A retrospective case-control study of gastrostomy use in children undergoing hematopoietic cell transplantation.


Journal

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

Informations de publication

Date de publication:
06 2023
Historique:
revised: 23 01 2023
received: 25 07 2022
accepted: 13 03 2023
medline: 17 5 2023
pubmed: 23 4 2023
entrez: 23 04 2023
Statut: ppublish

Résumé

Maintaining a good nutritional status during the hematopoietic cell transplantation (HCT) procedure is challenging in the pediatric population. In a multicentric retrospective study, we compared the outcome of nutritional status and HCT-related parameters in 227 pediatric patients during and after HCT between 2005 and 2015. 112 patients received a gastrostomy before the start of HCT (GS group), and 115 did not receive a gastrostomy (NGS). Data collection was performed at HCT, 3, 6, and 12 months post-HCT. At time point of HCT the Standard Deviation Score (SDS) of weight was 0.17 in the NGS group, and 0.71 in the GS group (p = .01) Patients in the NGS group lost more weight during the first 3 months after HCT than patients in the GS group. At 12 months, patients in the NGS remained at a lower weight, while patients in the GS group slightly increased their weight. There were no differences between the groups in the incidence of acute graft-versus-host-disease (GvHD), overall survival, and non-relapse mortality. However, the number of febrile episodes requiring intravenous treatment with antibiotics, was higher in the GS group as compared to the NGS group, during the first 3 months post-HCT (p < .001). Our results indicate that gastrostomy can be utilized in children undergoing HCT without any negative effects on mortality. Therefore, the use of a gastrostomy appears to be a safe option to maintain a good nutritional status during the HCT procedure.

Sections du résumé

BACKGROUND
Maintaining a good nutritional status during the hematopoietic cell transplantation (HCT) procedure is challenging in the pediatric population.
METHODS
In a multicentric retrospective study, we compared the outcome of nutritional status and HCT-related parameters in 227 pediatric patients during and after HCT between 2005 and 2015. 112 patients received a gastrostomy before the start of HCT (GS group), and 115 did not receive a gastrostomy (NGS). Data collection was performed at HCT, 3, 6, and 12 months post-HCT.
RESULTS
At time point of HCT the Standard Deviation Score (SDS) of weight was 0.17 in the NGS group, and 0.71 in the GS group (p = .01) Patients in the NGS group lost more weight during the first 3 months after HCT than patients in the GS group. At 12 months, patients in the NGS remained at a lower weight, while patients in the GS group slightly increased their weight. There were no differences between the groups in the incidence of acute graft-versus-host-disease (GvHD), overall survival, and non-relapse mortality. However, the number of febrile episodes requiring intravenous treatment with antibiotics, was higher in the GS group as compared to the NGS group, during the first 3 months post-HCT (p < .001).
CONCLUSIONS
Our results indicate that gastrostomy can be utilized in children undergoing HCT without any negative effects on mortality. Therefore, the use of a gastrostomy appears to be a safe option to maintain a good nutritional status during the HCT procedure.

Identifiants

pubmed: 37087694
doi: 10.1111/petr.14520
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e14520

Subventions

Organisme : ALF Uppsala
Organisme : Barncancerfonden
ID : PR2016-0017

Informations de copyright

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

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Auteurs

Karin Mellgren (K)

Department of Pediatric Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

Tom Nicolajsen (T)

Department of Paediatrics, NU-Sjukvården, Trollhättan, Sweden.

Tania Panagiota Christoforaki (TP)

Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden.

Sara Marin Juan (SM)

Department of Clinical Science, Intervention and Technology, Division of Paediatrics, Karolinska Institutet, Stockholm, Sweden.

Thomas Mårtensson (T)

Department of Women's and Children's Health, Uppsala University, Uppsala, Sweden.

Jacek Toporski (J)

Department of Pediatrics, Skåne University Hospital, Lund, Sweden.

Thomas H Casswall (TH)

Department of Clinical Science, Intervention and Technology, Division of Paediatrics, Karolinska Institutet, Stockholm, Sweden.

Britt Gustafsson (B)

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

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