Evolution of Ventricular Assist Device Support Strategy in Children With Univentricular Physiology

被引:9
作者
Merritt, Taylor
Gazit, Avihu Z.
Carvajal, Horacio
Montgomery, Brock K.
Shepard, Mark
Mehegan, Mary
Canter, Matthew
Miller, Jacob
Eghtesady, Pirooz
Nath, Dilip S.
机构
[1] St Louis Childrens Hosp, Heart Ctr, St Louis, MO 63178 USA
[2] Washington Univ, Sch Med St Louis, Div Pediat Cardiothorac Surg, St Louis, MO USA
[3] Washington Univ, Sch Med St Louis, Pediat Crit Care, St Louis, MO USA
[4] Washington Univ, Dept Pediat, Sch Med St Louis, St Louis, MO 63130 USA
关键词
MECHANICAL CIRCULATORY SUPPORT; TRANSPLANTATION; BRIDGE;
D O I
10.1016/j.athoracsur.2021.09.043
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Since 2012, we have supported 18 children with single ventricle (SV) physiology on ventricular assist devices (VADs) as a bridge to decision, transplantation, or recovery. We provide a detailed report of our cumulative surgical experience and lessons learned from these patients. METHODS We reviewed all SV-VADs between March 2012 and April 2020. Implanted SV-VADs intended for short-term support were excluded. Demographic and clinical data included palliation stage at the time of VAD implantation, cannulation configuration, device type, duration of support, circuit and device interventions, postoperative support, anticoagulation strategy, complications, mortality, and 1-year survival postdischarge. RESULTS Five SV newborns without prior surgical palliation, 8 infants post-Norwood/hybrid procedure, 4 infants post -Glenn, and 1 infant post-Fontan were initially supported with either continuous-flow (n = 13 of 18, 72%) or pulsatile-flow (n = 5 of 18, 28%) devices. Three (17%) of 18 transitioned to another device during support. Before VAD conversion, 9 (50%) of 18 were supported by extracorporeal membrane oxygenation. Outcomes included 7 (39%) of 18 who trans-planted, 2 (11%) of 18 who recovered, and 9 (50%) of 18 who died before discharge. Of these deaths, 2 occurred after transplantation and 2 after explantation, and 5 had redirection of care while on support secondary to previously un-diagnosed pulmonary venoocclusive disease (n = 2) or severe neurologic events (n = 3). Overall, 6 (33%) of 18 experienced neurologic injury. At last follow-up, 9 (50%) of 18 children were alive (median 1.2 [interquartile range, 0.8-4.3] years postexplantation/transplantation). CONCLUSIONS Our experience shows that SV children, including newborns, can be successfully bridged to desired endpoints with proper patient selection and using specific cannulation strategies. Continuing utilization of this strategy is warranted for future children requiring VAD support. (Ann Thorac Surg 2022;114:1739-45) (c) 2022 by The Society of Thoracic Surgeons
引用
收藏
页码:1739 / 1744
页数:6
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