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胺碘酮和决奈达隆导致的肝损伤具有不同的临床表现。

Amiodarone and Dronedarone Causes Liver Injury with Distinctly Different Clinical Presentations.

机构信息

Albert Einstein Medical Center, Sidney Kimmel Medical College, Philadelphia, PA, USA.

Thomas Jefferson University Hospital, Sidney Kimmel Medical College, Philadelphia, PA, USA.

出版信息

Dig Dis Sci. 2024 Apr;69(4):1479-1487. doi: 10.1007/s10620-023-08251-2. Epub 2024 Feb 28.

Abstract

OBJECTIVE

To describe hepatotoxicity due to amiodarone and dronedarone from the DILIN and the US FDA's surveillance database.

METHODS

Hepatotoxicity due to amiodarone and dronedarone enrolled in the U.S. Drug Induced Liver Injury Network (DILIN) from 2004 to 2020 are described. Dronedarone hepatotoxicity cases associated with liver biopsy results were obtained from the FDA Adverse Event Reporting System (FAERS) from 2009 to 2020.

RESULTS

Among DILIN's 10 amiodarone and 3 dronedarone DILIN cases, the latency for amiodarone was longer than with dronedarone (388 vs 119 days, p = 0.50) and the median ALT at DILI onset was significantly lower with amiodarone (118 vs 1191 U/L, p = 0.05). Liver biopsies in five amiodarone cases showed fibrosis, steatosis, and numerous Mallory-Denk bodies. Five patients died although only one from liver failure. One patient with dronedarone induced liver injury died of a non-liver related cause. Nine additional cases of DILI due to dronedarone requiring hospitalization were identified in the FAERS database. Three patients developed liver injury within a month of starting the medication. Two developed acute liver failure and underwent urgent liver transplant, one was evaluated for liver transplant but then recovered spontaneously, while one patient with cirrhosis died of liver related causes.

CONCLUSION

Amiodarone hepatotoxicity resembles that seen in alcohol related liver injury, with fatty infiltration and inflammation. Dronedarone is less predictable, typically without fat and with a shorter latency of use before presentation. These differences may be explained, in part, by the differing pharmacokinetics of the two drugs leading to different mechanisms of hepatotoxicity.

摘要

目的

描述来自 DILIN 和美国 FDA 监测数据库的胺碘酮和决奈达隆引起的肝毒性。

方法

描述了 2004 年至 2020 年期间美国药物性肝损伤网络(DILIN)中登记的胺碘酮和决奈达隆引起的肝毒性。从 2009 年至 2020 年,从 FDA 不良事件报告系统(FAERS)获得了与肝活检结果相关的决奈达隆肝毒性病例。

结果

在 DILIN 的 10 例胺碘酮和 3 例决奈达隆 DILIN 病例中,胺碘酮的潜伏期长于决奈达隆(388 天与 119 天,p=0.50),DILI 发病时的中位 ALT 水平明显低于胺碘酮(118 与 1191 U/L,p=0.05)。5 例胺碘酮病例的肝活检显示纤维化、脂肪变性和大量 Mallory-Denk 小体。尽管只有 1 例死于肝功能衰竭,但有 5 例患者死亡。1 例因决奈达隆引起的肝损伤患者死于非肝脏相关原因。在 FAERS 数据库中还确定了另外 9 例因决奈达隆导致的需要住院的 DILI 病例。3 例患者在开始用药后 1 个月内发生肝损伤。2 例发展为急性肝功能衰竭并接受紧急肝移植,1 例接受肝移植评估但随后自发恢复,而 1 例肝硬化患者死于与肝脏相关的原因。

结论

胺碘酮肝毒性类似于酒精相关肝损伤,表现为脂肪浸润和炎症。决奈达隆更不可预测,通常没有脂肪,在出现之前使用的潜伏期较短。这些差异可能部分解释为两种药物的不同药代动力学导致不同的肝毒性机制。

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