On the Treatment of Acute Poisoning With Paracetamol

Author:

Simonova A. Yu.1ORCID,Potskhveriya M. M.2ORCID,Belova M. V.3ORCID,Ilyashenko K. K.1ORCID,Kulabuhov V. V.4ORCID,Stolbova N. Y.4ORCID,Klyuev A. E.4ORCID

Affiliation:

1. Department of Acute Poisonings and Somatopsychiatric Disorders N.V. Sklifosovsky Research Institute for Emergency Medicine; Scientific and Practical Toxicology Center of Federal Medical and Biological Agency

2. Department of Acute Poisonings and Somatopsychiatric Disorders N.V. Sklifosovsky Research Institute for Emergency Medicine; Scientific and Practical Toxicology Center of Federal Medical and Biological Agency; Russian Medical Academy of Continuing Professional Education

3. Department of Acute Poisonings and Somatopsychiatric Disorders N.V. Sklifosovsky Research Institute for Emergency Medicine; Russian Medical Academy of Continuing Professional Education

4. Department of Acute Poisonings and Somatopsychiatric Disorders N.V. Sklifosovsky Research Institute for Emergency Medicine

Abstract

BACKGROUND Currently, despite the optimization of diagnostic methods in order to predict the development of liver damage, improvement of treatment protocols, paracetamol poisoning is a serious problem in medicine, being the most common cause of acute liver failure worldwide.AIM OF STUDY To determine the indications for the use of acetylcysteine in paracetamol poisoning and evaluate the effectiveness of the 21-hour protocol for its administration.MATERIAL AND METHODS We examined 20 patients with acute paracetamol poisoning (15 women and 5 men), the median age was 21.5 (19.8–32.3) years. ALT and AST were assessed during the entire period of stay in the hospital, the time period from the moment of taking paracetamol to hospitalization and the beginning of the administration of ACC, the concentration of paracetamol in the blood, and mortality. According to the level of ALT and AST in the blood, the patients were divided into 2 groups: Group I consisted of 14 patients, in whom the concentration of ALT and AST during the entire observation period did not exceed 50 U/L; in Group II (6 patients), an increase in the level of ALT and AST in the blood of more than 50 U/L was observed. To assess the risk of liver lesion, the Rumack-Matthew nomogram was used. To compare the concentrations of paracetamol in the blood of patients, the paracetamol index was used.RESULTS It was found that in 10 patients with a high risk of liver damage, who were treated with a 21-hour regimen of ACC administration, no hepatotoxic effect was found. The use of ACC according to a 21-hour protocol in patients with initially elevated ALT and AST levels of more than 50 U/L (n = 4) (25%) led to a rapid positive dynamics of laboratory and clinical parameters. It was found that in 2 patients, despite the introduction of ACC, the development of liver damage was observed. At the same time, the level of paracetamol in their blood was 6.6 and 10.6 fold higher than the “therapeutic” line of the nomogram, and the time from the moment of taking the drug to the beginning of the administration of ACC was 8 and 20 hours. High risk factors for the development of hepatotoxic effect in case of paracetamol poisoning are the time range from the moment of taking the drug to the beginning of the administration of ACC and the value of the paracetamol index.CONCLUSION Indications for the use of acetylcysteine in acute poisoning with paracetamol is a high risk of liver damage. Its criteria are high doses, increased concentrations of ALT and AST when patients are admitted to the hospital; if it is possible to determine the concentration of paracetamol in the blood, an increase in the value of the paracetamol index is more than 1. The use of a 21-hour protocol of intravenous administration of acetylcysteine is effective in case of paracetamol poisoning and its early use in the complex of treatment almost always prevents the development of acute liver failure.

Publisher

The Scientific and Practical Society of Emergency Medicine Physicians

Subject

Emergency Medicine

Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3