Prevalence of High On-treatment Platelet Reactivity in Diabetic Patients Treated with Aspirin

Abstract Background Randomized controlled trials have shown that ≤100 mg aspirin daily is not effective for primary prevention of cardiovascular events in diabetes; however, clinical and pharmacologic evidence suggests these patients need >100 mg for adequate antiplatelet activity. Although high...

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Veröffentlicht in:The American journal of medicine 2014, Vol.127 (1), p.95.e1-95.e9
Hauptverfasser: Simpson, Scot H., BSP, PharmD, MSc, Abdelmoneim, Ahmed S., BPharm, MSc, Omran, Dima, BSc(Pharm), Featherstone, Travis R., BSc(Pharm)
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container_end_page 95.e9
container_issue 1
container_start_page 95.e1
container_title The American journal of medicine
container_volume 127
creator Simpson, Scot H., BSP, PharmD, MSc
Abdelmoneim, Ahmed S., BPharm, MSc
Omran, Dima, BSc(Pharm)
Featherstone, Travis R., BSc(Pharm)
description Abstract Background Randomized controlled trials have shown that ≤100 mg aspirin daily is not effective for primary prevention of cardiovascular events in diabetes; however, clinical and pharmacologic evidence suggests these patients need >100 mg for adequate antiplatelet activity. Although high on-treatment platelet reactivity (HTPR) could explain the lack of benefit, prevalence of HTPR in diabetes is not known. This systematic review examined the relationship between daily aspirin dose and prevalence of HTPR in patients with diabetes. Methods Three electronic databases were searched until May 2013 using database-appropriate terms for aspirin, resistance, and diabetes. Studies were included if prevalence of HTPR was reported according to daily dose and diabetes status. Patients were stratified by daily aspirin dose and the weighted mean prevalence across studies was calculated. Where appropriate, pooled relative risks (RR) were calculated using a random-effects model. Results Data were available from 31 studies that enrolled 2147 diabetic patients. Overall, prevalence of HTPR was 21.9% (95% confidence interval [CI], 15.2%-28.5%) in diabetic patients and 15.8% (95% CI, 11.4%-20.3%) in nondiabetic patients (pooled RR 1.36; 95% CI, 1.08-1.71; I2 56%). Prevalence appeared to be dose related, with 398 (23.6%) of 1689 diabetic patients using ≤100 mg daily having HTPR compared with 64 (12.3%) of 518 diabetic patients using 101-325 mg daily (pooled RR 1.70; 95% CI, 1.07-2.72; I2 0%). Conclusions Although these observations should be verified in a clinical trial, the possibility that 1 in 4 patients have HTPR with doses commonly used in diabetes could have significant implications on overall effectiveness of aspirin.
doi_str_mv 10.1016/j.amjmed.2013.09.019
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Although high on-treatment platelet reactivity (HTPR) could explain the lack of benefit, prevalence of HTPR in diabetes is not known. This systematic review examined the relationship between daily aspirin dose and prevalence of HTPR in patients with diabetes. Methods Three electronic databases were searched until May 2013 using database-appropriate terms for aspirin, resistance, and diabetes. Studies were included if prevalence of HTPR was reported according to daily dose and diabetes status. Patients were stratified by daily aspirin dose and the weighted mean prevalence across studies was calculated. Where appropriate, pooled relative risks (RR) were calculated using a random-effects model. Results Data were available from 31 studies that enrolled 2147 diabetic patients. Overall, prevalence of HTPR was 21.9% (95% confidence interval [CI], 15.2%-28.5%) in diabetic patients and 15.8% (95% CI, 11.4%-20.3%) in nondiabetic patients (pooled RR 1.36; 95% CI, 1.08-1.71; I2 56%). Prevalence appeared to be dose related, with 398 (23.6%) of 1689 diabetic patients using ≤100 mg daily having HTPR compared with 64 (12.3%) of 518 diabetic patients using 101-325 mg daily (pooled RR 1.70; 95% CI, 1.07-2.72; I2 0%). Conclusions Although these observations should be verified in a clinical trial, the possibility that 1 in 4 patients have HTPR with doses commonly used in diabetes could have significant implications on overall effectiveness of aspirin.