Combination Therapy Improves Survival After Acute Myocardial Infarction in the Elderly with Chronic Kidney Disease

Background: Individuals with chronic kidney disease have a high mortality rate after acute myocardial infarction. It is not known how frequently these individuals are prescribed combination cardioprotective therapy and if survival is affected by such therapy after acute myocardial infarction. Method...

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Veröffentlicht in:Renal failure 2004-01, Vol.26 (6), p.715-725
Hauptverfasser: Krause, Michelle W., Massing, Mark, Kshirsagar, Abhijit, Rosamond, Wayne, Simpson, Ross J.
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container_end_page 725
container_issue 6
container_start_page 715
container_title Renal failure
container_volume 26
creator Krause, Michelle W.
Massing, Mark
Kshirsagar, Abhijit
Rosamond, Wayne
Simpson, Ross J.
description Background: Individuals with chronic kidney disease have a high mortality rate after acute myocardial infarction. It is not known how frequently these individuals are prescribed combination cardioprotective therapy and if survival is affected by such therapy after acute myocardial infarction. Methods: A retrospective cohort study of 1,342 Medicare recipients with acute myocardial infarction. Data were collected by medical chart abstraction as part of the Cooperative Cardiovascular Project in 60 hospitals in North Carolina during 5 30 1996-12 28 1997. We categorized cardioprotective medication use as aspirin alone, aspirin with beta-blockers, and aspirin with beta-blockers and ace-inhibitors. Chronic kidney disease was defined as a derived glomerular filtration rate (GFR) ranging from 15-89 mL min 1.73 m2. Cox proportional hazards regression analyses were performed to determine the effect of cardioprotective medication use on survival while controlling for potential explanatory variables. Results: The prevalence of cardioprotective medication use differed among levels of chronic kidney disease. Those with severe kidney disease (GFR 15-29 mL min 1.73 m2) were less frequently prescribed aspirin with beta-blockers, 27.1%, and only 8.6% were prescribed aspirin with beta-blockers and ace-inhibitors. Survival was improved with prescribed cardioprotective medication use. In severe kidney disease (GFR 15-29 mL min 1.73 m2), the hazards risk for death was 0.21 (0.08, 0.53) for aspirin alone, 0.17 (0.06, 0.51) for aspirin with beta-blockers, and 0.35 (0.09, 1.42) for aspirin with beta-blockers and ace-inhibitors. Conclusions: Individuals with chronic kidney disease benefit from combination cardioprotective therapy, but are less likely to be prescribed them after acute myocardial infarction. Further investigation is warranted to identify possible reasons for these observed treatment disparities.
doi_str_mv 10.1081/JDI-200037110
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It is not known how frequently these individuals are prescribed combination cardioprotective therapy and if survival is affected by such therapy after acute myocardial infarction. Methods: A retrospective cohort study of 1,342 Medicare recipients with acute myocardial infarction. Data were collected by medical chart abstraction as part of the Cooperative Cardiovascular Project in 60 hospitals in North Carolina during 5 30 1996-12 28 1997. We categorized cardioprotective medication use as aspirin alone, aspirin with beta-blockers, and aspirin with beta-blockers and ace-inhibitors. Chronic kidney disease was defined as a derived glomerular filtration rate (GFR) ranging from 15-89 mL min 1.73 m2. Cox proportional hazards regression analyses were performed to determine the effect of cardioprotective medication use on survival while controlling for potential explanatory variables. Results: The prevalence of cardioprotective medication use differed among levels of chronic kidney disease. Those with severe kidney disease (GFR 15-29 mL min 1.73 m2) were less frequently prescribed aspirin with beta-blockers, 27.1%, and only 8.6% were prescribed aspirin with beta-blockers and ace-inhibitors. Survival was improved with prescribed cardioprotective medication use. In severe kidney disease (GFR 15-29 mL min 1.73 m2), the hazards risk for death was 0.21 (0.08, 0.53) for aspirin alone, 0.17 (0.06, 0.51) for aspirin with beta-blockers, and 0.35 (0.09, 1.42) for aspirin with beta-blockers and ace-inhibitors. Conclusions: Individuals with chronic kidney disease benefit from combination cardioprotective therapy, but are less likely to be prescribed them after acute myocardial infarction. Further investigation is warranted to identify possible reasons for these observed treatment disparities.</description><identifier>ISSN: 0886-022X</identifier><identifier>EISSN: 1525-6049</identifier><identifier>DOI: 10.1081/JDI-200037110</identifier><identifier>PMID: 15600265</identifier><identifier>CODEN: REFAE8</identifier><language>eng</language><publisher>Colchester: Informa UK Ltd</publisher><subject>Adrenergic beta-Antagonists - therapeutic use ; Aged ; Aged, 80 and over ; Anesthesia. Intensive care medicine. Transfusions. 