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        <title>Paediatric Drugs 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 'Paediatric Drugs' source.</description>
        <link><![CDATA[http://www.medworm.com/rss/search.php?qu=Paediatric+Drugs&t=Paediatric+Drugs&s=Search&f=source]]></link>
        <lastBuildDate>Thu, 09 Feb 2012 01:09:39 +0100</lastBuildDate>
        <item>
            <title>Everolimus: in patients with subependymal giant cell astrocytoma associated with tuberous sclerosis complex.</title>
            <link>http://www.medworm.com/index.php?rid=5520715&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22136276%26dopt%3DAbstract</link>
            <description>Authors: Curran MP
    Abstract
    Everolimus is an orally administered inhibitor of the mammalian target of rapamycin (mTOR). Everolimus (starting dosage 3.0 mg/m2) was associated with a significant reduction in the volume of the largest subependymal giant cell astrocytoma (SEGA) in 28 patients aged ≥3 years with tuberous sclerosis complex (TSC) in a phase II trial (C2485). At 6 months, 32% of patients treated with everolimus had a ≥50% reduction in the volume of their largest SEGA lesion (assessed via an independent central radiology review); 75% had a ≥30% reduction. No patients developed new lesions. During the extension phase of this trial (median duration 34 months), the reduction in SEGA volume was maintained, with no everolimus recipient requiring surgery or other therapy ...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520715</comments>
            <pubDate>Tue, 20 Dec 2011 13:13:34 +0100</pubDate>
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        <item>
            <title>Drug exposure and pregnancy outcome in mozambique.</title>
            <link>http://www.medworm.com/index.php?rid=5520714&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22145781%26dopt%3DAbstract</link>
            <description>Conclusions: Drug exposure during pregnancy, including drugs with recognized potential pregnancy risk, was high in this rural area of southern Africa. The association of stillbirths with drug exposure might be a consequence of the disease that led to drug administration, although a direct causality of the drugs cannot be excluded. These findings emphasize the need for reinforcing pharmacovigilance systems in rural Africa, especially, or at least, in pregnant women.
    PMID: 22145781 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520714</comments>
            <pubDate>Tue, 20 Dec 2011 13:13:25 +0100</pubDate>
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        <item>
            <title>Defining juvenile idiopathic arthritis remission and optimum time for disease-modifying anti-rheumatic drug withdrawal: why we need a consensus.</title>
            <link>http://www.medworm.com/index.php?rid=5520713&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22149548%26dopt%3DAbstract</link>
            <description>Authors: Broughton T, Armon K
    Abstract
    Juvenile idiopathic arthritis (JIA) is an autoimmune disease of childhood requiring treatment with immune modulation therapy. It runs a relapsing and remitting course, with approximately half of affected children continuing with active disease into adult life. Defining clinical remission is challenging, but necessary, as it is critical in determining when potentially toxic therapy can be stopped. We found that preliminary consensus criteria for defining JIA remission are not being used in full by a representative sample of UK pediatric rheumatologists. Extending the period of remission, whilst on synthetic disease-modifying anti-rheumatic drug (DMARD) medication, beyond 6 months does not seem to reduce the risk of relapse once medication is st...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520713</comments>
            <pubDate>Tue, 20 Dec 2011 13:13:17 +0100</pubDate>
            <guid isPermaLink="false">5520713</guid>        </item>
        <item>
            <title>Anesthetic-related neurotoxicity and the developing brain: shall we change practice?</title>
            <link>http://www.medworm.com/index.php?rid=5520712&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22149549%26dopt%3DAbstract</link>
            <description>Authors: Vutskits L
    Abstract
    Millions of human infants receive general anesthetics for surgery or diagnostic procedures every year worldwide, and there is a growing inquietude regarding the safety of these drugs for the developing brain. In fact, accumulating experimental evidence together with recent epidemiologic observations suggest that general anesthetics might exert undesirable effects on the immature nervous system. The goal of this review is to highlight basic science issues as well as to critically present experimental data and clinical observations relevant to this possibility. By acting on a plethora of ligand-gated ion channels, general anesthetics are powerful modulators of neural activity. Since even brief interference with physiologic activity patterns during critica...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520712</comments>
            <pubDate>Tue, 20 Dec 2011 13:13:08 +0100</pubDate>
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        <item>
            <title>Celiac disease in pediatric patients with autoimmune hepatitis: etiology, diagnosis, and management.</title>
            <link>http://www.medworm.com/index.php?rid=5520711&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22149550%26dopt%3DAbstract</link>
            <description>Authors: Panetta F, Nobili V, Sartorelli MR, Papa RE, Ferretti F, Alterio A, Diamanti A
    Abstract
    Celiac disease (CD) is defined as a permanent intolerance to ingested wheat gliadins and other cereal prolamins, occurring in genetically susceptible people. Persistent elevation of serum aminotransferase activity is expression of liver damage related to CD, which occurs in two distinctive forms. The most frequent is a mild asymptomatic liver injury, with a moderate increase of serum aminotransferase activities and a mild inflammatory portal and lobular infiltrate on liver biopsy (celiac hepatitis), reversible on a gluten-free diet (GFD). More rarely, severe and progressive inflammatory liver damage, induced by an autoimmune process and identified as autoimmune hepatitis (AIH), can deve...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520711</comments>
            <pubDate>Tue, 20 Dec 2011 13:12:58 +0100</pubDate>
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        <item>
            <title>Candesartan cilexetil in children and adolescents aged 1 to</title>
            <link>http://www.medworm.com/index.php?rid=5520710&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22149551%26dopt%3DAbstract</link>
            <description>Authors: Hoy SM, Keating GM
    Abstract
    † Adapted and reproduced from the original article published in American Journal of Cardiovascular Drugs 2010; 10 (5): 335-42.[1].
    PMID: 22149551 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520710</comments>
            <pubDate>Tue, 20 Dec 2011 13:12:49 +0100</pubDate>
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        <item>
            <title>Meningococcal quadrivalent (serogroups a, C, w135, and y) conjugate vaccine (menveo®)†: profile report.</title>
            <link>http://www.medworm.com/index.php?rid=5520709&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22149552%26dopt%3DAbstract</link>
            <description>Authors: Deeks ED
    Abstract
    † Adapted and reproduced from the original article published in BioDrugs 2010; 24 (5): 287-97.[1].
    PMID: 22149552 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520709</comments>
            <pubDate>Tue, 20 Dec 2011 13:12:40 +0100</pubDate>
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        <item>
            <title>Pneumococcal polysaccharide conjugate vaccine (13-valent, adsorbed) [prevenar 13®]†: profile report.</title>
            <link>http://www.medworm.com/index.php?rid=5520708&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22149553%26dopt%3DAbstract</link>
            <description>Authors: Duggan ST
    Abstract
    † Adapted and reproduced from the original article published in Drugs 2010; 70 (15): 1973-86.
    PMID: 22149553 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520708</comments>
            <pubDate>Tue, 20 Dec 2011 13:12:30 +0100</pubDate>
            <guid isPermaLink="false">5520708</guid>        </item>
        <item>
            <title>Medical Management of Nocturnal Enuresis.</title>
            <link>http://www.medworm.com/index.php?rid=5520707&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D22168597%26dopt%3DAbstract</link>
            <description>Authors: Deshpande AV, Caldwell PH
    Abstract
    Nocturnal enuresis, or bedwetting, is the most common cause of urinary incontinence in children. It is known to have a significant psychosocial impact on the child as well as the family. Nocturnal enuresis typically presents as failure to become dry at night after successful daytime toilet training. It can be primary or secondary (developing after being successfully dry at night for at least 6 months). Children with nocturnal enuresis may have excessive nocturnal urine production, poor sleep arousal and/or reduced bladder capacity. Alarm therapy is the recommended first-line therapy, with treatment choices being influenced by the presence or absence of the abnormalities mentioned above. Children with nocturnal enuresis may also have dayti...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5520707</comments>
            <pubDate>Wed, 14 Dec 2011 05:00:00 +0100</pubDate>
            <guid isPermaLink="false">5520707</guid>        </item>
        <item>
            <title>Acknowledgment.</title>
            <link>http://www.medworm.com/index.php?rid=5385328&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999647%26dopt%3DAbstract</link>
            <description>Authors: 
    PMID: 21999647 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5385328</comments>
            <pubDate>Wed, 09 Nov 2011 14:01:36 +0100</pubDate>
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        <item>
            <title>Pediatric drug-resistant tuberculosis: a global perspective.</title>
            <link>http://www.medworm.com/index.php?rid=5385327&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999648%26dopt%3DAbstract</link>
            <description>This article was based on a presentation given at the 26th International Pediatric Association Conference of Pediatrics, Johannesburg, South Africa, 4-9 August 2010. In 2009, there were 9.4 million new cases of tuberculosis (TB) globally, and, of these, approximately 1 million were pediatric cases. Drug-resistant TB makes up a relatively small proportion of new TB cases, but is much more likely in previously treated cases. Pediatric TB remains difficult to diagnose microbiologically, with the result that detection of drug-resistant TB in children is an ongoing challenge. Since children diagnosed with TB predominantly represent recently acquired TB infection, they provide an important indication of drug-resistant TB prevalence and transmission within their communities. Drug-resistant TB...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5385327</comments>
            <pubDate>Wed, 09 Nov 2011 14:00:38 +0100</pubDate>
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        <item>
            <title>Medical management of chronic liver diseases in children (part I): focus on curable or potentially curable diseases.</title>
            <link>http://www.medworm.com/index.php?rid=5364605&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999649%26dopt%3DAbstract</link>
            <description>Authors: El-Shabrawi MH, Kamal NM
    Abstract
    The management of children with chronic liver disease (CLD) mandates a multidisciplinary approach. CLDs can be classified into 'potentially' curable, treatable non-curable, and end-stage diseases. Goals pertaining to the management of CLDs can be divided into prevention or minimization of progressive liver damage in curable CLD by treating the primary cause; prevention or control of complications in treatable CLD; and prediction of the outcome in end-stage CLD in order to deliver definitive therapy by surgical procedures, including liver transplantation. Curative, specific therapies aimed at the primary causes of CLDs are, if possible, best considered by a pediatric hepatologist. Medical management of CLDs in children will be reviewed in t...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5364605</comments>
            <pubDate>Thu, 03 Nov 2011 11:06:57 +0100</pubDate>
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        <item>
            <title>Medical Management of Chronic Liver Diseases (CLD) in Children (Part II): Focus on the Complications of CLD, and CLD that Require Special Considerations.</title>
            <link>http://www.medworm.com/index.php?rid=5364604&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999650%26dopt%3DAbstract</link>
            <description>Authors: El-Shabrawi MH, Kamal NM
    Abstract
    Treatment of the causes of many chronic liver diseases (CLDs) may not be possible. In this case, complications must be anticipated, prevented or at least controlled by the best available therapeutic modalities. There are three main goals for the management of portal hypertension: (i) prevention of the first episode of variceal bleeding largely by non-selective β-adrenoceptor antagonists, which is not generally recommended in children; (ii) control of bleeding by using a stepwise approach from the least to most invasive strategies; (iii) and prevention of re-bleeding using bypass operations, with particular enthusiasm for the use of meso-Rex bypass in the pediatric population. Hepatic encephalopathy management also consists of three main a...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5364604</comments>
            <pubDate>Thu, 03 Nov 2011 11:05:08 +0100</pubDate>
            <guid isPermaLink="false">5364604</guid>        </item>
        <item>
            <title>Acute bacterial meningitis in infants and children: epidemiology and management.</title>
            <link>http://www.medworm.com/index.php?rid=5364603&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999651%26dopt%3DAbstract</link>
            <description>Authors: Agrawal S, Nadel S
    Abstract
    Acute bacterial meningitis (ABM) continues to be associated with high mortality and morbidity, despite advances in antimicrobial therapy. The causative organism varies with age, immune function, immunization status, and geographic region, and empiric therapy for meningitis is based on these factors. Haemophilus influenzae type b (Hib), Streptococcus pneumoniae, and Neisseria meningitidis cause the majority of cases of ABM. Disease epidemiology is changing rapidly due to immunization practices and changing bacterial resistance patterns. Hib was the leading cause of meningitis in children prior to the introduction of an effective vaccination. In those countries where Hib vaccine is a part of the routine infant immunization schedule, Hib has now be...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5364603</comments>
            <pubDate>Thu, 03 Nov 2011 11:03:08 +0100</pubDate>
            <guid isPermaLink="false">5364603</guid>        </item>
        <item>
            <title>DTaP(5)-IPV-Hib Vaccine (Pediacel®).</title>
            <link>http://www.medworm.com/index.php?rid=5364602&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999652%26dopt%3DAbstract</link>
            <description>Authors: Frampton JE
    Abstract
    Pediacel® is a fully liquid formulation of a diphtheria, tetanus, five-component acellular pertussis, inactivated poliovirus and Haemophilus influenzae type b combination vaccine, which does not require reconstitution. Both vial and prefilled syringe presentations of Pediacel® are available for use in the EU. In active-controlled clinical trials, primary and/or booster vaccination with Pediacel® was highly immunogenic, eliciting strong and sustained serologic responses against all its component toxoids/antigens when administered according to a variety of different schedules. In particular, pivotal studies showed that Pediacel® was generally similar and/or noninferior to reconstituted pentavalent and hexavalent diphtheria, tetanus, and acellular per...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5364602</comments>
            <pubDate>Thu, 03 Nov 2011 11:01:28 +0100</pubDate>
            <guid isPermaLink="false">5364602</guid>        </item>
        <item>
            <title>Pharmacovigilance in Pediatrics: Current Challenges.</title>
            <link>http://www.medworm.com/index.php?rid=5385329&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21999612%26dopt%3DAbstract</link>
            <description>Authors: Neubert A
    PMID: 21999612 [PubMed - as supplied by publisher] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5385329</comments>
            <pubDate>Fri, 14 Oct 2011 04:00:00 +0100</pubDate>
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        <item>
            <title>The worldwide opioid epidemic: implications for treatment and research in pregnancy and the newborn.</title>
            <link>http://www.medworm.com/index.php?rid=5199647&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21888441%26dopt%3DAbstract</link>
            <description>Authors: Knoppert D
    PMID: 21888441 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5199647</comments>
            <pubDate>Sat, 10 Sep 2011 17:47:14 +0100</pubDate>
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        <item>
            <title>Drug treatment of hypertensive crisis in children.</title>
            <link>http://www.medworm.com/index.php?rid=5199646&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21888442%26dopt%3DAbstract</link>
            <description>Authors: Thomas CA
    Abstract
    Hypertensive crisis is a relatively rare event and is associated with significant morbidity and mortality in adults and pediatric patients alike. Rapid, safe, and effective treatment is imperative to alleviate immediate presenting clinical symptoms, prevent devastating morbidity, preserve long-term quality of life, and prevent mortality. Many medications in the hypertensive crisis arsenal have been used for nearly half a century. Nearly all treatment options have been utilized in children for decades, yet reliable data and sound clinical literature remain elusive. Every agent considered to be a first-line, second-line, or adjunctive option has yet to be evaluated in a randomized controlled trial in pediatric patients. With a paucity of clinical data to f...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5199646</comments>
            <pubDate>Sat, 10 Sep 2011 17:47:04 +0100</pubDate>
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        <item>
            <title>Clinical usefulness of second-generation antipsychotics in treating children and adolescents diagnosed with bipolar or schizophrenic disorders.</title>
            <link>http://www.medworm.com/index.php?rid=5199645&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21888443%26dopt%3DAbstract</link>
            <description>Authors: Gentile S
    Abstract
    The onset of severe, chronic or recurrent psychiatric illnesses, such as schizophrenia-spectrum and bipolar disorders, is a dramatic clinical event often detectable during adolescence and even in childhood. At any age, pharmacotherapy, along with enhancement of social skills and family support, is the mainstay for the management of such disorders. The aim of this review is to critically analyze findings from randomized controlled trials (RCTs) that have investigated the clinical utility of second-generation antipsychotics (SGAs) for the treatment of early-onset schizophrenia and bipolar disorders. Eighteen studies were considered, all of which were unfortunately impaired by methodologic limitations, such as the paucity of long-term data and lack of a thr...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5199645</comments>
            <pubDate>Sat, 10 Sep 2011 17:46:54 +0100</pubDate>
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        <item>
            <title>Antiretroviral therapy for children in resource-limited settings: current regimens and the role of newer agents.</title>
            <link>http://www.medworm.com/index.php?rid=5199644&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21888444%26dopt%3DAbstract</link>
            <description>Authors: Eley BS, Meyers T
    Abstract
    WHO antiretroviral treatment guidelines for HIV-infected children have influenced the design of treatment programmes in resource-limited settings. This review analyses the latest WHO first- and second-line regimen recommendations. The recommendation to use lopinavir/ritonavir-containing first-line regimens in young children with prior non-nucleoside reverse transcriptase inhibitor (NNRTI) exposure is based on good quality evidence. Recent research suggests that lopinavir/ritonavir-containing first-line regimens should be extended to all young children, irrespective of prior NNRTI exposure. Strategies for overcoming the adverse metabolic effects of rifampicin-containing anti-tuberculosis therapy on antiretroviral therapy regimens have been under-r...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5199644</comments>
            <pubDate>Sat, 10 Sep 2011 17:46:44 +0100</pubDate>
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        <item>
            <title>Drug Exposure during the Periconceptional Period: A Study of 1793 Women.</title>
            <link>http://www.medworm.com/index.php?rid=5199643&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21888445%26dopt%3DAbstract</link>
            <description>Conclusions: During the highest teratogenic risk period, 1.1% of women received a contraindicated drug, despite existence of a safer alternative drug. This may be partly accounted for by physicians not being aware of the pregnancy at the time the drug was administered and could be reduced by adding a section entitled 'women of child-bearing potential' to the SPC.
