- Research article
- Open Access
Childhood Arthritis and Rheumatology Research Alliance consensus clinical treatment plans for juvenile dermatomyositis with skin predominant disease
Pediatric Rheumatologyvolume 15, Article number: 1 (2017)
Juvenile dermatomyositis (JDM) is the most common form of the idiopathic inflammatory myopathies in children. A subset of children have the rash of JDM without significant weakness, and the optimal treatments for these children are unknown. The goal of this study was to describe the development of consensus clinical treatment plans (CTPs) for children with JDM who have active skin rashes, without significant muscle involvement, referred to as skin predominant JDM in this manuscript.
The Children’s Arthritis and Rheumatology Research Alliance (CARRA) is a North American consortium of pediatric rheumatology health care providers. CARRA members collaborated to determine consensus on typical treatments for JDM patients with skin findings without significant weakness, to develop CTPs for this subgroup of patients. We used a combination of Delphi surveys and nominal group consensus meetings to develop these CTPs.
Consensus was reached on patient characteristics and outcome assessment, and CTPs were developed and finalized for patients with skin predominant JDM. Treatment option A included hydroxychloroquine alone, Treatment option B included hydroxychloroquine and methotrexate, and Treatment option C included hydroxychloroquine, methotrexate and corticosteroids.
Three CTPs were developed for use in children with skin predominant JDM, which reflect typical treatment approaches. These are not considered to be specific recommendations or standard of care. Using the CARRA network and prospective data collection, we will be able to apply statistical methods in the future to allow comparisons of JDM patients following these consensus treatment plans.
Juvenile Dermatomyositis (JDM) is the most common form of the idiopathic inflammatory myopathies in children but is relatively rare, affecting about 1–3 per 1 million children annually in the United States [1, 2]. It is a diffuse vasculopathy with inflammation in skin and muscle, typically associated with weakness and physical limitations.
Classic cutaneous manifestations which are pathognomonic for the diagnosis of JDM include Gottron’s papules and heliotrope rash. Malar rash and nailbed capillary changes are also frequently present . JDM patients typically have proximal muscle weakness, but a subset of patients present with skin disease without any significant weakness or muscle inflammation [4, 5].
General designations for this subset of JDM patients have included: amyopathic dermatomyositis (DM), clinically amyopathic DM, DM sine myositis, and hypomyopathic DM, among others [5–9]. These generally have intended to describe the subset of DM patients with typical skin disease of DM but without clinically significant weakness. For this publication, we will use the term skin predominant JDM to describe the patient subtype under consideration.
The epidemiology, treatment and outcomes of skin predominant JDM are not well studied. The largest series of clinically amyopathic JDM patients published included 68 cases, of which about 25% progressed to classical JDM . Few patients with clinically amyopathic JDM in this series developed disease-related complications: only 4% developed calcinosis and no patients developed vasculopathy, interstitial lung disease or malignancy .
The best treatments for JDM and skin predominant JDM are not known, and treatments used are extremely variable . Proposed therapy of skin predominant JDM includes recommendations for topical and systemic therapies, without trial data or case experiences to support these approaches .
Presently available retrospective studies in JDM are limited by small sample sizes, lack of blinding, and lack of generalizability. Efforts to conduct a traditional randomized controlled trial to conclusively evaluate the best treatment of skin predominant JDM are associated with many challenges. First, the rarity of skin predominant JDM, which is a subset of an already uncommon condition, limits its successful study due to the inability to accrue sufficient numbers of patients from a reasonable number of sites, over a practical time period. In addition, there are significant cost and logistic issues involved in conducting traditional clinical trials in this uncommon condition.
To overcome these obstacles, the Children’s Arthritis and Rheumatology Research Alliance (CARRA) has worked to develop consensus treatment plans (CTPs) to study treatments in patients with rare rheumatic diseases like JDM [13–15] and other pediatric inflammatory conditions [16–18] to allow for pragmatic studies of treatments and outcomes. These have been termed consensus clinical treatment plans, as they have been developed by CARRA members, through consensus methods. These CTPs are meant to represent typical, commonly accepted treatment approaches used by pediatric rheumatologists to treat these illnesses. These commonly accepted treatment approaches are generally based on anecdotal experience and have not been studied in the context of any formal clinical trials.
