Literature DB >> 23684161

Extraanatomic bypass technique for the treatment of midaortic syndrome in children.

Roland Hetzer1, Daniel Absi, Oliver Miera, Natalia Solowjowa, Antonia Schulz, Mariano Francisco del Maria Javier, Eva Maria Delmo Walter.   

Abstract

BACKGROUND: This report aims to introduce the extraanatomic bypass technique to treat the midaortic syndrome and to document its long-term effectiveness and durability.
METHODS: Fourteen patients (mean age, 6.7 ± 3.76 years; range 8 months to 11 years) received diagnoses of midaortic syndrome, characterized by severe narrowing of the abdominal aorta with involvement of the renal and visceral branches. Angiography showed variable lengths of high-grade midaortic stenosis, with 7 children having visceral artery involvement and 9 having renal artery involvement. All children were hypertensive (mean blood pressure, 165 ± 15.7 mm Hg). Three had had previous nephrectomies. Six patients had had previous percutaneous transluminal renal artery angioplasties. The midaortic obstruction was relieved by descending abdominal aorta bypass (left thoracoabdominal approach) and by an ascending abdominal aorta bypass (median sternotomy and transabdominal approach) in 12 patients. No visceral artery revascularization was done.
RESULTS: There was a considerable blood pressure reduction in all patients and relief of intermittent claudication in 6 affected patients. One patient had a bilateral renal artery bypass 2 weeks postoperatively because of recurrence of renal hypertension. At a mean follow-up time of 5.8 ± 1.36 years (range, 9 months to 15 years), there was no further reoperation nor mortality. Twelve patients had complete relief of hypertension, and 2 had mild hypertension. All patients have normal renal function and no signs or symptoms of visceral malperfusion. Growth and development have proceeded normally. Follow-up magnetic resonance tomography showed patent grafts without any strictures.
CONCLUSIONS: Extraanatomic bypass provides very effective and long-term relief of hypertension and any malperfusion in midaortic syndrome.
Copyright © 2013 The Society of Thoracic Surgeons. Published by Elsevier Inc. All rights reserved.

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Year:  2013        PMID: 23684161     DOI: 10.1016/j.athoracsur.2013.03.025

Source DB:  PubMed          Journal:  Ann Thorac Surg        ISSN: 0003-4975            Impact factor:   4.330


  6 in total

1.  Descending aorta-external iliac artery bypass for middle aortic syndrome.

Authors:  Yuki Okamoto; Kazuo Yamamoto; Tsutomu Sugimoto; Fuyuki Asami; Ayako Nagasawa; Satoru Shiraiwa; Norihito Nakamura; Shinpei Yoshii
Journal:  Heart Vessels       Date:  2013-11-26       Impact factor: 2.037

2.  Unlikely culprit: congenital middle aortic syndrome diagnosed in the sixth decade of life.

Authors:  Muhammad Sajawal Ali; Stefan Tchernodrinski; Divyanshu Mohananey; Ahya Sajawal Ali
Journal:  BMJ Case Rep       Date:  2016-08-16

3.  Total arch replacement for aortic arch aneurysm with coexisting middle aortic syndrome.

Authors:  Zaiqiang Yu; Masahito Minakawa; Norihiro Kondo; Kazuyuki Daitoku; Ikuo Fukuda
Journal:  Int J Surg Case Rep       Date:  2018-11-24

4.  Severe midaortic syndrome: a stepwise approach to treatment with drug-eluting balloons: a case report.

Authors:  Peter Zartner; Christopher Hart; Martin B E Schneider
Journal:  Eur Heart J Case Rep       Date:  2019-02-25

5.  Long-segment thoracoabdominal aortic coarctation in a child with Down syndrome.

Authors:  Vladimir Tonello de Vasconcelos; Ruy Guilherme Rodrigues Cal; Adriano Luís Gomes; Simone Aguiar; Maria Fernanda Carvalho de Camargo; José Carlos Costa Baptista-Silva
Journal:  J Vasc Surg Cases       Date:  2015-06-19

Review 6.  Diagnosis and Management of Genetic Causes of Middle Aortic Syndrome in Children: A Comprehensive Literature Review.

Authors:  Cecilia Lazea; Camelia Al-Khzouz; Crina Sufana; Diana Miclea; Carmen Asavoaie; Ioana Filimon; Otilia Fufezan
Journal:  Ther Clin Risk Manag       Date:  2022-03-16       Impact factor: 2.423

  6 in total

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