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Diabetic patients treated with abciximab and intracoronary stenting
Diabetic patients are at greater risk for restenosis, recurrent ischemia, and complications following angioplasty than are their nondiabetic counterparts. This is a retrospective study identifying diabetic patients who were treated with abciximab and intracoronary stenting during the period of Janua...
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Published in: | Catheterization and cardiovascular interventions 2002-03, Vol.55 (3), p.321-325 |
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container_title | Catheterization and cardiovascular interventions |
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creator | Walton, Brian L. Mumm, Kim Taniuchi, Megumi Kurz, Howard I. Lasala, John M. |
description | Diabetic patients are at greater risk for restenosis, recurrent ischemia, and complications following angioplasty than are their nondiabetic counterparts. This is a retrospective study identifying diabetic patients who were treated with abciximab and intracoronary stenting during the period of January 1997 to December 1999. Abciximab was administered to 268 of 707 diabetic patients who received intracoronary stents from 1997 to 1999. The abciximab group contained a higher number of patients with severe ventricular dysfunction and high‐grade lesions. Primary endpoints of all‐cause mortality, same‐vessel revascularization, CABG, TVR, and postprocedural myocardial infarction were similar for both groups. The abciximab group had reduced rates of readmission for cardiac reasons during all follow‐up periods. The trends toward improvement of mortality, surgical or percutaneous revascularization, and cardiac readmissions suggest the effect of abciximab may provide benefit for up to 9 months for higher‐risk diabetic patients. Cathet Cardiovasc Intervent 2002;55:321–325. © 2002 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/ccd.10025 |
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This is a retrospective study identifying diabetic patients who were treated with abciximab and intracoronary stenting during the period of January 1997 to December 1999. Abciximab was administered to 268 of 707 diabetic patients who received intracoronary stents from 1997 to 1999. The abciximab group contained a higher number of patients with severe ventricular dysfunction and high‐grade lesions. Primary endpoints of all‐cause mortality, same‐vessel revascularization, CABG, TVR, and postprocedural myocardial infarction were similar for both groups. The abciximab group had reduced rates of readmission for cardiac reasons during all follow‐up periods. The trends toward improvement of mortality, surgical or percutaneous revascularization, and cardiac readmissions suggest the effect of abciximab may provide benefit for up to 9 months for higher‐risk diabetic patients. Cathet Cardiovasc Intervent 2002;55:321–325. © 2002 Wiley‐Liss, Inc.</description><identifier>ISSN: 1522-1946</identifier><identifier>EISSN: 1522-726X</identifier><identifier>DOI: 10.1002/ccd.10025</identifier><identifier>PMID: 11870935</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>abciximab ; Angioplasty, Balloon, Coronary - adverse effects ; Antibodies, Monoclonal - administration & dosage ; Biological and medical sciences ; Blood. Blood coagulation. Reticuloendothelial system ; Combined Modality Therapy ; Coronary Restenosis - etiology ; Coronary Restenosis - therapy ; Diabetes Complications ; diabetic ; Female ; Follow-Up Studies ; Humans ; Immunoglobulin Fab Fragments - administration & dosage ; Male ; Medical sciences ; Middle Aged ; Pharmacology. Drug treatments ; Retrospective Studies ; Risk ; stent ; Stents ; Time Factors</subject><ispartof>Catheterization and cardiovascular interventions, 2002-03, Vol.55 (3), p.321-325</ispartof><rights>Copyright © 2002 Wiley‐Liss, Inc.</rights><rights>2002 INIST-CNRS</rights><rights>Copyright 2002 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3895-8cbb60921d4d0d42379a7a96b51c5732121d623b99463b880720c4ea573411563</citedby><cites>FETCH-LOGICAL-c3895-8cbb60921d4d0d42379a7a96b51c5732121d623b99463b880720c4ea573411563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13521859$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11870935$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Walton, Brian L.</creatorcontrib><creatorcontrib>Mumm, Kim</creatorcontrib><creatorcontrib>Taniuchi, Megumi</creatorcontrib><creatorcontrib>Kurz, Howard I.</creatorcontrib><creatorcontrib>Lasala, John M.</creatorcontrib><title>Diabetic patients treated with abciximab and intracoronary stenting</title><title>Catheterization and cardiovascular interventions</title><addtitle>Cathet. Cardiovasc. Intervent</addtitle><description>Diabetic patients are at greater risk for restenosis, recurrent ischemia, and complications following angioplasty than are their nondiabetic counterparts. This is a retrospective study identifying diabetic patients who were treated with abciximab and intracoronary stenting during the period of January 1997 to December 1999. Abciximab was administered to 268 of 707 diabetic patients who received intracoronary stents from 1997 to 1999. The abciximab group contained a higher number of patients with severe ventricular dysfunction and high‐grade lesions. Primary endpoints of all‐cause mortality, same‐vessel revascularization, CABG, TVR, and postprocedural myocardial infarction were similar for both groups. The abciximab group had reduced rates of readmission for cardiac reasons during all follow‐up periods. The trends toward improvement of mortality, surgical or percutaneous revascularization, and cardiac readmissions suggest the effect of abciximab may provide benefit for up to 9 months for higher‐risk diabetic patients. Cathet Cardiovasc Intervent 2002;55:321–325. © 2002 Wiley‐Liss, Inc.