Loading…
Pretreatment with intragraft verapamil prior to percutaneous coronary intervention of saphenous vein graft lesions: results of the randomized, controlled vasodilator prevention on no-reflow (VAPOR) trial
Intragraft verapamil is effective in treating no-reflow during saphenous vein graft (SVG) percutaneous coronary intervention (PCI). In this study, we assessed the use of intragraft verapamil given pre-PCI to prevent no-reflow. Patients undergoing SVG PCI were randomized to receive intragraft 200 g v...
Saved in:
Published in: | The Journal of invasive cardiology 2002-06, Vol.14 (6), p.299-302 |
---|---|
Main Authors: | , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | 302 |
container_issue | 6 |
container_start_page | 299 |
container_title | The Journal of invasive cardiology |
container_volume | 14 |
creator | Michaels, Andrew D Appleby, Mark Otten, Matthew H Dauterman, Kent Ports, Thomas A Chou, Tony M Gibson, C Michael |
description | Intragraft verapamil is effective in treating no-reflow during saphenous vein graft (SVG) percutaneous coronary intervention (PCI). In this study, we assessed the use of intragraft verapamil given pre-PCI to prevent no-reflow.
Patients undergoing SVG PCI were randomized to receive intragraft 200 g verapamil or no verapamil immediately prior to PCI. Pre- and post-PCI, vessel flow was assessed using TIMI flow grade and TIMI frame count by blinded angiographic readers. Tissue level perfusion in the graft territory was assessed using the TIMI myocardial perfusion grade (TMPG). CK-MB or troponin I levels were measured 6 12 hours post-PCI.
Ten patients were randomized to the verapamil group and 12 were assigned to the placebo group. No-reflow occurred in 33.3% of the placebo group, compared to none of the verapamil patients (p = 0.10). The use of intragraft verapamil prior to SVG PCI increased flow rate in the vessel as assessed by TIMI frame count (53.3 22.4% faster in the verapamil group versus 11.5 38.9% in the placebo group; p = 0.016). There was a trend toward improved myocardial perfusion as assessed by TMPG. There was no difference in the incidence of cardiac biomarker release following PCI.
Intragraft administration of verapamil prior to saphenous vein graft PCI reduces no-reflow and is associated with a trend toward improved myocardial perfusion. |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_71768683</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71768683</sourcerecordid><originalsourceid>FETCH-LOGICAL-p122t-5e6d4c7a5d471d6e4dd4ce37755e879a42a5f133de13716d43c50343abf7b1d23</originalsourceid><addsrcrecordid>eNo9kN1KAzEQRvdCsbX6CpIrUXCh2exuWu9K8Q8KLaLelulm1kayyTrJtugr-lKmtHo1DN-ZM_AdJX0-zLNUjAXvJafefwyHGRdjfpL0eBaTko_6yc-CMBBCaNAGttVhzbQNBO8EdWAbJGih0Ya1pB2x4FiLVHUBLLrOs8qRs0BfuxukTVRoZ5mrmYd2jXaHbFBbtrcZ9DH2t4zQdyb4HRjWyAisco3-RnUTjfG7MwYV24B3ShsI8XFL-G-3zLqUsDZuy67eJov58zULpMGcJcc1GI_nhzlIXu_vXqaP6Wz-8DSdzNKWZ1lICyxVXkkoVC65KjFXcUUhZVHgSI4hz6CouRAKuZA8sqIqhiIXsKrliqtMDJLLvbcl99mhD8tG-wqN2beylFyWo3IkInhxALtVg2oZS2xiW8u_-sUvCXeHDw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71768683</pqid></control><display><type>article</type><title>Pretreatment with intragraft verapamil prior to percutaneous coronary intervention of saphenous vein graft lesions: results of the randomized, controlled vasodilator prevention on no-reflow (VAPOR) trial</title><source>Freely Accessible Science Journals</source><creator>Michaels, Andrew D ; Appleby, Mark ; Otten, Matthew H ; Dauterman, Kent ; Ports, Thomas A ; Chou, Tony M ; Gibson, C Michael</creator><creatorcontrib>Michaels, Andrew D ; Appleby, Mark ; Otten, Matthew H ; Dauterman, Kent ; Ports, Thomas A ; Chou, Tony M ; Gibson, C Michael</creatorcontrib><description>Intragraft verapamil is effective in treating no-reflow during saphenous vein graft (SVG) percutaneous coronary intervention (PCI). In this study, we assessed the use of intragraft verapamil given pre-PCI to prevent no-reflow.
