Gaensbauer James T, Dash Nabaneeta, Verma Sanjay, Hall D J, Adler-Shohet Felice C, Li Guyu, Lee Grace, Dinnes Laura, Wendorf Kristen
Mayo Clinic Center for Tuberculosis, Mayo Clinic, Rochester, MN, USA.
Division of Pediatric Infectious Diseases, Department of Pediatrics and Adolescent Medicine, Mayo Clinic, Rochester, MN, USA.
J Clin Tuberc Other Mycobact Dis. 2024 May 1;36:100449. doi: 10.1016/j.jctube.2024.100449. eCollection 2024 Aug.
Pediatric multidrug-resistant tuberculosis (MDR-TB) remains a significant global problem, and there are numerous barriers preventing children with MDR-TB from being identified, confirmed with microbiologic tests, and treated with a safe, practical, and effective regimen. However, several recent advances in diagnostics and treatment regimens have the promise to improve outcomes for children with MDR-TB. We introduce this review with two cases that exemplify both the challenges in management of MDR-TB in children, but also the potential to achieve a positive outcome. More than 30,000 cases of MDR-TB per year are believed to occur in children but less than 5% are confirmed microbiologically, contributing to poorer outcomes and excess mortality. Rapid molecular-based testing that provides information on rifampin susceptibility is increasingly globally available and recommended for all children suspected of TB disease--but remains limited by challenges obtaining appropriate samples and the paucibacillary nature of most pediatric TB. More complex assays allowing better characterization of drug-resistant isolates are emerging. For children diagnosed with MDR-TB, treatment regimens have traditionally been long and utilize multiple drugs associated with significant side effects, particularly injectable agents. Several new or repurposed drugs including bedaquiline, delamanid, clofazimine and linezolid now allow most treatment regimens to be shorter and all-oral. Yet data to support short, all-oral, novel regimens for young children containing pretomanid remain insufficient at present, and there is a compelling need to conduct pediatric trials of promising therapeutics and MDR-TB treatment regimens.
儿童耐多药结核病(MDR-TB)仍然是一个重大的全球性问题,存在众多障碍阻碍耐多药结核病儿童得到识别、通过微生物检测确诊以及接受安全、实用且有效的治疗方案。然而,诊断和治疗方案方面的一些最新进展有望改善耐多药结核病儿童的治疗结果。我们通过两个案例引入本综述,这两个案例既体现了儿童耐多药结核病管理中的挑战,也展现了取得积极结果的可能性。据信每年有超过30000例儿童耐多药结核病病例,但微生物确诊的病例不到5%,这导致了更差的治疗结果和更高的死亡率。基于快速分子检测可提供利福平敏感性信息,在全球范围内越来越容易获得,并被推荐用于所有疑似结核病的儿童——但仍受限于获取合适样本的挑战以及大多数儿童结核病的少菌性。能够更好地表征耐药菌株的更复杂检测方法正在出现。对于确诊为耐多药结核病的儿童,传统治疗方案疗程长,且使用多种有显著副作用的药物,尤其是注射剂。几种新的或重新利用的药物,包括贝达喹啉、地拉曼啶、氯法齐明和利奈唑胺,现在使大多数治疗方案得以缩短并可全口服。然而,目前支持含普瑞曼尼德的针对幼儿的短程、全口服新方案的数据仍然不足,迫切需要开展有前景的治疗方法和耐多药结核病治疗方案的儿科试验。