Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2010 Feb;62(2):219-25.
doi: 10.1002/acr.20071.

Protocols for the initial treatment of moderately severe juvenile dermatomyositis: results of a Children's Arthritis and Rheumatology Research Alliance Consensus Conference

Affiliations

Protocols for the initial treatment of moderately severe juvenile dermatomyositis: results of a Children's Arthritis and Rheumatology Research Alliance Consensus Conference

Adam M Huber et al. Arthritis Care Res (Hoboken). 2010 Feb.

Abstract

Objective: To use juvenile dermatomyositis (DM) survey data and expert opinion to develop a small number of consensus treatment protocols, which reflect current initial treatment of moderately severe juvenile DM.

Methods: A consensus meeting was held in Toronto, Ontario, Canada on December 1-2, 2007. Nominal group technique was used to achieve consensus on treatment protocols, which represented typical management of moderately severe juvenile DM. Consensus was also reached as to which patients these protocols would be applicable (inclusion and exclusion criteria), which initial investigations should be done prior to initiating one of these protocols, which data should be collected to evaluate these protocols, and the concomitant interventions required or recommended.

Results: Three protocols that described the first 2 months of treatment were developed. All protocols included corticosteroids and methotrexate. One protocol also included intravenous gamma globulin. Consensus was achieved for all issues that were addressed by conference participants, although there were some areas of controversy.

Conclusion: Despite considerable variation in clinical practice, it is possible to achieve consensus on the initial treatment of juvenile DM. Once these protocols are extended beyond 2 months, these protocols will be available for clinical use. By using methods that account for differences between patients (confounding by indication), the comparative effectiveness of the protocols will be evaluated. In the future, the goal will be to identify the optimal treatment of moderately severe juvenile DM.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Process followed for achieving consensus for each question considered.

Similar articles

Cited by

References

    1. Bitnum S, Daeschner C, Jr, Travis LB, Dodge WF, Hopps HC. Dermatomyositis. J Pediatr. 1964;64(1):101–31. - PubMed
    1. Huber AM, Lang B, LeBlanc CM, Birdi N, Bolaria R, Malleson P, et al. Medium- and Long-Term Functional Outcomes in a Multicenter Cohort of Children with Juvenile Dermatomyositis. Arthritis Rheum. 2001;43(3):541–9. - PubMed
    1. Stringer E, Ota S, Bohnsack J, Bowyer SL, Griffin TA, Huber AM, et al. Treatment approaches to juvenile dermatomyositis across North America: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) JDM treatment survey. 2009. - PubMed
    1. Horton J. Nominal group technique. A method of decision-making by committee. Anaesthesia. 1980;35(8):811–4. - PubMed
    1. Ruperto N, Ravelli A, Murray K, Lovell DJ, Andersson-Gare B, Feldman BM, et al. Preliminary core sets of measures for disease activity and damage assessment in juvenile systemic lupus erythematosus and juvenile dermatomyositis. Rheumatology. 2003;42(12):1452–9. - PubMed

Publication types

MeSH terms

LinkOut - more resources