Cowger Jennifer Ann, Castle Lindsay, Aaronson Keith David, Slaughter Mark S, Moainie Sina, Walsh Mary, Salerno Christopher
From the *Division of Cardiology, St. Vincent Heart Center of Indiana, Indianapolis, Indiana; †Division of Cardiovascular Medicine, University of Michigan Health System, Ann Arbor, Michigan; ‡Division of Cardiothoracic Surgery, University of Louisville, Louisville, Kentucky; and §Cardiothoracic Surgery, St. Vincent Heart Center of Indiana, Indianapolis, Indiana.
ASAIO J. 2016 May-Jun;62(3):281-5. doi: 10.1097/MAT.0000000000000362.
The aim of this study was to evaluate the performance of an adjusted HeartMate II risk score (HMRS) in Interagency Registry for Mechanically Assisted Circulatory Support (INTERMACS; n = 9,733) and in HeartWare Ventricular Assist Device (HVAD) bridge to transplant (BTT) trial patients (n = 360). Interagency Registry for Mechanically Assisted Circulatory Support data were used to calculate an adjusted HMRS, omitting center volume, for all patients on continuous-flow left ventricular assist device (LVAD) support. Ninety day mortality was then evaluated in INTERMACS and HVAD-BTT patients. Four risk groups were identified based on INTERMACS patient-adjusted HMRS: very low (<5%, 90 day mortality; score <0.20), low (5-10%, 90 day mortality; score 0.20-1.97), medium (10-20%, 90 day mortality; score 1.98-4.48), and high risk (>20%, 90 day mortality; score >4.48). Within INTERMACS, there were significant differences in survival between all-adjusted HMRS risk groups (p < 0.001 in pairwise comparisons). Controlling for known mortality correlates, the adjusted HMRS mortality hazard ratio was 1.19 (1.25-1.23) per unit HMRS increase. The HVAD cohort was a low-risk cohort with 90 day survivals for very low-, low-, and medium-risk patients of 100%, 97 ± 1.1%, and 90 ± 3.6%, respectively (p = 0.007). Patients in the very low- and low-risk group had significantly improved survival compared with medium-risk patients, respectively (both p < 0.05). The adjusted HMRS appropriately risk stratified a large cohort of INTERMACS patients and was predictive of survival in HeartWare-supported patients.
本研究的目的是评估调整后的HeartMate II风险评分(HMRS)在机构间机械辅助循环支持注册研究(INTERMACS;n = 9733)以及HeartWare心室辅助装置(HVAD)过渡到移植(BTT)试验患者(n = 360)中的表现。利用机构间机械辅助循环支持注册研究的数据,为所有接受连续流左心室辅助装置(LVAD)支持的患者计算调整后的HMRS,不包括中心容量。然后评估INTERMACS和HVAD-BTT患者的90天死亡率。根据INTERMACS患者调整后的HMRS确定了四个风险组:极低风险(90天死亡率<5%;评分<0.20)、低风险(90天死亡率5-10%;评分0.20-1.97)、中等风险(90天死亡率10-20%;评分1.98-4.48)和高风险(90天死亡率>20%;评分>4.48)。在INTERMACS中,所有调整后的HMRS风险组之间的生存率存在显著差异(两两比较p < 0.001)。在控制已知的死亡率相关因素后,调整后的HMRS死亡率风险比为每单位HMRS增加1.19(1.25-1.23)。HVAD队列是一个低风险队列,极低风险、低风险和中等风险患者的90天生存率分别为100%、97±1.1%和90±3.6%(p = 0.007)。极低风险和低风险组患者的生存率分别与中等风险患者相比有显著改善(均p < 0.05)。调整后的HMRS对大量INTERMACS患者进行了适当的风险分层,并可预测接受HeartWare支持患者的生存率。