Fecal microbiota transplantation in a toddler after heart transplant was a safe and effective treatment for recurrent Clostridiodes difficile infection: A case report.


Journal

Pediatric transplantation
ISSN: 1399-3046
Titre abrégé: Pediatr Transplant
Pays: Denmark
ID NLM: 9802574

Informations de publication

Date de publication:
02 2020
Historique:
received: 28 05 2019
revised: 19 08 2019
accepted: 01 09 2019
pubmed: 17 10 2019
medline: 26 1 2021
entrez: 17 10 2019
Statut: ppublish

Résumé

Pediatric recipients of SOT have a significantly increased risk of Clostridiodes (formerly Clostridium) difficile infection (CDI), which is associated with adverse outcomes after SOT. Alterations to the intestinal microbiota community structure increase the risk of CDI. FMT is a safe and effective treatment for recurrent CDI in immunocompetent children and adults. While there are increasing data that FMT in immunosuppressed patients is safe and effective without increased risk of infection, data regarding safety and efficacy of FMT in children after SOT are limited. To our knowledge, we report the youngest immunocompromised patient to undergo FMT and the third overall case of FMT in a child after HTx. Our patient presented with five episodes of rCDI in 6 months, and 16S rRNA genetic analysis revealed significant loss of overall microbiota community structure and diversity prior to FMT compared with a donor and a healthy, age-matched control. After FMT, marked and prolonged (at least 16 months) shifts in the recipient microbiota community structure and diversity were evident, approaching that of donor and healthy, age-matched control. FMT was well tolerated, restored microbial diversity without any graft or transplant complications, and prevented further rCDI episodes after more than 4 years of follow-up.

Identifiants

pubmed: 31617299
doi: 10.1111/petr.13598
pmc: PMC6982574
mid: NIHMS1051678
doi:

Types de publication

Case Reports

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13598

Subventions

Organisme : NIAID NIH HHS
ID : U01 AI124290
Pays : United States
Organisme : NIH HHS
ID : U01-AI24290
Pays : United States

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 Wiley Periodicals, Inc.

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Auteurs

Joseph A Spinner (JA)

Section of Pediatric Cardiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.

Claire E Bocchini (CE)

Section of Pediatric Infectious Disease, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.

Ruth A Luna (RA)

Department of Pathology and Immunology, Texas Children's Microbiome Center, Baylor College of Medicine, Houston, TX, USA.

Santosh Thapa (S)

Department of Pathology and Immunology, Texas Children's Microbiome Center, Baylor College of Medicine, Houston, TX, USA.

Miriam A Balderas (MA)

Department of Pathology and Immunology, Texas Children's Microbiome Center, Baylor College of Medicine, Houston, TX, USA.

Susan W Denfield (SW)

Section of Pediatric Cardiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.

William J Dreyer (WJ)

Section of Pediatric Cardiology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.

Dorottya Nagy-Szakal (D)

Section of Pediatric Gastroenterology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
USDA/ARS Children's Nutrition Research Center, Houston, TX, USA.

Faith D Ihekweazu (FD)

Section of Pediatric Gastroenterology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.

James Versalovic (J)

Department of Pathology and Immunology, Texas Children's Microbiome Center, Baylor College of Medicine, Houston, TX, USA.

Tor Savidge (T)

Department of Pathology and Immunology, Texas Children's Microbiome Center, Baylor College of Medicine, Houston, TX, USA.

Richard Kellermayer (R)

Section of Pediatric Gastroenterology, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
USDA/ARS Children's Nutrition Research Center, Houston, TX, USA.

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Classifications MeSH