    PMID: 21888445 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5199643</comments>
            <pubDate>Sat, 10 Sep 2011 17:46:34 +0100</pubDate>
            <guid isPermaLink="false">5199643</guid>        </item>
        <item>
            <title>47th Annual Meeting of the American Society of Clinical Oncology (ASCO), Chicago, IL, USA, 3-7 June 2011: Focus on Pediatric Oncology.</title>
            <link>http://www.medworm.com/index.php?rid=5199642&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21888446%26dopt%3DAbstract</link>
            <description>Authors: Wilde MI
    PMID: 21888446 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5199642</comments>
            <pubDate>Sat, 10 Sep 2011 17:46:24 +0100</pubDate>
            <guid isPermaLink="false">5199642</guid>        </item>
        <item>
            <title>Clonidine extended-release: in attention-deficit hyperactivity disorder.</title>
            <link>http://www.medworm.com/index.php?rid=5199641&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21888447%26dopt%3DAbstract</link>
            <description>Authors: Croxtall JD
    Abstract
    Clonidine, an α(2)-adrenergic agonist, is approved in the US as an extended-release (XR) tablet for the treatment of attention-deficit hyperactivity disorder (ADHD) in children and adolescents (aged 6-17 years). In two, randomized, double-blind, multicenter, phase III trials of 8 weeks' duration, clonidine XR improved the symptoms of ADHD in children and adolescents. Significantly greater reductions from baseline in ADHD rating scale IV (ADHD-RS-IV) total scores at week 5 (primary endpoint) were achieved by recipients of clonidine XR 0.2 and 0.4 mg/day monotherapy than by recipients of placebo. When added to patients' normal stimulant regimen, significantly greater reductions from baseline in ADHD-RS-IV total scores at week 5 (primary endpoint) were...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5199641</comments>
            <pubDate>Sat, 10 Sep 2011 17:46:14 +0100</pubDate>
            <guid isPermaLink="false">5199641</guid>        </item>
        <item>
            <title>17 α-Hydroxyprogesterone Caproate (Makena™): In the Prevention of Preterm Birth.</title>
            <link>http://www.medworm.com/index.php?rid=5199640&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21888448%26dopt%3DAbstract</link>
            <description>Authors: Deeks ED
    Abstract
    17 α-hydroxyprogesterone caproate is a synthetic progestin of which there is now a US FDA-approved formulation available for intramuscular administration (Makena™) to reduce the risk of preterm birth. Intramuscular 17 α-hydroxyprogesterone caproate (identical in formulation and manufacturing process to Makena™, thus hereafter referred to as Makena™) 250 mg once weekly, initiated at 16-20 weeks' gestation, was effective in reducing the risk of preterm birth in women with a singleton pregnancy at high risk of delivering preterm in a large, well designed, placebo-controlled trial (n = 463 randomized). Rates of delivery before 37 (primary endpoint), 35, or 32 weeks' gestation were significantly lower with Makena™ than with placebo, correspondi...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=5199640</comments>
            <pubDate>Sat, 10 Sep 2011 17:46:04 +0100</pubDate>
            <guid isPermaLink="false">5199640</guid>        </item>
        <item>
            <title>Genetic susceptibility in sepsis: implications for the pediatric population.</title>
            <link>http://www.medworm.com/index.php?rid=4983447&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692545%26dopt%3DAbstract</link>
            <description>Authors: Nadel S
    
    PMID: 21692545 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4983447</comments>
            <pubDate>Thu, 30 Jun 2011 10:30:30 +0100</pubDate>
            <guid isPermaLink="false">4983447</guid>        </item>
        <item>
            <title>Management of immune thrombocytopenic purpura in children: potential role of novel agents.</title>
            <link>http://www.medworm.com/index.php?rid=4983446&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692546%26dopt%3DAbstract</link>
            <description>Authors: Bredlau AL, Semple JW, Segel GB
    The treatment of immune thrombocytopenic purpura (ITP) in children is controversial, requiring individualized assessment of the patient and consideration of treatment options. If the platelet count is &amp;gt;10 000/μL and the patient is asymptomatic, a 'watch and wait' strategy is appropriate since most children with ITP will recover completely without pharmacotherapy. If therapy is indicated because of bleeding or a platelet count &amp;lt;10 000/μL, then treatment with glucocorticoids, intravenous immunoglobulin (IVIg), or anti-D are possible initial choices. Glucocorticoid treatment is the least expensive and is our usual first choice of therapy. Its use assumes that the blood counts and blood film have been evaluated to ensure the absence of e...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4983446</comments>
            <pubDate>Thu, 30 Jun 2011 10:30:25 +0100</pubDate>
            <guid isPermaLink="false">4983446</guid>        </item>
        <item>
            <title>Antidepressants and Psychostimulants in Pediatric Populations: Is there an Association with Mania?</title>
            <link>http://www.medworm.com/index.php?rid=4983445&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692547%26dopt%3DAbstract</link>
            <description>This article reviews the literature that examines whether exposure to psychostimulants or antidepressants precipitates or exacerbates manic symptoms, or decreases the age at onset of mania in pediatric populations. A PubMed search using relevant key words identified studies targeting five distinct clinical groups: (i) youth without a diagnosis of bipolar disorder (BD) at the time of exposure to psychostimulants; (ii) youth with a diagnosis of BD at the time of exposure to psychostimulants; (iii) youth without a diagnosis of BD at the time of exposure to antidepressants; (iv) youth with a diagnosis of BD at the time of exposure to antidepressants; and (v) youth who develop BD after exposure to these medications. In patients with attention-deficit hyperactivity disorder (ADHD), the risk for ...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4983445</comments>
            <pubDate>Thu, 30 Jun 2011 10:30:21 +0100</pubDate>
            <guid isPermaLink="false">4983445</guid>        </item>
        <item>
            <title>Pharmacologic management of high-risk neuroblastoma in children.</title>
            <link>http://www.medworm.com/index.php?rid=4983444&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692548%26dopt%3DAbstract</link>
            <description>Authors: Ganeshan VR, Schor NF
    Neuroblastoma is the most common extracranial solid tumor of childhood. It accounts for 15% of pediatric cancer deaths. Children with high-risk disease have a 3-year event-free survival rate of only 20%. Chemotherapy is the mainstay of treatment in children with advanced neuroblastoma. The aim of this article was to review and critically evaluate the pharmacotherapy of neuroblastoma, using peer reviewed and review literature from 2000-11. All peer reviewed, published human subject studies of therapy for neuroblastoma in children were included. Animal model and in vitro studies were included only if they added to the understanding of the mechanism of a proposed or existing human neuroblastoma therapy. Current therapeutic options for neuroblastoma involve i...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4983444</comments>
            <pubDate>Thu, 30 Jun 2011 10:30:16 +0100</pubDate>
            <guid isPermaLink="false">4983444</guid>        </item>
        <item>
            <title>Pediatric clinical trials in latin america and guyana: present views of local practitioners and ways to embrace the future.</title>
            <link>http://www.medworm.com/index.php?rid=4983443&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692549%26dopt%3DAbstract</link>
            <description>Conclusion: The survey indicated a considerable depth of interest in the improvement of the pediatric clinical research environment in Latin America. There is some momentum toward the development of a Latin American network for the facilitation and supervision of pediatric clinical research.
    PMID: 21692549 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4983443</comments>
            <pubDate>Thu, 30 Jun 2011 10:30:12 +0100</pubDate>
            <guid isPermaLink="false">4983443</guid>        </item>
        <item>
            <title>Long-term follow-up of statin treatment in a cohort of children with familial hypercholesterolemia: efficacy and tolerability.</title>
            <link>http://www.medworm.com/index.php?rid=4983442&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21692550%26dopt%3DAbstract</link>
            <description>Conclusions: In this large cohort of FH children, the efficacy and tolerability of pravastatin therapy in real-life conditions was demonstrated to be similar to that in randomized controlled studies.
    PMID: 21692550 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4983442</comments>
            <pubDate>Thu, 30 Jun 2011 10:30:07 +0100</pubDate>
            <guid isPermaLink="false">4983442</guid>        </item>
        <item>
            <title>Better medicines for 300 million children in china: report on recent progress.</title>
            <link>http://www.medworm.com/index.php?rid=4780520&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21500867%26dopt%3DAbstract</link>
            <description>Authors: Li Z, Wang L, Wang Y, Gui YH, Vinks AA, Macleod S
    
    PMID: 21500867 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4780520</comments>
            <pubDate>Wed, 04 May 2011 08:15:59 +0100</pubDate>
            <guid isPermaLink="false">4780520</guid>        </item>
        <item>
            <title>Targeting airway inflammation in cystic fibrosis in children: past, present, and future.</title>
            <link>http://www.medworm.com/index.php?rid=4780519&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21500868%26dopt%3DAbstract</link>
            <description>Authors: Pressler T
    Inflammation is a major component of the vicious cycle characterizing cystic fibrosis (CF) pulmonary disease. If untreated, this inflammatory process irreversibly damages the airways, leading to bronchiectasis and ultimately respiratory failure. Anti-inflammatory drugs for CF lung disease appear to have beneficial effects on disease progression. These agents include oral corticosteroids and ibuprofen, as well as azithromycin, which, in addition to its antimicrobial effects, also possess anti-inflammatory properties. Inhaled corticosteroids, antioxidants, nutritional supplements, and protease inhibitors have a limited impact on the disease. Adverse effects limit therapy with oral corticosteroids and ibuprofen. Azithromycin appears to be safe and effective, and is thu...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4780519</comments>
            <pubDate>Wed, 04 May 2011 08:15:46 +0100</pubDate>
            <guid isPermaLink="false">4780519</guid>        </item>
        <item>
            <title>Intestinal transplantation in children: a review of immunotherapy regimens.</title>
            <link>http://www.medworm.com/index.php?rid=4780518&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21500869%26dopt%3DAbstract</link>
            <description>Authors: Nayyar NS, McGhee W, Martin D, Sindhi R, Soltys K, Bond G, Mazariegos GV
    This review summarizes the outcomes and known adverse effects of current immunosuppression strategies in use in pediatric intestinal transplantation. Intestinal transplantation has evolved from an experimental therapy to a highly successful treatment for children with intestinal failure who have complications with total parenteral nutrition. Because of continued success with intestinal transplantation over the past decade, the focus of clinicians and researchers is shifting from short-term patient survival to optimizing long-term outcomes. Current 5-year patient and graft survival rates after intestinal transplantation are 58% and 40%, respectively, in the US; single centers have reported nearly 80% patie...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4780518</comments>
            <pubDate>Wed, 04 May 2011 08:15:23 +0100</pubDate>
            <guid isPermaLink="false">4780518</guid>        </item>
        <item>
            <title>Juvenile idiopathic arthritis: new insights into classification, measures of outcome, and pharmacotherapy.</title>
            <link>http://www.medworm.com/index.php?rid=4780517&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21500870%26dopt%3DAbstract</link>
            <description>Authors: Beresford MW
    Significant advances have taken place in recent years in our understanding of the aetiopathogenesis, management, and clinical outcome of juvenile idiopathic arthritis (JIA). Fundamental to this advancement has been international collaborative efforts of the clinical scientific community and all those involved in the multidisciplinary care of children and young people with JIA. A key factor has been facing the challenge of developing a robust classification system for JIA, a clinically very heterogeneous group of conditions. JIA illustrates the necessity of disease classification to enable scientific progress but also the iterative and evolving process this entails. What is emerging is the imperative to improve our understanding of the biologic and genetic basis of...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4780517</comments>
            <pubDate>Wed, 04 May 2011 08:15:19 +0100</pubDate>
            <guid isPermaLink="false">4780517</guid>        </item>
        <item>
            <title>Addendum.</title>
            <link>http://www.medworm.com/index.php?rid=4780516&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21500871%26dopt%3DAbstract</link>
            <description>Authors: 
    
    PMID: 21500871 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4780516</comments>
            <pubDate>Wed, 04 May 2011 08:15:15 +0100</pubDate>
            <guid isPermaLink="false">4780516</guid>        </item>
        <item>
            <title>Antiretroviral Drugs in Pediatric HIV-Infected Patients: Pharmacokinetic and Practical Challenges.</title>
            <link>http://www.medworm.com/index.php?rid=4780515&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21500872%26dopt%3DAbstract</link>
            <description>Authors: Phelps BR, Rakhmanina N
    Antiretroviral (ARV) therapy has been shown to achieve high therapeutic efficacy in treating pediatric HIV disease. The delivery of affordable, child friendly, and easy to store and administer ARV drugs is key to the successful management of HIV in children. In recent years, significant progress has been made in scaling up the access to pediatric ARV therapy among children worldwide. Despite the improved ARV drug access, multiple challenges remain concerning palatability and efficient delivery of ARV drugs to children from infancy into adolescence. Data are limited regarding developmental changes in pharmacokinetics of individual ARV drugs, and pediatric and adult fixed-dose combinations. This review provides a practical discussion regarding the pharmac...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4780515</comments>
            <pubDate>Wed, 04 May 2011 08:15:11 +0100</pubDate>
            <guid isPermaLink="false">4780515</guid>        </item>
        <item>
            <title>Aripiprazole: in the treatment of irritability associated with autistic disorder in pediatric patients.</title>
            <link>http://www.medworm.com/index.php?rid=4780514&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21500873%26dopt%3DAbstract</link>
            <description>Authors: Curran MP
    Aripiprazole is an atypical antipsychotic approved for the treatment of irritability associated with autistic disorder in pediatric patients aged 6-17 years. In two, randomized, double-blind, placebo-controlled studies in pediatric patients aged 6-17 years with irritability associated with autistic disorder, 8 weeks of treatment with aripiprazole 2-15 mg/day, compared with placebo, resulted in significant improvements in the Aberrant Behavior Checklist Irritability subscale score at endpoint (primary endpoint), and the mean Clinical Global Impression-Improvement score. Aripiprazole was generally well tolerated in this patient population in the two 8-week studies and a 52-week study, with most adverse events being mild to moderate in severity. Aripiprazole was assoc...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4780514</comments>
            <pubDate>Wed, 04 May 2011 08:15:07 +0100</pubDate>
            <guid isPermaLink="false">4780514</guid>        </item>
        <item>
            <title>Detecting unexpected adverse drug reactions in children.</title>
            <link>http://www.medworm.com/index.php?rid=4554094&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21351806%26dopt%3DAbstract</link>
            <description>Authors: Star K
    
    PMID: 21351806 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554094</comments>
            <pubDate>Mon, 07 Mar 2011 03:45:57 +0100</pubDate>
            <guid isPermaLink="false">4554094</guid>        </item>
        <item>
            <title>Multisystem langerhans cell histiocytosis in children: current treatment and future directions.</title>
            <link>http://www.medworm.com/index.php?rid=4554093&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21351807%26dopt%3DAbstract</link>
            <description>Authors: Minkov M
    Langerhans cell histiocytosis (LCH) is a rare (about 3-5 cases per million children aged 0-14 years), non-malignant disease characterized by proliferation and accumulation of clonal dendritic cells, extreme clinical heterogeneity, and an unpredictable course. Three large-scale, international, prospective therapeutic studies (LCH-I to III) for multisystem LCH (MS-LCH) have been conducted by the Histiocyte Society since 1991. The cumulative lessons from these studies are summarized in this review. Patients with MS-LCH represent a heterogeneous group with respect to disease severity and outcome, therefore treatment stratification and risk-tailored treatment are mandatory. The risk for mortality can be predicted based on involvement of 'risk organs' (e.g. hematopoietic sy...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554093</comments>
            <pubDate>Mon, 07 Mar 2011 03:45:51 +0100</pubDate>
            <guid isPermaLink="false">4554093</guid>        </item>
        <item>
            <title>Current management of primary sclerosing cholangitis in pediatric patients.</title>
            <link>http://www.medworm.com/index.php?rid=4554092&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21351808%26dopt%3DAbstract</link>
            <description>Authors: Ibrahim SH, Lindor KD
    Primary sclerosing cholangitis (PSC) is a chronic cholestatic condition affecting the extrahepatic and intrahepatic biliary tree. The incidence is seemingly increasing in children as a result of increased use of cholangiographic screening techniques in children with inflammatory bowel disease. The clinical presentation of PSC in childhood is variable and frequently without obvious cholestatic features, and cholangiography is essential for the diagnosis of this disorder. Histologic findings may help to exclude autoimmune sclerosing cholangitis. The underlying pathogenesis remains poorly understood and, as a result, therapeutic agents that halt disease progression and improve prognosis are lacking. PSC treatment is mainly supportive and directed at controll...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554092</comments>
            <pubDate>Mon, 07 Mar 2011 03:45:46 +0100</pubDate>
            <guid isPermaLink="false">4554092</guid>        </item>
        <item>
            <title>Rufinamide for pediatric patients with lennox-gastaut syndrome: a comprehensive overview.</title>
            <link>http://www.medworm.com/index.php?rid=4554091&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21351809%26dopt%3DAbstract</link>
            <description>Authors: Wier HA, Cerna A, So TY
    Rufinamide is a triazole derivative with broad-spectrum antiepileptic effects that is unrelated to any antiepileptic drug currently on the market. The European Commission and the US FDA approved rufinamide in 2007 and 2008, respectively, for adjunctive treatment of seizures associated with Lennox-Gastaut syndrome in children 4 years of age or older and adults. The mechanism of action of rufinamide is not completely understood but it is believed to prolong the inactive state of sodium channels, therefore limiting excessive firing of sodium-dependent action potentials. Rufinamide is well absorbed when taken with food, with an absolute bioavailability between 70% and 85%. The elimination half-life of the drug is around 6-10 hours, with a time to maximum pl...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554091</comments>
            <pubDate>Mon, 07 Mar 2011 03:45:41 +0100</pubDate>
            <guid isPermaLink="false">4554091</guid>        </item>
        <item>
            <title>Management of seizures in lennox-gastaut syndrome.</title>
            <link>http://www.medworm.com/index.php?rid=4554090&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21351810%26dopt%3DAbstract</link>
            <description>Authors: Crumrine PK
    Lennox-Gastaut syndrome is an epilepsy syndrome that begins in childhood (between 1 and 8 years of age), worsens during latency and persists frequently into adulthood, is refractory to antiepileptic medications, and results in cognitive decline and behavioral problems in affected individuals. Seizure types consist primarily of axial tonic, atonic, and atypical absence; nocturnal tonic seizures are the most common seizure pattern in this population, but often are not one of the initial seizure patterns. Some patients also have myoclonic seizures; this seizure pattern is less frequent than the three preceding types. Although there are some cases that are cryptogenic, most are symptomatic, arising during prenatal and perinatal periods from intrauterine infections, and...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554090</comments>
            <pubDate>Mon, 07 Mar 2011 03:45:35 +0100</pubDate>
            <guid isPermaLink="false">4554090</guid>        </item>
        <item>
            <title>Limited Capacity in US Pediatric Drug Trials: Qualitative Analysis of Expert Interviews.</title>
            <link>http://www.medworm.com/index.php?rid=4554089&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21351811%26dopt%3DAbstract</link>
            <description>Conclusions: Insufficient US PDT capacity may hinder the development of new drugs for children and limit studies on the safety and efficacy of drugs presently used to treat pediatric conditions. Further public policy initiatives may be needed to achieve the full promise of BPCA/PREA.
