Relationship between Haemoglobin A1c Values and Recurrent Cardiac Events: A Retrospective,Longitudinal Cohort Study
Objective: This study set out to analyse the impact of baseline glycosylated haemoglobin A 1c (HbA 1c ) values on the incidence of recurrent cardiac events in patients prescribed optimal secondary prevention medications and receiving aggressive cardiac risk factor management. Methods: This was a ret...
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Veröffentlicht in: | Clinical drug investigation 2008, Vol.28 (8), p.501-507 |
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creator | Kauffman, Amy B. Delate, Thomas Olson, Kari L. Cymbala, Alicia A. Hutka, Kara A. Kasten, Sheila L. Rasmussen, Jon R. |
description | Objective:
This study set out to analyse the impact of baseline glycosylated haemoglobin A
1c
(HbA
1c
) values on the incidence of recurrent cardiac events in patients prescribed optimal secondary prevention medications and receiving aggressive cardiac risk factor management.
Methods:
This was a retrospective study conducted at Kaiser Permanente Colorado and included adults followed by a clinical pharmacy specialist-managed cardiac risk service (CPCRS) with an incident cardiac event and an HbA
1c
value measured within 1 year prior or 60 days after the incident cardiac event was identified. Cox proportional hazards models were constructed to assess the relationship between HbA
1c
levels and recurrent cardiac events (assessed as continuous and categorical measures) after adjustment for potential confounding variables.
Results:
Of 5663 patients identified within an incident cardiac event between January 1999 and March 2005, 1270 (22.4%) patients had a baseline HbA
1c
value recorded. Of these 1270 patients, 215 (16.9%) had a recurrent cardiac event. Compared with the ‘no recurrent event’ cohort, the ‘recurrent event’ cohort were younger, less likely to have undergone an initial coronary artery bypass graft, and more likely to have undergone percutaneous coronary intervention with or without stent. The recurrent event cohort was also less likely to have purchased an HMG-CoA reductase inhibitor (‘statin’) [p = 0.043] at the time of the incident cardiac event. There was no significant difference in mean baseline HbA
1c
value between the cohorts. There were also no significant differences between the cohorts when categorized by baseline HbA
1c |
doi_str_mv | 10.2165/00044011-200828080-00005 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_69292749</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>69292749</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2235-229fa103549bd61420273cbc196b3987d59fd3c778cd00e2799b67ca1f5a65b63</originalsourceid><addsrcrecordid>eNqFkMlOwzAQhi0EolB4BeQTt8CME2_HqioUqRJSBVwtx3FKqjQpdgLi7QltgSOn2f7ZPkIowg1DwW8BIMsAMWEAiilQkAwp4EfkDFHqBDWq452fJoyLdETOY1wDoEDBTskIFdcKtDgj86WvbVe1TXyttjT33Yf3DZ1bv2lXdZtXDZ2goy-27n2ktino0rs-BN90dGpDUVlHZ-9DFC_ISWnr6C8Pdkye72ZP03myeLx_mE4WiWMs5QljurQIKc90XgjMGDCZutyhFnmqlSy4LovUSalcAeCZ1DoX0lksuRU8F-mYXO_nbkP7NhzVmU0Vna9r2_i2j0ZoppnM9CBUe6ELbYzBl2Ybqo0NnwbBfFM0PxTNL0Wzozi0Xh129PnGF3-NB2yDQO8FcSg1Kx_Muu1DM_z9__AvQqx8UQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>69292749</pqid></control><display><type>article</type><title>Relationship between Haemoglobin A1c Values and Recurrent Cardiac Events: A Retrospective,Longitudinal Cohort Study</title><source>MEDLINE</source><source>SpringerLink Journals - AutoHoldings</source><creator>Kauffman, Amy B. ; Delate, Thomas ; Olson, Kari L. ; Cymbala, Alicia A. ; Hutka, Kara A. ; Kasten, Sheila L. ; Rasmussen, Jon R.</creator><creatorcontrib>Kauffman, Amy B. ; Delate, Thomas ; Olson, Kari L. ; Cymbala, Alicia A. ; Hutka, Kara A. ; Kasten, Sheila L. ; Rasmussen, Jon R.</creatorcontrib><description>Objective:
This study set out to analyse the impact of baseline glycosylated haemoglobin A
1c
(HbA
1c
) values on the incidence of recurrent cardiac events in patients prescribed optimal secondary prevention medications and receiving aggressive cardiac risk factor management.
