Abstract

BackgroundRecent reports have suggested the efficacy of a double carbapenem (DC) combination, including ertapenem, for the treatment of carbapenem-resistant Klebsiella pneumoniae (CR-Kp) infections. We aimed to evaluate the clinical impact of such a regimen in critically ill patients.MethodsThis case–control (1:2), observational, two-center study involved critically ill adults with a microbiologically documented CR-Kp invasive infection treated with the DC regimen matched with those receiving a standard treatment (ST) (i.e., colistin, tigecycline, or gentamicin).ResultsThe primary end point was 28-day mortality. Secondary outcomes were clinical cure, microbiological eradication, duration of mechanical ventilation and of vasopressors, and 90-day mortality. Forty-eight patients treated with DC were matched with 96 controls. Occurrence of septic shock at infection and high procalcitonin levels were significantly more frequent in patients receiving DC treatment (p < 0.01). The 28-day mortality was significantly higher in patients receiving ST compared with the DC group (47.9% vs 29.2%, p = 0.04). Similarly, clinical cure and microbiological eradication were significantly higher when DC was used in patients infected with CR-Kp strains resistant to colistin (13/20 (65%) vs 10/32 (31.3%), p = 0.03 and 11/19 (57.9%) vs 7/27 (25.9%), p = 0.04, respectively). In the logistic regression and multivariate Cox-regression models, the DC regimen was associated with a reduction in 28-day mortality (OR 0.33, 95% CI 0.13–0.87 and OR 0.43, 95% CI 0.23–0.79, respectively).ConclusionsImproved 28-day mortality was associated with the DC regimen compared with ST for severe CR-Kp infections. A randomized trial is needed to confirm these observational results.Trial registrationClinicalTrials.gov NCT03094494. Registered 28 March 2017.

Highlights

  • Recent reports have suggested the efficacy of a double carbapenem (DC) combination, including ertapenem, for the treatment of carbapenem-resistant Klebsiella pneumoniae (CR-Kp) infections

  • Preventive strategies aimed at reducing the spread of CR-Kp in the intensive care unit (ICU) are essential in reducing the infection rate related to these bacteria, which are a serious challenge for ICU physicians due to the exiguous available therapeutic options [7,8,9,10]

  • Among 72 potentially eligible case patients receiving a DC regimen including ertapenem, alone or in combination with another “in vitro active antibiotic”, 24 patients were excluded and 48 patients were selected for the analysis (Additional file 1: Figure S1)

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Summary

Introduction

Recent reports have suggested the efficacy of a double carbapenem (DC) combination, including ertapenem, for the treatment of carbapenem-resistant Klebsiella pneumoniae (CR-Kp) infections. CR-Kp isolates are spreading worldwide in an ongoing dynamic process, constituting a new global health threat. Infections related to this pathogen are associated with increased mortality, longer hospital and intensive care unit (ICU) stay, and consequent increased cost of care [4, 5]. Among new antimicrobials, the use of novel beta-lactam/beta-lactamase inhibitor combinations (e.g., ceftazidime–avibactam) is still poor and is associated with the rapid emergence of resistance during treatment [15, 16]

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