Platelet Inhibitory Effect of Clopidogrel in Patients Treated With Omeprazole, Pantoprazole, and Famotidine: A Prospective, Randomized, Crossover Study. Issue 6 (29th April 2013)
- Record Type:
- Journal Article
- Title:
- Platelet Inhibitory Effect of Clopidogrel in Patients Treated With Omeprazole, Pantoprazole, and Famotidine: A Prospective, Randomized, Crossover Study. Issue 6 (29th April 2013)
- Main Title:
- Platelet Inhibitory Effect of Clopidogrel in Patients Treated With Omeprazole, Pantoprazole, and Famotidine: A Prospective, Randomized, Crossover Study
- Authors:
- Arbel, Yaron
Birati, Edo Y.
Finkelstein, Ariel
Halkin, Amir
Kletzel, Hanna
Abramowitz, Yigal
Berliner, Shlomo
Deutsch, Varda
Herz, Itzhak
Keren, Gad
Banai, Shmuel - Abstract:
- <abstract abstract-type="main"> <title>Abstract</title> <sec id="clc22117-sec-0001" sec-type="section"> <title>Background</title> <p>Concerns about an inhibitory effect of proton pump inhibitors (PPIs) on clopidogrel metabolism have been raised. Because the pharmacological effect of clopidogrel is dependent on genetically determined activity of the hepatic cytochrome P450 isoenzymes system, it is important to examine the interaction between different PPIs and high on‐treatment platelet reactivity (HPR) after controlling for genetic variability. The aim of the study was to assess the effect of 2 PPIs and a histamine‐2 (H2) receptor‐blocker on platelet reactivity in a crossover trial where each patient was alternately treated with each drug.</p> </sec> <sec id="clc22117-sec-0002" sec-type="section"> <title>Hypothesis</title> <p>Omeprazole reduces HPR more than other PPI or H<sub>2</sub> blockers.</p> </sec> <sec id="clc22117-sec-0003" sec-type="section"> <title>Methods</title> <p>Patients treated with aspirin and clopidogrel for at least 1 month were assigned to 3 consecutive 1‐month treatment periods during which they were treated with each of the 3 study medications twice daily: omeprazole 20 mg, famotidine 40 mg, and pantoprazole 20 mg. At the end of each treatment phase, platelet function was evaluated with the Verify Now system using 2 cutoff values (&gt;208 P2Y12 reaction units [PRUs] and &gt;230 PRUs) for the definition of HPR.</p> </sec> <sec id="clc22117-sec-0004"<abstract abstract-type="main"> <title>Abstract</title> <sec id="clc22117-sec-0001" sec-type="section"> <title>Background</title> <p>Concerns about an inhibitory effect of proton pump inhibitors (PPIs) on clopidogrel metabolism have been raised. Because the pharmacological effect of clopidogrel is dependent on genetically determined activity of the hepatic cytochrome P450 isoenzymes system, it is important to examine the interaction between different PPIs and high on‐treatment platelet reactivity (HPR) after controlling for genetic variability. The aim of the study was to assess the effect of 2 PPIs and a histamine‐2 (H2) receptor‐blocker on platelet reactivity in a crossover trial where each patient was alternately treated with each drug.</p> </sec> <sec id="clc22117-sec-0002" sec-type="section"> <title>Hypothesis</title> <p>Omeprazole reduces HPR more than other PPI or H<sub>2</sub> blockers.</p> </sec> <sec id="clc22117-sec-0003" sec-type="section"> <title>Methods</title> <p>Patients treated with aspirin and clopidogrel for at least 1 month were assigned to 3 consecutive 1‐month treatment periods during which they were treated with each of the 3 study medications twice daily: omeprazole 20 mg, famotidine 40 mg, and pantoprazole 20 mg. At the end of each treatment phase, platelet function was evaluated with the Verify Now system using 2 cutoff values (&gt;208 P2Y12 reaction units [PRUs] and &gt;230 PRUs) for the definition of HPR.</p> </sec> <sec id="clc22117-sec-0004" sec-type="section"> <title>Results</title> <p>Patients with HPR were older than those without HPR (62 ± 10 vs 55 ± 8 years, respectively, P = 0.03). HPR was more prevalent during omeprazole therapy compared to famotidine or pantoprazole (48%, 33%, and 31%, respectively, for the 208 PRU cutoff, P= 0.04; and 37%, 17%, and 23%, respectively, for the 230 PRU cutoff, P= 0.003).</p> </sec> <sec id="clc22117-sec-0005" sec-type="section"> <title>Conclusions</title> <p>After eliminating the effects of interindividual variability in clopidogrel metabolism, omeprazole therapy was associated with substantially more HPR than famotidine or pantoprazole.</p> </sec> </abstract> … (more)
- Is Part Of:
- Clinical cardiology. Volume 36:Issue 6(2013:Jun.)
- Journal:
- Clinical cardiology
- Issue:
- Volume 36:Issue 6(2013:Jun.)
- Issue Display:
- Volume 36, Issue 6 (2013)
- Year:
- 2013
- Volume:
- 36
- Issue:
- 6
- Issue Sort Value:
- 2013-0036-0006-0000
- Page Start:
- 342
- Page End:
- 346
- Publication Date:
- 2013-04-29
- Subjects:
- Cardiology -- Periodicals
616.12005 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1932-8737/issues ↗
http://www3.interscience.wiley.com/journal/113412417/home ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/clc.22117 ↗
- Languages:
- English
- ISSNs:
- 0160-9289
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.265000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4032.xml