Takajo Daiji, Critser Paul J, Cash Michelle, Magness Melissa, Hirsch Russel
Heart Institute Cincinnati Children's Hospital Medical Center Cincinnati OH USA.
Department of Pediatrics, College of Medicine University of Cincinnati Cincinnati OH USA.
J Am Heart Assoc. 2025 Jan 21;14(2):e037908. doi: 10.1161/JAHA.124.037908. Epub 2025 Jan 17.
Pulmonary vein stenosis in children is associated with a poor prognosis. However, the cause and risk factors for mortality remain uncertain.
This retrospective, single-center study identified children with primary and secondary pulmonary vein stenosis through a cardiac catheterization database. Kaplan-Meier analysis, log-rank tests, and Cox regression analysis were performed to assess outcome and identify significant predictors of mortality.
Among 56 children with pulmonary vein stenosis (33 male children, 59%), 20 (36%) died at a median age of 10 months (interquartile range, 4-24 months). All patients underwent cardiac catheterization, with 45 (80%) undergoing at least 1 interventional procedure. Causes of death included multiorgan failure (35%), progressive respiratory failure (20%), and sudden cardiac death (15%). Prematurity, chronic lung disease, a genetic syndrome, or the number of affected pulmonary veins did not significantly correlate with mortality. However, right ventricular (RV) systolic pressure greater than half systemic pressure was associated with mortality (hazard ratio [HR], 5.5 [95% CI, 2.2-14.1]; <0.001). The final predictive model for mortality included RV systolic pressure greater than half systemic pressure (HR, 4.0 [95% CI, 1.6-10.4]; =0.004), moderately or severely diminished RV systolic function (HR, 3.6 [95% CI, 1.1-11.5]; =0.032), and the presence of congenital heart disease (HR, 2.4 [95% CI, 0.9-6.7]; =0.084).
This report is the first to indicate that RV systolic pressure and RV dysfunction are significant independent predictors of mortality in children with pulmonary vein stenosis. A greater understanding of mortality in this population is necessary, particularly in those with RV systolic pressure less than half systemic.
儿童肺静脉狭窄与预后不良相关。然而,死亡率的原因和危险因素仍不确定。
这项回顾性单中心研究通过心脏导管插入术数据库确定了原发性和继发性肺静脉狭窄的儿童。进行了Kaplan-Meier分析、对数秩检验和Cox回归分析,以评估结局并确定死亡率的重要预测因素。
在56例肺静脉狭窄儿童中(33例男童,占59%),20例(36%)死亡,中位年龄为10个月(四分位间距为4 - 24个月)。所有患者均接受了心脏导管插入术,其中45例(80%)至少接受了1次介入手术。死亡原因包括多器官功能衰竭(35%)、进行性呼吸衰竭(20%)和心源性猝死(15%)。早产、慢性肺病、遗传综合征或受累肺静脉数量与死亡率无显著相关性。然而,右心室(RV)收缩压大于体循环压力的一半与死亡率相关(风险比[HR]为5.5[95%置信区间,2.2 - 14.1];P<0.001)。死亡率的最终预测模型包括右心室收缩压大于体循环压力的一半(HR为4.0[95%置信区间,1.6 - 10.4];P = 0.004)、右心室收缩功能中度或重度降低(HR为3.6[95%置信区间,1.1 - 11.5];P = 0.032)以及存在先天性心脏病(HR为2.4[95%置信区间,0.9 - 6.7];P = 0.084)。
本报告首次表明右心室收缩压和右心室功能障碍是儿童肺静脉狭窄死亡率的重要独立预测因素。有必要更深入了解该人群的死亡率,尤其是右心室收缩压低于体循环压力一半的患者。