Dynamic Changes in ST Segment Resolution After Myocardial Infarction and the Association with Microvascular Injury on Cardiac Magnetic Resonance Imaging

Background Persistent ST elevation after reperfused ST elevation myocardial infarction (STEMI) is believed to be related to poor microvascular perfusion. Cardiac magnetic resonance imaging (CMR) can evaluate microvascular obstruction (MVO) and intramyocardial haemorrhage (IMH) both of which represen...

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Veröffentlicht in:Heart, lung & circulation lung & circulation, 2011-02, Vol.20 (2), p.111-118
Hauptverfasser: Weaver, James C., FRACP, Ramsay, David D., FRACP, Rees, David, PhD, Binnekamp, Maurits F., FRACP, Prasan, Ananth M., PhD, McCrohon, Jane A., PhD
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container_end_page 118
container_issue 2
container_start_page 111
container_title Heart, lung & circulation
container_volume 20
creator Weaver, James C., FRACP
Ramsay, David D., FRACP
Rees, David, PhD
Binnekamp, Maurits F., FRACP
Prasan, Ananth M., PhD
McCrohon, Jane A., PhD
description Background Persistent ST elevation after reperfused ST elevation myocardial infarction (STEMI) is believed to be related to poor microvascular perfusion. Cardiac magnetic resonance imaging (CMR) can evaluate microvascular obstruction (MVO) and intramyocardial haemorrhage (IMH) both of which represent severe microvascular damage, have independent prognostic value and are dynamic and evolving over the first 48 hours after reperfusion. The aim of this study was to assess whether the development of MVO or IMH has an impact upon ST segment resolution. Methods Patients undergoing primary percutaneous coronary intervention (PCI) for STEMI had serial 12 lead electrocardiograms (ECG) from one hour after PCI until discharge. Persistent single lead maximal residual ST elevation (maxSTE) at each time point was calculated. ST segment deterioration (re-elevation) was calculated on each ECG until discharge compared with one hour post PCI ECG. CMR was performed within seven days post infarct utilising T2 weighted imaging to evaluate culprit artery area at risk (AAR) and IMH. Gadolinium delayed enhancement CMR quantified infarct size and MVO. Results In the 41 patients studied 58% had MVO and 41% had IMH. ST segment deterioration was more common in those with MVO or IMH ( p = 0.03 and p = 0.008 respectively). MaxSTE was higher at each time point after PCI in those with MVO but only became statistically significant after 24 hours. The measurement of maxSTE at 48 or 72 hours after revascularisation provided the best correlation with the combination of infarct size, AAR, MVO and intramyocardial haemorrhage. Conclusion Microvascular injury as defined on CMR is associated with dynamic changes and persistence of ST segment elevation in the first 72 hours after reperfusion.
