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初始治疗方式对慢性特发性荨麻疹长期控制的影响。

Influence of initial treatment modality on long-term control of chronic idiopathic urticaria.

机构信息

Division of Allergy and Clinical Immunology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

出版信息

PLoS One. 2013 Jul 23;8(7):e69345. doi: 10.1371/journal.pone.0069345. Print 2013.

Abstract

BACKGROUND

Chronic idiopathic urticaria (CIU) is a common cutaneous disorder but the influence of initial treatment modality on long-term control is not known. The aim of this study was to evaluate clinical features, and the influence of initial treatment modality on long-term control.

METHODS AND RESULTS

641 CIU patients were enrolled from the allergy clinic in a tertiary referral hospital. Disease duration, aggravating factors and treatment modality at each visit were evaluated. Times required to reach a controlled state were analyzed according to initial treatment modality, using Kaplan-Meier survival curves, the Cox proportional-hazards model, and propensity scores. Female to male ratio was 1.7: 1; mean age at onset was 40.5 years. The most common aggravating factors were food (33.5%), stress (31.5%) and fatigue (21.6%). Most patients (82.2%) used H1-antihistamines alone as initial treatment while 17% used a combination treatment with oral corticosteroids. There was no significant difference in the time taken to reach a controlled state between patients treated with single vs multiple H1-antihistamines or between those who received H1-antihistamine monotherapy vs. a combination therapy with oral corticosteroids.

CONCLUSION

The time required to control CIU is not reduced by use of multiple H1-antihistamines or oral corticosteroids in the initial treatment.

摘要

背景

慢性特发性荨麻疹(CIU)是一种常见的皮肤疾病,但初始治疗方式对长期控制的影响尚不清楚。本研究旨在评估临床特征,以及初始治疗方式对长期控制的影响。

方法和结果

从一家三级转诊医院的过敏诊所招募了 641 例 CIU 患者。评估了每次就诊时的疾病持续时间、加重因素和治疗方式。根据初始治疗方式,使用 Kaplan-Meier 生存曲线、Cox 比例风险模型和倾向评分分析达到控制状态所需的时间。男女比例为 1.7:1;发病年龄的平均值为 40.5 岁。最常见的加重因素是食物(33.5%)、压力(31.5%)和疲劳(21.6%)。大多数患者(82.2%)单独使用 H1 抗组胺药作为初始治疗,而 17%的患者使用 H1 抗组胺药联合口服皮质类固醇治疗。使用单一或多种 H1 抗组胺药或 H1 抗组胺药联合口服皮质类固醇治疗的患者达到控制状态所需的时间无显著差异。

结论

在初始治疗中使用多种 H1 抗组胺药或口服皮质类固醇并不能缩短 CIU 的控制时间。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f5/3720657/9cefcab216da/pone.0069345.g001.jpg

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