The intent of the CTP is that each treating clinician will be able to choose and follow a plan for the care of their individual patient, which is similar to their typical treatment approach. This will allow for increased standardization of treatment approaches between institution review board (IRB) approved CARRA centers and clinicians, and facilitate the prospective collection of data through CARRA’s detailed registry, including: patient demographics, clinical and lab characteristics, medication-related adverse events, as well as response to treatments and outcomes. Using patient characteristics and outcomes that will be collected prospectively, innovative statistical methods can be used to account for the selection biases of non-random assignment to CTP treatment groups, to estimate treatment effects comparable to those that might be obtained with traditional randomized controlled trials [19–23].
Previously, a CTP for children presenting with moderate JDM was published by CARRA [13, 14], and a pilot study using that CTP was recently completed and undergoing analysis. A second CTP was developed and recently published for skin resistant JDM, characterized by persistent skin rash despite resolution of muscle involvement . The goal of the present study is to describe the development of a third set of JDM CTPs for skin predominant JDM, which applies to the distinct subset of JDM patients, whose presentation is characterized by classic skin rash without significant muscle involvement.
CARRA is a North American organization, made up of pediatric rheumatologists and other medical professionals, interested in advancing research in pediatric rheumatic conditions. It is comprised of more than 400 individuals from more than 110 centers, which includes the majority of pediatric rheumatologists in North America. CARRA’s mission is to “conduct collaborative research to prevent, treat and cure pediatric rheumatic diseases”.
This CTP was developed over several years of collective work and consensus building, with our CARRA collaborators, to represent typical care provided in the pediatric rheumatology community. At each meeting, results from previous surveys, consensus meetings, as well as relevant literature were reviewed and presented to participants. Surveys were sent to the complete CARRA membership and members were asked to complete the survey if they treated patients with JDM and had sufficient expertise.
CARRA Annual Meeting, 2011—Miami, FL. During this meeting, approximately 36 members of the CARRA JDM Committee discussed the clinically relevant JDM phenotypes for which additional CTPs should be developed. It was agreed that “skin disease” in JDM was important and specifically patients presenting with rash but no clinical weakness were considered to be a clinically relevant subtype of JDM (so called “amyopathic and hypomyopathic” JDM), which would include newly diagnosed JDM patients. It was also agreed that patients with “resistant skin disease” (i.e. patients with typical JDM, who had persistent skin disease despite resolution of muscle involvement following treatment) were a distinct JDM subtype. It was agreed that these subgroups should be considered separately .
There was general discussion regarding patient characteristics of “amyopathic and hypomyopathic” JDM and at this meeting, and it was decided that the preferred descriptor for this subtype of JDM patient would be “skin predominant JDM”. In particular, since some cutaneous features of JDM are considered pathognomonic, initiating treatment for patients in this CTP with at least 6 weeks of skin findings was agreed upon.
CARRA Annual Meeting, 2012—Las Vegas, NV. A smaller core work group of 7 CARRA members from the JDM Committee met to begin developing components of the CTP, including the definition of skin predominant JDM, inclusion and exclusion criteria and a broad range of reasonable treatment regimens, and four candidate treatment arms were agreed upon. The initial candidate treatment arms included 1) hydroxychloroquine alone, 2) hydroxychloroquine and methotrexate, 3) hydroxychloroquine, methotrexate and intravenous immunoglobulin, and 4) hydroxychloroquine, methotrexate, intravenous immunoglobulin and corticosteroids.
