Retrospective Analysis of Systemic Corticosteroids for Alopecia Areata in Pediatric Patients

Tamazian Shant, Rogers Rachel, C. Leslie
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Abstract

Background: Therapy for alopecia areata (AA) in a pediatric patient population is challenging and controversial. Common treatments include a variety of topical or injected agents. Systemic steroid treatment in children is controversial due to concern of negative side effects. The purpose of this study was to evaluate the efficacy and safety of systemic corticosteroid therapy for the treatment of AA in pediatric patients. Methods: This retrospective chart review included patients treated with standard courses of oral corticosteroids (3-week taper starting at 1 mg/kg) for AA who were managed by the Dermatology Section at the Children’s Hospital of Philadelphia between 2015 and 2018. The following data was extracted from patients’ charts: Severity of disease measured by Severity of Alopecia Tool (SALT) scores for AA, treatment regimen, duration of treatment and number of steroid courses, side effects, age, gender, and weight percentiles. SALT scores and weight percentiles were recorded at pretreatment as well as at 3 months and 6 months after initiation of treatment. SALT scores, when available, were additionally recorded at 9, 12, and 15 months after initiation of treatment. Results: 82 pediatric subjects were included in the study. Subjects were grouped according to severity at pretreatment with systemic corticosteroids with < 50% SALT as mild and > 50% SALT as Severe. Subjects in the > 50% SALT score group followed at 5 intervals (pre-treatment, 3 months, 6 months, 9 months, 12 months, 15 months) showed statistically-significant improvement/lowering of SALT scores, while subjects in the < 50% SALT group did not over the same time period. No serious adverse side effects were documented in any subjects treated. However, 67 patients of a total of 82 studied relapsed during the time intervals observed. The average time to relapse was 21.9 weeks after initiation of treatment (standard deviation: 16.76 weeks; range: 4.71 to 73.43 Additionally, weight percentiles a statistically significant baseline. Conclusion: Patients with baseline SALT scores ≥ 50 improved significantly after a course of systemic steroids but relapsed on average 4-5 months later with concomitant weight gain.
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全身性皮质类固醇治疗儿科斑秃的回顾性分析
背景:儿科斑秃(AA)患者的治疗具有挑战性和争议性。常见的治疗方法包括各种局部或注射药物。由于担心副作用,儿童全身性类固醇治疗存在争议。本研究的目的是评估全身皮质类固醇治疗儿科AA患者的疗效和安全性。方法:本回顾性图表回顾包括2015年至2018年期间由费城儿童医院皮肤科管理的AA患者接受口服皮质类固醇标准疗程(3周逐渐减少,起始剂量为1mg /kg)。从患者的图表中提取以下数据:通过AA的脱发严重程度工具(SALT)评分测量的疾病严重程度,治疗方案,治疗持续时间和类固醇疗程数,副作用,年龄,性别和体重百分位数。在治疗前以及治疗开始后3个月和6个月记录SALT评分和体重百分位数。在治疗开始后9个月、12个月和15个月额外记录SALT评分。结果:82名儿童被纳入研究。受试者根据全身皮质类固醇预处理时的严重程度分组,< 50% SALT为轻度,> 50% SALT为重度。在治疗前、治疗前3个月、治疗后6个月、治疗后9个月、治疗后12个月、治疗后15个月,SALT评分> 50%组的受试者在治疗前5个月、治疗前3个月、治疗后6个月、治疗后9个月、治疗后12个月、治疗后15个月的受试者的SALT评分均有统计学意义的改善/降低。所有受试者均未发现严重的不良副作用。然而,在观察到的时间间隔内,总共82名患者中有67名复发。开始治疗后平均复发时间为21.9周(标准差:16.76周;范围:4.71至73.43此外,体重百分位数是具有统计学意义的基线。结论:基线SALT评分≥50的患者在全身性类固醇治疗一个疗程后显著改善,但平均4-5个月后复发并伴有体重增加。
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来源期刊
Archives of dermatology
Archives of dermatology 医学-皮肤病学
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4-8 weeks
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