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Prognostic value of perfusion cardiovascular magnetic resonance with adenosine triphosphate stress in stable coronary artery disease
Adenosine triphosphate (ATP) has been predominantly used in the Asia-Pacific region for stress perfusion cardiovascular magnetic resonance (CMR). We evaluated the prognosis of patients stressed using ATP, for which there are no current data. We performed a retrospective longitudinal study from Janua...
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Published in: | Journal of cardiovascular magnetic resonance 2021-06, Vol.23 (1), p.75-11, Article 75 |
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creator | Ng, Ming-Yen Chin, Chi Yeung Yap, Pui Min Wan, Eric Yuk Fai Hai, JoJo Siu Han Cheung, Stephen Tse, Hung Fat Bucciarelli-Ducci, Chiara Pennell, Dudley John Yiu, Kai-Hang |
description | Adenosine triphosphate (ATP) has been predominantly used in the Asia-Pacific region for stress perfusion cardiovascular magnetic resonance (CMR). We evaluated the prognosis of patients stressed using ATP, for which there are no current data.
We performed a retrospective longitudinal study from January 2016 to December 2020 and included 208 subjects with suspected obstructive coronary artery disease (CAD) who underwent ATP stress perfusion CMR. An inducible stress perfusion defect was defined as a subendocardial dark rim involving ≥ 1.5 segments that persisted for ≥ 6 beats during stress but not at rest. The primary outcome measure was a composite of major adverse cardiovascular events (MACE) including (1) cardiac death, (2) nonfatal myocardial infarction, (3) cardiac hospitalization, (4) late coronary revascularization. We compared outcomes in patients with and without perfusion defect using Kaplan-Meier and log rank tests. Significant predictors of MACE were identified using multivariable Cox regression analysis.
Median follow-up was 3.3 years. Patients with no stress perfusion defect had a lower incidence of MACE (p |
doi_str_mv | 10.1186/s12968-021-00770-z |
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We performed a retrospective longitudinal study from January 2016 to December 2020 and included 208 subjects with suspected obstructive coronary artery disease (CAD) who underwent ATP stress perfusion CMR. An inducible stress perfusion defect was defined as a subendocardial dark rim involving ≥ 1.5 segments that persisted for ≥ 6 beats during stress but not at rest. The primary outcome measure was a composite of major adverse cardiovascular events (MACE) including (1) cardiac death, (2) nonfatal myocardial infarction, (3) cardiac hospitalization, (4) late coronary revascularization. We compared outcomes in patients with and without perfusion defect using Kaplan-Meier and log rank tests. Significant predictors of MACE were identified using multivariable Cox regression analysis.
Median follow-up was 3.3 years. Patients with no stress perfusion defect had a lower incidence of MACE (p < 0.001), including lower cardiac hospitalization (p = 0.004), late coronary revascularization (p = 0.001) and cardiac death (p = 0.003). Significant independent predictors for MACE were stress induced perfusion defect (p < 0.001, hazard ratio [HR] = 3.63), lower left ventricular ejection fractino (LVEF) (p < 0.001, HR = 0.96) and infarct detected by late gadolinium enhancement (LGE) (p = 0.001, HR = 2.92).
