1 Divisions of Cardiology and Cardiothoracic Surgery The Children's Hospital of Philadelphia, Philadelphia PA.
2 Departments of Pediatrics and Surgery Perelman School of Medicine at the University of Pennsylvania Philadelphia PA.
J Am Heart Assoc. 2018 Oct 2;7(19):e009145. doi: 10.1161/JAHA.118.009145.
Background Prenatal diagnosis of single ventricle-type congenital heart disease is associated with improved clinical courses. Prenatal counseling allows for optimal delivery preparations and opportunity for prenatal intervention. Expectant parents frequently ask what the likelihood of survival through staged palliation is and the factors that influence outcome. Our goal was specifically to quantify peri- and postnatal outcomes in this population. Methods and Results We identified all patients with a prenatal diagnosis of single ventricle-type congenital heart disease presenting between July 2004 and December 2011 at our institution. Maternal data, fetal characteristics, and data from the postnatal clinical course were collected for each patient. Kaplan-Meier curves and multivariate analysis with logistic regression were used to evaluate variables associated with decreased transplant-free survival. Five hundred two patients were identified, consisting of 381 (76%) right ventricle- and 121 left ventricle-dominant lesions. After prenatal diagnosis, 42 patients did not follow up at our center; 79 (16%) chose termination of pregnancy, and 11 had intrauterine demise with 370 (74%) surviving to birth. Twenty-two (6%) underwent palliative care at birth. Among 348 surviving to birth with intention to treat, 234 (67%) survived to at least 6 months post-Fontan palliation. Presence of fetal hydrops, right ventricle dominance, presence of extracardiac anomalies, and low birthweight were significantly associated with decreased transplant-free survival. Conclusions In patients with a prenatal diagnosis of single ventricle-type congenital heart disease and intention to treat, 67% survive transplant-free to at least 6 months beyond Fontan operation. An additional 5% survive to 4 years of age without transplant or Fontan completion. Fetuses with right ventricle-dominant lesions, extracardiac anomalies, hydrops, or low birthweights have decreased transplant-free survival.
单心室型先天性心脏病的产前诊断与改善临床病程相关。产前咨询可使分娩准备和产前干预的机会最佳化。准父母经常询问通过分期姑息治疗存活的可能性以及影响结果的因素。我们的目标是专门量化该人群的围产期和产后结局。
我们确定了 2004 年 7 月至 2011 年 12 月期间在我们机构接受单心室型先天性心脏病产前诊断的所有患者。为每位患者收集了母亲数据、胎儿特征和产后临床过程数据。使用 Kaplan-Meier 曲线和多变量分析逻辑回归来评估与无移植存活相关的变量。确定了 502 例患者,其中 381 例(76%)为右心室优势病变,121 例为左心室优势病变。产前诊断后,42 例患者未在我们中心随访;79 例(16%)选择终止妊娠,11 例宫内死亡,370 例(74%)存活至分娩。22 例(6%)在出生时接受姑息治疗。在 348 例存活至分娩并打算接受治疗的患者中,234 例(67%)至少在 Fontan 姑息手术后 6 个月存活。胎儿水肿、右心室优势、存在心脏外畸形和低出生体重与无移植存活显著相关。
在有单心室型先天性心脏病产前诊断并打算接受治疗的患者中,67%无移植存活至 Fontan 手术后至少 6 个月。另有 5%无移植或 Fontan 完成存活至 4 岁。右心室优势病变、心脏外畸形、水肿或低出生体重的胎儿无移植存活减少。