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  4. Comparative effectiveness of vancomycin and metronidazole on event-free survival after initial infection in patients with Clostridioides difficile—a German multicentre cohort study
 
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2024
Journal Article
Title

Comparative effectiveness of vancomycin and metronidazole on event-free survival after initial infection in patients with Clostridioides difficile—a German multicentre cohort study

Abstract
Objectives: The objective of this study is to examine the comparative effectiveness of vancomycin and metronidazole in a confirmatory analysis of event-free survival (EFS) after initial infection in patients with Clostridioides difficile from a German multicentre cohort study. Methods: The IBIS multicentre cohort enrolled patients with an index episode of C. difficile infection between August 2017 and September 2020. The primary endpoint was EFS, defined as response to treatment with metronidazole or vancomycin within 10 days of initiation, absence of recurrence and death from any cause up to 90 days post-treatment. A Cox proportional hazards model with inverse probability of treatment weighting was used to investigate the comparative effectiveness of this outcome. Additionally, subgroup analyses were performed based on severe and non-severe infections. Results: Of the 489 patients included, 118 (24%) received initial treatment with metronidazole and 371 (76%) with vancomycin. Of these, 78/118 (66.1%) and 247/371 (66.6%), respectively, responded to treatment within 10 days, neither developed a recurrence nor died within 90 days and thus achieved the outcome of EFS. In the subgroup of non-severe infections, 74/293 patients (25.3%) received metronidazole, and 219/293 (74.7%) received vancomycin. Of these, 33/74 (44.6%) metronidazole patients and 150/219 (68.5%) vancomycin patients survived event free. The Cox proportional hazards model revealed differences in EFS for the overall population and both subgroups (reference metronidazole: all severity levels: hazard ratio [HR] 0.46, [95% CI, 0.33–0.65]; non-severe: HR 0.39; [95% CI, 0.24–0.60]; severe: HR 0.52; [95% CI, 0.28–0.95]). Discussion: Our analysis confirms current changes in guidelines, as it supports the superiority of vancomycin compared with metronidazole across all severity levels.
Author(s)
Conrad, Jana
Universitätsmedizin Mainz
Giesbrecht, Katharina
Universitätsklinikum Frankfurt
Aguilar, Rebeca Cruz
Uniklinik Köln
Gräfe, Stefanie K.
Uniklinik Köln
Ullah, Arhamhabib
Uniklinik Köln
Hunfeld, Klaus Peter
Northwest Medical Centre
Lübbert, Christoph
Universität Leipzig
Pützfeld, Stefan
Krankenhaus Porz am Rhein
Reuken, Philipp Alexander
Universitätsklinikum Jena und Medizinische Fakultät
Schmitz-Rode, Marieke
Evangelisches Krankenhaus Kalk gGmbH
Schalk, Enrico
Medizinische Fakultät und Uniklinikum Magdeburg
Schmidt-Wilcke, Tobias
District Hospital Mainkofen
Schmiedel, Stefan
Universitätsklinikum Hamburg-Eppendorf
Solbach, Philipp Christoph
Universitätsklinikum Schleswig-Holstein Campus Lübeck
Vehreschild, Maria J.Gt T.
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Journal
Clinical Microbiology and Infection  
Open Access
DOI
10.1016/j.cmi.2024.08.003
Additional link
Full text
Language
English
Fraunhofer-Institut für Translationale Medizin und Pharmakologie ITMP  
Keyword(s)
  • Clostridioides difficile infection

  • Germany

  • Guidelines

  • Metronidazole

  • Multicentre

  • Vancomycin

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