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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Veröffentlicht in:The Annals of pharmacotherapy 2003-10, Vol.37 (10), p.1375-1380
Hauptverfasser: Dobesh, Paul P, Lanfear, Sara L, Abu-Shanab, Joy R, Lakamp, Jonathan E, Gowda, Siddhesh, Haikal, Maged Y
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container_end_page 1380
container_issue 10
container_start_page 1375
container_title The Annals of pharmacotherapy
container_volume 37
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
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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&amp;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 &amp; 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 &amp; 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 &amp; dosage</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - antagonists &amp; inhibitors</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - therapeutic use</subject><subject>Retrospective Studies</subject><subject>Treatment Outcome</subject><subject>Tyrosine - administration &amp; dosage</subject><subject>Tyrosine - adverse effects</subject><subject>Tyrosine - analogs &amp; 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 &amp; 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 &amp; 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 &amp; dosage</topic><topic>Platelet Glycoprotein GPIIb-IIIa Complex - antagonists &amp; inhibitors</topic><topic>Platelet Glycoprotein GPIIb-IIIa Complex - therapeutic use</topic><topic>Retrospective Studies</topic><topic>Treatment Outcome</topic><topic>Tyrosine - administration &amp; dosage</topic><topic>Tyrosine - adverse effects</topic><topic>Tyrosine - analogs &amp; 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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