Recurrent

clostridioides difficile emerging infections program fecal microbiota transplantation real-world therapy utilization recurrent clostridioides difficile

Journal

Open forum infectious diseases
ISSN: 2328-8957
Titre abrégé: Open Forum Infect Dis
Pays: United States
ID NLM: 101637045

Informations de publication

Date de publication:
Jul 2024
Historique:
received: 12 03 2024
accepted: 12 06 2024
medline: 8 7 2024
pubmed: 8 7 2024
entrez: 8 7 2024
Statut: epublish

Résumé

Fecal microbiota transplantation (FMT) is recommended for the treatment of recurrent A retrospective community-wide cohort study was conducted using surveillance data from the Georgia Emerging Infections Program, the Georgia Discharge Data System, and locally maintained lists of FMTs completed across multiple institutions to evaluate all episodes of A total of 3038 (22%) of 13 852 patients with CDI had rCDI during this period. In a propensity-matched cohort, patients who received an FMT had lower rates of rCDI (odds ratio, 0.6 [95% confidence interval, .38-.96) and a lower mortality rate (0.26 [.08-.82]). Of patients with rCDI, only 6% had received FMT. Recipients were more likely to be young, white, and female and less likely to have renal disease, diabetes, or liver disease, though these chronic illnesses were associated with higher rates of rCDI. These data suggest FMT has been underused in a population-based assessment and that FMT substantially reduced risk of recurrence and death.

Sections du résumé

Background UNASSIGNED
Fecal microbiota transplantation (FMT) is recommended for the treatment of recurrent
Methods UNASSIGNED
A retrospective community-wide cohort study was conducted using surveillance data from the Georgia Emerging Infections Program, the Georgia Discharge Data System, and locally maintained lists of FMTs completed across multiple institutions to evaluate all episodes of
Results UNASSIGNED
A total of 3038 (22%) of 13 852 patients with CDI had rCDI during this period. In a propensity-matched cohort, patients who received an FMT had lower rates of rCDI (odds ratio, 0.6 [95% confidence interval, .38-.96) and a lower mortality rate (0.26 [.08-.82]). Of patients with rCDI, only 6% had received FMT. Recipients were more likely to be young, white, and female and less likely to have renal disease, diabetes, or liver disease, though these chronic illnesses were associated with higher rates of rCDI.
Conclusions UNASSIGNED
These data suggest FMT has been underused in a population-based assessment and that FMT substantially reduced risk of recurrence and death.

Identifiants

pubmed: 38975247
doi: 10.1093/ofid/ofae309
pii: ofae309
pmc: PMC11227225
doi:

Types de publication

Journal Article

Langues

eng

Pagination

ofae309

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America.

Déclaration de conflit d'intérêts

Potential conflicts of interest. C. S. K has served as a scientific advisor to Seres Therapeutics and a consultant to Ferring/Rebiotix. S. K. F. reports that Emory University has received a service agreement from Pfizer for public health research on Clostridioides difficile, starting in 2019 for 2 years. All other authors report no potential conflicts.

Auteurs

Nirja Mehta (N)

Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, USA.
Georgia Emerging Infections Program, Decatur, Georgia, USA.

Dana Goodenough (D)

Georgia Emerging Infections Program, Decatur, Georgia, USA.
Atlanta Veterans' Affairs Medical Center, Decatur, Georgia, USA.
Emory University School of Medicine, Atlanta, Georgia, USA.

Nitin K Gupta (NK)

Atlanta Gastroenterology Associates, Georgia, USA.
United Digestive, Atlanta, Georgia, USA.
Northside Hospital, Department of Gastroenterology, Atlanta, Georgia, USA.

Stepy Thomas (S)

Georgia Emerging Infections Program, Decatur, Georgia, USA.
Atlanta Veterans' Affairs Medical Center, Decatur, Georgia, USA.
Emory University School of Medicine, Atlanta, Georgia, USA.

Christina Mehta (C)

Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, USA.

Radhika Prakash (R)

Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, USA.

Michael H Woodworth (MH)

Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, USA.

Colleen S Kraft (CS)

Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, USA.
Department of Pathology and Laboratory Medicine, Emory University School of Medicine, Atlanta, Georgia, USA.

Scott K Fridkin (SK)

Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, USA.
Georgia Emerging Infections Program, Decatur, Georgia, USA.

Classifications MeSH