Methods:
This was a retrospective study conducted at Kaiser Permanente Colorado and included adults followed by a clinical pharmacy specialist-managed cardiac risk service (CPCRS) with an incident cardiac event and an HbA
1c
value measured within 1 year prior or 60 days after the incident cardiac event was identified. Cox proportional hazards models were constructed to assess the relationship between HbA
1c
levels and recurrent cardiac events (assessed as continuous and categorical measures) after adjustment for potential confounding variables.
Results:
Of 5663 patients identified within an incident cardiac event between January 1999 and March 2005, 1270 (22.4%) patients had a baseline HbA
1c
value recorded. Of these 1270 patients, 215 (16.9%) had a recurrent cardiac event. Compared with the ‘no recurrent event’ cohort, the ‘recurrent event’ cohort were younger, less likely to have undergone an initial coronary artery bypass graft, and more likely to have undergone percutaneous coronary intervention with or without stent. The recurrent event cohort was also less likely to have purchased an HMG-CoA reductase inhibitor (‘statin’) [p = 0.043] at the time of the incident cardiac event. There was no significant difference in mean baseline HbA
1c
value between the cohorts. There were also no significant differences between the cohorts when categorized by baseline HbA
1c
<7% as referent compared with ≥7% to <8%, ≥8% to <9%, ≥9 to <10%, and ≥10%. Moreover, there was no significant difference between cohorts when HbA
1c
values <7% were compared with values >7% in the unadjusted analysis. Results remained non-significant after adjustment for sex, incident cardiac event type, baseline age, β-blocker use, statin use and hyperlipidaemia.
Conclusion:
The results of this study suggest that an abnormal HbA
1c
is not predictive of recurrent cardiac events among patients with cardiovascular disease when other cardiovascular risk factors are being aggressively treated and appropriate secondary prevention medications are being taken. However, larger studies are warranted to validate these findings</description><identifier>ISSN: 1173-2563</identifier><identifier>EISSN: 1179-1918</identifier><identifier>DOI: 10.2165/00044011-200828080-00005</identifier><identifier>PMID: 18598096</identifier><language>eng</language><publisher>Cham: Springer International Publishing</publisher><subject>Adrenergic beta-Antagonists - therapeutic use ; Adult ; Angiotensin-Converting Enzyme Inhibitors - therapeutic use ; Aspirin - therapeutic use ; Cardiovascular Diseases - diagnosis ; Cardiovascular Diseases - prevention & control ; Colorado ; Female ; Glycated Hemoglobin A - analysis ; Humans ; Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use ; Hypoglycemic Agents - therapeutic use ; Internal Medicine ; Longitudinal Studies ; Male ; Medicine ; Medicine & Public Health ; Original Research Article ; Pharmacology/Toxicology ; Pharmacotherapy ; Platelet Aggregation Inhibitors ; Predictive Value of Tests ; Prognosis ; Recurrence ; Retrospective Studies ; Risk Assessment</subject><ispartof>Clinical drug investigation, 2008, Vol.28 (8), p.501-507</ispartof><rights>Adis Data Information BV 2008</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2235-229fa103549bd61420273cbc196b3987d59fd3c778cd00e2799b67ca1f5a65b63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.2165/00044011-200828080-00005$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.2165/00044011-200828080-00005$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,780,784,4023,27922,27923,27924,41487,42556,51318</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18598096$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kauffman, Amy B.</creatorcontrib><creatorcontrib>Delate, Thomas</creatorcontrib><creatorcontrib>Olson, Kari L.</creatorcontrib><creatorcontrib>Cymbala, Alicia A.</creatorcontrib><creatorcontrib>Hutka, Kara A.</creatorcontrib><creatorcontrib>Kasten, Sheila L.</creatorcontrib><creatorcontrib>Rasmussen, Jon R.</creatorcontrib><title>Relationship between Haemoglobin A1c Values and Recurrent Cardiac Events: A Retrospective,Longitudinal Cohort Study</title><title>Clinical drug investigation</title><addtitle>Clin. Drug Investig</addtitle><addtitle>Clin Drug Investig</addtitle><description>Objective:
This study set out to analyse the impact of baseline glycosylated haemoglobin A
1c
(HbA
1c
) values on the incidence of recurrent cardiac events in patients prescribed optimal secondary prevention medications and receiving aggressive cardiac risk factor management.
Methods:
This was a retrospective study conducted at Kaiser Permanente Colorado and included adults followed by a clinical pharmacy specialist-managed cardiac risk service (CPCRS) with an incident cardiac event and an HbA
1c
value measured within 1 year prior or 60 days after the incident cardiac event was identified. Cox proportional hazards models were constructed to assess the relationship between HbA
1c
levels and recurrent cardiac events (assessed as continuous and categorical measures) after adjustment for potential confounding variables.
