm329115puv01%2F</link>
            <description>This study aimed to evaluate factors that influence variability of X-ray exposure in children
 with congenital heart diseases during cardiac catheterization. The study included 107 children who underwent either diagnostic
 (n&amp;nbsp;=&amp;nbsp;46) or interventional (n&amp;nbsp;=&amp;nbsp;61) procedures. A custom-made sheet for patient and procedural characteristics was designed. Data were collected, and different
 correlations were applied to determine factors that influence variability of X-ray exposure. The flouroscopy time (FT) differed
 significantly between the diagnostic (8.9&amp;nbsp;±&amp;nbsp;6.3&amp;nbsp;min) and intervention (12.8&amp;nbsp;±&amp;nbsp;9.98&amp;nbsp;min) groups (P&amp;nbsp;=&amp;nbsp;0.032). The mean dose–area product (DAP) differed significantly between the two groups (3.775&amp;nbsp;±&amp;nbsp;2.5&amp;nbsp;Gy/cm2 ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5103797</comments>
            <pubDate>Tue, 02 Aug 2011 15:53:16 +0100</pubDate>
            <guid isPermaLink="false">5103797</guid>        </item>
        <item>
            <title>Aortic Exclusion: A Method of Handling Aortic Insufficiency in the Pediatric Population Needing Mechanical Circulatory Support</title>
            <link>http://www.medworm.com/index.php?rid=5103800&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe56014748471835g%2F</link>
            <description>We report the first case of aortic exclusion in an infant with moderate to severe aortic insufficiency
 in need of MCS.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0069-7Authors
		Kimberly L. Gandy, Children’s Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USAMichael E. Mitchell, Children’s Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USAAndrew N. Pelech, Children’s Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USARobert A. Niebler, Children’s Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USAGeorge Hoffman, Children’s Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USAStuart Berger, Children’s Mercy Hospital, 2401 Gillham Road, Kansas City, MO 64108, USA
	

	
		Journal Pediatric CardiologyOnline ISSN...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5103800</comments>
            <pubDate>Tue, 02 Aug 2011 06:12:59 +0100</pubDate>
            <guid isPermaLink="false">5103800</guid>        </item>
        <item>
            <title>Calcified Unruptured Sinus of Valsalva Aneurysm in a Child</title>
            <link>http://www.medworm.com/index.php?rid=5103799&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn263710h14324484%2F</link>
            <description>We present the management
 and outcome of such a case.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0068-8Authors
		Arul Dominic Furtado, Department of Cardio-Thoracic Surgery, Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bangalore, 560069 IndiaDevananda Nijagal Shivanna, Department of Cardio-Thoracic Surgery, Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bangalore, 560069 IndiaSyed Murfad Peer, Department of Cardio-Thoracic Surgery, Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bangalore, 560069 IndiaJayaranganath Mahimarangaiah, Department of Pediatric Cardiology, Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bangalore, 560069 India
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print IS...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5103799</comments>
            <pubDate>Tue, 02 Aug 2011 06:12:59 +0100</pubDate>
            <guid isPermaLink="false">5103799</guid>        </item>
        <item>
            <title>Isolated Junctional Tachycardia in a Child After Noncardiac Surgery: An Uncommon Clinical Presentation</title>
            <link>http://www.medworm.com/index.php?rid=5103798&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F7310n72l176862j4%2F</link>
            <description>This report describes the case of a 3-year-old boy with no cardiac history who experienced
 transient junctional tachycardia after a right pyeloplasty. Medical therapy was not prescribed initially due to lack of symptoms.
 However, symptomatic junctional tachycardia recurred, prompting institution of oral beta-blocker therapy. Isolated junctional
 tachycardia should not be overlooked in the differential diagnosis of pediatric supraventricular tachycardia after noncardiac
 surgery.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s00246-011-0072-zAuthors
		Chenni S. Sriram, Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USARoger D. White, Division of Cardio/Thoracic Anesthesia...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5103798</comments>
            <pubDate>Tue, 02 Aug 2011 06:12:59 +0100</pubDate>
            <guid isPermaLink="false">5103798</guid>        </item>
        <item>
            <title>The Quantitative and Qualitative Responses of Platelets in Pediatric Patients Undergoing Cardiopulmonary Bypass Surgery</title>
            <link>http://www.medworm.com/index.php?rid=5103801&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F6010m42m678p655m%2F</link>
            <description>This study provides a new foundation for future studies investigating requirements of platelet supplementation
 in the setting of pediatric CPB surgery.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s00246-011-0079-5Authors
		Vera Ignjatovic, Murdoch Childrens Research Institute, Flemington Road, Parkville, VIC 3052, AustraliaJenny Than, Department of Clinical Haematology, Royal Children’s Hospital, Melbourne, VIC, AustraliaRobyn Summerhayes, Murdoch Childrens Research Institute, Flemington Road, Parkville, VIC 3052, AustraliaFiona Newall, Murdoch Childrens Research Institute, Flemington Road, Parkville, VIC 3052, AustraliaSteve Horton, Department of Cardiac Surgery, Royal Children’s Hospital, Melbourne, VIC, AustraliaAndrew Cochrane, Department of Paediatrics, The University o...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5103801</comments>
            <pubDate>Tue, 02 Aug 2011 06:12:58 +0100</pubDate>
            <guid isPermaLink="false">5103801</guid>        </item>
        <item>
            <title>Successful Percutaneous Cardiac Resynchronization Despite an Occlusive Thebesian Valve</title>
            <link>http://www.medworm.com/index.php?rid=5088069&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fb121152716171120%2F</link>
            <description>We report the case of a patient with symptomatic heart failure referred after an unsuccessful attempt at cardiac resynchronization
 therapy. An occlusive Thebesian valve prevented entry into the coronary sinus ostium. Careful analysis of the patient’s cardiovascular
 physiology and anatomy revealed the “fortuitous” presence of a persistent left superior vena cava. Cannulation of this vessel
 permitted percutaneous retrograde placement of a left ventricular lead into a posterolateral cardiac venous branch resulting
 in successful cardiac resynchronization. This unique case provides strong evidence that thorough knowledge of cardiac embryology,
 anatomy, and physiology plays a pivotal role in percutaneous electromechanical intervention for drug-refractory heart failure.
