综合工具包整合生活方式和临床问卷,通过直肠拭子分析肠道微生物群:在重症监护肝硬化患者中的应用。

Julie Marin, Mohamed Ghalayini, Younes Kaoudji, Samira Dziri, Cecile Zylberfajn, Lorraine Blaise, Astrid Hoogvorst, Stephane Charpentier, Virginie Chaillou, Sylvie Beauchamp, Séverine Donneger, Nathalie Barget, Mathilde Touvier, Pierre Nahon, Roland Amathieu, Mathilde Lescat
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引用次数: 0

摘要

介绍。肠道菌群的研究现在是许多临床研究的一个重要方面。例如,微生物群多样性调查可以通过识别严重程度标记和识别可能的病原体来源,帮助我们更好地管理肝硬化患者。假设/差距语句。对重症监护病房脆弱病人(如肝硬化患者)进行肠道菌群的临床研究具有重大挑战。在这项研究中,我们开发了一个综合工具包,通过直肠拭子结合直接的生活方式和临床问卷来调查脆弱患者的肠道微生物群。方法。我们将这种前瞻性方法应用于49例表型良好的肝硬化患者,作为其代偿状态的函数(门诊招募的代偿患者与重症监护病房的代偿失代偿患者)。结果。我们的结果与文献一致,表明肝功能损害与微生物群多样性降低有关。此外,我们监测失代偿肝硬化患者的需氧微生物群,观察在这些病原体引起严重感染之前,产生扩展谱β -内酰胺酶(ESBL)的大肠杆菌侵入肠道的需氧微生物群。我们提出这种实用的方法用于更大规模的队列研究,旨在通过使用微生物群分析作为相关病理严重程度的预测工具和鉴定导致严重感染的药物来加强对免疫功能低下患者的监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive toolkit integrating lifestyle and clinical questionnaires with gut microbiota profiling via rectal swabs: application in intensive care cirrhotic patients.

Introduction. The study of gut microbiota is now an essential dimension in many clinical studies. For instance, microbiota diversity investigation can help us to better manage cirrhotic patients by the identification of markers of severity and the identification of possible sources of pathogens.Hypothesis/Gap Statement. Conducting clinical research on gut microbiota for fragile patients in intensive care units, such as cirrhotic patients, poses significant challenges.Aim. In this study, we developed a comprehensive toolkit for investigating gut microbiota in fragile patients using rectal swabbing combined with straightforward lifestyle and clinical questionnaires.Methodology . We applied this prospective approach to 49 well-phenotyped cirrhotic patients as a function of their compensation status (compensated patients with outpatients' recruitment vs decompensated patients in intensive care units).Results . Our results, consistent with the literature, showed that liver function impairment is associated with lower microbiota diversity. Additionally, we monitored aerobic microbiota in decompensated cirrhotic patients, observing the invasion of extended spectrum beta-lactamase (ESBL)-producing Escherichia coli in the gut's aerobic microbiota prior to severe infection caused by these pathogens.Conclusion. We propose this pragmatic methodology for larger cohort studies, aiming to enhance the monitoring of immunocompromised patients by using microbiota analysis as a predictive tool for the severity of associated pathologies and the identification of agents responsible for severe infections.

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