Delphi Survey, Spring 2013— An electronic survey was sent to all CARRA members (n = 400), to present the consensus results from the 2012 meeting for clarification regarding issues that had not been satisfactorily addressed in the meetings. These issues included whether skin predominant JDM was broadly considered to be an important clinical issue, and if members would consider using a CTP for the treatment of this JDM subtype. Complete responses were received from 97 CARRA members (73 pediatric rheumatologists, 7 internal medicine/pediatric rheumatologists and 17 pediatric rheumatology fellows). Of these, 31% had 0–4 years, 26% had 5–10 years and 43% had >10 years of experience caring for patients with JDM. More than 82% of respondents considered themselves to be moderately or very experienced in the care of JDM. The majority of respondents agreed that skin predominant JDM was an important clinical issue, and would consider using a CTP to treat this JDM subtype (92% and 98%, respectively). In addition, 91% of respondents agreed that rash for ≥ 6 weeks was sufficient to include a patient in this CTP.
CARRA Annual Meeting, 2013—Chicago, IL. Building on the results from the consensus meeting from the previous year and the Delphi survey results, a core group of 21 members of the CARRA JDM Committee met. Nominal group methods  were used to come to consensus, which was set at ≥75%. Issues addressed included clarification of patient inclusion and exclusion criteria, minimum evaluation for inclusion into these CTPs, interval of monitoring and data collection, medications to be included, the use of topical therapies, and the role of additional diagnostic testing, including imaging and biopsies. After additional review and discussion of the candidate treatment arms, consensus was reached to exclude the treatment option that included IVIG, decreasing the number of treatment arms to three. During the course of this meeting, concern was expressed regarding the rarity of skin predominant JDM, and it was suggested that perhaps pediatric dermatologists were independently seeing and managing this JDM subtype.
January 2014— Additional expertise was requested and obtained from Pediatric Dermatology (PeDRA) members in 2014. An electronic survey was sent out to all PeDRA members (n = 146) to better understand the degree to which they were managing and treating skin predominant JDM. Forty PeDRA members responded to the survey: 39 (98%) of the respondents practiced in an academic setting. Most had been in practice more than 5 years: 7 (18.0%) for 6–9 years and 17 (43.6%) for >10 years. All respondents agreed that better treatment and understanding of this JDM subtype was important. Thirty five (90%) reported that they refer all JDM patients to a pediatric rheumatologist, and 30 (77%) estimated that they see 1–5 amyopathic JDM patients within the past 5 years.
CARRA Annual Meeting, 2014—Orlando, FL. Twelve members of the CARRA JDM Committee met to further develop the CTPs and formally review the PeDRA survey results. Nominal group methods  were used to come to consensus, which was set at ≥75%. Further decisions regarding treatment arms, medication dosing, use of topical therapies and outcome assessment were made.
CARRA Annual Meeting, 2015—Austin, TX. Ten members of the CARRA JDM Committee met to finalize the proposed CTP. In addition, 2 PeDRA members and one patient/parent representative from CureJM participated in the meeting. The proposed CTP was presented and using nominal group methods  the complete CTP proposal was finalized.
A number of modifications were considered in this meeting. Clarification regarding the age of JDM patients and duration of symptoms needed were made. Inclusion criteria were discussed in detail, especially the definition of normal strength and how it is determined by clinicians in light of the challenges of strength testing in young children. The three treatment arms were finalized, and all participants agreed that topical therapies would be explicitly monitored with this CTP. All respondents agreed that presently available and validated tools should be used to assess skin activity. Final consensus was reached regarding recommendations on steroid dose.
It was agreed that patients would be withdrawn from this CTP if they developed weakness during the course of treatment or required additional systemic therapy. We reviewed and summarized our work to date in order to develop CTPs which reflected CARRA consensus on typical treatments for JDM patients with skin predominant disease.
The CTPs presented in this manuscript are intended for patients with skin predominant JDM. CARRA members reached consensus on the clinical characteristics of patients to be included in this subgroup of JDM (Table 1). These patients are defined as children with cutaneous manifestations of JDM skin disease for at least 6 weeks, without any weakness detected by the patient/parent or clinician. All patients included in this CTP require one of the hallmark rashes of JDM, namely, Gottron’s papules or heliotrope rash, with or without other cutaneous manifestations (e.g. Shawl sign, V-sign, malar rash, periungal erythema, vasculopathic changes in the nail bed capillaries, etc.).
