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Detection of individual responses to clopidogrel: Validation of a novel, rapid analysis using thrombelastography 6s
Bartosz Olechowski1,2, Richard T Dalton2, Vikram Khanna1,2
1Coronary Research Group, University Hospital Southampton NHS Foundation Trust, Southampton, UK.
Insights
This study validates the Thrombelastography 6s assay for assessing P2Y12 inhibitor response, showing its novel AUC15 parameter offers a faster, reliable alternative to MA for personalized antiplatelet therapy.
Area of Science:
- Cardiovascular Medicine
- Clinical Pathology
- Pharmacology
Background:
- Assessing individual response to P2Y12 inhibitors is crucial for predicting risks in percutaneous coronary intervention.
- Current methods may not be optimal for rapid clinical decision-making.
Purpose of the Study:
- To validate a novel point-of-care (POC) assay, Thrombelastography (TEG) 6s, for detecting changes in adenosine diphosphate (ADP)-induced clotting.
- To compare a new rapid parameter, area under the curve at 15 minutes (AUC15), with the traditional maximum clot amplitude (MA) using TEG 6s.
Main Methods:
- ADP-induced clotting was measured in 25 participants (healthy volunteers and ACS patients) receiving clopidogrel.
- Samples were analyzed using both conventional TEG 5000 and the POC TEG 6S.
- The novel AUC15 parameter was compared with MA in the TEG 6S.
Main Results:
- TEG 5000 and TEG 6s demonstrated agreement in detecting changes in ADP-induced platelet activation.
- A strong correlation was found between MA and AUC15 in TEG 6s (R² = 0.867, R = 0.936).
- AUC15 results were available approximately 13.3 minutes sooner than MA.
Conclusions:
- Thrombelastography 6s is a rapid, accurate POC assay for ADP-induced clotting, validated against TEG 5000.
- The novel AUC15 parameter is a viable, time-saving alternative to MA.
- These findings support the potential of TEG 6s and AUC15 in guiding personalized P2Y12 inhibitor therapy.
Introduction:
There is potential value in testing individual response to P2Y12 inhibitors to predict ischemic and bleeding risk in patients undergoing percutaneous coronary intervention. The aims of this study were: (1) to validate the ability of a novel point of care (POC) assay, thrombelastography (TEG) 6s, to detect changes in adenosine diphosphate (ADP)-induced whole blood clotting in volunteers and patients given clopidogrel using TEG 5000 as a reference and (2) to compare a novel, rapid parameter, area under the curve at 15 minutes (AUC15), with the traditional maximum clot amplitude (MA) in TEG 6s.
Methods:
A total of 25 participants were included in whom ADP-induced clotting was measured at 4 time points: (1) 12 healthy volunteers given 600 mg of clopidogrel; (2) 12 patients with ACS given 600 mg of clopidogrel; (3) 1 healthy volunteer given 600 mg of clopidogrel on 5 separate occasions. All samples were tested using conventional TEG 5000 and the new POC TEG 6S, and a new parameter called AUC15 was compared with MA in TEG 6s.
Results:
(1) TEG 5000 and TEG 6s both detected changes in ADP-induced platelet activation. Bland-Altman analysis demonstrated a good level of agreement between them. (2) For TEG 6S, correlation between MA and the novel AUC15 was strong for both thrombin and ADP channels (R2 = 0.867, R = .936, P < .001), and the AUC15 result was available on average 13.3 minutes earlier.
Conclusions:
Thrombelastography 6s is a rapid, easy to use and accurate test of ADP-induced clotting using TEG 5000 as a reference. A novel parameter, AUC15, is a viable, time-saving option for this test and has potential value in personalized P2Y12 inhibitor therapy.
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