TY - JOUR
T1 - Comparative Outcomes of Percutaneous Coronary Intervention for ST-Segment-Elevation Myocardial Infarction Among Medicare Beneficiaries With Multivessel Coronary Artery Disease
T2 - An National Cardiovascular Data Registry Research to Practice Project
AU - Secemsky, Eric A.
AU - Butala, Neel
AU - Raja, Aishwarya
AU - Khera, Rohan
AU - Wang, Yongfei
AU - Curtis, Jeptha P.
AU - Maddox, Thomas M.
AU - Virani, Salim S.
AU - Armstrong, Ehrin J.
AU - Shunk, Kendrick A.
AU - Brindis, Ralph G.
AU - Bhatt, Deepak
AU - Yeh, Robert W.
N1 - Funding Information:
Dr Secemsky reports the following: Consulting/Speakers Bureau/Advisory Board: Bard, Cook, CSI, Janssen, Medtronic, Philips; Grants to Institution: As-traZeneca, Bard, Boston Scientific, Cook, CSI, Medtronic, Philips. Dr Butala reports the following: Consulting: Hilabs, Ownership interest: Hilabs. Dr Curtis has a contract with the American College of Cardiology for his role as Senior Medical Officer, National Cardiovascular Data Registry (NCDR); receives salary support from the American College of Cardiology, NCDR; receives funding from the Centers for Medicare & Medicaid Services to develop and maintain performance measures that are used for public reporting; holds equity interest in Medtronic. Dr Maddox discloses current grant funding from the National Institutes of Health (NIH) National Center for Advancing Translational Sciences (NCATS; 1U24TR002306-01: A National Center for Digital Health Informatics Innovation), current consulting for Creative Educational Concepts, Inc, and Atheneum Partners, and honoraria and/or expense reimbursement in the past 3 years from the University of Utah (May 2017), New York Presbyterian (September 2017), Westchester Medical Center (October 2017), Sentara Heart Hospital (December 2018), the Henry Ford health system (March 2019), and the University of California San Diego (January 2020). He is currently employed as a cardiologist and the executive director of the Healthcare Innovation Lab at BJC HealthCare/Washington University School of Medicine. In this capacity, he is advising Myia Labs, for which his employer is receiving equity compensation in the company. He is receiving no individual compensation from the company. He is also a compensated director for a New Mexico-based foundation, the J.F Maddox Foundation. Dr Virani discloses the following: research support from Department of Veterans Affairs, World Heart Federation, Tahir and Jooma Family. Honorarium: American College of Cardiology (Associate Editor for Innovations, acc.org). Steering Committee member: Patient and Provider Assessment of Lipid Management (PALM) registry at the Duke Clinical Research Institute (no financial remuneration). Dr Armstrong discloses the following: consultant/ advisory board for Abbott Vascular, Boston Scientific, Cardiovascular Systems, Gore, Intact Vascular, Medtronic, and Philips. Dr Shunk discloses institutional research support from Siemens Medical Systems, Medinol Ltd, Svelte Medical Systems, Cardiovascular Systems, Inc, Boston Scientific, and Regeneron Pharmaceuticals, Inc; consulting for Terumo, PercAssist and TransAortic Medical, Inc; and equity options in TransAortic Medical and PercAssist. Dr Brindis has a contract with the American College of Cardiology for