Outcomes According to Cardiac Catheterization Referral and Clopidogrel Use Among Medicare Patients With Non-ST-Segment Elevation Myocardial Infarction Discharged Without In-hospital Revascularization.
dc.contributor.author | Hess, Connie N | |
dc.contributor.author | Hellkamp, Anne S | |
dc.contributor.author | Roe, Matthew T | |
dc.contributor.author | Thomas, Laine | |
dc.contributor.author | Scirica, Benjamin M | |
dc.contributor.author | Peng, S Andrew | |
dc.contributor.author | Peterson, Eric D | |
dc.contributor.author | Wang, Tracy Y | |
dc.coverage.spatial | England | |
dc.date.accessioned | 2017-07-06T13:26:37Z | |
dc.date.available | 2017-07-06T13:26:37Z | |
dc.date.issued | 2016-03-14 | |
dc.description.abstract | BACKGROUND: While use of P2Y12 receptor inhibitor is recommended by guidelines, few studies have examined its effectiveness among older non-ST-segment elevation myocardial infarction patients who did not undergo coronary revascularization. METHODS AND RESULTS: We included unrevascularized non-ST-segment elevation myocardial infarction patients ≥65 years discharged home from 463 ACTION Registry-GWTG hospitals from 2007 to 2010. Rates of discharge clopidogrel use were described for patients with no angiography, angiography without obstructive coronary artery disease (CAD; ≥50% stenosis in ≥1 vessel), and angiography with obstructive CAD. Two-year outcomes were ascertained from linked Medicare data and included composite major adverse cardiac events (defined as all-cause death, myocardial infarction readmission, or revascularization), and individual components. Outcomes associated with clopidogrel use were adjusted using inverse probability-weighted propensity modeling. Of 14 154 unrevascularized patients, 54.7% (n=7745) did not undergo angiography, 10.6% (n=1494) had angiography without CAD, and 34.7% (n=4915) had angiography with CAD. Discharge clopidogrel was prescribed for 42.2% of all unrevascularized patients: 37.8% without angiography, 34.1% without obstructive CAD at angiography, and 51.6% with obstructive CAD at angiography. Discharge clopidogrel use was not associated with major adverse cardiac events in any group: without angiography (adjusted hazard ratio [95% CI]: 0.99 [0.93-1.06]), angiography without CAD (1.04 [0.74-1.47]), and angiography with CAD (1.12 [1.00-1.25], Pinteraction=0.20). CONCLUSIONS: We found no association between discharge clopidogrel use and long-term risk of major adverse cardiac events among older, unrevascularized non-ST-segment elevation myocardial infarction patients. Clopidogrel use in this population requires further prospective evaluation. | |
dc.identifier | ||
dc.identifier | JAHA.115.002784 | |
dc.identifier.eissn | 2047-9980 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.publisher | Ovid Technologies (Wolters Kluwer Health) | |
dc.relation.ispartof | J Am Heart Assoc | |
dc.relation.isversionof | 10.1161/JAHA.115.002784 | |
dc.subject | P2Y12 receptor inhibitor | |
dc.subject | effectiveness | |
dc.subject | unrevascularized non–ST‐segment elevation myocardial infarction patients | |
dc.subject | Age Factors | |
dc.subject | Aged | |
dc.subject | Aged, 80 and over | |
dc.subject | Cardiac Catheterization | |
dc.subject | Coronary Angiography | |
dc.subject | Coronary Artery Disease | |
dc.subject | Female | |
dc.subject | Humans | |
dc.subject | Male | |
dc.subject | Medicare | |
dc.subject | Myocardial Infarction | |
dc.subject | Myocardial Revascularization | |
dc.subject | Patient Discharge | |
dc.subject | Platelet Aggregation Inhibitors | |
dc.subject | Purinergic P2Y Receptor Antagonists | |
dc.subject | Referral and Consultation | |
dc.subject | Registries | |
dc.subject | Risk Factors | |
dc.subject | Ticlopidine | |
dc.subject | Time Factors | |
dc.subject | Treatment Outcome | |
dc.subject | United States | |
dc.title | Outcomes According to Cardiac Catheterization Referral and Clopidogrel Use Among Medicare Patients With Non-ST-Segment Elevation Myocardial Infarction Discharged Without In-hospital Revascularization. | |
dc.type | Journal article | |
duke.contributor.orcid | Peterson, Eric D|0000-0002-5415-4721 | |
pubs.author-url | ||
pubs.begin-page | e002784 | |
pubs.issue | 3 | |
pubs.organisational-group | Basic Science Departments | |
pubs.organisational-group | Biostatistics & Bioinformatics | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Clinical Research Institute | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Medicine, Cardiology | |
pubs.organisational-group | School of Medicine | |
pubs.publication-status | Published online | |
pubs.volume | 5 |
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