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It is not known how frequently these individuals are prescribed combination cardioprotective therapy and if survival is affected by such therapy after acute myocardial infarction. Methods: A retrospective cohort study of 1,342 Medicare recipients with acute myocardial infarction. Data were collected by medical chart abstraction as part of the Cooperative Cardiovascular Project in 60 hospitals in North Carolina during 5 30 1996-12 28 1997. We categorized cardioprotective medication use as aspirin alone, aspirin with beta-blockers, and aspirin with beta-blockers and ace-inhibitors. Chronic kidney disease was defined as a derived glomerular filtration rate (GFR) ranging from 15-89 mL min 1.73 m2. Cox proportional hazards regression analyses were performed to determine the effect of cardioprotective medication use on survival while controlling for potential explanatory variables. Results: The prevalence of cardioprotective medication use differed among levels of chronic kidney disease. Those with severe kidney disease (GFR 15-29 mL min 1.73 m2) were less frequently prescribed aspirin with beta-blockers, 27.1%, and only 8.6% were prescribed aspirin with beta-blockers and ace-inhibitors. Survival was improved with prescribed cardioprotective medication use. In severe kidney disease (GFR 15-29 mL min 1.73 m2), the hazards risk for death was 0.21 (0.08, 0.53) for aspirin alone, 0.17 (0.06, 0.51) for aspirin with beta-blockers, and 0.35 (0.09, 1.42) for aspirin with beta-blockers and ace-inhibitors. Conclusions: Individuals with chronic kidney disease benefit from combination cardioprotective therapy, but are less likely to be prescribed them after acute myocardial infarction. Further investigation is warranted to identify possible reasons for these observed treatment disparities.</description><subject>Adrenergic beta-Antagonists - therapeutic use</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</subject><subject>Aspirin - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cardioprotective medication use</subject><subject>Cardiotonic Agents - therapeutic use</subject><subject>Cardiovascular disease</subject><subject>Chronic kidney disease</subject><subject>Cohort Studies</subject><subject>Confidence Intervals</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Geriatric Assessment</subject><subject>Humans</subject><subject>Kidney Failure, Chronic - diagnosis</subject><subject>Kidney Failure, Chronic - epidemiology</subject><subject>Kidney Failure, Chronic - therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Myocardial Infarction - diagnosis</subject><subject>Myocardial Infarction - drug therapy</subject><subject>Myocardial Infarction - mortality</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Prognosis</subject><subject>Registries</subject><subject>Renal Dialysis - adverse effects</subject><subject>Renal Dialysis - methods</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Survival Analysis</subject><subject>Treatment Outcome</subject><issn>0886-022X</issn><issn>1525-6049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kUFv1DAQRi0EokvhyBX5Qm8BO4kd73G1LbBQxIEicbNsZ6y4cuzFdrbKvydlFyoOPY00et9o5g1Cryl5R4mg7z9f7qqaENJ0lJInaEVZzSpO2vVTtCJC8IrU9c8z9CLnW0IoE139HJ1RxgmpOVuhtI2jdkEVFwO-GSCp_Yx34z7FA2T8fUoHd1Aeb2yBhDdmKoC_ztGo1LulvQtWJfMn6wIuA-Ar30PyM75zZcDbIcXgDP7i-gAzvnQZVIaX6JlVPsOrUz1HPz5c3Ww_VdffPu62m-vKtIyVygKlWnRgFAdN-ZppZixoDj1RrQYrbMsbbVvRMCK4VhqIIX1LeQ-cWto05-jiOHc55tcEucjRZQPeqwBxypJ3tKN1ew9WR9CkmHMCK_fJjSrNkhJ5L1kukuU_yQv_5jR40iP0D_TJ6gK8PQEqG-VtUsG4_MDxek055wsnjpwLNqZR3cXke1nU7GP6G2oe26H7LzqA8mVY_gLyNk4pLGIf2f43B1iqvA</recordid><startdate>20040101</startdate><enddate>20040101</enddate><creator>Krause, Michelle W.</creator><creator>Massing, Mark</creator><creator>Kshirsagar, Abhijit</creator><creator>Rosamond, Wayne</creator><creator>Simpson, Ross J.</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</general><scope>IQODW</scope><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>20040101</creationdate><title>Combination Therapy Improves Survival After Acute Myocardial Infarction in the Elderly with Chronic Kidney Disease</title><author>Krause, Michelle W. ; Massing, Mark ; Kshirsagar, Abhijit ; Rosamond, Wayne ; Simpson, Ross J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c455t-fe11b87eca6eb1695b5cfeb6ed0a4bef8f463bf4835086babe0c0d416de61f133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Adrenergic beta-Antagonists - therapeutic use</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Angiotensin-Converting Enzyme Inhibitors - therapeutic use</topic><topic>Aspirin - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Cardioprotective medication use</topic><topic>Cardiotonic Agents - therapeutic use</topic><topic>Cardiovascular