Management of aortic arch hypoplasia in neonates and infants

dc.contributor.authorOnalan, Mehmet A.
dc.contributor.authorTemur, Bahar
dc.contributor.authorAydin, Selim
dc.contributor.authorBasgoze, Serdar
dc.contributor.authorGuzelmeric, Fusun
dc.contributor.authorOdemis, Ender
dc.contributor.authorErek, Ersin
dc.date.accessioned2023-02-21T12:32:25Z
dc.date.available2023-02-21T12:32:25Z
dc.date.issued2021-01-01
dc.description.abstractObjectives Surgical management of aortic arch hypoplasia (AAH) with associated intracardiac anomalies is a challenge in newborns. We reviewed the characteristics and outcomes of neonates and infants who underwent pulmonary artery banding concomitant to arch repair and single-stage total repair at our institution. Methods Medical records of 60 patients undergoing aortic arch reconstruction for AAH from 2014 to 2019 were retrospectively reviewed. Twenty-five patients were female (41.6\%), and the age of the patients ranged from 4 to 120 days (median, 19.5 days). The patients were divided into two groups: Group 1 (23 patients) underwent pulmonary artery banding concomitant to arch repair, and Group 2 (37 patients) underwent single-stage total repair in addition to arch repair. All arch repair procedures consisted of an extended (to the midportion of the ascending aorta) patch aortoplasty. Results Postoperative early mortality occurred in 12 patients, eight in Group 1 (34.8\%) and four in Group 2 (10.8\%). There was an early survival advantage in Group 2 (p = .019). Recoarctation occurred in 13 cases (21.6\%), and 11 (18.3\%) of them required reintervention (balloon angioplasty: 7, reoperation: 4). On univariate analysis, risk factors associated with death were pulmonary artery banding (hazard ratio {[}HR], 0.44
dc.description.abstractconfidence interval {[}CI], 0.09-2
dc.description.abstractp = .019), prematurity (HR, 4.67
dc.description.abstractCI, 1.34-16.18
dc.description.abstractp = <.001), preoperative mechanical ventilation support requirement (HR, 0.048
dc.description.abstractCI, 0.52-6.39
dc.description.abstractp = .048), and functional single ventricle (HR, 0.43
dc.description.abstractCI, 0.1-1.86
dc.description.abstractp = .006). The mean duration of follow-up was 21.9 +/- 15.1 months, and there was no late death in either group. Conclusion Single-stage repair of AAH with intracardiac pathologies has better results than palliation, according to survival rates and postoperative results. The use of the patch augmentation technique in AAH is valid and associated with an acceptable incidence of recurrent arch obstruction.
dc.description.issue1
dc.description.issueJAN
dc.description.pages124-133
dc.description.volume36
dc.identifier.doi10.1111/jocs.15212
dc.identifier.urihttps://hdl.handle.net/11443/1063
dc.identifier.urihttp://dx.doi.org/10.1111/jocs.15212
dc.identifier.wosWOS:000591267300001
dc.publisherWILEY
dc.relation.ispartofJOURNAL OF CARDIAC SURGERY
dc.subjectaortic arch plasty
dc.subjectcongenital heart disease
dc.subjecthypoplastic aortic arch
dc.titleManagement of aortic arch hypoplasia in neonates and infants
dc.typeArticle

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