Outcomes of Surgical Repair of Vascular Rings and Slings in Children: A Word for the Asymptomatic.


Journal

Seminars in thoracic and cardiovascular surgery
ISSN: 1532-9488
Titre abrégé: Semin Thorac Cardiovasc Surg
Pays: United States
ID NLM: 8917640

Informations de publication

Date de publication:
Historique:
received: 21 08 2020
accepted: 08 09 2020
pubmed: 26 9 2020
medline: 3 7 2021
entrez: 25 9 2020
Statut: ppublish

Résumé

Vascular rings (VRs) are rare aortic arch anomalies that may present with a wide variety of symptoms related to esophageal and/or airway compression. We reviewed our surgical experience in both symptomatic and asymptomatic children. All children (n = 58) who underwent surgical repair of VRs or slings (mean age 27.4 ± 45.60 months; 36 males [62%]) between March 2000 and April 2020 were included. The most common anatomic variant was a right aortic arch (RAA) with aberrant left subclavian artery (ALSCA) (n = 29; 50%). Kommerell's diverticulum was present in 23 of these patients (79%). The second most common variant was a double aortic arch (n = 22; 38%), followed by pulmonary artery sling (n = 4; 6%), RAA with mirror image branching and left ligamentum arteriosum (n = 3; 5.2%), and left aortic arch (LAA) with aberrant right subclavian artery (n = 1; 1.7%). One patient had a double ring with pulmonary artery sling and RAA with ALSCA. Symptoms were present in 42 patients (72%). Left lateral thoracotomy was the approach in 50 patients (86%), while sternotomy was used in 8 (14%). Symptomatic improvement occurred in the majority of symptomatic patients (93%). There was one perioperative mortality (1.7%) in the symptomatic group which was non-VR related. Morbidities included recurrent laryngeal nerve injury in three patients (5.2%) and transient chylothorax in two (3.4%). Persistence/recurrence of symptoms resulted in one early and one late reoperation. The mean follow-up was 3 ± 5 years. In the current era, VR repair in children including asymptomatic ones can be performed with excellent results. We recommend complete repair of RAA with aberrant LSCA by resection of Kommerell's diverticulum and translocation of the ALSCA to avoid recurrence.

Identifiants

pubmed: 32977012
pii: S1043-0679(20)30286-0
doi: 10.1053/j.semtcvs.2020.09.013
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

492-500

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2020 Elsevier Inc. All rights reserved.

Auteurs

Sameh M Said (SM)

Divisions of Pediatric Cardiovascular Surgery, Masonic Children's Hospital, University of Minnesota, Minneapolis, Minnesota; Department of Cardiothoracic Surgery, Faculty of Medicine, Alexandria University, Alexandria, Egypt. Electronic address: ssaid@umn.edu.

Gamal Marey (G)

Divisions of Pediatric Cardiovascular Surgery, Masonic Children's Hospital, University of Minnesota, Minneapolis, Minnesota.

Stacie Knutson (S)

Pediatric Cardiology, Masonic Children's Hospital, University of Minnesota, Minneapolis, Minnesota.

Nathan Rodgers (N)

Pediatric Cardiology, Masonic Children's Hospital, University of Minnesota, Minneapolis, Minnesota.

Martina Richtsfeld (M)

Pediatric Anestheiology, Masonic Children's Hospital, University of Minnesota, Minneapolis, Minnesota.

Brian Joy (B)

Pediatric Critical Care, Masonic Children's Hospital, University of Minnesota, Minneapolis, Minnesota.

Massimo Griselli (M)

Divisions of Pediatric Cardiovascular Surgery, Masonic Children's Hospital, University of Minnesota, Minneapolis, Minnesota.

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