Outcomes with Changes in Prescribing of Glycoprotein IIb/IIIa Inhibitors in PCI
Background Glycoprotein IIb/IIIa receptor antagonists have been shown to have an impact on the outcomes of death/myocardial infarction (MI) in patients undergoing percutaneous coronary intervention. At our institution, tirofiban has largely replaced abciximab in an attempt to decrease costs. Objecti...
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creator | Dobesh, Paul P Lanfear, Sara L Abu-Shanab, Joy R Lakamp, Jonathan E Gowda, Siddhesh Haikal, Maged Y |
description | Background
Glycoprotein IIb/IIIa receptor antagonists have been shown to have an impact on the outcomes of death/myocardial infarction (MI) in patients undergoing percutaneous coronary intervention. At our institution, tirofiban has largely replaced abciximab in an attempt to decrease costs.
Objective
To assess the impact of this change on patient outcomes in the absence of head-to-head trials.
Methods
Medical records were reviewed and telephone follow-ups were conducted on patients receiving tirofiban (n = 83) at our facility between February and November 1999. Death/MI at 30 days and 6 months after infusion were recorded. Safety and length of stay (LOS) were also assessed. These data were compared using χ2 analysis with results obtained from a previous review of abciximab use (n = 83) collected between May 1997 and November 1998.
Results
There was no difference in the baseline incidence of (1) cardiovascular risk factors, (2) prior revascularization, (3) prior MI, (4) the number of vessels with atherosclerotic disease assessed by angiography, and (5) the number of vessels receiving procedures. Death/MI trended to be worse with tirofiban versus abciximab at our institution at 30 days (4.8% abciximab vs. 12% tirofiban; p = 0.163) and 6 months (6% abciximab vs. 18.1% tirofiban; p = 0.032). Bleeding and median LOS (3 d abciximab vs. 3 d tirofiban) were not different. Despite an increase in pharmacy cost, the use of abciximab provided these outcomes without an increase in total hospital cost.
Conclusions
The perceived economically driven change in medication selection from abciximab to tirofiban may not have been appropriate based on the negative trends seen in this review. To maintain optimal patient outcomes, this change should be reevaluated. |
doi_str_mv | 10.1345/aph.1C363 |
format | Article |
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Glycoprotein IIb/IIIa receptor antagonists have been shown to have an impact on the outcomes of death/myocardial infarction (MI) in patients undergoing percutaneous coronary intervention. At our institution, tirofiban has largely replaced abciximab in an attempt to decrease costs.
Objective
To assess the impact of this change on patient outcomes in the absence of head-to-head trials.
Methods
Medical records were reviewed and telephone follow-ups were conducted on patients receiving tirofiban (n = 83) at our facility between February and November 1999. Death/MI at 30 days and 6 months after infusion were recorded. Safety and length of stay (LOS) were also assessed. These data were compared using χ2 analysis with results obtained from a previous review of abciximab use (n = 83) collected between May 1997 and November 1998.
Results
There was no difference in the baseline incidence of (1) cardiovascular risk factors, (2) prior revascularization, (3) prior MI, (4) the number of vessels with atherosclerotic disease assessed by angiography, and (5) the number of vessels receiving procedures. Death/MI trended to be worse with tirofiban versus abciximab at our institution at 30 days (4.8% abciximab vs. 12% tirofiban; p = 0.163) and 6 months (6% abciximab vs. 18.1% tirofiban; p = 0.032). Bleeding and median LOS (3 d abciximab vs. 3 d tirofiban) were not different. Despite an increase in pharmacy cost, the use of abciximab provided these outcomes without an increase in total hospital cost.