Patients undergoing SVG PCI were randomized to receive intragraft 200 g verapamil or no verapamil immediately prior to PCI. Pre- and post-PCI, vessel flow was assessed using TIMI flow grade and TIMI frame count by blinded angiographic readers. Tissue level perfusion in the graft territory was assessed using the TIMI myocardial perfusion grade (TMPG). CK-MB or troponin I levels were measured 6 12 hours post-PCI.
Ten patients were randomized to the verapamil group and 12 were assigned to the placebo group. No-reflow occurred in 33.3% of the placebo group, compared to none of the verapamil patients (p = 0.10). The use of intragraft verapamil prior to SVG PCI increased flow rate in the vessel as assessed by TIMI frame count (53.3 22.4% faster in the verapamil group versus 11.5 38.9% in the placebo group; p = 0.016). There was a trend toward improved myocardial perfusion as assessed by TMPG. There was no difference in the incidence of cardiac biomarker release following PCI.
Intragraft administration of verapamil prior to saphenous vein graft PCI reduces no-reflow and is associated with a trend toward improved myocardial perfusion.</description><identifier>ISSN: 1042-3931</identifier><identifier>PMID: 12042618</identifier><language>eng</language><publisher>United States</publisher><subject>Aged ; Angioplasty, Balloon, Coronary - methods ; Cardiac Catheterization ; Coronary Angiography ; Female ; Graft Occlusion, Vascular - diagnostic imaging ; Graft Occlusion, Vascular - drug therapy ; Graft Occlusion, Vascular - surgery ; Humans ; Male ; Middle Aged ; Myocardial Reperfusion - methods ; Preoperative Care ; Regional Blood Flow ; Saphenous Vein - transplantation ; Treatment Outcome ; Vasodilator Agents - administration & dosage ; Verapamil - administration & dosage</subject><ispartof>The Journal of invasive cardiology, 2002-06, Vol.14 (6), p.299-302</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12042618$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Michaels, Andrew D</creatorcontrib><creatorcontrib>Appleby, Mark</creatorcontrib><creatorcontrib>Otten, Matthew H</creatorcontrib><creatorcontrib>Dauterman, Kent</creatorcontrib><creatorcontrib>Ports, Thomas A</creatorcontrib><creatorcontrib>Chou, Tony M</creatorcontrib><creatorcontrib>Gibson, C Michael</creatorcontrib><title>Pretreatment with intragraft verapamil prior to percutaneous coronary intervention of saphenous vein graft lesions: results of the randomized, controlled vasodilator prevention on no-reflow (VAPOR) trial</title><title>The Journal of invasive cardiology</title><addtitle>J Invasive Cardiol</addtitle><description>Intragraft verapamil is effective in treating no-reflow during saphenous vein graft (SVG) percutaneous coronary intervention (PCI). In this study, we assessed the use of intragraft verapamil given pre-PCI to prevent no-reflow.
Patients undergoing SVG PCI were randomized to receive intragraft 200 g verapamil or no verapamil immediately prior to PCI. Pre- and post-PCI, vessel flow was assessed using TIMI flow grade and TIMI frame count by blinded angiographic readers. Tissue level perfusion in the graft territory was assessed using the TIMI myocardial perfusion grade (TMPG). CK-MB or troponin I levels were measured 6 12 hours post-PCI.
Ten patients were randomized to the verapamil group and 12 were assigned to the placebo group. No-reflow occurred in 33.3% of the placebo group, compared to none of the verapamil patients (p = 0.10). The use of intragraft verapamil prior to SVG PCI increased flow rate in the vessel as assessed by TIMI frame count (53.3 22.4% faster in the verapamil group versus 11.5 38.9% in the placebo group; p = 0.016). There was a trend toward improved myocardial perfusion as assessed by TMPG. There was no difference in the incidence of cardiac biomarker release following PCI.
