Sheikh Farooq H, Ravichandran Ashwin K, Goldstein Daniel J, Agarwal Richa, Ransom John, Bansal Aditya, Kim Gene, Cleveland Joseph C, Uriel Nir, Sheridan Brett C, Chomsky Don, Patel Snehal R, Dirckx Nick, Franke Abi, Mehra Mandeep R
Medstar Heart and Vascular Institute, Washington, DC (F.H.S.).
Ascension St Vincent, Indianapolis, IN (A.K.R.).
Circ Heart Fail. 2021 Oct;14(10):e008360. doi: 10.1161/CIRCHEARTFAILURE.120.008360. Epub 2021 Sep 16.
Heart failure disproportionately affects Black patients. Whether differences among race influence outcomes in advanced heart failure with use of a fully magnetically levitated continuous-flow left ventricular assist device remains uncertain.
We included 515 IDE (Investigational Device Exemption) clinical trial patients and 500 Continued Access Protocol patients implanted with the HeartMate 3 left ventricular assist device in the MOMENTUM 3 study (Multicenter Study of MagLev Technology in Patients Undergoing Mechanical Circulatory Support Therapy With HeartMate 3). Outcomes were compared between Black and White left ventricular assist device recipients for the primary end point of survival free of disabling stroke or reoperation to replace or remove a malfunctioning device at 2 years, overall survival, adverse events, 6-minute walk distance, and quality of life scores.
Of 1015 HeartMate 3 patients, 675 were self-identified as White and 285 as Black individuals. The Black patient cohort was younger, more obese and with a history of hypertension, and more nonischemic cause of heart failure, relative to the White patient group. Black and White patients did not experience a difference in the primary end point (81.1% versus 77.9%; hazard ratio, 1.08 [95% CI, 0.76-1.54], =0.6568). Black patients were at higher risk of adverse events (calculated as events per 100 patient-years), including bleeding (75.4 versus 63.5; <0.0001), stroke (9.5 versus 7.2; =0.0183), and hypertension (10.1 versus 3.2; <0.0001). The 6-minute walk distance was not different at baseline and 6 months between the groups, however, the absolute change from baseline was greater for White patients (median: +183.0 [interquartile range, 42.0-335.3] versus +163.8 [interquartile range, 42.3-315.0] meters, =0.01). The absolute quality of life measurement (EuroQoL group, 5-dimension, 5-level instrument visual analog scale) at baseline and 6 months was better in the Black patient group, but relative improvement from baseline to 6 months was greater in White patients (median: +20.0 [interquartile range, 5.0-40.0] versus +25.0 [interquartile range, 10.0-45.0]; =0.0298).
Although the survival free of disabling stroke or reoperation to replace/remove a malfunctioning device at 2 years with the HM 3 left ventricular assist device did not differ by race, Black HeartMate 3 patients experienced a higher morbidity burden and smaller gains in functional capacity and quality of life when compared with White patients. These findings require efforts designed to better understand and overcome these gaps through systematic identification and tackling of putative factors. Registration: URL: https://www.clinicaltrials.gov; Unique identifiers: NCT02224755 and NCT02892955.
心力衰竭对黑人患者的影响尤为严重。种族差异是否会影响使用完全磁悬浮连续流左心室辅助装置治疗晚期心力衰竭的预后仍不确定。
我们纳入了MOMENTUM 3研究(使用HeartMate 3进行机械循环支持治疗的患者的磁悬浮技术多中心研究)中515名接受研究器械豁免(IDE)临床试验的患者和500名接受持续接入方案的患者,这些患者均植入了HeartMate 3左心室辅助装置。比较了黑人和白人左心室辅助装置接受者在2年时无致残性中风或再次手术以更换或移除故障装置的生存这一主要终点、总生存率、不良事件、6分钟步行距离和生活质量评分方面的差异。
在1015名HeartMate 3患者中,675名自述为白人,285名自述为黑人。与白人患者组相比,黑人患者队列更年轻、更肥胖且有高血压病史,且因非缺血性原因导致心力衰竭的比例更高。黑人和白人患者在主要终点方面无差异(81.1%对77.9%;风险比,1.08[95%CI,0.76 - 1.54],P = 0.6568)。黑人患者发生不良事件的风险更高(以每100患者年的事件数计算),包括出血(75.4对63.5;P < 0.0001)、中风(9.5对7.2;P = 0.0183)和高血压(10.1对3.2;P < 0.0001)。两组在基线和6个月时的6分钟步行距离无差异,然而,白人患者从基线的绝对变化更大(中位数:+183.0[四分位间距,42.0 - 335.3]对+163.8[四分位间距,42.3 - 315.0]米,P = 0.01)。在基线和6个月时,黑人患者组的绝对生活质量测量值(欧洲生活质量小组,5维度、5水平仪器视觉模拟量表)更好,但白人患者从基线到6个月的相对改善更大(中位数:+20.0[四分位间距,5.0 - 40.0]对+25.0[四分位间距,10.0 - 45.0];P = 0.0298)。
尽管使用HM 3左心室辅助装置在2年时无致残性中风或再次手术以更换/移除故障装置的生存率在种族上没有差异,但与白人患者相比,黑人HeartMate 3患者的发病负担更高,功能能力和生活质量的改善更小。这些发现需要通过系统识别和解决假定因素来努力更好地理解和克服这些差距。注册:网址:https://www.clinicaltrials.gov;唯一标识符:NCT02224755和NCT02892955。