Prognostic factors of severe community-acquired staphylococcal pneumonia in France
- PMID: 33833037
- PMCID: PMC8859977
- DOI: 10.1183/13993003.04445-2020
Prognostic factors of severe community-acquired staphylococcal pneumonia in France
Abstract
Purpose: Staphylococcus aureus causes severe forms of community-acquired pneumonia (CAP), namely staphylococcal pleuropneumonia in young children and staphylococcal necrotising pneumonia in older patients. Methicillin resistance and the Panton-Valentine leukocidin (PVL) toxin, as well as less specific factors, have been associated with poor outcome in severe CAP, but their roles are unclear.
Methods: A prospective multicentre cohort study of severe staphylococcal CAP was conducted in 77 paediatric and adult intensive care units in France between January 2011 and December 2016. After age-clustering, risk factors for mortality, including pre-existing conditions, clinical presentation, laboratory features, strain genetic lineage, PVL, other virulence factors and methicillin resistance were assessed using univariate and multivariable Cox and LASSO (least absolute shrinkage and selection operator) regressions.
Results: Out of 163 included patients, aged 1 month to 87 years, 85 (52.1%) had PVL-positive CAP; there were 20 (12.3%) patients aged <3 years (hereafter "toddlers"), among whom 19 (95%) had PVL-positive CAP. The features of PVL-positive CAP in toddlers matched with the historical description of staphylococcal pleuropneumonia, with a lower mortality (three (15%) out of 19) compared to PVL-positive CAP in older patients (31 (47%) out of 66). Mortality in older patients was predicted by PVL-positivity (hazard ratio (HR) 1.81, 95% CI 1.03-3.17) and methicillin resistance (HR 2.37, 95% CI 1.29-4.34) independently from S. aureus lineages and the presence of other determinants of virulence.
Conclusion: PVL was associated with staphylococcal pleuropneumonia in toddlers and was a risk factor for mortality in older patients with severe CAP, independently of methicillin resistance, S. aureus genetic background and other virulence factors.
Copyright ©The authors 2021.
Conflict of interest statement
Conflict of interest: Y. Gillet has nothing to disclose. Conflict of interest: A. Tristan has nothing to disclose. Conflict of interest: J-P. Rasigade reports personal fees from MSD and Pfizer, grants from bioMérieux, outside the submitted work. Conflict of interest: M. Saadatian-Elahi has nothing to disclose. Conflict of interest: C. Bouchiat has nothing to disclose. Conflict of interest: M. Bès has nothing to disclose. Conflict of interest: O. Dumitrescu has nothing to disclose. Conflict of interest: M. Leloire has nothing to disclose. Conflict of interest: C. Dupieux has nothing to disclose. Conflict of interest: F. Laurent has nothing to disclose. Conflict of interest: G. Lina has nothing to disclose. Conflict of interest: J. Etienne has nothing to disclose. Conflict of interest: P. Vanhems reports personal fees from Astellas, Biosciences and Pfizer, grants from Anios and MSD, outside the submitted work. Conflict of interest: L. Argaud has nothing to disclose. Conflict of interest: F. Vandenesch has nothing to disclose.
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