    PMID: 21351811 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554089</comments>
            <pubDate>Mon, 07 Mar 2011 03:45:29 +0100</pubDate>
            <guid isPermaLink="false">4554089</guid>        </item>
        <item>
            <title>The 26th international pediatric association congress of pediatrics, johannesburg, South Africa, 4-9 august 2010.</title>
            <link>http://www.medworm.com/index.php?rid=4554088&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21351812%26dopt%3DAbstract</link>
            <description>Authors: Wilde MI
    
    PMID: 21351812 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554088</comments>
            <pubDate>Mon, 07 Mar 2011 03:45:24 +0100</pubDate>
            <guid isPermaLink="false">4554088</guid>        </item>
        <item>
            <title>Aztreonam lysine for inhalation solution in cystic fibrosis†: profile report.</title>
            <link>http://www.medworm.com/index.php?rid=4554087&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21351813%26dopt%3DAbstract</link>
            <description>Authors: Plosker GL
    † Adapted and reproduced from the original article published in Drugs 2010; 70 (14): 1843-55.[1].
    PMID: 21351813 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554087</comments>
            <pubDate>Mon, 07 Mar 2011 03:45:19 +0100</pubDate>
            <guid isPermaLink="false">4554087</guid>        </item>
        <item>
            <title>Spotlight on tdap(5) vaccine (covaxis®) as a single-booster immunization for the prevention of tetanus, diphtheria, and pertussis: in children (aged ≥4 years), adolescents, and adults†.</title>
            <link>http://www.medworm.com/index.php?rid=4554086&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21351814%26dopt%3DAbstract</link>
            <description>Authors: Scott LJ
    Covaxis® (also licensed as Triaxis® or Adacel® in individual countries) is a Tdap(5) (i.e. combined tetanus toxoid, reduced diphtheria toxoid, five component acellular pertussis [namely detoxified pertussis toxin, filamentous hemagglutinin, pertactin, and fimbriae types 2 and 3]) vaccine for the prevention of diphtheria, tetanus, and pertussis. It is approved for use in Europe as a single intramuscular booster dose in children (aged ≥4 years), adolescents, and adults, and in the US it is approved for use in individuals aged 11-64 years. In large, randomized, controlled clinical trials conducted in the UK and North America, a single intramuscular booster dose of Covaxis® induced robust immune responses for all of its component antigens when given to children (age...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554086</comments>
            <pubDate>Mon, 07 Mar 2011 03:45:13 +0100</pubDate>
            <guid isPermaLink="false">4554086</guid>        </item>
        <item>
            <title>Folate Fortification and Survival of Children with Acute Lymphoblastic Leukemia.</title>
            <link>http://www.medworm.com/index.php?rid=4554085&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21366358%26dopt%3DAbstract</link>
            <description>Conclusion: These data suggest that folate fortification does not appear to have caused an increase in therapeutic failures in children with ALL.
    PMID: 21366358 [PubMed - as supplied by publisher] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4554085</comments>
            <pubDate>Wed, 02 Mar 2011 00:00:00 +0100</pubDate>
            <guid isPermaLink="false">4554085</guid>        </item>
        <item>
            <title>Pharmacologic management of acutely agitated pediatric patients.</title>
            <link>http://www.medworm.com/index.php?rid=4289168&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21162596%26dopt%3DAbstract</link>
            <description>Authors: Sonnier L, Barzman D
    Acute agitation is a state of behavioral dyscontrol that requires intervention. Medications available in rapid delivery formats are frequently administered to treat acute agitation, either as a chemical restraint or on a voluntary basis. Prior to initiating treatment, the etiology of agitation must be evaluated. In choosing a medication, general pharmacologic principles should be followed. Medication should be selected based on the underlying cause in conjunction with weighing the risks, benefits, and side effects of medications. There are three classes of medications administered to children and adolescents to treat agitation: antihistamines, benzodiazepines, and antipsychotics. The most concerning short-term side effects of antipsychotics are their adver...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4289168</comments>
            <pubDate>Sun, 26 Dec 2010 16:30:38 +0100</pubDate>
            <guid isPermaLink="false">4289168</guid>        </item>
        <item>
            <title>Pediatric asthma controller therapy.</title>
            <link>http://www.medworm.com/index.php?rid=4289167&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21162597%26dopt%3DAbstract</link>
            <description>Authors: Anselmo M
    The treatment of children with asthma has historically relied upon expert opinion using data extrapolated from adult studies. Over the past few years, landmark studies have been completed providing healthcare professionals with evidence on which a reasonable approach can be made for children suffering from this common and serious disease. Asthmatic phenotype in children, unlike adults, tends to differ according to age, which must be taken into account as well as triggers, severity, and level of control. The care of the child with asthma is complex, but accumulating data have demonstrated that we are on the right path for optimizing control while reducing the burden of side effects. The newest Global Initiative for Asthma (GINA) guidelines, as well as recent updates f...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4289167</comments>
            <pubDate>Sun, 26 Dec 2010 16:30:30 +0100</pubDate>
            <guid isPermaLink="false">4289167</guid>        </item>
        <item>
            <title>Pharmacologic considerations for oseltamivir disposition: focus on the neonate and young infant.</title>
            <link>http://www.medworm.com/index.php?rid=4289166&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21162598%26dopt%3DAbstract</link>
            <description>Authors: Abdel-Rahman SM, Newland JG, Kearns GL
    Across much of the world, pandemic H1N1 infection has produced a significant healthcare crisis, reflected in significant morbidity and mortality. Statistics reveal that infection-associated deaths among individuals without pre-existing conditions (e.g. immunosuppression) are clustered in pregnant women and young infants. In developing countries where the availability of influenzae vaccine is limited, the only currently available pharmacologic counter-measure for H1N1 disease is oseltamivir, a neuraminidase inhibitor with excellent in vitro activity against the virus. This drug is available in oral solid and liquid formulations, has excellent peroral bioavailability in adults, and generally has a very favorable safety profile. Many observa...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4289166</comments>
            <pubDate>Sun, 26 Dec 2010 16:30:23 +0100</pubDate>
            <guid isPermaLink="false">4289166</guid>        </item>
        <item>
            <title>Disease registries and outcomes research in children: focus on lysosomal storage disorders.</title>
            <link>http://www.medworm.com/index.php?rid=4289165&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21162599%26dopt%3DAbstract</link>
            <description>Authors: Jones S, James E, Prasad S
    Assessing medicines specifically for use in children has been neglected in the past, with the majority of formal clinical studies being conducted in adults. Clinical trials are a pivotal part of the drug approval process; however, they are not always applicable to the diverse populations - including children - that receive the drug after approval. They may not be the most informative assessment tool, especially in rare (or orphan) disorders where there are few patients, due to a lack of existing natural history data and the challenges of designing appropriately powered statistical analyses. Disease registries, which can collect clinical information in larger, more heterogeneous populations than can be included in a clinical trial, are becoming increa...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4289165</comments>
            <pubDate>Sun, 26 Dec 2010 16:30:15 +0100</pubDate>
            <guid isPermaLink="false">4289165</guid>        </item>
        <item>
            <title>Calcineurin inhibitor-free immunosuppression in pediatric renal transplantation: a viable option?</title>
            <link>http://www.medworm.com/index.php?rid=4289164&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21162600%26dopt%3DAbstract</link>
            <description>Authors: Höcker B, Tönshoff B
    The introduction, in the mid-1980s, of calcineurin inhibitors - namely ciclosporin (cyclosporine) and later tacrolimus - has significantly improved short-term renal graft survival by lowering acute rejection rates in both adult and pediatric kidney transplantation. Nonetheless, long-term transplant survival is still not satisfactory, with calcineurin inhibitor-induced chronic nephrotoxicity being one of the main causes of progressive nephron loss and declining renal transplant function. Hence, different immunosuppressant regimens have been proposed to avoid or ameliorate calcineurin inhibitor-induced nephrotoxicity. These comprise the use of non-depleting or depleting antibodies for calcineurin inhibitor minimization, calcineurin inhibitor avoidance, or ...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4289164</comments>
            <pubDate>Sun, 26 Dec 2010 16:30:09 +0100</pubDate>
            <guid isPermaLink="false">4289164</guid>        </item>
        <item>
            <title>Acknowledgment.</title>
            <link>http://www.medworm.com/index.php?rid=4119965&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21028913%26dopt%3DAbstract</link>
            <description>Authors: 
    
    PMID: 21028913 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4119965</comments>
            <pubDate>Sat, 30 Oct 2010 13:45:31 +0100</pubDate>
            <guid isPermaLink="false">4119965</guid>        </item>
        <item>
            <title>New antimicrobial strategies in cystic fibrosis.</title>
            <link>http://www.medworm.com/index.php?rid=4119964&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21028914%26dopt%3DAbstract</link>
            <description>This article focuses on recent developments in the field of new antimicrobial strategies for CF. It is clear that studies on new classes of antibiotics or antimicrobial-like drugs are scarce, and that most studies involve new (inhalation) formulations, new routes of delivery, or analogs of existing classes of antibiotics. Studies of new antibiotic-like drugs are, in most cases, in preclinical phases of development and only a few of these agents may reach the market. Importantly, new inhaled antibiotics, e.g. aztreonam, levofloxacin, and fosfomycin, and new, more efficient delivery systems such as dry powder inhalation and liposomes for current antibiotics are in the clinical phase of development. These developments will be of great importance in improving effective treatment and reducing t...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4119964</comments>
            <pubDate>Sat, 30 Oct 2010 13:45:27 +0100</pubDate>
            <guid isPermaLink="false">4119964</guid>        </item>
        <item>
            <title>Pain management in newborns: from prevention to treatment.</title>
            <link>http://www.medworm.com/index.php?rid=4119963&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21028915%26dopt%3DAbstract</link>
            <description>Authors: Walter-Nicolet E, Annequin D, Biran V, Mitanchez D, Tourniaire B
    All neonates in the Neonatal Intensive Care Unit (NICU) or during the first days of life undergo painful and stressful procedures. Epidemiologic studies have shown that pain induced by these procedures is not effectively prevented or is inadequately treated. Pain experienced during the neonatal period may lead to negative outcomes, especially in preterm neonates. Prevention is the first step of pain management, and practical guidelines should be used in the NICU. Assessment must be done with adequate tools that take into account the infant's pathology and gestational age. Distinguishing between acute and prolonged pain is important for both assessment and treatment. The most common drugs that have been studied fo...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4119963</comments>
            <pubDate>Sat, 30 Oct 2010 13:45:23 +0100</pubDate>
            <guid isPermaLink="false">4119963</guid>        </item>
        <item>
            <title>Tumor necrosis factor inhibitors in the management of juvenile idiopathic arthritis: an evidence-based review.</title>
            <link>http://www.medworm.com/index.php?rid=4119962&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21028916%26dopt%3DAbstract</link>
            <description>Authors: Shenoi S, Wallace CA
    Juvenile idiopathic arthritis (JIA) is a chronic inflammatory disorder of unknown origin that is often treated with a variety of disease-modifying agents. Tumor necrosis factor (TNF) inhibitors are a group of genetically engineered biologic agents that target the proinflammatory cytokine TNF. This review focuses on the use of TNF inhibitors in JIA. Etanercept was the first TNF inhibitor approved for use in children with moderate to severe polyarticular-course JIA following encouraging results from a randomized, double-blind, placebo-controlled, multicenter trial in children. Open-label extension studies of the original trial involving 8 years of follow-up demonstrated the long-term safety and efficacy of etanercept in children. Other studies from establish...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4119962</comments>
            <pubDate>Sat, 30 Oct 2010 13:45:19 +0100</pubDate>
            <guid isPermaLink="false">4119962</guid>        </item>
        <item>
            <title>The use of triptans for pediatric migraines.</title>
            <link>http://www.medworm.com/index.php?rid=4119961&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21028917%26dopt%3DAbstract</link>
            <description>Authors: Eiland LS, Hunt MO
    Migraine headaches frequently occur in the pediatric population, with a prevalence of 3% in children 2-7 years of age, 4-11% in children 7-11 years of age, and 8-23% in children 11 years of age and older. Migraine without aura is more than twice as common as migraine with aura in children. Headaches are the third leading cause of emergency room referrals and rank in the top five health problems of children. The 2004 American Academy of Neurology's treatment parameter for migraine in children and adolescents recommended that nasal sumatriptan be considered for acute treatment; however, data were lacking to make a decision regarding the available oral triptans at that time. The more recently released European guidelines discuss three different triptans for use...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4119961</comments>
            <pubDate>Sat, 30 Oct 2010 13:45:15 +0100</pubDate>
            <guid isPermaLink="false">4119961</guid>        </item>
        <item>
            <title>Strategies to prevent cellular rejection in pediatric heart transplant recipients.</title>
            <link>http://www.medworm.com/index.php?rid=4119960&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21028918%26dopt%3DAbstract</link>
            <description>Authors: Denfield SW
    Despite more than 40 years' experience in pediatric heart transplantation, cellular rejection remains a significant cause of morbidity and mortality. In this review, strategies and agents to prevent acute cellular rejection are discussed. Strategies to prevent rejection are divided into two phases - induction and maintenance therapies. Currently, the most commonly used induction agents are polyclonal antibodies (rabbit or equine antithymocyte globulin) and interleukin-2 receptor antibodies (daclizumab or basiliximab). Induction therapies have reduced early rejection, are renal sparing, and can reduce corticosteroid exposure, but have not yet been shown to have a longer term survival benefit. Multiple maintenance immunosuppressants are available. Nearly all regimens...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4119960</comments>
            <pubDate>Sat, 30 Oct 2010 13:45:11 +0100</pubDate>
            <guid isPermaLink="false">4119960</guid>        </item>
        <item>
            <title>Ondansetron dosing in pediatric gastroenteritis: a prospective cohort, dose-response study.</title>
            <link>http://www.medworm.com/index.php?rid=4119959&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D21028919%26dopt%3DAbstract</link>
            <description>Conclusions: Within the dose range of 0.13-0.26 mg/kg, higher doses of ondansetron were not superior to lower doses, nor were they associated with increased side effects. Thus, ondansetron in this dose range was shown to result in a similar reduction in emesis in children with acute gastroenteritis.
