Journal of Pediatric Cardiology and Cardiac Surgery

Online ISSN: 2433-1783 Print ISSN: 2433-2720
Japanese Society of Pediatric Cardiology and Cardiac Surgery
Japanese Society of Pediatric Cardiology and Cardiac Surgery Academy Center, 358-5 Yamabuki-cho, Shinju-ku, Tokyo 162-0801, Japan
Journal of Pediatric Cardiology and Cardiac Surgery 4(2): 75-79 (2020)
doi:10.24509/jpccs.19-006

Case ReportCase Report

Staged Treatment Using Right Ventricular Outflow Tract Stenting for Effective Augmentation of Native Pulmonary Arteries in a Case of Tetralogy of Fallot with Major Aortopulmonary Collateral Arteries

1Department of Cardiology, Shizuoka Children’s Hospital ◇ Shizuoka, Japan

2Department of Cardiovascular Surgery, Shizuoka Children’s Hospital ◇ Shizuoka, Japan

*1

Current affiliation: Kurashiki Central Hospital, 1–1–1 Miwa Kurashiki-city, Okayama710–8602, Japan

受付日:2019年10月31日Received: October 31, 2019
受理日:2020年2月13日Accepted: February 13, 2020
発行日:2020年7月1日Published: July 1, 2020
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Stenting of the right ventricular outflow tract (RVOT) is an emerging alternative for the management of cyanotic tetralogy of Fallot (TOF) in the neonatal or early infancy stage. We describe our treatment of a TOF in the early infancy stage, using RVOT, in a patient for whom the TOF physiology was associated with major aortopulmonary collateral arteries (MAPCAs), all of which had a dual blood supply from the pulmonary arteries. The procedure was successful, with sufficient antegrade blood flow of the native pulmonary arteries achieved for occlusion of all MAPCAs. RVOT stenting provided an effective strategy for the management of cyanotic TOF, without the need for unifocalization, in the presence of MAPCAs with dual blood supply.

Key words: RVOT stenting; TOF; MAPCAs; unifocalization

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