TY - JOUR
T1 - Variation in Antithrombotic Therapy and Clinical Outcomes in Patients With Preexisting Atrial Fibrillation Undergoing Transcatheter Aortic Valve Replacement
T2 - Insights From the Society of Thoracic Surgeons/American College of Cardiology Transcatheter Valve Therapy Registry
AU - Sherwood, Matthew W.
AU - Gupta, Aakriti
AU - Vemulapalli, Sreekanth
AU - Li, Zhuokai
AU - Piccini, Jonathan
AU - Harrison, J. Kevin
AU - Dai, David
AU - Vora, Amit N.
AU - Mack, Michael J.
AU - Holmes, David R.
AU - Rumsfeld, John S.
AU - Cohen, David J.
AU - Thourani, Vinod H.
AU - Kirtane, Ajay J.
AU - Peterson, Eric D.
N1 - Funding Information:
Dr Gupta is supported by the National Institutes of Health training grant T32 HL007854.
Funding Information:
Dr Sherwood reports personal fees from Medtronic outside the submitted work. Dr Gupta reports other from Edwards Lifesciences, Arnold & Porter law firm, Ben C. Martin law firm, and Heartbeat Health, Inc, outside the submitted work. Dr Ve-mulapalli reports grants from the American College of Cardiology and Society of Thoracic Surgeons during the conduct of the study; grants and personal fees from Boston Scientific; grants from Abbott outside the submitted work; and National Institutes of Health (R01 and SBIR), Janssen (advisory board), Boston Scientific (advisory board), HeartFlow (consulting), and American College of Physicians (consulting). Dr Piccini reports grants from Abbott, Bayer, American Heart Association, Philips, and Boston Scientific and other from Medtronic outside the submitted work. Dr Harrison reports grants from Edwards Lifesciences, Medtronic, Inc, Abbott/St. Jude, and Boston Scientific during the conduct of the study. Dr Vora reports personal fees from Medtronic during the conduct of the study. Dr Mack reports nonfinancial support from Abbott, Edwards Lifesciences, and Medtronic during the conduct of the study. Dr Cohen reports grants and personal fees from Edwards Lifesciences, Medtronic, Boston Scientific, and Abbott outside the submitted work. Dr Kirtane reports Institutional funding to the Columbia University or Cardiovascular Research Foundation from Medtronic, Boston Scientific, Abbott Vascular, Abiomed, Cardiovascular Systems, Inc, CathWorks, Siemens, Philips, and ReCor Medical. In addition to research grants, institutional funding includes fees paid to the Columbia University or Cardiovascular Research Foundation for speaking engagements and consulting. Personal: consulting at Neurotronic; travel expenses/meals from Medtronic, Boston Scientific, Abbott Vascular, Abiomed, Cardiovascular Systems, Inc, CathWorks, Siemens, Philips, ReCor Medical, Chiesi, OpSens, Zoll, and Regeneron. Dr Peterson reports grants and personal fees from Bristol Myers Squibb, Janssen, Pfizer, AstraZeneca, and Amgen and grants from Sanofi during the conduct of the study. The other authors report no conflicts.
Publisher Copyright:
© 2021 Lippincott Williams and Wilkins. All rights reserved.
