The Impact of Generic Clopidogrel Bisulfate on Platelet Inhibition in Patients with Coronary Artery Stents: Results of the ACCEL-GENERIC Study

Background/Aims: In patients with coronary artery stents, the cost of clopidogrel has been cited as a factor in the premature discontinuation of therapy. Thus, the introduction of lower-cost generic clopidogrel may increase patient compliance. However, platelet inhibition by generic clopidogrel has...

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Veröffentlicht in:The Korean journal of internal medicine 2010-06, Vol.25 (2), p.154
Hauptverfasser: Young Hoon Jeong, Jin Sin Koh, Min Kyung Kang, Yeon Jeong Ahn, In Suk Kim, Yong Whi Park, Seok Jae Hwang, Choong Hwan Kwak, Jin Yong Hwang
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container_end_page
container_issue 2
container_start_page 154
container_title The Korean journal of internal medicine
container_volume 25
creator Young Hoon Jeong
Jin Sin Koh
Min Kyung Kang
Yeon Jeong Ahn
In Suk Kim
Yong Whi Park
Seok Jae Hwang
Choong Hwan Kwak
Jin Yong Hwang
description Background/Aims: In patients with coronary artery stents, the cost of clopidogrel has been cited as a factor in the premature discontinuation of therapy. Thus, the introduction of lower-cost generic clopidogrel may increase patient compliance. However, platelet inhibition by generic clopidogrel has not been compared to the original clopidogrel formulation in patients with coronary artery stents. Methods: We prospectively enrolled 20 patients receiving chronic therapy with the original clopidogrel bisulfate (Plavix(R)). After assessing patient compliance with Plavix(R), maintenance therapy was switched to generic clopidogrel bisulfate (Plavitor(R)). Platelet reactivity was assessed at baseline and 30-day after the switch using conventional aggregometry and the VerifyNow P2Y12 assay. Results: All patients completed maintenance therapy with Plavitor(R). Before and after switching therapy maximal (36.5±7.9% vs. 39.8±16.2%, p=0.280) and late platelet aggregation (23.5±10.9% vs. 29.1±18.3%, p=0.156) with 5 μmol/L adenosine diphosphate (ADP) stimulus did not differ. Likewise, 20 μmol/L ADP-induced platelet aggregation and P2Y12 reaction unit in patients on Plavitor(R) therapy was comparable to that in patients on Plavix(R) therapy. However, Bland-Altman analysis showed wide limits of agreement between measured platelet reactivity on Plavix(R) vs. Plavitor(R) therapies. Conclusions: Among patients on Plavix(R) maintenance therapy with coronary stents, replacement with Plavitor(R) shows a comparable inhibition of ADP-induced platelet aggregation. However, due to poor inter-therapy agreement, between two regimens, physicians may be cautious when introducing generic clopidogrel bisulfate. (Korean J Intern Med 2010;25:154-161)
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Thus, the introduction of lower-cost generic clopidogrel may increase patient compliance. However, platelet inhibition by generic clopidogrel has not been compared to the original clopidogrel formulation in patients with coronary artery stents. Methods: We prospectively enrolled 20 patients receiving chronic therapy with the original clopidogrel bisulfate (Plavix(R)). After assessing patient compliance with Plavix(R), maintenance therapy was switched to generic clopidogrel bisulfate (Plavitor(R)). Platelet reactivity was assessed at baseline and 30-day after the switch using conventional aggregometry and the VerifyNow P2Y12 assay. Results: All patients completed maintenance therapy with Plavitor(R). Before and after switching therapy maximal (36.5±7.9% vs. 39.8±16.2%, p=0.280) and late platelet aggregation (23.5±10.9% vs. 29.1±18.3%, p=0.156) with 5 μmol/L adenosine diphosphate (ADP) stimulus did not differ. Likewise, 20 μmol/L ADP-induced platelet aggregation and P2Y12 reaction unit in patients on Plavitor(R) therapy was comparable to that in patients on Plavix(R) therapy. However, Bland-Altman analysis showed wide limits of agreement between measured platelet reactivity on Plavix(R) vs. Plavitor(R) therapies. Conclusions: Among patients on Plavix(R) maintenance therapy with coronary stents, replacement with Plavitor(R) shows a comparable inhibition of ADP-induced platelet aggregation. However, due to poor inter-therapy agreement, between two regimens, physicians may be cautious when introducing generic clopidogrel bisulfate. 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Thus, the introduction of lower-cost generic clopidogrel may increase patient compliance. However, platelet inhibition by generic clopidogrel has not been compared to the original clopidogrel formulation in patients with coronary artery stents. Methods: We prospectively enrolled 20 patients receiving chronic therapy with the original clopidogrel bisulfate (Plavix(R)). After assessing patient compliance with Plavix(R), maintenance therapy was switched to generic clopidogrel bisulfate (Plavitor(R)). Platelet reactivity was assessed at baseline and 30-day after the switch using conventional aggregometry and the VerifyNow P2Y12 assay. Results: All patients completed maintenance therapy with Plavitor(R). Before and after switching therapy maximal (36.5±7.9% vs. 39.8±16.2%, p=0.280) and late platelet aggregation (23.5±10.9% vs. 29.1±18.3%, p=0.156) with 5 μmol/L adenosine diphosphate (ADP) stimulus did not differ. Likewise, 20 μmol/L ADP-induced platelet aggregation and P2Y12 reaction unit in patients on Plavitor(R) therapy was comparable to that in patients on Plavix(R) therapy. However, Bland-Altman analysis showed wide limits of agreement between measured platelet reactivity on Plavix(R) vs. Plavitor(R) therapies. Conclusions: Among patients on Plavix(R) maintenance therapy with coronary stents, replacement with Plavitor(R) shows a comparable inhibition of ADP-induced platelet aggregation. However, due to poor inter-therapy agreement, between two regimens, physicians may be cautious when introducing generic clopidogrel bisulfate. 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source KoreaMed Synapse; DOAJ Directory of Open Access Journals; PubMed Central Open Access; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Blood platelets
Clopidogrel
Drugs
generic
Purinoceptor P2Y12
title The Impact of Generic Clopidogrel Bisulfate on Platelet Inhibition in Patients with Coronary Artery Stents: Results of the ACCEL-GENERIC Study
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