Abstract

This paper presents the immediate outcomes of valve-sparing operations on the aortic valve and ascending aorta in radical correction of congenital and acquired heart disease. Materials and methods. The study enrolled 50 patients with aortic insufficiency who were operated upon at Shumakov National Medical Research Center of Transplantology and Artificial Organs from 2011 to 2019. The mean age was 48 ± 16 years, 64% of them were men (n = 32). The study included patients with tricuspid (n = 36, 72%) and bicuspid (n = 14, 28%) aortic valves. Aortic valve reimplantation was performed in 32 (64%) patients, aortic root remodeling - in 1 (2%). 17 (34%) patients had no aortic root reconstruction or remodeling. Aortic valve reimplantation was done in 4 (8%) cases in combination with coronary artery bypass grafting, and in 4 (8%) with mitral and tricuspid valve repair. Results. Thirty-day mortality was 0%. In 1 case (2%), a permanent pacemaker was installed due to complete atrioventricular block. There were no neurological and coronary events, and cases of endocarditis. In all patients (100%), aortic valve insufficiency after surgical correction did not exceed grade 1 according to echocardiographic follow-up examination. On aortic valve mean and peak gradients were 8 ± 6 and 15 ± 7 mm Hg, respectively. Findings. Type I and II valve-sparing reconstructive surgery (for bicuspid and tricuspid aortic valves) is an excellent alternative to prosthetic repair with great postoperative outcomes, low valve-associated complications and low mortality.

Highlights

  • Valve-sparing operations on the aortic valve and the ascending aorta: radical correction of congenital and acquired heart diseases

  • This paper presents the immediate outcomes of valve-sparing operations on the aortic valve and ascending aorta in radical correction of congenital and acquired heart disease

  • Aortic valve reimplantation was performed in 32 (64%) patients, aortic root remodeling - in 1 (2%). 17 (34%) patients had no aortic root reconstruction or remodeling

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Summary

Материалы и методы

В исследование вошли 50 пациентов с аортальной недостаточностью, оперированные в нашем центре с 2011-го по 2019 г. В исследование вошли пациенты с трехстворчатым (n = 36, 72%) и дву­ створ­чатым (n = 14, 28%) аортальными клапанами. У 5 пациентов (10%) был диагностированный синд­ ром Марфана. Всем пациентам до операции были проведены стандартные обследования (электрокардиография, эхокардиография, рентгеновская спиральная компьютерная томография органов грудной клетки с контрастированием, а также обследования для исключения сопутствующей патологии). 1. У 47 пациентов коррекция порока выполнена через срединную стернотомию (94%), в остальных – через верхнюю срединную мини-стернотомию. Канюляция проводилась в аорту и правое предсердие, дренирование левого желудочка проводили через правую верхнюю легочную вену. При сочетанной и комбинированной патологии использовались две канюли в нижнюю и верхнюю полые вены. При изолированном поражении проводилась кровяная гиперкалиевая кардиоплегия по методике Калафиори, при сочетанной патологии – кустодиол. Объемы и кратность введения варьировались в зависимости от характеристики пациента и объема выполняемого хирургического вмешательства

Клиническое наблюдение
Непосредственные результаты
Findings
Surgical correction and postoperative indicators
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