doi_str_mv 10.1016/j.hlc.2010.09.006
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Cardiac magnetic resonance imaging (CMR) can evaluate microvascular obstruction (MVO) and intramyocardial haemorrhage (IMH) both of which represent severe microvascular damage, have independent prognostic value and are dynamic and evolving over the first 48 hours after reperfusion. The aim of this study was to assess whether the development of MVO or IMH has an impact upon ST segment resolution. Methods Patients undergoing primary percutaneous coronary intervention (PCI) for STEMI had serial 12 lead electrocardiograms (ECG) from one hour after PCI until discharge. Persistent single lead maximal residual ST elevation (maxSTE) at each time point was calculated. ST segment deterioration (re-elevation) was calculated on each ECG until discharge compared with one hour post PCI ECG. CMR was performed within seven days post infarct utilising T2 weighted imaging to evaluate culprit artery area at risk (AAR) and IMH. Gadolinium delayed enhancement CMR quantified infarct size and MVO. Results In the 41 patients studied 58% had MVO and 41% had IMH. ST segment deterioration was more common in those with MVO or IMH ( p = 0.03 and p = 0.008 respectively). MaxSTE was higher at each time point after PCI in those with MVO but only became statistically significant after 24 hours. The measurement of maxSTE at 48 or 72 hours after revascularisation provided the best correlation with the combination of infarct size, AAR, MVO and intramyocardial haemorrhage. Conclusion Microvascular injury as defined on CMR is associated with dynamic changes and persistence of ST segment elevation in the first 72 hours after reperfusion.</description><identifier>ISSN: 1443-9506</identifier><identifier>EISSN: 1444-2892</identifier><identifier>DOI: 10.1016/j.hlc.2010.09.006</identifier><identifier>PMID: 20943440</identifier><language>eng</language><publisher>Australia: Elsevier B.V</publisher><subject>Aged ; Angioplasty ; Cardiac magnetic resonance ; Cardiovascular ; Coronary Circulation ; Electrocardiography ; Female ; Humans ; Intramyocardial haemorrhage ; Magnetic Resonance Imaging ; Male ; Microcirculation ; Microvascular obstruction ; Middle Aged ; Myocardial Infarction - diagnostic imaging ; Myocardial Infarction - physiopathology ; Myocardial Infarction - therapy ; Myocardial Reperfusion ; Radiography ; ST segment resolution ; Time Factors</subject><ispartof>Heart, lung &amp; circulation, 2011-02, Vol.20 (2), p.111-118</ispartof><rights>2010</rights><rights>2010. Published by Elsevier Inc. on behalf of Australasian Society of Cardiac and Thoracic Surgeons and the Cardiac Society of Australia and New Zealand. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c407t-67325033608dcabbd4a362be156c61ee6a1a261ce5d18b07bfa6ce70b6463ea23</citedby><cites>FETCH-LOGICAL-c407t-67325033608dcabbd4a362be156c61ee6a1a261ce5d18b07bfa6ce70b6463ea23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.hlc.2010.09.006$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,781,785,3551,27925,27926,45996</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20943440$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Weaver, James C., FRACP</creatorcontrib><creatorcontrib>Ramsay, David D., FRACP</creatorcontrib><creatorcontrib>Rees, David, PhD</creatorcontrib><creatorcontrib>Binnekamp, Maurits F., FRACP</creatorcontrib><creatorcontrib>Prasan, Ananth M., PhD</creatorcontrib><creatorcontrib>McCrohon, Jane A., PhD</creatorcontrib><title>Dynamic Changes in ST Segment Resolution After Myocardial Infarction and the Association with Microvascular Injury on Cardiac Magnetic Resonance Imaging</title><title>Heart, lung &amp; circulation</title><addtitle>Heart Lung Circ</addtitle><description>Background Persistent ST elevation after reperfused ST elevation myocardial infarction (STEMI) is believed to be related to poor microvascular perfusion. Cardiac magnetic resonance imaging (CMR) can evaluate microvascular obstruction (MVO) and intramyocardial haemorrhage (IMH) both of which represent severe microvascular damage, have