Retrograde Flow to Aortic Root Predicts Inferior Cardiopulmonary Performance and Restrictive Lung Physiology in Fontan Circulation

Henri Juhani Pyykkönen MSc , Otto Rahkonen MD, PhD , Heikki Tikkanen MD, PhD , Karim Khanji MSc , Päivi Piirilä MD, PhD , Olli Pitkänen-Argillander MD, PhD
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Abstract

Background

Cardiac output in Fontan circulation depends on systemic venous pressure, pulmonary vascular resistance, and ventricular function. Because myocardial function is dependent on coronary perfusion, we studied whether retrograde flow to aortic root in the mitral/aortic atresia subgroup of hypoplastic left heart syndrome (HLHS) affects cardiopulmonary performance.

Methods

We studied 26 stable Fontan patients (14.4 ± 2.4 years) with right (RV, n = 17) and left (LV, n = 9) systemic ventricle morphology. All RV patients had HLHS and were subdivided according to postnatal flow to the hypoplastic ascending aorta being antegrade (HLHS-A) or retrograde (HLHS-R) due to valve atresia. Physical activity was assessed by questionnaire (LASERI, a questionnaire for Finnish children regarding physical activity), cardiopulmonary exercise test (1-minute ramp protocol), body composition (Biacorpus RX 4000), and muscle fitness (EUROFIT). These data were correlated with the postnatal aorta size and current branch pulmonary artery size index (McGoon index).

Results

Patients with HLHS-R seldom self-reported engagement in vigorous physical activity and had significantly lower cardiopulmonary performance (peak oxygen uptake [VO2peak]) than patients with LV morphology (P = 0.037), but not compared with patients with HLHS-A. Branch pulmonary artery size did not correlate with VO2peak. Patients with HLHS-R had most severe lung restrictions (forced vital capacity z-score –3 ± 0.9, P = 0.0073; forced expiratory volume in 1 second z-score –3.3 ± 1.1, P = 0.001).

Conclusions

Young Fontan patients with LV had better cardiopulmonary performance than patients with HLHS. Patients with HLHS-R were the least active and had the lowest VO2peak and most restrictive lungs. It is important to recognize postnatally single ventricle patients at high risk for inactivity to promote an active and healthy lifestyle.
主动脉根部逆行血流预测方坦循环中较差的心肺功能和限制性肺生理
方丹循环的心输出量取决于全身静脉压、肺血管阻力和心室功能。由于心肌功能依赖于冠状动脉灌注,我们研究了左心发育不全综合征(HLHS)二尖瓣/主动脉闭锁亚组的主动脉根部逆行血流是否影响心肺功能。方法选取右侧(RV, n = 17)和左侧(LV, n = 9)系统脑室形态稳定的Fontan患者26例(14.4±2.4年)。所有RV患者均有HLHS,并根据出生后流向发育不全的升主动脉分为顺行(HLHS- a)或因瓣膜闭锁而逆行(HLHS- r)。身体活动通过问卷(LASERI,芬兰儿童关于身体活动的问卷)、心肺运动测试(1分钟斜坡方案)、身体成分(Biacorpus RX 4000)和肌肉健康(EUROFIT)进行评估。这些数据与出生后主动脉大小和当前肺动脉分支大小指数(McGoon指数)相关。结果HLHS-R患者很少自我报告参与剧烈体育活动,心肺功能(峰值摄氧量[VO2peak])显著低于左室形态患者(P = 0.037),但与HLHS-A患者相比差异无统计学意义。肺动脉分支大小与VO2peak无相关性。HLHS-R患者肺功能受限最严重(强迫肺活量z-score -3±0.9,P = 0.0073;1 s用力呼气量z评分-3.3±1.1,P = 0.001)。结论年轻Fontan左室患者心肺功能优于HLHS患者。HLHS-R患者最不活跃,vo2峰值最低,肺限制最多。重要的是要认识到产后单心室患者缺乏运动的高风险,以促进积极和健康的生活方式。
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