Study of antitubercular drugs on liver function tests in newly diagnosed tuberculosis

Anitha N, Raju Dasari, Suresh Cherlopalli, Sujana Sriram
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Abstract

Background: Particularly in areas where both tuberculosis and liver illness are prominent, it is necessary to determine the factors that put patients at risk for developing anti-tuberculosis drug-induced hepatotoxicity (anti-TB-DIH). In this study, both the prevalence of anti-TB-DIH and the factors that contribute to its development were studied. As a consequence of this, the purpose of the present study was to explore the abnormal liver function test in patients who were being treated for tuberculosis. Aims and Objectives: (i) To investigate hepatotoxicity in antitubercular patients. (ii) To protect the liver from chemotherapy drug side effects through early detection. (iii) To understand drug-induced hepatotoxicity risk factors. Materials and Methods: This is a prospective study of one hundred patients who were treated at the Department of Pulmonary Medicine and the Department of Pharmacology at the Rajiv Gandhi Institute of Medical Sciences in Kadapa between January 2022 and January 2023. Results: Patients varying in age from 15 to 30 years comprised 21 (21%) of the study, 31–50 years comprised 31% of the study, 51–70 years comprised 38% of the study, and 71–80 years comprised 10% of the study, with 68 (68%) males and 32 (32%) females. When compared to the levels that were present before therapy, the levels of aspartate aminotransferase (AST), alanine aminotransferase (ALT), and alkaline phosphatase (ALP) exhibited a substantial increase after 2 months of treatment. A comparison of the patient’s levels of AST, ALT, ALP, and gammaglutamyl transpeptidase (GGT) before treatment and after treatment for 6 months demonstrated a considerable rise in all of these enzymes’ activities. Conclusion: Because it was established that the majority of patients suffer hepatotoxicity within the first 14 days of beginning antituberculosis therapy (ATT) medication, it is imperative that the liver function of patients be monitored in the initial days in which treatment with ATT is being initiated.
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抗结核药物对新诊断结核患者肝功能检查的影响
背景:特别是在结核病和肝脏疾病都很突出的地区,有必要确定使患者处于发生抗结核药物性肝毒性(anti-TB-DIH)风险的因素。在本研究中,研究了抗结核- dih的患病率及其发展的因素。因此,本研究的目的是探讨正在接受结核病治疗的患者的肝功能检查异常。目的和目的:(1)研究抗结核患者的肝毒性。(ii)通过早期发现保护肝脏免受化疗药物副作用的影响。(iii)了解药物性肝毒性危险因素。材料和方法:这是一项前瞻性研究,纳入了2022年1月至2023年1月期间在卡达帕拉吉夫甘地医学科学研究所肺医学系和药学系接受治疗的100名患者。结果:年龄在15 - 30岁的患者占21例(21%),31-50岁的患者占31%,51-70岁的患者占38%,71-80岁的患者占10%,其中男性68例(68%),女性32例(32%)。与治疗前相比,治疗2个月后,天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)和碱性磷酸酶(ALP)水平显著升高。比较患者治疗前和治疗后6个月的AST、ALT、ALP和γ -氨酰转肽酶(GGT)水平显示,所有这些酶的活性都显著升高。结论:由于已经确定大多数患者在开始抗结核治疗(ATT)的最初14天内出现肝毒性,因此在开始抗结核治疗的最初几天监测患者的肝功能是必要的。
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