 
 
	Content Ty...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088069</comments>
            <pubDate>Sat, 30 Jul 2011 15:52:34 +0100</pubDate>
            <guid isPermaLink="false">5088069</guid>        </item>
        <item>
            <title>Cardiac Lymphangioma in an Infant</title>
            <link>http://www.medworm.com/index.php?rid=5088071&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk7n4v68786782t4u%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0061-2Authors
		Hala Almarsafawy, Department of Pediatrics, Mansoura University, Mansoura, EgyptMohamed Matter, Department of Pediatrics, Mansoura University, Mansoura, EgyptMohamed-Adel Elgamal, Department of Congenital and Pediatric Cardiac Surgery, Mansoura University, Mansoura, EgyptKhaled Zalata, Department of Pathology, Mansoura University, Mansoura, Egypt
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088071</comments>
            <pubDate>Sat, 30 Jul 2011 05:56:24 +0100</pubDate>
            <guid isPermaLink="false">5088071</guid>        </item>
        <item>
            <title>Anomalous Hepatic Vein Draining into the Coronary Sinus</title>
            <link>http://www.medworm.com/index.php?rid=5088070&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fuj7710402317577v%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0063-0Authors
		Can Vuran, Department of Cardiovascular Surgery, Baskent University, Istanbul Hospital, Oymaci Sk, No: 7, Altunizade/Istanbul, TurkeyEmre Ozker, Department of Cardiovascular Surgery, Baskent University, Istanbul Hospital, Oymaci Sk, No: 7, Altunizade/Istanbul, TurkeyBurcak Gumus, Department of Radiology, Baskent University, Istanbul Hospital, Oymaci Sk, No: 7, Altunizade/Istanbul, TurkeyRiza Turkoz, Department of Cardiovascular Surgery, Baskent University, Istanbul Hospital, Oymaci Sk, No: 7, Altunizade/Istanbul, Turkey
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088070</comments>
            <pubDate>Sat, 30 Jul 2011 05:56:24 +0100</pubDate>
            <guid isPermaLink="false">5088070</guid>        </item>
        <item>
            <title>Dilated Tortuous Right Coronary Artery to Coronary Sinus Fistula</title>
            <link>http://www.medworm.com/index.php?rid=5088072&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu765732362364606%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0055-0Authors
		Feyza Ayşenur Paç, Department of Pediatric Cardiology, Turkiye Yuksek Ihtisas Education and Research Hospital, Kizilay S, No: 4, Sihhiye, 06100 Ankara, Turkeyİbrahim Ece, Department of Pediatric Cardiology, Turkiye Yuksek Ihtisas Education and Research Hospital, Kizilay S, No: 4, Sihhiye, 06100 Ankara, TurkeyŞevket Ballı, Department of Pediatric Cardiology, Turkiye Yuksek Ihtisas Education and Research Hospital, Kizilay S, No: 4, Sihhiye, 06100 Ankara, Turkey
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088072</comments>
            <pubDate>Fri, 29 Jul 2011 16:07:55 +0100</pubDate>
            <guid isPermaLink="false">5088072</guid>        </item>
        <item>
            <title>Acute Kidney Injury After Cardiac Surgery in Infants and Children: Evaluation of the Role of Angiotensin-Converting Enzyme Inhibitors</title>
            <link>http://www.medworm.com/index.php?rid=5088074&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fk70x61536kv885t6%2F</link>
            <description>This study
 sought to evaluate the role of angiotensin-converting enzyme (ACE) inhibitors and other nephrotoxic medications in the risk
 for the development of AKI in neonates and children undergoing cardiac surgery. A retrospective review of all patients younger
 than 2&amp;nbsp;years admitted to the cardiac intensive care unit after cardiac surgery from March 2007 to September 2008 was conducted.
 Patients were included in the review if they received furosemide alone or in combination with an ACE inhibitor. Creatinine
 clearance was calculated, and the patient’s maximal degree of AKI was classified by pRIFLE. A P value less than 0.05 was considered significant. Of the 319 patients who met the inclusion criteria, 149 (47%) received furosemide
 therapy alone and 170 (53%) received a combinat...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088074</comments>
            <pubDate>Thu, 28 Jul 2011 15:57:11 +0100</pubDate>
            <guid isPermaLink="false">5088074</guid>        </item>
        <item>
            <title>Surgical Management of Congenital Heart Disease: Contribution of the Aristotle Complexity Score to Planning and Budgeting in the German Diagnosis-Related Groups System</title>
            <link>http://www.medworm.com/index.php?rid=5088073&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu67n165w0770956g%2F</link>
            <description>This study
 investigated how this performance evolved during years 2006 to 2010. Hospital costs and reimbursements correlated highly with
 Aristotle comprehensive complexity levels (Spearman r&amp;nbsp;=&amp;nbsp;1). Mean costs and reimbursement reached 35,050&amp;#8364;&amp;nbsp;±&amp;nbsp;32,665&amp;#8364; and 31,283&amp;#8364;&amp;nbsp;±&amp;nbsp;34,732&amp;#8364;, respectively, for an underfunding of
 10.7%. Basic and comprehensive unit surgical performances were respectively 3036&amp;nbsp;±&amp;nbsp;1009 and 3891&amp;nbsp;±&amp;nbsp;1591 points in 2006. Both
 performances increased in sigmoid fashion to reach 3883&amp;nbsp;±&amp;nbsp;1344 and 5335&amp;nbsp;±&amp;nbsp;1314 points, respectively, in 2010. Top performances
 would be achieved in year 2011, and extrapolated costs would comprise about 19,434,094.92&amp;#8364; (95% confidence interval, 11,961,4...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088073</comments>
            <pubDate>Thu, 28 Jul 2011 15:57:11 +0100</pubDate>
            <guid isPermaLink="false">5088073</guid>        </item>
        <item>
            <title>Commotio Cordis Presenting as a Temporary Complete Atrioventricular Block in a 2-Year-Old Girl With Congenitally Corrected Transposition of the great Arteries</title>
            <link>http://www.medworm.com/index.php?rid=5088075&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbj416379m0763788%2F</link>
            <description>This report describes a 2-year-old girl with congenitally corrected transposition of the great arteries (ccTGA) who presented
 with transient complete atrioventricular (AV) block after a mild chest blow. Running around the house with her older sister,
 she fell to the floor. Her sister also fell and landed on her. The girl became cyanotic and pale and experienced a transient
 loss of consciousness. At arrival to the emergency department, she had regained consciousness, but she remained pale. An electrocardiogram
