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慢性荨麻疹中的非镇静性H1抗组胺药。

Nonsedating H1 antihistamines in chronic urticaria.

作者信息

Monroe E W

机构信息

Department of Dermatology, Medical College of Wisconsin, Milwaukee.

出版信息

Ann Allergy. 1993 Dec;71(6):585-91.

PMID:7903515
Abstract

Histamine type 1 (H1) receptor antagonists are the principal therapy for chronic urticaria. Their usefulness, however, is sometimes compromised by undesirable central nervous system (CNS) side effects such as daytime sedation and anticholinergic side effects such as dry mouth. Second-generation, nonsedating antihistamines (terfenadine, astemizole, loratadine, and cetirizine hydrochloride) are just as effective as the potent first-generation antihistamines such as hydroxyzine. Yet they do not cause the CNS and anticholinergic side effects seen with the older agents. Cardiovascular side effects, which have been recently reported with terfenadine and astemizole, are dose related and rare, generally occurring in patients who overdose or who take concomitant medications that increase serum antihistamine levels. The second-generation antihistamines also offer twice daily and once daily dosage schedules, which are more convenient than the two- to four-times daily schedules of the older agents. They should therefore be considered first-line agents for the treatment of chronic urticaria. This article is a review of the role of the nonsedating antihistamines in the treatment of chronic urticaria.

摘要

组胺1型(H1)受体拮抗剂是慢性荨麻疹的主要治疗方法。然而,它们的效用有时会受到不良中枢神经系统(CNS)副作用(如日间镇静)和抗胆碱能副作用(如口干)的影响。第二代非镇静性抗组胺药(特非那定、阿司咪唑、氯雷他定和盐酸西替利嗪)与强效第一代抗组胺药(如羟嗪)一样有效。然而,它们不会引起 older agents 所出现的中枢神经系统和抗胆碱能副作用。最近报道的特非那定和阿司咪唑的心血管副作用与剂量相关且罕见,通常发生在过量用药或同时服用增加血清抗组胺药水平的药物的患者中。第二代抗组胺药还提供每日两次和每日一次的给药方案,这比 older agents 每日两到四次的给药方案更方便。因此,它们应被视为治疗慢性荨麻疹的一线药物。本文是对非镇静性抗组胺药在慢性荨麻疹治疗中的作用的综述。

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