Dart Richard C, Bailey Elise
Rocky Mountain Poison and Drug Center, Denver Health and Hospital Authority, Denver, Colorado 80204, USA.
Pharmacotherapy. 2007 Sep;27(9):1219-30. doi: 10.1592/phco.27.9.1219.
To compare the reported occurrence of liver failure in subjects in prospective trials with that in patients in retrospective reports after repeated use of therapeutic dosages of acetaminophen.
Systematic review of the medical literature.
MEDLINE and EMBASE biomedical and pharmacologic databases.
Adults who received repeated dosing of acetaminophen 4 g/day or lower for at least 24 hours.
Articles written in several languages were abstracted by trained personnel using a structured abstraction form. Data were categorized by methodology (prospective vs retrospective), acetaminophen dosage, and type of liver effect. A total of 791 articles were identified, which included 30,865 subjects in prospective studies and 9337 patients in retrospective reports. The prospective studies reported no cases of fulminant hepatic injury, liver transplantation, or death due to acetaminophen. Of the 30,865 subjects in these studies, 129 (0.4%) were identified who had a serum aminotransferase level that exceeded the upper limit of normal, including 61 subjects in randomized trials in which the proportion of serum aminotransferase level increase was the same as or less than that in the placebo group and 68 subjects in trials without a placebo group. In addition, 4263 (13.8%) received the maximum recommended therapeutic dosage (3.9-4 g/day). In the retrospective reports, 96 patients (1.0%) had a serum alanine aminotransferase level that exceeded the upper limit of normal, one (0.01%) underwent liver transplantation, and six (0.06%) died. Causality relationship of acetaminophen for each retrospective case was assessed with the Naranjo adverse drug reaction probability scale. The mean +/- SD Naranjo score for all 103 retrospective cases was 3.2 +/- 1.9, indicating a possible relationship between the increased aminotransferase levels and acetaminophen use. Some retrospective reports contained information suggesting that the patient had ingested an overdose despite a history of therapeutic use.
Prospective studies indicated that repeated use of a true therapeutic acetaminophen dosage may slightly increase the level of serum aminotransferase activity, but hepatic failure or death was not reported. Retrospective reports indicated a higher rate of increased serum aminotransferase levels, and several reported associated liver injury and death. The differing results and presence of evidence indicating inaccurate acetaminophen dosage information in some case reports suggests that these cases may be inadvertent overdoses, rather than true therapeutic dosages.
比较前瞻性试验中受试者重复使用治疗剂量对乙酰氨基酚后报告的肝衰竭发生率与回顾性报告中患者的发生率。
对医学文献进行系统评价。
MEDLINE和EMBASE生物医学与药理学数据库。
每天接受4克或更低剂量对乙酰氨基酚重复给药至少24小时的成年人。
由经过培训的人员使用结构化摘要表格提取多种语言撰写的文章。数据按方法(前瞻性与回顾性)、对乙酰氨基酚剂量和肝效应类型进行分类。共识别出791篇文章,其中前瞻性研究中有30865名受试者,回顾性报告中有9337名患者。前瞻性研究未报告暴发性肝损伤、肝移植或因对乙酰氨基酚导致的死亡病例。在这些研究的30865名受试者中,有129名(0.4%)血清转氨酶水平超过正常上限,其中包括随机试验中的61名受试者,其血清转氨酶水平升高的比例与安慰剂组相同或更低,以及无安慰剂组试验中的68名受试者。此外,4263名(13.8%)接受了最大推荐治疗剂量(3.9 - 4克/天)。在回顾性报告中,96名患者(1.0%)血清丙氨酸转氨酶水平超过正常上限,1名(0.01%)接受了肝移植,6名(0.06%)死亡。使用Naranjo药物不良反应概率量表评估每个回顾性病例中对乙酰氨基酚的因果关系。所有103例回顾性病例的平均±标准差Naranjo评分为3.2±1.9,表明转氨酶水平升高与对乙酰氨基酚使用之间可能存在关联。一些回顾性报告包含的信息表明,尽管有治疗用药史,但患者摄入了过量药物。
前瞻性研究表明,重复使用真正的治疗剂量对乙酰氨基酚可能会使血清转氨酶活性水平略有升高,但未报告肝衰竭或死亡情况。回顾性报告显示血清转氨酶水平升高的发生率更高,且有几例报告了相关的肝损伤和死亡。结果不同以及一些病例报告中存在对乙酰氨基酚剂量信息不准确的证据表明,这些病例可能是意外过量用药,而非真正的治疗剂量用药。