Rosemarie Peri1,2, Rebeca Cruz Aguilar1,2, Kester Tüffers3, Andreas Erhardt4, Alexander Link5, Philipp Ehlermann6, Wolfgang Angeli7, Thorsten Frank8, Martin Storr9, Thomas Glück10, Andreas Sturm11, Ulrich Rosien12, Frank Tacke13, Oliver Bachmann14,15, Philipp Solbach14,15, Andreas Stallmach16, Felix Goeser2,17, Maria Jgt Vehreschild1,2,18. 1. Department I of Internal Medicine, University Hospital Cologne, Cologne, Germany. 2. German Centre for Infection Research (DZIF), Bonn-Cologne, Germany. 3. Department II of Internal Medicine, St. Johannes Hospital, Dortmund, Germany. 4. Department II of Internal Medicine, St. Petrus Hospital, Wuppertal, Germany. 5. Department of Gastroenterology, Hepatology and Infectious Diseases, University Hospital Magdeburg, Magdeburg, Germany. 6. Department of Internal Medicine, SRH Kurpfalzkrankenhaus Heidelberg, Heidelberg, Germany. 7. Department of Gastroenterology, Kempten-Oberallgäu Clinic, Kempten, Germany. 8. Department of Internal Medicine II, St. Katharinen Hospital, Frechen, Germany. 9. Department of Gastroenterology, Ludwig-Maximilians-University, Munich, and Center of Endoscopy, Starnberg, Germany. 10. Department of Internal Medicine, Trostberg Clinic, Trostberg, Germany. 11. Department of Internal Medicine and Gastroenterology, DRK Kliniken Westend, Berlin, Germany. 12. Visceral Medical Center, Israelitic Hospital Hamburg, Hamburg, Germany. 13. Department of Medicine III, University Hospital Aachen, Aachen, Germany. 14. Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany. 15. German Centre for Infection Research (DZIF), Hannover, Germany. 16. Department of Internal Medicine IV (Gastroenterology, Hepatology and Infectiology), University Hospital Jena, Jena, Germany. 17. Department of Internal Medicine I, University Hospital Bonn, Bonn, Germany. 18. Department of Internal Medicine, Infectious Diseases, University Hospital Frankfurt, Frankfurt am Main, Germany These authors contributed equally.
Abstract
Introduction: Fecal microbiota transfer (FMT) is highly effective in the treatment and prevention of recurrent Clostridioides difficile infection (rCDI) with cure rates of about 80% after a single treatment. Nevertheless, the reasons for failure in the remaining 20% remain largely elusive. The aim of the present study was to investigate different potential clinical predictors of response to FMT in Germany. Methods: Information was extracted from the MicroTrans Registry (NCT02681068), a retrospective observational multicenter study, collecting data from patients undergoing FMT for recurrent or refractory CDI in Germany. We performed binary logistic regression with the following covariates: age, gender, ribotype 027, Eastern Co-operative Oncology Group score, immunosuppression, preparation for FMT by use of proton pump inhibitor, antimotility agents and bowel lavage, previous recurrences, severity of CDI, antibiotic induction treatment, fresh or frozen FMT preparation, and route of application. Results: Treatment response was achieved in 191/240 evaluable cases (79.6%) at day 30 (D30) post FMT and 78.1% at day 90 (D90) post FMT. Assessment of clinical predictors for FMT failure by forward and confirmatory backward-stepwise regression analysis yielded higher age as an independent predictor of FMT failure (p = 0.001; OR 1.060; 95%CI 1.025-1.097). Conclusion: FMT in Germany is associated with high cure rates at D30 and D90. No specific pre-treatment, preparation or application strategy had an impact on FMT success. Only higher age was identified as an independent risk factor for treatment failure. Based on these and external findings, future studies should focus on the assessment of microbiota and microbiota-associated metabolites as factors determining FMT success.
Introduction: Fecal microbiota transfer (FMT) is highly effective in the treatment and prevention of recurrent Clostridioides difficile infection (rCDI) with cure rates of about 80% after a single treatment. Nevertheless, the reasons for failure in the remaining 20% remain largely elusive. The aim of the present study was to investigate different potential clinical predictors of response to FMT in Germany. Methods: Information was extracted from the MicroTrans Registry (NCT02681068), a retrospective observational multicenter study, collecting data from patients undergoing FMT for recurrent or refractory CDI in Germany. We performed binary logistic regression with the following covariates: age, gender, ribotype 027, Eastern Co-operative Oncology Group score, immunosuppression, preparation for FMT by use of proton pump inhibitor, antimotility agents and bowel lavage, previous recurrences, severity of CDI, antibiotic induction treatment, fresh or frozen FMT preparation, and route of application. Results: Treatment response was achieved in 191/240 evaluable cases (79.6%) at day 30 (D30) post FMT and 78.1% at day 90 (D90) post FMT. Assessment of clinical predictors for FMT failure by forward and confirmatory backward-stepwise regression analysis yielded higher age as an independent predictor of FMT failure (p = 0.001; OR 1.060; 95%CI 1.025-1.097). Conclusion:FMT in Germany is associated with high cure rates at D30 and D90. No specific pre-treatment, preparation or application strategy had an impact on FMT success. Only higher age was identified as an independent risk factor for treatment failure. Based on these and external findings, future studies should focus on the assessment of microbiota and microbiota-associated metabolites as factors determining FMT success.
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