his role as Senior Medical Officer, NCDR. Dr Bhatt discloses the following relationships—Advisory Board: Cardax, Cereno Scientific, Elsevier Practice Update Cardiology, Medscape Cardiology, PhaseBio, PLx Pharma, Regado Biosciences; Board of Directors: Boston VA Research Institute, Society of Cardiovascular Patient Care, TobeSoft; Chair: American Heart Association Quality Oversight Committee; Data Monitoring Committees: Baim Institute for Clinical Research (formerly Harvard Clinical Research Institute, for the PORTICO trial, funded by St. Jude Medical, now Abbott), Cleveland Clinic (including for the ExCEED trial, funded by Edwards), Duke Clinical Research Institute, Mayo Clinic, Mount Sinai School of Medicine (for the ENVISAGE trial, funded by Daiichi Sankyo), Population Health Research Institute; Honoraria: American College of Cardiology (Senior Associate Editor, Clinical Trials and News, ACC.org; Vice-Chair, American College of Cardiology Accreditation Committee), Baim Institute for Clinical Research (formerly Harvard Clinical Research Institute; RE-DUAL PCI clinical trial steering committee funded by Boehringer Ingelheim; AEGIS-II executive committee funded by CSL Behring), Belvoir Publications (Editor in Chief, Harvard Heart Letter), Duke Clinical Research Institute (clinical trial steering committees, including for the PRONOUNCE trial, funded by Ferring Pharmaceuticals), HMP Global (Editor in Chief, Journal of Invasive Cardiology), Journal of the American College of Cardiology (Guest Editor; Associate Editor), Medtelligence/ReachMD (CME steering committees), MJH Life Sciences, Population Health Research Institute (for the COMPASS operations committee, publications committee, steering committee, and USA national co-leader, funded by Bayer), Slack Publications (Chief Medical Editor, Cardiology Today’s Intervention), Society of Cardiovascular Patient Care (Secretary/Treasurer), WebMD (CME steering committees); Other: Clinical Cardiology (Deputy Editor), NCDR-ACTION Registry Steering Committee (Chair), VA CART Research and Publications Committee (Chair); Research Funding: Abbott, Afimmune, Amarin, Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Bristol-Myers Squibb, Cardax, Chiesi, CSL Behring, Eisai, Ethicon, Ferring Pharmaceuticals, Forest Laboratories, Fractyl, Idorsia, Ironwood, Ischemix, Lexicon, Lilly, Medtronic, Pfizer, PhaseBio, PLx Pharma, Regeneron, Roche, Sanofi Aventis, Synaptic, The Medicines Company; Royal- ties: Elsevier (Editor, Cardiovascular Intervention: A Companion to Braunwald’s Heart Disease); Site Co-Investigator: Biotronik, Boston Scientific, CSI, St. Jude Medical (now Abbott), Svelte; Trustee: American College of Cardiology; Unfunded Research: FlowCo, Merck, Novo Nordisk, Takeda. Dr Yeh discloses the following: Consulting/Scientific Advisory Board/Research Grants from Abbott Vascular, AstraZeneca, Boston Scientific, Medtronic, and Research Grants from Bard, Cook, Philips. The other authors report no conflicts.
Funding Information:
This study was funded by the National Cardiovascular Data Registry (NCDR). Dr Secemsky is funded in part by National Institutes of Health (NIH)/National Heart, Lung, and Blood Institute (NHLBI) K23HL150290.
Publisher Copyright:
© 2021 Lippincott Williams and Wilkins. All rights reserved.
