Literature DB >> 27798062

Long-term outcomes of complete vascular ring division in children: a 36-year experience from a single institution.

Phillip S Naimo1,2,3, Tyson A Fricke1,2,3, Julia S Donald1, Elie Sawan1, Yves d'Udekem1,2,3, Christian P Brizard1,2,3, Igor E Konstantinov1,2,3.   

Abstract

Objectives: Complete vascular rings are rare and cause tracheoesophageal compression. Following surgical division, some patients have persisting tracheomalacia. We aim to assess the long-term outcomes of complete vascular ring division.
Methods: All patients (n = 132) who underwent surgical division of a complete vascular ring between 1978 and 2014 were identified from the hospital database and retrospectively reviewed.
Results: Complete vascular rings consisted of a double aortic arch (n = 80), right aortic arch with an aberrant subclavian artery and left ligamentum arteriosum (n = 50), right aortic arch with mirror image branching and left ligamentum arteriosum (n = 1), and a left aortic arch with right descending aorta and right ligamentum arteriosum (n = 1). Kommerell's diverticulum was identified in 10 patients. Preoperative tracheomalacia was identified via bronchoscopy in 25 patients. Concomitant tracheal reconstruction was not performed in any patient. Kommerell's diverticulum was resected in 1 patient. The hospital mortality rate was 1.5% (2/132). There were no late deaths. The overall survival rate was 98.3 ± 1.2% (95% CI: 93.4, 99.6) at 20 years. Postoperatively, persistent tracheal compression was reported in 3 patients, and tracheomalacia in 16 patients. The rate of freedom from reoperation was 88.6 ± 4.0% (95% CI: 77.9, 94.3) at 20 years. No patient required tracheal surgery during the follow-up period. Follow-up was 92% (121/132) complete, with a median follow-up of 11.4 years (range 44 days to 36 years). At the last follow-up, 7 patients had mild tracheomalacia. Conclusions: Outcomes of division of a complete vascular ring are excellent. Tracheomalacia often improves following division of the vascular ring. Respiratory symptoms following complete vascular ring division are uncommon.
© The Author 2016. Published by Oxford University Press on behalf of the European Association for Cardio-Thoracic Surgery. All rights reserved.

Entities:  

Keywords:  Complete vascular ring; Congenital heart disease; Surgery

Mesh:

Year:  2017        PMID: 27798062     DOI: 10.1093/icvts/ivw344

Source DB:  PubMed          Journal:  Interact Cardiovasc Thorac Surg        ISSN: 1569-9285


  5 in total

1.  Stridor serving as a harbinger of the mirror-image right aortic arch carrying three anatomic dispositions contributing to a noosing vascular ring.

Authors:  Meng-Luen Lee; Ming-Sheng Lee; Albert D Yang; Ming-Che Chang; Ying-Cheng Chen
Journal:  Anatol J Cardiol       Date:  2021-04       Impact factor: 1.596

2.  Resection of Kommerell's diverticulum in an infant with prenatal diagnosis of right aortic arch.

Authors:  Kenji Suzuki; Takashi Sasaki; Shinobu Kunugi; Yoshio Shima; Ryuji Fukazawa; Akira Shimizu; Takashi Nitta
Journal:  Surg Case Rep       Date:  2019-11-06

3.  Prenatal diagnosis of vascular rings and outcome.

Authors:  Shweta Bakhru; Nageswara Rao Koneti; Sujata Patil; Bhargavi Dhulipudi; Tapan Dash; Geeta Kolar; Suseela Vavilala
Journal:  Ann Pediatr Cardiol       Date:  2021-02-16

4.  Long-term outcomes in children undergoing vascular ring division: a multi-institution experience.

Authors:  Di Yu; Zhangke Guo; Xin You; Wei Peng; Jirong Qi; Jian Sun; Kaihong Wu; Xiaofeng Li; Xuming Mo
Journal:  Eur J Cardiothorac Surg       Date:  2022-02-18       Impact factor: 4.191

5.  Vocal cord dysfunction after pediatric cardiac surgery: A prospective implementation study.

Authors:  Louise Kenny; Amy McIntosh; Karen Jardine; Jessica Suna; Kathryn Versluis; Nicola Slee; Gareth Lloyd; Robert Justo; Greg Merlo; Mary Wilson; Tristan Reddan; Jennifer Powell; Prem Venugopal; Kim Betts; Nelson Alphonso
Journal:  JTCVS Open       Date:  2022-06-09
  5 in total

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