TY - JOUR
T1 - Combination versus monotherapy as definitive treatment for Pseudomonas aeruginosa bacteraemia
T2 - A multicentre retrospective observational cohort study
AU - Babich, Tanya
AU - Naucler, Pontus
AU - Valik, John Karlsson
AU - Giske, Christian G.
AU - Benito, Natividad
AU - Cardona, Ruben
AU - Rivera, Alba
AU - Pulcini, Celine
AU - Abdel Fattah, Manal
AU - Haquin, Justine
AU - MacGowan, Alasdair
AU - Grier, Sally
AU - Gibbs, Julie
AU - Chazan, Bibiana
AU - Yanovskay, Anna
AU - Ami, Ronen Ben
AU - Landes, Michal
AU - Nesher, Lior
AU - Zaidman-Shimshovitz, Adi
AU - McCarthy, Kate
AU - Paterson, David L.
AU - Tacconelli, Evelina
AU - Buhl, Michael
AU - Mauer, Susanna
AU - Rodriguez-Bano, Jesus
AU - Morales, Isabel
AU - Oliver, Antonio
AU - Ruiz De Gopegui, Enrique
AU - Cano, Angela
AU - MacHuca, Isabel
AU - Gozalo-Marguello, Monica
AU - Martinez, Luis Martinez
AU - Gonzalez-Barbera, Eva M.
AU - Alfaro, Iris Gomez
AU - Salavert, Miguel
AU - Beovic, Bojana
AU - Saje, Andreja
AU - Mueller-Premru, Manica
AU - Pagani, Leonardo
AU - Vitrat, Virginie
AU - Kofteridis, Diamantis
AU - Zacharioudaki, Maria
AU - Maraki, Sofia
AU - Weissman, Yulia
AU - Paul, Mical
AU - Dickstein, Yaakov
AU - Leibovici, Leonard
AU - Yahav, Dafna
N1 - Publisher Copyright:
© 2021 The Author(s) 2021. Published by Oxford University Press on behalf of the British Society for Antimicrobial Chemotherapy. All rights reserved. For permissions, please email: [email protected].
PY - 2021/7/15
Y1 - 2021/7/15
N2 - Background: Pseudomonas aeruginosa bacteraemia is a common and serious infection. No consensus exists regarding whether definitive combination therapy is superior to monotherapy. We aimed to evaluate the impact of combination therapy on mortality. Methods: This was a multicentre retrospective study (nine countries, 25 centres), including 1277 patients with P. aeruginosa bacteraemia during 2009-15. We evaluated the association between β-lactam plus aminoglycoside or quinolone combination therapy versus β-lactam monotherapy and mortality. The primary outcome was 30 day all-cause mortality. Univariate and multivariate Cox regression analyses were conducted, introducing combination as a time-dependent variable. Propensity score was conducted to adjust for confounding for choosing combination therapy over monotherapy. Results: Of 1119 patients included, 843 received definitive monotherapy and 276 received combination therapy (59% aminoglycoside and 41% quinolone). Mortality at 30 days was 16.9% (189/1119) and was similar between combination (45/276; 16.3%) and monotherapy (144/843; 17.1%) groups (P = 0.765). In multivariate Cox regression, combination therapy was not associated with reduced mortality (HR 0.98, 95% CI 0.64-1.53). No advantage in terms of clinical failure, microbiological failure or recurrent/persistent bacteraemia was demonstrated using combination therapy. Likewise, adverse events and resistance development were similar for the two regimens. Conclusions: In this retrospective cohort, no mortality advantage was demonstrated using combination therapy over monotherapy for P. aeruginosa bacteraemia. Combination therapy did not improve clinical or microbiological failure rates, nor affect adverse events or resistance development. Our finding of no benefit with combination therapy needs confirmation in well-designed randomized controlled trials.
AB - Background: Pseudomonas aeruginosa bacteraemia is a common and serious infection. No consensus exists regarding whether definitive combination therapy is superior to monotherapy. We aimed to evaluate the impact of combination therapy on mortality. Methods: This was a multicentre retrospective study (nine countries, 25 centres), including 1277 patients with P. aeruginosa bacteraemia during 2009-15. We evaluated the association between β-lactam plus aminoglycoside or quinolone combination therapy versus β-lactam monotherapy and mortality. The primary outcome was 30 day all-cause mortality. Univariate and multivariate Cox regression analyses were conducted, introducing combination as a time-dependent variable. Propensity score was conducted to adjust for confounding for choosing combination therapy over monotherapy. Results: Of 1119 patients included, 843 received definitive monotherapy and 276 received combination therapy (59% aminoglycoside and 41% quinolone). Mortality at 30 days was 16.9% (189/1119) and was similar between combination (45/276; 16.3%) and monotherapy (144/843; 17.1%) groups (P = 0.765). In multivariate Cox regression, combination therapy was not associated with reduced mortality (HR 0.98, 95% CI 0.64-1.53). No advantage in terms of clinical failure, microbiological failure or recurrent/persistent bacteraemia was demonstrated using combination therapy. Likewise, adverse events and resistance development were similar for the two regimens. Conclusions: In this retrospective cohort, no mortality advantage was demonstrated using combination therapy over monotherapy for P. aeruginosa bacteraemia. Combination therapy did not improve clinical or microbiological failure rates, nor affect adverse events or resistance development. Our finding of no benefit with combination therapy needs confirmation in well-designed randomized controlled trials.
UR - http://www.scopus.com/inward/record.url?scp=85112125127&partnerID=8YFLogxK
U2 - 10.1093/jac/dkab134
DO - 10.1093/jac/dkab134
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C2 - 33993273
AN - SCOPUS:85112125127
SN - 0305-7453
VL - 76
SP - 2172
EP - 2181
JO - Journal of Antimicrobial Chemotherapy
JF - Journal of Antimicrobial Chemotherapy
IS - 8
ER -