 (ECG) demonstrated complete AV block with a heart rate of 78 beats per minute (bpm). The ECG after admission showed a Wenckebach-type
 second-degree AV block. Day 2 after admission, a 12-lead ECG showed significant ST and T-wave abnormalities in the precordial
 leads, but the girl...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088075</comments>
            <pubDate>Wed, 27 Jul 2011 18:48:17 +0100</pubDate>
            <guid isPermaLink="false">5088075</guid>        </item>
        <item>
            <title>Serum Levels After Everolimus-Stent Implantation and Paclitaxel-Balloon Angioplasty in an Infant with Recurrent Pulmonary Vein Obstruction After Repaired Total Anomalous Pulmonary Venous Connection</title>
            <link>http://www.medworm.com/index.php?rid=5088076&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyl45778557437584%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Everolimus-eluting stents and paclitaxel-coated balloons are used in the interventional treatment of coronary artery disease
 in adults to reduce the restenosis rate and in small-vessel disease. Both substances are released into the circulation. We
 report systemic drug exposure after implantation of one everolimus-eluting stent and dilation with one paclitaxel-coated balloon
 in an 8-month-old infant, which was used as an innovative therapy for recurrent pulmonary vein stenosis.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s00246-011-0054-1Authors
		Matthias J. Müller, Department for Pediatric Cardiology and Intensive Care Medicine, Georg-August-University Göttingen, Robert-Koch-Str. 40, 37075 Göttingen, GermanyUlrich Krause, Department for Pediatric Cardio...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088076</comments>
            <pubDate>Wed, 27 Jul 2011 15:50:39 +0100</pubDate>
            <guid isPermaLink="false">5088076</guid>        </item>
        <item>
            <title>Formation of Ventricular Aneurysm After Endocarditis in a Child With Methicillin-Resistant Staphylococcus aureus (MRSA) Bacteremia</title>
            <link>http://www.medworm.com/index.php?rid=5088078&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fhu7176xrt5n57tv5%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0044-3Authors
		Lasya Gaur, Pediatric Cardiology, Children’s National Medical Center, 111 Michigan Avenue NW, Washington, DC 20010, USAShobhit Madan, Department of Radiology, Children’s Hospital of Pittsburgh of UPMC, 4401 Penn Avenue, Suite Floor 2, Pittsburgh, PA 15224, USAVictor Morell, Division of Pediatric Cardiothoracic Surgery, Children’s Hospital of Pittsburgh of UPMC, 4401 Penn Avenue, Suite Floor 3, Pittsburgh, PA 15224, USAGaurav Arora, Division of Pediatric Cardiology, Children’s Hospital of Pittsburgh of UPMC, 4401 Penn Avenue, Suite Floor 3, Pittsburgh, PA 15224, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088078</comments>
            <pubDate>Tue, 26 Jul 2011 05:47:08 +0100</pubDate>
            <guid isPermaLink="false">5088078</guid>        </item>
        <item>
            <title>Successful Treatment with Bosentan for Pulmonary Hypertension and Reduced Peripheral Circulation in Juvenile Systemic Sclerosis</title>
            <link>http://www.medworm.com/index.php?rid=5088077&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fr42t7r67h8120n2t%2F</link>
            <description>We describe a case of juvenile SSc–PAH successfully treated with bosentan. The present case shows that bosentan
 ameliorated PAH and peripheral circulation as evaluated by cold stress thermography. No bosentan-related adverse events such
 as liver dysfunction were observed. Prospective randomized trials are required to validate the effectiveness of bosentan for
 patients with juvenile SSc; however, bosentan might be useful for the management of patients with juvenile SSc.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0056-zAuthors
		Masaki Shimizu, Department of Pediatrics, School of Medicine, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, JapanYoko Hashida, Department of Pediatrics, School of Medicine, Institute of Medical, Ph...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5088077</comments>
            <pubDate>Tue, 26 Jul 2011 05:47:08 +0100</pubDate>
            <guid isPermaLink="false">5088077</guid>        </item>
        <item>
            <title>Relationship of Pulmonary Artery Wedge Pressure to Left Atrial Pressure and Pulmonary Vascular Resistance in Preoperative Fontan Patients</title>
            <link>http://www.medworm.com/index.php?rid=5070126&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fm1517626466q4w87%2F</link>
            <description>This study was to validate PAWp as an accurate estimate of LAp for calculating pulmonary
 vascular resistance in single-ventricle patients after the bidirectional Glenn operation. A prospective study measuring direct
 branch pulmonary artery pressures, ipsilateral PAWp, and direct LAp to calculate pulmonary and systemic blood flows was conducted.
 Pulmonary vascular resistance (PVR) was calculated for each patient using the PAWp and compared to the PVR calculated by direct
 LAp measurements. Twenty-eight patients were enrolled; 27 were eligible for study inclusion. Ages ranged from 21 to 60&amp;nbsp;months
 and weights ranged from 9.5 to 20.8&amp;nbsp;kg. Underlying congenital heart defect diagnoses varied, with all patients either functionally
 or anatomically univentricular. Left mPAWp measured ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5070126</comments>
            <pubDate>Mon, 25 Jul 2011 15:44:26 +0100</pubDate>
            <guid isPermaLink="false">5070126</guid>        </item>
        <item>
            <title>Prospective, Longitudinal Study of Plastic Bronchitis Cast Pathology and Responsiveness to Tissue Plasminogen Activator</title>
            <link>http://www.medworm.com/index.php?rid=5063503&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fuv47q3vt661428t8%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Plastic bronchitis (PB) is a rare disease that often occurs in patients with congenital heart disease (CHD) who have undergone
 staged single-ventricle palliation. It is characterized by the formation of rubbery “casts” in the airways. PB treatment frequently
 includes inhaled tissue plasminogen activator (tPA). However, the efficacy of tPA to reduce cast burden is unknown. This is
 further complicated by our lack of knowledge of cast composition. We obtained spontaneously expectorated PB casts from children
 (n&amp;nbsp;=&amp;nbsp;4) with CHD and one adult patient with idiopathic PB. Pathological assessment was made from paraffin-preserved samples.
