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Multicenter Study
. 2021 Nov 11;58(5):2004445.
doi: 10.1183/13993003.04445-2020. Print 2021 Nov.

Prognostic factors of severe community-acquired staphylococcal pneumonia in France

Collaborators, Affiliations
Multicenter Study

Prognostic factors of severe community-acquired staphylococcal pneumonia in France

Yves Gillet et al. Eur Respir J. .

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.

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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.

Figures

FIGURE 1
FIGURE 1
Mortality of patients with Staphylococcus aureus community-acquired pneumonia (CAP) according to age and the presence of the Panton–Valentine leukocidin (PVL). a, c) Density estimates of the occurrence of pneumonia in all patients of the considered group and in deceased patients. b, d) Estimates of mortality rate. Shaded areas present bootstrap-based 95% confidence bands of the estimates. Analyses were conducted separately for patients with a, b) PVL-positive CAP and c, d) PVL-negative CAP.
FIGURE 2
FIGURE 2
Survival of 143 patients aged ≥3 years with Staphylococcus aureus pneumonia. Survival after intensive care unit admission according to whether the causative strain was methicillin-resistant (MRSA) or -susceptible (MSSA) and whether it harboured the Panton–Valentine leukocidin (PVL) toxin is shown. +: censored (discharged) patients. Log-rank test, p=0.0007.

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