PY - 2021/4/1
Y1 - 2021/4/1
N2 - Background: Optimal antithrombotic management of patients with preexisting atrial fibrillation undergoing transcatheter aortic valve replacement is challenging given the need to balance the risk of bleeding and thromboembolism. We aimed to examine variation in care and association of antithrombotic therapies with 1-year outcomes of stroke, bleeding, and mortality in patients undergoing transcatheter aortic valve replacement with concomitant atrial fibrillation in the United States. Methods: Patients who underwent transcatheter aortic valve replacement with preexisting atrial fibrillation from November 2011 through September 2015 in the Society of Thoracic Surgeons/American College of Cardiology Transcatheter Valve Therapy registry linked to the Medicare database were examined according to receipt of oral anticoagulants (OACs) or antiplatelet therapies (APTs) or a combination of these (OAC+APT) at discharge. To assess the associations of antithrombotic therapies with 1-year outcomes of stroke, bleeding, and mortality, we utilized inverse probability weighting for antithrombotic therapies and multivariable regression modeling to adjust for patient- and hospital-level variables. Results: In the 11 382 patients included in our study, 5833 (51.2%) were discharged on OAC+APT, 4786 (42.0%) on APT alone, and 763 (6.7%) on OAC alone. There was significant variability in discharge medication patterns, including 42% of patients discharged without OAC therapy. In adjusted analyses, the risk for all-cause mortality and stroke was not significantly different when comparing the 3 different antithrombotic strategies. Risk of bleeding was higher with OAC+APT compared with APT alone (hazard ratio, 1.16 [95% CI, 1.05-1.27]) and similar compared with OAC alone (hazard ratio, 1.17 [95% CI, 0.93-1.47]). Conclusions: There was significant variability in discharge medication patterns across US sites in patients with atrial fibrillation undergoing transcatheter aortic valve replacement, including significant underuse of OAC in this high-risk cohort. The use of OAC+APT (versus OAC alone or APT alone) was not associated with a lower risk of stroke or mortality but was associated with increased risk of bleeding complications at 1 year compared with APT alone.
AB - Background: Optimal antithrombotic management of patients with preexisting atrial fibrillation undergoing transcatheter aortic valve replacement is challenging given the need to balance the risk of bleeding and thromboembolism. We aimed to examine variation in care and association of antithrombotic therapies with 1-year outcomes of stroke, bleeding, and mortality in patients undergoing transcatheter aortic valve replacement with concomitant atrial fibrillation in the United States. Methods: Patients who underwent transcatheter aortic valve replacement with preexisting atrial fibrillation from November 2011 through September 2015 in the Society of Thoracic Surgeons/American College of Cardiology Transcatheter Valve Therapy registry linked to the Medicare database were examined according to receipt of oral anticoagulants (OACs) or antiplatelet therapies (APTs) or a combination of these (OAC+APT) at discharge. To assess the associations of antithrombotic therapies with 1-year outcomes of stroke, bleeding, and mortality, we utilized inverse probability weighting for antithrombotic therapies and multivariable regression modeling to adjust for patient- and hospital-level variables. Results: In the 11 382 patients included in our study, 5833 (51.2%) were discharged on OAC+APT, 4786 (42.0%) on APT alone, and 763 (6.7%) on OAC alone. There was significant variability in discharge medication patterns, including 42% of patients discharged without OAC therapy. In adjusted analyses, the risk for all-cause mortality and stroke was not significantly different when comparing the 3 different antithrombotic strategies. Risk of bleeding was higher with OAC+APT compared with APT alone (hazard ratio, 1.16 [95% CI, 1.05-1.27]) and similar compared with OAC alone (hazard ratio, 1.17 [95% CI, 0.93-1.47]). Conclusions: There was significant variability in discharge medication patterns across US sites in patients with atrial fibrillation undergoing transcatheter aortic valve replacement, including significant underuse of OAC in this high-risk cohort. The use of OAC+APT (versus OAC alone or APT alone) was not associated with a lower risk of stroke or mortality but was associated with increased risk of bleeding complications at 1 year compared with APT alone.
KW - atrial fibrillation
KW - cohort studies
KW - hospitals
KW - probability
KW - transcatheter aortic valve replacement
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U2 - 10.1161/CIRCINTERVENTIONS.120.009963
DO - 10.1161/CIRCINTERVENTIONS.120.009963
M3 - Article
C2 - 33877866
AN - SCOPUS:85104851055
SN - 1941-7640
VL - 14
SP - E009963
JO - Circulation: Cardiovascular Interventions
JF - Circulation: Cardiovascular Interventions
IS - 4
ER -