 Casts were treated with phosphate-buffered saline (PBS) or tPA. Cast response to tPA was assessed by changes in cast weight
 ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063503</comments>
            <pubDate>Sat, 23 Jul 2011 15:49:04 +0100</pubDate>
            <guid isPermaLink="false">5063503</guid>        </item>
        <item>
            <title>Outcomes of Hypoplastic Left Heart Syndrome in Low-Birth-Weight Patients</title>
            <link>http://www.medworm.com/index.php?rid=5063504&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fu130608x70487j06%2F</link>
            <description>The objective of this study was to assess outcomes of hypoplastic left heart syndrome (HLHS) patients weighing ≤2.5&amp;nbsp;kg throughout
 staged palliation. We performed a single-center retrospective review. Abstracted data included gestational age, birth weight,
 presence of noncardiac anomalies, and survival through Fontan. Fifty-two patients met inclusion criteria, with a median birth
 weight of 2.14&amp;nbsp;kg and gestational age of 36&amp;nbsp;weeks. Five patients received comfort care only. Of 47 patients who underwent
 initial surgical palliation, 51% survived to initial hospital discharge. Birth weight and gestational age (GA) were similar
 between survivors and nonsurvivors. Compared with survivors, risk factors for death prior to initial hospital discharge were
 as follows: small for GA...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063504</comments>
            <pubDate>Fri, 22 Jul 2011 17:07:11 +0100</pubDate>
            <guid isPermaLink="false">5063504</guid>        </item>
        <item>
            <title>Congenital Subclavian Steal Syndrome Associated With Heterotaxy Syndrome and Atrioventricular Septal Defect</title>
            <link>http://www.medworm.com/index.php?rid=5063505&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F2100643823p63502%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;An infant under follow-up evaluation since the fetal stage was detected to have subclavian steal syndrome (SSS) associated
 with heterotaxy syndrome and atrioventricular septal defect. Such a complex association has not been reported previously.
 Congenital SSS occurs as a result of a subclavian artery originating from the main pulmonary artery through the ductus instead
 of the aortic arch. In rare cases, as in the reported case, it may occur due to proximal segment atresia of the left subclavian
 artery.
 
 
	Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0048-zAuthors
		Murat Ciftel, Department of Pediatric Cardiology, Faculty of Medicine, Akdeniz University, Antalya, TurkeyFirat Kardelen, Department of Pediatric Cardiology, Faculty of Medicine, Akdeniz ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063505</comments>
            <pubDate>Thu, 21 Jul 2011 18:10:47 +0100</pubDate>
            <guid isPermaLink="false">5063505</guid>        </item>
        <item>
            <title>Exercise-Induced Intraventricular Obstruction in a Child with Near Syncope and Chest Pain During Exercise</title>
            <link>http://www.medworm.com/index.php?rid=5063508&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyr77280q69140863%2F</link>
            <description>We report the case of a 10-year-old girl with two episodes of light-headedness and chest pain during exercise. She had an
 unremarkable clinical record, physical examination, ECG, and echocardiogram. Noninvasive ischemia tests were positive, but
 coronary angiography was normal. Exercise stress echocardiogram revealed an exercise-induced intra-left-ventricular obstruction
 with a peak gradient of 78&amp;nbsp;mmHg and replicated her symptoms. After starting beta-blocker therapy her clinical status improved
 and no residual obstruction was detected. The authors review this unsuspected clinical condition, seldom reported in the adult
 population and, to our knowledge, never before in a child.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s00246-011-0052-3Authors
		Artur Lopes, Cardiology ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063508</comments>
            <pubDate>Thu, 21 Jul 2011 18:10:44 +0100</pubDate>
            <guid isPermaLink="false">5063508</guid>        </item>
        <item>
            <title>Exercise-Induced Myocardial Ischemia in a Case of Anomalous Origin of the Left Main Coronary Artery from the Noncoronary Sinus of Valsalva</title>
            <link>http://www.medworm.com/index.php?rid=5063507&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F00745757280043h1%2F</link>
            <description>We report a case of anomalous origin of the left main coronary artery (LCA) from the noncoronary sinus of valsalva (LCANCS)
 in a young healthy patient who presented with syncope and cardiopulmonary arrest during exercise. The enhanced computed tomography
 showed acute angle take-off (AAT) of LCA, and the exercise stress thallium-201 myocardial scintigraphy demonstrated a large
 defect at the LCA perfusion region. We propose that the coexistence of AAT and resulting ischemia causes sudden cardiac death
 during exercise in the patients with LCANCS.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s00246-011-0051-4Authors
		Mitsunori Nishiyama, Graduate School of Medicine, Tokyo Medical and Dental University, Tokyo, JapanShouzaburo Doi, Graduate School of Medicine, Tokyo Medical and Den...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063507</comments>
            <pubDate>Thu, 21 Jul 2011 18:10:44 +0100</pubDate>
            <guid isPermaLink="false">5063507</guid>        </item>
        <item>
            <title>Accuracy of Doppler-Derived Estimation of Pulmonary Vascular Resistance in Congenital Heart Disease: An Index of Operability</title>
            <link>http://www.medworm.com/index.php?rid=5063506&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fg1117h1t4046v071%2F</link>
            <description>In conclusion, Doppler-derived TRV/VTIm ratio is a reliable index that may be helpful as a supplementary diagnostic tool for the selection of modality of treatment
 and follow-up of patients with PAH and increased PVR.
 
 
	Content Type Journal ArticlePages 1-7DOI 10.1007/s00246-011-0035-4Authors
		Gholam Hossein Ajami, Department of Pediatrics, Division of Pediatric Cardiology, Namazi Hospital, Shiraz University of Medical Sciences, 71937-11351 Shiraz, IranSirous Cheriki, Department of Pediatrics, Division of Pediatric Cardiology, Namazi Hospital, Shiraz University of Medical Sciences, 71937-11351 Shiraz, IranHamid Amoozgar, Department of Pediatrics, Division of Pediatric Cardiology, Namazi Hospital, Shiraz University of Medical Sciences, 71937-11351 Shiraz, IranMohammad Borzouee, Departm...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063506</comments>
            <pubDate>Thu, 21 Jul 2011 18:10:44 +0100</pubDate>
            <guid isPermaLink="false">5063506</guid>        </item>
        <item>
            <title>Infliximab Treatment for Pediatric Refractory Kawasaki Disease</title>
            <link>http://www.medworm.com/index.php?rid=5063509&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F802157778k134234%2F</link>
            <description>Content Type Journal ArticlePages 1-5DOI 10.1007/s00246-011-0045-2Authors
		Laura L. Blaisdell, Department of Pediatrics, Maine Medical Center, 887 Congress Street Suite 310, Portland, ME 04102, USAJennifer A. Hayman, Barbara Bush Children’s Hospital, Maine Medical Center, 887 Congress Street Suite 310, Portland, ME 04102, USAAdrian M. Moran, Division of Pediatric Cardiology, Department of Pediatrics, Maine Medical Center, 887 Congress Street Suite 310, Portland, ME 04102, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5063509</comments>
            <pubDate>Wed, 20 Jul 2011 12:27:41 +0100</pubDate>
            <guid isPermaLink="false">5063509</guid>        </item>
        <item>
            <title>Coronary Artery-to-Pulmonary Artery Fistula in a Case of Pulmonary Atresia With Ventricular Septal Defect</title>
            <link>http://www.medworm.com/index.php?rid=5052648&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F48w1jtvg56x6wu23%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Pulmonary atresia with ventricular septal defect (PA-VSD) can be associated with varying pulmonary artery connections. The
 origin of pulmonary blood flow can vary greatly among patients, and some case reports have described the presence of left
 coronary artery-to-pulmonary artery fistula. Two cases of patients found to have coronary artery-to-pulmonary artery fistula
 in the settings of PA-VSD are reported.
