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与使用塞来昔布和罗非昔布相关的肾衰竭。

Renal failure associated with the use of celecoxib and rofecoxib.

作者信息

Ahmad Syed R, Kortepeter Cindy, Brinker Allen, Chen Min, Beitz Julie

机构信息

Division of Drug Risk Evaluation, Office of Drug Safety, Center for Drug Evaluation and Research, Food and Drug Administration, Rockville, Maryland 20857, USA.

出版信息

Drug Saf. 2002;25(7):537-44. doi: 10.2165/00002018-200225070-00007.

Abstract

OBJECTIVE

Celecoxib and rofecoxib are two relatively new nonsteroidal anti-inflammatory drugs (NSAIDs) that selectively inhibit the cyclo-oxygenase-2 (COX-2) isoenzyme at therapeutic concentrations. The nephrotoxic potential of selective COX-2 inhibitors has not been clearly established. This study was conducted in order to understand the association between acute renal failure and the two COX-2 inhibitors celecoxib and rofecoxib.

METHODS

A search was performed in the US Food and Drug Administration's (FDA) Adverse Event Reporting System (AERS) to identify cases of renal failure submitted to the FDA. A MEDLINE search of the English language literature was also performed to identify published cases of renal failure associated with celecoxib and rofecoxib.

RESULTS

One hundred twenty-two and 142 domestic US cases of celecoxib and rofecoxib-associated renal failure, respectively, were identified in the AERS database. The literature search identified 19 cases of acute renal impairment in association with celecoxib and rofecoxib. In addition, drug regulatory authorities in the UK, Canada, and Australia have received about 50 reports of renal failure with celecoxib and rofecoxib. Descriptive statistics of the AERS cases have been summarised in this report.

CONCLUSIONS

Data from AERS and published case reports suggest that use of both these drugs is associated with renal effects similar to that of conventional nonselective NSAIDs. Physicians should be aware that serious or life-threatening renal failure has been reported in patients with normal or impaired renal function after short-term therapy with celecoxib and rofecoxib. Patients at greatest risk for renal injury are those with pre-existing renal impairment, heart failure, liver dysfunction, those taking diuretics and/or ACE inhibitors, and the elderly. Kidney function should be monitored closely for any signs of potential renal injuries soon after initiating treatment with these agents, especially in high-risk populations. In addition, healthcare practitioners should adequately warn patients of the signs and symptoms of serious renal toxicity, and of the need for them to see their physician promptly if they occur. Celecoxib and rofecoxib are not recommended for use in patients with advanced renal disease.

摘要

目的

塞来昔布和罗非昔布是两种相对较新的非甾体抗炎药(NSAIDs),在治疗浓度下可选择性抑制环氧化酶-2(COX-2)同工酶。选择性COX-2抑制剂的肾毒性潜力尚未明确确定。进行本研究以了解急性肾衰竭与两种COX-2抑制剂塞来昔布和罗非昔布之间的关联。

方法

在美国食品药品监督管理局(FDA)的不良事件报告系统(AERS)中进行检索,以识别提交给FDA的肾衰竭病例。还对英文文献进行了MEDLINE检索,以识别与塞来昔布和罗非昔布相关的已发表的肾衰竭病例。

结果

在AERS数据库中分别识别出122例和142例美国国内与塞来昔布和罗非昔布相关的肾衰竭病例。文献检索发现19例与塞来昔布和罗非昔布相关的急性肾功能损害病例。此外,英国、加拿大和澳大利亚的药品监管当局已收到约50例与塞来昔布和罗非昔布相关的肾衰竭报告。本报告总结了AERS病例的描述性统计数据。

结论

来自AERS和已发表病例报告的数据表明,使用这两种药物与传统非选择性NSAIDs的肾脏效应相似。医生应意识到,在短期使用塞来昔布和罗非昔布治疗后,肾功能正常或受损的患者中均有严重或危及生命的肾衰竭报告。肾损伤风险最高的患者是那些已有肾功能损害、心力衰竭、肝功能不全、正在服用利尿剂和/或ACE抑制剂的患者以及老年人。在开始使用这些药物治疗后,应密切监测肾功能,以发现潜在肾损伤的任何迹象,尤其是在高危人群中。此外,医护人员应充分警告患者严重肾毒性的体征和症状,以及如果出现这些症状需要及时就医的必要性。不建议晚期肾病患者使用塞来昔布和罗非昔布。

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