少年局限性硬皮病:一项来自三级保健中心的大型回顾性队列研究。

IF 2.8 3区 医学 Q1 PEDIATRICS
Bugra Han Egeli, Johnathan Dallas, Diana B Reusch, Katharina S Shaw, Stephen Gellis, Robert Sundel, Mary Beth Son, Ruth Ann Vleugels, Fatma Dedeoglu
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引用次数: 0

摘要

背景:青少年局限性硬皮病是一种罕见的儿童炎症性疾病,主要影响皮肤和皮下组织,但也有可能影响更深的组织,并可能与皮外表现相关,导致严重损害和残疾。管理方法各不相同,但近年来,专家小组试图通过共识治疗计划来简化护理方法。方法:本回顾性队列研究纳入了美国一家三级儿科医院21年(1999-2020年)随访≥3年的儿童少年局限性硬皮病患者。对人口统计学、疾病特征和治疗趋势的数据进行分析,重点关注2012年儿童关节炎和风湿病研究联盟青少年局限性硬皮病共识治疗计划发表前后的全身与局部治疗和治疗趋势。结果:101例青少年局限性硬皮病患者符合纳入标准。63例患者接受全身治疗,38例接受局部治疗。接受全身治疗的患者更常在风湿病-皮肤病联合项目(67%)或风湿病诊所(30%)接受治疗,而接受局部治疗的患者主要在皮肤病诊所接受治疗(71%)。从2013年开始,接受联合方案治疗的患者比例显著增加(47%对20%,p = 0.008),接受全身治疗的患者比例显著增加(78%对55%,p)。该青少年局限性硬皮病队列是单一中心报道的最大队列之一,显示了2012年儿童关节炎和风湿病研究联盟青少年局限性硬皮病共识治疗计划发表后全身治疗的使用增加。有必要对长期治疗结果和一线治疗失败时采用的治疗方法进行进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Juvenile localized scleroderma: a large retrospective cohort study from a tertiary care center.

Background: Juvenile localized scleroderma is a rare pediatric inflammatory disease that primarily affects the skin and subcutaneous tissue but also has the potential to impact deeper tissues and can be associated with extracutaneous manifestations, leading to substantial impairment and disability. Management approaches vary, but in recent years, expert groups have attempted to streamline the approach to care with consensus treatment plans.

Methods: This retrospective cohort study included pediatric juvenile localized scleroderma patients with ≥ 3 years of follow-up identified within a 21-year period (1999-2020) at a single tertiary care pediatric hospital in the USA. Data on demographics, disease characteristics, and treatment trends were analyzed, with a focus on systemic versus topical therapy and treatment trends before and after the publication of the Childhood Arthritis and Rheumatology Research Alliance juvenile localized scleroderma consensus treatment plan in 2012.

Results: A total of 101 juvenile localized scleroderma patients fulfilled our inclusion criteria. Sixty-three patients were treated with systemic therapy, and 38 were treated with topical therapy. Patients on systemic therapy were more commonly treated in a combined rheumatology-dermatology program (67%) or rheumatology clinic (30%), whereas those on topical therapy were primarily treated in a dermatology clinic (71%). Starting in 2013, a significantly greater percentage of all patients were treated in the combined program (47% vs. 20%, p = 0.008), and a significantly greater percentage of patients received systemic therapy (78% vs. 55%, p < 0.05).

Conclusion: This juvenile localized scleroderma cohort is one of the largest reported from a single center and demonstrated an increase in the use of systemic therapy following the publication of the Childhood Arthritis and Rheumatology Research Alliance juvenile localized scleroderma consensus treatment plan in 2012. Further studies on long-term treatment outcomes and therapeutic approaches utilized when first-line treatment failures occur are warranted.

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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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