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,Francesco Giuseppe De Rosa,Matteo Bassetti,Accurso Giuseppe,Bavaro Davide Fiore,Stefania Chiappetta,Faliero Domenico,Fumarola Benedetta,G G Nicholas,Giovannenze Francesca,Maccaro Angelo,M Lingua Andrea,Merli Marco,Pagani Gabriele,Sardanelli Alessia,Scaglione Vincenzo,Tontodonati Monica,Vassia Veronica
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.