Division of Congenital Heart Surgery, Department of Surgery, Baylor College of Medicine and Texas Children's Hospital, Houston, Tex.
Division of Congenital Heart Surgery, Department of Surgery, Baylor College of Medicine and Texas Children's Hospital, Houston, Tex.
J Thorac Cardiovasc Surg. 2022 Feb;163(2):387-395.e3. doi: 10.1016/j.jtcvs.2021.03.058. Epub 2021 Apr 2.
Previous studies have demonstrated increased early mortality and pulmonary vein reintervention for patients with total anomalous pulmonary venous connection (TAPVC) and heterotaxy syndrome (HTX+) compared with patients with TAPVC without heterotaxy syndrome (HTX-). We aimed to evaluate the longitudinal risk of pulmonary vein reintervention and mortality in HTX + patients.
A retrospective review was performed to identify longitudinal interventions in patients with TAPVC seen at a single center from 1995 to 2019. The mean cumulative interventions were described for all patients using the Nelson-Aalen estimator. Survival with TAPVC was described using Kaplan-Meier estimates.
A total of 336 patients were identified with TAPVC, of whom 118 (35%) had heterotaxy syndrome. Functional single ventricles were identified in 106 of these 118 HTX + patients (90%) and in 14 of 218 HTX- patients (6%) (P < .001). Obstructed TAPVC (OBS+) was present in 49 of 118 HTX + patients (42%) and in 87 of 218 HTX- patients (40%) (P = .89). The median duration of follow-up was 6.5 years. Five-year survival was 69% for HTX+/OBS + patients, 72% for HTX+/OBS- patients, 86% for HTX-/OBS + patients, and 95% for HTX-/OBS- patients (P < .0001, log-rank test). The mean number of pulmonary vein interventions at the median follow-up time was greater in the HTX+/OBS + patients compared with HTX+/OBS- patients (mean, 2.0 vs 1.1; P = .030), HTX-/OBS + patients (mean, 1.3; P = .033), and HTX-/OBS- patients (mean, 1.3; P = .029).
Among the 4 cohorts, HTX+ was associated with a higher rate of mortality, and HTX+/OBS+ was associated with a greater number of pulmonary vein interventions. This may be due in part to the high prevalence of single ventricle physiology in the HTX + cohort.
先前的研究表明,与非异构综合征(HTX-)患者相比,完全性肺静脉异常连接(TAPVC)和异构综合征(HTX+)患者的早期死亡率和肺静脉再介入更高。我们旨在评估 HTX+患者肺静脉再介入和死亡率的纵向风险。
对 1995 年至 2019 年在单一中心接受 TAPVC 治疗的患者进行回顾性分析,采用 Nelson-Aalen 估计值描述所有患者的平均累积干预措施。采用 Kaplan-Meier 估计值描述 TAPVC 患者的生存情况。
共确定 336 例 TAPVC 患者,其中 118 例(35%)存在异构综合征。在这 118 例 HTX+患者中,106 例(90%)存在功能性单心室,218 例 HTX-患者中 14 例(6%)存在功能性单心室(P<.001)。49 例 HTX+患者(42%)存在梗阻性 TAPVC(OBS+),218 例 HTX-患者中有 87 例(40%)存在 OBS+(P=.89)。中位随访时间为 6.5 年。HTX+/OBS+患者的 5 年生存率为 69%,HTX+/OBS-患者为 72%,HTX-/OBS+患者为 86%,HTX-/OBS-患者为 95%(P<.0001,对数秩检验)。在中位随访时间时,HTX+/OBS+患者的肺静脉干预次数明显多于 HTX+/OBS-患者(平均值,2.0 比 1.1;P=.030)、HTX-/OBS+患者(平均值,1.3;P=.033)和 HTX-/OBS-患者(平均值,1.3;P=.029)。
在这 4 组中,HTX+与死亡率较高相关,而 HTX+/OBS+与肺静脉介入次数较多相关。这可能部分归因于 HTX+患者中单心室生理学的高患病率。