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系统评价:布洛芬所致肝损伤。

Systematic review: ibuprofen-induced liver injury.

机构信息

Unidad de Gestión Clínica de Aparato Digestivo, Hospital Universitario Virgen de la Victoria, Instituto de Investigación Biomédica de Málaga, Universidad de Málaga, Málaga, Spain.

Department of Pharmacology and Toxicology, Maastricht University Medical Center, Maastricht, The Netherlands.

出版信息

Aliment Pharmacol Ther. 2020 Mar;51(6):603-611. doi: 10.1111/apt.15645. Epub 2020 Jan 27.

Abstract

BACKGROUND

Nonsteroidal anti-inflammatory drugs (NSAIDs) are a leading cause of drug-induced liver injury (DILI) across the world. Ibuprofen is one of the most commonly used and safest NSAIDs, nevertheless reports on ibuprofen-induced hepatotoxicity are available.

AIM

To analyse previously published information on ibuprofen-induced liver injury for a better characterisation of its phenotypic expression.

METHOD

A systematic search was performed and information on ibuprofen-induced liver injury included in case series and case reports, in terms of demographic, clinical, biochemical and outcome data, was analysed.

RESULTS

Twenty-two idiosyncratic ibuprofen hepatotoxicity cases were identified in the literature, suggesting a very low prevalence of this type of DILI. These patients had a mean age of 31 years and 55% were females. Mean cumulative dose of ibuprofen and time to onset were 30 g and 12 days, respectively. Hepatocellular injury was the most frequently involved liver injury pattern. Six cases developed vanishing bile duct syndrome. Full recovery occurred in 11 patients after a mean time of 14 weeks, whereas five cases evolved to acute liver failure leading to death/liver transplantation.

CONCLUSIONS

When assessing potential hepatotoxicity cases, physicians should keep in mind that ibuprofen has been associated with hepatotoxicity in the literature. Ibuprofen-associated DILI presents commonly as hepatocellular damage after a short latency period. Published reports on ibuprofen hepatotoxicity leading to liver failure resulting in liver transplantation or death are available. However, due to the apparent low absolute risk of ibuprofen-induced liver complications, ibuprofen can be regarded as an efficacious and safe NSAID.

摘要

背景

非甾体抗炎药(NSAIDs)是全球范围内导致药物性肝损伤(DILI)的主要原因。布洛芬是最常用和最安全的 NSAIDs 之一,但已有关于布洛芬引起的肝毒性的报道。

目的

分析已发表的关于布洛芬引起的肝损伤的信息,以更好地描述其表型表达。

方法

进行了系统搜索,并分析了病例系列和病例报告中包含的布洛芬引起的肝损伤的信息,包括人口统计学、临床、生化和结局数据。

结果

文献中确定了 22 例特发性布洛芬肝毒性病例,提示这种类型的 DILI 发生率非常低。这些患者的平均年龄为 31 岁,女性占 55%。布洛芬的累积剂量和发病时间的平均值分别为 30g 和 12 天。肝细胞损伤是最常见的肝损伤模式。6 例发生胆汁消失综合征。11 例患者在平均 14 周后完全恢复,而 5 例患者发展为急性肝衰竭导致死亡/肝移植。

结论

在评估潜在的肝毒性病例时,医生应牢记布洛芬在文献中与肝毒性有关。布洛芬相关的 DILI 通常在潜伏期短后表现为肝细胞损伤。已有关于导致肝衰竭导致肝移植或死亡的布洛芬肝毒性的报告。然而,由于布洛芬引起的肝并发症的明显低绝对风险,布洛芬可被视为一种有效且安全的 NSAID。

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