Coarctation repair through left thoracotomy in neonates and infants
Автор: Belyaeva Maria M., Ilyin Vladimir N., Kornoukhov Oleg Yu., Kornoukhov Yury Yu., Kalinina Oxana I.
Журнал: Патология кровообращения и кардиохирургия @journal-meshalkin
Рубрика: Специальная тема: детская кардиохирургия
Статья в выпуске: 4 т.22, 2018 года.
Бесплатный доступ
Aim. A growing interest in the use of sternotomy and perfusion for repair of aortic coarctation in neonates and infants has enabled us to retrospectively review our own experience in this practice. Our purpose was to determine the efficacy of coarctation repair with extended end-to-end anastomosis through left thoracotomy focusing on a re-intervention rate and dynamics of transverse aortic arch growth during long-term follow-up. Methods. One hundred and twenty-four patients under 3 months old who underwent coarctation repair (between 2008 and 2016) were enrolled in this study. In 43 patients (35%), aorta coarctation was combined with ventricular septal defect, 49 patients (39.5%) had transversal aortic arch hypoplasia (Z-score less than -2). All operations were carried out by using extended “end-to-end” anastomosis technique via thoracotomy. In patients with concomitant ventricular septal defect, PA-banding was performed simultaneously. Overall follow-up was 3.6 (0.3-8.0) years. Results. Early mortality was 1.6%. Late survival rate was 93.5%. Recurrent aortic arch obstruction was revealed in 10 (8%) patients, on the average, in 6.5 (3.5-15) months after coarctation repair. Management of re-stenosis with balloon aortoplasty was effective in all cases and had no complications. A statistically significant growth (p function show_eabstract() { $('#eabstract1').hide(); $('#eabstract2').show(); $('#eabstract_expand').hide(); }
Aortic arch hypoplasia, coarctation of the aorta, congenital heart disease, extended end-to-end anastomosis, left thoracotomy
Короткий адрес: https://sciup.org/142230669
IDR: 142230669 | DOI: 10.21688/1681-3472-2018-4-12-20