Perfusion defects on ATP stress are predictive of MACE which is driven primarily by cardiac hospitalization, late coronary revascularization and cardiac death. Significant independent predictors of MACE were stress induced perfusion defect, lower LVEF and infarct detected by LGE.</description><identifier>ISSN: 1097-6647</identifier><identifier>ISSN: 1532-429X</identifier><identifier>EISSN: 1532-429X</identifier><identifier>DOI: 10.1186/s12968-021-00770-z</identifier><identifier>PMID: 34162392</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Adenosine Triphosphate ; ATP ; Cardiology ; Cardiovascular disease ; Cardiovascular magnetic resonance ; Contrast Media ; Coronary artery ; Coronary artery bypass ; Coronary artery disease ; Coronary Artery Disease - diagnostic imaging ; Coronary vessels ; Death ; Gadolinium ; Heart ; Heart attack ; Humans ; Longitudinal Studies ; Magnetic resonance ; Magnetic Resonance Imaging, Cine ; Magnetic Resonance Spectroscopy ; Mortality ; Muscle proteins ; Myocardial infarction ; Patients ; Perfusion ; Predictive Value of Tests ; Prognosis ; Rank tests ; Regression analysis ; Resonance ; Retrospective Studies ; Risk Assessment ; Risk Factors ; Standard deviation ; Stress ; Vasodilator Agents ; Ventricle</subject><ispartof>Journal of cardiovascular magnetic resonance, 2021-06, Vol.23 (1), p.75-11, Article 75</ispartof><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-3bcb4e68f5fc23a28972248519469f4fc023505e5ba7b670f4e6224c543dc3343</citedby><cites>FETCH-LOGICAL-c594t-3bcb4e68f5fc23a28972248519469f4fc023505e5ba7b670f4e6224c543dc3343</cites><orcidid>0000-0001-9533-3892</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8223349/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2552824321?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,725,778,782,883,25740,27911,27912,36999,37000,44577,53778,53780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34162392$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ng, Ming-Yen</creatorcontrib><creatorcontrib>Chin, Chi Yeung</creatorcontrib><creatorcontrib>Yap, Pui Min</creatorcontrib><creatorcontrib>Wan, Eric Yuk Fai</creatorcontrib><creatorcontrib>Hai, JoJo Siu Han</creatorcontrib><creatorcontrib>Cheung, Stephen</creatorcontrib><creatorcontrib>Tse, Hung Fat</creatorcontrib><creatorcontrib>Bucciarelli-Ducci, Chiara</creatorcontrib><creatorcontrib>Pennell, Dudley John</creatorcontrib><creatorcontrib>Yiu, Kai-Hang</creatorcontrib><title>Prognostic value of perfusion cardiovascular magnetic resonance with adenosine triphosphate stress in stable coronary artery disease</title><title>Journal of cardiovascular magnetic resonance</title><addtitle>J Cardiovasc Magn Reson</addtitle><description>Adenosine triphosphate (ATP) has been predominantly used in the Asia-Pacific region for stress perfusion cardiovascular magnetic resonance (CMR). We evaluated the prognosis of patients stressed using ATP, for which there are no current data.
We performed a retrospective longitudinal study from January 2016 to December 2020 and included 208 subjects with suspected obstructive coronary artery disease (CAD) who underwent ATP stress perfusion CMR. An inducible stress perfusion defect was defined as a subendocardial dark rim involving ≥ 1.5 segments that persisted for ≥ 6 beats during stress but not at rest. The primary outcome measure was a composite of major adverse cardiovascular events (MACE) including (1) cardiac death, (2) nonfatal myocardial infarction, (3) cardiac hospitalization, (4) late coronary revascularization. We compared outcomes in patients with and without perfusion defect using Kaplan-Meier and log rank tests. Significant predictors of MACE were identified using multivariable Cox regression analysis.
Median follow-up was 3.3 years. Patients with no stress perfusion defect had a lower incidence of MACE (p < 0.001), including lower cardiac hospitalization (p = 0.004), late coronary revascularization (p = 0.001) and cardiac death (p = 0.003). Significant independent predictors for MACE were stress induced perfusion defect (p < 0.001, hazard ratio [HR] = 3.63), lower left ventricular ejection fractino (LVEF) (p < 0.001, HR = 0.96) and infarct detected by late gadolinium enhancement (LGE) (p = 0.001, HR = 2.92).
