TY - JOUR
T1 - Temporal Changes and Institutional Variation in Use of Percutaneous Coronary Intervention for ST-Elevation Myocardial Infarction with Multivessel Coronary Artery Disease in the United States
T2 - An NCDR 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:
reported grants and personal fees from Cook, BD, Medtronic, Philips, and CSI; grants from Boston Scientific and AstraZeneca; personal fees from Janssen and Abbott Vascular outside the submitted work. Dr Butala reported receiving consulting fees from and holding an ownership interest in Hilabs. Dr Curtis reported having a contract with the American College of Cardiology for his role as senior medical officer of the National Cardiovascular Data Registry and receiving salary support from the American College of Cardiology and National Cardiovascular Data Registry, during the conduct of this study; and receiving funding from the Centers for Medicare & Medicaid Services to develop and maintain performance measures that are used for public reporting and holding equity interest in Medtronic outside the submitted work. Dr Maddox discloses current grant funding from the National Center for Advancing Translational Sciences (grant 1U24TR002306-01); current consulting for Creative Educational Concepts Inc and Atheneum Partners; honoraria and/or expense reimbursement in the past 3 years from the University of Utah, NewYork Presbyterian, Westchester Medical Center, Sentara Heart Hospital, the Henry Ford Health System, and the University of California San Diego; current employment as a cardiologist and the executive director of the Healthcare Innovation Lab at BJC HealthCare/Washington University School of Medicine, including advising Myia Labs, for which his employer is receiving equity compensation in the company; and serving as a compensated director for the J. F. Maddox Foundation. Dr Virani reported grants from the Department of Veterans Affairs, World Heart Federation, and the Tahir and Jooma Family; honoraria from the American College of Cardiology as an associate editor for Innovations (acc.org); and participation as a steering committee member Patient and Provider Assessment of Lipid Management (PALM) registry at the Duke Clinical Research Institute (with no financial remuneration)
Funding Information:
outside the submitted work. Dr Armstrong disclosures consultant/advisory board participation for Abbott Vascular, Boston Scientific, Cardiovascular Systems, Gore, Intact Vascular, Medtronic, and Philips. Dr Shunk disclosed 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 a senior medical officer in the National Cardiovascular Data Registry. Dr Bhatt reports participation in advisory boards for Cardax, Cereno Scientific, Elsevier Practice Update Cardiology, Medscape Cardiology, PhaseBio, PLx Pharma, Regado Biosciences; on boards of directors for the Boston VA Research Institute, Society of Cardiovascular Patient Care, and TobeSoft; as a chairperson for the American Heart Association Quality Oversight Committee; as a member of data monitoring committees for 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), and Population Health Research Institute. Dr Bhatt has received honoraria from the American College of Cardiology (senior associate editor, Clinical Trials and News [acc.org]; vice-chair, ACC Accreditation Committee), Baim Institute for Clinical Research (formerly the 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 (as editor in chief of Harvard Heart Letter), Duke Clinical Research Institute (clinical trial steering committees, including for the PRONOUNCE trial, funded by Ferring Pharmaceuticals), HMP Global (as editor in chief of Journal of Invasive Cardiology), Journal of the American College of Cardiology (as a guest editor and associate editor), Medtelligence/ReachMD (on continuing medical education steering committees), MJH Life Sciences, Population Health Research Institute (for the COMPASS operations committee, publications committee, and steering committee and as US national coleader; funded by Bayer), Slack Publications (chief medical editor for Cardiology Today’s Intervention), Society of Cardiovascular Patient Care (secretary-treasurer), WebMD (continuing medical education steering committees). In addition, he is involved with Clinical Cardiology (as a deputy editor), the NCDR-ACTION Registry steering committee (as a chair), the VA Clinical Assessment, Reporting and Tracking System for Cath Labs Research and Publications Committee (as a chair); has received research funding from Abbott, Afimmune, Amarin, Amgen, AstraZeneca, Bayer, Boehringer Ingelheim, Bristol Myers Squibb, Cardax, Chiesi, CSL Behring, Eisai, Ethicon, Ferring Pharmaceuticals, Forest Laboratories/AstraZeneca, Fractyl, Idorsia, Ironwood, Ischemix, Lexicon, Lilly, Medtronic, Pfizer, PhaseBio, PLx Pharma, Regeneron, Roche, Sanofi Aventis, Synaptic, The Medicines Company; has received royalties from Elsevier (editor, Cardiovascular Intervention: A Companion to Braunwald’s Heart Disease); served as a site coinvestigator for Biotronik, Boston Scientific, CSI, St Jude Medical (now Abbott), and Svelte; has been a trustee of the American College of Cardiology; has completed unfunded research with FlowCo, Merck, Novo Nordisk, and Takeda; and has received personal fees from Level Ex, Contego Medical, CellProthera, and K2P, outside the submitted work. Dr Yeh reported grants and personal fees from Abbott Vascular, AstraZeneca, Medtronic, and Boston Scientific outside the submitted work. No other disclosures were reported.
Funding Information:
Funding/Support: This study was funded by the
Publisher Copyright:
© 2021 American Medical Association. All rights reserved.
