Jansen van Vuuren Jocelyn, Crocker-Buque Tim, Berry Catherine, Viatushka Dzmitry, Usmanova Ruzilya, Nyang'wa Bern-Thomas, Parpieva Nargiza, Liverko Irina, Solodovnikova Varvara, Sinha Animesh
Médecins sans Frontières, United Kingdom & Netherlands.
London School of Hygiene & Tropical Medicine, London, United Kingdom.
PLOS Glob Public Health. 2024 Sep 24;4(9):e0003057. doi: 10.1371/journal.pgph.0003057. eCollection 2024.
Tuberculosis (TB) and chronic hepatitis C virus infection (HCV) remain significant global health challenges, especially in low- and middle-income countries. In Eastern Europe, a considerable percentage of multi-drug resistant (MDR) and rifampicin resistant (RR) TB populations show high HCV prevalence. Current WHO guidelines do not routinely advise HCV testing during MDR-TB treatment, despite HCV being a risk factor for drug-induced liver complications in TB patients. This study investigates the co-treatment of MDR/RR-TB and HCV, using data from the TB-PRACTECAL trial. Data were collected as part of the TB-PRACTECAL clinical trial. All participants were screened for HCV at baseline. Participants who were HCV antibody positive and those who were treated for hepatitis C with Direct Acting Antivirals (DAAs) were extracted and compared to overall cohort characteristics. The characteristics of participants concomitantly treated with direct-acting antivirals are described including hepatitis treatment outcomes and adverse events. Among 552 participants from Belarus, Uzbekistan, and South Africa, 24 (4.3%) were HCV antibody positive. Unfavourable TB treatment outcomes were noted in 106/523 (22%) of the HCV-negative, 8/18 (44%) of the HCV-seropositive, and 2/7 (29%) of HCV-confirmed participants treated with DAAs. Of the six participants who received concurrent HCV and MDR/RR TB treatment, three were cured of HCV and three had no post-treatment HCV RNA test, five completed TB treatment and one discontinued treatment due to a severe adverse reaction. Concurrent treatment of MDR-TB and HCV, including in HIV patients, showed promising outcomes with no significant adverse events. The findings support the potential benefits of integrating HCV care into MDR-TB management.
结核病(TB)和慢性丙型肝炎病毒感染(HCV)仍然是重大的全球健康挑战,尤其是在低收入和中等收入国家。在东欧,相当比例的耐多药(MDR)和利福平耐药(RR)结核病患者中HCV感染率很高。尽管HCV是结核病患者药物性肝并发症的一个危险因素,但世界卫生组织目前的指南并不常规建议在耐多药结核病治疗期间进行HCV检测。本研究利用结核病实践(TB-PRACTECAL)试验的数据,对耐多药/利福平耐药结核病和HCV的联合治疗进行了调查。数据是作为结核病实践临床试验的一部分收集的。所有参与者在基线时都接受了HCV筛查。提取HCV抗体呈阳性的参与者以及接受直接作用抗病毒药物(DAA)治疗丙型肝炎的参与者,并与整个队列的特征进行比较。描述了同时接受直接作用抗病毒药物治疗的参与者的特征,包括肝炎治疗结果和不良事件。在来自白俄罗斯、乌兹别克斯坦和南非的552名参与者中,24名(4.3%)HCV抗体呈阳性。在HCV阴性的523名参与者中有106名(22%)、HCV血清学阳性的18名参与者中有8名(44%)以及接受DAA治疗的HCV确诊参与者中有2名(29%)出现了不良的结核病治疗结果。在同时接受HCV和耐多药/利福平耐药结核病治疗的6名参与者中,3名HCV治愈,3名未进行治疗后HCV RNA检测,5名完成了结核病治疗,1名因严重不良反应而中断治疗。耐多药结核病和HCV的联合治疗,包括在艾滋病毒患者中,显示出有前景的结果,且无重大不良事件。这些发现支持了将HCV护理纳入耐多药结核病管理的潜在益处。