Kiernan Michael S, Grandin E Wilson, Brinkley Marshall, Kapur Navin K, Pham Duc Thinh, Ruthazer Robin, Rame J Eduardo, Atluri Pavan, Birati Edo Y, Oliveira Guilherme H, Pagani Francis D, Kirklin James K, Naftel David, Kormos Robert L, Teuteberg Jeffrey J, DeNofrio David
From the Cardiovascular Center, Tufts Medical Center, Boston, MA (M.S.K., N.K.K., D.D.); Cardiovascular Institute, Beth Israel Deaconess Medical Center, Boston, MA (E.W.G.); Heart and Vascular Institute, Vanderbilt University Medical Center, Nashville, TN (M.B.); Division of Cardiothoracic Surgery, Northwestern Memorial Hospital, Chicago, IL (D.T.P.); Clinical and Translational Science Institute, Tufts University, Boston, MA (R.R.); Heart and Vascular Institute, University of Pennsylvania, Philadelphia (J.E.R., E.Y.B.); Division of Cardiology, University Hospitals, Cleveland, OH (P.A., G.H.O.); Division of Cardiothoracic Surgery, University of Michigan School of Medicine, Ann Arbor (F.D.P.); Division of Cardiothoracic Surgery, University of Alabama Birmingham School of Medicine (J.K.K.); University of Alabama Birmingham School of Public Health (D.N.); and Heart and Vascular Institute, University of Pittsburgh Medical Center, PA (R.L.K., J.J.T.).
Circ Heart Fail. 2017 Oct;10(10). doi: 10.1161/CIRCHEARTFAILURE.117.003863.
To investigate preimplant risk factors associated with early right ventricular assist device (RVAD) use in patients undergoing continuous-flow left ventricular assist device (LVAD) surgery.
Patients in the Interagency Registry for Mechanically Assisted Circulatory Support who underwent primary continuous-flow-LVAD surgery were examined for concurrent or subsequent RVAD implantation within 14 days of LVAD. Risk factors for RVAD implantation and the combined end point of RVAD or death within 14 days of LVAD were assessed with stepwise logistic regression. We compared survival between patients with and without RVAD using Kaplan-Meier method and Cox proportional hazards modeling. Of 9976 patients undergoing continuous-flow-LVAD implantation, 386 patients (3.9%) required an RVAD within 14 days of LVAD surgery. Preimplant characteristics associated with RVAD use included interagency registry for mechanically assisted circulatory support patient profiles 1 and 2, the need for preoperative extracorporeal membrane oxygenation or renal replacement therapy, severe preimplant tricuspid regurgitation, history of cardiac surgery, and concomitant procedures other than tricuspid valve repair at the time of LVAD. Hemodynamic determinants included elevated right atrial pressure, reduced pulmonary artery pulse pressure, and reduced stroke volume. The final model demonstrated good performance for both RVAD implant (area under the curve, 0.78) and the combined end point of RVAD or death within 14 days (area under the curve, 0.73). Compared with patients receiving an isolated LVAD, patients requiring RVAD had decreased 1- and 6-month survival: 78.1% versus 95.8% and 63.6% versus 87.9%, respectively (<0.0001 for both).
The need for RVAD implantation after LVAD is associated with indices of global illness severity, markers of end-organ dysfunction, and profiles of hemodynamic instability.
探讨在接受连续流左心室辅助装置(LVAD)手术的患者中,与早期使用右心室辅助装置(RVAD)相关的植入前风险因素。
对机构间机械辅助循环支持注册中心中接受初次连续流LVAD手术的患者,在LVAD植入后14天内进行了同期或后续RVAD植入情况的检查。采用逐步逻辑回归评估RVAD植入的风险因素以及LVAD植入后14天内RVAD或死亡的联合终点。我们使用Kaplan-Meier方法和Cox比例风险模型比较了使用和未使用RVAD患者的生存率。在9976例接受连续流LVAD植入的患者中,386例(3.9%)在LVAD手术后14天内需要RVAD。与使用RVAD相关的植入前特征包括机构间机械辅助循环支持患者档案1和2、术前需要体外膜肺氧合或肾脏替代治疗、植入前严重三尖瓣反流、心脏手术史以及LVAD植入时除三尖瓣修复外的其他伴随手术。血流动力学决定因素包括右心房压力升高、肺动脉脉压降低和每搏量减少。最终模型对RVAD植入(曲线下面积,0.78)和LVAD植入后14天内RVAD或死亡的联合终点(曲线下面积,0.73)均显示出良好的性能。与仅接受LVAD的患者相比,需要RVAD的患者在术后1个月和6个月的生存率降低:分别为78.1%对95.8%和63.6%对87.9%(两者均<0.0001)。
LVAD术后需要植入RVAD与整体疾病严重程度指标、终末器官功能障碍标志物以及血流动力学不稳定情况有关。