Serial Transverse Enteroplasty (STEP) for Short Bowel Syndrome (SBS) in Children: A Multicenter Study on Long-term Outcomes.

STEP Serial transverse enteroplasty Short bowel syndrome (SBS)

Journal

Journal of pediatric surgery
ISSN: 1531-5037
Titre abrégé: J Pediatr Surg
Pays: United States
ID NLM: 0052631

Informations de publication

Date de publication:
26 Sep 2024
Historique:
received: 10 03 2024
revised: 31 08 2024
accepted: 04 09 2024
medline: 6 10 2024
pubmed: 6 10 2024
entrez: 5 10 2024
Statut: aheadofprint

Résumé

Short Bowel Syndrome (SBS), secondary to various underlying diseases, is one of the main causes of intestinal failure in children. Surgical management by serial transverse enteroplasty (STEP), is feasible in selected cases, but results on long-term follow-up are scarce. The aim of this study was to report long-term outcomes of the STEP procedure in children with SBS. We performed a multicenter national retrospective study reviewing medical charts of children who underwent a STEP technique between 2000 and 2022 in 6 university hospitals. Collected data included demographics, SBS history, surgical procedures, nutritional support (enteral or parenteral), STEP management, complications, and outcomes (nutritional support, digestive symptoms, growth). STEP was performed in 36 SBS, resulting from 14 gastroschisis, 10 intestinal atresia, 8 necrotizing enterocolitis (NEC), 2 midgut volvulus, and 2 intestinal Hirschsprung disease. Median age at first STEP was 10.8 months [4.5; 63.8]. Bowel length significantly increased (47 vs 70 cm, p < 0.01), with a median gain of 16 cm [11; 25] or 34%. At surgery, 33 children had parenteral nutrition (PN). A second STEP was performed in 11 patients, at a median age of 4.2 years [2.8; 6.8]. One patient underwent a third STEP. Two children required intestinal transplantation. Median follow-up was 7 years [4.4;11.4]. Out of 33 children requiring PN before surgery, 14 children were weaned off PN. The remaining 19 children still required PN, but their dependency decreased by 19%. Out of 17 children presenting severe intestinal dilations and bacterial overgrowth, 12 became asymptomatic. Out of 20 with chronic obstructive symptoms, 8 patients still required supplementary PN whereas 12 achieved complete enteral autonomy, including 3 requiring supplementary enteral support. STEP technique remains a surgical option in the management of these children, enabling a decrease in PN dependency, resulting in weaning off PN in some cases, as well as an improvement of clinical symptoms. Retrospective multicenter observational study. Level 3.

Identifiants

pubmed: 39368852
pii: S0022-3468(24)00811-X
doi: 10.1016/j.jpedsurg.2024.161909
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

161909

Informations de copyright

Copyright © 2024 The Author(s). Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest The authors declare that they have no conflicts of interest.

Auteurs

Claire Dagorno (C)

Department of Pediatric Surgery, Robert-Debré Children's University Hospital, APHP, Paris, France; Department of General Pediatric Surgery, Necker-Enfants Malades Hospital, APHP, Paris, France.

Louise Montalva (L)

Department of Pediatric Surgery, Robert-Debré Children's University Hospital, APHP, Paris, France; Paris-Cité University, Paris, France; NeuroDiderot, INSERM UMR1141, Paris, France.

Carmen Capito (C)

Department of General Pediatric Surgery, Necker-Enfants Malades Hospital, APHP, Paris, France; Paris-Cité University, Paris, France.

Frederic Lavrand (F)

Department of General Pediatric Surgery, Children Hospital, CHU de Bordeaux, France.

Audrey Guinot (A)

Department of General Pediatric Surgery, Children and Mother Hospital, CHU de Nantes, France.

Stéphan De Napoli Cocci (S)

Department of General Pediatric Surgery, Children and Mother Hospital, CHU de Nantes, France.

Thomas Gelas (T)

Department of General Pediatric Surgery, Hospices Civils de Lyon, Children and Mother Hospital, CHU de Lyon, France.

Rémi Dubois (R)

Department of General Pediatric Surgery, Hospices Civils de Lyon, Children and Mother Hospital, CHU de Lyon, France.

Anne Dariel (A)

Department of General Pediatric Surgery, Timone Hospital, CHU de Marseille, France.

Emmanuelle Dugelay (E)

Department of Pediatric Gastro-enterology, Robert-Debré Children's University Hospital, APHP, Paris, France.

Christophe Chardot (C)

Department of General Pediatric Surgery, Necker-Enfants Malades Hospital, APHP, Paris, France; Paris-Cité University, Paris, France.

Arnaud Bonnard (A)

Department of Pediatric Surgery, Robert-Debré Children's University Hospital, APHP, Paris, France; Paris-Cité University, Paris, France; NeuroDiderot, INSERM UMR1141, Paris, France. Electronic address: arnaud.bonnard@aphp.fr.

Classifications MeSH