Patients may have mild calcinosis, determined by the judgement of the treating clinician, but should not have lipodystrophy or skin ulceration, since it was agreed that patients with these findings have greater disease severity beyond the context of this CTP. In addition, patients should not have systemic involvement or findings of other major organ involvement, including parenchymal lung disease, dysphagia, aspiration, intestinal vasculitis, or myocarditis, as assessed by the treating clinician.
Medication therapy in each of the CTPs is summarized in Table 2. All treatment plans include hydroxychloroquine at 5mg/kg/day (maximum 400mg), with this as monotherapy in Treatment option A. Treatment option B includes the additional use of methotrexate, administered by the parenteral route (preferred), at a dose of 15 mg/m2 or 1 mg/kg (maximum 40 mg) once weekly. Treatment option C includes oral corticosteroids (prednisone at 1–2 mg/kg/day, maximum 60 mg) in conjunction with weekly methotrexate, and daily oral hydroxychloroquine in the same doses as treatment Plan B.
In all CTPs, appropriate sun avoidance and maximization of sunscreen use, including broad spectrum products with SPF ≥ 30, were recommended for all patients, with specific recommendations according to the treating clinician. It was agreed that details regarding topical therapies, which would include any topical steroids and topical calcineurin inhibitors, including various formulations and potencies, would be collected and recorded in a detailed manner in the CARRA registry.
Since these CTPs deal with skin disease as the major manifestation of JDM and resolution of skin features is the primary outcome measure, there was extensive discussion about how skin disease would be assessed. Use of presently available assessment tools [25–29] was weighed against the development of a novel assessment tool more applicable to these specific CTPs. It was decided that the cutaneous disease activity visual analogue scale (VAS) from the Myositis Disease Activity Assessment Tool (MDAAT) would serve as the primary outcome [25, 30]. It was agreed that the development of a novel tool was outside the scope of this current work. This was a consensus decision supported by 91% of respondents in the initial Delphi survey and 100% of participants during the 2015 CARRA meeting.
Baseline investigations and data collection at follow-up visits were common to all 3 CTPs (Table 3). It was agreed that all patients would have basic investigations at enrollment and at follow-up visits, suggested at a 3 to 4 month interval, to minimize the burden on busy clinicians. In addition, centers would have the option of collecting additional data including autoantibody studies and either the PRINTO or IMACS core set activity measures [25, 31, 32] at baseline and at follow-up.
It was agreed that treatment failure was defined as the addition of any additional disease-modifying antirheumatic drugs to any of the three treatment options, or any of the following: decline in the MDAAT, MD Global, Extramuscular Disease Activity by ≥ 2 cm or worsening of muscle enzymes by ≥20%. These patients would be withdrawn from the CTP.
We present a set of consensus clinical treatment plans (CTPs) for children with JDM who have typical skin rashes but no significant muscle weakness, which we call skin predominant JDM.
Skin disease as a component of JDM is important since it reflects disease activity and may contribute to morbidity, including physical disfigurement, calcinosis and lipodystophy. Skin disease is a manifestation of active vasculopathy in JDM that is important to monitor and treat [33, 34]. It has been reported that early severe skin disease activity in JDM may predict cardiac dysfunction better than muscle disease , and persistently active skin disease at 3 and 6 months after diagnosis is predictive of continued active disease . These data support the importance of adequate treatment of JDM-related skin disease, since it may predict worse outcomes [33–36]. There is limited knowledge of patients with skin predominant JDM and optimal treatment approaches, and studying this rare condition using traditional clinical trials is not possible.
These CTPs are meant to represent typical, reasonable treatment approaches taken by pediatric rheumatologists. They are not standard of care, and do not replace clinical judgment or decision making between the treating physician and patient. The intent of these CTPs are to provide clinicians with reasonable medication options for treating patients with skin predominant JDM, in hopes of diminishing differences in treatment approaches between clinicians across multiple CARRA centers. This in turn will allow for improved prospective data collection of patient responses to treatments through the CARRA registry. Using statistical methods [22, 23], this prospective and uniform data collection will allow us to compare differences in patient outcomes in the three different CTP options, which may estimate treatment effects similar to those obtained with traditional randomized controlled trials.
