Hackensack University Medical Center, New Jersey, USA.
Arthritis Care Res (Hoboken). 2012 Aug;64(8):1175-85. doi: 10.1002/acr.21687.
Juvenile localized scleroderma (LS) is a chronic inflammatory skin disorder associated with substantial morbidity and disability. Although a wide range of therapeutic strategies has been reported in the literature, a lack of agreement on treatment specifics and accepted methods for clinical assessment has made it difficult to compare approaches and identify optimal therapy. Our objective was to develop standardized treatment plans, clinical assessments, and response criteria for active, moderate to high severity juvenile LS.
A core group of pediatric rheumatologists, dermatologists, and a lay advisor was engaged by the Childhood Arthritis and Rheumatology Research Alliance (CARRA) to develop standardized treatment plans and assessment parameters for juvenile LS using consensus methods/nominal group techniques. Recommendations were validated in 2 face-to-face conferences with a larger group of practitioners with expertise in juvenile LS and with the full membership of CARRA, which encompasses the majority of pediatric rheumatologists in the US and Canada.
Consensus was achieved on standardized treatment plans that reflect the prevailing treatment practices of CARRA members. Standardized clinical assessment methods and provisional treatment response criteria were also developed. Greater than 90% of pediatric rheumatologists responding to a survey (66% of CARRA membership) affirmed the final recommendations and agreed to utilize these consensus plans to treat patients with juvenile LS.
Using consensus methodology, we have developed standardized treatment plans and assessment methods for juvenile LS. The high level of support among pediatric rheumatologists will support future comparative effectiveness studies and enable the development of evidence-based guidelines for the treatment of juvenile LS.
青少年局限性硬皮病(LS)是一种慢性炎症性皮肤疾病,与较高的发病率和致残率相关。尽管文献中报道了广泛的治疗策略,但由于缺乏对治疗细节的共识以及临床评估的公认方法,使得比较各种方法和确定最佳治疗方案变得困难。我们的目标是为活动期、中重度青少年 LS 制定标准化的治疗方案、临床评估和反应标准。
儿童关节炎和风湿病研究联盟(CARRA)的一组核心儿科风湿病学家、皮肤科医生和一名非专业顾问通过共识方法/名义小组技术参与制定了青少年 LS 的标准化治疗方案和评估参数。建议在与具有青少年 LS 专业知识的更广泛实践医生以及包括美国和加拿大大多数儿科风湿病学家的 CARRA 全体成员的 2 次面对面会议上进行了验证。
就反映 CARRA 成员当前治疗实践的标准化治疗方案达成了共识。还制定了标准化临床评估方法和暂定治疗反应标准。对调查做出回应的儿科风湿病学家中(占 CARRA 成员的 66%)有超过 90%肯定了最终建议,并同意使用这些共识方案来治疗青少年 LS 患者。
我们使用共识方法制定了青少年 LS 的标准化治疗方案和评估方法。儿科风湿病学家的高度支持将支持未来的比较有效性研究,并为青少年 LS 的治疗制定基于证据的指南。