    PMID: 21028919 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=4119959</comments>
            <pubDate>Sat, 30 Oct 2010 13:45:07 +0100</pubDate>
            <guid isPermaLink="false">4119959</guid>        </item>
        <item>
            <title>Hepatic veno-occlusive disease: a chemotherapy-related toxicity in children with malignancies.</title>
            <link>http://www.medworm.com/index.php?rid=3921654&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20799757%26dopt%3DAbstract</link>
            <description>Authors: Cefalo MG, Maurizi P, Arlotta A, Scalzone M, AttinÃ  G, Ruggiero A, Riccardi R
    Hepatic veno-occlusive disease (VOD) is a major manifestation of liver toxicity associated with conventional and high-dose chemotherapy in children affected by hematologic malignancies and certain solid tumors. Clinically, patients present with jaundice, painful hepatomegaly, and fluid retention, which may evolve into multi-organ failure, a hallmark of severe disease. The pathogenesis is complex and not completely understood, but the damage to sinusoidal endothelium, typically caused by toxic metabolites released from antineoplastic drugs, is thought to play a crucial role, together with cytokine activation, immune deregulation, and coagulopathy. Diagnosis is based on clinical criteria supported b...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3921654</comments>
            <pubDate>Thu, 02 Sep 2010 04:57:23 +0100</pubDate>
            <guid isPermaLink="false">3921654</guid>        </item>
        <item>
            <title>Antivirals for influenza: strategies for use in pediatrics.</title>
            <link>http://www.medworm.com/index.php?rid=3921653&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20799758%26dopt%3DAbstract</link>
            <description>Authors: Smith SM, Gums JG
    Influenza infection is annually responsible for significant morbidity and mortality, particularly among the very young and old. Recently updated guidelines recommend influenza vaccination of all children aged 6 months to 18 years; however, childhood vaccination remains underutilized. Furthermore, concerns over the reduced efficacy of vaccination in children have further heightened the need for effective treatment schemes. Antiviral therapies have emerged as attractive options in the battle against influenza infection. These agents include the adamantanes (amantadine and rimantadine) and neuraminidase inhibitors (zanamivir, oseltamivir, and peramivir). Broad-scale use of adamantane antivirals has been severely limited in recent years because of high resistance...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3921653</comments>
            <pubDate>Thu, 02 Sep 2010 04:57:19 +0100</pubDate>
            <guid isPermaLink="false">3921653</guid>        </item>
        <item>
            <title>Pentoxifylline in preterm neonates: a systematic review.</title>
            <link>http://www.medworm.com/index.php?rid=3921652&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20799759%26dopt%3DAbstract</link>
            <description>Authors: Harris E, Schulzke SM, Patole SK
    Sepsis, necrotizing enterocolitis (NEC), and chronic lung disease (CLD) in preterm neonates are associated with significant mortality and morbidity, including long-term neurodevelopmental impairment and socioeconomic burden. Safe and effective drugs for the prevention and treatment of these conditions are urgently needed. Pentoxifylline, a synthetic theobromine derivative, is a non-steroidal immunomodulating agent with unique hemorrheologic effects which has been used in a range of infectious, vascular, and inflammatory conditions in adults and children. The unique properties of pentoxifylline explain its potential benefits in preterm neonates with sepsis, NEC, and CLD, conditions characterized by activation of the inflammatory cytokine cascade...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3921652</comments>
            <pubDate>Thu, 02 Sep 2010 04:57:14 +0100</pubDate>
            <guid isPermaLink="false">3921652</guid>        </item>
        <item>
            <title>Ketoprofen pharmacokinetics, efficacy, and tolerability in pediatric patients.</title>
            <link>http://www.medworm.com/index.php?rid=3921651&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20799760%26dopt%3DAbstract</link>
            <description>In conclusion, ketoprofen is effective and well tolerated in children for the control of post-surgical pain and for the control of pain and fever in inflammatory conditions.
    PMID: 20799760 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3921651</comments>
            <pubDate>Thu, 02 Sep 2010 04:57:10 +0100</pubDate>
            <guid isPermaLink="false">3921651</guid>        </item>
        <item>
            <title>Clinical Significance of Medication Reconciliation in Children Admitted to a UK Pediatric Hospital: Observational Study of Neurosurgical Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3921650&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20799761%26dopt%3DAbstract</link>
            <description>Conclusions: The introduction of medication reconciliation in children on admission to hospital has the potential to reduce discomfort or clinical deterioration by reducing unintentional changes to repeat prescribed medication. Consequently, there is no justification for the omission of children from the NICE-NPSA guidance concerning medication reconciliation in hospitals, and costing tools should include pediatric patients.
    PMID: 20799761 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3921650</comments>
            <pubDate>Thu, 02 Sep 2010 04:57:06 +0100</pubDate>
            <guid isPermaLink="false">3921650</guid>        </item>
        <item>
            <title>Mometasone Furoate in Children with Mild to Moderate Persistent Asthma: A Review of the Evidence.</title>
            <link>http://www.medworm.com/index.php?rid=3723749&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20593906%26dopt%3DAbstract</link>
            <description>Authors: Milgrom H
    The high prevalence of asthma in pediatric patients underscores the need for effective and safe treatment in this population. Current treatment guidelines recommend inhaled corticosteroids (ICSs) as a preferred treatment for the control of mild to moderate persistent asthma in patients of all ages, including young children. Clinical efficacy, systemic safety, and ease of use are desirable attributes of an ICS used to treat children with persistent asthma. Recently, mometasone furoate administered via a dry powder inhaler (MF-DPI) 110 mug once daily in the evening (delivered dose of 100 mug) was approved by the US FDA for the maintenance treatment of asthma in children 4-11 years of age. Data from the clinical trial program for MF-DPI that establish the efficacy, long...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3723749</comments>
            <pubDate>Sun, 04 Jul 2010 16:48:30 +0100</pubDate>
            <guid isPermaLink="false">3723749</guid>        </item>
        <item>
            <title>Understanding Developmental Pharmacodynamics: Importance for Drug Development and Clinical Practice.</title>
            <link>http://www.medworm.com/index.php?rid=3723748&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20593907%26dopt%3DAbstract</link>
            <description>Authors: Mulla H
    Developmental pharmacodynamics is the study of age-related maturation of the structure and function of biologic systems and how this affects response to pharmacotherapy. This may manifest as a change in the potency, efficacy, or therapeutic range of a drug. The paucity of studies exploring developmental pharmacodynamics reflects the lack of suitable juvenile animal models and the ethical and practical constraints of conducting studies in children. However, where data from animal models are available, valuable insight has been gained into how response to therapy can change through the course of development. For example, animal neurodevelopmental models have revealed that temporal differences in the maturation of norepinephrine and serotonin neurotransmitter systems may ...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3723748</comments>
            <pubDate>Sun, 04 Jul 2010 16:48:24 +0100</pubDate>
            <guid isPermaLink="false">3723748</guid>        </item>
        <item>
            <title>Rotavirus Infections and Vaccines: Burden of Illness and Potential Impact of Vaccination.</title>
            <link>http://www.medworm.com/index.php?rid=3723747&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20593908%26dopt%3DAbstract</link>
            <description>Authors: Grimwood K, Lambert SB, Milne RJ
    Rotaviruses are the most common cause of severe gastroenteritis in children. By 5 years of age virtually every child worldwide will have experienced at least one rotavirus infection. This leads to an enormous disease burden, where every minute a child dies because of rotavirus infection and another four are hospitalized, at an annual societal cost in 2007 of $US2 billion. Most of the annual 527 000 deaths are in malnourished infants living in rural regions of low and middle income countries. In contrast, most measurable costs arise from medical expenses and lost parental wages in high income countries. Vaccines are the only public health prevention strategy likely to control rotavirus disease. They were developed to mimic the immunity following...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3723747</comments>
            <pubDate>Sun, 04 Jul 2010 16:48:19 +0100</pubDate>
            <guid isPermaLink="false">3723747</guid>        </item>
        <item>
            <title>Hereditary Angioedema in Childhood: An Approach to Management.</title>
            <link>http://www.medworm.com/index.php?rid=3723746&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20593909%26dopt%3DAbstract</link>
            <description>Authors: Ebo DG, Verweij MM, De Knop KJ, Hagendorens MM, Bridts CH, De Clerck LS, Stevens WJ
    Hereditary angioedema (HAE) is an inherited disorder characterized by recurrent, circumscribed, non-pitting, non-pruritic, and rather painful subepithelial swelling of sudden onset, which fades during the course of 48-72 hours, but can persist for up to 1 week. Lesions can be solitary or multiple, and primarily involve the extremities, larynx, face, esophagus, and bowel wall. Patients with HAE experience angioedema because of a defective control of the plasma kinin-forming cascade that is activated through contact with negatively charged endothelial macromolecules leading to binding and auto-activation of coagulation factor XII, activation of prekallikrein to kallikrein by factor XIIa, and clea...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3723746</comments>
            <pubDate>Sun, 04 Jul 2010 16:48:13 +0100</pubDate>
            <guid isPermaLink="false">3723746</guid>        </item>
        <item>
            <title>A Randomized Trial of Propranolol versus Sodium Valproate for the Prophylaxis of Migraine in Pediatric Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3723745&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20593910%26dopt%3DAbstract</link>
            <description>Conclusion: This prospective study supports the efficacy of propranolol and sodium valproate as prophylaxis for pediatric migraine without aura, based on IHS criteria. There were no significant differences between these two drugs in all evaluated parameters except for the mean headache frequency per month, which was lower with propranolol than with sodium valproate.
    PMID: 20593910 [PubMed - as supplied by publisher] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3723745</comments>
            <pubDate>Sun, 04 Jul 2010 16:48:08 +0100</pubDate>
            <guid isPermaLink="false">3723745</guid>        </item>
        <item>
            <title>Foreword.</title>
            <link>http://www.medworm.com/index.php?rid=3723752&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20590167%26dopt%3DAbstract</link>
            <description>Authors: Dagan R
    
    PMID: 20590167 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3723752</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3723752</guid>        </item>
        <item>
            <title>Appropriate treatment of acute otitis media in the era of antibiotic resistance.</title>
            <link>http://www.medworm.com/index.php?rid=3723751&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20590168%26dopt%3DAbstract</link>
            <description>Authors: Dagan R
    The outcome of treatment for acute otitis media (AOM) differs between various antibiotic drugs. Outcome depends upon the drugs' pharmacokinetics, but in the case of infectious diseases also on the susceptibility of the organism and the interaction between the drug and the organisms at the specific site of infection (pharmacodynamics). In the era of antibiotic resistance, it is thus important to understand the pharmacokinetics/pharmacodynamics of the various available drugs in the context of AOM and its main two pathogens, Streptococcus pneumoniae and non-typeable Haemophilus influenzae. In terms of clinical outcome, it is also important to realize that AOM is a self-limiting disease in most cases, so that response to treatment is always compared with the expected backg...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3723751</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3723751</guid>        </item>
        <item>
            <title>The Viriato Study: Update on Antimicrobial Resistance of Microbial Pathogens Responsible for Community-Acquired Respiratory Tract Infections in Portugal.</title>
            <link>http://www.medworm.com/index.php?rid=3723750&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20590169%26dopt%3DAbstract</link>
            <description>Authors: Melo-Cristino J, Santos L, Silva-Costa C, FriÃ£es A, Pinho MD, Ramirez M, 
    The Viriato study is a prospective, multicentre laboratory-based surveillance study of antimicrobial susceptibility in which 30 microbiology laboratories throughout Portugal are asked to isolate, identify and submit to a central laboratory for testing Streptococcus pneumoniae, Haemophilus influenzae and Moraxella catarrhalis responsible for community-acquired lower respiratory tract infections and Streptococcus pyogenes from tonsillitis. To monitor changes in antimicrobial resistance patterns of these frequent respiratory pathogens. Susceptibility was determined by disk diffusion (Kirby-Bauer) or using Etest strips following the Clinical and Laboratory Standards Institute guidelines. From 1999 to 2007...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3723750</comments>
            <pubDate>Mon, 28 Jun 2010 23:00:00 +0100</pubDate>
            <guid isPermaLink="false">3723750</guid>        </item>
        <item>
            <title>Mifamurtide: a review of its use in the treatment of osteosarcoma.</title>
            <link>http://www.medworm.com/index.php?rid=3588895&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20481644%26dopt%3DAbstract</link>
            <description>Authors: Frampton JE
    Mifamurtide (liposomal muramyl tripeptide phosphatidyl ethanolamine; Mepact(R)) is an immunomodulator with antitumor effects that appear to be mediated via activation of monocytes and macrophages. In the EU, mifamurtide is indicated in children, adolescents, and young adults for the treatment of high-grade, resectable, non-metastatic osteosarcoma after macroscopically complete surgical resection; it is administered by intravenous infusion in conjunction with postoperative multiagent chemotherapy. In the US, mifamurtide is currently an investigational agent that holds orphan drug status for the treatment of osteosarcoma. In a large, randomized, open-label, multicenter, phase III trial, the addition of adjuvant (postoperative) mifamurtide to three- or four-drug combi...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3588895</comments>
            <pubDate>Sat, 22 May 2010 15:27:17 +0100</pubDate>
            <guid isPermaLink="false">3588895</guid>        </item>
        <item>
            <title>Escitalopram: in the treatment of major depressive disorder in adolescent patients.</title>
            <link>http://www.medworm.com/index.php?rid=3588894&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20481645%26dopt%3DAbstract</link>
            <description>Authors: Yang LP, Scott LJ
    Escitalopram is a selective serotonin reuptake inhibitor (SSRI), and is the second antidepressant to be approved for use in treating major depressive disorder (MDD) in adolescent patients (aged 12-17 years) in the US. In a randomized, double-blind, flexible-dose, multicenter trial, once-daily escitalopram 10-20 mg (n = 154) for 8 weeks was significantly better than placebo (n = 157) in improving the severity of depressive symptoms (as assessed by the change in the Children's Depression Rating Scale-Revised [CDRS-R] total score) in adolescent patients with MDD. Preliminary data from a combined analysis of the double-blind data from this trial and double-blind data from a 16-week, fixed-dose, extension study suggest a significant difference between escitalopram...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3588894</comments>
            <pubDate>Sat, 22 May 2010 15:27:14 +0100</pubDate>
            <guid isPermaLink="false">3588894</guid>        </item>
        <item>
            <title>Cardiovascular Effects of Medications for the Treatment of Attention-Deficit Hyperactivity Disorder: What is Known and How Should it Influence Prescribing in Children?</title>
            <link>http://www.medworm.com/index.php?rid=3588893&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20481646%26dopt%3DAbstract</link>
            <description>Authors: Elia J, Vetter VL
    The effective medications currently marketed for attention-deficit hyperactivity disorder (ADHD) have central and peripheral catecholaminergic effects that have been shown to result in statistically significant increases in heart rate and blood pressure. The impact of these medications on serious cardiovascular events in healthy children is unknown, but serious cardiovascular events related to ADHD medications are considered rare. However, children with cardiac pathology may be at greater risk given that increased sympathetic tone has been reported as a causal factor in generating ventricular arrhythmias in adults with coronary artery disease, and physical exercise has been consistently reported as a trigger for increased risk of sudden cardiac death in athle...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3588893</comments>
            <pubDate>Sat, 22 May 2010 15:27:12 +0100</pubDate>
            <guid isPermaLink="false">3588893</guid>        </item>
        <item>
            <title>Impact of Antiretroviral Therapy on Growth, Body Composition and Metabolism in Pediatric HIV Patients.</title>
            <link>http://www.medworm.com/index.php?rid=3588892&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20481647%26dopt%3DAbstract</link>
            <description>Authors: Kim RJ, Rutstein RM
    Highly active antiretroviral therapy improves survival and growth in children with HIV infection. However, its use can be associated with adverse changes in body composition and metabolism. Bone mineral density can be adversely affected in HIV-positive children due to nutritional compromise or certain antiretrovirals. HIV-associated lipodystrophy, consisting of redistribution of adipose tissue, insulin resistance, and dyslipidemia, has also been described in children. Pediatric HIV patients may be at greater risk for these problems because of their longer potential lifetime exposure to these agents and because childhood is normally a period of rapid growth and tissue accretion. Healthcare providers for children with HIV infection must be aware of the potent...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3588892</comments>
            <pubDate>Sat, 22 May 2010 15:27:09 +0100</pubDate>
            <guid isPermaLink="false">3588892</guid>        </item>
        <item>
            <title>Levetiracetam in childhood epilepsy.</title>
            <link>http://www.medworm.com/index.php?rid=3588891&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20486734%26dopt%3DAbstract</link>
            <description>In conclusion, results from clinical trials to date suggest that levetiracetam has a full spectrum of efficacy as well as a favorable safety profile, and this drug can be considered a valuable option in the treatment of epilepsy in pediatric patients.