PY - 2021/8/1
Y1 - 2021/8/1
N2 - Background: Prior studies on the use of multivessel percutaneous coronary intervention (MV PCI) for patients with ST-segment-elevation myocardial infarction (STEMI) and multivessel coronary artery disease have yielded heterogeneous results. The recent COMPLETE trial (Complete Versus Culprit-Only Revascularization Strategies to Treat Multivessel Disease After Early PCI for STEMI) demonstrated that MV PCI was superior to culprit-only PCI among patients with STEMI. It is unclear how these trial results apply to clinical decisions encountered in routine practice. Methods: We studied STEMI admissions among patients >65 years with multivessel disease and Centers for Medicare and Medicaid Services-linked data in the National Cardiovascular Data Registry CathPCI Registry from July 1, 2009 to December 31, 2017. MV PCI was defined as PCI to a nonculprit lesion ≤45 days of the index procedure. The primary outcome was the composite of death, myocardial infarction, and revascularization from 45 days through 1 year. To account for unmeasured confounders, an instrumental variable analysis was used to compare treatment strategies. The instrument was institutional rates of MV PCI. A falsification end point of postdischarge major bleeding was utilized to assess for residual confounding. Results: Of 56 332 admissions from 1102 institutions, 37.7% received MV PCI ≤45 days of index STEMI PCI. Of those undergoing MV PCI, 74.8% received complete revascularization. In unadjusted analysis, MV PCI was associated with a lower cumulative incidence of the composite outcome between 45 days and 1 year (13.9% versus 18.2% for non-MV PCI, P<0.01). In the instrumental variable analysis, there was no association between MV PCI and the composite outcome (adjusted risk difference, -0.97% [95% CI, -3.52% to 1.59%]; P=0.46). An association between MV PCI and the falsification end point of major bleeding was not observed (adjusted risk difference, -2.54% [95% CI, -5.30% to 0.22%]; P=0.07). Conclusions: In this large, nationwide analysis, we did not find benefit of MV PCI by 1 year among older STEMI patients. The clinical benefit of MV PCI may not extend equally outside of trials to include all patients, including those with more extreme ages and more complex decision-making.
AB - Background: Prior studies on the use of multivessel percutaneous coronary intervention (MV PCI) for patients with ST-segment-elevation myocardial infarction (STEMI) and multivessel coronary artery disease have yielded heterogeneous results. The recent COMPLETE trial (Complete Versus Culprit-Only Revascularization Strategies to Treat Multivessel Disease After Early PCI for STEMI) demonstrated that MV PCI was superior to culprit-only PCI among patients with STEMI. It is unclear how these trial results apply to clinical decisions encountered in routine practice. Methods: We studied STEMI admissions among patients >65 years with multivessel disease and Centers for Medicare and Medicaid Services-linked data in the National Cardiovascular Data Registry CathPCI Registry from July 1, 2009 to December 31, 2017. MV PCI was defined as PCI to a nonculprit lesion ≤45 days of the index procedure. The primary outcome was the composite of death, myocardial infarction, and revascularization from 45 days through 1 year. To account for unmeasured confounders, an instrumental variable analysis was used to compare treatment strategies. The instrument was institutional rates of MV PCI. A falsification end point of postdischarge major bleeding was utilized to assess for residual confounding. Results: Of 56 332 admissions from 1102 institutions, 37.7% received MV PCI ≤45 days of index STEMI PCI. Of those undergoing MV PCI, 74.8% received complete revascularization. In unadjusted analysis, MV PCI was associated with a lower cumulative incidence of the composite outcome between 45 days and 1 year (13.9% versus 18.2% for non-MV PCI, P<0.01). In the instrumental variable analysis, there was no association between MV PCI and the composite outcome (adjusted risk difference, -0.97% [95% CI, -3.52% to 1.59%]; P=0.46). An association between MV PCI and the falsification end point of major bleeding was not observed (adjusted risk difference, -2.54% [95% CI, -5.30% to 0.22%]; P=0.07). Conclusions: In this large, nationwide analysis, we did not find benefit of MV PCI by 1 year among older STEMI patients. The clinical benefit of MV PCI may not extend equally outside of trials to include all patients, including those with more extreme ages and more complex decision-making.
KW - Medicare
KW - coronary artery disease
KW - death
KW - myocardial infarction
KW - percutaneous coronary intervention
UR - http://www.scopus.com/inward/record.url?scp=85113779208&partnerID=8YFLogxK
U2 - 10.1161/CIRCINTERVENTIONS.120.010323
DO - 10.1161/CIRCINTERVENTIONS.120.010323
M3 - Article
C2 - 34372676
AN - SCOPUS:85113779208
SN - 1941-7640
VL - 14
SP - E010323
JO - Circulation: Cardiovascular Interventions
JF - Circulation: Cardiovascular Interventions
IS - 8
ER -