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.

IF 5.7 1区 医学 Q1 CRITICAL CARE MEDICINE
Jean-David Pommier, Benoît Tressieres, Pascal Blanchet, Frederic Desmoulins, Pascale Piednoir, Nejla Aissa, Frederic Martino, Marc Valette, Alexandre Demoule, Sebastien Breurec, Laurent Camous
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引用次数: 0

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.

加勒比地区患有坏死性软组织感染的危重患者:2014-2023年回顾性队列的无监督分析,确定与死亡率相关的因素。
背景:关于热带地区坏死性软组织感染(NSTIs)的流行病学数据很少。在这里,我们的目的是描述热带地区重症监护病房(ICU)收治的NSTIs危重患者的临床和生物学特征以及结果。此外,我们分析了这些发现,以确定不同的临床表型,并探讨其与患者预后的关系。方法:本回顾性观察研究纳入2014年1月至2023年12月在瓜德罗普大学医院ICU收治的所有NSTIs患者。通过无监督聚类(混合数据的因子分析和主成分的分层聚类)确定具有相似临床概况的患者亚组。单因素和多因素分析确定了与90天死亡率相关的因素。结果:研究期间共有91例NSTI患者入住ICU。简化急性生理评分(SAPS) II的中位数为45分[IQR 40-66],入院至首次手术清创的中位数时间为8小时[IQR 6-10小时]。而在ICU, 65%的患者进行机械通气,75%的患者发生休克,34%的患者接受肾脏替代治疗。90天死亡率为32%。无监督聚类显示出轻度NSTI (n = 23, 25%)、重度NSTI (n = 49, 54%)和暴发性NSTI (n = 19, 21%)这三种聚类与不同的ICU病程和结局相关。皮下肺气肿和败血症相关脑病是影响聚类识别的关键成分。多因素分析显示,死亡率与SAPS II、皮下肺气肿、入院至首次手术之间bbb8小时以及免疫功能低下有关。结论:对热带地区NSTIs危重患者的无监督分析显示,三种不同的患者群表现出独特的表型特征和临床结果。入院后,NSTIs患者应仔细筛查败血症相关脑病、皮下肺气肿和血小板减少症。目前的探索性结果必须在更大的多中心队列中得到证实。
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来源期刊
Annals of Intensive Care
Annals of Intensive Care CRITICAL CARE MEDICINE-
CiteScore
14.20
自引率
3.70%
发文量
107
审稿时长
13 weeks
期刊介绍: Annals of Intensive Care is an online peer-reviewed journal that publishes high-quality review articles and original research papers in the field of intensive care medicine. It targets critical care providers including attending physicians, fellows, residents, nurses, and physiotherapists, who aim to enhance their knowledge and provide optimal care for their patients. The journal's articles are included in various prestigious databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, OCLC, PubMed, PubMed Central, Science Citation Index Expanded, SCOPUS, and Summon by Serial Solutions.
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