TY - JOUR
T1 - Impact of Race on Clinical Outcomes after Implantation with a Fully Magnetically Levitated Left Ventricular Assist Device
T2 - An Analysis from the MOMENTUM 3 Trial
AU - Sheikh, Farooq H.
AU - Ravichandran, Ashwin K.
AU - Goldstein, Daniel J.
AU - Agarwal, Richa
AU - Ransom, John
AU - Bansal, Aditya
AU - Kim, Gene
AU - Cleveland, Joseph C.
AU - Uriel, Nir
AU - Sheridan, Brett C.
AU - Chomsky, Don
AU - Patel, Snehal R.
AU - Dirckx, Nick
AU - Franke, Abi
AU - Mehra, Mandeep R.
N1 - Funding Information:
Dr Sheikh reports speaker honorarium and institutional research support from Abbott. Dr Ravichandran is a speaker honorarium from Abbott and Medtronic. Dr Goldstein is an educator and surgical proctor for Abbott and consultant for Medtronic. Dr Agarwal is an educator for Abbott. Dr Bansal is a consultant and advisory board member for Abbott, AbioMed, and TandemLife, recipient of research grant from TandemLife, and advisory board member for VADovations. Dr Cleveland is a member of clinical events committee for ARIES and data safety monitoring board for repair MR; both are Abbott-sponsored studies. Dr Uriel is part of the Medical Advisory Board of Livemetric. Dr Sheridan is a proctor for Abbott. N. Dirckx is an employee of Abbott. Dr Franke is an employee of Abbott. Dr Mehra reports payment made to his institution from Abbott for consulting and consulting fees from Portola, Bayer, Triple Gene, and Baim Institute for Clinical Research and is an advisory board member for Medtronic, Janssen, NuPulseCV, Leviticus, FineHeart, and Mesoblast. The other authors report no conflicts.
Publisher Copyright:
© 2021 Lippincott Williams and Wilkins. All rights reserved.
PY - 2021/10/1
Y1 - 2021/10/1
N2 - Background: 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. Methods: 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. Results: 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], P=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; P<0.0001), stroke (9.5 versus 7.2; P=0.0183), and hypertension (10.1 versus 3.2; P<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, P=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]; P=0.0298). Conclusions: 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.
AB - Background: 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. Methods: 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. Results: 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], P=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; P<0.0001), stroke (9.5 versus 7.2; P=0.0183), and hypertension (10.1 versus 3.2; P<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, P=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]; P=0.0298). Conclusions: 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.
KW - heart failure
KW - quality of life
KW - race factors
KW - thoracic surgery
KW - treatment outcome
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U2 - 10.1161/CIRCHEARTFAILURE.120.008360
DO - 10.1161/CIRCHEARTFAILURE.120.008360
M3 - Article
C2 - 34525837
AN - SCOPUS:85119458182
SN - 1941-3297
VL - 14
SP - E008360
JO - Circulation: Heart Failure
JF - Circulation: Heart Failure
IS - 10
ER -