Implementation of guidelines for management of possible multidrug-resistant pneumonia in intensive care: an observational, multicentre cohort study
- PMID: 21256086
- DOI: 10.1016/S1473-3099(10)70314-5
Implementation of guidelines for management of possible multidrug-resistant pneumonia in intensive care: an observational, multicentre cohort study
Abstract
Background: The American Thoracic Society and Infectious Diseases Society of America provide guidelines for management of hospital-acquired, ventilator-associated, and health-care-associated pneumonias, consisting of empirical antibiotic regimens for patients at risk for multidrug-resistant pathogens. We aimed to improve compliance with these guidelines and assess outcomes.
Methods: We implemented a performance-improvement initiative in four academic medical centres in the USA with protocol-based education and prospective observation of outcomes. Patients were assessed for severity of illness and followed up until death, hospital discharge, or day 28. We included patients in intensive-care units who were at risk for multidrug-resistant pneumonia and were treated empirically.
Findings: 303 patients at risk for multidrug-resistant pneumonia were treated empirically, and prescribed treatment was guideline compliant in 129 patients and non-compliant in 174 patients. 44 (34%) patients died before 28 days in the compliance group and 35 (20%) died in the non-compliance group. Five patients in the compliance group and seven in the non-compliance group were lost to follow-up after day 14. Kaplan-Meier estimated survival to 28 days was 65% in the compliance group and 79% in the non-compliance group (p=0·0042). This difference persisted after adjustment for severity of illness. Median length of stay and duration of mechanical ventilation did not differ between groups. Compliance failures included non-use of dual treatment for Gram-negative pathogens in 154 patients and absence of meticillin-resistant Staphylococcus aureus coverage in 24 patients. For patients in whom pathogens were subsequently identified, empirical treatment was active in 79 (81%) of 97 of patients receiving compliant therapy compared with 109 (85%) of 128 of patients receiving non-compliant therapy.
Interpretation: Because adherence with empirical treatment was associated with increased mortality, we recommend a randomised trial be done before further implementation of these guidelines.
Funding: Pfizer, US Medical.
Copyright © 2011 Elsevier Ltd. All rights reserved.
Comment in
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Nosocomial pneumonia: de-escalation is what matters.Lancet Infect Dis. 2011 Mar;11(3):155-7. doi: 10.1016/S1473-3099(11)70003-2. Epub 2011 Jan 20. Lancet Infect Dis. 2011. PMID: 21256087 No abstract available.
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Treatment of hospital-acquired pneumonia.Lancet Infect Dis. 2011 Oct;11(10):728-9; author reply 731-2. doi: 10.1016/S1473-3099(11)70261-4. Lancet Infect Dis. 2011. PMID: 21958574 No abstract available.
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Treatment of hospital-acquired pneumonia.Lancet Infect Dis. 2011 Oct;11(10):728; author reply 731-2. doi: 10.1016/S1473-3099(11)70260-2. Lancet Infect Dis. 2011. PMID: 21958575 No abstract available.
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Treatment of hospital-acquired pneumonia.Lancet Infect Dis. 2011 Oct;11(10):729; author reply 731-2. doi: 10.1016/S1473-3099(11)70262-6. Lancet Infect Dis. 2011. PMID: 21958576 No abstract available.
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Treatment of hospital-acquired pneumonia.Lancet Infect Dis. 2011 Oct;11(10):729-30. doi: 10.1016/S1473-3099(11)70263-8. Lancet Infect Dis. 2011. PMID: 21958577 No abstract available.
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Treatment of hospital-acquired pneumonia.Lancet Infect Dis. 2011 Oct;11(10):730-1; author reply 731-2. doi: 10.1016/S1473-3099(11)70264-X. Lancet Infect Dis. 2011. PMID: 21958578 No abstract available.
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