independent prognostic value and are dynamic and evolving over the first 48 hours after reperfusion. The aim of this study was to assess whether the development of MVO or IMH has an impact upon ST segment resolution. Methods Patients undergoing primary percutaneous coronary intervention (PCI) for STEMI had serial 12 lead electrocardiograms (ECG) from one hour after PCI until discharge. Persistent single lead maximal residual ST elevation (maxSTE) at each time point was calculated. ST segment deterioration (re-elevation) was calculated on each ECG until discharge compared with one hour post PCI ECG. CMR was performed within seven days post infarct utilising T2 weighted imaging to evaluate culprit artery area at risk (AAR) and IMH. Gadolinium delayed enhancement CMR quantified infarct size and MVO. Results In the 41 patients studied 58% had MVO and 41% had IMH. ST segment deterioration was more common in those with MVO or IMH ( p = 0.03 and p = 0.008 respectively). MaxSTE was higher at each time point after PCI in those with MVO but only became statistically significant after 24 hours. The measurement of maxSTE at 48 or 72 hours after revascularisation provided the best correlation with the combination of infarct size, AAR, MVO and intramyocardial haemorrhage. Conclusion Microvascular injury as defined on CMR is associated with dynamic changes and persistence of ST segment elevation in the first 72 hours after reperfusion.</description><subject>Aged</subject><subject>Angioplasty</subject><subject>Cardiac magnetic resonance</subject><subject>Cardiovascular</subject><subject>Coronary Circulation</subject><subject>Electrocardiography</subject><subject>Female</subject><subject>Humans</subject><subject>Intramyocardial haemorrhage</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Microcirculation</subject><subject>Microvascular obstruction</subject><subject>Middle Aged</subject><subject>Myocardial Infarction - diagnostic imaging</subject><subject>Myocardial Infarction - physiopathology</subject><subject>Myocardial Infarction - therapy</subject><subject>Myocardial Reperfusion</subject><subject>Radiography</subject><subject>ST segment resolution</subject><subject>Time Factors</subject><issn>1443-9506</issn><issn>1444-2892</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9Uk2P0zAQjRCI_YAfwAX5xinFX3EaISFVhYVKWyHR5WxNnEnqkDiLnSzKP-Hn4rQLBw6cxp55741m3iTJK0ZXjDL1tl0dO7PiNP5psaJUPUkumZQy5euCPz29RVpkVF0kVyG0lLJciuJ5csFpIYWU9DL59WF20FtDtkdwDQZiHTnckQM2PbqRfMUwdNNoB0c29Yie7OfBgK8sdGTnavDmVANXkfGIZBPCYCyccj_teCR7a_zwAMFMHfjIaCc_k1jcnjQM2UPjcIztl0YOnEGy66GxrnmRPKuhC_jyMV4n324-3m0_p7dfPu22m9vUSJqPqcoFz6gQiq4rA2VZSRCKl8gyZRRDVMCAK2Ywq9i6pHlZgzKY01JJJRC4uE7enHXv_fBjwjDq3gaDXQcOhynotcxEwTImIpKdkXGkEDzW-t7bHvysGdWLH7rV0Q-9-KFpoaMfkfP6UX0qe6z-Mv4YEAHvzgCMMz5Y9DoYi3EPlfVoRl0N9r_y7_9hm846a6D7jjOGdpi8i8vTTAeuqT4sB7HcA4unEIMUvwFFlLI2</recordid><startdate>20110201</startdate><enddate>20110201</enddate><creator>Weaver, James C., FRACP</creator><creator>Ramsay, David D., FRACP</creator><creator>Rees, David, PhD</creator><creator>Binnekamp, Maurits F., FRACP</creator><creator>Prasan, Ananth M., PhD</creator><creator>McCrohon, Jane A., PhD</creator><general>Elsevier B.V</general><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>20110201</creationdate><title>Dynamic Changes in ST Segment Resolution After Myocardial Infarction and the Association with Microvascular Injury on Cardiac Magnetic Resonance Imaging</title><author>Weaver, James C., FRACP ; Ramsay, David D., FRACP ; Rees, David, PhD ; Binnekamp, Maurits F., FRACP ; Prasan, Ananth M., PhD ; McCrohon, Jane A., PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-67325033608dcabbd4a362be156c61ee6a1a261ce5d18b07bfa6ce70b6463ea23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Aged</topic><topic>Angioplasty</topic><topic>Cardiac magnetic resonance</topic><topic>Cardiovascular</topic><topic>Coronary Circulation</topic><topic>Electrocardiography</topic><topic>Female</topic><topic>Humans</topic><topic>Intramyocardial haemorrhage</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Microcirculation</topic><topic>Microvascular