Colistin and Rifampicin Compared With Colistin Alone for the Treatment of Serious Infections Due to Extensively Drug-Resistant Acinetobacter baumannii: A Multicenter, Randomized Clinical Trial

Autor: Maria De Cristoforo, Matteo Bassetti, Raffaele Zarrilli, Annunziata Mattei, Emanuele Durante-Mangoni, Giuseppe Signoriello, Claudio Viscoli, Nicola Galdieri, Antonio Corcione, Roberto Andini, Nicola Petrosillo, Paolo Malacarne, Paola Elvira Mocavero, Riccardo Utili, Patrizia Murino, Ciro Gallo
Přispěvatelé: DURANTE MANGONI, Emanuele, Signoriello, Giuseppe, Andini, R, Mattei, A, De Cristoforo, M, Murino, P, Bassetti, M, Malacarne, P, Petrosillo, N, Galdieri, N, Mocavero, P, Corcione, A, Viscoli, C, Zarrilli, R, Gallo, Ciro, Utili, Riccardo, Durante Mangoni, E, Signoriello, G, De Cristofaro, Mg, Zarrilli, Raffaele, Gallo, C, Utili, R.
Rok vydání: 2013
Předmět:
Acinetobacter baumannii
Male
Drug Resistance
Drug resistance
Antimicrobial therapy
law.invention
Tertiary Care Centers
Randomized controlled trial
law
Drug Resistance
Multiple
Bacterial

80 and over
polycyclic compounds
Aged
80 and over

biology
Bacterial
Ventilator-associated pneumonia
Middle Aged
Intensive care unit
Anti-Bacterial Agents
Intensive Care Units
Treatment Outcome
Infectious Diseases
Combination
Drug Therapy
Combination

Female
Rifampin
Multiple
Mortality
Treatment efficacy
Treatment safety
Acinetobacter Infections
Adult
Aged
Colistin
Critical Illness
Humans
Length of Stay
Survival Analysis
Microbiology (medical)
medicine.drug
medicine.medical_specialty
Drug Therapy
Internal medicine
Intensive care
medicine
business.industry
biochemical phenomena
metabolism
and nutrition

bacterial infections and mycoses
biology.organism_classification
medicine.disease
Surgery
mortality
ventilator-associated pneumonia
antimicrobial therapy
treatment efficacy
treatment safety

bacteria
business
Rifampicin
Zdroj: Clinical Infectious Diseases. 57:349-358
ISSN: 1537-6591
1058-4838
Popis: Background Extensively drug-resistant (XDR) Acinetobacter baumannii may cause serious infections in critically ill patients. Colistin often remains the only therapeutic option. Addition of rifampicin to colistin may be synergistic in vitro. In this study, we assessed whether the combination of colistin and rifampicin reduced the mortality of XDR A. baumannii infections compared to colistin alone. Methods This multicenter, parallel, randomized, open-label clinical trial enrolled 210 patients with life-threatening infections due to XDR A. baumannii from intensive care units of 5 tertiary care hospitals. Patients were randomly allocated (1:1) to either colistin alone, 2 MU every 8 hours intravenously, or colistin (as above), plus rifampicin 600 mg every 12 hours intravenously. The primary end point was overall 30-day mortality. Secondary end points were infection-related death, microbiologic eradication, and hospitalization length. Results Death within 30 days from randomization occurred in 90 (43%) subjects, without difference between treatment arms (P = .95). This was confirmed by multivariable analysis (odds ratio, 0.88 [95% confidence interval, .46-1.69], P = .71). A significant increase of microbiologic eradication rate was observed in the colistin plus rifampicin arm (P = .034). No difference was observed for infection-related death and length of hospitalization. Conclusions In serious XDR A. baumannii infections, 30-day mortality is not reduced by addition of rifampicin to colistin. These results indicate that, at present, rifampicin should not be routinely combined with colistin in clinical practice. The increased rate of A. baumannii eradication with combination treatment could still imply a clinical benefit. Clinical trials registration NCT01577862.
Databáze: OpenAIRE