    PMID: 20486734 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3588891</comments>
            <pubDate>Sat, 22 May 2010 15:27:06 +0100</pubDate>
            <guid isPermaLink="false">3588891</guid>        </item>
        <item>
            <title>Epidemiology and management of insomnia in children with autistic spectrum disorders.</title>
            <link>http://www.medworm.com/index.php?rid=3359659&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20218744%26dopt%3DAbstract</link>
            <description>Authors: Miano S, Ferri R
    Insomnia is the predominant sleep concern in children with autistic spectrum disorder (ASD), and its nature is most likely multifactorial, with neurochemical (abnormalities in serotonergic transmission or melatonin levels), psychiatric (anxiety), and behavioral (poor sleep habits) etiological factors involved. Children with ASD experience sleep problems similar to those of typically developing children, although the prevalence is markedly higher, occurring in 44-83% of school-aged children with ASD. Caregivers usually report that insomnia is the most frequent sleep disorder, described as disorders of initiating and maintaining sleep, restless sleep, bedtime resistance, co-sleeping, alterations of sleep hygiene, and early awakenings in the morning. Many actigra...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3359659</comments>
            <pubDate>Sat, 13 Mar 2010 00:40:21 +0100</pubDate>
            <guid isPermaLink="false">3359659</guid>        </item>
        <item>
            <title>Current approaches to the management of pediatric hodgkin lymphoma.</title>
            <link>http://www.medworm.com/index.php?rid=3359658&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20218745%26dopt%3DAbstract</link>
            <description>Authors: Freed J, Kelly KM
    Hodgkin lymphoma is one of the few cancers that affect both adults and children. Cure rates for Hodgkin lymphoma remain among the best for pediatric cancers. However, cure is often associated with significant delayed effects of therapy, including an elevated risk for second malignancies, cardiotoxicity, pulmonary toxicity, and gonadal and non-gonadal endocrine dysfunction. Therefore, the aim of current treatment strategies is to further improve outcomes while minimizing therapy-related complications. At diagnosis, patients are classified into risk groups based on disease stage, and the presence of clinical, biologic, and serologic risk factors. In general, the most recent trials have intensified therapy in those patients with high-risk disease to improve dise...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3359658</comments>
            <pubDate>Sat, 13 Mar 2010 00:40:18 +0100</pubDate>
            <guid isPermaLink="false">3359658</guid>        </item>
        <item>
            <title>Published pediatric randomized drug trials in developing countries, 1996-2002.</title>
            <link>http://www.medworm.com/index.php?rid=3359657&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20218746%26dopt%3DAbstract</link>
            <description>Authors: Nor Aripin KN, Sammons HM, Choonara I
    The greatest burden of disease in children lies in the developing world; however, previous reviews have suggested that few randomized controlled trials (RCTs) involving children take place in developing countries. Children in developing countries deserve the same standard of medicines as those in developed countries, i.e. appropriate medications for the specific diseases that occur. To elucidate published pediatric therapeutic RCTs that have taken place in the developing world and to determine whether they are appropriate for the major diseases occurring there, and to explore their approach to safety monitoring. A previously assembled database of pediatric RCTs published between 1996 and 2002, from journals indexed in MEDLINE, was analyzed...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3359657</comments>
            <pubDate>Sat, 13 Mar 2010 00:40:15 +0100</pubDate>
            <guid isPermaLink="false">3359657</guid>        </item>
        <item>
            <title>Efficacy and safety of besifloxacin ophthalmic suspension 0.6% in children and adolescents with bacterial conjunctivitis: a post hoc, subgroup analysis of three randomized, double-masked, parallel-group, multicenter clinical trials.</title>
            <link>http://www.medworm.com/index.php?rid=3359656&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20218747%26dopt%3DAbstract</link>
            <description>Authors: Comstock TL, Paterno MR, Usner DW, Pichichero ME
    Acute conjunctivitis is the most frequent eye disorder seen by primary care physicians and one that often affects children. Besifloxacin is a new topical fluoroquinolone, the first chlorofluoroquinolone, for the treatment of bacterial conjunctivitis. To examine the efficacy and safety of besifloxacin ophthalmic suspension 0.6% in patients aged 1-17 years with bacterial conjunctivitis. This was a post hoc analysis of a subgroup of pediatric patients aged 1-17 years who had participated in three previously reported, randomized, double-masked, parallel-group, multicenter, clinical trials evaluating the safety and efficacy of besifloxacin in the treatment of bacterial conjunctivitis. The studies were conducted in a community setting...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3359656</comments>
            <pubDate>Sat, 13 Mar 2010 00:40:12 +0100</pubDate>
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        <item>
            <title>Darunavir: In Treatment-Experienced Pediatric Patients with HIV-1 Infection.</title>
            <link>http://www.medworm.com/index.php?rid=3359655&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20218748%26dopt%3DAbstract</link>
            <description>Authors: McKeage K, Scott LJ
    Darunavir is a nonpeptidic HIV type 1 (HIV-1) protease inhibitor (PI) that binds with high affinity to the HIV-1 protease, including multi-drug resistant proteases. This drug is highly potent against a range of laboratory strains and clinical isolates of wild-type and multidrug-resistant HIV and has limited potential to cause cytotoxicity. Darunavir did not display cross-resistance with other PIs in vitro. The coadministration of a low boosting dose of ritonavir with darunavir (boosted darunavir) increases the bioavailablity of darunavir. The drug is also administered together with other highly active antiretroviral agents. The efficacy of twice-daily boosted darunavir (11-19 mg/kg plus ritonavir 1.5-2.5 mg/kg) in treatment-experienced pediatric patients (a...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3359655</comments>
            <pubDate>Sat, 13 Mar 2010 00:40:09 +0100</pubDate>
            <guid isPermaLink="false">3359655</guid>        </item>
        <item>
            <title>Colesevelam: in pediatric patients with heterozygous familial hypercholesterolemia.</title>
            <link>http://www.medworm.com/index.php?rid=3359654&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20218749%26dopt%3DAbstract</link>
            <description>Authors: Perry CM
    Colesevelam hydrochloride (colesevelam), a non-absorbed, synthetic, lipid-lowering polymer, is a bile acid sequestrant. Colesevelam binds with high affinity to bile acids within the gastrointestinal tract, thereby inhibiting the reabsorption of bile acids, resulting in decreases in serum low-density lipoprotein cholesterol (LDL-C) levels. Colesevelam is available as tablets and as powder for oral suspension. At dosages of 3.75 g once daily or 1.875 g twice daily, colesevelam is approved in the US for the treatment of pediatric patients aged 10-17 years with heterozygous familial hypercholesterolemia. Colesevelam may be administered as monotherapy or in combination with an HMG-CoA reductase inhibitor (statin). A 32-week trial was conducted and consisted of a stabliliza...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3359654</comments>
            <pubDate>Sat, 13 Mar 2010 00:40:06 +0100</pubDate>
            <guid isPermaLink="false">3359654</guid>        </item>
        <item>
            <title>Breastfeeding in HIV-Positive Women: What Can be Recommended?</title>
            <link>http://www.medworm.com/index.php?rid=3121192&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20034337%26dopt%3DAbstract</link>
            <description>Authors: Slater M, Stringer EM, Stringer JS
    Breastfeeding remains a common practice in parts of the world where the burden of HIV is highest and the fewest alternative feeding options exist. The impossible dilemma faced by HIV-positive mothers is whether to breastfeed their infants in keeping with cultural norms but in doing so risk transmitting the virus through breast milk, or to pursue formula feeding, which comes with its own set of risks, including a higher rate of infant mortality from diarrheal illnesses, while reducing transmission of HIV. Treatment of mothers and/or their infants with antiretroviral drugs is a strategy that has been employed for several decades to reduce HIV transmission through pregnancy and delivery, but the effect of these agents when taken during breastfee...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3121192</comments>
            <pubDate>Sat, 26 Dec 2009 13:08:18 +0100</pubDate>
            <guid isPermaLink="false">3121192</guid>        </item>
        <item>
            <title>Juvenile Myelomonocytic Leukemia: Epidemiology, Etiopathogenesis, Diagnosis, and Management Considerations.</title>
            <link>http://www.medworm.com/index.php?rid=3121191&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20034338%26dopt%3DAbstract</link>
            <description>Authors: Yoshimi A, Kojima S, Hirano N
    Juvenile myelomonocytic leukemia (JMML) is a rare hematopoietic malignancy of early childhood with features characteristic of both myelodysplastic and myeloproliferative disorders. Recent studies clearly show that the deregulated activation of the RAS signaling pathway plays a central role in the pathogenesis of JMML. Somatic defects in either RAS, PTPN11 or NF1 genes involved in this pathway are detected in 70-80% of JMML patients, allowing a molecular diagnosis to be made in the majority of cases. Patients with JMML respond poorly to chemotherapy, and the probability of survival without allogeneic hematopoietic stem cell transplantation (HSCT) is less than 10%. Recent studies show that the event-free survival after HSCT is between 24 and 54%, wi...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3121191</comments>
            <pubDate>Sat, 26 Dec 2009 13:08:15 +0100</pubDate>
            <guid isPermaLink="false">3121191</guid>        </item>
        <item>
            <title>Juvenile-Onset Clinically Amyopathic Dermatomyositis: An Overview of Recent Progress in Diagnosis and Management.</title>
            <link>http://www.medworm.com/index.php?rid=3121190&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20034339%26dopt%3DAbstract</link>
            <description>Authors: Walling HW, Gerami P, Sontheimer RD
    Juvenile-onset amyopathic dermatomyositis is an uncommon variant of juvenile-onset dermatomyositis (JDM), characterized by the hallmark cutaneous features of dermatomyositis for at least 6 months without clinical or laboratory evidence of muscle disease. Cutaneous calcinosis, vasculopathy, and interstitial lung disease frequently complicate the course of classic JDM (typical JDM with myositis) but are infrequent in amyopathic JDM. Recent literature suggests that approximately 75% of amyopathic JDM patients will remain free from muscle disease after years of follow-up, while approximately 25% of patients will evolve to having classic JDM. No clinical, laboratory, or ancillary parameters have been found to be predictive for this transition to ...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3121190</comments>
            <pubDate>Sat, 26 Dec 2009 13:08:13 +0100</pubDate>
            <guid isPermaLink="false">3121190</guid>        </item>
        <item>
            <title>Adverse Effects of Immunosuppression in Pediatric Solid Organ Transplantation.</title>
            <link>http://www.medworm.com/index.php?rid=3121189&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20034340%26dopt%3DAbstract</link>
            <description>Authors: Schonder KS, Mazariegos GV, Weber RJ
    Solid organ transplantation is a life-saving treatment for end-stage organ failure in children. Immunosuppressant medications are used to prevent rejection of the organ transplant. However, these medications are associated with significant adverse effects that impact growth and development, quality of life (QOL), and sometimes long-term survival after transplantation. Adverse effects can differ between the immunosuppressants, but many result from the overall state of immunosuppression. Strategies to manage immunosuppressant adverse effects often involve minimizing exposure to the drugs while balancing the risk for rejection. Early recognition of immunosuppressant adverse effects may help to reduce morbidities associated with solid organ tra...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3121189</comments>
            <pubDate>Sat, 26 Dec 2009 13:08:10 +0100</pubDate>
            <guid isPermaLink="false">3121189</guid>        </item>
        <item>
            <title>Optimizing Emetic Control in Children Receiving Antineoplastic Therapy: Beyond the Guidelines.</title>
            <link>http://www.medworm.com/index.php?rid=3121188&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20034341%26dopt%3DAbstract</link>
            <description>Authors: Dupuis LL, Nathan PC
    Existing guidelines for the prevention of antineoplastic chemotherapy-induced nausea and vomiting (CINV) in children are constrained by the lack of robust evidence. Current guidelines recommend the use of a serotonin 5-HT(3) receptor antagonist plus a corticosteroid to prevent acute CINV. Consequently, antiemetic agents that are recommended for use in adult cancer patients do not appear in the current pediatric guidelines. In addition, there is no information to guide the selection of alternative antiemetic agents for children who either cannot receive the recommended agents or who do not respond adequately to the treatment. Possible barriers to adherence to the pediatric antiemetic selection guidelines that are currently available are discussed, and publi...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3121188</comments>
            <pubDate>Sat, 26 Dec 2009 13:08:08 +0100</pubDate>
            <guid isPermaLink="false">3121188</guid>        </item>
        <item>
            <title>Bosentan: In Pediatric Patients with Pulmonary Arterial Hypertension.</title>
            <link>http://www.medworm.com/index.php?rid=3121187&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D20034342%26dopt%3DAbstract</link>
            <description>Authors: Carter NJ, Keating GM
    Bosentan is a dual endothelin-1 (ET-1) receptor antagonist that has affinity for ET-1 receptors A and B. In the EU, oral bosentan (Tracleer(R)) is indicated to improve exercise capacity and symptoms in patients with pulmonary arterial hypertension (PAH) of WHO functional class III; benefits have also been seen in patients with WHO functional class II PAH. Bosentan is available as film-coated tablets, and a new dispersible formulation of bosentan has also recently been approved in the EU for the treatment of PAH in children aged &amp;gt;/=2 years. A noncomparative, multicenter, phase III trial (FUTURE-1), which was primarily designed to investigate the pharmacokinetics of dispersible bosentan in pediatric patients, demonstrated that increasing the dosage of bo...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=3121187</comments>
            <pubDate>Sat, 26 Dec 2009 13:08:05 +0100</pubDate>
            <guid isPermaLink="false">3121187</guid>        </item>
        <item>
            <title>Acknowledgment.</title>
            <link>http://www.medworm.com/index.php?rid=2957937&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19877721%26dopt%3DAbstract</link>
            <description>Authors: 
    
    PMID: 19877721 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2957937</comments>
            <pubDate>Wed, 04 Nov 2009 16:10:02 +0100</pubDate>
            <guid isPermaLink="false">2957937</guid>        </item>
        <item>
            <title>Juvenile dermatomyositis: advances in pathogenesis, evaluation, and treatment.</title>
            <link>http://www.medworm.com/index.php?rid=2957936&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19877722%26dopt%3DAbstract</link>
            <description>Authors: Huber AM
    Juvenile dermatomyositis (JDM) is a rare, presumably autoimmune illness that causes proximal muscle weakness and a variety of typical cutaneous features. The study of this illness has been hampered by its rarity but, in recent years, important developments have increased our understanding of JDM. Genetic factors are likely important in the pathogenesis of JDM. These include several Human Leukocyte Antigen alleles, in particular those associated with the 8.1 ancestral haplotype and the tumor necrosis factor-alpha gene 308 polymorphism. Microchimerism, activation of plasmacytoid dendritic cells, and upregulation of type-1 interferon inducible genes also appear to play an important role in the pathogenesis of JDM. The study of JDM has also been limited by a lack of valid...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2957936</comments>
            <pubDate>Wed, 04 Nov 2009 16:10:02 +0100</pubDate>
            <guid isPermaLink="false">2957936</guid>        </item>
        <item>
            <title>Vasculitis in children and adolescents: clinical presentation, etiopathogenesis, and treatment.</title>
            <link>http://www.medworm.com/index.php?rid=2957935&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19877723%26dopt%3DAbstract</link>
            <description>Authors: Tullus K, Marks SD
