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American Heart Association

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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
Meeting Info:

Scientific Sessions 2024

2024

Chicago, Illinois

Session Info:

Platelet Function and ACS

Saturday, 11/16/2024 , 02:50PM - 04:15PM

Moderated Digital Poster Session

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