Rotundo Laura, Pyrsopoulos Nikolaos
Department of Medicine, Rutgers New Jersey Medical School, Newark, NJ 07103, United States.
Department of Gastroenterology and Hepatology, Rutgers New Jersey Medical School, Newark, NJ 07103, United States.
World J Hepatol. 2020 Apr 27;12(4):125-136. doi: 10.4254/wjh.v12.i4.125.
Drug induced liver injury (DILI) is a common cause of acute liver injury. Paracetamol, also known as acetaminophen, is a widely used anti-pyretic that has long been established to cause liver toxicity once above therapeutic levels. Hepatotoxicity from paracetamol overdose, whether intentional or non-intentional, is the most common cause of DILI in the United States and remains a global issue. Given the increased prevalence of combination medications in the form of pain relievers and antihistamines, paracetamol can be difficult to identify and remains a significant cause of acute hepatotoxicity, as evidenced by its contribution to over half of all acute liver failure cases in the United States. This is especially concerning given that, when co-ingested with other medications, the rise in serum paracetamol levels may be delayed past the 4-hour post-ingestion mark that is currently used to determine patients that require medical therapy. This review serves to describe the clinical and pathophysiologic features of hepatotoxicity secondary to paracetamol and provide an update on current available knowledge and treatment options.
药物性肝损伤(DILI)是急性肝损伤的常见原因。对乙酰氨基酚,又称醋氨酚,是一种广泛使用的退烧药,长期以来已确定一旦超过治疗水平就会导致肝毒性。对乙酰氨基酚过量导致的肝毒性,无论有意或无意,是美国DILI最常见的原因,并且仍然是一个全球性问题。鉴于以止痛药和抗组胺药形式存在的复方药物的患病率增加,对乙酰氨基酚可能难以识别,并且仍然是急性肝毒性的重要原因,美国超过一半的急性肝衰竭病例都与其有关,这证明了这一点。鉴于与其他药物同时摄入时,血清对乙酰氨基酚水平的升高可能会延迟到目前用于确定需要药物治疗的患者的摄入后4小时标记之后,这尤其令人担忧。这篇综述旨在描述对乙酰氨基酚继发肝毒性的临床和病理生理特征,并提供当前现有知识和治疗选择的最新信息。