A two-stage approach to correct aortic coarctation combined with aortic root aneurysm and bicuspid aortic valve in an adult patient

Coarctation of the aorta (CoA) is a congenital heart disease (CHD) that may remain undiagnosed until adulthood. Its clinical manifestations vary depending on the anatomical severity of the narrowing and the degree of collateral circulation development. The management of CoA, particularly when associated with additional CHDs or acquired cardiovascular pathology in adult patients, necessitates a comprehensive and individualised treatment strategy. We present a clinical case of a 33-year-old female diagnosed with CoA, complicated by an aortic root aneurysm and bicuspid aortic valve (BAV) insufficiency. Given the complexity of her condition, a staged hybrid approach was implemented. In the first stage, the patient underwent surgical valve-sparing aortic root replacement (David procedure), preserving the native valve function. Three weeks later, thoracic endovascular aortic repair (TEVAR) was performed to address the CoA. The patient's postoperative recovery was uneventful. Follow-up imaging, including computed tomography angiography (СТА) and transthoracic echocardiography at 3 months post-discharge, demonstrated an optimal surgical outcome, confirming the efficacy of this tailored two-stage strategy.

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Publication Details

Journal
Perfusion
Published
2025-06-09
DOI
https://doi.org/10.1177/02676591251351212
Primary Topic
Congenital Heart Disease Studies
Type
article
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article

A two-stage approach to correct aortic coarctation combined with aortic root aneurysm and bicuspid aortic valve in an adult patient

Almas Tolegenuly, Abay K. Baigenzhin, Aidos Yerpashov, Bulat Kupenov et al.
Perfusion
Congenital Heart Disease Studies
article

A two-stage approach to correct aortic coarctation combined with aortic root aneurysm and bicuspid aortic valve in an adult patient

Almas Tolegenuly, Abay K. Baigenzhin, Aidos Yerpashov, Bulat Kupenov, Alimzhan Yelzhasov, Diana Argynkyzy, Adil Abdinurov, Daut Tolen
article en

Abstract

Coarctation of the aorta (CoA) is a congenital heart disease (CHD) that may remain undiagnosed until adulthood. Its clinical manifestations vary depending on the anatomical severity of the narrowing and the degree of collateral circulation development. The management of CoA, particularly when associated with additional CHDs or acquired cardiovascular pathology in adult patients, necessitates a comprehensive and individualised treatment strategy. We present a clinical case of a 33-year-old female diagnosed with CoA, complicated by an aortic root aneurysm and bicuspid aortic valve (BAV) insufficiency. Given the complexity of her condition, a staged hybrid approach was implemented. In the first stage, the patient underwent surgical valve-sparing aortic root replacement (David procedure), preserving the native valve function. Three weeks later, thoracic endovascular aortic repair (TEVAR) was performed to address the CoA. The patient's postoperative recovery was uneventful. Follow-up imaging, including computed tomography angiography (СТА) and transthoracic echocardiography at 3 months post-discharge, demonstrated an optimal surgical outcome, confirming the efficacy of this tailored two-stage strategy.

Perfusion
National Medical Holding (KZ)
Good health and well-being
Openalex Percentile: Top 81%
Congenital Heart Disease Studies
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