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Comparison of Multiplate and VerifyNow platelet function tests in predicting clinical outcome in patients with acute coronary syndromes

Authors :
Ana Holley
Peter D. Larsen
Sarah Fairley
A. Al-Sinan
Scott A. Harding
Alexander Sasse
Source :
Thrombosis Research. 152:14-19
Publication Year :
2017
Publisher :
Elsevier BV, 2017.

Abstract

Introduction This study examined the ability of two widely used “point of care” platelet function assays, VerifyNow and Multiplate, to predict adverse outcomes in patients with acute coronary syndromes (ACS). Methods We examined platelet reactivity using VerifyNow and Multiplate P2Y 12 assays in patients with ACS and the relationship between platelet reactivity and both MACE (defined as a composite of death, myocardial infarction, stroke, stent thrombosis and unplanned revascularisation) and TIMI major bleeding at 1 year. Results In 619 ACS patients, 65 patients (10.5%) had experienced MACE at 1 year and 6 patients (1%) had TIMI major bleeding events. The two measures of platelet reactivity were only moderately correlated (Rho = 0.43, p = 0.0001). Both measures demonstrated a statistically significant relationship with MACE, with area under the curve for VerifyNow of 0.632 (0.001) and for Multiplate of 0.577 ( p = 0.04), and neither measure showed a significant relationship with bleeding. Logistic regression analysis found that only VerifyNow was a statistical predictor of MACE ( p = 0.01). MACE occurred in 16% of those classified as having HPR using VerifyNow compared to 7% in those without HPR (odds ratio of 2.6 (95% CI 1.5–4.4, p = 0.001). In those classified as having HPR by the Multiplate assay, MACE occurred in 13% compared to 9% of those without HPR (Odds ratio 1.5 95% CI 0.9–2.5, p = 0.11). Conclusion The two points of care platelet function tests examined in this study were only moderately correlated. The VerifyNow assay demonstrated a stronger relationship to MACE than the Multiplate assay.

Details

ISSN :
00493848
Volume :
152
Database :
OpenAIRE
Journal :
Thrombosis Research
Accession number :
edsair.doi.dedup.....b82b962dbca3e0d0af17b9319383fcf8