The Effect of Botulinum Toxin Type A Injections on Stricture Formation, Leakage Rates, Esophageal Elongation, and Anastomotic Healing Following Primary Anastomosis in a Long- and Short-Gap Esophageal Atresia Model - A Protocol for a Randomized, Controlled, Blinded Trial in Pigs.

anastomotic stricture botulinum toxin oesophageal atresia

Journal

International journal of surgery protocols
ISSN: 2468-3574
Titre abrégé: Int J Surg Protoc
Pays: England
ID NLM: 101758186

Informations de publication

Date de publication:
2021
Historique:
received: 13 07 2021
accepted: 27 07 2021
entrez: 26 8 2021
pubmed: 27 8 2021
medline: 27 8 2021
Statut: epublish

Résumé

Esophageal atresia (EA) is a congenital malformation affecting 1:3000-4500 newborns. Approximately 15% have a long-gap EA (LGEA), in which case a primary anastomosis is often impossible to achieve. To create continuity of the esophagus patients instead have to undergo lengthening procedures or organ interpositions; methods associated with high morbidity and poor functional outcomes. Esophageal injections of Botulinum Toxin Type A (BTX-A) could enable primary anastomosis and mitigate stricture formation through decreased tissue tension. In this randomized controlled blinded animal trial, 24 pigs are divided into a long- or short-gap EA group (LGEA and SGEA, respectively) and randomized to receive BTX-A or isotonic saline injections. In the LGEA group, injections are given endoscopically in the esophageal musculature. After seven days, a 3 cm esophageal resection and primary anastomosis is performed. In the SGEA group, a 1 cm esophageal resection and primary anastomosis is performed, followed by intraoperative injections of BTX-A or isotonic saline. After 14 days, stricture formation, presence of leakage, and esophageal compliance is assessed using endoscopic and manometric techniques, and in vivo and ex vivo contrast radiography. Tissue elongation is evaluated in a stretch-tension test, and the esophagus is assessed histologically to evaluate anastomotic healing. The study complies with the ARRIVE guidelines for animal studies and has been approved by the Danish Animal Experimentation Council. Results will be published in peer-reviewed journals and presented at national and international conferences. The optimal management of long-gap esophageal atresia remains controversialPrimary anastomosis could improve functional outcomes and reduce complicationsBotulinum Toxin Type A decreases tissue tension and could facilitate anastomosisReduced tension could further abate the risk for anastomotic stricture and leakageWe present a model to evaluate the method in long- and short-gap esophageal atresia.

Sections du résumé

BACKGROUND BACKGROUND
Esophageal atresia (EA) is a congenital malformation affecting 1:3000-4500 newborns. Approximately 15% have a long-gap EA (LGEA), in which case a primary anastomosis is often impossible to achieve. To create continuity of the esophagus patients instead have to undergo lengthening procedures or organ interpositions; methods associated with high morbidity and poor functional outcomes. Esophageal injections of Botulinum Toxin Type A (BTX-A) could enable primary anastomosis and mitigate stricture formation through decreased tissue tension.
METHODS AND ANALYSIS METHODS
In this randomized controlled blinded animal trial, 24 pigs are divided into a long- or short-gap EA group (LGEA and SGEA, respectively) and randomized to receive BTX-A or isotonic saline injections. In the LGEA group, injections are given endoscopically in the esophageal musculature. After seven days, a 3 cm esophageal resection and primary anastomosis is performed. In the SGEA group, a 1 cm esophageal resection and primary anastomosis is performed, followed by intraoperative injections of BTX-A or isotonic saline. After 14 days, stricture formation, presence of leakage, and esophageal compliance is assessed using endoscopic and manometric techniques, and in vivo and ex vivo contrast radiography. Tissue elongation is evaluated in a stretch-tension test, and the esophagus is assessed histologically to evaluate anastomotic healing.
ETHICS AND DISSEMINATION BACKGROUND
The study complies with the ARRIVE guidelines for animal studies and has been approved by the Danish Animal Experimentation Council. Results will be published in peer-reviewed journals and presented at national and international conferences.
HIGHLIGHTS CONCLUSIONS
The optimal management of long-gap esophageal atresia remains controversialPrimary anastomosis could improve functional outcomes and reduce complicationsBotulinum Toxin Type A decreases tissue tension and could facilitate anastomosisReduced tension could further abate the risk for anastomotic stricture and leakageWe present a model to evaluate the method in long- and short-gap esophageal atresia.

Identifiants

pubmed: 34435166
doi: 10.29337/ijsp.156
pmc: PMC8362621
doi:

Types de publication

Journal Article

Langues

eng

Pagination

171-177

Informations de copyright

Copyright: © 2021 The Author(s).

Déclaration de conflit d'intérêts

The authors have no competing interests to declare.

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Auteurs

Emma Svensson (E)

Pediatric surgery, Department of Clinical Sciences Lund, Faculty of Medicine, Lund University. Skane University Hospital Lund, 221 84 Lund, Sweden.

Peter Zvara (P)

Research Unit for Urology, Department of Clinical Research, University of Southern Denmark, J. B. Winsløws Vej 4, 5000 Odense C, Denmark.

Niels Qvist (N)

Research Unit for Surgery, Odense University Hospital, University of Southern Denmark, J. B. Winsløws Vej 4, 5000 Odense C, Denmark.

Lars Hagander (L)

Pediatric surgery, Department of Clinical Sciences Lund, Faculty of Medicine, Lund University. Skane University Hospital Lund, 221 84 Lund, Sweden.

Sören Möller (S)

OPEN - Open Patient data Explorative Network, Odense University Hospital; Department of Clinical Research, University of Southern Denmark, J. B. Winsløws Vej 9A, 5000 Odense C, Denmark.

Lars Rasmussen (L)

Research Unit for Surgery, Odense University Hospital, University of Southern Denmark, J. B. Winsløws Vej 4, 5000 Odense C, Denmark.

Henrik Daa Schrøder (HD)

Department of Pathology, Odense University Hospital, University of Southern Denmark, J.B. Winsløws Vej 15, 5000 Odense, Denmark.

Eva Kildall Hejbøl (EK)

Department of Pathology, Odense University Hospital, University of Southern Denmark, J.B. Winsløws Vej 15, 5000 Odense, Denmark.

Niels Bjørn (N)

Research Unit for Surgery, Odense University Hospital, University of Southern Denmark, J. B. Winsløws Vej 4, 5000 Odense C, Denmark.

Súsanna Petersen (S)

Research Unit for Surgery, Odense University Hospital, University of Southern Denmark, J. B. Winsløws Vej 4, 5000 Odense C, Denmark.

Kristine Cederstrøm Larsen (KC)

Research Unit for Surgery, Odense University Hospital, University of Southern Denmark, J. B. Winsløws Vej 4, 5000 Odense C, Denmark.

Jan Krhut (J)

Department of Surgical Studies, Medical Faculty, Ostrava University, Syllabova 19, 703 00, Ostrava, Czech Republic.
Department of Urology, University Hospital, 17.listopadu 1790, 708 52 Ostrava, Czech Republic.

Oliver J Muensterer (OJ)

Department of Pediatric Surgery, Dr. von Hauner Children's Hospital of the Ludwig-Maximilians-University Munich, Lindwurmstraße 4, 80337 Munich, Germany.

Mark Bremholm Ellebæk (MB)

Research Unit for Surgery, Odense University Hospital, University of Southern Denmark, J. B. Winsløws Vej 4, 5000 Odense C, Denmark.

Classifications MeSH