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半数以上被认为因过量服用而导致急性肝衰竭的患者的血浆中检测不到对乙酰氨基酚。

Acetaminophen is Undetectable in Plasma From More Than Half of Patients Believed to Have Acute Liver Failure Due to Overdose.

机构信息

Division of Gastroenterology and Hepatology, University of Kansas Medical Center, Kansas City, Kansas.

Public Health Sciences, Medical University of South Carolina, Charleston, South Caroline.

出版信息

Clin Gastroenterol Hepatol. 2019 Sep;17(10):2110-2116. doi: 10.1016/j.cgh.2019.01.040. Epub 2019 Feb 5.

Abstract

BACKGROUND & AIMS: Evaluation of patients with acute liver injury (ALI) or acute liver failure (ALF) often includes measurement of plasma levels of acetaminophen, to determine exposure and/or toxicity. However, once liver injury has developed, acetaminophen might be undetectable in plasma. We investigated the association between level of acetaminophen measured and outcomes of patients designated as having ALF or ALI due to acetaminophen toxicity.

METHODS

We performed a retrospective analysis of data from 434 subjects in the Acute Liver Failure Study Group who met criteria for ALF (coagulopathy and hepatic encephalopathy within 26 weeks of the first symptoms, without pre-existing liver disease) or ALI (severe liver injury with coagulopathy but no encephalopathy) due to acetaminophen toxicity from January 1, 2010 through December 31, 2014. We collected data on patient demographics, biochemical features, reported acetaminophen use, N-acetylcysteine therapy, liver transplant, and outcomes. Descriptive statistics were used to assess patient demographics, clinical characteristics, and outcomes whereas differences in continuous variables between patients with vs without acetaminophen detection on admission were analyzed using the Wilcoxon rank-sum test. The primary aim was to determine the proportion of patients with detectable plasma levels of acetaminophen.

RESULTS

Acetaminophen was undetectable in serum samples from 227 patients (52%). There were no significant differences between groups of patients with detectable vs undetectable levels in demographic features, alcohol use, median levels of alanine aspartate, or use of N-acetylcysteine (given to 94.7% of patients with detectable acetaminophen vs 95.9% of those with undetectable acetaminophen; P=.63). We observed a significant difference in median dose taken between patients with detectable (29,500 mg; interquartile range, 15,000 mg-50,007 mg) vs no detectable parent compound (14,950 mg; interquartile range, 3960 mg-25,000) (P=.003). A lower proportion of patients with detectable plasma levels of acetaminophen (72.3%) survived without a liver transplant than of patients with undetectable levels (86.3%) in univariate analysis (P=.0006), although this was not significant in multivariable analysis (P=.12). Although most patients had unintentional overdoses, a higher proportion of patients with suicidal overdoses (43%) had detectable levels of acetaminophen than patients with accidental overdoses (29.3%; P=.01).

CONCLUSION

More than half of patients who present at the hospital with acetaminophen-induced ALI or ALF have undetectable levels of acetaminophen. Clinicians should not exclude acetaminophen toxicity because of undetectable levels or withhold N-acetylcysteine for patients with ALI or ALF when acetaminophen toxicity is suspected.

摘要

背景与目的

评估急性肝损伤(ALI)或急性肝衰竭(ALF)患者时,常需检测血浆中对乙酰氨基酚水平,以判断接触情况和/或毒性。但一旦发生肝损伤,血浆中可能检测不到对乙酰氨基酚。本研究旨在探讨对乙酰氨基酚测定值与确诊为对乙酰氨基酚中毒所致 ALF 或 ALI 患者结局之间的关系。

方法

我们对 2010 年 1 月 1 日至 2014 年 12 月 31 日期间因对乙酰氨基酚中毒而符合 ALF(首发症状后 26 周内出现凝血功能障碍和肝性脑病,无既往肝脏疾病)或 ALI(严重肝损伤伴凝血功能障碍但无脑功能障碍)标准的急性肝衰竭研究组 434 例患者的数据进行了回顾性分析。我们收集了患者人口统计学、生化特征、报告的对乙酰氨基酚使用情况、N-乙酰半胱氨酸治疗、肝移植和结局等数据。采用描述性统计方法评估患者的人口统计学、临床特征和结局,采用 Wilcoxon 秩和检验分析入院时对乙酰氨基酚检测阳性与阴性患者的连续变量差异。主要目的是确定可检测到血浆中对乙酰氨基酚水平的患者比例。

结果

227 例患者(52%)的血清样本中未检测到对乙酰氨基酚。在可检测到与未检测到对乙酰氨基酚水平的患者组中,在人口统计学特征、酒精使用、丙氨酸氨基转移酶中位数或 N-乙酰半胱氨酸使用方面(94.7%检测到对乙酰氨基酚的患者和 95.9%未检测到对乙酰氨基酚的患者均接受了 N-乙酰半胱氨酸治疗;P=.63)均无显著差异。我们观察到可检测到(29500 mg;四分位距 15000 mg-50007 mg)和未检测到(14950 mg;四分位距 3960 mg-25000)母体化合物的患者中位剂量之间存在显著差异(P=.003)。在单变量分析中,与未检测到血浆水平对乙酰氨基酚的患者(72.3%)相比,可检测到对乙酰氨基酚水平的患者(86.3%)无肝移植生存的比例较低(P=.0006),但在多变量分析中,差异无统计学意义(P=.12)。尽管大多数患者为意外过量,但与意外过量(29.3%)的患者相比,自杀过量(43%)患者中可检测到对乙酰氨基酚的比例更高(P=.01)。

结论

在因对乙酰氨基酚导致的 ALI 或 ALF 而就诊的患者中,超过一半的患者无法检测到对乙酰氨基酚。当怀疑对乙酰氨基酚中毒时,临床医生不应该因为未检测到对乙酰氨基酚或未检测到对乙酰氨基酚而排除对乙酰氨基酚毒性,也不应该为 ALI 或 ALF 患者 withholding N-acetylcysteine。

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