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Volume 35, Issue 4, Pages 375-381 (April 2010)


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Patterns of antimicrobial therapy in severe nosocomial infections: empiric choices, proportion of appropriate therapy, and adaptation rates—a multicentre, observational survey in critically ill patients

Dirk Vogelaersa, David De Belsb, Frédéric Forêtc, Sophie Crand, Eric Gilberte, Karen Schoonheydtf, Stijn BlotaCorresponding Author Informationemail address, for the ANTHICUS Study Investigators1

Received 17 September 2009; accepted 23 November 2009. published online 01 February 2010.

Abstract 

This prospective, observational multicentre (n=24) study investigated relationships between antimicrobial choices and rates of empiric appropriate or adequate therapy, and subsequent adaptation of therapy in 171 ICU patients with severe nosocomial infections. Appropriate antibiotic therapy was defined as in vitro susceptibility of the causative pathogen and clinical response to the agent administered. In non-microbiologically documented infections, therapy was considered adequate in the case of favourable clinical response <5 days. Patients had pneumonia (n=127; 66 ventilator-associated), intra-abdominal infection (n=23), and bloodstream infection (n=21). Predominant pathogens were Pseudomonas aeruginosa (n=29) Escherichia coli (n=26), Staphylococcus aureus (n=22), and Enterobacter aerogenes (n=21). In 49.6% of infections multidrug-resistant (MDR) bacteria were involved, mostly extended-spectrum β-lactamase (EBSL)-producing Enterobacteriaceae and MDR non-fermenting Gram-negative bacteria. Prior antibiotic exposure and hospitalisation in a general ward prior to ICU admission were risk factors for MDR. Empiric therapy was appropriate/adequate in 63.7% of cases. Empiric schemes were classified according to coverage of (i) ESBL-producing Enterobacteriaceae and non-fermenting Gram-negative bacteria (“meropenem-based”), (ii) non-fermenting Gram-negative bacteria (schemes with an antipseudomonal agent), and (iii) first-line agents not covering ESBL-Enterobacteriaceae nor non-fermenting Gram-negative bacteria. Meropenem-based schemes allowed for significantly higher rates of appropriate/adequate therapy (p<0.001). This benefit remained when only patients without risk factors for MDR were considered (p=0.021). In 106 patients (61%) empiric therapy was modified: in 60 cases following initial inappropriate/inadequate therapy, in 46 patients in order to refine empiric therapy. In this study reflecting real-life practice, first-line use of meropenem provided significantly higher rates of the appropriate/adequate therapy, irrespective of presence of risk factors for MDR.

a General Internal Medicine & Infectious Diseases, Ghent University Hospital, De Pintelaan 185, 9000 Ghent, Belgium

b Intensive Care Department, Brugmann University Hospital, Brussels, Belgium

c Department of Internal Medicine – Intensive Care Unit, CHR St. Joseph-Warquignies, Boussu, Belgium

d Intensive Care Department, CHIREC, Brussels, Belgium

e Intensive Care Department, CHR du Tournaisis, Tournai, Belgium

f Intensive Care Department, Ziekenhuisnetwerk Antwerpen, Antwerp, Belgium

Corresponding Author InformationCorresponding author. Tel.: +32 9 332 62 16.

1 The ANTHICUS Study Investigators are: O. Abid (RHMS, Ath, Belgium), S. Cran (CHIREC, Brussels, Belgium), D. De Bels (CHU Brugmann, Brussels, Belgium), F. De Leener (CHR St. joseph-Warquignies, Boussu, Belgium), L. Finianos (Clinique St. Joseph, Liège, Belgium), F. Forêt (CHR St. Joseph-Warquignies, Mons, Belgium), M. Genard (CIU Ambroise Paré, Mons, Belgium), E. Gilbert (CHR du Tournaisis, Tournai, Belgium), E. Khodadadi (IRIS Sud-Bracops, Brussels, Belgium), S. Machayekhi (CH Hornu Frameries, Hornu), D. Mircev (IRIS Sud-Etterbeek-Ixelles, Brussels, Belgium), D. Neuberg (CH de L’Ardenne, Libramont, Belgium), J.-Y. Piette (CH Bois de l’Abbaye, Seraign, Belgium), P. Serpe (CH ND Bruyères, Chenee, Belgium), F. Beernaert (H. Hart Ziekenhuis, Eeklo, Belgium), K. De Decker (Antwerp University Hospital, Antwerp, Belgium), K. De Ridder (AZ Maria Middelares, Sint-Niklaas, Belgium), C. Declercq (St. Josef Ziekenhuis, Izegem, Belgium), I. Demeyer (OLV Aalst, Aalst, Belgium), B. Nonneman (ASZ, Aalst, Belgium), K. Schoonheydt (ZNA, Antwerp, Belgium, W. Swinnen (AZ St. Blasius, Dendermonde, Belgium), and L. Wosteyn (ASZ, Roeselaere, Belgium).

PII: S0924-8579(09)00549-4

doi:10.1016/j.ijantimicag.2009.11.015


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