Results:
Of 5663 patients identified within an incident cardiac event between January 1999 and March 2005, 1270 (22.4%) patients had a baseline HbA
1c
value recorded. Of these 1270 patients, 215 (16.9%) had a recurrent cardiac event. Compared with the ‘no recurrent event’ cohort, the ‘recurrent event’ cohort were younger, less likely to have undergone an initial coronary artery bypass graft, and more likely to have undergone percutaneous coronary intervention with or without stent. The recurrent event cohort was also less likely to have purchased an HMG-CoA reductase inhibitor (‘statin’) [p = 0.043] at the time of the incident cardiac event. There was no significant difference in mean baseline HbA
1c
value between the cohorts. There were also no significant differences between the cohorts when categorized by baseline HbA
1c
<7% as referent compared with ≥7% to <8%, ≥8% to <9%, ≥9 to <10%, and ≥10%. Moreover, there was no significant difference between cohorts when HbA
1c
values <7% were compared with values >7% in the unadjusted analysis. Results remained non-significant after adjustment for sex, incident cardiac event type, baseline age, β-blocker use, statin use and hyperlipidaemia.
Conclusion:
The results of this study suggest that an abnormal HbA
1c
is not predictive of recurrent cardiac events among patients with cardiovascular disease when other cardiovascular risk factors are being aggressively treated and appropriate secondary prevention medications are being taken. However, larger studies are warranted to validate these findings</description><subject>Adrenergic beta-Antagonists - therapeutic use</subject><subject>Adult</subject><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Aspirin - therapeutic use</subject><subject>Cardiovascular Diseases - diagnosis</subject><subject>Cardiovascular Diseases - prevention & control</subject><subject>Colorado</subject><subject>Female</subject><subject>Glycated Hemoglobin A - analysis</subject><subject>Humans</subject><subject>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</subject><subject>Hypoglycemic Agents - therapeutic use</subject><subject>Internal Medicine</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Original Research Article</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacotherapy</subject><subject>Platelet Aggregation Inhibitors</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Recurrence</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><issn>1173-2563</issn><issn>1179-1918</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkMlOwzAQhi0EolB4BeQTt8CME2_HqioUqRJSBVwtx3FKqjQpdgLi7QltgSOn2f7ZPkIowg1DwW8BIMsAMWEAiilQkAwp4EfkDFHqBDWq452fJoyLdETOY1wDoEDBTskIFdcKtDgj86WvbVe1TXyttjT33Yf3DZ1bv2lXdZtXDZ2goy-27n2ktino0rs-BN90dGpDUVlHZ-9DFC_ISWnr6C8Pdkye72ZP03myeLx_mE4WiWMs5QljurQIKc90XgjMGDCZutyhFnmqlSy4LovUSalcAeCZ1DoX0lksuRU8F-mYXO_nbkP7NhzVmU0Vna9r2_i2j0ZoppnM9CBUe6ELbYzBl2Ybqo0NnwbBfFM0PxTNL0Wzozi0Xh129PnGF3-NB2yDQO8FcSg1Kx_Muu1DM_z9__AvQqx8UQ</recordid><startdate>2008</startdate><enddate>2008</enddate><creator>Kauffman, Amy B.</creator><creator>Delate, Thomas</creator><creator>Olson, Kari L.</creator><creator>Cymbala, Alicia A.</creator><creator>Hutka, Kara A.</creator><creator>Kasten, Sheila L.</creator><creator>Rasmussen, Jon R.</creator><general>Springer International Publishing</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>7X8</scope></search><sort><creationdate>2008</creationdate><title>Relationship between Haemoglobin A1c Values and Recurrent Cardiac Events</title><author>Kauffman, Amy B. ; Delate, Thomas ; Olson, Kari L. ; Cymbala, Alicia A. ; Hutka, Kara A. ; Kasten, Sheila L. ; Rasmussen, Jon R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2235-229fa103549bd61420273cbc196b3987d59fd3c778cd00e2799b67ca1f5a65b63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adrenergic beta-Antagonists - therapeutic use</topic><topic>Adult</topic><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Aspirin - therapeutic use</topic><topic>Cardiovascular Diseases - diagnosis</topic><topic>Cardiovascular Diseases - prevention & control</topic><topic>Colorado</topic><topic>Female</topic><topic>Glycated Hemoglobin A - analysis</topic><topic>Humans</topic><topic>Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use</topic><topic>Hypoglycemic Agents - therapeutic use</topic><topic>Internal Medicine</topic><topic>Longitudinal Studies</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Original Research Article</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacotherapy</topic><topic>Platelet Aggregation Inhibitors</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Recurrence</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kauffman, Amy B.