    The childhood vasculitides are a group of diseases affecting small to large blood vessels. The two most common conditions are Henoch-Sch&amp;#xF6;nlein purpura (HSP) and Kawasaki disease (KD). HSP is diagnosed on the basis of typical clinical findings and is mostly a self-limiting disease. KD is the most common vasculitis in infants and the development of coronary artery aneurysms is the major complication. Early treatment with intravenous immunoglobulin and aspirin (acetylsalicylic acid) is required to minimize this risk. All other vasculitides are very rare in children and include anti-neutrophil cytoplasmic autoantibody (ANCA)-associated vasculitis, polyarteritis nodosa and Takayasu disease. The etiology of all these vasculitic diseases is generally unknown a...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2957935</comments>
            <pubDate>Wed, 04 Nov 2009 16:10:02 +0100</pubDate>
            <guid isPermaLink="false">2957935</guid>        </item>
        <item>
            <title>Treatment strategies to minimize or prevent chronic allograft dysfunction in pediatric renal transplant recipients: an overview.</title>
            <link>http://www.medworm.com/index.php?rid=2957934&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19877724%26dopt%3DAbstract</link>
            <description>Authors: H&amp;#xF6;cker B, T&amp;#xF6;nshoff B
    Long-term allograft survival poses a major problem in pediatric renal transplantation, with allograft nephropathy being the principal cause of graft failure after the first post-transplant year. The mechanisms of nephron loss resulting in graft dysfunction are multiple, comprising both immunologic factors such as acute and chronic antibody- or T-cell-mediated rejection and non-immunologic components. The latter include peri-transplant injuries and renovascular lesions (renal artery stenosis, thrombosis) as well as cardiovascular risk factors such as arterial hypertension and hyperlipidemia. Another relevant issue leading to progressive nephron loss and declining kidney transplant function is acute and chronic nephrotoxicity induced by the calcine...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2957934</comments>
            <pubDate>Wed, 04 Nov 2009 16:10:02 +0100</pubDate>
            <guid isPermaLink="false">2957934</guid>        </item>
        <item>
            <title>Pediatric safety of tizanidine: clinical adverse event database and retrospective chart assessment.</title>
            <link>http://www.medworm.com/index.php?rid=2957933&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19877725%26dopt%3DAbstract</link>
            <description>Authors: Henney HR, Chez M
    Tizanidine is an imidazoline with central alpha(2)-adrenoceptor agonist activity at both spinal and supraspinal levels, which is indicated as a short-acting drug for the management of spasticity. Despite being used in pediatric populations, there is no adequate information or well controlled studies to document the safety and efficacy of tizanidine in this group. To evaluate the safety of tizanidine in the pediatric population. We compared spontaneous adverse event reports in the Acorda Therapeutics worldwide clinical adverse event database for children (&amp;lt;/=16 years; n = 99) and adults (&amp;gt;16 years; n = 1153) who had received tizanidine and for whom at least one adverse event was reported, and performed a retrospective chart review of the safety of tizani...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2957933</comments>
            <pubDate>Wed, 04 Nov 2009 16:10:02 +0100</pubDate>
            <guid isPermaLink="false">2957933</guid>        </item>
        <item>
            <title>Topical pimecrolimus: a review of its use in the management of pediatric atopic dermatitis.</title>
            <link>http://www.medworm.com/index.php?rid=2957932&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19877726%26dopt%3DAbstract</link>
            <description>Authors: Yang LP, Curran MP
    Topical pimecrolimus 1% cream (Elidel(R)) [hereafter referred to as topical pimecrolimus] is a nonsteroidal alternative in the treatment of pediatric atopic dermatitis. In vehicle-controlled, short-term, continuous-use trials in pediatric patients with mild to moderate atopic dermatitis, topical pimecrolimus was effective in treating disease symptoms. Topical pimecrolimus was effective in preventing disease flares and reducing the need for topical corticosteroids in longer term, intermittent-use trials. In addition, topical pimecrolimus was associated with improvements in the health-related quality of life (HR-QOL) of pediatric patients with atopic dermatitis and their parents. In vehicle-controlled trials, topical pimecrolimus was generally as well tolerate...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2957932</comments>
            <pubDate>Wed, 04 Nov 2009 16:10:02 +0100</pubDate>
            <guid isPermaLink="false">2957932</guid>        </item>
        <item>
            <title>Epidemiology and management of essential tremor in children.</title>
            <link>http://www.medworm.com/index.php?rid=2763528&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19725596%26dopt%3DAbstract</link>
            <description>Authors: Ferrara J, Jankovic J
    Essential tremor (ET) is a common, often familial, movement disorder characterized by tremor of the limbs, head, and voice. Epidemiological surveys indicate that up to 5% of the adult population has ET, and 5-30% of adults with ET report symptom onset during childhood. There is, however, little published regarding ET in the pediatric population, and no prospective studies targeted specifically to children. Retrospective studies from subspecialty movement disorder clinics indicate that childhood-onset ET is usually hereditary, begins at a mean age of 6 years, and affects boys three times as often as girls. While ET occasionally results in disability during childhood, only one-quarter of children seeing a neurologist for ET require pharmacotherapy. Small ca...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2763528</comments>
            <pubDate>Fri, 04 Sep 2009 16:22:02 +0100</pubDate>
            <guid isPermaLink="false">2763528</guid>        </item>
        <item>
            <title>Antivirals for cytomegalovirus infection in neonates and infants: focus on pharmacokinetics, formulations, dosing, and adverse events.</title>
            <link>http://www.medworm.com/index.php?rid=2763527&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19725597%26dopt%3DAbstract</link>
            <description>Authors: Marshall BC, Koch WC
    Cytomegalovirus (CMV) infection is very common throughout the world, and has become more of a pediatric clinical concern given the high incidence of congenital CMV infections as well as the increasing numbers of immunocompromised patients. Because of this, the need for antiviral therapies in infants and neonates is growing. Currently, there are four antivirals available that are active against CMV: ganciclovir, valganciclovir, foscarnet, and cidofovir. At this time, none have approved indications for use in children. Although there are limited data regarding the dose, pharmacokinetics (PK), safety, and adverse events for some of these antivirals, ganciclovir, and its oral prodrug valganciclovir, have been the best studied in the infant and neonate populati...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2763527</comments>
            <pubDate>Fri, 04 Sep 2009 16:22:02 +0100</pubDate>
            <guid isPermaLink="false">2763527</guid>        </item>
        <item>
            <title>Pharmacotherapy in pediatric critical illness: a prospective observational study.</title>
            <link>http://www.medworm.com/index.php?rid=2763526&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19725598%26dopt%3DAbstract</link>
            <description>Authors: McDonnell C, Hum S, Frndova H, Parshuram CS
    Pharmacotherapy is an under-evaluated element of critical care medicine. In order to better understand pharmacotherapy in pediatric critical illness, we evaluated a cohort of emergency admissions to a university-affiliated pediatric intensive care unit (PICU). A prospective, observational study was performed. Eligible patients were admitted to this medical-surgical ICU for at least 24 hours. The primary outcomes were the number of drug orders written, the number of different medications ordered, and the number of drug administrations. Multiple regression analyses were used to identify factors independently associated with each primary outcome. We studied 100 patients with a median age of 40 months (interquartile range [IQR] 9-82), wh...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2763526</comments>
            <pubDate>Fri, 04 Sep 2009 16:22:02 +0100</pubDate>
            <guid isPermaLink="false">2763526</guid>        </item>
        <item>
            <title>Pediatric Pharmacy Advocacy Group International Pediatric Pharmacy and Pharmacology Symposium, 24-26 April 2009; Orlando, Florida, USAdagger.</title>
            <link>http://www.medworm.com/index.php?rid=2763525&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19725599%26dopt%3DAbstract</link>
            <description>Authors: Wilde MI
    
    PMID: 19725599 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2763525</comments>
            <pubDate>Fri, 04 Sep 2009 16:22:02 +0100</pubDate>
            <guid isPermaLink="false">2763525</guid>        </item>
        <item>
            <title>Pneumococcal Polysaccharide Protein D-Conjugate Vaccine (Synflorix; PHiD-CV).</title>
            <link>http://www.medworm.com/index.php?rid=2763524&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19725600%26dopt%3DAbstract</link>
            <description>Authors: Croxtall JD, Keating GM
    black triangle The pneumococcal polysaccharide protein D-conjugate vaccine (PHiD-CV; Synflorix) contains ten capsular polysaccharide serotypes from the bacterium Streptococcus pneumoniae, eight of which are conjugated to a nonlipidated cell-surface liporotein (protein D) of non-typeable Haemophilus influenzae (NTHi) and two of which are conjugated to either tetanus or diphtheria toxoid. black triangle In a three-dose primary vaccination schedule in infants aged &amp;lt;6 months, PHiD-CV elicited high immune responses against all pneumococcal serotypes contained in the vaccine and was noninferior to an approved 7-valent pneumococcal conjugate vaccine (7vCRM) for eight of the ten serotypes (five of the seven common to both vaccines). Moreover, functional anti...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2763524</comments>
            <pubDate>Fri, 04 Sep 2009 16:22:02 +0100</pubDate>
            <guid isPermaLink="false">2763524</guid>        </item>
        <item>
            <title>Multidisciplinarity goes mainstream: orlando meeting of the pediatric pharmacy advocacy group focuses attention on the need for multidisciplinary networks.</title>
            <link>http://www.medworm.com/index.php?rid=2664519&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19566106%26dopt%3DAbstract</link>
            <description>Authors: Macleod S, Knoppert D
    
    PMID: 19566106 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2664519</comments>
            <pubDate>Tue, 04 Aug 2009 09:22:02 +0100</pubDate>
            <guid isPermaLink="false">2664519</guid>        </item>
        <item>
            <title>Non-infectious pediatric uveitis: an update on immunomodulatory management.</title>
            <link>http://www.medworm.com/index.php?rid=2664518&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19566107%26dopt%3DAbstract</link>
            <description>Authors: Sharma SM, Dick AD, Ramanan AV
    Pediatric non-infectious uveitis remains a rare but potentially sight-threatening group of diseases. However, early screening and treatment can improve outcomes. No single agent has proven to be efficacious in all cases. A wide variety of long-term immunomodulatory treatments are available; these agents differ in both their potency and side effect profiles. Corticosteroids remain an extremely valuable form of treatment in the short-term management of uveitis. Other major groups of immunomodulatory treatments include the calcineurin inhibitors and antimetabolites such as methotrexate, which is frequently used as the first-line agent. The biologics, including anti-tumor necrosis factor agents and interferons, are newer and potentially very useful t...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2664518</comments>
            <pubDate>Tue, 04 Aug 2009 09:22:02 +0100</pubDate>
            <guid isPermaLink="false">2664518</guid>        </item>
        <item>
            <title>Variations in amoxicillin pharmacokinetic/pharmacodynamic parameters may explain treatment failures in acute otitis media.</title>
            <link>http://www.medworm.com/index.php?rid=2664517&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19566108%26dopt%3DAbstract</link>
            <description>The objective of this review was to define the biologic variations in amoxicillin PK/PD parameters for the treatment of AOM in children and assess whether these variations could explain why the commonly employed amoxicillin PK/PD model is imperfect in predicting outcome for every patient in this clinical setting. To this end, a literature search of MEDLINE (1966-2006) and EMBASE (1974-2006) was conducted to identify studies that evaluated ampicillin or amoxicillin intestinal absorption, serum concentrations, and/or middle ear fluid (MEF) concentrations. Analysis of studies identified for review showed that the intestinal bioavailability of amoxicillin depends on passive diffusion and a saturable 'pump' mechanism that produces variable serum concentrations of the antibacterial agent. Indeed...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2664517</comments>
            <pubDate>Tue, 04 Aug 2009 09:22:02 +0100</pubDate>
            <guid isPermaLink="false">2664517</guid>        </item>
        <item>
            <title>Caspofungin: in pediatric patients with fungal infections.</title>
            <link>http://www.medworm.com/index.php?rid=2664516&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19566110%26dopt%3DAbstract</link>
            <description>Authors: Garnock-Jones KP, Keam SJ
    black triangle Caspofungin is the first echinocandin to be approved for the treatment of fungal infections in pediatric patients. The antifungal properties of caspofungin result from interference with fungal cell-wall integrity. black triangle In vitro, caspofungin is fungicidal against Candida spp. and fungistatic against Aspergillus spp., but has little or no fungicidal or fungistatic activity against Cryptococcus neoformans, the Zygomycetes, Fusarium spp., or Trichosporon beigelii. black triangle Caspofungin was effective as empirical antifungal therapy in pediatric patients with persistent fever and neutropenia. Almost half (46%) of caspofungin recipients and one-third (32%) of liposomal amphotericin B recipients achieved an overall favorable resp...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2664516</comments>
            <pubDate>Tue, 04 Aug 2009 09:22:02 +0100</pubDate>
            <guid isPermaLink="false">2664516</guid>        </item>
        <item>
            <title>Micafungin: a review of its use in the prophylaxis and treatment of invasive Candida infections in pediatric patients.</title>
            <link>http://www.medworm.com/index.php?rid=2664515&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19566111%26dopt%3DAbstract</link>
            <description>Authors: Carter NJ, Keating GM
    Intravenous micafungin (Mycamine(R); Funguard(R)) is an echinocandin indicated in Japan and the EU for the treatment of pediatric patients (including neonates) with invasive candidiasis and as prophylaxis against Candida infection in pediatric patients undergoing allogeneic hematopoietic stem cell transplantation (HSCT). In the EU, micafungin is also indicated in pediatric patients who are expected to have neutropenia for &amp;gt;/=10 days. In Japan, children may also receive micafungin for the treatment of, or as prophylaxis against, invasive Aspergillus infection. Micafungin is not currently approved for use in pediatric patients in the US. Micafungin has very good antifungal activity against a wide range of Candida spp. in vitro. It has a favorable pharmac...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2664515</comments>
            <pubDate>Tue, 04 Aug 2009 09:22:02 +0100</pubDate>
            <guid isPermaLink="false">2664515</guid>        </item>
        <item>
            <title>Potential Vitamin-Drug Interactions in Children: At a Pediatric Emergency Department.</title>
            <link>http://www.medworm.com/index.php?rid=2571661&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19566109%26dopt%3DAbstract</link>
            <description>Authors: Goldman RD, Vohra S, Rogovik AL
    A significant increase in vitamin use has been observed in recent years and interactions between vitamins and medications have been reported. To determine the frequency and types of potential interactions between vitamins and medications in children arriving at a large tertiary, pediatric emergency department. We also compared family characteristics of children with potential interactions with those of children with no potential interactions, in order to determine children at a higher risk. A cross-sectional study in which a survey was conducted of parents/caregivers and/or patients aged 0-18 years registered at a large pediatric emergency department in Canada. A total of 1804 families underwent a face-to-face interview. The main outcome measure...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2571661</comments>
            <pubDate>Sun, 05 Jul 2009 21:00:06 +0100</pubDate>
            <guid isPermaLink="false">2571661</guid>        </item>
        <item>
            <title>The dutch medicines for children research network: a new resource for clinical trials.</title>
            <link>http://www.medworm.com/index.php?rid=2538134&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19445544%26dopt%3DAbstract</link>
            <description>Authors: Weber EH, Timmermans IT, Offringa M
    In Europe, several national networks have been established to undertake clinical research of medicines for children. In the Netherlands, the Dutch Medicines for Children Research Network (MCRN) was launched in September 2008. The purpose of the Dutch MCRN is to improve the speed, quality, and coordination of clinical drug research in children, ultimately resulting in better patient care.
