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. 2025 Jun 2;15(1):77.
doi: 10.1186/s13613-025-01488-2.

Critically ill patients with necrotizing soft tissue infections in the Caribbean area: unsupervised analysis of a retrospective cohort (2014-2023) with identification of factors associated with mortality

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Critically ill patients with necrotizing soft tissue infections in the Caribbean area: unsupervised analysis of a retrospective cohort (2014-2023) with identification of factors associated with mortality

Jean-David Pommier et al. Ann Intensive Care. .

Abstract

Background: Scarce epidemiological data are available regarding necrotizing soft tissue infections (NSTIs) in tropical areas. Here we aimed to describe the clinical and biological features, and outcomes, of critically ill patients with NSTIs admitted to an intensive care unit (ICU) in a tropical setting. Furthermore, we analyzed these findings to identify distinct clinical phenotypes and explore their associations with patient outcomes.

Methods: This retrospective observational study included all patients with NSTIs admitted to the ICU of the University Hospital of Guadeloupe between January 2014 and December 2023. Subgroups of patients having similar clinical profiles were identified through unsupervised clustering (factor analysis for mixed data, and hierarchical clustering on principal components). Univariate and multivariate analyses identified factors associated with 90-day mortality.

Results: During the study period, 91 NSTI patients were admitted to the ICU. The median Simplified Acute Physiology Score (SAPS) II was 45 [IQR 40-66], and the median time between hospital admission and first surgical debridement was 8 h [IQR 6-10 h]. While in the ICU, 65% of patients were mechanically ventilated, 75% experienced shock, and 34% underwent renal replacement therapy. The 90-day mortality rate was 32%. Unsupervised clustering revealed three clusters-mild NSTI (n = 23, 25%), severe NSTI (n = 49, 54%), and fulminant NSTI (n = 19, 21%)-which were associated with different ICU courses and outcomes. Subcutaneous emphysema and sepsis-associated encephalopathy were key components influencing cluster identification. Multivariate analysis revealed that mortality was associated with SAPS II, subcutaneous emphysema, >8 h between hospital admission and first surgery, and immunocompromised status.

Conclusion: Unsupervised analysis of critically ill patients with NSTIs in tropical settings revealed three distinct patient clusters that exhibited unique phenotypic characteristics and clinical outcomes. Upon hospital admission, patients with NSTIs should be carefully screened for sepsis-associated encephalopathy, subcutaneous emphysema, and thrombopenia. The present exploratory results must be confirmed in larger multicentric cohorts.

Keywords: Fasciitis; Intensive care unit; Multiple-organ failure; Necrotizing soft tissue infection; Septic shock.

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Conflict of interest statement

Declarations. Ethics approval and consent to participate: This retrospective study was performed in accordance with the declaration of Helsinki for research including human data. The study was approved by the local ethics committee, which waived consent for retrospective anonymous data collection, in accordance with French Law, and was registered under the number A26_20/02/2024. This study is reported following the Strengthening the Reporting of Observational Studies in Epidemiology (STROBE) statement. All authors have given consent for publication of this manuscript in Annals of Intensive Care. Competing interests: The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
Bacteria and fungi identified from soft tissues samples or blood cultures from all patients with necrotizing soft tissue infections who had at least one identified microorganism (N = 84/91), and according to cluster: cluster 1 (N = 19/23), cluster 2 (N = 46/49), and cluster 3 (N = 19/19)
Fig. 2
Fig. 2
Cumulative survival rates. Kaplan–Meier survival curves of patients admitted to the intensive care unit with necrotizing soft tissue infections, stratified according to the presence or absence of subcutaneous emphysema (A), time from hospital admission to surgical debridement (within or over 8 h) (B), and immunocompromised status (C)

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