There are important limitations to consider with this work. We chose to include patients with classic skin findings of JDM for a minimum of 6 weeks. Though most case definitions of this patient subtype suggest 6 months before formal classification , we note that in clinical practice, treatment is usually initiated in a JDM patient based on clinical indication, rather than an exact duration of symptoms. Therefore we felt that inclusion of these early patients for this CTP was reasonable and reflected CARRA member practice patterns. In addition, we are aware that nearly 25% of patients with skin predominant JDM progress to classic JDM with weakness, over time. Thus, we included criteria for treatment failure, and guidelines for withdrawal from this CTP, expecting that some patients would evolve to classic JDM with weakness over time. We hypothesize that early introduction of systemic treatment in skin predominant JDM may delay or prevent the development of weakness, so formal study of this is planned in the context of this work.
We involved a large number of pediatric rheumatologists in this consensus process, over the course of several years. Responses to online surveys from CARRA and PeDRA members were about 24 and 27%, respectively, which can be considered a low response rate. We found that survey responses pertaining to this topic are lower compared to earlier surveys from CARRA [13, 14, 16, 17], however, it should be noted that our present survey response rates are comparable to current reported online survey response rates [37, 38]. The surveys were sent to the full CARRA and PeDRA membership, and not a specific subset of JDM experts, but it is reasonable to postulate that clinicians with more exposure and expertise to JDM were more likely to respond to the surveys. We postulate that survey respondents were likely clinicians who have the most interest and expertise in JDM, so it is possible that these findings are not representative of all CARRA and PeDRA members. In this regard, additional Delphi survey of the full participating group could have been administered after finalizing the CTPs; however, given the general response to the earlier Delphi surveys, this was not performed. A previous CARRA survey, which collected information on medications used by pediatric rheumatologists in North America to treat skin predominant JDM, reported medications combinations which overlap considerably with the CTPs developed here . Therefore, we are confident our CTPS can be used broadly in clinical practice and for larger scale, future study.
Topical therapies (sunscreens, steroids, calcineurin inhibitors, etc.) are not explicitly included among the separate treatment arms. The focus on systemic therapy in this CTP, reflects consensus among the participating pediatric rheumatologists, who generally treat these patients with systemic therapy, rather than topical therapies alone. In addition, we recognized that the power to detect a difference between the CTP options would be further diminished if various combinations of topical therapies were included. However, since we cannot discount the role of topical therapies, which are used broadly in the treatment of skin predominant JDM, we plan to keep a strict record the various topical therapies used. We will also account for topical therapies in the final analysis, to assess if patients treated with various topical therapies (e.g., topical corticosteroids and calcineurin inhibitors at varying formulations and potencies) are associated with a difference in outcome.
We note that we have not included all the treatment options available, including early use of intravenous immunoglobulin therapy. Based on patient and clinician preferences, these CTPs may not be applicable to all patients with skin predominant JDM. These CTPs include systemic therapies, and are less immunosuppressive compared to previously published CTPs developed for patients with moderate weakness or ongoing rash, which included more potent medications including, high dose oral corticosteroids, pulse corticosteroids and intravenous gammaglobulin [13–15].
In conclusion, we present CTPs which are complementary to other treatment plans previously developed by the various disease-specific committees of CARRA [13–18]. It is hoped that these CTPs can be used prospectively to improve the understanding of the best treatment approaches for this skin predominant subgroup of JDM patients and improve outcomes.