Perfusion defects on ATP stress are predictive of MACE which is driven primarily by cardiac hospitalization, late coronary revascularization and cardiac death. Significant independent predictors of MACE were stress induced perfusion defect, lower LVEF and infarct detected by LGE.</description><subject>Adenosine Triphosphate</subject><subject>ATP</subject><subject>Cardiology</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular magnetic resonance</subject><subject>Contrast Media</subject><subject>Coronary artery</subject><subject>Coronary artery bypass</subject><subject>Coronary artery disease</subject><subject>Coronary Artery Disease - diagnostic imaging</subject><subject>Coronary vessels</subject><subject>Death</subject><subject>Gadolinium</subject><subject>Heart</subject><subject>Heart attack</subject><subject>Humans</subject><subject>Longitudinal Studies</subject><subject>Magnetic resonance</subject><subject>Magnetic Resonance Imaging, Cine</subject><subject>Magnetic Resonance Spectroscopy</subject><subject>Mortality</subject><subject>Muscle proteins</subject><subject>Myocardial infarction</subject><subject>Patients</subject><subject>Perfusion</subject><subject>Predictive Value of Tests</subject><subject>Prognosis</subject><subject>Rank tests</subject><subject>Regression analysis</subject><subject>Resonance</subject><subject>Retrospective Studies</subject><subject>Risk Assessment</subject><subject>Risk Factors</subject><subject>Standard deviation</subject><subject>Stress</subject><subject>Vasodilator Agents</subject><subject>Ventricle</subject><issn>1097-6647</issn><issn>1532-429X</issn><issn>1532-429X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkk1rFTEUhgdRbK3-ARcSEMTN1HxnshFK8aNQ0IWCu5DJnNxJmZtck5krdu0PN7e31l6RLBJOnvfNyeFtmucEnxLSyTeFUC27FlPSYqwUbq8fNMdEMNpyqr89rGesVSslV0fNk1KuMCZaYfW4OWKcSMo0PW5-fc5pFVOZg0NbOy2AkkcbyH4pIUXkbB5C2trilslmtLarCDs0Q0nRRgfoR5hHZAeoHiECmnPYjKlsRjsDKnPlCgqxnmw_AXIpV1n-iWyeoW5DKGALPG0eeTsVeHa7nzRf37_7cv6xvfz04eL87LJ1QvO5Zb3rOcjOC-8os7TTilLeCaK51J57hykTWIDoreqlwr7CFXCCs8ExxtlJc7H3HZK9Mpsc1rUXk2wwN4WUV6Y2FtwERnbUe2BWwsA5V1ITbjEG7QV46u3O6-3ea7P0axgcxDnb6cD08CaG0azS1nSU1l50NXh9a5DT9wXKbNahOJgmGyEtxVDBeac00V1FX_6DXqUlxzqqSgnaUc4o-UutbP1AiD7Vd93O1JzJOimJmVCVOv0PVdcA6-BSBB9q_UDw6p5gBDvNY0nTMtd8lEOQ7kGXUykZ_N0wCDa7wJp9YE0NrLkJrLmuohf3x3gn-ZNQ9htKF-f-</recordid><startdate>20210624</startdate><enddate>20210624</enddate><creator>Ng, Ming-Yen</creator><creator>Chin, Chi Yeung</creator><creator>Yap, Pui Min</creator><creator>Wan, Eric Yuk Fai</creator><creator>Hai, JoJo Siu Han</creator><creator>Cheung, Stephen</creator><creator>Tse, Hung Fat</creator><creator>Bucciarelli-Ducci, Chiara</creator><creator>Pennell, Dudley John</creator><creator>Yiu, Kai-Hang</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>Elsevier</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>3V.</scope><scope>7SC</scope><scope>7SP</scope><scope>7U5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JQ2</scope><scope>K9.</scope><scope>L7M</scope><scope>LK8</scope><scope>L~C</scope><scope>L~D</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>M7Z</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-9533-3892</orcidid></search><sort><creationdate>20210624</creationdate><title>Prognostic value of perfusion cardiovascular magnetic resonance with adenosine triphosphate stress in stable coronary artery disease</title><author>Ng, Ming-Yen ; Chin, Chi Yeung ; Yap, Pui Min ; Wan, Eric Yuk Fai ; Hai, JoJo Siu Han ; Cheung, Stephen ; Tse, Hung Fat ; Bucciarelli-Ducci, Chiara ; Pennell, Dudley John ; Yiu, Kai-Hang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-3bcb4e68f5fc23a28972248519469f4fc023505e5ba7b670f4e6224c543dc3343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adenosine Triphosphate</topic><topic>ATP</topic><topic>Cardiology</topic><topic>Cardiovascular disease</topic><topic>Cardiovascular magnetic resonance</topic><topic>Contrast Media</topic><topic>Coronary artery</topic><topic>Coronary artery bypass</topic><topic>Coronary artery disease</topic><topic>Coronary Artery Disease - diagnostic imaging</topic><topic>Coronary vessels</topic><topic>Death</topic><topic>Gadolinium</topic><topic>Heart</topic><topic>Heart attack</topic><topic>Humans</topic><topic>Longitudinal Studies</topic><topic>Magnetic resonance</topic><topic>Magnetic Resonance Imaging, Cine</topic><topic>Magnetic Resonance Spectroscopy</topic><topic>Mortality</topic><topic>Muscle proteins</topic><topic>Myocardial infarction</topic><topic>Patients</topic><topic>Perfusion</topic><topic>Predictive Value of Tests</topic><topic>Prognosis</topic><topic>Rank tests</topic><topic>Regression analysis</topic><topic>Resonance</topic><topic>Retrospective Studies</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Standard deviation</topic><topic>Stress</topic><topic>Vasodilator Agents</topic><topic>Ventricle</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ng, Ming-Yen</creatorcontrib><creatorcontrib>Chin, Chi Yeung</creatorcontrib><creatorcontrib>Yap, Pui