Conclusions
The perceived economically driven change in medication selection from abciximab to tirofiban may not have been appropriate based on the negative trends seen in this review. To maintain optimal patient outcomes, this change should be reevaluated.</description><identifier>ISSN: 1060-0280</identifier><identifier>EISSN: 1542-6270</identifier><identifier>DOI: 10.1345/aph.1C363</identifier><identifier>PMID: 14519056</identifier><identifier>CODEN: APHRER</identifier><language>eng</language><publisher>Los Angeles, CA: Harvey Whitney Books</publisher><subject><![CDATA[Angioplasty, Balloon, Coronary ; Antibodies, Monoclonal - administration & dosage ; Antibodies, Monoclonal - economics ; Antibodies, Monoclonal - therapeutic use ; Biological and medical sciences ; Cardiovascular system ; Female ; Humans ; Immunoglobulin Fab Fragments - administration & dosage ; Immunoglobulin Fab Fragments - economics ; Immunoglobulin Fab Fragments - therapeutic use ; Male ; Medical sciences ; Middle Aged ; Miscellaneous ; Myocardial Infarction - mortality ; Myocardial Infarction - therapy ; Pharmacology. Drug treatments ; Platelet Glycoprotein GPIIb-IIIa Complex - administration & dosage ; Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors ; Platelet Glycoprotein GPIIb-IIIa Complex - therapeutic use ; Retrospective Studies ; Treatment Outcome ; Tyrosine - administration & dosage ; Tyrosine - adverse effects ; Tyrosine - analogs & derivatives]]></subject><ispartof>The Annals of pharmacotherapy, 2003-10, Vol.37 (10), p.1375-1380</ispartof><rights>2003 SAGE Publications</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c334t-c694b6cdbbeed31e2b5bbb8dce19ef5f4311f79c708bd07248da37ca3a3b953a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1345/aph.1C363$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1345/aph.1C363$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,776,780,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15183521$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14519056$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dobesh, Paul P</creatorcontrib><creatorcontrib>Lanfear, Sara L</creatorcontrib><creatorcontrib>Abu-Shanab, Joy R</creatorcontrib><creatorcontrib>Lakamp, Jonathan E</creatorcontrib><creatorcontrib>Gowda, Siddhesh</creatorcontrib><creatorcontrib>Haikal, Maged Y</creatorcontrib><title>Outcomes with Changes in Prescribing of Glycoprotein IIb/IIIa Inhibitors in PCI</title><title>The Annals of pharmacotherapy</title><addtitle>Ann Pharmacother</addtitle><description>Background
Glycoprotein IIb/IIIa receptor antagonists have been shown to have an impact on the outcomes of death/myocardial infarction (MI) in patients undergoing percutaneous coronary intervention. At our institution, tirofiban has largely replaced abciximab in an attempt to decrease costs.
Objective
To assess the impact of this change on patient outcomes in the absence of head-to-head trials.
Methods
Medical records were reviewed and telephone follow-ups were conducted on patients receiving tirofiban (n = 83) at our facility between February and November 1999. Death/MI at 30 days and 6 months after infusion were recorded. Safety and length of stay (LOS) were also assessed. These data were compared using χ2 analysis with results obtained from a previous review of abciximab use (n = 83) collected between May 1997 and November 1998.
Results
There was no difference in the baseline incidence of (1) cardiovascular risk factors, (2) prior revascularization, (3) prior MI, (4) the number of vessels with atherosclerotic disease assessed by angiography, and (5) the number of vessels receiving procedures. Death/MI trended to be worse with tirofiban versus abciximab at our institution at 30 days (4.8% abciximab vs. 12% tirofiban; p = 0.163) and 6 months (6% abciximab vs. 18.1% tirofiban; p = 0.032). Bleeding and median LOS (3 d abciximab vs. 3 d tirofiban) were not different. Despite an increase in pharmacy cost, the use of abciximab provided these outcomes without an increase in total hospital cost.