Intragraft administration of verapamil prior to saphenous vein graft PCI reduces no-reflow and is associated with a trend toward improved myocardial perfusion.</description><subject>Aged</subject><subject>Angioplasty, Balloon, Coronary - methods</subject><subject>Cardiac Catheterization</subject><subject>Coronary Angiography</subject><subject>Female</subject><subject>Graft Occlusion, Vascular - diagnostic imaging</subject><subject>Graft Occlusion, Vascular - drug therapy</subject><subject>Graft Occlusion, Vascular - surgery</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Myocardial Reperfusion - methods</subject><subject>Preoperative Care</subject><subject>Regional Blood Flow</subject><subject>Saphenous Vein - transplantation</subject><subject>Treatment Outcome</subject><subject>Vasodilator Agents - administration & dosage</subject><subject>Verapamil - administration & dosage</subject><issn>1042-3931</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNo9kN1KAzEQRvdCsbX6CpIrUXCh2exuWu9K8Q8KLaLelulm1kayyTrJtugr-lKmtHo1DN-ZM_AdJX0-zLNUjAXvJafefwyHGRdjfpL0eBaTko_6yc-CMBBCaNAGttVhzbQNBO8EdWAbJGih0Ya1pB2x4FiLVHUBLLrOs8qRs0BfuxukTVRoZ5mrmYd2jXaHbFBbtrcZ9DH2t4zQdyb4HRjWyAisco3-RnUTjfG7MwYV24B3ShsI8XFL-G-3zLqUsDZuy67eJov58zULpMGcJcc1GI_nhzlIXu_vXqaP6Wz-8DSdzNKWZ1lICyxVXkkoVC65KjFXcUUhZVHgSI4hz6CouRAKuZA8sqIqhiIXsKrliqtMDJLLvbcl99mhD8tG-wqN2beylFyWo3IkInhxALtVg2oZS2xiW8u_-sUvCXeHDw</recordid><startdate>200206</startdate><enddate>200206</enddate><creator>Michaels, Andrew D</creator><creator>Appleby, Mark</creator><creator>Otten, Matthew H</creator><creator>Dauterman, Kent</creator><creator>Ports, Thomas A</creator><creator>Chou, Tony M</creator><creator>Gibson, C Michael</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200206</creationdate><title>Pretreatment with intragraft verapamil prior to percutaneous coronary intervention of saphenous vein graft lesions: results of the randomized, controlled vasodilator prevention on no-reflow (VAPOR) trial</title><author>Michaels, Andrew D ; Appleby, Mark ; Otten, Matthew H ; Dauterman, Kent ; Ports, Thomas A ; Chou, Tony M ; Gibson, C Michael</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p122t-5e6d4c7a5d471d6e4dd4ce37755e879a42a5f133de13716d43c50343abf7b1d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Aged</topic><topic>Angioplasty, Balloon, Coronary - methods</topic><topic>Cardiac Catheterization</topic><topic>Coronary Angiography</topic><topic>Female</topic><topic>Graft Occlusion, Vascular - diagnostic imaging</topic><topic>Graft Occlusion, Vascular - drug therapy</topic><topic>Graft Occlusion, Vascular - surgery</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Myocardial Reperfusion - methods</topic><topic>Preoperative Care</topic><topic>Regional Blood Flow</topic><topic>Saphenous Vein - transplantation</topic><topic>Treatment Outcome</topic><topic>Vasodilator Agents - administration & dosage</topic><topic>Verapamil - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Michaels, Andrew D</creatorcontrib><creatorcontrib>Appleby, Mark</creatorcontrib><creatorcontrib>Otten, Matthew H</creatorcontrib><creatorcontrib>Dauterman, Kent</creatorcontrib><creatorcontrib>Ports, Thomas A</creatorcontrib><creatorcontrib>Chou, Tony M</creatorcontrib><creatorcontrib>Gibson, C Michael</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of invasive cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Michaels, Andrew D</au><au>Appleby, Mark</au><au>Otten, Matthew H</au><au>Dauterman, Kent</au><au>Ports, Thomas A</au><au>Chou, Tony M</au><au>Gibson, C Michael</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pretreatment with intragraft verapamil prior to percutaneous coronary intervention of saphenous vein graft lesions: results of the randomized, controlled vasodilator prevention on no-reflow (VAPOR) trial</atitle><jtitle>The Journal of invasive cardiology</jtitle><addtitle>J Invasive Cardiol</addtitle><date>2002-06</date><risdate>2002</risdate><volume>14</volume><issue>6</issue><spage>299</spage><epage>302</epage><pages>299-302</pages><issn>1042-3931</issn><abstract>Intragraft verapamil is effective in treating no-reflow during saphenous vein graft (SVG) percutaneous coronary intervention (PCI). In this study, we assessed the use of intragraft verapamil given pre-PCI to prevent no-reflow.