    PMID: 19445544 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2538134</comments>
            <pubDate>Sat, 27 Jun 2009 20:47:04 +0100</pubDate>
            <guid isPermaLink="false">2538134</guid>        </item>
        <item>
            <title>Multimodal Treatments versus Pharmacotherapy Alone in Children with Psychiatric Disorders: Implications of Access, Effectiveness, and Contextual Treatment.</title>
            <link>http://www.medworm.com/index.php?rid=2538132&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19445545%26dopt%3DAbstract</link>
            <description>Authors: Reeves G, Anthony B
    Practice guidelines for the treatment of youth with mental health problems tend to endorse integrating psychopharmacologic treatment with psychosocial interventions, such as psychotherapy and parent skills training. However, poor access to pediatric mental health specialists and inadequate training of primary care physicians in psychosocial interventions make it difficult for families to receive this standard of care. Large pediatric randomized, multicenter trials, including the Multimodal Treatment Study of ADHD (attention deficit hyperactivity disorder) [MTA] and the Treatment for Adolescents with Depression Study (TADS), have begun to identify specific advantages of multimodal treatment compared with psychopharmacology alone. Advantages of combined treat...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2538132</comments>
            <pubDate>Sat, 27 Jun 2009 20:47:04 +0100</pubDate>
            <guid isPermaLink="false">2538132</guid>        </item>
        <item>
            <title>Pediatric generalized anxiety disorder: epidemiology, diagnosis, and management.</title>
            <link>http://www.medworm.com/index.php?rid=2538130&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19445546%26dopt%3DAbstract</link>
            <description>Authors: Keeton CP, Kolos AC, Walkup JT
    Pediatric generalized anxiety disorder (GAD) is characterized by excessive and uncontrollable worry about a variety of events and is accompanied by physical symptoms such as headaches, tension, restlessness, gastrointestinal distress, and heart palpitations. Symptoms impose marked distress and interfere with social, emotional, and educational functioning. GAD occurs in over 10% of children and adolescents, has an average age of onset of 8.5 years, and is more often reported in girls. Common co-occurring conditions include separation anxiety disorder and social phobia. Assessment involves a multi-informant, multi-method approach involving the child, parents, and school teachers. A clinical interview should be conducted to assess for the three prim...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2538130</comments>
            <pubDate>Sat, 27 Jun 2009 20:47:04 +0100</pubDate>
            <guid isPermaLink="false">2538130</guid>        </item>
        <item>
            <title>Current pharmacological management of gastro-esophageal reflux in children: an evidence-based systematic review.</title>
            <link>http://www.medworm.com/index.php?rid=2538128&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19445547%26dopt%3DAbstract</link>
            <description>Authors: Tighe MP, Afzal NA, Bevan A, Beattie RM
    Gastro-esophageal reflux (GER) is a common phenomenon, characterized by the regurgitation of the gastric contents into the esophagus. Gastro-esophageal reflux disease (GERD) is the term applied when GER is associated with sequelae or faltering growth. The main aims of treatment are to alleviate symptoms, promote normal growth, and prevent complications. Medical treatments for children include (i) altering the viscosity of the feeds with alginates; (ii) altering the gastric pH with antacids, histamine H(2) receptor antagonists, and proton pump inhibitors; and (iii) altering the motility of the gut with prokinetics, such as metoclopramide and domperidone. Our aim was to systematically review the evidence base for the medical treatment of g...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2538128</comments>
            <pubDate>Sat, 27 Jun 2009 20:47:04 +0100</pubDate>
            <guid isPermaLink="false">2538128</guid>        </item>
        <item>
            <title>Atomoxetine: a review of its use in attention-deficit hyperactivity disorder in children and adolescents.</title>
            <link>http://www.medworm.com/index.php?rid=2538126&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19445548%26dopt%3DAbstract</link>
            <description>Authors: Garnock-Jones KP, Keating GM
    Atomoxetine (Strattera(R)) is a selective norepinephrine (noradrenaline) reuptake inhibitor that is not classified as a stimulant, and is indicated for use in patients with attention-deficit hyperactivity disorder (ADHD). Atomoxetine is effective and generally well tolerated. It is significantly more effective than placebo and standard current therapy and does not differ significantly from or is noninferior to immediate-release methylphenidate; however, it is significantly less effective than the extended-release methylphenidate formulation OROS(R) methylphenidate (hereafter referred to as osmotically released methylphenidate) and extended-release mixed amfetamine salts. Atomoxetine can be administered either as a single daily dose or split into tw...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2538126</comments>
            <pubDate>Sat, 27 Jun 2009 20:47:04 +0100</pubDate>
            <guid isPermaLink="false">2538126</guid>        </item>
        <item>
            <title>Anti-diarrheal effects of diosmectite in the treatment of acute diarrhea in children: a review.</title>
            <link>http://www.medworm.com/index.php?rid=2291050&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19301931%26dopt%3DAbstract</link>
            <description>Authors: Dupont C, Vernisse B
    Acute diarrhea caused by an infectious organism is highly prevalent, particularly in developing countries, and is usually self-limiting. The condition is a major contributor to the global disease burden and is associated with a significant economic cost. The disease is common in children aged &amp;lt;5 years. It occurs as the result of exposure to a diarrheogenic agent that alters intestinal absorption and/or secretion, resulting in an increase in the volume of water that enters the colon beyond that which can be absorbed. Diarrhea almost always occurs by one or more of four mechanisms: disruption of osmotic forces in the intestine; disruption of normal secretory processes; disruption of epithelial cells or the epithelial tight junctions; or motility disorders...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2291050</comments>
            <pubDate>Thu, 26 Mar 2009 16:43:42 +0100</pubDate>
            <guid isPermaLink="false">2291050</guid>        </item>
        <item>
            <title>The role of inhaled corticosteroids in the management of cystic fibrosis.</title>
            <link>http://www.medworm.com/index.php?rid=2291049&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19301932%26dopt%3DAbstract</link>
            <description>Authors: Ross KR, Chmiel JF, Konstan MW
    The lung disease of cystic fibrosis (CF) is characterized by a vicious cycle of airway obstruction, chronic bacterial infection, and vigorous inflammation, which ultimately results in bronchiectasis. Recognition that excessive and persistent inflammation is a key factor in lung destruction has prompted investigation into anti-inflammatory therapies. Although effective, the use of systemic corticosteroids has been limited by the unacceptable adverse effect profile. Inhaled corticosteroids (ICS) are a widely prescribed anti-inflammatory agent in CF, likely as a result of clinicians' familiarity with these agents and their excellent safety profile at low doses in asthmatic patients. However, while multiple studies are limited by small sample size an...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2291049</comments>
            <pubDate>Thu, 26 Mar 2009 16:43:42 +0100</pubDate>
            <guid isPermaLink="false">2291049</guid>        </item>
        <item>
            <title>Etiology, diagnosis, and pharmacologic treatment of pediatric pulmonary hypertension.</title>
            <link>http://www.medworm.com/index.php?rid=2291047&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19301933%26dopt%3DAbstract</link>
            <description>This article reviews the current knowledge about the etiology, investigation, and treatment of children with pulmonary hypertension in the clinical setting.
    PMID: 19301933 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2291047</comments>
            <pubDate>Thu, 26 Mar 2009 16:43:42 +0100</pubDate>
            <guid isPermaLink="false">2291047</guid>        </item>
        <item>
            <title>Pediatric palliative care: use of opioids for the management of pain.</title>
            <link>http://www.medworm.com/index.php?rid=2291042&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19301934%26dopt%3DAbstract</link>
            <description>Authors: Zernikow B, Michel E, Craig F, Anderson BJ
    Pediatric palliative care (PPC) is provided to children experiencing life-limiting diseases (LLD) or life-threatening diseases (LTD). Sixty to 90% of children with LLD/LTD undergoing PPC receive opioids at the end of life. Analgesia is often insufficient. Reasons include a lack of knowledge concerning opioid prescribing and adjustment of opioid dose to changing requirements. The choice of first-line opioid is based on scientific evidence, pain pathophysiology, and available administration modes. Doses are calculated on a bodyweight basis up to a maximum absolute starting dose. Morphine remains the gold standard starting opioid in PPC. Long-term opioid choice and dose administration is determined by the pathology, analgesic effectivene...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2291042</comments>
            <pubDate>Thu, 26 Mar 2009 16:43:42 +0100</pubDate>
            <guid isPermaLink="false">2291042</guid>        </item>
        <item>
            <title>Incidence, Preventability, and Impact of Adverse Drug Events (ADEs) and Potential ADEs in Hospitalized Children in New Zealand: A Prospective Observational Cohort Study.</title>
            <link>http://www.medworm.com/index.php?rid=2291037&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19301935%26dopt%3DAbstract</link>
            <description>Authors: Kunac DL, Kennedy J, Austin N, Reith D
    Adverse drug events (ADEs) are an important problem in all hospitalized patients as these events represent medication-related patient harm. Few epidemiologic data exist regarding ADEs in the pediatric inpatient setting and, in particular, the economic impact of such ADEs upon the healthcare sector. To evaluate the incidence, preventability, and seriousness of ADEs and potential ADEs occurring in hospitalized children and to examine the cost implications of these ADEs. This was a prospective observational cohort study conducted in the pediatric, neonatal intensive care unit (NICU), and postnatal wards of a university-affiliated urban general hospital in Dunedin, New Zealand (NZ). The study population was all patients admitted to these ward...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2291037</comments>
            <pubDate>Thu, 26 Mar 2009 16:43:42 +0100</pubDate>
            <guid isPermaLink="false">2291037</guid>        </item>
        <item>
            <title>Establishing an international collaborative network in pediatric pharmacology. Proceedings of the Toronto Satellite in Pediatric Pharmacology, a satellite meeting of the IXth World Conference on Clinical Pharmacology and Therapeutics. July 25-26, 2008. Toronto, Ontario, Canada.</title>
            <link>http://www.medworm.com/index.php?rid=2242024&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19266625%26dopt%3DAbstract</link>
            <description>Authors: 
    
    PMID: 19266625 [PubMed - indexed for MEDLINE] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2242024</comments>
            <pubDate>Sat, 07 Mar 2009 14:02:06 +0100</pubDate>
            <guid isPermaLink="false">2242024</guid>        </item>
        <item>
            <title>The global alliance for pediatric pharmacology: the future is here and now.</title>
            <link>http://www.medworm.com/index.php?rid=2168487&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127940%26dopt%3DAbstract</link>
            <description>Authors: Koren G, Rieder M, MacLeod SM
    The vast majority of drugs prescribed for children have not been approved by regulatory agencies for the pediatric age group and, in many cases, have not been studied appropriately. In July 2008, at a meeting of pediatric pharmacologists from over 30 countries and 5 continents in Toronto, ON, Canada, it became apparent that numerous pediatric drug studies are being conducted, often duplicating studies done elsewhere. This is also true for pharmacokinetic and pharmacodynamic studies, as well as for the development of pediatric formulations. Finding simple ways to inform the world about existing data may save time and facilitate efforts.
    PMID: 19127940 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2168487</comments>
            <pubDate>Sun, 08 Feb 2009 21:00:10 +0100</pubDate>
            <guid isPermaLink="false">2168487</guid>        </item>
        <item>
            <title>Australian report on pediatric medication issues: is any magic happening in the 'land of oz' to save the therapeutic orphan?</title>
            <link>http://www.medworm.com/index.php?rid=2168486&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127951%26dopt%3DAbstract</link>
            <description>Authors: Beggs S
    Australian prescribers have faced many of the same issues as those in other developed countries in relation to medicines for children. Australia represents &amp;lt;1% of the world pharmaceutical market, with the pediatric market being a fraction of this. Thus, Australia's ability to influence the global market has been seen as limited, and it had been hoped that Australian children would benefit from international efforts in the area of medicines for children. This, however, has not eventuated, with there being very little change in the availability of medications for children in Australia over the past 2 decades. A number of reviews have been undertaken looking at the issue of medication for children in Australia and what could be done. Recently, two significant events ha...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2168486</comments>
            <pubDate>Sun, 08 Feb 2009 21:00:10 +0100</pubDate>
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        <item>
            <title>Delivering better medicines to children: need for better integration between the science, the policy, and the practice.</title>
            <link>http://www.medworm.com/index.php?rid=2168485&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127952%26dopt%3DAbstract</link>
            <description>Authors: Gazarian M
    We are experiencing an exciting and unprecedented period in the history of children's medicines globally. Milestone developments unfolding in recent years include the formation of the International Alliance for Better Medicines for Children in 2006 and landmark initiatives by the EU, the World Health Assembly (WHA), and the WHO in 2007. However, the challenges of optimizing the development, wider availability, and routine use of effective, safe, and affordable medicines addressing important child health needs are considerable. Each aspect of this continuum has so far received differential attention. Major initiatives in the US and EU have focused on stimulating research into children's medicines, largely driven by drug regulatory reforms, but with important gaps rem...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2168485</comments>
            <pubDate>Sun, 08 Feb 2009 21:00:10 +0100</pubDate>
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        <item>
            <title>Training pediatric clinical pharmacology and therapeutics specialists of the future: the needs, the reality, and opportunities for international networking.</title>
            <link>http://www.medworm.com/index.php?rid=2168484&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127959%26dopt%3DAbstract</link>
            <description>Authors: Gazarian M
    In recent years there has been a rapid and marked increase in global recognition of the need for better medicines for children, with various initiatives being implemented at global and regional levels. These exciting developments are matched by recognition of the need to build greater capacity in the field of pediatric clinical pharmacology and therapeutics to help deliver on the promise of better medicines for children. A range of pediatric medicines researchers, educators, clinical therapeutics practitioners, and experts in drug evaluation, regulation, and broader medicines policy are needed on a larger scale, in both developed and developing world settings. The current and likely future training needs to meet these diverse challenges, the current realities of try...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2168484</comments>
            <pubDate>Sun, 08 Feb 2009 21:00:10 +0100</pubDate>
            <guid isPermaLink="false">2168484</guid>        </item>
        <item>
            <title>Clinical investigation in pediatrics: challenges and opportunities in Toronto, Canada.</title>
            <link>http://www.medworm.com/index.php?rid=2168483&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127960%26dopt%3DAbstract</link>
            <description>Authors: Ito S
    We discuss the challenges and opportunities we face at The Hospital for Sick Children in Toronto, ON, Canada in conducting clinical investigation in children. Three areas are discussed: (i) the program structure of the Research Institute; (ii) the Toronto Centre for Phenogenomics as a common platform for preclinical studies across the university campus; and (iii) evolving clinical research infrastructure. Because preclinical and clinical investigation are becoming increasingly resource-intensive, we are witnessing a trend toward functional amalgamation of research teams, centralization of major experimental facilities, and the expansion of research infrastructure at local and national levels. Although these trends are common to clinical research in all age groups, pediat...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2168483</comments>
            <pubDate>Sun, 08 Feb 2009 21:00:10 +0100</pubDate>
            <guid isPermaLink="false">2168483</guid>        </item>
        <item>
            <title>Physiology and experimental medicine: translational research at the Toronto Hospital For Sick Children.</title>
            <link>http://www.medworm.com/index.php?rid=2168482&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127961%26dopt%3DAbstract</link>
            <description>Authors: Ottaviani PT
    Physiology and Experimental Medicine at The Hospital For Sick Children (Toronto, ON, Canada) is a multidisciplinary program that brings together significant interdisciplinary and interprofessional activity from different study areas such as: lung and cardiovascular physiology; imaging; metabolism and nutrition; pharmacology; and experimental medicine. The program is comprised of researchers, clinicians, and educators who focus on the study of complex, integrated bodily systems. Special emphasis is placed on investigations which bridge in vitro and in vivo approaches, basic science with clinical applications, experimental models with human disease, and human subject research.
    PMID: 19127961 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2168482</comments>
            <pubDate>Sun, 08 Feb 2009 21:00:10 +0100</pubDate>
            <guid isPermaLink="false">2168482</guid>        </item>
        <item>
            <title>Training clinicians in Maternal-Fetal Pharmacology: closing a conceptual gap.</title>
            <link>http://www.medworm.com/index.php?rid=2168481&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127962%26dopt%3DAbstract</link>
            <description>Authors: Koren G
    Developmental pharmacology is a science that does not start at birth, but rather preconceptionally. However, training for obstetricians, perinatologists, and neonatologists in this field is almost nonexistent. The novel Summer Institute in Maternal-Fetal Pharmacology is presented, with preliminary indications that it fulfils its mandate.
    PMID: 19127962 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2168481</comments>
            <pubDate>Sun, 08 Feb 2009 21:00:10 +0100</pubDate>
            <guid isPermaLink="false">2168481</guid>        </item>
        <item>
            <title>Rotavirus vaccine RIX4414 (Rotarix): a review of its use in the prevention of rotavirus gastroenteritis.</title>
            <link>http://www.medworm.com/index.php?rid=2168480&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127963%26dopt%3DAbstract</link>
            <description>Authors: McCormack PL, Keam SJ, Bernstein DI, Grimwood K, Linhares AC, Madhi SA, Nakagomi O, Vesikari T
    Rotavirus vaccine RIX4414 is an oral vaccine composed of a monovalent, live, attenuated, human rotavirus strain of G1P[8] type. RIX4414 vaccination in infants aged 6-17 weeks at enrolment provided protection against rotavirus gastroenteritis (RVGE) of any severity and high-level protection against severe RVGE requiring hospitalization in large, randomized clinical trials conducted in a wide range of geographic regions. Protective efficacy was evident over the period (2 months) between the first and second doses of vaccine, and the protection afforded by the full two-dose course was sustained for at least 2 years, the limit to which efficacy was assessed. RIX4414 displayed protective ...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2168480</comments>
            <pubDate>Sun, 08 Feb 2009 21:00:10 +0100</pubDate>
            <guid isPermaLink="false">2168480</guid>        </item>
        <item>
            <title>Improving drug treatment for children: are we making an impact?</title>
            <link>http://www.medworm.com/index.php?rid=2093280&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127939%26dopt%3DAbstract</link>
            <description>Authors: Macleod SM
    At the beginning of 2009, we are on the threshold of mobilizing expertise in child health care and pediatric pharmacy and pharmacology in pursuit of worldwide major improvements in drug therapy for children. Momentum is built on progressive legislation on pediatric drug therapy from the US and Europe and on recent advances promoted by the WHO, including publication of an essential medicines list for children. Opportunities abound for research, educational initiatives, and practice improvements likely to bear early fruit in the form of better pharmacotherapy for children and youth. The most pressing challenge remaining is mobilization of a critical mass of caregivers, pharmacologists, pharmacists, and other child health professionals prepared to address their skills ...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093280</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093280</guid>        </item>
        <item>
            <title>The Global Alliance for Pediatric Pharmacology : The Future is Here and Now.</title>
            <link>http://www.medworm.com/index.php?rid=2093279&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127940%26dopt%3DAbstract</link>
            <description>Authors: Koren G, Rieder M, Macleod SM
    The vast majority of drugs prescribed for children have not been approved by regulatory agencies for the pediatric age group and, in many cases, have not been studied appropriately. In July 2008, at a meeting of pediatric pharmacologists from over 30 countries and 5 continents in Toronto, ON, Canada, it became apparent that numerous pediatric drug studies are being conducted, often duplicating studies done elsewhere. This is also true for pharmacokinetic and pharmacodynamic studies, as well as for the development of pediatric formulations. Finding simple ways to inform the world about existing data may save time and facilitate efforts.
    PMID: 19127940 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093279</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093279</guid>        </item>
        <item>
            <title>Pediatric pharmacotherapy issues in Africa.</title>
            <link>http://www.medworm.com/index.php?rid=2093278&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127941%26dopt%3DAbstract</link>
            <description>Authors: Gray A
    Pediatric pharmacotherapy in Africa is constrained by a variety of factors, not all of them unique to the continent. While affordability of medicines and the availability of sustainable financing for healthcare are constant challenges to African health systems, other issues of particular importance for pediatric care are also hampering access. These include the burden of disease in such settings, the lack of appropriate human resources for health, and the lack of child-appropriate dosage forms, especially for ambulatory care. Access to medicines for children has been recognized as a global priority. Examples of developments that have the potential to improve pediatric pharmacotherapy in resource-constrained settings are the WHO Essential Medicines List for Children and ...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093278</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093278</guid>        </item>
        <item>
            <title>The European paediatric initiative: 1 year of experience.</title>
            <link>http://www.medworm.com/index.php?rid=2093277&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127942%26dopt%3DAbstract</link>
            <description>Authors: Saint-Raymond A, Seigneuret N
    The European Regulation on medicines for pediatric use entered into force on 26 January 2007. It changes dramatically the way medicines are developed for children. This regulation will increase availability of and information on pediatric medicines through high quality, ethical research.