obstruction</topic><topic>Middle Aged</topic><topic>Myocardial Infarction - diagnostic imaging</topic><topic>Myocardial Infarction - physiopathology</topic><topic>Myocardial Infarction - therapy</topic><topic>Myocardial Reperfusion</topic><topic>Radiography</topic><topic>ST segment resolution</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Weaver, James C., FRACP</creatorcontrib><creatorcontrib>Ramsay, David D., FRACP</creatorcontrib><creatorcontrib>Rees, David, PhD</creatorcontrib><creatorcontrib>Binnekamp, Maurits F., FRACP</creatorcontrib><creatorcontrib>Prasan, Ananth M., PhD</creatorcontrib><creatorcontrib>McCrohon, Jane A., PhD</creatorcontrib><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>Heart, lung &amp; circulation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Weaver, James C., FRACP</au><au>Ramsay, David D., FRACP</au><au>Rees, David, PhD</au><au>Binnekamp, Maurits F., FRACP</au><au>Prasan, Ananth M., PhD</au><au>McCrohon, Jane A., PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dynamic Changes in ST Segment Resolution After Myocardial Infarction and the Association with Microvascular Injury on Cardiac Magnetic Resonance Imaging</atitle><jtitle>Heart, lung &amp; circulation</jtitle><addtitle>Heart Lung Circ</addtitle><date>2011-02-01</date><risdate>2011</risdate><volume>20</volume><issue>2</issue><spage>111</spage><epage>118</epage><pages>111-118</pages><issn>1443-9506</issn><eissn>1444-2892</eissn><abstract>Background Persistent ST elevation after reperfused ST elevation myocardial infarction (STEMI) is believed to be related to poor microvascular perfusion. Cardiac magnetic resonance imaging (CMR) can evaluate microvascular obstruction (MVO) and intramyocardial haemorrhage (IMH) both of which represent severe microvascular damage, have independent prognostic value and are dynamic and evolving over the first 48 hours after reperfusion. The aim of this study was to assess whether the development of MVO or IMH has an impact upon ST segment resolution. Methods Patients undergoing primary percutaneous coronary intervention (PCI) for STEMI had serial 12 lead electrocardiograms (ECG) from one hour after PCI until discharge. Persistent single lead maximal residual ST elevation (maxSTE) at each time point was calculated. ST segment deterioration (re-elevation) was calculated on each ECG until discharge compared with one hour post PCI ECG. CMR was performed within seven days post infarct utilising T2 weighted imaging to evaluate culprit artery area at risk (AAR) and IMH. Gadolinium delayed enhancement CMR quantified infarct size and MVO. Results In the 41 patients studied 58% had MVO and 41% had IMH. ST segment deterioration was more common in those with MVO or IMH ( p = 0.03 and p = 0.008 respectively). MaxSTE was higher at each time point after PCI in those with MVO but only became statistically significant after 24 hours. The measurement of maxSTE at 48 or 72 hours after revascularisation provided the best correlation with the combination of infarct size, AAR, MVO and intramyocardial haemorrhage. Conclusion Microvascular injury as defined on CMR is associated with dynamic changes and persistence of ST segment elevation in the first 72 hours after reperfusion.</abstract><cop>Australia</cop><pub>Elsevier B.V</pub><pmid>20943440</pmid><doi>10.1016/j.hlc.2010.09.006</doi><tpages>8</tpages></addata></record>
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subjects Aged
Angioplasty
Cardiac magnetic resonance
Cardiovascular
Coronary Circulation
Electrocardiography
Female
Humans
Intramyocardial haemorrhage
Magnetic Resonance Imaging
Male
Microcirculation
Microvascular obstruction
Middle Aged
Myocardial Infarction - diagnostic imaging
Myocardial Infarction - physiopathology
Myocardial Infarction - therapy
Myocardial Reperfusion
Radiography
ST segment resolution
Time Factors
title Dynamic Changes in ST Segment Resolution After Myocardial Infarction and the Association with Microvascular Injury on Cardiac Magnetic Resonance Imaging
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