</description><identifier>ISSN: 0002-9343</identifier><identifier>EISSN: 1555-7162</identifier><identifier>DOI: 10.1016/j.amjmed.2013.09.019</identifier><identifier>PMID: 24384107</identifier><identifier>CODEN: AJMEAZ</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Aspirin ; Aspirin - administration &amp; dosage ; Aspirin - therapeutic use ; Blood platelets ; Blood Platelets - drug effects ; Cardiovascular Diseases - prevention &amp; control ; Diabetes ; Diabetes Complications - prevention &amp; control ; Dose-Response Relationship, Drug ; Drug Administration Schedule ; Drug dosages ; Drug resistance ; Humans ; Internal Medicine ; Medical Records Systems, Computerized ; Platelet Aggregation Inhibitors - administration &amp; dosage ; Platelet Aggregation Inhibitors - therapeutic use ; Prevalence ; Primary Prevention - methods ; Systematic review</subject><ispartof>The American journal of medicine, 2014, Vol.127 (1), p.95.e1-95.e9</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Jan 2014</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c445t-fc978664b6ec7e8e2e839987422ca4f09343ed7d1955dd8e6e5ee9b5d56d7fee3</citedby><cites>FETCH-LOGICAL-c445t-fc978664b6ec7e8e2e839987422ca4f09343ed7d1955dd8e6e5ee9b5d56d7fee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0002934313008437$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,4009,27902,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24384107$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Simpson, Scot H., BSP, PharmD, MSc</creatorcontrib><creatorcontrib>Abdelmoneim, Ahmed S., BPharm, MSc</creatorcontrib><creatorcontrib>Omran, Dima, BSc(Pharm)</creatorcontrib><creatorcontrib>Featherstone, Travis R., BSc(Pharm)</creatorcontrib><title>Prevalence of High On-treatment Platelet Reactivity in Diabetic Patients Treated with Aspirin</title><title>The American journal of medicine</title><addtitle>Am J Med</addtitle><description>Abstract Background Randomized controlled trials have shown that ≤100 mg aspirin daily is not effective for primary prevention of cardiovascular events in diabetes; however, clinical and pharmacologic evidence suggests these patients need &gt;100 mg for adequate antiplatelet activity. Although high on-treatment platelet reactivity (HTPR) could explain the lack of benefit, prevalence of HTPR in diabetes is not known. This systematic review examined the relationship between daily aspirin dose and prevalence of HTPR in patients with diabetes. Methods Three electronic databases were searched until May 2013 using database-appropriate terms for aspirin, resistance, and diabetes. Studies were included if prevalence of HTPR was reported according to daily dose and diabetes status. Patients were stratified by daily aspirin dose and the weighted mean prevalence across studies was calculated. Where appropriate, pooled relative risks (RR) were calculated using a random-effects model. Results Data were available from 31 studies that enrolled 2147 diabetic patients. Overall, prevalence of HTPR was 21.9% (95% confidence interval [CI], 15.2%-28.5%) in diabetic patients and 15.8% (95% CI, 11.4%-20.3%) in nondiabetic patients (pooled RR 1.36; 95% CI, 1.08-1.71; I2 56%). Prevalence appeared to be dose related, with 398 (23.6%) of 1689 diabetic patients using ≤100 mg daily having HTPR compared with 64 (12.3%) of 518 diabetic patients using 101-325 mg daily (pooled RR 1.70; 95% CI, 1.07-2.72; I2 0%). Conclusions Although these observations should be verified in a clinical trial, the possibility that 1 in 4 patients have HTPR with doses commonly used in diabetes could have significant implications on overall effectiveness of aspirin.</description><subject>Aspirin</subject><subject>Aspirin - administration &amp; dosage</subject><subject>Aspirin - therapeutic use</subject><subject>Blood platelets</subject><subject>Blood Platelets - drug effects</subject><subject>Cardiovascular Diseases - prevention &amp; control</subject><subject>Diabetes</subject><subject>Diabetes Complications - prevention &amp; control</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Administration Schedule</subject><subject>Drug dosages</subject><subject>Drug resistance</subject><subject>Humans</subject><subject>Internal Medicine</subject><subject>Medical Records Systems, Computerized</subject><subject>Platelet Aggregation Inhibitors - administration &amp; dosage</subject><subject>Platelet Aggregation Inhibitors - therapeutic use</subject><subject>Prevalence</subject><subject>Primary Prevention - methods</subject><subject>Systematic review</subject><issn>0002-9343</issn><issn>1555-7162</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkl1rFDEUhoModlv9ByIBb7yZMZ-TyY1QqrVCoYvWSwnZ5IzNOB_bJLuy_94M2yL0xqsQ8rxvch6C0BtKakpo86Gv7diP4GtGKK-JrgnVz9CKSikrRRv2HK0IIazSXPATdJpSX7ZEy-YlOmGCt4IStUI_1xH2doDJAZ47fBV-3eGbqcoRbB5hyng92AwDZPwNrMthH_IBhwl_CnYDOTi8tjkULuHbJQIe_wn5Dp-nbYhheoVedHZI8PphPUM_Lj_fXlxV1zdfvl6cX1dOCJmrzmnVNo3YNOAUtMCg5Vq3SjDmrOjIMgJ45amW0vsWGpAAeiO9bLzqAPgZen_s3cb5fgcpmzEkB8NgJ5h3yVChiaKatbyg756g_byLU3ldoVTLGiJ0WyhxpFycU4rQmW0Mo40HQ4lZ9JveHPWbRb8h2hT9Jfb2oXy3Wc4eQ4--C_DxCECxsQ8QTXJhke9DBJeNn8P_bnha4IYwBWeH33CA9G8Wk5gh5vvyBRZ9lBPSCq74XxD_rHY</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Simpson, Scot H., BSP, PharmD, MSc</creator><creator>Abdelmoneim, Ahmed S., BPharm, MSc</creator><creator>Omran, Dima, BSc(Pharm)</creator><creator>Featherstone, Travis R., BSc(Pharm)</creator><general>Elsevier Inc</general><general>Elsevier Sequoia S.A</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>7TK</scope><scope>7TO</scope><scope>7TS</scope><scope>7U9</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>2014</creationdate><title>Prevalence