Potential risk of liver injury in epileptic patients during COVID-19 pandemic.

Nasim Tabrizi, Athena Sharifi-Razavi
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Abstract

Most of the antiseizure medications (ASMs) are metabolized in liver and many of them particularly first-generation ASMs have the potential to increase liver enzymes or induce liver injury. Hence, treatment of new onset seizures or epilepsy by ASMs during the course of coronavirus disease 2019 (COVID-19), which could potentially be complicated by hepatic dysfunction, is a challenging clinical issue. Intravenous form of levetiracetam which has no significant hepatic metabolism or drug-drug interaction is often a favorable option to control seizures in acute phase of COVID-19. Administration of enzyme inducer ASMs and valproate with the well-known hepatotoxicity and common drug interactions is not generally recommended. In patients with epilepsy who are under control with potentially hepatotoxic ASMs, close observation and cautious dose reduction or drug switch should be considered if any evidence of hepatic impairment exists. However, risks of possible breakthrough seizures should be weighed against benefits of lowering the hazard of liver injury. In patients with epilepsy who receive polytherapy with ASMs, transient dose modification with the tendency to increase the dose of ASMs with more favorable safety profile and less drug interaction and decrease the dose of drugs with main hepatic metabolism, high protein binding, potential to cause liver injury and known drug-drug reaction should be considered. Finally, decision making should be individualized based on patients' conditions and course of illness.

Abstract Image

COVID-19 大流行期间癫痫患者肝损伤的潜在风险。
大多数抗癫痫药物(ASMs)在肝脏代谢,其中许多药物尤其是第一代ASMs有可能增加肝酶或诱发肝损伤。因此,在2019年冠状病毒病(COVID-19)病程中使用ASM治疗新发癫痫发作或癫痫,有可能因肝功能异常而并发症,这是一个具有挑战性的临床问题。静脉注射形式的左乙拉西坦没有明显的肝脏代谢或药物间相互作用,通常是控制 COVID-19 急性期癫痫发作的有利选择。一般不推荐使用酶诱导剂 ASM 和丙戊酸钠,因为它们具有众所周知的肝毒性和常见的药物相互作用。对于使用具有潜在肝毒性的 ASMs 可控制病情的癫痫患者,如果有任何肝功能损害的证据,应考虑密切观察并谨慎减量或换药。不过,应权衡可能出现突破性癫痫发作的风险与降低肝损伤危害的益处。对于接受 ASMs 多药治疗的癫痫患者,应考虑短暂的剂量调整,倾向于增加安全性较好、药物相互作用较少的 ASMs 的剂量,减少主要肝脏代谢、蛋白结合率高、可能导致肝损伤和已知药物间反应的药物的剂量。最后,应根据患者的病情和病程做出个体化决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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