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特异质性药物性肝损伤的流行病学及危险因素

Epidemiology and risk factors for idiosyncratic drug-induced liver injury.

作者信息

Björnsson Einar S

机构信息

Department of Internal Medicine, The Division of Gastroenterology and Hepatology, The National University Hospital of Iceland, Reykjavik, Iceland.

出版信息

Semin Liver Dis. 2014 May;34(2):115-22. doi: 10.1055/s-0034-1375953. Epub 2014 May 31.

Abstract

Idiosyncratic drug-induced liver injury (DILI) is, like other adverse effects of drugs, underreported and underestimated in most epidemiological studies based on registries of DILI cases and reporting systems (e.g., Medwatch). The same is probably true for prospective population-based studies, although they are much more likely to mirror the true incidence of DILI. Despite these challenges, the epidemiology of DILI remains of utmost importance and is gradually coming into better focus. A recent population based study found a crude incidence of ∼19 cases per 100,000 per year. Certain agents are particularly noteworthy for their DILI risk. Amoxicillin-clavulanate continues to be the most commonly implicated agent occurring in ∼1 out of 2,300 users. Some others that standout with significantly higher risk include azathioprine and infliximab. Although statin-induced hepatotoxicity has been well documented, the risk is probably quite low. Overall, the majority of DILI in children and adults is associated with either antibiotics or anticonvulsants. Drug-induced liver injury associated with intravenously given drugs does not show any major differences from DILI due to orally administered agents. Unfortunately, our understanding of pretherapy risk assessment remains rudimentary for the most part.

摘要

特异质性药物性肝损伤(DILI)与药物的其他不良反应一样,在大多数基于DILI病例登记和报告系统(如Medwatch)的流行病学研究中,报告不足且被低估。前瞻性人群研究可能也是如此,尽管它们更有可能反映DILI的真实发病率。尽管存在这些挑战,但DILI的流行病学仍然至关重要,并且正逐渐受到更多关注。最近一项基于人群的研究发现,每年每10万人中约有19例的粗略发病率。某些药物因其DILI风险尤其值得关注。阿莫西林-克拉维酸仍然是最常涉及的药物,约每2300名使用者中就有1例发生。其他一些风险显著更高的药物包括硫唑嘌呤和英夫利昔单抗。尽管他汀类药物引起的肝毒性已有充分记录,但风险可能相当低。总体而言,儿童和成人中的大多数DILI与抗生素或抗惊厥药有关。静脉给药引起的药物性肝损伤与口服药物引起的DILI没有任何重大差异。不幸的是,在很大程度上,我们对治疗前风险评估的理解仍然很基础。

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