Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, State Key Laboratory for Diagnosis and Treatment of Infectious Diseases, Department of Infectious Diseases, The First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China.
Virus Res. 2019 Sep;270:197664. doi: 10.1016/j.virusres.2019.197664. Epub 2019 Jul 14.
China has a high prevalence of tuberculosis and hepatitis B virus infection. The purpose of this study was to determine whether HBV coinfection increases the risk of incidence of drug-induced hepatotoxicity among patients on anti-tuberculosis therapy.
This retrospective study was carried out at the First Affiliated Hospital, School of Medicine, Zhejiang University, from 2013 to 2017. All enrolled patients were confirmed HBsAg-positive for a duration of at least 6 months and coinfected with mycobacterium tuberculosis.
A cohort of 90 patients was analyzed. The incidence of liver damage and liver failure was 51.11% (n = 46) and 22.22% (n = 20), respectively. By multivariate analysis, initial albumin <35 g/l (P = 0.004, odds ratio 6.162, 95% confidence interval 1.767-21.486) was an independent risk factor for liver failure, but prophylactic antiviral treatment (P < 0.001, odds ratio 0.033, 95% confidence interval 0.007-0.154) was an independent protective factor for liver failure. Of the 90 patients, 20 developed liver failure, none of the patients with liver failure received prophylactic antiviral therapy, and 6 of those patients died of liver failure.
Prophylactic antiviral treatment reduces the incidence of liver failure in patients coinfected with Mycobacterium tuberculosis and hepatitis B virus; therefore, it is recommended that prophylactic antiviral treatment be administered while receiving anti-tuberculosis treatment in patients coinfected with Mycobacterium tuberculosis and hepatitis B virus.
中国结核病和乙型肝炎病毒感染的患病率很高。本研究旨在确定乙型肝炎病毒(HBV)合并感染是否会增加抗结核治疗患者药物性肝毒性发病的风险。
这项回顾性研究于 2013 年至 2017 年在浙江大学医学院附属第一医院进行。所有入组患者均为 HBsAg 阳性至少 6 个月并合并结核分枝杆菌感染。
分析了一个 90 例患者的队列。肝损伤和肝功能衰竭的发生率分别为 51.11%(n=46)和 22.22%(n=20)。多变量分析显示,初始白蛋白<35g/L(P=0.004,比值比 6.162,95%置信区间 1.767-21.486)是肝功能衰竭的独立危险因素,但预防性抗病毒治疗(P<0.001,比值比 0.033,95%置信区间 0.007-0.154)是肝功能衰竭的独立保护因素。90 例患者中有 20 例发生肝功能衰竭,无一例肝功能衰竭患者接受预防性抗病毒治疗,其中 6 例患者死于肝功能衰竭。
预防性抗病毒治疗可降低结核分枝杆菌和乙型肝炎病毒合并感染患者肝功能衰竭的发生率;因此,建议在结核分枝杆菌和乙型肝炎病毒合并感染患者接受抗结核治疗时给予预防性抗病毒治疗。