</creatorcontrib><creatorcontrib>Delate, Thomas</creatorcontrib><creatorcontrib>Olson, Kari L.</creatorcontrib><creatorcontrib>Cymbala, Alicia A.</creatorcontrib><creatorcontrib>Hutka, Kara A.</creatorcontrib><creatorcontrib>Kasten, Sheila L.</creatorcontrib><creatorcontrib>Rasmussen, Jon R.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical drug investigation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kauffman, Amy B.</au><au>Delate, Thomas</au><au>Olson, Kari L.</au><au>Cymbala, Alicia A.</au><au>Hutka, Kara A.</au><au>Kasten, Sheila L.</au><au>Rasmussen, Jon R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relationship between Haemoglobin A1c Values and Recurrent Cardiac Events: A Retrospective,Longitudinal Cohort Study</atitle><jtitle>Clinical drug investigation</jtitle><stitle>Clin. Drug Investig</stitle><addtitle>Clin Drug Investig</addtitle><date>2008</date><risdate>2008</risdate><volume>28</volume><issue>8</issue><spage>501</spage><epage>507</epage><pages>501-507</pages><issn>1173-2563</issn><eissn>1179-1918</eissn><abstract>Objective:
This study set out to analyse the impact of baseline glycosylated haemoglobin A
1c
(HbA
1c
) values on the incidence of recurrent cardiac events in patients prescribed optimal secondary prevention medications and receiving aggressive cardiac risk factor management.
Methods:
This was a retrospective study conducted at Kaiser Permanente Colorado and included adults followed by a clinical pharmacy specialist-managed cardiac risk service (CPCRS) with an incident cardiac event and an HbA
1c
value measured within 1 year prior or 60 days after the incident cardiac event was identified. Cox proportional hazards models were constructed to assess the relationship between HbA
1c
levels and recurrent cardiac events (assessed as continuous and categorical measures) after adjustment for potential confounding variables.
Results:
Of 5663 patients identified within an incident cardiac event between January 1999 and March 2005, 1270 (22.4%) patients had a baseline HbA
1c
value recorded. Of these 1270 patients, 215 (16.9%) had a recurrent cardiac event. Compared with the ‘no recurrent event’ cohort, the ‘recurrent event’ cohort were younger, less likely to have undergone an initial coronary artery bypass graft, and more likely to have undergone percutaneous coronary intervention with or without stent. The recurrent event cohort was also less likely to have purchased an HMG-CoA reductase inhibitor (‘statin’) [p = 0.043] at the time of the incident cardiac event. There was no significant difference in mean baseline HbA
1c
value between the cohorts. There were also no significant differences between the cohorts when categorized by baseline HbA
1c
<7% as referent compared with ≥7% to <8%, ≥8% to <9%, ≥9 to <10%, and ≥10%. Moreover, there was no significant difference between cohorts when HbA
1c
values <7% were compared with values >7% in the unadjusted analysis. Results remained non-significant after adjustment for sex, incident cardiac event type, baseline age, β-blocker use, statin use and hyperlipidaemia.
Conclusion:
The results of this study suggest that an abnormal HbA
1c
is not predictive of recurrent cardiac events among patients with cardiovascular disease when other cardiovascular risk factors are being aggressively treated and appropriate secondary prevention medications are being taken. However, larger studies are warranted to validate these findings</abstract><cop>Cham</cop><pub>Springer International Publishing</pub><pmid>18598096</pmid><doi>10.2165/00044011-200828080-00005</doi><tpages>7</tpages></addata></record> |
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ispartof | Clinical drug investigation, 2008, Vol.28 (8), p.501-507 |
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language | eng |
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source | MEDLINE; SpringerLink Journals - AutoHoldings |
subjects | Adrenergic beta-Antagonists - therapeutic use Adult Angiotensin-Converting Enzyme Inhibitors - therapeutic use Aspirin - therapeutic use Cardiovascular Diseases - diagnosis Cardiovascular Diseases - prevention & control Colorado Female Glycated Hemoglobin A - analysis Humans Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use Hypoglycemic Agents - therapeutic use Internal Medicine Longitudinal Studies Male Medicine Medicine & Public Health Original Research Article Pharmacology/Toxicology Pharmacotherapy Platelet Aggregation Inhibitors Predictive Value of Tests Prognosis Recurrence Retrospective Studies Risk Assessment |
title | Relationship between Haemoglobin A1c Values and Recurrent Cardiac Events: A Retrospective,Longitudinal Cohort Study |
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