氯法齐明
脓肿分枝杆菌
医学
非结核分枝杆菌
内科学
文化转换
莫西沙星
龟分枝杆菌
痰培养
利福平
痰
抗生素
相伴的
肺结核
结核分枝杆菌
抗药性
养生
外科
乙胺丁醇
克拉霉素
分枝杆菌
免疫学
微生物学
生物
麻风病
病理
幽门螺杆菌
作者
Herman Pfaeffle,Reem Alameer,Mary H. Marshall,Eric R. Houpt,Dana Albon,Scott K. Heysell
标识
DOI:10.1016/j.pupt.2021.102058
摘要
Nontuberculous mycobacteria (NTM) infections are increasingly detected but difficult to cure given complex drug-resistance patterns. Select U.S. centers have incorporated clofazimine in the treatment of NTM but experience is limited as procurement restrictions hamper widespread use. A prospective cohort study was performed in patients diagnosed with pulmonary or extrapulmonary NTM infection and treated with clofazimine between February 2015 and April 2019 at a tertiary referral hospital. Treatment success was defined by a combined outcome of clinical stabilization, microbiologic cure and radiologic improvement. Secondary outcomes included all-cause mortality and time to sputum culture conversion. Uni/multi-variate regression were used to define associations between pre-determined predictor variables and overall treatment outcome. Of 44 patients enrolled, 39 (89 %) received clofazimine along with a median of 3 concomitant antibiotics. Thirty-one (80 %) of patients had pulmonary NTM infection, with Mycobacterium abscessus group and Mycobacterium avium complex being the most common species groups identified. Of 36 people with evaluable outcomes, 35 (97 %) survived and 22 (58 %) had treatment success, including 12 of 19 (63 %) with Mycobacterium abscessus group. In multivariate analysis, patients with Mycobacterium abscessus group were more likely to experience treatment success (OR 18.22, 95%CI 0.972–341.43, p = 0.052), while macrolide resistance predicted a lack of treatment success (OR 0.053, 95%CI 0.003–0.841, p = 0.037). Clofazimine was well-tolerated. Adding clofazimine to multi-class antibiotic regimens for drug-resistant NTM infection led to treatment success in the majority treated. Randomized controlled studies are needed to determine the individual impact of clofazimine within an otherwise optimized drug regimen.
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