School of Medicine, College of Health Sciences, Mekelle University, Mekelle, Ethiopia.
School of Public Health, College of Health Sciences, Mekelle University, Mekelle, Ethiopia.
PLoS One. 2020 Nov 10;15(11):e0241346. doi: 10.1371/journal.pone.0241346. eCollection 2020.
Short-course chemotherapy comprising isoniazid, rifampicin, ethambutol, and pyrazinamide has proved to be highly effective in the treatment of tuberculosis (TB). However, the most common adverse effect of this regimen leading to interruption of therapy is hepatotoxicity. There is a paucity of evidence in Tigray region on anti-tuberculosis drug-induced hepatitis. Therefore, this study aims to determine the magnitude, outcomes, and associated factors of drug-induced hepatitis in Ayder specialized comprehensive hospital tuberculosis clinic.
An institution-based cross-sectional study was done on 188 cases of patients who took anti-tuberculosis drugs from August 4, 2015 to June 30, 2018 in tuberculosis clinic, Ayder Comprehensive Specialized Hospital, Northern Ethiopia. Data on socio-demography, clinical characteristics and magnitude of the incidence and outcome of anti-tuberculosis drugs-induced hepatitis were collected using structured checklist from patients' records using census method. Then, we entered and analyzed the data using statistical packages for social sciences (SPSS) statistical software version 21. Descriptive statistics were done in tables, counts, proportions, median and range. Bivariate and multivariable regression analyses were done to identify factors that are associated with drug-induced hepatitis. Confidence interval was taken at 95% and p-value of less than 0.05 was used to denote significance.
We approached a total of 226 patients' records, and we collected data from188 records (83.2%response rate). Anti-tuberculosis drug-induced hepatitis was found in 26 (13.8%) of the patients, of which 3 (11.54%) have died. Using multivariable logistic regression analyses, preexisting liver disease (AOR: 42.01, 95% CI: 4.22-417.49), taking other hepatotoxic drugs (AOR: 23.66, 95% CI: 1.77-314.79), and having lower serum albumin (AOR: 10.55, 95% CI: 2.57-43.32) were found to be significantly associated with the development of anti-tuberculosis drug-induced hepatitis.
The incidence of anti-tuberculosis drug-induced hepatitis was high. Patients with low baseline serum albumin, taking other hepatotoxic drugs and having preexisting liver disease should be followed with serial liver enzymes after initiation of anti-tuberculosis medications. These patients should be followed with frequent measurement of liver enzymes to assess for the development of drug-induced hepatitis.
包含异烟肼、利福平、乙胺丁醇和吡嗪酰胺的短程化疗已被证明在结核病(TB)治疗中非常有效。然而,该方案导致治疗中断的最常见不良反应是肝毒性。在提格雷地区,关于抗结核药物引起的肝炎的证据很少。因此,本研究旨在确定 Ayder 综合专科医院结核科抗结核药物引起肝炎的发生率、结局和相关因素。
这是一项在 2015 年 8 月 4 日至 2018 年 6 月 30 日期间在 Ayder 综合专科医院结核科接受抗结核药物治疗的 188 例患者中进行的基于机构的横断面研究。使用从患者记录中使用普查方法收集的结构化清单,收集社会人口统计学、临床特征以及抗结核药物引起肝炎的发生率和结局的数据。然后,我们使用统计软件包(SPSS)统计软件版本 21 输入和分析数据。使用表格、计数、比例、中位数和范围进行描述性统计。进行了单变量和多变量回归分析,以确定与药物性肝炎相关的因素。置信区间为 95%,p 值<0.05 表示有统计学意义。
我们总共接触了 226 份患者记录,并从 188 份记录中收集了数据(83.2%的回应率)。发现 26 名(13.8%)患者出现抗结核药物性肝炎,其中 3 名(11.54%)死亡。使用多变量逻辑回归分析,发现存在先前存在的肝脏疾病(AOR:42.01,95%CI:4.22-417.49)、服用其他肝毒性药物(AOR:23.66,95%CI:1.77-314.79)和血清白蛋白水平较低(AOR:10.55,95%CI:2.57-43.32)与抗结核药物引起的肝炎的发展显著相关。
抗结核药物引起肝炎的发生率很高。基线血清白蛋白水平较低、服用其他肝毒性药物和患有先前存在的肝脏疾病的患者应在开始抗结核治疗后定期检测肝酶。这些患者应经常测量肝酶以评估药物性肝炎的发生。