    PMID: 19127942 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093277</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093277</guid>        </item>
        <item>
            <title>German Paediatric Research Network (PAED-Net).</title>
            <link>http://www.medworm.com/index.php?rid=2093276&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127943%26dopt%3DAbstract</link>
            <description>Authors: Seibert-Grafe M, Butzer R, Zepp F
    Clinical trials in children are mandatory to generate data on new drugs as well as on drugs used off-label or for unlicensed indications. The EU Paediatric Regulation introduced in 2007 provides the background, goals, and requirements for pediatric clinical trials. The German Paediatric Network (PAED-Net) was established in 2002 with a public grant from the German Ministry of Education and Research with the aim of developing competence, infrastructure, networking, and education for pediatric clinical trials. The network, consisting of six pediatric clinical units and a coordinating office, has progressed very well and has achieved valuable improvements concerning the conduct of pediatric clinical trials. In addition, training programs have enc...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093276</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093276</guid>        </item>
        <item>
            <title>The national institute for health research medicines for children research network.</title>
            <link>http://www.medworm.com/index.php?rid=2093275&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127944%26dopt%3DAbstract</link>
            <description>Authors: Nunn T
    The UK has established the National Institute for Health Research Medicines for Children Research Network to provide infrastructure to facilitate the conduct of randomized trials and other well designed studies sponsored by the pharmaceutical industry and public funding bodies. Clinical Studies Groups of experts establish priorities and assist in the development of protocols whilst Local Research Networks and an Extended Neonatal Network facilitate their implementation and conduct. Two Clinical Trials Units and a co-ordinating center assist in the development and conduct of studies and performance manage the network. Work streams on formulation and experimental medicine have been established. As of August 2008, 16 commercially sponsored studies had been adopted (from 12...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093275</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093275</guid>        </item>
        <item>
            <title>Drug therapy for children in china.</title>
            <link>http://www.medworm.com/index.php?rid=2093274&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127945%26dopt%3DAbstract</link>
            <description>Authors: Li Z, Wang Y
    The population of China is huge and includes 400 million children. For China, as for other countries in the world, there remain a number of questions from the past about drug therapy for children, such as unlicensed and off-label drug usage. Recently, China has updated Good Clinical Practice (GCP) guidelines, including those for pediatric drug clinical trials. Pediatric pharmacology research units need to be set up throughout the country. To provide better medicines to children in China is an enormous undertaking.
    PMID: 19127945 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093274</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093274</guid>        </item>
        <item>
            <title>The Task-force in Europe for Drug Development for the Young (TEDDY) Network of Excellence.</title>
            <link>http://www.medworm.com/index.php?rid=2093273&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127946%26dopt%3DAbstract</link>
            <description>Authors: Ceci A, Giaquinto C, Aboulker JP, Baiardi P, Bonifazi F, Della Pasqua O, Nicolosi A, Taruscio D, Sturkenboom M, Wong I
    The Task-force in Europe for Drug Development for the Young (TEDDY) was established in 2005 to contribute to the promotion of safe and efficacious medicines for children in the context of the impending European Paediatric Regulation that finally came into force in January 2007. The project includes seven objectives and 12 Work-Packages encompassing the main aspects of the development and use of pediatric drugs. TEDDY represents a new entity in the pediatric pharmaceutical field, differing from a Scientific Society, a network for developing research or trials, or a consultative regulatory body. The ambition of TEDDY is to support the existing pediatric networks...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093273</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093273</guid>        </item>
        <item>
            <title>Both parental psychopathology and prenatal maternal alcohol dependency can predict the behavioral phenotype in children.</title>
            <link>http://www.medworm.com/index.php?rid=2093272&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127947%26dopt%3DAbstract</link>
            <description>CONCLUSION: Parental psychopathology and prenatal exposure to maternal alcohol can contribute to the child's behavioral phenotype as measured by the CBCL. Therefore, the CBCL can be used to screen for such behaviors.
    PMID: 19127947 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093272</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093272</guid>        </item>
        <item>
            <title>Potential role of the placenta in fetal alcohol spectrum disorder.</title>
            <link>http://www.medworm.com/index.php?rid=2093271&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127948%26dopt%3DAbstract</link>
            <description>CONCLUSIONS: Identical maternal ethanol exposure levels produced differing levels of fetal exposure in a dizygotic human twin pair and a series of guinea pig littermates as evidenced through FAEE meconium analysis. These data indicate that the placenta may have a previously unappreciated role in mediating ethanol-induced fetal injury.
    PMID: 19127948 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093271</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093271</guid>        </item>
        <item>
            <title>Passive environmental exposure to cocaine in canadian children.</title>
            <link>http://www.medworm.com/index.php?rid=2093270&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127949%26dopt%3DAbstract</link>
            <description>CONCLUSION: Measurement of cocaine hair concentrations can allow estimation of the degree of environmental drug exposure in young children. Infants seem to have a disproportionately increased risk for systemic exposure, compared with older children.
    PMID: 19127949 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093270</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093270</guid>        </item>
        <item>
            <title>Pediatric clinical pharmacology studies in chagas disease: focus on Argentina.</title>
            <link>http://www.medworm.com/index.php?rid=2093269&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127950%26dopt%3DAbstract</link>
            <description>Authors: Garcia-Bournissen F, Altcheh J, Giglio N, Mastrantonio G, Omar Della V&amp;#xE9;dova C, Koren G
    Chagas disease is a neglected parasitic disease endemic in the Americas. It mainly affects impoverished populations and the acute phase of the infection mostly affects children. Many cases have also been detected in nonendemic countries as a result of recent migratory trends. The chronic phase is relatively asymptomatic, but 30% of patients with chronic infection eventually develop cardiac and digestive complications that commonly lead to death or disability. Only two drugs are available for the treatment of Chagas disease, benznidazole and nifurtimox. These drugs have been shown to be effective in the treatment of both acute and early chronic phases in children, but the pharmacokinetic...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093269</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093269</guid>        </item>
        <item>
            <title>Australian report on pediatric medication issues : is any magic happening in the 'land of oz' to save the therapeutic orphan?</title>
            <link>http://www.medworm.com/index.php?rid=2093268&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127951%26dopt%3DAbstract</link>
            <description>Authors: Beggs S
    Australian prescribers have faced many of the same issues as those in other developed countries in relation to medicines for children. Australia represents &amp;lt;1% of the world pharmaceutical market, with the pediatric market being a fraction of this. Thus, Australia's ability to influence the global market has been seen as limited, and it had been hoped that Australian children would benefit from international efforts in the area of medicines for children. This, however, has not eventuated, with there being very little change in the availability of medications for children in Australia over the past 2 decades. A number of reviews have been undertaken looking at the issue of medication for children in Australia and what could be done. Recently, two significant events ha...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093268</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093268</guid>        </item>
        <item>
            <title>Delivering better medicines to children : need for better integration between the science, the policy, and the practice.</title>
            <link>http://www.medworm.com/index.php?rid=2093267&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127952%26dopt%3DAbstract</link>
            <description>Authors: Gazarian M
    We are experiencing an exciting and unprecedented period in the history of children's medicines globally. Milestone developments unfolding in recent years include the formation of the International Alliance for Better Medicines for Children in 2006 and landmark initiatives by the EU, the World Health Assembly (WHA), and the WHO in 2007. However, the challenges of optimizing the development, wider availability, and routine use of effective, safe, and affordable medicines addressing important child health needs are considerable. Each aspect of this continuum has so far received differential attention. Major initiatives in the US and EU have focused on stimulating research into children's medicines, largely driven by drug regulatory reforms, but with important gaps rem...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093267</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093267</guid>        </item>
        <item>
            <title>The national institutes of health and the best pharmaceuticals for children act.</title>
            <link>http://www.medworm.com/index.php?rid=2093266&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127953%26dopt%3DAbstract</link>
            <description>Authors: Zajicek A
    The majority of drugs used to treat children are not labeled for use in children. The Best Pharmaceuticals for Children Act of 2002, re-authorized as the US FDA Amendments Act of 2007, directs the National Institutes of Health (NIH) to sponsor pediatric clinical trials of drugs lacking patent protection, if the FDA request for studies has been declined. The NIH is currently sponsoring 17 clinical studies. Challenges encountered include a paucity of investigators who are trained in pediatric clinical pharmacology; inadequate knowledge of the mechanisms of drug action in a growing child; and lack of pediatric formulations.
    PMID: 19127953 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093266</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
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        <item>
            <title>Optimal drug therapy for children: canadian initiatives.</title>
            <link>http://www.medworm.com/index.php?rid=2093265&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127954%26dopt%3DAbstract</link>
            <description>Authors: Rieder M
    Canada has a long tradition of undertaking research and training in pediatric clinical pharmacology, and has one of the longest continuous enterprises in this field in the world. Training in pediatric clinical pharmacology in Canada is nationally accredited and rigorous. Canada has the largest number of pediatric clinical pharmacologists per capita of any country on earth, but to date there have been no federally supported initiatives for child-focused drug research. The recent development of a unique national network focused on drug safety - the Genotypic Approaches to Therapy in Children - has provided a framework that it hopes will facilitate networking as well as the development of coordinated national and hopefully international initiatives in pediatric therapeut...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093265</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093265</guid>        </item>
        <item>
            <title>Medication errors in children.</title>
            <link>http://www.medworm.com/index.php?rid=2093264&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127955%26dopt%3DAbstract</link>
            <description>Authors: Kozer E
    Medication errors commonly involve children, with dosing errors being the most common. Medication errors are more frequent among the most sick patients who have urgent and complex medical conditions. Physicians who are less experienced, tired, depressed, and burnt out make more errors. The systems approach views every medical error as a system failure. The focus is on how to change the system in order to prevent errors. Adopting the systems approach will enhance patients' safety. Strategies that have been found to be effective in reducing medication errors include the use of computerized physician order entry systems, pre-printed order forms, color-coded systems, and involving pharmacists in clinical care.
    PMID: 19127955 [PubMed - in process] (Source: Paediatric Dr...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093264</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093264</guid>        </item>
        <item>
            <title>Pediatric formulations: international issues and potential solutions.</title>
            <link>http://www.medworm.com/index.php?rid=2093263&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127956%26dopt%3DAbstract</link>
            <description>Authors: Knoppert DC
    Appropriate dosage forms of medication are often not available for use in newborns, infants, and young children. This is a worldwide phenomenon, but especially in developing countries. The WHO's 'Make medicines child size' campaign emphasizes this shortcoming. Professional organizations, industry, and government from the international arena have the resources to address this and need to work together to create solutions.
    PMID: 19127956 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093263</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093263</guid>        </item>
        <item>
            <title>Challenges in pediatric drug development: a pharmaceutical industry perspective.</title>
            <link>http://www.medworm.com/index.php?rid=2093262&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127957%26dopt%3DAbstract</link>
            <description>Authors: Rose K
    A paradigm change is taking place from protecting children against clinical research to protecting them through research. It is based on a better scientific understanding of the child's physiology, on the increasing potential of biomedical interventions, and on an evolving conviction of children's right to benefit from scientific and pharmaceutical progress. The WHO campaign 'Make medicines child size' is contributing to expand this to a global vision of the health of all children. Research-based pharmaceutical industry develops innovative new medicines for serious and life-threatening diseases. It has built up competency in pediatric drug development and has welcomed US and EU pediatric legislation as well as the WHO campaign. More diseases without effective therapy in...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093262</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093262</guid>        </item>
        <item>
            <title>Training clinicians in pediatric pharmacology-toxicology: the toronto model.</title>
            <link>http://www.medworm.com/index.php?rid=2093261&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127958%26dopt%3DAbstract</link>
            <description>Authors: Koren G
    Established in 1979, the Toronto Program in Pediatric Pharmacology has trained pediatricians and pharmacists from over 30 countries and five continents. Within the training guidelines of the Royal College of Physicians and Surgeons of Canada, the philosophy of the program is tailoring the goals to meet the specific needs and career goals of each trainee. The program will continue to prepare pediatricians for the rapidly changing challenges of rational drug therapy for children.
    PMID: 19127958 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093261</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093261</guid>        </item>
        <item>
            <title>Training pediatric clinical pharmacology and therapeutics specialists of the future : the needs, the reality, and opportunities for international networking.</title>
            <link>http://www.medworm.com/index.php?rid=2093260&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127959%26dopt%3DAbstract</link>
            <description>Authors: Gazarian M
    In recent years there has been a rapid and marked increase in global recognition of the need for better medicines for children, with various initiatives being implemented at global and regional levels. These exciting developments are matched by recognition of the need to build greater capacity in the field of pediatric clinical pharmacology and therapeutics to help deliver on the promise of better medicines for children. A range of pediatric medicines researchers, educators, clinical therapeutics practitioners, and experts in drug evaluation, regulation, and broader medicines policy are needed on a larger scale, in both developed and developing world settings. The current and likely future training needs to meet these diverse challenges, the current realities of try...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093260</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093260</guid>        </item>
        <item>
            <title>Clinical investigation in pediatrics : challenges and opportunities in toronto, Canada.</title>
            <link>http://www.medworm.com/index.php?rid=2093259&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127960%26dopt%3DAbstract</link>
            <description>Authors: Ito S
    We discuss the challenges and opportunities we face at The Hospital for Sick Children in Toronto, ON, Canada in conducting clinical investigation in children. Three areas are discussed: (i) the program structure of the Research Institute; (ii) the Toronto Centre for Phenogenomics as a common platform for preclinical studies across the university campus; and (iii) evolving clinical research infrastructure. Because preclinical and clinical investigation are becoming increasingly resource-intensive, we are witnessing a trend toward functional amalgamation of research teams, centralization of major experimental facilities, and the expansion of research infrastructure at local and national levels. Although these trends are common to clinical research in all age groups, pediat...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093259</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093259</guid>        </item>
        <item>
            <title>Physiology and experimental medicine : translational research at the toronto hospital for sick children.</title>
            <link>http://www.medworm.com/index.php?rid=2093258&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127961%26dopt%3DAbstract</link>
            <description>Authors: Ottaviani PT
    Physiology and Experimental Medicine at The Hospital For Sick Children (Toronto, ON, Canada) is a multidisciplinary program that brings together significant interdisciplinary and interprofessional activity from different study areas such as: lung and cardiovascular physiology; imaging; metabolism and nutrition; pharmacology; and experimental medicine. The program is comprised of researchers, clinicians, and educators who focus on the study of complex, integrated bodily systems. Special emphasis is placed on investigations which bridge in vitro and in vivo approaches, basic science with clinical applications, experimental models with human disease, and human subject research.
    PMID: 19127961 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093258</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093258</guid>        </item>
        <item>
            <title>Training clinicians in maternal-fetal pharmacology : closing a conceptual gap.</title>
            <link>http://www.medworm.com/index.php?rid=2093257&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127962%26dopt%3DAbstract</link>
            <description>Authors: Koren G
    Developmental pharmacology is a science that does not start at birth, but rather preconceptionally. However, training for obstetricians, perinatologists, and neonatologists in this field is almost nonexistent. The novel Summer Institute in Maternal-Fetal Pharmacology is presented, with preliminary indications that it fulfils its mandate.
    PMID: 19127962 [PubMed - in process] (Source: Paediatric Drugs)</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093257</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
            <guid isPermaLink="false">2093257</guid>        </item>
        <item>
            <title>Rotavirus Vaccine RIX4414 (Rotarixtrade mark): A Review of its Use in the Prevention of Rotavirus Gastroenteritis.</title>
            <link>http://www.medworm.com/index.php?rid=2093256&amp;cid=s_36854_33_f&amp;fid=36854&amp;url=http%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fentrez%2Fquery.fcgi%3Ftmpl%3DNoSidebarfile%26db%3DPubMed%26cmd%3DRetrieve%26list_uids%3D19127963%26dopt%3DAbstract</link>
            <description>Authors: McCormack PL, Keam SJ
    Rotavirus vaccine RIX4414 is an oral vaccine composed of a monovalent, live, attenuated, human rotavirus strain of G1P[8] type.RIX4414 vaccination in infants aged 6-17 weeks at enrolment provided protection against rotavirus gastroenteritis (RVGE) of any severity and high-level protection against severe RVGE requiring hospitalization in large, randomized clinical trials conducted in a wide range of geographic regions. Protective efficacy was evident over the period (2 months) between the first and second doses of vaccine, and the protection afforded by the full two-dose course was sustained for at least 2 years, the limit to which efficacy was assessed. RIX4414 displayed protective efficacy against the common rotavirus G, P[8] types (G1P[8], G3P[8], G4P[8...</description>
            <author>Paediatric Drugs</author>
            <type>journals</type>
        <comments>http://www.medworm.com/rss/comments.php?id=2093256</comments>
            <pubDate>Sat, 10 Jan 2009 11:41:10 +0100</pubDate>
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