Min</creatorcontrib><creatorcontrib>Wan, Eric Yuk Fai</creatorcontrib><creatorcontrib>Hai, JoJo Siu Han</creatorcontrib><creatorcontrib>Cheung, Stephen</creatorcontrib><creatorcontrib>Tse, Hung Fat</creatorcontrib><creatorcontrib>Bucciarelli-Ducci, Chiara</creatorcontrib><creatorcontrib>Pennell, Dudley John</creatorcontrib><creatorcontrib>Yiu, Kai-Hang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Computer and Information Systems Abstracts</collection><collection>Electronics & Communications Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Computer Science Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>ProQuest Biological Science Collection</collection><collection>Computer and Information Systems Abstracts Academic</collection><collection>Computer and Information Systems Abstracts Professional</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biochemistry Abstracts 1</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of cardiovascular magnetic resonance</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ng, Ming-Yen</au><au>Chin, Chi Yeung</au><au>Yap, Pui Min</au><au>Wan, Eric Yuk Fai</au><au>Hai, JoJo Siu Han</au><au>Cheung, Stephen</au><au>Tse, Hung Fat</au><au>Bucciarelli-Ducci, Chiara</au><au>Pennell, Dudley John</au><au>Yiu, Kai-Hang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic value of perfusion cardiovascular magnetic resonance with adenosine triphosphate stress in stable coronary artery disease</atitle><jtitle>Journal of cardiovascular magnetic resonance</jtitle><addtitle>J Cardiovasc Magn Reson</addtitle><date>2021-06-24</date><risdate>2021</risdate><volume>23</volume><issue>1</issue><spage>75</spage><epage>11</epage><pages>75-11</pages><artnum>75</artnum><issn>1097-6647</issn><issn>1532-429X</issn><eissn>1532-429X</eissn><abstract>Adenosine triphosphate (ATP) has been predominantly used in the Asia-Pacific region for stress perfusion cardiovascular magnetic resonance (CMR). We evaluated the prognosis of patients stressed using ATP, for which there are no current data.
We performed a retrospective longitudinal study from January 2016 to December 2020 and included 208 subjects with suspected obstructive coronary artery disease (CAD) who underwent ATP stress perfusion CMR. An inducible stress perfusion defect was defined as a subendocardial dark rim involving ≥ 1.5 segments that persisted for ≥ 6 beats during stress but not at rest. The primary outcome measure was a composite of major adverse cardiovascular events (MACE) including (1) cardiac death, (2) nonfatal myocardial infarction, (3) cardiac hospitalization, (4) late coronary revascularization. We compared outcomes in patients with and without perfusion defect using Kaplan-Meier and log rank tests. Significant predictors of MACE were identified using multivariable Cox regression analysis.
Median follow-up was 3.3 years. Patients with no stress perfusion defect had a lower incidence of MACE (p < 0.001), including lower cardiac hospitalization (p = 0.004), late coronary revascularization (p = 0.001) and cardiac death (p = 0.003). Significant independent predictors for MACE were stress induced perfusion defect (p < 0.001, hazard ratio [HR] = 3.63), lower left ventricular ejection fractino (LVEF) (p < 0.001, HR = 0.96) and infarct detected by late gadolinium enhancement (LGE) (p = 0.001, HR = 2.92).
Perfusion defects on ATP stress are predictive of MACE which is driven primarily by cardiac hospitalization, late coronary revascularization and cardiac death. Significant independent predictors of MACE were stress induced perfusion defect, lower LVEF and infarct detected by LGE.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>34162392</pmid><doi>10.1186/s12968-021-00770-z</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0001-9533-3892</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenosine Triphosphate ATP Cardiology Cardiovascular disease Cardiovascular magnetic resonance Contrast Media Coronary artery Coronary artery bypass Coronary artery disease Coronary Artery Disease - diagnostic imaging Coronary vessels Death Gadolinium Heart Heart attack Humans Longitudinal Studies Magnetic resonance Magnetic Resonance Imaging, Cine Magnetic Resonance Spectroscopy Mortality Muscle proteins Myocardial infarction Patients Perfusion Predictive Value of Tests Prognosis Rank tests Regression analysis Resonance Retrospective Studies Risk Assessment Risk Factors Standard deviation Stress Vasodilator Agents Ventricle |
title | Prognostic value of perfusion cardiovascular magnetic resonance with adenosine triphosphate stress in stable coronary artery disease |
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