Early recognition and improved outcomes of ischemic heart disease has resulted in an aging population and a global increase in the prevalence of heart failure (HF).1 Consequently, the burden of stage D heart failure (HF), which is unresponsive to conventional medical therapy, has surpassed the availability of the finite donor organ pool. 2 Significant advances in the field of mechanical circulatory support has made destination therapy (DT) with left ventricular assist devices (LVADs) a promising alternative to heart transplantation, with 1-year postimplant actuarial survival at about 80% with a continuous flow LVAD (CF-LVAD).
3However, despite newer technology and greater familiarity with patient management, physicians continue to be confronted by early and/or late right ventricular failure (RVF) that significantly impacts survival post-LVAD implantation. As none of the current mechanical circulatory support (MCS) devices are approved for DT for solitary right heart support or biventricular support, it is critical to identify preoperative predictors of right heart failure post-LVAD implant.
Definition and Incidence of Right Ventricular Failure after LVAD PlacementIn the absence of a universally agreed-upon definition of RVF after LVAD placement, its reported incidence varies with the institutional practice, the United Network for Organ Sharing (UNOS) indication for MCS, the device type, and the criteria used to define failure. Additionally, it is now recognized that RVF is a progressive condition that can occur beyond the immediate postoperative period. However, this emerging concept of "late RVF" remains ill-defined and difficult to predict. The Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS) defines RVF as persistent signs and symptoms of RV dysfunction evident by central venous pressure (CVP) > 18 mm Hg with a cardiac index (CI) < 2.0 L/min/m 2 in the absence of increased left atrial filling pressure/pulmonary capillary wedge pressure (PCWP) > 18 mm Hg, cardiac tamponade, ventricular arrhythmias, and/or pneumothorax requiring either right ventricular assist device (RVAD) implantation or inhaled nitric oxide or inotropic therapy for ≥ 14 days after LVAD implantation. 4 According to INTERMACS, RVF severity is described as follows:• Severe, when there is a need for RVAD; • Moderate, when inotropes or intravenous or inhaled pulmonary vasodilators are used; and • Mild, when a combination of ≥ 2 signs and symptoms are present but without the need for RVAD or inotropic and/ or vasodilator support. Signs and symptoms include CVP > 18 mm Hg, CI < 2.3 L/min/m 2 , ascites, moderate to severe peripheral edema, or evidence of high CVP on physical exam or transthoracic echocardiogram.The incidence of severe RVF necessitating RVAD placement after LVAD or preemptive BiVAD support is reported to be anywhere from 9.4% to 37.0%. [5][6][7][8][9] Most studies have reported the incidence encompassing the need for inotropic support with or without RVAD (≥ 14 days) after LVAD implant, with a range of b...