 
 
	Content Type Journal ArticlePages 1-6DOI 10.1007/s00246-011-0043-4Authors
		Shyam K. Sathanandam, The Heart Institute for Children, Advocate Hope Children’s Hospital, 4440 W 95th Street, Oak Lawn, IL 60453, USARohit S. Loomba, Children’s Hospital of Wisconsin, Medical College of Wisconsin Affiliated Hospitals, 9000 Wisconsin Avenue, Wauwatosa, WI 53226, U...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5052648</comments>
            <pubDate>Mon, 18 Jul 2011 15:53:47 +0100</pubDate>
            <guid isPermaLink="false">5052648</guid>        </item>
        <item>
            <title>Postoperative Mass in the Left Atrium From a Transesophageal Echocardiography: An Omitted Myxoma or Thrombus?</title>
            <link>http://www.medworm.com/index.php?rid=5039167&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fbh6347726n764164%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0047-0Authors
		Silin Pan, Children’s Hospital, Qingdao University, Heart Center, Qingdao, ChinaQuansheng Xing, Children’s Hospital, Qingdao University, Heart Center, Qingdao, ChinaShuhua Duan, Children’s Hospital, Qingdao University, Heart Center, Qingdao, China
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5039167</comments>
            <pubDate>Thu, 14 Jul 2011 16:56:28 +0100</pubDate>
            <guid isPermaLink="false">5039167</guid>        </item>
        <item>
            <title>Results From Extrapleural Clipping of a Patent Ductus Arteriosus in Seriously Ill Preterm Infants</title>
            <link>http://www.medworm.com/index.php?rid=5039168&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F57764n1326646412%2F</link>
            <description>This study reports the immediate postoperative clinical
 outcomes for 24 extrapleurally clipped premature infants presenting with congestive heart failure in high-risk comorbidity
 status between March 2007 and November 2010. The demographics, preoperative clinical characteristics, and postoperative outcomes
 of the patients, including echocardiographic assessments, were evaluated. No surgery-related mortalities occurred. Four mortalities
 occurred after surgery due to sepsis and bleeding diathesis. All 20 surviving patients exhibited normal left ventricular dimensions
 and systolic function in the immediate follow-up period. The study shows that extrapleural clip closure in seriously ill premature
 infants has an acceptable overall short-term mortality and complication rate with a high ra...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5039168</comments>
            <pubDate>Thu, 14 Jul 2011 06:03:07 +0100</pubDate>
            <guid isPermaLink="false">5039168</guid>        </item>
        <item>
            <title>Murmur and Doppler Alternans in Critical Pulmonary Stenosis</title>
            <link>http://www.medworm.com/index.php?rid=5030267&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fq0048055521q85l4%2F</link>
            <description>This report describes a case of murmur
 alternans in critical pulmonary stenosis that also showed Doppler alternans on echocardiography. The underlying cause was
 right ventricular systolic dysfunction.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s00246-011-0033-6Authors
		Mehnaz Atiq, Department of Pediatrics and Child Health, Aga Khan University Hospital, P.O. Box 3500, Stadium Road, Karachi, 74800 PakistanSaleem Akhter, Department of Pediatrics and Child Health, Aga Khan University Hospital, P.O. Box 3500, Stadium Road, Karachi, 74800 PakistanSheikh Abdul Sattar, Department of Pediatrics and Child Health, Aga Khan University Hospital, P.O. Box 3500, Stadium Road, Karachi, 74800 PakistanShazia Mohsin, Department of Pediatrics and Child Health, Aga Khan University Hospital, P.O....</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5030267</comments>
            <pubDate>Tue, 12 Jul 2011 05:57:11 +0100</pubDate>
            <guid isPermaLink="false">5030267</guid>        </item>
        <item>
            <title>Treatment of Acute Heart Failure Using Levosimendan for a Patient With Dilated Cardiomyopathy, Chronic Renal Failure, and Hypertension</title>
            <link>http://www.medworm.com/index.php?rid=5030268&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl4l8x57506032n84%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The clinical and hemodynamic effects of compassionate therapy with levosimendan were evaluated in a 14-year–old patient with
 end-stage renal disease and arterial hypertension secondary to glycogenosis type Ia. The patient previously had normal heart
 function but experienced acute development of severe myocardial dysfunction resistant to diuretic therapy and inotropic support.
 Levosimendan administration was followed by a marked clinical and echocardiographic improvement. The authors believe that
 levosimendan may be useful for cases of resistant acute heart failure with arterial hypertension. Although administration
 of levosimendan is not recommended for patients with chronic renal disease, no adverse effect was observed. Therapeutic action
 for these patients see...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5030268</comments>
            <pubDate>Sun, 10 Jul 2011 05:53:05 +0100</pubDate>
            <guid isPermaLink="false">5030268</guid>        </item>
        <item>
            <title>Heart Rate Variability and Exercise Capacity of Patients With Repaired Tetralogy of Fallot</title>
            <link>http://www.medworm.com/index.php?rid=5020364&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fyr62u33268700257%2F</link>
            <description>This study investigated the correlation
 between HRV and exercise capacity in 30 patients with TOF after surgery for total correction. The median age of the patients
 was 14&amp;nbsp;years (range, 9–25&amp;nbsp;years), and the median follow-up period was 11.6&amp;nbsp;months (range, 5.3–20.2&amp;nbsp;months). Low- and high-frequency-domain
 HRV significantly correlated with VO2 peak (r&amp;nbsp;=&amp;nbsp;0.56, P&amp;nbsp;=&amp;nbsp;0.001 and r&amp;nbsp;=&amp;nbsp;0.44, P&amp;nbsp;=&amp;nbsp;0.02, respectively). After the 1-year follow-up evaluation, VO2 peak and HRV analysis did not differ from those at entry to the study. However, low- and high-frequency-domain HRV still
 correlated significantly with VO2 peak (r&amp;nbsp;=&amp;nbsp;0.43, P&amp;nbsp;=&amp;nbsp;0.03 and r&amp;nbsp;=&amp;nbsp;0.52, P&amp;nbsp;=&amp;nbsp;0.007, respectively). Left ventricular early...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020364</comments>
            <pubDate>Fri, 08 Jul 2011 06:37:23 +0100</pubDate>
            <guid isPermaLink="false">5020364</guid>        </item>
        <item>
            <title>Management of Warfarin in Children With Heart Disease</title>
            <link>http://www.medworm.com/index.php?rid=5020365&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8400971120713225%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s00246-011-0042-5Authors
		Sophie Jones, Department of Clinical Haematology, Royal Children’s Hospital, Parkville, AustraliaFiona Newall, Department of Clinical Haematology, Royal Children’s Hospital, Parkville, Australia
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5020365</comments>
            <pubDate>Thu, 07 Jul 2011 05:45:38 +0100</pubDate>
            <guid isPermaLink="false">5020365</guid>        </item>
        <item>
            <title>The Contribution of Chromosomal Abnormalities to Congenital Heart Defects: A Population-Based Study</title>
            <link>http://www.medworm.com/index.php?rid=5009799&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl452046618gt4200%2F</link>
            <description>In conclusion, in our study, approximately 1 in 8 infants with a CHD had a chromosomal abnormality. Clinicians should have
 a low threshold at which to obtain testing for chromosomal abnormalities in infants with CHDs, especially those with certain
 types of CHDs. Use of new technologies that have become recently available (e.g., chromosomal microarray) may increase the
 identified contribution of chromosomal abnormalities even further.
