School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Iranian Research Center for HIV/AIDS, Iranian Institute for Reduction of High-Risk Behaviors, Tehran University of Medical Sciences, Tehran, Iran.
Arch Iran Med. 2024 Mar 1;27(3):122-126. doi: 10.34172/aim.2024.19.
Tuberculosis (TB) is one of the oldest and most well-known diseases that has been associated with humans for many years and remains a global health challenge today. Timely diagnosis and proper treatment are crucial for controlling and preventing the spread of the disease. While anti-TB drugs offer many benefits, inadequate monitoring can lead to a range of side effects, including hepatotoxicity, which is a major concern and can cause treatment discontinuation. The aim of this study was to determine the approach to the hepatotoxicity of anti-TB drugs and to investigate potential relationships between demographic factors, underlying medical conditions, and successful retreatment outcomes for hepatotoxicity induced by anti-TB drugs.
For this study, we reviewed the medical records of patients who experienced hepatotoxicity due to anti-TB treatment and were admitted to the infectious ward of Imam Khomeini Hospital between April 2015 and February 2019. The data were collected using a questionnaire.
The findings indicated that the female gender, weight loss at the beginning of hospitalization, , , heart disease, and high levels of aspartate aminotransferase (AST) and alanine transaminase (ALT) at the beginning of hepatotoxicity are risk factors for failure to the retreatment of hepatotoxicity. There were two different approaches to the anti-TB retreatment regimen. The first approach involved gradually starting the drugs in full dose, while the second approach encompassed starting the drugs in the minimum dose and then increasing to the maximum dose. The results demonstrated no significant difference between the two approaches to managing hepatotoxicity induced by anti-TB drugs.
Drug-induced hepatotoxicity is a common occurrence that often results in treatment discontinuation. Understanding the prevalence of this complication and identifying appropriate methods of rechallenge treatment is crucial to reducing complications and mortality rates.
结核病(TB)是一种古老而著名的疾病,与人类已有多年的历史,至今仍是全球健康挑战。及时诊断和适当的治疗对于控制和预防疾病的传播至关重要。虽然抗结核药物有很多好处,但监测不足会导致一系列副作用,包括肝毒性,这是一个主要关注点,可能导致治疗中断。本研究旨在确定抗结核药物肝毒性的处理方法,并探讨潜在的人口统计学因素、基础医学状况和抗结核药物引起的肝毒性成功再治疗结果之间的关系。
在这项研究中,我们回顾了 2015 年 4 月至 2019 年 2 月期间因抗结核治疗而导致肝毒性并入住伊玛目霍梅尼医院传染病病房的患者的病历。数据使用问卷收集。
研究结果表明,女性、住院时体重减轻、,, 心脏病和肝毒性开始时天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)水平较高是肝毒性再治疗失败的危险因素。抗结核再治疗方案有两种不同的方法。第一种方法是逐渐开始全剂量用药,第二种方法是开始用最小剂量用药,然后增加到最大剂量。结果表明,两种方法在处理抗结核药物引起的肝毒性方面没有显著差异。
药物性肝毒性是一种常见的并发症,常常导致治疗中断。了解这种并发症的发生率并确定适当的再挑战治疗方法对于降低并发症和死亡率至关重要。