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口服胺碘酮后出现致命性肝毒性。

Fatal hepatotoxicity following oral administration of amiodarone.

作者信息

Richer M, Robert S

机构信息

Ecole de Pharmacie, Université Laval, Québec, Canada.

出版信息

Ann Pharmacother. 1995 Jun;29(6):582-6. doi: 10.1177/106002809502900605.

Abstract

OBJECTIVE

To report a case of fatal hepatotoxicity associated with the chronic use of oral amiodarone.

CASE SUMMARY

Long-term administration of amiodarone for the control of intractable ventricular tachycardia was associated with fatal hepatotoxicity in a patient receiving amiodarone for 14 months.

DISCUSSION

Although most hepatic adverse effects associated with amiodarone are transient and reversible with time, deaths resulting from amiodarone-induced hepatotoxicity have been reported. The relation of hepatotoxicity to cumulative dose and duration of therapy is debated. The histopathologic features of amiodarone-induced hepatotoxicity include Mallory bodies, steatosis, intralobular inflammatory infiltrates, fibrosis, and phospholipidosis.

CONCLUSIONS

Evidence pertaining to both mild and severe amiodarone toxicity indicates that cumulative dose may correlate with overall toxicity and, therefore, maintenance doses should be kept as low as possible. Patients should be followed with monitoring of liver function test results every 3-6 months.

摘要

目的

报告一例与长期口服胺碘酮相关的致命性肝毒性病例。

病例摘要

一名患者接受胺碘酮治疗14个月,长期服用胺碘酮控制顽固性室性心动过速,出现了致命性肝毒性。

讨论

尽管与胺碘酮相关的大多数肝脏不良反应是短暂的,且随时间可逆转,但已有胺碘酮诱发肝毒性导致死亡的报道。肝毒性与累积剂量及治疗持续时间的关系存在争议。胺碘酮诱发肝毒性的组织病理学特征包括马洛里小体、脂肪变性、小叶内炎性浸润、纤维化和磷脂沉积症。

结论

有关胺碘酮轻、重度毒性的证据表明,累积剂量可能与总体毒性相关,因此维持剂量应尽可能低。应每3至6个月对患者进行随访并监测肝功能检查结果。

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