 
 
	Content Type Journal ArticlePages 1-11DOI 10.1007/s00246-011-0034-5Authors
		Robert J. Hartman, National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention, 1600 Clifton Road, MS E-86, Atlanta, GA, USASonja A. Rasmussen, National Center on Birth Defects and Developmental Disabilities, Centers for Disease ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5009799</comments>
            <pubDate>Tue, 05 Jul 2011 05:34:18 +0100</pubDate>
            <guid isPermaLink="false">5009799</guid>        </item>
        <item>
            <title>Outcomes and Risk Factors for Mortality in Premature Neonates With Critical Congenital Heart Disease</title>
            <link>http://www.medworm.com/index.php?rid=4993633&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fy378u74448464327%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We sought to describe contemporary outcomes and identify risk factors for hospital mortality in premature neonates with critical
 congenital heart disease who were referred for early intervention. Neonates who were born before 37&amp;nbsp;weeks’ gestation with
 critical congenital heart disease and admitted to our institution from 2002 to 2008 were included in this retrospective cohort
 study. Critical congenital heart disease was defined as a defect requiring surgical or transcatheter cardiac intervention
 or a defect resulting in death within the first 28&amp;nbsp;days of life. Logistic regression analyses were performed to identify risk
 factors for mortality before hospital discharge. The study included 180 premature neonates, of whom 37 (21%) died during their
 initial h...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993633</comments>
            <pubDate>Tue, 28 Jun 2011 15:49:47 +0100</pubDate>
            <guid isPermaLink="false">4993633</guid>        </item>
        <item>
            <title>Successful Treatment of a Newborn With Genetically Confirmed Long QT Syndrome 3 and Repetitive Torsades De Pointes Tachycardia</title>
            <link>http://www.medworm.com/index.php?rid=4993634&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F65871355528335qr%2F</link>
            <description>Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0037-2Authors
		Christian Paech, Department for Pediatric Cardiology, University of Leipzig––Heart Center, 04289 Leipzig, GermanyPhilipp Suchowerskyj, Department for Pediatric Cardiology, University of Leipzig––Heart Center, 04289 Leipzig, GermanyRoman Anton Gebauer, Department for Pediatric Cardiology, University of Leipzig––Heart Center, 04289 Leipzig, Germany
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4993634</comments>
            <pubDate>Tue, 28 Jun 2011 15:49:43 +0100</pubDate>
            <guid isPermaLink="false">4993634</guid>        </item>
        <item>
            <title>Benign Outcome of Pulmonary Hypertension in Neonates With a Restrictive Patent Foramen Ovale Versus Result for Neonates With an Unrestrictive Patent Foramen Ovale</title>
            <link>http://www.medworm.com/index.php?rid=4985714&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F84861657hn0ghg2r%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Premature closure or restriction of foramen ovale (FO) is a rare but known entity. FO diameter &amp;lt;2&amp;nbsp;mm and Doppler velocity
 &amp;gt;120&amp;nbsp;cm/s, diameter &amp;lt;3&amp;nbsp;mm with Doppler velocity measured gradient &amp;gt;5&amp;nbsp;mmHg have all being used by various authors to describe
 this entity. Some neonates with restrictive FO have been noted to have severe pulmonary hypertension with no clinical signs
 or symptoms and with spontaneous resolution without any intervention. Seven consecutive neonates were indentified in the database
 between 01/01/2003 and 06/30/2010 with diagnosis of restrictive PFO (diameter &amp;lt;2&amp;nbsp;mm) with structurally normal heart and their
 initial and follow-up echocardiogram as well as hospital medical records were reviewed. As a control, seven ...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4985714</comments>
            <pubDate>Mon, 27 Jun 2011 17:51:15 +0100</pubDate>
            <guid isPermaLink="false">4985714</guid>        </item>
        <item>
            <title>Tako-Tsubo Syndrome in a 12-Year-Old Girl: Exhausted Heart, Not Broken Heart</title>
            <link>http://www.medworm.com/index.php?rid=4985715&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fx1135738v4244n31%2F</link>
            <description>We report the case of a 12-year-old girl with Tako-tsubo cardiomyopathy. She was successfully treated in our Pediatric Intensive
 Care Unit for acute left ventricular failure, which occurred after a brief submersion in sea water. At 2-month follow-up she
 showed an almost complete recovery of cardiac function. We consider Tako-tsubo syndrome, which is rarely reported in the pediatric
 population, to be the most likely diagnosis.
 
 
	Content Type Journal ArticlePages 1-4DOI 10.1007/s00246-011-0038-1Authors
		Sandro Dessardo, University Hospital Center Rijeka, T. Strizica 3, 51000 Rijeka, CroatiaVjekoslav Tomulić, University Hospital Center Rijeka, T. Strizica 3, 51000 Rijeka, CroatiaNada Sindičić Dessardo, University Hospital Center Rijeka, T. Strizica 3, 51000 Rijeka, Croatia
	

	
		Jo...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4985715</comments>
            <pubDate>Mon, 27 Jun 2011 17:51:14 +0100</pubDate>
            <guid isPermaLink="false">4985715</guid>        </item>
        <item>
            <title>Quality of Life Experienced by Adolescents and Young Adults With Congenital Heart Disease</title>
            <link>http://www.medworm.com/index.php?rid=4985716&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fe035813741r26j20%2F</link>
            <description>This study aimed to assess the quality of life (QOL) experienced by adolescents and young adults with congenital heart disease
 (CHD) and to determine which factors negatively affect adjustment and which factors increase resilience. The participants
 in the study were 74 patients with CHD (41 males and 33 females) ranging in age from 12 to 26&amp;nbsp;years (mean age, 18.76&amp;nbsp;±&amp;nbsp;3.86&amp;nbsp;years).
