COVID-19 中临床和微生物学参数的预后价值:COMEPA 研究

Nicola Veronese, M. Noale, Anna La Carrubba, Luca Carruba, Stefano Ciriminna, Francesco Pollicino, Dario Saguto, Simona De Grazia, Federica Cacioppo, G. M. Giammanco, Claudio Costantino, Francesco Vitale, Marco Affronti, Maria Chiara Morgante, Giusi Randazzo, Ligia J Dominguez, Stefania Maggi, Mario Barbagallo, the COMEPA study authors
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摘要

目的。聚类分析可能显示出不同的表型和症状特征,这可能是由于 COVID-19 的病理生理学不同,需要采用不同的临床方法。然而,结合临床和微生物学信息的聚类研究仍然有限。我们的研究旨在探讨集群的预后作用,包括临床和微生物学参数对肺部受累严重程度、院内死亡率和长COVID发生率的影响。研究方法有关 COVID-19、死亡率、肺部受累严重程度的信息来自病历;长 COVID 症状通过电话确认。考虑到入院时出现的 COVID-19 典型症状和 SarsCov2 变体,采用 k-means 聚类方法将数据划分为若干组。结果我们的分析在 414 名患者(平均年龄:65 岁;男性:59.9%)中发现了四个不同的群组。群组 1:入院时呼吸道 COVID 症状的发病率较高;群组 2:非呼吸道 COVID 症状的发病率较高,阿尔法变异体的发病率较高;群组 3:年龄较大且多为男性,报告的病情较重,野生型变异体的发病率较高;群组 4:入院时报告全身和胃肠道 COVID 症状较多的患者。从预后的角度来看,第 3 组患者更常见于死亡和入住疗养院,而出现长期 COVID 症状的比例明显较低。结论是结合临床和微生物学信息,COVID-19住院患者的群组不仅特征不同,而且预后价值也不同,在长期COVID方面也是如此。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic value of clinical and microbiological parameters in COVID-19: the COMEPA study
Purpose. Clusters’ analysis may indicate distinct phenotypes and symptom profiles potentially due to differing pathophysiology and needing different clinical approaches in COVID-19. However, the research about clusters combining clinical and microbiological information is still limited. The purpose of our study was to examine the prognostic role of clusters, including clinical and microbiological parameters in terms of severity of lung involvement, in-hospital mortality, and the occurrence of long COVID. Methods. Information regarding COVID-19, mortality, severity of lung involvement derived from medical records; long COVID symptomatology was ascertained using phone calls. A k-means clustering method was considered to partition data into clusters considering typical symptoms of COVID-19 present at hospital admission and SarsCov2 variants. Results. Our analysis identified among 414 patients (mean age: 65 years; males: 59.9%) four different clusters. Cluster 1: higher prevalence of respiratory COVID symptoms at hospital admission; Cluster 2: higher frequency of non-respiratory COVID symptoms and a higher prevalence of the Alpha variant; Cluster 3: older subjects and more frequently men, reporting more severe medical conditions and with a higher prevalence of Wild type variant; Cluster 4: patients that more often reported general and gastrointestinal COVID symptoms at the admission. From a prognostic point of view, patients in cluster 3 more frequently died and were admitted in a nursing home, with significantly lower presence of long COVID symptomatology. Conclusions. Clusters combining clinical and microbiological information in individuals hospitalized with COVID-19 that had different not only different profiles, but also different prognostic values, also in terms of long COVID.
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