{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,27]],"date-time":"2026-02-27T08:39:14Z","timestamp":1772181554130,"version":"3.50.1"},"reference-count":17,"publisher":"Texas Heart Institute Journal","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2016,12]]},"abstract":"<jats:p>Isolated left subclavian artery is one of the rarer aortic arch anomalies. It has been associated with other congenital heart diseases, typically tetralogy of Fallot, double-outlet right ventricle, and atrial and ventricular septal defects. Its significant clinical implications include a left-to-right shunt from the vertebrobasilar system, which causes pulmonary overcirculation and subclavian steal. We present an unusual case of a premature infant who was diagnosed prenatally with congenital complete atrioventricular block and tricuspid atresia and was found to have an isolated left subclavian artery postnatally. The patient underwent implantation of a permanent single-chamber epicardial pacing system. To our knowledge, this combination of lesions has not been reported\u2014and in our case, it influenced our surgical planning.<\/jats:p>","DOI":"10.14503\/thij-15-5692","type":"journal-article","created":{"date-parts":[[2016,12,16]],"date-time":"2016-12-16T23:13:42Z","timestamp":1481930022000},"page":"546-549","source":"Crossref","is-referenced-by-count":5,"title":["Isolated Left Subclavian Artery, Complete Atrioventricular Block, and Tricuspid Atresia in a Neonate"],"prefix":"10.14503","volume":"43","author":[{"given":"Kanupriya","family":"Chaturvedi","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Deepa","family":"Prasad","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ravi","family":"Ashwath","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"James P.","family":"Strainic","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Christopher S.","family":"Snyder","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"5628","reference":[{"issue":"3","key":"i1526-6702-43-6-546-b1","series-title":"Mayo Clin Proc","first-page":"407","article-title":"Right aortic arch with isolation of the left subclavian artery: case report and review of the literature","volume":"65","year":"1990","unstructured":"Luetmer\n              PH\n            , MillerGM.\n          Right aortic arch with isolation of the left subclavian artery: case report and review of the literature. 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Cardiol Young2014;24(1):134\u20135."},{"issue":"1","key":"i1526-6702-43-6-546-b17","series-title":"World J Pediatr Congenit Heart Surg","first-page":"98","article-title":"Absent pulmonary valve, tricuspid atresia, and congenital heart block","volume":"6","year":"2015","unstructured":"Juaneda\n              I\n            , RychikJ, FullerS, WeinbergPM, RomeJJ, MahleWT, GaynorJW.\n          Absent pulmonary valve, tricuspid atresia, and congenital heart block. 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