One and One-Half Ventricle Repair: Role for Restricting Antegrade Pulmonary Blood Flow

被引:3
|
作者
Prasanna, Anagha
Tan, Corinne W.
Anastasopulos, Alexandra
Beroukhim, Rebecca S.
Emani, Sitaram M.
机构
[1] Harvard Med Sch, Boston, MA 02115 USA
[2] Harvard Med Sch, Boston Childrens Hosp, Dept Cardiovasc Surg, Boston, MA 02115 USA
[3] Boston Childrens Hosp, SIMPeds, Boston, MA 02115 USA
[4] Harvard TH Chan Sch Publ Hlth, Dept Global Hlth & Populat, Boston, MA USA
[5] Boston Childrens Hosp, Dept Cardiol, Boston, MA 02115 USA
来源
ANNALS OF THORACIC SURGERY | 2022年 / 114卷 / 01期
关键词
BIDIRECTIONAL CAVOPULMONARY ANASTOMOSIS; VENOUS COLLATERAL DEVELOPMENT; SUPERIOR VENA-CAVA; ARTERIOVENOUS-MALFORMATIONS; GLENN;
D O I
10.1016/j.athoracsur.2021.04.058
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND In patients with hypoplastic subpulmonary ventricles, the one and one-half ventricle (1.5V) repair is an alternative to the Fontan procedure. However, in 1.5V-treated patients with pulsatile pulmonary blood flow, superior vena cava (SVC) hypertension or right atrial hypertension may develop. This study aimed to (1) describe patient outcomes after 1.5V repair and (2) determine whether pulmonary artery septation at 1.5V repair confers a lower risk of SVC or right atrial hypertension. METHODS This study retrospectively reviewed patients who underwent a 1.5V repair between 1989 and 2020. The primary outcome was transplant-free survival. Secondary outcomes were postoperative SVC hypertension (defined by mean Glenn pressures greater than 17 mm Hg, SVC flow reversal or pulsatility, venovenous collateral vessels, or SVC syndrome) and right atrial hypertension (defined as mean right atrial pressures greater than 10 mm Hg with inferior vena cava and hepatic vein dilation or flow reversal). RESULTS A total of 74 patients underwent 1.5V repair at a median age of 29.6 months (interquartile range, 8.9 to 45.5 months). Median follow-up time was 39.9 months (interquartile range, 11.4 to 178.1 months). Transplant-free survival at 10 years was 92.4%. Among survivors, 12% (8 of 69) had right atrial hypertension and 39% (27 of 69) had SVC hypertension on follow-up. Survivors with unseptated pulmonary arteries had a greater risk of SVC hypertension compared with patients with septated pulmonary arteries (44% vs 10%; P [.04). No difference was found in right atrial hypertension between the 2 groups. CONCLUSIONS Patients with 1.5V repair avoid Fontan-associated complications with favorable transplant-free survival. However, SVC hypertension remains a significant long-term complication. Pulmonary artery septation at 1.5V repair may reduce the risk of SVC hypertension. (C) 2022 by The Society of Thoracic Surgeons
引用
收藏
页码:176 / 183
页数:8
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