Congenital Heart Surgery, Texas Children's Hospital, Baylor College of Medicine, Houston, Tex.
Congenital Heart Surgery, Texas Children's Hospital, Baylor College of Medicine, Houston, Tex.
J Thorac Cardiovasc Surg. 2019 Apr;157(4):1609-1617.e2. doi: 10.1016/j.jtcvs.2018.12.045. Epub 2018 Dec 27.
Our institutional policy is to continue centrifugal-flow ventricular assist device support for 3 months or more without activation on the transplant wait-list for physical recovery and assessment of possible myocardial recovery. We evaluated our single-institutional outcomes with centrifugal-flow ventricular assist device support in children.
Prospectively collected outcomes data in consecutive patients aged 18 years or less with centrifugal-flow ventricular assist device support were reviewed.
There were 40 implantations in 39 patients (28 with cardiomyopathy, 11 with congenital heart disease, including 3 with univentricular physiology). The median support was 8 months (range, 1-79), with 13 patients (33%) supported for 12 months or more and a cumulative duration of 41 patient-years. The median age and weight at implantation were 11 (4-18) years and 35 (14-98) kg, respectively. The median body surface area was 1.1 (0.7-2.2) m, with 16 patients (40%) having a body surface area less than 1.0 m. Thirty-four patients (85%) had Interagency Registry for Mechanically Assisted Circulatory Support 1 or 2. Children with congenital heart disease were significantly smaller (P < .01) and had more prior cardiac interventions (P < .01) than those with cardiomyopathy. There were 2 early mortalities (5%) in children with cardiomyopathy. Of the 38 patients with successful implantations, 36 (95%) were discharged home and managed as outpatients. Overall adverse event rates were 5.1 (bleeding), 0.8 (device malfunction), 6.1 (infection), 3.9 (neurologic dysfunction), and 1.0 (renal dysfunction) (per 100 patient-month). In the 21 patients with cardiomyopathy supported for 3 months or more, 5 (24%) experienced normalization of left ventricular function; 4 underwent successful explantation, and 1 remains on support.
This study demonstrates favorable outcomes of centrifugal-flow ventricular assist device support in children, including those with congenital heart disease, with an increased incidence of cardiac recovery.
我们的机构政策是在等待移植期间,如果患者的身体状况恢复,且有可能出现心肌恢复,继续为心室内离心流辅助装置支持 3 个月或更长时间。我们评估了我们机构内使用心室内离心流辅助装置支持治疗儿童的结果。
回顾性收集连续接受心室内离心流辅助装置支持治疗的年龄在 18 岁或以下的患者的前瞻性采集的结果数据。
39 例患者中进行了 40 例植入术(28 例心肌病,11 例先天性心脏病,包括 3 例单心室生理)。中位支持时间为 8 个月(范围 1-79),13 例(33%)患者支持 12 个月或更长时间,累计患者时间为 41 人年。植入时的中位年龄和体重分别为 11 岁(4-18 岁)和 35 千克(14-98 千克)。中位体表面积为 1.1(0.7-2.2)m,16 例(40%)患者体表面积小于 1.0m。34 例(85%)患者为 Interagency Registry for Mechanically Assisted Circulatory Support 1 或 2 级。先天性心脏病患儿明显更小(P<.01),且有更多的既往心脏介入(P<.01)。在患有心肌病的 2 例早期死亡(5%)患儿中。38 例成功植入的患者中,36 例(95%)出院并作为门诊患者进行管理。总体不良事件发生率为 5.1%(出血)、0.8%(设备故障)、6.1%(感染)、3.9%(神经功能障碍)和 1.0%(肾功能障碍)(每 100 人月)。在接受 3 个月或更长时间支持的 21 例心肌病患者中,5 例(24%)左心室功能正常化;4 例成功进行了心脏移植,1 例仍在支持治疗中。
本研究表明,心室内离心流辅助装置在儿童中的支持效果良好,包括先天性心脏病患儿,心脏恢复的发生率增加。