Scientific Sessions 2024
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Platelet Function and ACS
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Evolving Trends and Outcomes of P2Y12 Inhibitor Pretreatment in Non-ST-Elevation Acute Coronary Syndrome in the United States: Insights from the NCDR Chest Pain-MI Registry
American Heart Association
2
0
Final ID: MDP294
Evolving Trends and Outcomes of P2Y12 Inhibitor Pretreatment in Non-ST-Elevation Acute Coronary Syndrome in the United States: Insights from the NCDR Chest Pain-MI Registry
Abstract Body (Do not enter title and authors here): Background Although high rates of P2Y12 inhibitor pretreatment for non-ST-elevation acute coronary syndrome (NSTE-ACS) have been reported, contemporary practice pattern in the U.S. are not well studied. Objectives To investigate the temporal trends, variability, and clinical outcomes of P2Y12 inhibitor pretreatment in NSTE-ACS across U.S. Methods Consecutive patients that underwent early invasive strategy for NSTE-ACS (coronary angiogram ≤ 24 hours of arrival) in National Cardiovascular Data Registry (NCDR) Chest Pain-Myocardial Infarction (MI) registry was analyzed. Initially, a time-trend analysis was conducted on the complete cohort from January 1, 2013, to March 31, 2023. Subsequently, a more recent cohort (January 1, 2019, to March 31, 2023), with a complete set of variables, was used to construct a hierarchical regression model to quantify variability in the use of pretreatment among institutions and hospital regions. For this contemporary cohort, instrumental variable analysis was performed to compare in-hospital outcomes between patients who received pretreatment and those who did not. Results Use of P2Y12 inhibitor pretreatment has decreased from 24.8% in 2013Q1 to 12.4% in 2023Q3. Among the contemporary cohort of 110,148 patients (2019-23; mean age, 63.9 [SD 12.5] years; 33.0% female), 17,509 (15.9%) received pretreatment. Significant variability in P2Y12 inhibitor pretreatment was observed (range: 0-100%): hierarchical regression model demonstrated that two identical patients would have more than a three-fold difference in the odds of pretreatment by changing institution or hospital region (OR 3.63; 95% CI, 3.51-3.74 and 3.21; 95% CI, 2.90-3.54, respectively). Instrumental variable analysis demonstrated no significant differences in in-hospital all-cause death (1.5% vs 1.7%; p=0.071), recurrent MI (0.56% vs 0.57%; p=0.98), or major bleeding (2.7% vs 2.8%; p=0.98) between the two groups. However, in patients who underwent coronary artery bypass surgery, pretreatment was associated with a longer length of stay (11.2 ± 5.1 days vs 9.8 ± 5.0 days; p < 0.001). Conclusions Within the nationwide registry in the U.S., we observed a significant variability in the use of P2Y12 inhibitor pretreatment among NSTE-ACS patients in the U.S. Given the lack of clear advantages and the potential for prolonged hospital stays, our findings highlight the importance of efforts to improve standardization.
Ueyama, Hiroki
( Emory University
, Atlanta
, Georgia
, United States
)
Kennedy, Kevin
( St. Luke's Hospital
, Kansas City
, Missouri
, United States
)
Rymer, Jennifer
( Duke
, Chapel Hill
, North Carolina
, United States
)
Sandhu, Alexander
( Stanford University
, Millbrae
, California
, United States
)
Kuno, Toshiki
( Montefiore Medical Center
, Bronx
, New York
, United States
)
Masoudi, Frederick
( Ascension
, Denver
, Colorado
, United States
)
Spertus, John
( Saint Lukes Mid America Heart Inst
, Kansas City
, Missouri
, United States
)
Kohsaka, Shun
( Keio University
, Tokyo
, Japan
)
Author Disclosures:
Hiroki Ueyama:DO NOT have relevant financial relationships
| kevin kennedy:No Answer
| Jennifer Rymer:DO NOT have relevant financial relationships
| Alexander Sandhu:DO have relevant financial relationships
;
Consultant:Lexicon Pharmaceuticals:Past (completed)
; Research Funding (PI or named investigator):Bayer:Expected (by end of conference)
; Research Funding (PI or named investigator):Novo Nordisk:Expected (by end of conference)
; Research Funding (PI or named investigator):Astra Zeneca:Expected (by end of conference)
; Consultant:Reprieve Cardiovascular:Active (exists now)
; Research Funding (PI or named investigator):Novartis:Active (exists now)
| Toshiki Kuno:DO NOT have relevant financial relationships
| Frederick Masoudi:DO have relevant financial relationships
;
Consultant:Bristol Meyers Squibb:Active (exists now)
; Researcher:NIH/NHLBI:Active (exists now)
; Other (please indicate in the box next to the company name):Massachusetts Medical Society (JournalWatch Cardiology Editor):Active (exists now)
; Other (please indicate in the box next to the company name):UpToDate (section editor):Active (exists now)
; Consultant:CPC Research:Active (exists now)
| John Spertus:DO have relevant financial relationships
;
Consultant:Bristol Meyers Squibb:Active (exists now)
; Consultant:Edwards Healthscients:Past (completed)
; Consultant:Abbott:Past (completed)
; Consultant:Bayer:Past (completed)
; Consultant:Terrumo:Active (exists now)
; Royalties/Patent Beneficiary:Outcomes Instruments - Copyright to SAQ, KCCQ, and PAQ:Active (exists now)
; Consultant:Alnylam:Past (completed)
; Other (please indicate in the box next to the company name):Board of Directors for Blue Cross Blue Shield of Kansas City:Active (exists now)
; Research Funding (PI or named investigator):Janssen:Active (exists now)
; Consultant:Janssen:Active (exists now)
; Consultant:Sanofi Aventis:Past (completed)
; Consultant:Imbria Pharmaceuticals:Active (exists now)
; Consultant:Cytokinetics:Active (exists now)
; Research Funding (PI or named investigator):Bristol Meyers Squibb:Active (exists now)
| Shun Kohsaka:No Answer