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未识别的对乙酰氨基酚毒性是不明原因急性肝衰竭的一个原因。

Unrecognized acetaminophen toxicity as a cause of indeterminate acute liver failure.

机构信息

Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX 75390-8887, USA.

出版信息

Hepatology. 2011 Feb;53(2):567-76. doi: 10.1002/hep.24060. Epub 2011 Jan 10.

Abstract

UNLABELLED

Despite extensive investigations, the cause of liver injury in 14% of patients with acute liver failure remains unknown (indeterminate). In a pilot study using a novel assay, highly specific acetaminophen-cysteine adducts were detected in 7 of 36 indeterminate patients (19%). To extend these observations, sera from 110 subjects enrolled in the Acute Liver Failure Study Group registry with indeterminate acute liver failure were analyzed with a similar but more efficient and sensitive adduct assay. As positive controls, another 199 patients with known or presumed acetaminophen-induced liver failure were assessed for the presence and quantity of adducts. Clinical, laboratory, and outcome data were compared for the two groups. On the basis of previous data for known therapeutic exposures and acetaminophen overdoses, an adduct concentration ≥1.0 nmol/mL of serum indicated a definite acetaminophen overdose. Among the 110 indeterminate cases, 18% had assay values ≥1.0 with a median level of 9.2 nmol/mL; 94.5% of the positive controls (known acetaminophen cases) had values ≥1.0 nmol/mL. Regardless of the initial diagnosis, subjects with elevated adduct levels demonstrated the clinical profile and hyperacute biochemical injury pattern associated with acetaminophen overdose: a predominance of female gender, very high aminotransferase levels, and low bilirubin levels.

CONCLUSION

These data confirm and extend previous observations regarding the high (18%) prevalence of unrecognized or uncertain acetaminophen toxicity among subjects with indeterminate acute liver failure. N-Acetylcysteine use was limited in this group, presumably because of the lack of a specific diagnosis of acetaminophen toxicity.

摘要

背景

尽管进行了广泛的调查,但仍有 14%的急性肝衰竭患者的肝损伤原因不明(不确定)。在一项使用新检测方法的初步研究中,在 36 名不确定的急性肝衰竭患者中发现了 7 例(19%)高度特异性的对乙酰氨基酚-半胱氨酸加合物。为了扩展这些观察结果,对急性肝衰竭研究组登记册中 110 例不确定的急性肝衰竭患者的血清进行了类似但更有效和敏感的加合物检测。作为阳性对照,对 199 例已知或推定的对乙酰氨基酚诱导的肝衰竭患者进行了加合物的存在和数量评估。比较了两组的临床、实验室和转归数据。基于先前对已知治疗性暴露和对乙酰氨基酚过量的研究数据,血清中加合物浓度≥1.0 nmol/ml 表明明确的对乙酰氨基酚过量。在 110 例不确定的病例中,18%的检测值≥1.0,中位数为 9.2 nmol/ml;94.5%的阳性对照(已知对乙酰氨基酚病例)的检测值≥1.0 nmol/ml。无论初始诊断如何,加合物水平升高的患者表现出与对乙酰氨基酚过量相关的临床特征和超急性生化损伤模式:女性为主、转氨酶水平极高、胆红素水平极低。

结论

这些数据证实并扩展了先前的观察结果,即在不确定的急性肝衰竭患者中,未被识别或不确定的对乙酰氨基酚毒性的发生率较高(18%)。在该组中,由于缺乏对乙酰氨基酚毒性的明确诊断,N-乙酰半胱氨酸的使用受到限制。

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