Serveur d'exploration Chloroquine

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Treatment approaches to juvenile dermatomyositis (JDM) across North America: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) JDM Treatment Survey.

Identifieur interne : 000137 ( Ncbi/Merge ); précédent : 000136; suivant : 000138

Treatment approaches to juvenile dermatomyositis (JDM) across North America: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) JDM Treatment Survey.

Auteurs : Elizabeth Stringer [Canada] ; John Bohnsack ; Suzanne L. Bowyer ; Thomas A. Griffin ; Adam M. Huber ; Bianca Lang ; Carol B. Lindsley ; Sylvia Ota ; Clarissa Pilkington ; Ann M. Reed ; Rosie Scuccimarri ; Brian M. Feldman

Source :

RBID : pubmed:20595275

Descripteurs français

English descriptors

Abstract

There are a number of different approaches to the initial treatment of juvenile dermatomyositis (JDM). We assessed the therapeutic approaches of North American pediatric rheumatologists to inform future studies of therapy in JDM.

DOI: 10.3899/jrheum.090953
PubMed: 20595275

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pubmed:20595275

Le document en format XML

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<title xml:lang="en">Treatment approaches to juvenile dermatomyositis (JDM) across North America: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) JDM Treatment Survey.</title>
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<name sortKey="Pilkington, Clarissa" sort="Pilkington, Clarissa" uniqKey="Pilkington C" first="Clarissa" last="Pilkington">Clarissa Pilkington</name>
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<term>Adrenal Cortex Hormones (therapeutic use)</term>
<term>Antirheumatic Agents (therapeutic use)</term>
<term>Arthritis, Juvenile (drug therapy)</term>
<term>Child</term>
<term>Cyclophosphamide (therapeutic use)</term>
<term>Dermatomyositis (drug therapy)</term>
<term>Humans</term>
<term>Immunoglobulins, Intravenous (therapeutic use)</term>
<term>Methotrexate (therapeutic use)</term>
<term>Research Design</term>
<term>Therapeutic Human Experimentation</term>
<term>Treatment Outcome</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Antirhumatismaux (usage thérapeutique)</term>
<term>Arthrite juvénile (traitement médicamenteux)</term>
<term>Cyclophosphamide (usage thérapeutique)</term>
<term>Dermatomyosite (traitement médicamenteux)</term>
<term>Enfant</term>
<term>Expérimentation thérapeutique humaine</term>
<term>Hormones corticosurrénaliennes (usage thérapeutique)</term>
<term>Humains</term>
<term>Immunoglobulines par voie veineuse (usage thérapeutique)</term>
<term>Méthotrexate (usage thérapeutique)</term>
<term>Plan de recherche</term>
<term>Résultat thérapeutique</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="therapeutic use" xml:lang="en">
<term>Adrenal Cortex Hormones</term>
<term>Antirheumatic Agents</term>
<term>Cyclophosphamide</term>
<term>Immunoglobulins, Intravenous</term>
<term>Methotrexate</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>Arthritis, Juvenile</term>
<term>Dermatomyositis</term>
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<term>Arthrite juvénile</term>
<term>Dermatomyosite</term>
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<term>Antirhumatismaux</term>
<term>Cyclophosphamide</term>
<term>Hormones corticosurrénaliennes</term>
<term>Immunoglobulines par voie veineuse</term>
<term>Méthotrexate</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Child</term>
<term>Humans</term>
<term>Research Design</term>
<term>Therapeutic Human Experimentation</term>
<term>Treatment Outcome</term>
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<term>Enfant</term>
<term>Expérimentation thérapeutique humaine</term>
<term>Humains</term>
<term>Plan de recherche</term>
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<front>
<div type="abstract" xml:lang="en">There are a number of different approaches to the initial treatment of juvenile dermatomyositis (JDM). We assessed the therapeutic approaches of North American pediatric rheumatologists to inform future studies of therapy in JDM.</div>
</front>
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<PMID Version="1">20595275</PMID>
<DateCompleted>
<Year>2011</Year>
<Month>02</Month>
<Day>14</Day>
</DateCompleted>
<DateRevised>
<Year>2013</Year>
<Month>11</Month>
<Day>21</Day>
</DateRevised>
<Article PubModel="Print-Electronic">
<Journal>
<ISSN IssnType="Print">0315-162X</ISSN>
<JournalIssue CitedMedium="Internet">
<Volume>37</Volume>
<Issue>9</Issue>
<PubDate>
<Year>2010</Year>
<Month>Sep</Month>
</PubDate>
</JournalIssue>
<Title>The Journal of rheumatology</Title>
<ISOAbbreviation>J. Rheumatol.</ISOAbbreviation>
</Journal>
<ArticleTitle>Treatment approaches to juvenile dermatomyositis (JDM) across North America: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) JDM Treatment Survey.</ArticleTitle>
<Pagination>
<MedlinePgn>1953-61</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.3899/jrheum.090953</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">There are a number of different approaches to the initial treatment of juvenile dermatomyositis (JDM). We assessed the therapeutic approaches of North American pediatric rheumatologists to inform future studies of therapy in JDM.</AbstractText>
<AbstractText Label="METHODS" NlmCategory="METHODS">A survey describing clinical cases of JDM was sent to pediatric rheumatologists. The cases described children with varying severity of typical disease, disease with atypical features, or refractory disease. Three open-ended questions were asked following each case: (1) What additional investigations would you order; (2) What medicine(s) would you start (dose, route, frequency, adjustment over time); and (3) What nonmedication treatment(s) would you start.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The response rate was 84% (141/167). For typical cases of JDM, regardless of severity, almost all respondents used corticosteroids and another medication, methotrexate (MTX) being the most commonly used. The route and pattern of corticosteroid administration was variable. Intravenous immunoglobulin (IVIG) was used more frequently for more severe disease, for refractory disease, and for prominent cutaneous disease. Hydroxychloroquine was often used in milder cases and cases principally characterized by rash. Cyclophosphamide was reserved for ulcerative disease and JDM complicated by lung disease.</AbstractText>
<AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">For the majority of North American pediatric rheumatologists, corticosteroids and MTX appear to be the standard of care for typical cases of JDM. There is variability, however, in the route of administration of corticosteroids and use of IVIG and hydroxychloroquine.</AbstractText>
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<Country>Canada</Country>
<MedlineTA>J Rheumatol</MedlineTA>
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