Patients undergoing SVG PCI were randomized to receive intragraft 200 g verapamil or no verapamil immediately prior to PCI. Pre- and post-PCI, vessel flow was assessed using TIMI flow grade and TIMI frame count by blinded angiographic readers. Tissue level perfusion in the graft territory was assessed using the TIMI myocardial perfusion grade (TMPG). CK-MB or troponin I levels were measured 6 12 hours post-PCI.
Ten patients were randomized to the verapamil group and 12 were assigned to the placebo group. No-reflow occurred in 33.3% of the placebo group, compared to none of the verapamil patients (p = 0.10). The use of intragraft verapamil prior to SVG PCI increased flow rate in the vessel as assessed by TIMI frame count (53.3 22.4% faster in the verapamil group versus 11.5 38.9% in the placebo group; p = 0.016). There was a trend toward improved myocardial perfusion as assessed by TMPG. There was no difference in the incidence of cardiac biomarker release following PCI.
Intragraft administration of verapamil prior to saphenous vein graft PCI reduces no-reflow and is associated with a trend toward improved myocardial perfusion.</abstract><cop>United States</cop><pmid>12042618</pmid><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1042-3931 |
ispartof | The Journal of invasive cardiology, 2002-06, Vol.14 (6), p.299-302 |
issn | 1042-3931 |
language | eng |
recordid | cdi_proquest_miscellaneous_71768683 |
source | Freely Accessible Science Journals |
subjects | Aged Angioplasty, Balloon, Coronary - methods Cardiac Catheterization Coronary Angiography Female Graft Occlusion, Vascular - diagnostic imaging Graft Occlusion, Vascular - drug therapy Graft Occlusion, Vascular - surgery Humans Male Middle Aged Myocardial Reperfusion - methods Preoperative Care Regional Blood Flow Saphenous Vein - transplantation Treatment Outcome Vasodilator Agents - administration & dosage Verapamil - administration & dosage |
title | Pretreatment with intragraft verapamil prior to percutaneous coronary intervention of saphenous vein graft lesions: results of the randomized, controlled vasodilator prevention on no-reflow (VAPOR) trial |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-22T09%3A56%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pretreatment%20with%20intragraft%20verapamil%20prior%20to%20percutaneous%20coronary%20intervention%20of%20saphenous%20vein%20graft%20lesions:%20results%20of%20the%20randomized,%20controlled%20vasodilator%20prevention%20on%20no-reflow%20(VAPOR)%20trial&rft.jtitle=The%20Journal%20of%20invasive%20cardiology&rft.au=Michaels,%20Andrew%20D&rft.date=2002-06&rft.volume=14&rft.issue=6&rft.spage=299&rft.epage=302&rft.pages=299-302&rft.issn=1042-3931&rft_id=info:doi/&rft_dat=%3Cproquest_pubme%3E71768683%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-p122t-5e6d4c7a5d471d6e4dd4ce37755e879a42a5f133de13716d43c50343abf7b1d23%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=71768683&rft_id=info:pmid/12042618&rfr_iscdi=true |