Dipartimento di Sicurezza e Bioetica-Sezione di Malattie Infettive, Università Cattolica del Sacro Cuore, Rome, Italy.
Department of Public Health and Infectious Diseases, Sapienza University of Rome, Rome, Italy.
J Antimicrob Chemother. 2024 Feb 1;79(2):453-461. doi: 10.1093/jac/dkad404.
To assess the impact of piperacillin/tazobactam MICs on in-hospital 30 day mortality in patients with third-generation cephalosporin-resistant Escherichia coli bloodstream infection treated with piperacillin/tazobactam, compared with those treated with carbapenems.
A multicentre retrospective cohort study was conducted in three large academic hospitals in Italy between 2018 and 2022. The study population comprised patients with monomicrobial third-generation cephalosporin-resistant E. coli bloodstream infection, who received either piperacillin/tazobactam or carbapenem therapy within 48 h of blood culture collection. The primary outcome was in-hospital 30 day all-cause mortality. A propensity score was used to estimate the likelihood of receiving empirical piperacillin/tazobactam treatment. Cox regression models were performed to ascertain risk factors independently associated with in-hospital 30 day mortality.
Of the 412 consecutive patients included in the study, 51% received empirical therapy with piperacillin/tazobactam, while 49% received carbapenem therapy. In the propensity-adjusted multiple Cox model, the Pitt bacteraemia score [HR 1.38 (95% CI, 0.85-2.16)] and piperacillin/tazobactam MICs of 8 mg/L [HR 2.35 (95% CI, 1.35-3.95)] and ≥16 mg/L [HR 3.69 (95% CI, 1.86-6.91)] were significantly associated with increased in-hospital 30 day mortality, while the empirical use of piperacillin/tazobactam was not found to predict in-hospital 30 day mortality [HR 1.38 (95% CI, 0.85-2.16)].
Piperacillin/tazobactam use might not be associated with increased mortality in treating third-generation cephalosporin-resistant E. coli bloodstream infections when the MIC is <8 mg/L.
评估哌拉西林/他唑巴坦 MIC 值对接受哌拉西林/他唑巴坦治疗与碳青霉烯类药物治疗的第三代头孢菌素耐药大肠埃希菌血流感染患者住院 30 天病死率的影响。
本研究为意大利三家大型学术医院于 2018 年至 2022 年开展的一项多中心回顾性队列研究。研究人群为接受哌拉西林/他唑巴坦或碳青霉烯类药物治疗的单一致病菌第三代头孢菌素耐药大肠埃希菌血流感染患者,且在采集血培养后 48 小时内接受治疗。主要结局为住院 30 天全因死亡率。采用倾向评分法估计接受经验性哌拉西林/他唑巴坦治疗的可能性。采用 Cox 回归模型确定与住院 30 天死亡率独立相关的危险因素。
本研究共纳入 412 例连续患者,其中 51%接受经验性哌拉西林/他唑巴坦治疗,49%接受碳青霉烯类药物治疗。在倾向评分调整后的多 Cox 模型中,Pitt 菌血症评分[HR 1.38(95%CI,0.85-2.16)]和哌拉西林/他唑巴坦 MIC 值为 8mg/L[HR 2.35(95%CI,1.35-3.95)]和≥16mg/L[HR 3.69(95%CI,1.86-6.91)]与住院 30 天病死率增加显著相关,而经验性使用哌拉西林/他唑巴坦与住院 30 天病死率无关[HR 1.38(95%CI,0.85-2.16)]。
当哌拉西林/他唑巴坦 MIC 值<8mg/L 时,治疗第三代头孢菌素耐药大肠埃希菌血流感染时,哌拉西林/他唑巴坦的使用与死亡率增加无关。