Conclusions
The perceived economically driven change in medication selection from abciximab to tirofiban may not have been appropriate based on the negative trends seen in this review. To maintain optimal patient outcomes, this change should be reevaluated.</description><subject>Angioplasty, Balloon, Coronary</subject><subject>Antibodies, Monoclonal - administration & dosage</subject><subject>Antibodies, Monoclonal - economics</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular system</subject><subject>Female</subject><subject>Humans</subject><subject>Immunoglobulin Fab Fragments - administration & dosage</subject><subject>Immunoglobulin Fab Fragments - economics</subject><subject>Immunoglobulin Fab Fragments - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Miscellaneous</subject><subject>Myocardial Infarction - mortality</subject><subject>Myocardial Infarction - therapy</subject><subject>Pharmacology. Drug treatments</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - administration & dosage</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><subject>Tyrosine - administration & dosage</subject><subject>Tyrosine - adverse effects</subject><subject>Tyrosine - analogs & derivatives</subject><issn>1060-0280</issn><issn>1542-6270</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkMlOwzAQQC0EomU58AMoF0Ac0nqJ4-SIIiiRKpUDnC3bcRpXWYqdKOrfY0ilXrh4PJo3ix4AdwguEInoUuyrBcpITM7AHNEIhzFm8Nz_YQxDiBM4A1fO7SCEKcLpJZihiKIU0ngONpuhV12jXTCavgqySrRbn5g2-LDaKWukabdBVwar-qC6ve167Wt5Lpd5nosgbytP9J2dWrL8BlyUonb69hivwdfb62f2Hq43qzx7WYeKkKgPVZxGMlaFlFoXBGksqZQyKZRGqS5pGRGESpYqBhNZQIajpBCEKUEEkSn17zV4nOb6k74H7XreGKd0XYtWd4PjjDJMMY48-DyBynbOWV3yvTWNsAeOIP-1x709_mfPs_fHoYNsdHEij7o88HAEhFOiLq1olXEnjqKEUIxO1zmx1XzXDbb1Mv7d-DSBldlWo7Gau0bUtd-P-DiOhE09jJIf_iCREg</recordid><startdate>20031001</startdate><enddate>20031001</enddate><creator>Dobesh, Paul P</creator><creator>Lanfear, Sara L</creator><creator>Abu-Shanab, Joy R</creator><creator>Lakamp, Jonathan E</creator><creator>Gowda, Siddhesh</creator><creator>Haikal, Maged Y</creator><general>Harvey Whitney Books</general><general>SAGE Publications</general><general>Whitney</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>20031001</creationdate><title>Outcomes with Changes in Prescribing of Glycoprotein IIb/IIIa Inhibitors in PCI</title><author>Dobesh, Paul P ; Lanfear, Sara L ; Abu-Shanab, Joy R ; Lakamp, Jonathan E ; Gowda, Siddhesh ; Haikal, Maged Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c334t-c694b6cdbbeed31e2b5bbb8dce19ef5f4311f79c708bd07248da37ca3a3b953a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Angioplasty, Balloon, Coronary</topic><topic>Antibodies, Monoclonal - administration & dosage</topic><topic>Antibodies, Monoclonal - economics</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Cardiovascular system</topic><topic>Female</topic><topic>Humans</topic><topic>Immunoglobulin Fab Fragments - administration & dosage</topic><topic>Immunoglobulin Fab Fragments - economics</topic><topic>Immunoglobulin Fab Fragments - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Miscellaneous</topic><topic>Myocardial Infarction - mortality</topic><topic>Myocardial Infarction - therapy</topic><topic>Pharmacology. Drug treatments</topic><topic>Platelet Glycoprotein GPIIb-IIIa Complex - administration & dosage</topic><topic>Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors</topic><topic>Platelet Glycoprotein GPIIb-IIIa Complex - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Treatment Outcome</topic><topic>Tyrosine - administration & dosage</topic><topic>Tyrosine - adverse effects</topic><topic>Tyrosine - analogs & derivatives</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Dobesh, Paul P</creatorcontrib><creatorcontrib>Lanfear, Sara L</creatorcontrib><creatorcontrib>Abu-Shanab, Joy