Single-drug versus combination antimicrobial therapy in critically ill patients with hospital-acquired pneumonia and ventilator-associated pneumonia due to Gram-negative pathogens: a multicenter retrospective cohort study

In this study including 391 critically ill patients with nosocomial pneumonia due to Gram-negative pathogens, combination therapy was not associated with a reduced hazard of death at Day 28 or a greater likelihood of clinical cure at Day 14. No over-risk of AKI was observed in patients receiving com...

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Veröffentlicht in:Critical care (London, England) England), 2024-01, Vol.28 (1), p.10-10, Article 10
Hauptverfasser: Barbier, François, Dupuis, Claire, Buetti, Niccolò, Schwebel, Carole, Azoulay, Élie, Argaud, Laurent, Cohen, Yves, Hong Tuan Ha, Vivien, Gainnier, Marc, Siami, Shidasp, Forel, Jean-Marie, Adrie, Christophe, de Montmollin, Étienne, Reignier, Jean, Ruckly, Stéphane, Zahar, Jean-Ralph, Timsit, Jean-François
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Sprache:eng
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Zusammenfassung:In this study including 391 critically ill patients with nosocomial pneumonia due to Gram-negative pathogens, combination therapy was not associated with a reduced hazard of death at Day 28 or a greater likelihood of clinical cure at Day 14. No over-risk of AKI was observed in patients receiving combination therapy. The benefits and harms of combination antimicrobial therapy remain controversial in critically ill patients with hospital-acquired pneumonia (HAP), ventilated HAP (vHAP) or ventilator-associated pneumonia (VAP) involving Gram-negative bacteria. We included all patients in the prospective multicenter OutcomeRea database with a first HAP, vHAP or VAP due to a single Gram-negative bacterium and treated with initial adequate single-drug or combination therapy. The primary endpoint was Day-28 all-cause mortality. Secondary endpoints were clinical cure rate at Day 14 and a composite outcome of death or treatment-emergent acute kidney injury (AKI) at Day 7. The average effects of combination therapy on the study endpoints were investigated through inverse probability of treatment-weighted regression and multivariable regression models. Subgroups analyses were performed according to the resistance phenotype of the causative pathogens (multidrug-resistant or not), the pivotal (carbapenems or others) and companion (aminoglycosides/polymyxins or others) drug classes, the duration of combination therapy (
ISSN:1364-8535
1466-609X
1364-8535
1366-609X
DOI:10.1186/s13054-023-04792-0