Department of Medical and Toxicological Critical Care, APHP, Lariboisière Hospital, Paris University, INSERM UMRS-1144, Paris, France.
Department of Gastroenterology, APHP, Beaujon Hospital, Paris University, INSERM UMRS-1148, Clichy, France.
United European Gastroenterol J. 2021 Jun;9(5):571-580. doi: 10.1002/ueg2.12093.
Acetaminophen is a common cause of poisoning and liver injury worldwide; however, patient stratification is suboptimal. We aimed to assess the contribution of admission plasma procalcitonin concentration (PCT) to better identify acetaminophen-poisoned patients likely to develop liver injury.
We conducted a prospective observational cohort study including all acetaminophen-poisoned patients requiring N-acetylcysteine admitted in a toxicological intensive care unit between 2012 and 2017. Multivariate analysis was performed using a Cox regression model to investigate factors associated with liver injury, defined as an increase in alanine aminotransferase (ALT) >100 IU/L.
One hundred seventeen patients (age, 32 years (21-53), median [25th-75th percentiles]) were included after self-ingesting 16 g (9-30) acetaminophen and received N-acetylcysteine infusion administered within a median 6 h-delay (4-12) from exposure. Co-ingestions were reported in 77% of patients. Rumack-Matthew nomogram was non-interpretable in 47% cases. Liver injury occurred in 38 patients (32%) with a median peak ALT of 2020 IU/L (577-4248). In liver injury patients, admission PCT was significantly increased in comparison to patients without liver injury (21.5 ng/ml (3.2-44.9) versus 0.1 ng/ml (0-0.4), respectively, p < 0.01). The increase in PCT preceded the increase in ALT by 33 h (10-74). In a multivariate analysis, PCT > 1 ng/ml was significantly associated with liver injury (hazard ratio, 7.2 [95% confidence interval, 2.3-22.6; p < 0.001]). PCT (area under the receiver-operating characteristics curve, 0.91 [95%CI: 0.84-0.97]) predicted liver injury with sensitivity, specificity, negative, and positive predictive values of 0.92, 0.84, 0.96, and 0.73, respectively.
PCT on admission is associated with liver injury in acetaminophen poisoning. PCT might be used as a predictive tool of liver injury to improve clinical decision-making.
对乙酰氨基酚是全球范围内导致中毒和肝损伤的常见原因,但目前对患者的分层效果并不理想。本研究旨在评估入院时血浆降钙素原(PCT)浓度对更好地识别可能发生肝损伤的乙酰氨基酚中毒患者的作用。
我们进行了一项前瞻性观察队列研究,纳入了 2012 年至 2017 年间在毒理学重症监护病房因乙酰氨基酚中毒而需要接受 N-乙酰半胱氨酸治疗的所有患者。采用 Cox 回归模型进行多变量分析,以探讨与肝损伤相关的因素,肝损伤定义为丙氨酸氨基转移酶(ALT)升高>100IU/L。
共纳入 117 例(年龄 32 岁(21-53 岁),中位数[25 百分位数-75 百分位数])患者,这些患者因自服 16g(9-30)乙酰氨基酚后中毒,在中位 6 小时(4-12 小时)延迟后接受 N-乙酰半胱氨酸输注治疗。77%的患者存在合并用药。47%的患者的 Rumack-Matthew 列线图无法解释。38 例(32%)患者发生肝损伤,中位 ALT 峰值为 2020IU/L(577-4248IU/L)。与无肝损伤的患者相比,肝损伤患者的入院时 PCT 显著升高(分别为 21.5ng/ml(3.2-44.9)和 0.1ng/ml(0-0.4),p<0.01)。PCT 升高早于 ALT 升高 33 小时(10-74 小时)。多变量分析显示,PCT>1ng/ml 与肝损伤显著相关(危险比 7.2[95%置信区间 2.3-22.6;p<0.001])。PCT(受试者工作特征曲线下面积 0.91[95%CI:0.84-0.97])预测肝损伤的敏感性、特异性、阴性预测值和阳性预测值分别为 0.92、0.84、0.96 和 0.73。
入院时的 PCT 与乙酰氨基酚中毒患者的肝损伤有关。PCT 可作为预测肝损伤的工具,以改善临床决策。