Infectious Diseases Department, Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Passeig Vall d'Hebron 119-129, 08035, Barcelona, Spain.
Spanish Network for Research in Infectious Diseases (REIPI), Madrid, Spain.
Infection. 2018 Aug;46(4):461-468. doi: 10.1007/s15010-018-1133-5. Epub 2018 Mar 28.
The aim of this study was to evaluate the effectiveness of ceftolozane/tazobactam (C/T) for treating extensively drug-resistant Pseudomonas aeruginosa (XDR-PA) infections, and to analyze whether high C/T dosing (2 g ceftolozane and 1 g tazobactam every 8 h) and infection source control have an impact on outcome.
Retrospective study of all consecutive patients treated with C/T for XDR-PA infection at a tertiary referral hospital (November 2015-July 2017). Main clinical and microbiological variables were analyzed.
Thirty-eight patients were included. Median age was 59.5 years and Charlson Comorbidity Index was 3.5. Fourteen (36.8%) patients had respiratory tract infection, six (15.8%) soft tissue, and six (15.8%) urinary tract infection. Twenty-three (60.5%) received high-dose C/T and in 24 (63.2%) C/T was combined with other antibiotics. At completion of treatment, 33 (86.8%) patients showed clinical response. At 90 days of follow-up, 26 (68.4%) achieved clinical cure, and 12 (31.6%) had clinical failure because of persistent infection in one patient, death attributable to the XDR-PA infection in four, and clinical recurrence in seven. All-cause mortality was 5 (13.2%). Lower C/T MIC and adequate infection source control were the only variables significantly associated with clinical cure.
C/T should be considered for treating XDR-PA infections, with infection source control being an important factor to avoid failure and resistance.
本研究旨在评估头孢他啶/他唑巴坦(C/T)治疗广泛耐药铜绿假单胞菌(XDR-PA)感染的疗效,并分析高剂量 C/T 给药(2 g 头孢他啶和 1 g 他唑巴坦,每 8 小时 1 次)和感染源控制是否对结果有影响。
对一家三级转诊医院(2015 年 11 月至 2017 年 7 月)接受 C/T 治疗 XDR-PA 感染的所有连续患者进行回顾性研究。分析主要的临床和微生物学变量。
共纳入 38 例患者。中位年龄为 59.5 岁,Charlson 合并症指数为 3.5。14 例(36.8%)患者患有呼吸道感染,6 例(15.8%)患有软组织感染,6 例(15.8%)患有尿路感染。23 例(60.5%)接受高剂量 C/T 治疗,24 例(63.2%)C/T 与其他抗生素联合使用。治疗完成时,33 例(86.8%)患者显示临床反应。90 天随访时,26 例(68.4%)达到临床治愈,12 例(31.6%)因 1 例持续感染、4 例归因于 XDR-PA 感染的死亡和 7 例临床复发而临床失败。总死亡率为 5 例(13.2%)。较低的 C/T MIC 和适当的感染源控制是与临床治愈显著相关的唯一变量。
C/T 可用于治疗 XDR-PA 感染,感染源控制是避免失败和耐药的重要因素。