PY - 2021/5
Y1 - 2021/5
N2 - Importance: After disparate results from observational and small randomized studies, the COMPLETE trial demonstrated superiority of multivessel (MV) percutaneous coronary intervention (PCI) over culprit-only PCI for ST-elevation myocardial infarction (STEMI). Objective: To describe temporal trends and institutional variation of MV PCI use for STEMI in the United States to inform how new evidence may influence clinical practice. Design, Setting, and Participants: This cohort study included STEMI admissions involving MV disease from 1598 institutions in the National Cardiovascular Data Registry CathPCI Registry from the third quarter of 2009 to the first quarter of 2018. An MV PCI was defined as a PCI to a nonculprit lesion within 45 days of the index procedure. Exposures: Multivessel PCI, defined as placement of coronary stents in 2 or more major epicardial vessels or the staged placement of 1 or more coronary stents in a major epicardial vessel distinct from the index culprit vessel, within 45 days of the index PCI. Main Outcomes and Measures: Outcomes included the proportional use of MV PCI among STEMI admissions with MV disease, and the timing of MV PCI (an index procedure, a staged procedure during index hospitalization, or a postdischarge procedure within 45 days). Results: Among 359879 admissions with STEMI and MV disease, MV PCI was performed in 38.5% (n = 138380; mean [SD] age of patients, 62.3 [12.3] years; 102266 men [73.9%]) within 45 days. Of those receiving MV PCIs, 30.8% (n = 42629) had a procedure performed during the index procedure, 31.6% (n = 43696) as a staged procedure during the index hospitalization, and 37.6% (n = 52055) within 45 days of discharge. Complete revascularization of all diseased arteries was performed in 76.2% (n = 105389). From the third quarter of 2009 to the second quarter of 2013, MV PCI use declined by 10%, from 42.7% (3230 of 7572 cases) to a nadir of 32.7% (3386 of 10342 cases), followed by an increase to 44.0% (5062 of 11497 cases) by the fourth quarter of 2017. During this time, there was a 13.6% decline in use of postdischarge staged MV PCI (from 23.4% of STEMI cases [1772 of 7572 cases] in the third quarter of 2009 to 9.9% [1094 of 11171 cases] in the fourth quarter of 2014) and an 12.5% increase in MV PCI performed during the index admission (from 19.3% [1458 of 7572 cases] in the third quarter of 2009 to 31.8% [3557 of 11171 cases] in the first quarter of 2018). Multivessel PCI use varied substantially across institutions, with a median use of 37.9% (interquartile range, 30.0%-46.5%). Conclusions and Relevance: In this large, nationwide analysis, MV PCI use for patients with STEMI has been increasing through early 2018 but was used in the minority of patients and with wide variability across US institutions. The adoption of new trial results into guidelines and practice may further promote the growth of MV PCI..
AB - Importance: After disparate results from observational and small randomized studies, the COMPLETE trial demonstrated superiority of multivessel (MV) percutaneous coronary intervention (PCI) over culprit-only PCI for ST-elevation myocardial infarction (STEMI). Objective: To describe temporal trends and institutional variation of MV PCI use for STEMI in the United States to inform how new evidence may influence clinical practice. Design, Setting, and Participants: This cohort study included STEMI admissions involving MV disease from 1598 institutions in the National Cardiovascular Data Registry CathPCI Registry from the third quarter of 2009 to the first quarter of 2018. An MV PCI was defined as a PCI to a nonculprit lesion within 45 days of the index procedure. Exposures: Multivessel PCI, defined as placement of coronary stents in 2 or more major epicardial vessels or the staged placement of 1 or more coronary stents in a major epicardial vessel distinct from the index culprit vessel, within 45 days of the index PCI. Main Outcomes and Measures: Outcomes included the proportional use of MV PCI among STEMI admissions with MV disease, and the timing of MV PCI (an index procedure, a staged procedure during index hospitalization, or a postdischarge procedure within 45 days). Results: Among 359879 admissions with STEMI and MV disease, MV PCI was performed in 38.5% (n = 138380; mean [SD] age of patients, 62.3 [12.3] years; 102266 men [73.9%]) within 45 days. Of those receiving MV PCIs, 30.8% (n = 42629) had a procedure performed during the index procedure, 31.6% (n = 43696) as a staged procedure during the index hospitalization, and 37.6% (n = 52055) within 45 days of discharge. Complete revascularization of all diseased arteries was performed in 76.2% (n = 105389). From the third quarter of 2009 to the second quarter of 2013, MV PCI use declined by 10%, from 42.7% (3230 of 7572 cases) to a nadir of 32.7% (3386 of 10342 cases), followed by an increase to 44.0% (5062 of 11497 cases) by the fourth quarter of 2017. During this time, there was a 13.6% decline in use of postdischarge staged MV PCI (from 23.4% of STEMI cases [1772 of 7572 cases] in the third quarter of 2009 to 9.9% [1094 of 11171 cases] in the fourth quarter of 2014) and an 12.5% increase in MV PCI performed during the index admission (from 19.3% [1458 of 7572 cases] in the third quarter of 2009 to 31.8% [3557 of 11171 cases] in the first quarter of 2018). Multivessel PCI use varied substantially across institutions, with a median use of 37.9% (interquartile range, 30.0%-46.5%). Conclusions and Relevance: In this large, nationwide analysis, MV PCI use for patients with STEMI has been increasing through early 2018 but was used in the minority of patients and with wide variability across US institutions. The adoption of new trial results into guidelines and practice may further promote the growth of MV PCI..
UR - http://www.scopus.com/inward/record.url?scp=85095882894&partnerID=8YFLogxK
U2 - 10.1001/jamacardio.2020.5354
DO - 10.1001/jamacardio.2020.5354
M3 - Article
C2 - 33146666
AN - SCOPUS:85095882894
SN - 2380-6583
VL - 6
SP - 574
EP - 580
JO - JAMA Cardiology
JF - JAMA Cardiology
IS - 5
ER -