Delayed sequential abdominal wall closure in pediatric liver transplantation to overcome "large for size" scenarios.


Journal

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

Informations de publication

Date de publication:
Feb 2022
Historique:
revised: 13 08 2021
received: 29 06 2021
accepted: 23 08 2021
pubmed: 3 9 2021
medline: 3 3 2022
entrez: 2 9 2021
Statut: ppublish

Résumé

Primary abdominal wall closure after pediatric liver transplantation (PLT) is neither always possible nor advisable, given the graft-recipient size discrepancy and its potential large-for-size scenario. Our objective was to report the experience accumulated with delayed sequential closure (DSC) guided by Doppler ultrasound control. Retrospective analysis of DSC performed from 2013 to March 2020. Twenty-seven DSC (26.5%) were identified out of 102 PLT. Transplant indications and type of grafts were similar among both groups. In patients with DSC, mean weight and GRWR were 9.4 ± 5.5 kg (3.1-26 kg) and 4.7 ± 2.4 (1.9-9.7), significantly lower and higher than the primary closure cohort, respectively. The median time to achieve definitive closure was 6 days (range 3-23 days), and the median number of procedures was 4 (range 2-9). Patients with DSC had longer overall PICU (22.5 ± 16.9 vs. 9.1 ± 9.7 days, p < .05) and hospital stay (33.4 ± 19.1 vs 23, 9 ± 19.8 days (p < .05). These differences are less remarkable if the analysis is performed in a subgroup of patients weighing less than 10 kg. Two patients presented vascular complications (7.4%) within DSC group. No differences were seen when comparing overall, 3-year graft and patient survival (96% and 96% in the DSC group). DSC is a simple and safe technique to ensure satisfactory clinical outcomes to overcome "large for size" scenarios in PLT. In addition, we were able to avoid using a permanent biological material for closing the abdomen.

Sections du résumé

BACKGROUND BACKGROUND
Primary abdominal wall closure after pediatric liver transplantation (PLT) is neither always possible nor advisable, given the graft-recipient size discrepancy and its potential large-for-size scenario. Our objective was to report the experience accumulated with delayed sequential closure (DSC) guided by Doppler ultrasound control.
METHODS METHODS
Retrospective analysis of DSC performed from 2013 to March 2020.
RESULTS RESULTS
Twenty-seven DSC (26.5%) were identified out of 102 PLT. Transplant indications and type of grafts were similar among both groups. In patients with DSC, mean weight and GRWR were 9.4 ± 5.5 kg (3.1-26 kg) and 4.7 ± 2.4 (1.9-9.7), significantly lower and higher than the primary closure cohort, respectively. The median time to achieve definitive closure was 6 days (range 3-23 days), and the median number of procedures was 4 (range 2-9). Patients with DSC had longer overall PICU (22.5 ± 16.9 vs. 9.1 ± 9.7 days, p < .05) and hospital stay (33.4 ± 19.1 vs 23, 9 ± 19.8 days (p < .05). These differences are less remarkable if the analysis is performed in a subgroup of patients weighing less than 10 kg. Two patients presented vascular complications (7.4%) within DSC group. No differences were seen when comparing overall, 3-year graft and patient survival (96% and 96% in the DSC group).
CONCLUSIONS CONCLUSIONS
DSC is a simple and safe technique to ensure satisfactory clinical outcomes to overcome "large for size" scenarios in PLT. In addition, we were able to avoid using a permanent biological material for closing the abdomen.

Identifiants

pubmed: 34472687
doi: 10.1111/petr.14132
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14132

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 Wiley Periodicals LLC.

Références

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Auteurs

José Andrés Molino (JA)

Paediatric Surgery Department, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Ernest Hidalgo (E)

HPB Surgery and Transplants Department, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Jesús Quintero (J)

Paediatric Hepatology and Liver Transplant Unit, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Ana Coma (A)

Paediatric Radiology Unit, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Juan Ortega (J)

Paediatric Intensive Care Unit, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Javier Juamperez (J)

Paediatric Hepatology and Liver Transplant Unit, Vall d´Hebron Hospital Campus, Barcelona, Spain.

María Mercadal-Hally (M)

Paediatric Hepatology and Liver Transplant Unit, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Lluis Riera (L)

Paediatric Radiology Unit, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Lucia Riaza (L)

Paediatric Radiology Unit, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Itxarone Bilbao (I)

HPB Surgery and Transplants Department, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Cristina Dopazo (C)

HPB Surgery and Transplants Department, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Mireia Caralt (M)

HPB Surgery and Transplants Department, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Elisabeth Pando (E)

HPB Surgery and Transplants Department, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Concepción Gómez-Gavara (C)

HPB Surgery and Transplants Department, Vall d´Hebron Hospital Campus, Barcelona, Spain.

Ramón Charco (R)

HPB Surgery and Transplants Department, Vall d´Hebron Hospital Campus, Barcelona, Spain.

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