Sotgiu Giovanni, D'Ambrosio Lia, Centis Rosella, Tiberi Simon, Esposito Susanna, Dore Simone, Spanevello Antonio, Migliori Giovanni Battista
Clinical Epidemiology and Medical Statistics Unit, Department of Biomedical Sciences, University of Sassari-Research, Medical Education and Professional Development Unit, AOU Sassari, Sassari 07100, Italy.
World Health Organization Collaborating Centre for Tuberculosis and Lung Diseases, Fondazione S. Maugeri, IRCCS (Istituto di Ricovero e Cura a Carattere Sceintifico), Via Roncaccio 16, Tradate 21049, Italy.
Int J Mol Sci. 2016 Mar 12;17(3):373. doi: 10.3390/ijms17030373.
Carbapenems (ertapenem, imipenem, meropenem) are used to treat multidrug-resistant (MDR-) and extensively drug-resistant tuberculosis (XDR-TB), even if the published evidence is limited, particularly when it is otherwise difficult to identify the recommended four active drugs to be included in the regimen. No systematic review to date has ever evaluated the efficacy, safety, and tolerability of carbapenems.
A search of peer-reviewed, scientific evidence was carried out, aimed at evaluating the efficacy/effectiveness, safety, and tolerability of carbapenem-containing regimens in individuals with pulmonary/extra-pulmonary disease which was bacteriologically confirmed as M/XDR-TB. We used PubMed to identify relevant full-text, English manuscripts up to the 20 December 2015, excluding editorials and reviews.
Seven out of 160 studies satisfied the inclusion criteria: two on ertapenem, one on imipenem, and four on meropenem, all published between 2005 and 2016. Of seven studies, six were retrospective, four were performed in a single center, two enrolled children, two had a control group, and six reported a proportion of XDR-TB cases higher than 20%. Treatment success was higher than 57% in five studies with culture conversion rates between 60% and 94.8%.
The safety and tolerability is very good, with the proportion of adverse events attributable to carbapenems below 15%.
碳青霉烯类药物(厄他培南、亚胺培南、美罗培南)用于治疗耐多药(MDR-)和广泛耐药结核病(XDR-TB),尽管已发表的证据有限,尤其是在难以确定方案中推荐的四种有效药物时。迄今为止,尚无系统评价评估碳青霉烯类药物的疗效、安全性和耐受性。
检索经同行评审的科学证据,旨在评估含碳青霉烯类方案对细菌学确诊为M/XDR-TB的肺/肺外疾病患者的疗效/有效性、安全性和耐受性。我们使用PubMed检索截至2015年12月20日的相关英文全文手稿,排除社论和综述。
160项研究中有7项符合纳入标准:2项关于厄他培南,1项关于亚胺培南,4项关于美罗培南,均发表于2005年至2016年之间。在这7项研究中,6项为回顾性研究,4项在单一中心进行,2项纳入儿童,2项有对照组,6项报告XDR-TB病例比例高于20%。5项研究的治疗成功率高于57%,培养转化率在60%至94.8%之间。
安全性和耐受性非常好,碳青霉烯类药物所致不良事件的比例低于15%。