Peng Ed, O'Sullivan John J, Griselli Massimo, Roysam Chandrika, Crossland David, Chaudhari Milind, Wrightson Neil, Butt Tanveer, Parry Gareth, MacGowan Guy A, Schueler Stephan, Hasan Asif
Children's Heart Unit, Freeman Hospital, Newcastle Upon Tyne, United Kingdom; Cardiopulmonary Transplant Unit, Freeman Hospital, Newcastle Upon Tyne, United Kingdom.
Children's Heart Unit, Freeman Hospital, Newcastle Upon Tyne, United Kingdom.
Ann Thorac Surg. 2014 Dec;98(6):2122-9. doi: 10.1016/j.athoracsur.2014.06.054. Epub 2014 Oct 22.
The systemic morphologic right ventricle (RV) in congenitally corrected transposition of the great arteries or after atrial switch for transposition of the great arteries is associated with late ventricular failure. Although the role of the left ventricular assist device (LVAD) in supporting the failing LV is established, the indications and outcomes of using LVAD in a systemic RV remain unclear. We assessed the role of a third-generation LVAD for systemic RV support.
Seven patients (mean age, 36 years) received the HeartWare (HeartWare International Inc, Framingham, MA) VAD for systemic RV failure (congenitally corrected transposition of the great arteries in 1 and after atrial switch in 6). Four patients (57%) had severe subpulmonic LV failure, and aggressive perioperative diuresis with or without hemofiltration was used to offload the subpulmonic LV. The indications of VAD were (1) bridge to transplant in 3 and (2) bridge to decision for a high transpulmonary gradient in 4. Transplantation outcome was compared with systemic RV failure without VAD bridge in 19 patients (years 1989 to 2013).
Systemic RV support alone was achieved in all patients, with no early deaths (≤30 days). Overall, 6 (86%) returned home, 3 (44%) received a transplant, 2 (28%) died of noncardiac causes, and 2 (28%) continue on VAD support (median support, 232 days). Repeat catheterization (n = 4) showed an improved median transpulmonary gradient in 3 patients (median 18.5 mm Hg pre-VAD vs 8.0 mm Hg post-VAD). Two bridge-to-decision patients received transplants at 640 and 685 days. The stroke rate on VAD support was 43% (2 thromboembolic and 1 hemorrhagic; 3 with satisfactory recovery). De novo aortic regurgitation was 29% (n = 2; 1 valve replacement). All patients (n = 3) survived transplantation (vs 10.5% early mortality without VAD bridge; p = 1.00) and were well at follow-up (range, 53 to 700 days).
The third-generation VAD provides durable support for systemic RV failure as a bridge to transplant and as a strategy to reduce pulmonary vascular resistance. Although concomitant subpulmonic LV failure is common, systemic RV support alone was achieved in all patients.
在大动脉转位矫正型先天性心脏病或大动脉转位心房调转术后,形态学上的体循环右心室(RV)与晚期心室衰竭相关。虽然左心室辅助装置(LVAD)在支持衰竭的左心室方面的作用已得到确立,但在体循环右心室中使用LVAD的适应证和结果仍不明确。我们评估了第三代LVAD对体循环右心室的支持作用。
7例患者(平均年龄36岁)因体循环右心室衰竭接受了HeartWare(HeartWare International Inc,弗雷明汉,马萨诸塞州)VAD治疗(1例为大动脉转位矫正型先天性心脏病,6例为心房调转术后)。4例患者(57%)存在严重的肺下左心室衰竭,采用积极的围手术期利尿,伴或不伴血液滤过,以减轻肺下左心室负荷。VAD的适应证为:(1)3例用于过渡到移植;(2)4例用于在高跨肺压差情况下过渡到决策。将移植结果与19例(1989年至2013年)未使用VAD过渡的体循环右心室衰竭患者进行比较。
所有患者均实现了单纯体循环右心室支持,无早期死亡(≤30天)。总体而言,6例(86%)患者回家,3例(44%)接受了移植,2例(28%)死于非心脏原因,2例(28%)继续接受VAD支持(中位支持时间232天)。4例患者再次进行心导管检查显示,3例患者的跨肺压差中位数有所改善(VAD植入前中位数为18.5 mmHg,VAD植入后为8.0 mmHg)。2例过渡到决策的患者分别在640天和685天接受了移植。VAD支持期间的卒中发生率为43%(2例血栓栓塞和1例出血;3例恢复良好)。新发主动脉瓣反流发生率为29%(n = 2;1例进行了瓣膜置换)。所有3例接受移植的患者均存活(未使用VAD过渡的患者早期死亡率为10.5%;p = 1.00),随访时情况良好(范围为53至700天)。
第三代VAD可为体循环右心室衰竭提供持久支持,作为过渡到移植的手段以及降低肺血管阻力的策略。虽然肺下左心室衰竭很常见,但所有患者均实现了单纯体循环右心室支持。