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酗酒者急性对乙酰氨基酚过量服用后肝毒性的估计风险。

Estimated risk of hepatotoxicity after an acute acetaminophen overdose in alcoholics.

作者信息

Ali Fahad M, Boyer Edward W, Bird Steven B

机构信息

Division of Medical Toxicology, Department of Emergency Medicine, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655, USA.

出版信息

Alcohol. 2008 May;42(3):213-8. doi: 10.1016/j.alcohol.2007.11.005. Epub 2008 Mar 20.

Abstract

A published logistic regression model based on the Canadian Acetaminophen Overdose Study registry was used to calculate the risk of hepatotoxicity after an acute acetaminophen overdose and to estimate a treatment threshold line for alcoholic patients who did not co-ingest alcohol (i.e., abstinent alcoholics) on the Rumack-Matthew nomogram. The risk of hepatotoxicity in nonalcoholic and abstinent alcoholic patients was calculated at the acetaminophen concentration of 150 microg/ml at 4h (37.5 microg/ml at 12h) treatment threshold line. This corresponds to the "possible risk" line on the Rumack-Matthew nomogram and represents a 1.6% risk of hepatotoxicity for nonalcoholic patients at or below this line. At or below this same 150 microg/ml at 4-h line, abstinent alcoholic patients have a hepatotoxicity risk of 10.7%. The risk of hepatotoxicity in abstinent alcoholics' equivalent to that of nonalcoholics (i.e., 1.6%) occurs at a lower acetaminophen concentrations treatment threshold line, that is, 104 microg/ml at 4h (26 microg/ml at 12h). Because of difficulties plotting this new line on the familiar Rumack-Matthew semilogarithmic scale, a line connecting 100 microg/ml at 4h (25 microg/ml at 12h) is proposed. This line equates to a 1.1% risk of hepatotoxicity in abstinent alcoholic patients. The analysis supports the observation that based on the published model abstinent alcoholics might have a greater risk of hepatotoxicity after an acute acetaminophen overdose. This proposed new risk line can be used in hypothesis generation for future clinical studies in this alcohol related problem.

摘要

基于加拿大对乙酰氨基酚过量研究登记处发布的逻辑回归模型,用于计算急性对乙酰氨基酚过量后发生肝毒性的风险,并在鲁马克 - 马修列线图上为未同时摄入酒精的酒精性肝病患者(即戒酒的酗酒者)估计治疗阈值线。在对乙酰氨基酚浓度为4小时150微克/毫升(12小时37.5微克/毫升)的治疗阈值线时,计算非酒精性和戒酒的酗酒者发生肝毒性的风险。这对应于鲁马克 - 马修列线图上的“可能风险”线,代表在此线及以下的非酒精性患者发生肝毒性的风险为1.6%。在4小时150微克/毫升这条相同的线及以下,戒酒的酗酒者发生肝毒性的风险为10.7%。戒酒的酗酒者发生与非酒精性患者相同肝毒性风险(即1.6%)时,对乙酰氨基酚浓度的治疗阈值线更低,即4小时104微克/毫升(12小时26微克/毫升)。由于难以在熟悉的鲁马克 - 马修半对数尺度上绘制这条新线,建议绘制一条连接4小时100微克/毫升(12小时25微克/毫升)的线。这条线相当于戒酒的酗酒者发生肝毒性的风险为1.1%。该分析支持以下观察结果:根据已发表的模型,戒酒的酗酒者在急性对乙酰氨基酚过量后可能有更高的肝毒性风险。这条建议的新风险线可用于针对这个酒精相关问题的未来临床研究的假设生成。

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