Division of Allergy and Immunology, Department of Pediatrics, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla, Thailand.
Asian Pac J Allergy Immunol. 2022 Jun;40(2):121-125. doi: 10.12932/AP-030619-0573.
A standard dose of second-generation H1 -antihistamines is recommended as the first-line treatment of chronic spontaneous urticaria (CSU), previous studies have found that approximately 20-50% of CSU children fail to control their symptoms and required step-up treatments.
To evaluate the predictors of uncontrolled symptoms with first-line medication and describe the treatment outcomes of CSU children in the southern region of Thailand.
This retrospective chart review of CSU patients, aged 2-18 years, who were initially treated with the standard dose of second-generation H1 -antihistamine at the Pediatric Allergy Clinic, Songkhlanagarind Hospital, from January 2008 to July 2018. The data were collected at the initial visit (demographic data, onset of rash, frequency of urticaria, presence of angioedema, previous resolved CU, laboratory investigation results) and follow-up visits (treatment outcome, time to controlled urticaria).
The medical records of 192 CSU children were reviewed; their median age were 8.5 years and the mean frequency of rash was 4 days/week. Forty-seven children (24.4%) fail to controlled symptoms with a standard dose of second -generation H1 -antihistamines and a factor significantly associated was frequency of rash for more than 4 days per week (OR = 4.36, P < 0.001). The median time to controlled urticaria was 1.28 months.
Most of CSU children in the southern region of Thailand experienced controlled symptoms with a standard dose of second-generation H1 -antihistamines, and the frequency of urticaria for more than 4 days per week was a factor associated with uncontrolled symptoms that regimen.
推荐第二代 H1 抗组胺药标准剂量作为慢性自发性荨麻疹(CSU)的一线治疗方法,先前的研究发现,约 20-50%的 CSU 儿童无法控制其症状,需要进行升级治疗。
评估一线药物治疗控制不佳症状的预测因素,并描述泰国南部地区 CSU 儿童的治疗结果。
这是一项对 2008 年 1 月至 2018 年 7 月期间在宋卡哈林那格医院儿科过敏诊所接受标准剂量第二代 H1 抗组胺药初始治疗的 CSU 患者(年龄 2-18 岁)的回顾性图表审查。数据收集于初次就诊时(人口统计学数据、皮疹发作、荨麻疹发作频率、血管性水肿、既往缓解性 CU、实验室检查结果)和随访就诊时(治疗结果、控制荨麻疹的时间)。
共回顾了 192 例 CSU 儿童的病历;他们的中位年龄为 8.5 岁,皮疹发作频率平均为每周 4 天。47 例(24.4%)儿童在使用第二代 H1 抗组胺药标准剂量治疗后症状仍未得到控制,其中皮疹发作频率超过每周 4 天是与症状未控制显著相关的因素(OR = 4.36,P < 0.001)。控制荨麻疹的中位时间为 1.28 个月。
泰国南部地区的大多数 CSU 儿童使用第二代 H1 抗组胺药标准剂量后症状得到控制,每周皮疹发作超过 4 天是与未控制症状相关的因素。