Institute of Social and Preventive Medicine (ISPM), University of Bern, Bern, Switzerland; Swiss Tropical and Public Health Institute, Basel, Switzerland; University of Basel, Basel, Switzerland.
Institute of Social and Preventive Medicine (ISPM), University of Bern, Bern, Switzerland.
Lancet Infect Dis. 2019 Mar;19(3):298-307. doi: 10.1016/S1473-3099(18)30673-X. Epub 2019 Feb 8.
Drug resistance is a challenge for the global control of tuberculosis. We examined mortality in patients with tuberculosis from high-burden countries, according to concordance or discordance of results from drug susceptibility testing done locally and in a reference laboratory.
This multicentre cohort study was done in Côte d'Ivoire, Democratic Republic of the Congo, Kenya, Nigeria, South Africa, Peru, and Thailand. We collected Mycobacterium tuberculosis isolates and clinical data from adult patients aged 16 years or older. Patients were stratified by HIV status and tuberculosis drug resistance. Molecular or phenotypic drug susceptibility testing was done locally and at the Swiss National Center for Mycobacteria, Zurich, Switzerland. We examined mortality during treatment according to drug susceptibility test results and treatment adequacy in multivariable logistic regression models adjusting for sex, age, sputum microscopy, and HIV status.
We obtained M tuberculosis isolates from 871 patients diagnosed between 2013 and 2016. After exclusion of 237 patients, 634 patients with tuberculosis were included in this analysis; the median age was 33·2 years (IQR 26·9-42·5), 239 (38%) were women, 272 (43%) were HIV-positive, and 69 (11%) patients died. Based on the reference laboratory drug susceptibility test, 394 (62%) strains were pan-susceptible, 45 (7%) monoresistant, 163 (26%) multidrug-resistant (MDR), and 30 (5%) had pre-extensively or extensively drug resistant (pre-XDR or XDR) tuberculosis. Results of reference and local laboratories were concordant for 513 (81%) of 634 patients and discordant for 121 (19%) of 634. Overall, sensitivity to detect any resistance was 90·8% (95% CI 86·5-94·2) and specificity 84·3% (80·3-87·7). Mortality ranged from 6% (20 of 336) in patients with pan-susceptible tuberculosis treated according to WHO guidelines to 57% (eight of 14) in patients with resistant strains who were under-treated. In logistic regression models, compared with concordant drug susceptibility test results, the adjusted odds ratio of death was 7·33 (95% CI 2·70-19·95) for patients with discordant results potentially leading to under-treatment.
Inaccurate drug susceptibility testing by comparison with a reference standard leads to under-treatment of drug-resistant tuberculosis and increased mortality. Rapid molecular drug susceptibility test of first-line and second-line drugs at diagnosis is required to improve outcomes in patients with MDR tuberculosis and pre-XDR or XDR tuberculosis.
National Institutes of Allergy and Infectious Diseases, Swiss National Science Foundation, Swiss National Center for Mycobacteria.
耐药性是全球结核病控制面临的一项挑战。我们根据当地和参考实验室的药敏试验结果是否一致,来检测来自高负担国家的结核病患者的死亡率。
本多中心队列研究在科特迪瓦、刚果民主共和国、肯尼亚、尼日利亚、南非、秘鲁和泰国进行。我们从年龄在 16 岁及以上的成年结核病患者中收集结核分枝杆菌分离株和临床数据。根据 HIV 状况和结核病药物耐药性对患者进行分层。在当地和瑞士苏黎世国家分枝杆菌中心进行分子或表型药物敏感性测试。我们通过多变量逻辑回归模型,根据药敏试验结果和治疗充足性,在校正性别、年龄、痰显微镜检查和 HIV 状况后,检测治疗期间的死亡率。
我们从 2013 年至 2016 年期间诊断的 871 名患者中获得了 M 结核分枝杆菌分离株。排除 237 名患者后,本分析纳入了 634 名结核病患者;中位年龄为 33.2 岁(IQR 26.9-42.5),239 名(38%)为女性,272 名(43%)为 HIV 阳性,69 名(11%)患者死亡。根据参考实验室药敏试验,394 株(62%)菌株为全敏感,45 株(7%)为单耐药,163 株(26%)为多药耐药(MDR),30 株(5%)为耐多药/广泛耐药(pre-XDR 或 XDR)结核病。634 名患者中,513 名(81%)患者的参考和本地实验室结果一致,121 名(19%)患者的结果不一致。总体而言,检测任何耐药性的敏感性为 90.8%(95%CI 86.5-94.2),特异性为 84.3%(80.3-87.7)。死亡率从全敏感结核病患者(按世卫组织指南治疗)的 6%(336 例中的 20 例)到耐药菌株患者(治疗不足)的 57%(14 例中的 8 例)不等。在逻辑回归模型中,与药敏试验结果一致相比,结果不一致可能导致治疗不足的患者的死亡调整比值比为 7.33(95%CI 2.70-19.95)。
与参考标准相比,不准确的药敏试验导致耐药结核病治疗不足和死亡率增加。在诊断时需要快速进行一线和二线药物的分子药敏试验,以改善耐多药结核病和耐多药/广泛耐药结核病患者的结局。
美国国立过敏和传染病研究所、瑞士国家科学基金会、瑞士国家分枝杆菌中心。