Department of Surgery, Division of Cardiothoracic Surgery, University of Colorado Anschutz Medical Center, Aurora, Colorado 80045, USA.
J Heart Lung Transplant. 2011 Aug;30(8):862-9. doi: 10.1016/j.healun.2011.04.004. Epub 2011 May 31.
Patients requiring biventricular assist device (BiVAD) for mechanical circulatory support (MCS) have substantially worse outcomes than patients requiring left VAD (LVAD) support only. Patient-specific risk factors have yet to be consistently identified in a large, multicenter registry, which may underlie the poorer outcomes for BiVAD patients. The Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS) is a registry of U.S. Food and Drug Administration-approved durable MCS devices used for bridge-to-transplantation, destination therapy, or recovery. The purposes of this study were to 1) identify the underlying pre-implant characteristics of the population requiring BiVAD support that contribute to reduced survival, and 2) identify differences in postoperative outcomes with respect to adverse events compared with patients supported with LVAD alone.
From June 2006 to September 2009, 1,646 patients were entered into the INTERMACS database in which adverse events and outcomes were recorded for primary implants with LVAD or BiVAD. Competing outcomes methodology was used to estimate the time-related probability of death, transplant, or recovery. Overall survival for all groups was analyzed with Kaplan-Meier methods and Cox proportional regression analysis.
The distribution of primary device implants included 1,440 LVADs and 206 BiVADs. BiVAD patients presented with a lower INTERMACS profile 93% in INTERMACS 1 or 2, compared with 73% for LVAD patients (p < 0.001). Survival at 6 months was 86% for LVADs and 56% for BiVADs (p < .0001). Adverse event rates, expressed as episodes/100 patient-months for the BiVAD group compared with LVAD, were significantly higher for infection (33.2 vs 14.3), bleeding (71.6 vs 15.5), neurologic events (7.9 vs 2.6), and for device failure (4.9 vs 2.0).
Patients requiring BiVAD support at the time of durable MCS implant are more critically ill at the time of MCS implant. BiVAD patients experience worse survival than patients supported with LVAD alone and higher rates of serious adverse events. Characteristics of the population present at the time of BiVAD implant likely influence post-implant MCS outcomes.
需要双心室辅助装置(BiVAD)进行机械循环支持(MCS)的患者的预后明显比仅需要左心室辅助装置(LVAD)支持的患者差。在一个大型多中心注册中心中,尚未一致确定患者特异性的风险因素,这可能是 BiVAD 患者预后较差的原因。机械循环辅助机构间注册(INTERMACS)是美国食品和药物管理局批准的用于桥接移植、终末期治疗或恢复的耐用性机械循环支持设备的注册中心。本研究的目的是:1)确定需要 BiVAD 支持的人群的基础植入前特征,这些特征导致生存率降低;2)与仅接受 LVAD 支持的患者相比,确定术后不良事件的结果差异。
2006 年 6 月至 2009 年 9 月,共有 1646 例患者被纳入 INTERMACS 数据库,其中记录了 LVAD 或 BiVAD 原发性植入的不良事件和结果。使用竞争风险方法估计与死亡、移植或恢复相关的时间相关概率。使用 Kaplan-Meier 方法和 Cox 比例风险回归分析对所有组的总生存率进行分析。
原发性设备植入的分布包括 1440 例 LVAD 和 206 例 BiVAD。BiVAD 患者的 INTERMACS 评分较低,93%为 INTERMACS 1 或 2 级,而 LVAD 患者为 73%(p <0.001)。LVAD 组的 6 个月生存率为 86%,BiVAD 组为 56%(p <0.0001)。BiVAD 组的不良事件发生率(以每 100 例患者-月的发生率表示)与 LVAD 组相比,感染(33.2 比 14.3)、出血(71.6 比 15.5)、神经系统事件(7.9 比 2.6)和设备故障(4.9 比 2.0)显著更高。
在接受耐用性 MCS 植入时需要 BiVAD 支持的患者在 MCS 植入时的病情更危急。BiVAD 患者的生存率比仅接受 LVAD 支持的患者差,严重不良事件的发生率更高。BiVAD 植入时人群的特征可能会影响植入后的 MCS 结果。