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Aortic-to-Right Ventricle Shunting for Rare Cardiovascular Conditions

The Annals of thoracic surgery, 2022-12, Vol.114 (6), p.e455-e458 [Peer Reviewed Journal]

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Title:
Aortic-to-Right Ventricle Shunting for Rare Cardiovascular Conditions
Author: Miwa, Koji ; Iwai, Shigemitsu ; Nagashima, Toshiaki
Subjects: Heart Defects, Congenital - epidemiology ; Heart Defects, Congenital - surgery ; Heart Septal Defects ; Heart Septal Defects, Ventricular - diagnostic imaging ; Heart Septal Defects, Ventricular - surgery ; Heart Ventricles - abnormalities ; Heart Ventricles - diagnostic imaging ; Heart Ventricles - surgery ; Humans ; Pulmonary Atresia - surgery
Is Part Of: The Annals of thoracic surgery, 2022-12, Vol.114 (6), p.e455-e458
Description: Pulmonary atresia with hypoplastic right ventricle and ventricular septal defect with right ventricle–dependent coronary circulation are very rare congenital heart anomalies. This report describes the case of a patient in whom aortic-right ventricle shunting was surgically established with a satisfactory postoperative course. Aortic–right ventricle shunting can enhance oxygenation of the sinusoidal communication and reduce the incidence of myocardial ischemia without influencing the left ventricular volume load through the ventricular septal defect despite preservation of the septal defect.
Publisher: Netherlands: Elsevier Inc
Language: English
Identifier: ISSN: 0003-4975
EISSN: 1552-6259
DOI: 10.1016/j.athoracsur.2022.02.023
PMID: 35231433
Source: MEDLINE
Alma/SFX Local Collection

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