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非甾体抗炎药的严重皮肤不良反应:文献综述。

Severe adverse skin reactions to nonsteroidal antiinflammatory drugs: A review of the literature.

机构信息

College of Pharmacy, University of Rhode Island, Kingston, RI 02881, USA.

出版信息

Am J Health Syst Pharm. 2010 Feb 1;67(3):206-13. doi: 10.2146/ajhp080603.

DOI:10.2146/ajhp080603
PMID:20101062
Abstract

PURPOSE

Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) associated with the use of nonsteroidal antiinflammatory drugs (NSAIDs) are described.

SUMMARY

A search of the English- language medical literature was conducted to identify studies and cases of SJS and TEN associated with NSAIDs and cyclooxygenase-2-selective NSAIDs available in the United States. Several epidemiologic studies, case reports, and case series involving SJS and TEN associated with NSAIDs were identified. Of the available NSAIDs, oxicam derivatives appeared to have the greatest association with SJS and TEN. The relative risks reported with other NSAIDs are much lower. The risk with cyclooxygenase-2-selective NSAIDs and meloxicam is less clear, since all were introduced after the completion of the epidemiologic studies. SJS or TEN from NSAIDs and cyclooxygenase-2-selective NSAIDs appears to affect the same patient population as other medications that cause SJS or TEN. The risk of SJS or TEN caused by NSAIDs is extremely low (less than 2 per 1 million users per week for oxicam derivatives, less than 1 per 1 million users per week for other NSAIDs, and 6 cases per 1 million person-years for celecoxib). Aspirin is not typically associated with SJS or TEN. Of the other salicylates, SJS or TEN has only been reported with diflunisal.

CONCLUSION

The risk of SJS or TEN in patients receiving NSAIDs is extremely low; older patients, women, and patients within the first month of treatment initiation appear to have the greatest risk. Health care providers and patients should be aware of the signs and symptoms of SJS and TEN.

摘要

目的

本文描述了与非甾体抗炎药(NSAIDs)相关的史蒂文斯-约翰逊综合征(SJS)和中毒性表皮坏死松解症(TEN)。

摘要

检索了英文医学文献,以确定与美国可用的 NSAIDs 和环氧化酶-2 选择性 NSAIDs 相关的 SJS 和 TEN 的研究和病例。确定了几项涉及 NSAIDs 相关 SJS 和 TEN 的流行病学研究、病例报告和病例系列。在可用的 NSAIDs 中,昔康衍生物似乎与 SJS 和 TEN 的关联性最大。其他 NSAIDs 的报告相对风险要低得多。环氧化酶-2 选择性 NSAIDs 和美洛昔康的风险不太明确,因为它们都是在完成流行病学研究后推出的。来自 NSAIDs 和环氧化酶-2 选择性 NSAIDs 的 SJS 或 TEN 似乎影响与其他引起 SJS 或 TEN 的药物相同的患者群体。NSAIDs 引起的 SJS 或 TEN 的风险极低(每周每 100 万使用者中昔康衍生物不到 2 例,其他 NSAIDs 不到 1 例,塞来昔布每 100 万人年 6 例)。阿司匹林通常与 SJS 或 TEN 无关。在其他水杨酸盐中,只有 diflunisal 与 SJS 或 TEN 有关。

结论

接受 NSAIDs 治疗的患者发生 SJS 或 TEN 的风险极低;老年患者、女性和治疗开始后第一个月内的患者风险最大。医疗保健提供者和患者应了解 SJS 和 TEN 的症状和体征。

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