PMID- 20595275 OWN - NLM STAT- MEDLINE DCOM- 20110214 LR - 20131121 IS - 1499-2752 (Electronic) IS - 0315-162X (Linking) VI - 37 IP - 9 DP - 2010 Sep TI - Treatment approaches to juvenile dermatomyositis (JDM) across North America: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) JDM Treatment Survey. PG - 1953-61 LID - 10.3899/jrheum.090953 [doi] AB - 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. 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. 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. CONCLUSION: 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. FAU - Stringer, Elizabeth AU - Stringer E AD - IWK Health Centre, 5850 University Avenue, Halifax, Nova Scotia B3K 6R8. Elizabeth.stringer@iwk.nshealth.ca FAU - Bohnsack, John AU - Bohnsack J FAU - Bowyer, Suzanne L AU - Bowyer SL FAU - Griffin, Thomas A AU - Griffin TA FAU - Huber, Adam M AU - Huber AM FAU - Lang, Bianca AU - Lang B FAU - Lindsley, Carol B AU - Lindsley CB FAU - Ota, Sylvia AU - Ota S FAU - Pilkington, Clarissa AU - Pilkington C FAU - Reed, Ann M AU - Reed AM FAU - Scuccimarri, Rosie AU - Scuccimarri R FAU - Feldman, Brian M AU - Feldman BM LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20100701 PL - Canada TA - J Rheumatol JT - The Journal of rheumatology JID - 7501984 RN - 0 (Adrenal Cortex Hormones) RN - 0 (Antirheumatic Agents) RN - 0 (Immunoglobulins, Intravenous) RN - 8N3DW7272P (Cyclophosphamide) RN - YL5FZ2Y5U1 (Methotrexate) SB - IM MH - Adrenal Cortex Hormones/therapeutic use MH - Antirheumatic Agents/*therapeutic use MH - Arthritis, Juvenile/*drug therapy MH - Child MH - Cyclophosphamide/therapeutic use MH - Dermatomyositis/*drug therapy MH - Humans MH - Immunoglobulins, Intravenous/therapeutic use MH - Methotrexate/therapeutic use MH - *Research Design MH - Therapeutic Human Experimentation MH - Treatment Outcome EDAT- 2010/07/03 06:00 MHDA- 2011/02/15 06:00 CRDT- 2010/07/03 06:00 PHST- 2010/07/03 06:00 [entrez] PHST- 2010/07/03 06:00 [pubmed] PHST- 2011/02/15 06:00 [medline] AID - jrheum.090953 [pii] AID - 10.3899/jrheum.090953 [doi] PST - ppublish SO - J Rheumatol. 2010 Sep;37(9):1953-61. doi: 10.3899/jrheum.090953. Epub 2010 Jul 1.