 Demographic information and a complete clinical history were obtained. The participants were interviewed regarding topics
 such as social support, family educational style, self-image, and physical limitations. They responded to questions in a standardized
 psychiatric interview (SADS-L) and completed a self-report questionnaire (WHOQOL-BREF) for assessment of QOL. Compared with
 the Portugue...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4985716</comments>
            <pubDate>Mon, 27 Jun 2011 17:51:12 +0100</pubDate>
            <guid isPermaLink="false">4985716</guid>        </item>
        <item>
            <title>Upcoming Events in Pediatric Cardiology</title>
            <link>http://www.medworm.com/index.php?rid=4970150&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fv62n401200420373%2F</link>
            <description>Content Type Journal ArticlePages 1-1DOI 10.1007/s00246-011-0031-8

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4970150</comments>
            <pubDate>Tue, 21 Jun 2011 16:41:46 +0100</pubDate>
            <guid isPermaLink="false">4970150</guid>        </item>
        <item>
            <title>From Other Journals</title>
            <link>http://www.medworm.com/index.php?rid=4970149&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F534n3r7047l71m03%2F</link>
            <description>Content Type Journal ArticlePages 1-5DOI 10.1007/s00246-011-0030-9Authors
		Sanjiv Gandhi, 1507 W. Harrison St, Chicago, IL 60607, USAOmar M. Khalid, 1507 W. Harrison St, Chicago, IL 60607, USA
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4970149</comments>
            <pubDate>Tue, 21 Jun 2011 16:41:46 +0100</pubDate>
            <guid isPermaLink="false">4970149</guid>        </item>
        <item>
            <title>Congenital Aorta Right Atrial Fistula: Successful Transcatheter Closure With the Amplatzer Occluder</title>
            <link>http://www.medworm.com/index.php?rid=4946478&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F556670t36w117803%2F</link>
            <description>Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0026-5Authors
		Sharad Chandra, Department of Cardiology, Chhatarpati Shahuji Maharaj Medical University (CSMMU), King George Medical College (KGMC), Lucknow, IndiaSudarshan Vijay, Department of Cardiology, Chhatarpati Shahuji Maharaj Medical University (CSMMU), King George Medical College (KGMC), Lucknow, IndiaDaljeet Kaur, Department of Cardiology, Chhatarpati Shahuji Maharaj Medical University (CSMMU), King George Medical College (KGMC), Lucknow, IndiaSudhanshu Dwivedi, Department of Cardiology, Chhatarpati Shahuji Maharaj Medical University (CSMMU), King George Medical College (KGMC), Lucknow, India
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4946478</comments>
            <pubDate>Fri, 17 Jun 2011 12:01:39 +0100</pubDate>
            <guid isPermaLink="false">4946478</guid>        </item>
        <item>
            <title>Influence of Chromosome 22q11.2 Microdeletion on Postoperative Calcium Level After Cardiac-Correction Surgery</title>
            <link>http://www.medworm.com/index.php?rid=4946479&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F8lr0741638974830%2F</link>
            <description>This study included 22 children diagnosed with del22q11.2
 syndrome and 110 children without del22q11.2 syndrome from Nanjing Children’s Hospital. Clinical examinations and blood ionized
 calcium testing were reviewed retrospectively. A comparative study of postoperative calcium levels and complications of del22q11.2
 patients with nondeletion patients was performed. Association between postoperative hypocalcaemia and adverse incidents after
 cardiac correction was also examined. Postoperative hypocalcaemia was observed among 86.4% of del22q11.2 patients and among
 only 47.3% of nondeletion subjects. The difference was statistically significant (P&amp;nbsp;=&amp;nbsp;0.0017). Patients with del22q11.2 syndrome also had a much sharper decrease in serum calcium levels during the first 6&amp;nbsp;h
 aft...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4946479</comments>
            <pubDate>Thu, 16 Jun 2011 05:53:07 +0100</pubDate>
            <guid isPermaLink="false">4946479</guid>        </item>
        <item>
            <title>Takayasu’s Arteritis Mimicking Unilateral Pulmonary Artery Agenesis in a Child With Severe Pulmonary Hypertension and Right Heart Failure: A Diagnostic Dilemma</title>
            <link>http://www.medworm.com/index.php?rid=4946480&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F71u2k622632g260v%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Affliction of the pulmonary arteries in Takayasu’s arteritis is uncommon. Moreover the incidence of pulmonary artery involvement
 in this condition is often underestimated because of asymptomatic nature in most patients. Severe involvement may however
 present with pulmonary artery hypertension and hemoptysis, which may prove to be fatal. This case report describes a 9-year-old
 girl with severe pulmonary hypertension and right heart failure secondary to total occlusion of the right pulmonary artery.
 Detailed clinical examination and computed tomography (CT) angiography confirmed this diagnosis.
 
 
	Content Type Journal ArticlePages 1-5DOI 10.1007/s00246-011-0025-6Authors
		Sudeep Kumar, Department of Cardiology, Sanjay Gandhi Postgraduate Institute of Medical Scien...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4946480</comments>
            <pubDate>Wed, 15 Jun 2011 06:19:01 +0100</pubDate>
            <guid isPermaLink="false">4946480</guid>        </item>
        <item>
            <title>Significance of Circulating Hepatocyte Growth Factor in Protein-Losing Enteropathy After Fontan Operation</title>
            <link>http://www.medworm.com/index.php?rid=4936692&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fcmw2217v0431m48g%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;The purpose of this study was to measure serum hepatocyte growth factor (HGF) and elucidate the relationship between HGF and
 protein-losing enteropathy (PLE) after Fontan operation (FO). Ten patients with PLE (mean age 15.7&amp;nbsp;±&amp;nbsp;8.7&amp;nbsp;years) who underwent
 FO were enrolled. Control group 1 comprised 20 patients without PLE after FO, and control group 2 comprised 10 patients with
 nephrotic syndrome (NS). Serum HGF, vascular endothelial growth factor, albumin, and random stool alpha-1 antitrypsin concentration
 were measured. Transthoracic echocardiography was completed. Serum HGF level was significantly greater in the PLE patients
 (0.61&amp;nbsp;±&amp;nbsp;0.27&amp;nbsp;ng/ml) after FO than in the two control groups (0.41&amp;nbsp;±&amp;nbsp;0.12&amp;nbsp;ng/ml [P&amp;nbsp;=&amp;nbsp;0....</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4936692</comments>
            <pubDate>Sat, 11 Jun 2011 06:04:22 +0100</pubDate>
            <guid isPermaLink="false">4936692</guid>        </item>
        <item>
            <title>A Case of Left Main Pulmonary Artery Aneurysm Associated with Valvular Pulmonary Stenosis in a Child</title>
            <link>http://www.medworm.com/index.php?rid=4936691&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fl25250883n066261%2F</link>
            <description>We report here a pediatric case of left pulmonary artery aneurysm associated with valvular pulmonary stenosis and
 a hypoplastic right pulmonary artery, which we confirmed via multidetector computed tomography angiography.