R</creatorcontrib><creatorcontrib>Lakamp, Jonathan E</creatorcontrib><creatorcontrib>Gowda, Siddhesh</creatorcontrib><creatorcontrib>Haikal, Maged Y</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>The Annals of pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Dobesh, Paul P</au><au>Lanfear, Sara L</au><au>Abu-Shanab, Joy R</au><au>Lakamp, Jonathan E</au><au>Gowda, Siddhesh</au><au>Haikal, Maged Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Outcomes with Changes in Prescribing of Glycoprotein IIb/IIIa Inhibitors in PCI</atitle><jtitle>The Annals of pharmacotherapy</jtitle><addtitle>Ann Pharmacother</addtitle><date>2003-10-01</date><risdate>2003</risdate><volume>37</volume><issue>10</issue><spage>1375</spage><epage>1380</epage><pages>1375-1380</pages><issn>1060-0280</issn><eissn>1542-6270</eissn><coden>APHRER</coden><abstract>Background
Glycoprotein IIb/IIIa receptor antagonists have been shown to have an impact on the outcomes of death/myocardial infarction (MI) in patients undergoing percutaneous coronary intervention. At our institution, tirofiban has largely replaced abciximab in an attempt to decrease costs.
Objective
To assess the impact of this change on patient outcomes in the absence of head-to-head trials.
Methods
Medical records were reviewed and telephone follow-ups were conducted on patients receiving tirofiban (n = 83) at our facility between February and November 1999. Death/MI at 30 days and 6 months after infusion were recorded. Safety and length of stay (LOS) were also assessed. These data were compared using χ2 analysis with results obtained from a previous review of abciximab use (n = 83) collected between May 1997 and November 1998.
Results
There was no difference in the baseline incidence of (1) cardiovascular risk factors, (2) prior revascularization, (3) prior MI, (4) the number of vessels with atherosclerotic disease assessed by angiography, and (5) the number of vessels receiving procedures. Death/MI trended to be worse with tirofiban versus abciximab at our institution at 30 days (4.8% abciximab vs. 12% tirofiban; p = 0.163) and 6 months (6% abciximab vs. 18.1% tirofiban; p = 0.032). Bleeding and median LOS (3 d abciximab vs. 3 d tirofiban) were not different. Despite an increase in pharmacy cost, the use of abciximab provided these outcomes without an increase in total hospital cost.
Conclusions
The perceived economically driven change in medication selection from abciximab to tirofiban may not have been appropriate based on the negative trends seen in this review. To maintain optimal patient outcomes, this change should be reevaluated.</abstract><cop>Los Angeles, CA</cop><pub>Harvey Whitney Books</pub><pmid>14519056</pmid><doi>10.1345/aph.1C363</doi><tpages>6</tpages></addata></record> |
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subjects | Angioplasty, Balloon, Coronary Antibodies, Monoclonal - administration & dosage Antibodies, Monoclonal - economics Antibodies, Monoclonal - therapeutic use Biological and medical sciences Cardiovascular system Female Humans Immunoglobulin Fab Fragments - administration & dosage Immunoglobulin Fab Fragments - economics Immunoglobulin Fab Fragments - therapeutic use Male Medical sciences Middle Aged Miscellaneous Myocardial Infarction - mortality Myocardial Infarction - therapy Pharmacology. Drug treatments Platelet Glycoprotein GPIIb-IIIa Complex - administration & dosage Platelet Glycoprotein GPIIb-IIIa Complex - antagonists & inhibitors Platelet Glycoprotein GPIIb-IIIa Complex - therapeutic use Retrospective Studies Treatment Outcome Tyrosine - administration & dosage Tyrosine - adverse effects Tyrosine - analogs & derivatives |
title | Outcomes with Changes in Prescribing of Glycoprotein IIb/IIIa Inhibitors in PCI |
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