</description><subject>abciximab</subject><subject>Angioplasty, Balloon, Coronary - adverse effects</subject><subject>Antibodies, Monoclonal - administration & dosage</subject><subject>Biological and medical sciences</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>Combined Modality Therapy</subject><subject>Coronary Restenosis - etiology</subject><subject>Coronary Restenosis - therapy</subject><subject>Diabetes Complications</subject><subject>diabetic</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>Immunoglobulin Fab Fragments - administration & dosage</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Pharmacology. Drug treatments</subject><subject>Retrospective Studies</subject><subject>Risk</subject><subject>stent</subject><subject>Stents</subject><subject>Time Factors</subject><issn>1522-1946</issn><issn>1522-726X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNp1kElP5DAQhS0EAgY48AdQLiDNIeAljuMjCkyDxCKxCMTFKjtuMKSTxnYL-t-PoQOcONWT6nu1PIS2Cd4nGNMDY5pPwZfQOuGU5oKW98uDJrIo19CfEJ4xxrKkchWtEVIJLBlfR_WRA22jM9kUorNdDFn0FqJtsjcXnzLQxr27CegMuiZzXfRget934OdZiIl33eMmWhlDG-zWUDfQ7b_jm_okP7scndaHZ7lhleR5ZbQusaSkKRrcFJQJCQJkqTkxXDBKUqekTMt0MNNVhQXFprCQegUhvGQbaG8xd-r715kNUU1cMLZtobP9LChBikrSAifw7wI0vg_B27Ga-vSDnyuC1UdQKiX2KXhid4ahMz2xzQ85RJSA3QGAYKAde-iMCz8c45RUXCbuYMG9udbOf9-o6vroa3W-cLiU5Pu3A_yLKgUTXN1djFQxIlf31fW5emD_AZPKjz8</recordid><startdate>200203</startdate><enddate>200203</enddate><creator>Walton, Brian L.</creator><creator>Mumm, Kim</creator><creator>Taniuchi, Megumi</creator><creator>Kurz, Howard I.</creator><creator>Lasala, John M.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><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>200203</creationdate><title>Diabetic patients treated with abciximab and intracoronary stenting</title><author>Walton, Brian L. ; Mumm, Kim ; Taniuchi, Megumi ; Kurz, Howard I. ; Lasala, John M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3895-8cbb60921d4d0d42379a7a96b51c5732121d623b99463b880720c4ea573411563</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>abciximab</topic><topic>Angioplasty, Balloon, Coronary - adverse effects</topic><topic>Antibodies, Monoclonal - administration & dosage</topic><topic>Biological and medical sciences</topic><topic>Blood. Blood coagulation. Reticuloendothelial system</topic><topic>Combined Modality Therapy</topic><topic>Coronary Restenosis - etiology</topic><topic>Coronary Restenosis - therapy</topic><topic>Diabetes Complications</topic><topic>diabetic</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>Immunoglobulin Fab Fragments - administration & dosage</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Pharmacology. Drug treatments</topic><topic>Retrospective Studies</topic><topic>Risk</topic><topic>stent</topic><topic>Stents</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Walton, Brian L.</creatorcontrib><creatorcontrib>Mumm, Kim</creatorcontrib><creatorcontrib>Taniuchi, Megumi</creatorcontrib><creatorcontrib>Kurz, Howard I.</creatorcontrib><creatorcontrib>Lasala, John M.</creatorcontrib><collection>Istex</collection><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>Catheterization and cardiovascular interventions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Walton, Brian L.</au><au>Mumm, Kim</au><au>Taniuchi, Megumi</au><au>Kurz, Howard I.</au><au>Lasala, John M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diabetic patients treated with abciximab and intracoronary stenting</atitle><jtitle>Catheterization and cardiovascular interventions</jtitle><addtitle>Cathet. Cardiovasc. Intervent</addtitle><date>2002-03</date><risdate>2002</risdate><volume>55</volume><issue>3</issue><spage>321</spage><epage>325</epage><pages>321-325</pages><issn>1522-1946</issn><eissn>1522-726X</eissn><abstract>Diabetic patients are at greater risk for restenosis, recurrent ischemia, and complications following angioplasty than are their nondiabetic counterparts. This is a retrospective study identifying diabetic patients who were treated with abciximab and intracoronary stenting during the period of January 1997 to December 1999. Abciximab was administered to 268 of 707 diabetic patients who received intracoronary stents from 1997 to 1999. The abciximab group contained a higher number of patients with severe ventricular dysfunction and high‐grade lesions. Primary endpoints of all‐cause mortality, same‐vessel revascularization, CABG, TVR, and postprocedural myocardial infarction were similar for both groups. The abciximab group had reduced rates of readmission for cardiac reasons during all follow‐up periods. The trends toward improvement of mortality, surgical or percutaneous revascularization, and cardiac readmissions suggest the effect of abciximab may provide benefit for up to 9 months for higher‐risk diabetic patients. Cathet Cardiovasc Intervent 2002;55:321–325. © 2002 Wiley‐Liss, Inc.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>11870935</pmid><doi>10.1002/ccd.10025</doi><tpages>5</tpages></addata></record> |
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subjects | abciximab Angioplasty, Balloon, Coronary - adverse effects Antibodies, Monoclonal - administration & dosage Biological and medical sciences Blood. Blood coagulation. Reticuloendothelial system Combined Modality Therapy Coronary Restenosis - etiology Coronary Restenosis - therapy Diabetes Complications diabetic Female Follow-Up Studies Humans Immunoglobulin Fab Fragments - administration & dosage Male Medical sciences Middle Aged Pharmacology. Drug treatments Retrospective Studies Risk stent Stents Time Factors |
title | Diabetic patients treated with abciximab and intracoronary stenting |
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