Childhood Arthritis and Rheumatology Research Alliance
Childhood Health Assessment Questionnaire
Childhood Myositis Assessment Scale
Clinical Treatment Plan
Myositis Disease Activity Assessment Tool
Magnetic resonance imaging
Pediatric Rheumatology International Trials Organization
Visual Analog Scale
Mendez EP, Lipton R, Ramsey-Goldman R, Roettcher P, Bowyer S, Dyer A, et al. US incidence of juvenile dermatomyositis, 1995–1998: Results from the National Institute of Arthritis and Musculoskeletal and Skin Diseases Registry. Arthritis Rheum. 2003;49:300–5.
Symmons DP, Sills JA, Davis SM. The incidence of juvenile dermatomyositis: results from a nation-wide study. Br J Rheumatol. 1995;34:732–6.
Shah M, Mamyrova G, Targoff IN, Huber AM, Malley JD, Rice MM, et al. The clinical phenotypes of the juvenile idiopathic inflammatory myopathies. Medicine (Baltimore). 2013;92:25–41.
Robinson AB, Hoeltzel MF, Wahezi DM, Becker ML, Kessler EA, Schmeling H, et al. Clinical characteristics of children with juvenile dermatomyositis: the Childhood Arthritis and Rheumatology Research Alliance Registry. Arthritis Care Res (Hoboken). 2014;66:404–10.
Gerami P, Schope JM, McDonald L, Walling HW, Sontheimer RD. A systematic review of adult-onset clinically amyopathic dermatomyositis (dermatomyositis siné myositis): A missing link within the spectrum of the idiopathic inflammatory myopathies. J Am Acad Dermatol. 2006;54:597–613.
Bailey EE, Fiorentino DF. Amyopathic dermatomyositis: definitions, diagnosis, and management. Curr Rheumatol Rep. 2014;16:465.
Sato S, Kuwana M. Clinically amyopathic dermatomyositis. Curr Opin Rheumatol. 2010;22:639–43.
Euwer RL, Sontheimer RD. Amyopathic dermatomyositis: a review. J Invest Dermatol. 1993;100:124S–7S.
Sontheimer RD. Would a new name hasten the acceptance of amyopathic dermatomyositis (dermatomyositis siné myositis) as a distinctive subset within the idiopathic inflammatory dermatomyopathies spectrum of clinical illness? J Am Acad Dermatol. 2002;46:626–36.
Gerami P, Walling HW, Lewis J, Doughty L, Sontheimer RD. A systematic review of juvenile-onset clinically amyopathic dermatomyositis. Br J Dermatol. 2007;157:637–44.
Stringer E, Bohnsack J, Bowyer SL, Griffin TA, Huber AM, Lang B, et al. Treatment approaches to juvenile dermatomyositis (JDM) across North America: The Childhood Arthritis and Rheumatology Research Alliance (CARRA) JDM treatment survey. J Rheumatol. 2010;37:1953–61.
Walling HW, Gerami P, Sontheimer RD. Juvenile-onset clinically amyopathic dermatomyositis: an overview of recent progress in diagnosis and management. Paediatr Drugs. 2010;12:23–34.
Huber AM, Giannini EH, Bowyer SL, Kim S, Lang B, Lindsley CB, et al. Protocols for the initial treatment of moderately severe Juvenile dermatomyositis: Results of a children’s Arthritis and Rheumatology Research Alliance consensus conference. Arthritis Care Res. (Hoboken). 2010;62:219–25.
Huber AM, Robinson AB, Reed AM, Abramson L, Bout-Tabaku S, Carrasco R, et al. Consensus treatments for moderate juvenile dermatomyositis: beyond the first two months. Results of the second Childhood Arthritis and Rheumatology Research Alliance consensus conference. Arthritis Care Res (Hoboken). 2012;64:546–53.
Huber AM, Kim S, Reed AM, Carrasco R, Feldman BM, Hong SD, Kahn P, Rahimi H, Robinson AB, Vehe RK, Weiss JE SC. Childhood Arthritis andRheumatology Research Alliance Consensus Clinical Treatment Plans for Juvenile Dermatomyositis with Persistent Skin Rash. J.Rheumatol. 2016; in press.
