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Current management of juvenile dermatomyositis in Germany and Austria: an online survey of pediatric rheumatologists and pediatric neurologists

机译:德国和奥地利少年皮质肌炎的目前管理:对儿科风湿病学家和儿科神经科学家的在线调查

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Abstract Background Juvenile Dermatomyositis (JDM) is a rare pediatric autoimmune disease with broad variations of the individual course. Data on the optimal management are mostly lacking. Currently treatment decisions are often based on experts’ opinions. In order to develop consensus-based treatment strategies for JDM in Germany a survey was pursued to analyze the current clinical practice. Methods An online survey addressing all members of the Society for Pediatric Rheumatology (GKJR) in Germany and Austria and pediatric neurologists with expertise in JDM was performed in February/March of 2016. The questionnaire consisted of 5 case scenarios including diagnostic criteria, treatment of moderate, severe and refractory JDM, using either multiple choice or a 5-point Likert scale. Basic descriptive statistics were used to analyze the findings. Results The survey was completed by 60 pediatric rheumatologists and 7 pediatric neurologists experienced in the management of JDM. Typical findings allowing a diagnosis were considered to be: typical skin changes, proximal muscle weakness, MRI findings, elevated muscle enzymes, nailfold capillary changes, presence of calcinosis and muscle biopsy. Regarding induction treatment of moderate/severe JDM: 59%/74% opted for intermittent intravenous methylprednisolone (IVMP) pulse therapy, and 21%/40% for conventional high-dose oral glucocorticoids. Methotrexate (MTX) was the preferred disease-modifying conventional anti-rheumatic drug (cDMARD) for moderate and severe JDM. Regarding the management of refractory moderate or severe JDM, intravenous immune globulins, mycophenolate mofetil and rituximab were preferred treatment options. Conclusion There is consensus about the diagnosis of JDM strongly supported by classic clinical and MRI findings. There is great variety in the treatment of JDM in Germany regarding both induction and maintenance therapy. The development of consensus-based treatment strategies for JDM based on harmonization of current clinical practice is essential in order to allow comparative effectiveness research in the future.
机译:抽象背景儿童皮肌炎(JDM)是一种罕见的儿科自身免疫性疾病与个体当然广泛的变化。在优化管理数据大多缺乏。目前治疗决策往往是根据专家的意见。为了开发JDM共识为基础的治疗策略,在德国的一个调查奉行分析当前临床实践。方法在2016年2月/ 3月进行的一项在线调查处理在德国和奥地利,并在JDM专长小儿神经科医师协会儿科风湿病(GKJR)的所有成员的问卷包括5个例场景,包括诊断标准,治疗中度,严重的和顽固JDM,即使用多选或一个5点Likert量表。基本描述性统计来分析结果。结果本次调查由60个小儿风湿病和JDM的管理经历了7名小儿神经科医师完成。典型的发现允许诊断被认为是:典型的皮肤变化,近端肌无力,MRI发现,升高的肌肉酶,甲襞毛细管的变化,钙质沉着和肌肉活检的存在。关于中度/重度JDM的诱导治疗:对于传统的高剂量口服糖皮质激素的59%/ 74%选择间断静脉甲泼尼龙(IVMP)脉冲疗法,和21%/ 40%。氨甲蝶呤(MTX)是为中度和重度JDM优选疾病修饰常规抗风湿药(cDMARD)。对于难治性中度或重度JDM,静脉注射免疫球蛋白,霉酚酸酯和利妥昔单抗的管理是首选的治疗方案。结论是关于JDM由经典的临床和MRI表现强烈支持诊断共识。目前在德国关于诱导和维持治疗治疗JDM的种类繁多。基于目前的临床实践的统一为JDM共识为基础的治疗策略的发展是至关重要的,以允许在未来比较效益研究。

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