Impact of adequate empirical combination therapy on mortality in septic shock due to Pseudomonas aeruginosa bloodstream infections: a multicentre retrospective cohort study

感染性休克 医学 回顾性队列研究 养生 内科学 比例危险模型 铜绿假单胞菌 菌血症 联合疗法 抗生素 队列 队列研究 休克(循环) 重症监护医学 败血症 微生物学 细菌 生物 遗传学
作者
Antonio Vena,Michela Schenone,Silvia Corcione,Maddalena Giannella,Renato Pascale,Daniele Roberto Giacobbe,Marco Muccio,Simone Mornese Pinna,Bianca Pari,Francesca Giovannenze,Nicholas Geremia,Małgorzata Mikulska,Eleonora Taddei,Flavio Sangiorgi,Davide Fiore Bavaro,Vincenzo Scaglione,Veronica Vassia,Marco Merli,Michele Bartoletti,Pierluigi Viale
出处
期刊:Journal of Antimicrobial Chemotherapy [Oxford University Press]
被引量:7
标识
DOI:10.1093/jac/dkae296
摘要

Abstract Objectives To determine the association of adequate empirical combination therapy (AECT) with 30-day all-cause mortality in patients with septic shock due to Pseudomonas aeruginosa bloodstream infections (BSI). Methods This multicentre, retrospective cohort study analysed data from 14 public hospitals in Italy, including all consecutive adult patients admitted during 2021–2022 with septic shock due to P. aeruginosa BSI. We compared the outcomes of patients receiving AECT to those on adequate empirical monotherapy (AEMT) using Cox regression analyses. Results Of the 98 patients who received adequate empirical antibiotic treatment for septic shock due to P. aeruginosa BSI, 24 underwent AECT and 74 were given AEMT. AECT was associated with a lower 30-day all-cause mortality (25%, six out of 24) compared to AEMT (56.8%, 42 out of 74; P = 0.007). Multivariate Cox regression analysis indicated AECT as the only factor significantly associated with improved survival (aHR 0.30; 95% CI 0.12–0.71; P = 0.006). By contrast, the use of monotherapy or combination therapy in the definitive regimen did not influence mortality (aHR 0.73; 95% CI 0.25–2.14; P = 0.568). Conclusions AECT may be associated with reduced mortality compared to monotherapy in septic shock patients due to P. aeruginosa BSI. However, the administration of definitive adequate monotherapy or combination therapy yields similar outcomes, suggesting that once susceptibility is documented, switching to a single active in vitro drug is safe and feasible. Further studies are recommended to validate these findings.
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