Li SC, Torok KS, Pope E, Dedeoglu F, Hong S, Jacobe HT, et al. Development of consensus treatment plans for juvenile localized scleroderma: a roadmap toward comparative effectiveness studies in juvenile localized scleroderma. Arthritis Care Res (Hoboken). 2012;64:1175–85.
DeWitt EM, Kimura Y, Beukelman T, Nigrovic PA, Onel K, Prahalad S, et al. Consensus treatment plans for new-onset systemic juvenile idiopathic arthritis. Arthritis Care Res (Hoboken). 2012;64:1001–10.
Ringold S, Weiss PF, Colbert RA, DeWitt EM, Lee T, Onel K, et al. Childhood Arthritis and Rheumatology Research Alliance consensus treatment plans for new-onset polyarticular juvenile idiopathic arthritis. Arthritis Care Res (Hoboken). 2014;66:1063–72.
Johnson SR, Fransen J, Khanna D, Baron M, van den Hoogen F, Medsger TA, et al. Validation of potential classification criteria for systemic sclerosis. Arthritis Care Res (Hoboken). 2012;64:358–67.
Kawut SM, Horn EM, Berekashvili KK, Garofano RP, Goldsmith RL, Widlitz AC, et al. New predictors of outcome in idiopathic pulmonary arterial hypertension. Am J Cardiol. 2005;95:199–203.
Frank H, Mlczoch J, Huber K, Schuster E, Gurtner HP, Kneussl M. The effect of anticoagulant therapy in primary and anorectic drug-induced pulmonary hypertension. Chest. 1997;112:714–21.
Johnson SR, Feldman BM, Pope JE, Tomlinson GA. Shifting our thinking about uncommon disease trials: the case of methotrexate in scleroderma. J Rheumatol. 2009;36:323–9.
Gupta S, Faughnan ME, Tomlinson GA, Bayoumi AM. A framework for applying unfamiliar trial designs in studies of rare diseases. J Clin Epidemiol. 2011;64:1085–94.
Ruperto N, Meiorin S, Iusan SM, Ravelli A, Pistorio A, Martini A. Consensus procedures and their role in pediatric rheumatology. Curr Rheumatol Rep. 2008;10:142–6.
Rider LG, Werth VP, Huber AM, Alexanderson H, Rao AP, Ruperto N, et al. Measures of adult and juvenile dermatomyositis, polymyositis, and inclusion body myositis: Physician and Patient/Parent Global Activity, Manual Muscle Testing (MMT), Health Assessment Questionnaire (HAQ)/Childhood Health Assessment Questionnaire (C-HAQ). Arthritis Care Res (Hoboken). 2011;63:S118–57.
Huber AM, Dugan EM, Lachenbruch PA, Feldman BM, Perez MD, Zemel LS, et al. The Cutaneous Assessment Tool: development and reliability in juvenile idiopathic inflammatory myopathy. Rheumatology (Oxford). 2007;46:1606–11.
Huber AM, Dugan EM, Lachenbruch PA, Feldman BM, Perez MD, Zemel LS, et al. Preliminary validation and clinical meaning of the Cutaneous Assessment Tool in juvenile dermatomyositis. Arthritis Rheum. 2008;59:214–21.
Huber AM, Lachenbruch PA, Dugan EM, Miller FW, Rider LG. Alternative scoring of the Cutaneous Assessment Tool in juvenile dermatomyositis: results using abbreviated formats. Arthritis Rheum. 2008;59:352–6.
Klein RQ, Bangert CA, Costner M, Connolly MK, Tanikawa A, Okawa J, et al. Comparison of the reliability and validity of outcome instruments for cutaneous dermatomyositis. Br J Dermatol. 2008;159:887–94.
Sultan SM, Allen E, Oddis CV, Kiely P, Cooper RG, Lundberg IE, et al. Reliability and validity of the myositis disease activity assessment tool. Arthritis Rheum. 2008;58:3593–9.
Miller FW, Rider LG, Chung YL, Cooper R, Danko K, Farewell V, et al. Proposed preliminary core set measures for disease outcome assessment in adult and juvenile idiopathic inflammatory myopathies. Rheumatology (Oxford). 2001;40:1262–73.
