Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
Department of Pharmacology and Therapeutics, Faculty of Medicine, Universitas Indonesia, Jakarta, Indonesia.
PLoS One. 2021 Mar 4;16(3):e0248017. doi: 10.1371/journal.pone.0248017. eCollection 2021.
Adverse events (AEs) during drug-resistant tuberculosis (DR-TB) treatment, especially with human immunodeficiency virus (HIV) co-infection, remains a major threat to poor DR-TB treatment adherence and outcomes. This meta-analysis aims to investigate the effect of HIV infection on the development of AEs during DR-TB treatment.
Eligible studies evaluating the association between HIV seropositivity and risks of AE occurrence in DR-TB patients were included in this systematic review. Interventional and observational studies were assessed for risk of bias using the Risk of Bias in Nonrandomized Studies of Intervention and Newcastle-Ottawa Scale tool, respectively. Random-effects meta-analysis was performed to estimate the pooled risk ratio (RR) along with their 95% confidence intervals (CIs).
A total of 37 studies involving 8657 patients were included in this systematic review. We discovered that HIV infection independently increased the risk of developing AEs in DR-TB patients by 12% (RR 1.12 [95% CI: 1.02-1.22]; I2 = 0%, p = 0.75). In particular, the risks were more accentuated in the development of hearing loss (RR 1.44 [95% CI: 1.18-1.75]; I2 = 60%), nephrotoxicity (RR 2.45 [95% CI: 1.20-4.98], I2 = 0%), and depression (RR 3.53 [95% CI: 1.38-9.03]; I2 = 0%). Although our findings indicated that the augmented risk was primarily driven by antiretroviral drug usage rather than HIV-related immunosuppression, further studies investigating their independent effects are required to confirm our findings.
HIV co-infection independently increased the risk of developing AEs during DR-TB treatment. Increased pharmacovigilance through routine assessments of audiological, renal, and mental functions are strongly encouraged to enable prompt diagnosis and treatment in patients experiencing AEs during concomitant DR-TB and HIV treatment.
耐药结核病(DR-TB)治疗期间的不良事件(AEs),尤其是合并人类免疫缺陷病毒(HIV)感染,仍然是导致 DR-TB 治疗依从性和结局较差的主要威胁。本荟萃分析旨在研究 HIV 感染对 DR-TB 治疗期间 AEs 发生的影响。
本系统评价纳入了评估 HIV 血清阳性与 DR-TB 患者发生 AE 风险之间关联的研究。干预性和观察性研究分别使用非随机干预研究的偏倚风险和纽卡斯尔-渥太华量表工具进行风险评估。采用随机效应荟萃分析估计汇总风险比(RR)及其 95%置信区间(CI)。
本系统评价共纳入 37 项研究,涉及 8657 名患者。我们发现,HIV 感染使 DR-TB 患者发生 AEs 的风险独立增加了 12%(RR 1.12 [95% CI:1.02-1.22];I2 = 0%,p = 0.75)。特别是在听力损失(RR 1.44 [95% CI:1.18-1.75];I2 = 60%)、肾毒性(RR 2.45 [95% CI:1.20-4.98],I2 = 0%)和抑郁(RR 3.53 [95% CI:1.38-9.03];I2 = 0%)的发展中风险更为明显。虽然我们的研究结果表明,这种增加的风险主要是由抗逆转录病毒药物的使用引起的,而不是由 HIV 相关免疫抑制引起的,但需要进一步研究来确定它们的独立影响。
HIV 合并感染使 DR-TB 治疗期间发生 AEs 的风险独立增加。强烈鼓励通过常规评估听觉、肾脏和精神功能来加强药物警戒,以便在同时接受 DR-TB 和 HIV 治疗的患者出现 AEs 时能够及时诊断和治疗。