Hospital Universitario Reina Sofía-IMIBIC-University of Córdoba, (Spanish Network for Research in Infectious Diseases (REIPI)), Córdoba, Spain.
Hospitales Universitarios Virgen del Rocío-IBIS, (REIPI), Seville, Spain.
Clin Microbiol Infect. 2018 Jun;24(6):630-634. doi: 10.1016/j.cmi.2017.09.016. Epub 2017 Sep 29.
To assess the association of survival and treatment with colistin and tigecycline in critically ill patients with carbapenem-resistant Acinetobacter baumannii bacteraemia.
An observational cohort study was carried out. Targeted therapy consisted of monotherapy with colistin (9 million UI/day) or combined therapy with colistin and tigecycline (100 g/day). The primary outcome was 30-day crude mortality. The association between combined targeted therapy and mortality was controlled for empirical therapy with colistin, propensity score of combined therapy and other potential confounding variables in a multivariate Cox regression analysis.
A total of 118 cases were analysed. Seventy-six patients (64%) received monotherapy and 42 patients (36%) received combined therapy. The source of bacteraemia was primary in 18% (21/118) of the patients, ventilator-associated pneumonia in 64% (76/118) and other sources in 14% (16/118). The 30-day crude mortality rate was 62% (42/76) for monotherapy and 57% (24/42) for combined therapy. The variables associated with 30-day crude mortality were: Charlson index (hazard ratio (HR) 1.16, 95% CI 1.02-1.32; p 0.028), empirical therapy with colistin (HR 2.25, 95% CI 1.33-3.80; p 0.003) and renal dysfunction before treatment (HR 1.91, 95% CI 1.01-3.61; p 0.045). Combined targeted therapy was not associated with lower adjusted 30-day crude mortality (adjusted HR 1.29, 95% CI 0.64-2.58; p 0.494).
Combined targeted therapy with high-dose colistin and standard dose tigecycline was not associated with lower crude mortality of bacteraemia due to carbapenem-resistant A. baumannii in critically ill patients.
Registered in ClinicalTrials.gov. Identifier: NCT02573064.
评估在重症耐碳青霉烯鲍曼不动杆菌血流感染患者中,联合使用多黏菌素和替加环素治疗与生存的关系。
进行了一项观察性队列研究。目标治疗包括多黏菌素单药治疗(900 万单位/天)或多黏菌素联合替加环素治疗(100mg/天)。主要结局为 30 天的粗死亡率。在多变量 Cox 回归分析中,将联合靶向治疗与死亡率的关系与经验性多黏菌素治疗、联合治疗的倾向评分和其他潜在混杂变量进行了控制。
共分析了 118 例患者。76 例(64%)患者接受单药治疗,42 例(36%)患者接受联合治疗。血培养的来源在 18%(21/118)的患者中为原发性,在 64%(76/118)的患者中为呼吸机相关性肺炎,在 14%(16/118)的患者中为其他来源。单药治疗的 30 天粗死亡率为 62%(76/118),联合治疗的 30 天粗死亡率为 57%(24/42)。与 30 天粗死亡率相关的变量包括:Charlson 指数(危险比(HR)1.16,95%置信区间(CI)1.02-1.32;p=0.028)、经验性多黏菌素治疗(HR 2.25,95%CI 1.33-3.80;p=0.003)和治疗前肾功能障碍(HR 1.91,95%CI 1.01-3.61;p=0.045)。联合靶向治疗与调整后的 30 天粗死亡率无显著相关性(调整后的 HR 1.29,95%CI 0.64-2.58;p=0.494)。
在重症耐碳青霉烯鲍曼不动杆菌血流感染患者中,联合使用高剂量多黏菌素和标准剂量替加环素治疗并未降低粗死亡率。
ClinicalTrials.gov 注册。标识符:NCT02573064。