Ruperto N, Ravelli A, Pistorio A, Ferriani V, Calvo I, Ganser G, et al. The provisional Paediatric Rheumatology International Trials Organisation/American College of Rheumatology/European League Against Rheumatism Disease activity core set for the evaluation of response to therapy in juvenile dermatomyositis: a prospective va. Arthritis Rheum. 2008;59:4–13.
Christen-Zaech S, Seshadri R, Sundberg J, Paller AS, Pachman LM. Persistent association of nailfold capillaroscopy changes and skin involvement over thirty-six months with duration of untreated disease in patients with juvenile dermatomyositis. Arthritis Rheum. 2008;58:571–6.
Smith RL, Sundberg J, Shamiyah E, Dyer A, Pachman LM. Skin involvement in juvenile dermatomyositis is associated with loss of end row nailfold capillary loops. J Rheumatol. 2004;31:1644–9.
Schwartz T, Sanner H, Gjesdal O, Flatø B, Sjaastad I. In juvenile dermatomyositis, cardiac systolic dysfunction is present after long-term follow-up and is predicted by sustained early skin activity. Ann Rheum Dis. 2014;73:1805–10.
Stringer E, Singh-Grewal D, Feldman BM. Predicting the course of juvenile dermatomyositis: significance of early clinical and laboratory features. Arthritis Rheum. 2008;58:3585–92.
Cunningham CT, Quan H, Hemmelgarn B, Noseworthy T, Beck CA, Dixon E, et al. Exploring physician specialist response rates to web-based surveys. BMC Med Res Methodol. 2015;15:32.
Nota SPFT, Strooker JA, Ring D. Differences in response rates between mail, e-mail, and telephone follow-up in hand surgery research. Hand (N Y). 2014;9:504–10.
CARRA is supported in part by grants from the Arthritis Foundation, NIAMS, Duke Clinical Research Institute, the WASIE Foundation, and CureJM. Dr. Rider is supported in part by the intramural research program of the National Institutes of Health, National Institute of Environmental Health Sciences. We thank Dr. Alison Ehrlich for critical reading of the manuscript. We also would like to thank our PeDRA collaborators and Dermatology Colleagues who helped to review and distribute the survey, including Dr. Shielagh Maguiness, Dr. Ruth Ann Vleugels, Dr. Jennifer Huang, Dr. Yvonne Chiu, Dr. Michele Ramien, Dr. Jérôme Coulombe, MD, Dr. Regina-Celeste Ahmad, Dr. Lisa M. Arkin and Dr. Reagan Hunt. Mitali Dave is acknowledged for her insights and contribution as a parent of a child with JDM to our CTP development, as well as Dr. Fatma Dedeoglu, Dr. Andrew Eichenfield, Dr. Donald Goldsmith, Dr. Peri Pepmueller, Dr. Kathryn Phillippi, Dr. Kara Schmidt, Dr. Rosie Scuccimarri and Dr. Amy Woodward were active participants in the development of this CTP.
This project received no direct funding.
Availability of data and materials
The survey data obtained during and/or analysed during the current study are available from the corresponding author on reasonable request.
SK and AMH are accountable for all aspects of the work in ensuring that the questions related to the accuracy or integrity of the work are appropirately investigated and resolved. SK, PK, ABR, CHS, LGR and AMH made substantial contributions to conception and design, acquisition of data, analysis and interpretation of data, and have been involved in drafting the manuscript or revising it critically for important intellectual content. BL, AS, EJO, KS, MLC, and LBA made substantial contributions to conception, acquisition of data, and have been involved in critically revising the manuscript for important intellectual content. Authors agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All authors read and approved the final manuscript.
The author(s) are all members CARRA and declare(s) that they have no competing interests.
Consent for publication
Not applicable; No patient data was included in this work.
Ethics approval and consent to participate
Ethics board approval and consent was obtained for this work from the Institutional Review Board of Boston Children’s Hospital (#00016698).