of High On-treatment Platelet Reactivity in Diabetic Patients Treated with Aspirin</title><author>Simpson, Scot H., BSP, PharmD, MSc ; Abdelmoneim, Ahmed S., BPharm, MSc ; Omran, Dima, BSc(Pharm) ; Featherstone, Travis R., BSc(Pharm)</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c445t-fc978664b6ec7e8e2e839987422ca4f09343ed7d1955dd8e6e5ee9b5d56d7fee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aspirin</topic><topic>Aspirin - administration &amp; dosage</topic><topic>Aspirin - therapeutic use</topic><topic>Blood platelets</topic><topic>Blood Platelets - drug effects</topic><topic>Cardiovascular Diseases - prevention &amp; control</topic><topic>Diabetes</topic><topic>Diabetes Complications - prevention &amp; control</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Administration Schedule</topic><topic>Drug dosages</topic><topic>Drug resistance</topic><topic>Humans</topic><topic>Internal Medicine</topic><topic>Medical Records Systems, Computerized</topic><topic>Platelet Aggregation Inhibitors - administration &amp; dosage</topic><topic>Platelet Aggregation Inhibitors - therapeutic use</topic><topic>Prevalence</topic><topic>Primary Prevention - methods</topic><topic>Systematic review</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Simpson, Scot H., BSP, PharmD, MSc</creatorcontrib><creatorcontrib>Abdelmoneim, Ahmed S., BPharm, MSc</creatorcontrib><creatorcontrib>Omran, Dima, BSc(Pharm)</creatorcontrib><creatorcontrib>Featherstone, Travis R., BSc(Pharm)</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Physical Education Index</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>The American journal of medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Simpson, Scot H., BSP, PharmD, MSc</au><au>Abdelmoneim, Ahmed S., BPharm, MSc</au><au>Omran, Dima, BSc(Pharm)</au><au>Featherstone, Travis R., BSc(Pharm)</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence of High On-treatment Platelet Reactivity in Diabetic Patients Treated with Aspirin</atitle><jtitle>The American journal of medicine</jtitle><addtitle>Am J Med</addtitle><date>2014</date><risdate>2014</risdate><volume>127</volume><issue>1</issue><spage>95.e1</spage><epage>95.e9</epage><pages>95.e1-95.e9</pages><issn>0002-9343</issn><eissn>1555-7162</eissn><coden>AJMEAZ</coden><abstract>Abstract Background Randomized controlled trials have shown that ≤100 mg aspirin daily is not effective for primary prevention of cardiovascular events in diabetes; however, clinical and pharmacologic evidence suggests these patients need &gt;100 mg for adequate antiplatelet activity. Although high on-treatment platelet reactivity (HTPR) could explain the lack of benefit, prevalence of HTPR in diabetes is not known. This systematic review examined the relationship between daily aspirin dose and prevalence of HTPR in patients with diabetes. Methods Three electronic databases were searched until May 2013 using database-appropriate terms for aspirin, resistance, and diabetes. Studies were included if prevalence of HTPR was reported according to daily dose and diabetes status. Patients were stratified by daily aspirin dose and the weighted mean prevalence across studies was calculated. Where appropriate, pooled relative risks (RR) were calculated using a random-effects model. Results Data were available from 31 studies that enrolled 2147 diabetic patients. Overall, prevalence of HTPR was 21.9% (95% confidence interval [CI], 15.2%-28.5%) in diabetic patients and 15.8% (95% CI, 11.4%-20.3%) in nondiabetic patients (pooled RR 1.36; 95% CI, 1.08-1.71; I2 56%). Prevalence appeared to be dose related, with 398 (23.6%) of 1689 diabetic patients using ≤100 mg daily having HTPR compared with 64 (12.3%) of 518 diabetic patients using 101-325 mg daily (pooled RR 1.70; 95% CI, 1.07-2.72; I2 0%). Conclusions Although these observations should be verified in a clinical trial, the possibility that 1 in 4 patients have HTPR with doses commonly used in diabetes could have significant implications on overall effectiveness of aspirin.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24384107</pmid><doi>10.1016/j.amjmed.2013.09.019</doi></addata></record>
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subjects Aspirin
Aspirin - administration & dosage
Aspirin - therapeutic use
Blood platelets
Blood Platelets - drug effects
Cardiovascular Diseases - prevention & control
Diabetes
Diabetes Complications - prevention & control
Dose-Response Relationship, Drug
Drug Administration Schedule
Drug dosages
Drug resistance
Humans
Internal Medicine
Medical Records Systems, Computerized
Platelet Aggregation Inhibitors - administration & dosage
Platelet Aggregation Inhibitors - therapeutic use
Prevalence
Primary Prevention - methods
Systematic review
title Prevalence of High On-treatment Platelet Reactivity in Diabetic Patients Treated with Aspirin
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