 
 
	Content Type Journal ArticlePages 1-2DOI 10.1007/s00246-011-0021-xAuthors
		Ran Lee, Department of Pediatrics, School of Medicine, Konkuk University, Gwangjin-gu, Seoul, KoreaJae Sung Son, Department of Pediatrics, School of Medicine, Konkuk University, Gwangjin-gu, Seoul, KoreaYong Mean Park, Department of Pediatrics, School of Medicine, Konkuk University, Gwangjin-gu, Seoul, Korea
	

	
		Journal Pediatric CardiologyOnline ISSN 1432-1971Print ISSN 0172-0643 (Source: Pediatric Cardiology)</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4936691</comments>
            <pubDate>Sat, 11 Jun 2011 06:04:22 +0100</pubDate>
            <guid isPermaLink="false">4936691</guid>        </item>
        <item>
            <title>Oral Budesonide Treatment for Protein-Losing Enteropathy in Fontan-Palliated Patients</title>
            <link>http://www.medworm.com/index.php?rid=4936693&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2Fn583837412623397%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;Protein-losing enteropathy (PLE) is a rare complication of Fontan palliation associated with significant morbidity and mortality.
 It is characterized by the loss of serum proteins into the intestinal lumen, and its pathophysiology likely involves enteral
 inflammation. Budesonide, an oral steroid, is an attractive treatment option because of its potent enteral activity and minimal
 systemic side effects. A single-center, retrospective review of Fontan-palliated PLE patients treated with oral budesonide
 for 6&amp;nbsp;months or longer was performed. The patient characteristics reviewed were demographics, anatomic diagnosis, budesonide
 treatment (dose and duration), other medications and therapeutic interventions, hospitalizations, serum albumin levels, medical
 complicati...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4936693</comments>
            <pubDate>Fri, 10 Jun 2011 06:35:55 +0100</pubDate>
            <guid isPermaLink="false">4936693</guid>        </item>
        <item>
            <title>Unmasking of Neonatal Renovascular Hypertension by Milrinone Used for Cardiac Dysfunction</title>
            <link>http://www.medworm.com/index.php?rid=4923184&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F20650112729221q7%2F</link>
            <description>We present this case to
 alert clinicians to the rarer causes of left-ventricular dysfunction and to point out that its etiology, i.e., hypertension,
 may not be apparent until there is improvement in the systolic function of the left ventricle.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0027-4Authors
		Prema Ramaswamy, Division of Pediatric Cardiology, Maimonides Infants and Children’s Hospital of Brooklyn, Brooklyn, NY, USASusan Schulman, Department of Pediatrics, Maimonides Infants and Children’s Hospital of Brooklyn, Brooklyn, NY, USAPanayot Filipov, Division of Neonatology, Maimonides Infants and Children’s Hospital of Brooklyn, Brooklyn, NY, USAJuan C. Kupferman, Division of Pediatric Nephrology, Maimonides Infants and Children’s Hospital of Brooklyn, Br...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923184</comments>
            <pubDate>Wed, 08 Jun 2011 15:45:29 +0100</pubDate>
            <guid isPermaLink="false">4923184</guid>        </item>
        <item>
            <title>Total Anomalous Pulmonary Venous Drainage Complicated by Tracheoesophageal Fistula</title>
            <link>http://www.medworm.com/index.php?rid=4923185&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F1482r18044702601%2F</link>
            <description>Abstract&amp;nbsp;&amp;nbsp;We provided emergency treatment to a 1-day-old neonate (1600&amp;nbsp;g) with tracheoesophageal fistula (gross classification, type
 C) and total anomalous pulmonary venous drainage (infracardiac type) complicated by pulmonary venous obstruction. Emergency
 surgery was required because the tracheoesophageal fistula would have caused respiratory failure. Here we report the perioperative
 management techniques we used, including the surgical strategy.
 
 
	Content Type Journal ArticlePages 1-3DOI 10.1007/s00246-011-0011-zAuthors
		Toru Okamura, Department of Cardiovascular Surgery, School of Medicine, Ehime University, Shitsukawa, Toon city, Ehime 791-0295, JapanMitsugi Nagashima, Department of Cardiovascular Surgery, School of Medicine, Ehime University, Shitsukawa, Toon cit...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923185</comments>
            <pubDate>Wed, 08 Jun 2011 15:45:27 +0100</pubDate>
            <guid isPermaLink="false">4923185</guid>        </item>
        <item>
            <title>Establishment of Secondary Iron Overloaded Mouse Model: Evaluation of Cardiac Function and Analysis According to Iron Concentration</title>
            <link>http://www.medworm.com/index.php?rid=4923187&amp;cid=s_33303_7_f&amp;fid=33303&amp;url=http%3A%2F%2Fwww.springerlink.com%2Fcontent%2F041440545g0rn213%2F</link>
            <description>In this study, we established murine model of secondary iron overload, studied the changes
 in cardiac function with echocardiography, and examined the histopathologic changes. Three experimental groups of the six
 week-old C57/BL mice (H-2b) were injected intraperitoneally with 10&amp;nbsp;mg of iron dextran daily 5&amp;nbsp;days a week for 2, 4, and 6&amp;nbsp;weeks. Cumulative doses of
 iron for the three experimental groups were 100, 200, and 300&amp;nbsp;mg, while the control groups were injected with the same amounts
 of phosphate-buffered saline. We studied the cardiac function under anesthesia with echocardiography using a GE Vivid7 Dimension
 system. Plasma iron levels and liver iron contents were measured. The hearts and livers were harvested and stained with H&amp;E
 and Perls Prussian blue for iro...</description>
            <author>Pediatric Cardiology</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4923187</comments>
            <pubDate>Wed, 08 Jun 2011 15:45:26 +0100</pubDate>
            <guid isPermaLink="false">4923187</guid>        </item>
    </channel>
</rss>