disease</topic><topic>Chronic kidney disease</topic><topic>Cohort Studies</topic><topic>Confidence Intervals</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Geriatric Assessment</topic><topic>Humans</topic><topic>Kidney Failure, Chronic - diagnosis</topic><topic>Kidney Failure, Chronic - epidemiology</topic><topic>Kidney Failure, Chronic - therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Myocardial Infarction - diagnosis</topic><topic>Myocardial Infarction - drug therapy</topic><topic>Myocardial Infarction - mortality</topic><topic>Nephrology. Urinary tract diseases</topic><topic>Prognosis</topic><topic>Registries</topic><topic>Renal Dialysis - adverse effects</topic><topic>Renal Dialysis - methods</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Survival Analysis</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Krause, Michelle W.</creatorcontrib><creatorcontrib>Massing, Mark</creatorcontrib><creatorcontrib>Kshirsagar, Abhijit</creatorcontrib><creatorcontrib>Rosamond, Wayne</creatorcontrib><creatorcontrib>Simpson, Ross J.</creatorcontrib><collection>Pascal-Francis</collection><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>Renal failure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Krause, Michelle W.</au><au>Massing, Mark</au><au>Kshirsagar, Abhijit</au><au>Rosamond, Wayne</au><au>Simpson, Ross J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Combination Therapy Improves Survival After Acute Myocardial Infarction in the Elderly with Chronic Kidney Disease</atitle><jtitle>Renal failure</jtitle><addtitle>Ren Fail</addtitle><date>2004-01-01</date><risdate>2004</risdate><volume>26</volume><issue>6</issue><spage>715</spage><epage>725</epage><pages>715-725</pages><issn>0886-022X</issn><eissn>1525-6049</eissn><coden>REFAE8</coden><abstract>Background: Individuals with chronic kidney disease have a high mortality rate after acute myocardial infarction. It is not known how frequently these individuals are prescribed combination cardioprotective therapy and if survival is affected by such therapy after acute myocardial infarction. Methods: A retrospective cohort study of 1,342 Medicare recipients with acute myocardial infarction. Data were collected by medical chart abstraction as part of the Cooperative Cardiovascular Project in 60 hospitals in North Carolina during 5 30 1996-12 28 1997. We categorized cardioprotective medication use as aspirin alone, aspirin with beta-blockers, and aspirin with beta-blockers and ace-inhibitors. Chronic kidney disease was defined as a derived glomerular filtration rate (GFR) ranging from 15-89 mL min 1.73 m2. Cox proportional hazards regression analyses were performed to determine the effect of cardioprotective medication use on survival while controlling for potential explanatory variables. Results: The prevalence of cardioprotective medication use differed among levels of chronic kidney disease. Those with severe kidney disease (GFR 15-29 mL min 1.73 m2) were less frequently prescribed aspirin with beta-blockers, 27.1%, and only 8.6% were prescribed aspirin with beta-blockers and ace-inhibitors. Survival was improved with prescribed cardioprotective medication use. In severe kidney disease (GFR 15-29 mL min 1.73 m2), the hazards risk for death was 0.21 (0.08, 0.53) for aspirin alone, 0.17 (0.06, 0.51) for aspirin with beta-blockers, and 0.35 (0.09, 1.42) for aspirin with beta-blockers and ace-inhibitors. Conclusions: Individuals with chronic kidney disease benefit from combination cardioprotective therapy, but are less likely to be prescribed them after acute myocardial infarction. Further investigation is warranted to identify possible reasons for these observed treatment disparities.</abstract><cop>Colchester</cop><pub>Informa UK Ltd</pub><pmid>15600265</pmid><doi>10.1081/JDI-200037110</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
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subjects Adrenergic beta-Antagonists - therapeutic use
Aged
Aged, 80 and over
Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy
Angiotensin-Converting Enzyme Inhibitors - therapeutic use
Aspirin - therapeutic use
Biological and medical sciences
Cardioprotective medication use
Cardiotonic Agents - therapeutic use
Cardiovascular disease
Chronic kidney disease
Cohort Studies
Confidence Intervals
Drug Therapy, Combination
Female
Geriatric Assessment
Humans
Kidney Failure, Chronic - diagnosis
Kidney Failure, Chronic - epidemiology
Kidney Failure, Chronic - therapy
Male
Medical sciences
Myocardial Infarction - diagnosis
Myocardial Infarction - drug therapy
Myocardial Infarction - mortality
Nephrology. Urinary tract diseases
Prognosis
Registries
Renal Dialysis - adverse effects
Renal Dialysis - methods
Retrospective Studies
Risk Assessment
Survival Analysis
Treatment Outcome
title Combination Therapy Improves Survival After Acute Myocardial Infarction in the Elderly with Chronic Kidney Disease
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