Addressing extreme size mismatch in pediatric intestinal transplantation: Outcomes of intestinal length reduction.


Journal

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

Informations de publication

Date de publication:
08 2023
Historique:
revised: 25 01 2023
received: 09 08 2022
accepted: 22 03 2023
medline: 24 7 2023
pubmed: 19 6 2023
entrez: 19 6 2023
Statut: ppublish

Résumé

Bench liver reduction, with or without intestinal length reduction (LR) (coupled with delayed closure and abdominal wall prostheses), has been a strategy adopted by our program for small children due to the limited availability of size-matched donors. This report describes the short, medium, and long-term outcomes of this graft reduction strategy. A single-center, retrospective analysis of children that underwent intestinal transplantation (April 1993 to December 2020) was performed. Patients were grouped according to whether they received an intestinal graft of full length (FL) or following LR. Overall, 105 intestinal transplants were performed. The LR group (n = 10) was younger (14.5 months vs. 40.0 months, p = .012) and smaller (8.7 kg vs. 13.0 kg, p = .032) compared to the FL group (n = 95). Similar abdominal closure rates were achieved after LR, without any increase in abdominal compartment syndrome (1/10 vs. 7/95, p = .806). The 90-day graft and patient survival were similar (9/10, 90% vs. 83/95, 86%; p = .810). Medium and long-term graft survival at 1 year (8/10, 80% vs. 65/90, 71%; p = .599), and 5 years (5/10, 50% vs. 42/84, 50%; p = 1.00) was similar. LR of intestinal grafts appears to be a safe strategy for infants and small children requiring intestinal transplantation. This technique should be considered in the situation of significant size mismatch of intestine containing grafts.

Sections du résumé

BACKGROUND
Bench liver reduction, with or without intestinal length reduction (LR) (coupled with delayed closure and abdominal wall prostheses), has been a strategy adopted by our program for small children due to the limited availability of size-matched donors. This report describes the short, medium, and long-term outcomes of this graft reduction strategy.
METHODS
A single-center, retrospective analysis of children that underwent intestinal transplantation (April 1993 to December 2020) was performed. Patients were grouped according to whether they received an intestinal graft of full length (FL) or following LR.
RESULTS
Overall, 105 intestinal transplants were performed. The LR group (n = 10) was younger (14.5 months vs. 40.0 months, p = .012) and smaller (8.7 kg vs. 13.0 kg, p = .032) compared to the FL group (n = 95). Similar abdominal closure rates were achieved after LR, without any increase in abdominal compartment syndrome (1/10 vs. 7/95, p = .806). The 90-day graft and patient survival were similar (9/10, 90% vs. 83/95, 86%; p = .810). Medium and long-term graft survival at 1 year (8/10, 80% vs. 65/90, 71%; p = .599), and 5 years (5/10, 50% vs. 42/84, 50%; p = 1.00) was similar.
CONCLUSION
LR of intestinal grafts appears to be a safe strategy for infants and small children requiring intestinal transplantation. This technique should be considered in the situation of significant size mismatch of intestine containing grafts.

Identifiants

pubmed: 37334497
doi: 10.1111/petr.14528
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14528

Subventions

Organisme : Catherine Marie Enright Kelly Memorial Research Scholarship
Organisme : Sir Jules Thorn Biomedical Research Charity

Informations de copyright

© 2023 The Authors. Pediatric Transplantation published by Wiley Periodicals LLC.

Références

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Auteurs

Angus Hann (A)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.
Liver and Intestinal Transplant Unit, Birmingham Children's Hospital, Birmingham, UK.
Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.

Girish L Gupte (GL)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.

Adithya Pathanki (A)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.
Liver and Intestinal Transplant Unit, Birmingham Children's Hospital, Birmingham, UK.

Maria Coelho (M)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.

Sue Beath (S)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.

Jane Hartley (J)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.

Deirdre Kelly (D)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.
Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.

Jean De Ville De Goyet (J)

Department for the Treatment and Study of Pediatric Abdominal Diseases and Abdominal Transplantation, ISMETT, Palermo, Italy.

Ye H Oo (YH)

Liver and Intestinal Transplant Unit, Birmingham Children's Hospital, Birmingham, UK.

Hermien Hartog (H)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.
Liver and Intestinal Transplant Unit, Birmingham Children's Hospital, Birmingham, UK.

Thamara P R Perera (TPR)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.
Liver and Intestinal Transplant Unit, Birmingham Children's Hospital, Birmingham, UK.

Khalid Sharif (K)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.

Darius F Mirza (DF)

Liver Unit, Queen Elizabeth Hospital, Birmingham, UK.
Liver and Intestinal Transplant Unit, Birmingham Children's Hospital, Birmingham, UK.
Centre for Liver and Gastrointestinal Research, Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.

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