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对乙酰氨基酚过量的管理:当前的争议

Management of paracetamol overdose: current controversies.

作者信息

Kozer E, Koren G

机构信息

Division of Clinical Pharmacology and Toxicology, The Hospital for Sick Children, Toronto, Ontario, Canada.

出版信息

Drug Saf. 2001;24(7):503-12. doi: 10.2165/00002018-200124070-00003.

Abstract

Paracetamol (acetaminophen) is one of the most frequently used analgesics, and is the most commonly used substance in self-poisoning in the US and UK. Paracetamol toxicity is manifested primarily in the liver. Treatment with N-acetyl-cysteine (NAC), if started within 10 hours from ingestion, can prevent hepatic damage in most cases. Pharmacokinetic data relating plasma paracetamol concentration to time after ingestion have been used to generate a 'probable hepatoxicity line' to predict which cases of paracetamol overdose will result in hepatotoxicity and should be treated with NAC. However, later studies use a 25% lower line as their 'possible hepatotoxicity line'. Although adopting the original line may save considerable resources, further studies are needed to determine whether such an approach is safe. On the basis of the metabolism of paracetamol, several risk factors for paracetamol toxicity have been proposed. These risk factors include long term alcohol (ethanol) ingestion, fasting and treatment with drugs that induce the cytochrome P450 2E1 enzyme system. Although some studies have suggested that these risk factors may be associated with worse prognosis, the data are inconclusive. However, until further evidence is available, we suggest that the lower line should be used when risk factors are present. In Canada and the UK, the intravenous regimen for NAC is used almost exclusively; in the US, an oral regimen is used. Both regimens have been shown to be effective. There is no large scale study with direct comparison between these 2 therapeutic protocols and controversy still exists as to which regimen is superior. During the last few years there has been an increase in the number of reports of liver failure associated with prolonged paracetamol administration for therapeutic reasons. The true incidence of this phenomenon is not known. We suggest testing liver enzyme levels if a child has received more than 75 mg/kg/day of paracetamol for more than 24 hours during febrile illness, and to treat with NAC when transaminase levels are elevated. Paracetamol overdose during pregnancy should be treated with either oral or intravenous NAC according to the regular protocols in order to prevent maternal, and potentially fetal, toxicity. Unless severe maternal toxicity develops, paracetamol overdose does not appear to increase the risk for adverse pregnancy outcome.

摘要

对乙酰氨基酚是最常用的镇痛药之一,也是美国和英国自我中毒中最常用的物质。对乙酰氨基酚毒性主要表现在肝脏。如果在摄入后10小时内开始用N - 乙酰半胱氨酸(NAC)治疗,大多数情况下可预防肝损伤。将血浆对乙酰氨基酚浓度与摄入后时间相关的药代动力学数据已被用于生成一条“可能肝毒性线”,以预测哪些对乙酰氨基酚过量病例会导致肝毒性,以及哪些病例应接受NAC治疗。然而,后来的研究使用低25%的线作为其“可能肝毒性线”。虽然采用原来的线可能节省大量资源,但需要进一步研究以确定这种方法是否安全。基于对乙酰氨基酚的代谢,已提出了几个对乙酰氨基酚毒性的危险因素。这些危险因素包括长期摄入酒精(乙醇)、禁食以及用诱导细胞色素P450 2E1酶系统的药物治疗。虽然一些研究表明这些危险因素可能与更差的预后相关,但数据尚无定论。然而,在有进一步证据之前,我们建议当存在危险因素时应使用较低的线。在加拿大和英国,几乎只使用NAC的静脉给药方案;在美国,则使用口服给药方案。两种方案均已证明有效。尚无对这两种治疗方案进行直接比较的大规模研究,关于哪种方案更优仍存在争议。在过去几年中,因治疗原因长期服用对乙酰氨基酚导致肝衰竭的报告数量有所增加。这种现象的真实发生率尚不清楚。我们建议,如果儿童在发热性疾病期间接受对乙酰氨基酚超过75mg/kg/天超过24小时,应检测肝酶水平,当转氨酶水平升高时用NAC治疗。孕期对乙酰氨基酚过量应根据常规方案用口服或静脉NAC治疗,以预防母体及潜在胎儿的毒性。除非发生严重的母体毒性,对乙酰氨基酚过量似乎不会增加不良妊娠结局的风险。

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