Prevention of Early Ventilator-Associated Pneumonia after Cardiac Arrest
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Titre | Prevention of Early Ventilator-Associated Pneumonia after Cardiac Arrest |
Type de publication | Journal Article |
Year of Publication | 2019 |
Auteurs | Francois B., Cariou A., Clere-Jehl R., Dequin P.-F, Renon-Carron F., Daix T., Guitton C., Deye N., Legriel S., Plantefeve G., Quenot J.-P, Desachy A., Kamel T., Bedon-Carte S., Diehl J.-L, Chudeau N., Karam E., Durand-Zaleski I., Giraudeau B., Vignon P., Le Gouge A., ANTHARTIC CRICS-TRIGGERSEPNetwork |
Journal | NEW ENGLAND JOURNAL OF MEDICINE |
Volume | 381 |
Pagination | 1831-1842 |
Date Published | NOV 7 |
Type of Article | Article |
ISSN | 0028-4793 |
Résumé | Patients treated with targeted temperature management (32 to 34 degrees C) after cardiac arrest are at increased risk for early ventilator-associated pneumonia. In this multicenter trial, intravenous amoxicillin-clavulanate for 48 hours after cardiac arrest resulted in a lower incidence of early ventilator-associated pneumonia than placebo but did not affect ventilator-free days or mortality at day 28. Background Patients who are treated with targeted temperature management after out-of-hospital cardiac arrest with shockable rhythm are at increased risk for ventilator-associated pneumonia. The benefit of preventive short-term antibiotic therapy has not been shown. Methods We conducted a multicenter, double-blind, randomized, placebo-controlled trial involving adult patients (>18 years of age) in intensive care units (ICUs) who were being mechanically ventilated after out-of-hospital cardiac arrest related to initial shockable rhythm and treated with targeted temperature management at 32 to 34 degrees C. Patients with ongoing antibiotic therapy, chronic colonization with multidrug-resistant bacteria, or moribund status were excluded. Either intravenous amoxicillin-clavulanate (at doses of 1 g and 200 mg, respectively) or placebo was administered three times a day for 2 days, starting less than 6 hours after the cardiac arrest. The primary outcome was early ventilator-associated pneumonia (during the first 7 days of hospitalization). An independent adjudication committee determined diagnoses of ventilator-associated pneumonia. Results A total of 198 patients underwent randomization, and 194 were included in the analysis. After adjudication, 60 cases of ventilator-associated pneumonia were confirmed, including 51 of early ventilator-associated pneumonia. The incidence of early ventilator-associated pneumonia was lower with antibiotic prophylaxis than with placebo (19 patients [19%] vs. 32 [34%]; hazard ratio, 0.53; 95% confidence interval, 0.31 to 0.92; P=0.03). No significant differences between the antibiotic group and the control group were observed with respect to the incidence of late ventilator-associated pneumonia (4% and 5%, respectively), the number of ventilator-free days (21 days and 19 days), ICU length of stay (5 days and 8 days if patients were discharged and 7 days and 7 days if patients had died), and mortality at day 28 (41% and 37%). At day 7, no increase in resistant bacteria was identified. Serious adverse events did not differ significantly between the two groups. Conclusions A 2-day course of antibiotic therapy with amoxicillin-clavulanate in patients receiving a 32-to-34 degrees C targeted temperature management strategy after out-of-hospital cardiac arrest with initial shockable rhythm resulted in a lower incidence of early ventilator-associated pneumonia than placebo. No significant between-group differences were observed for other key clinical variables, such as ventilator-free days and mortality at day 28. (Funded by the French Ministry of Health; ANTHARTIC ClinicalTrials.gov number, NCT02186951.) |
DOI | 10.1056/NEJMoa1812379 |