{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T16:04:55Z","timestamp":1790352295342,"version":"4.1.0"},"reference-count":0,"publisher":"European Association of Cardiothoracic Surgery (EACTS Publishing Ltd)","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["MMCTS"],"published-print":{"date-parts":[[2026,9,25]]},"abstract":"<jats:p>The cervical aortic arch, first described by Reid, is a rare congenital anomaly of the aortic arch. We report the surgical management of a neonate with a right cervical arch with coarctation, a contralateral descending thoracic aorta, and severely reduced left ventricular function. Arch repair with aortic uncrossing was performed under whole-body perfusion, achieved by simultaneously cannulating the aortic arch and the descending thoracic aorta.<\/jats:p>","DOI":"10.1510\/mmcts.2026.038","type":"journal-article","created":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T15:26:33Z","timestamp":1790349993000},"source":"Crossref","is-referenced-by-count":0,"title":["Cervical aortic arch with severe left ventricular dysfunction in a neonate: successful repair using whole-body perfusion"],"prefix":"10.1510","member":"10966","published-online":{"date-parts":[[2026,9,25]]},"container-title":["Multimedia Manual of Cardio-Thoracic Surgery"],"original-title":[],"deposited":{"date-parts":[[2026,9,25]],"date-time":"2026-09-25T15:26:34Z","timestamp":1790349994000},"score":1,"resource":{"primary":{"URL":"https:\/\/mmcts.org\/case-report\/2242"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026,9,25]]},"references-count":0,"URL":"https:\/\/doi.org\/10.1510\/mmcts.2026.038","relation":{},"ISSN":["1813-9175"],"issn-type":[{"value":"1813-9175","type":"electronic"}],"subject":[],"published":{"date-parts":[[2026,9,25]]}}}