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Pulmonary microbiome patterns correlate with the course of disease in patients with sepsis-induced ARDS following major abdominal surgery

F. C.F. Schmitt*, A. Lipinski, S. Hofer, F. Uhle, C. Nusshag, T. Hackert, A. H. Dalpke, M. A. Weigand, T. Brenner, S. Boutin

*Korrespondierende/r Autor/-in für diese Arbeit

Abstract

Background: Patients with sepsis-induced acute respiratory distress syndrome (ARDS) have a high mortality rate. Early, targeted antibiotic therapy is crucial for patient survival. The clinical use of a next-generation sequencing (NGS)-based approach for pathogen identification may lead to improved diagnostic performance. Therefore, the objectives of this study were to examine changes in the pulmonary microbiome and resulting influences on patient outcome in sepsis-induced ARDS, and to compare NGS- and culture-based diagnostic methods for pathogen identification. Methods: In total, 30 patients in two groups were enrolled in the study: 15 patients with sepsis-induced ARDS following major abdominal surgery and 15 patients undergoing oesophageal resection (serving as controls). In the ARDS group, blood samples were collected at ARDS onset (day 0), and 5 and 10 days later. Bronchoalveolar lavage (BAL) was performed at the same timepoints to collect epithelial lining fluid for culture- and NGS-based analyses, and to evaluate longitudinal changes in the pulmonary microbiome. In the control group, only one BAL and one blood sample were collected. Results: Patients with ARDS showed significantly lower α-diversity (P=0.007) and increased dominance (P=0.012) in their pulmonary microbiome compared with the controls. The α-diversity index correlated with the length of stay in the intensive care unit (P=0.015) and the need for mechanical ventilation (P=0.009). In 42.9% of patients with ARDS, culture-based results were negative while NGS findings indicated bacterial colonization. Conclusion: Sepsis-induced ARDS is associated with significant dysbiosis of the patient's pulmonary microbiome, which is closely correlated with the clinical course of disease.

OriginalspracheEnglisch
ZeitschriftJournal of Hospital Infection
Jahrgang105
Ausgabenummer3
Seiten (von - bis)438-446
Seitenumfang9
ISSN0195-6701
DOIs
PublikationsstatusVeröffentlicht - 07.2020

Fördermittel

This study was funded by the Department of Anaesthesiology, the Department of General and Transplant Surgery and the Department of Infectious Diseases, Medical Microbiology and Hygiene at Heidelberg University Hospital, Heidelberg, Germany. Further support was provided by the German Ministry for Education and Research (82DZL00401, 82DZL004A1). This study was funded by the Department of Anaesthesiology, the Department of General and Transplant Surgery and the Department of Infectious Diseases, Medical Microbiology and Hygiene at Heidelberg University Hospital , Heidelberg, Germany. Further support was provided by the German Ministry for Education and Research (82DZL00401, 82DZL004A1).

TrägerTrägernummer
Bundesministerium für Bildung und Forschung82DZL004A1, 82DZL00401

    UN SDGs

    Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

    1. SDG 3 – Gesundheit und Wohlergehen
      SDG 3 – Gesundheit und Wohlergehen

    Strategische Forschungsbereiche und Zentren

    • Forschungsschwerpunkt: Infektion und Entzündung - Zentrum für Infektions- und Entzündungsforschung Lübeck (ZIEL)

    DFG-Fachsystematik

    • 2.21-03 Medizinische Mikrobiologie und Mykologie, Hygiene, Molekulare Infektionsbiologie
    • 2.21-05 Immunologie

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