Electrocardiographic detection of left ventricular hypertrophy by the simple QRS voltage-duration product
Objectives. The object of this study was to assess the hypothesis that the product of QRS voltage and duration, as an approximation of the time-voltage integral of the QRS complex, can improve the electrocardiographic (ECG) identification of left ventricular hypertrophy. Background. Electrocardiogra...
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description | Objectives. The object of this study was to assess the hypothesis that the product of QRS voltage and duration, as an approximation of the time-voltage integral of the QRS complex, can improve the electrocardiographic (ECG) identification of left ventricular hypertrophy.
Background. Electrocardiographic identification of left ventricular hypertrophy has been limited by the poor sensitivity of standard voitage criteria. However, increases in left ventricular mass can be more closely related to increases in the time-voltage integral of the summed left ventricular dipole than to changes in voltage or QRS duration alone.
Methods. Antemortem ECGs were compared with left ventricular mass at autopsy in 220 patients. There were 95 patients with left ventricular hypertrophy, defined by left ventricular mass index 118 g/m2in men and 104 g/m2in women. The voltage-duration product was calculated as the product of QRS duration and Cornell voltage (Cornell product) and the 12-lead sum of QRS voltage (12-lead product).
Results. At partitions with a matched specificity of 95%, each voltage-duration product significantly improved sensitivity for the detection of left ventricular hypertrophy when compared with simple voltage criteria alone (Cornell product 51 % [48 of 95] vs. Cornell voltage 36% [34 of 95], p < 0.005 and 12-lead product 45% [43 of 95] vs. 12-lead voltage 31% [30 of 95], p < 0.001). Sensitivity of both the Cornell product and 12-lead product was significantly greater than that found for QRS duration alone (28%, 27 of 95, p< 0.005) and the Romhilt-Estes point score (27%, 28 of 95, p < 0.005), and compared favorably with the sensitivity of hie complex Cornell multivariate score (44%, 42 of 95, p = NS). Comparison of receiver operating characteristic curves demonstrated that improved performance of the voltage-duration products for the detection of left ventricular hypertrophy was independent of test partition selection. In addition, test performance of the voltage-duration products was not significantly affected by the presence or absence of a bundle branch block.
Conclusions. These data suggest that the simple product of either Cornell or 12-lead voltage and QRS duration can identify left ventricular hypertrophy more accurately than can voltage or QRS duration criteria alone and may approach or exceed the performance of more complex multiple regression analyses. |
doi_str_mv | 10.1016/0735-1097(92)90376-X |
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Background. Electrocardiographic identification of left ventricular hypertrophy has been limited by the poor sensitivity of standard voitage criteria. However, increases in left ventricular mass can be more closely related to increases in the time-voltage integral of the summed left ventricular dipole than to changes in voltage or QRS duration alone.
Methods. Antemortem ECGs were compared with left ventricular mass at autopsy in 220 patients. There were 95 patients with left ventricular hypertrophy, defined by left ventricular mass index 118 g/m2in men and 104 g/m2in women. The voltage-duration product was calculated as the product of QRS duration and Cornell voltage (Cornell product) and the 12-lead sum of QRS voltage (12-lead product).
Results. At partitions with a matched specificity of 95%, each voltage-duration product significantly improved sensitivity for the detection of left ventricular hypertrophy when compared with simple voltage criteria alone (Cornell product 51 % [48 of 95] vs. Cornell voltage 36% [34 of 95], p < 0.005 and 12-lead product 45% [43 of 95] vs. 12-lead voltage 31% [30 of 95], p < 0.001). Sensitivity of both the Cornell product and 12-lead product was significantly greater than that found for QRS duration alone (28%, 27 of 95, p< 0.005) and the Romhilt-Estes point score (27%, 28 of 95, p < 0.005), and compared favorably with the sensitivity of hie complex Cornell multivariate score (44%, 42 of 95, p = NS). Comparison of receiver operating characteristic curves demonstrated that improved performance of the voltage-duration products for the detection of left ventricular hypertrophy was independent of test partition selection. In addition, test performance of the voltage-duration products was not significantly affected by the presence or absence of a bundle branch block.
Conclusions. These data suggest that the simple product of either Cornell or 12-lead voltage and QRS duration can identify left ventricular hypertrophy more accurately than can voltage or QRS duration criteria alone and may approach or exceed the performance of more complex multiple regression analyses.</description><identifier>ISSN: 0735-1097</identifier><identifier>EISSN: 1558-3597</identifier><identifier>DOI: 10.1016/0735-1097(92)90376-X</identifier><identifier>PMID: 1401620</identifier><identifier>CODEN: JACCDI</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Biological and medical sciences ; Bundle-Branch Block - diagnosis ; Bundle-Branch Block - epidemiology ; Bundle-Branch Block - pathology ; Cardiac dysrhythmias ; Cardiology. Vascular system ; Chi-Square Distribution ; Electrocardiography - methods ; Electrocardiography - statistics & numerical data ; Female ; Heart ; Heart Ventricles - pathology ; Humans ; Hypertrophy, Left Ventricular - diagnosis ; Hypertrophy, Left Ventricular - epidemiology ; Hypertrophy, Left Ventricular - pathology ; Least-Squares Analysis ; Male ; Medical sciences ; Middle Aged ; Organ Size ; ROC Curve</subject><ispartof>Journal of the American College of Cardiology, 1992-11, Vol.20 (5), p.1180-1186</ispartof><rights>1992</rights><rights>1993 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c487t-13fcd51c4eec44e8f603f5e7624b6c3588e2e41bbbd62f24753b10b410ba39b83</citedby><cites>FETCH-LOGICAL-c487t-13fcd51c4eec44e8f603f5e7624b6c3588e2e41bbbd62f24753b10b410ba39b83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0735-1097(92)90376-X$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,778,782,3539,27907,27908,45978</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=4448561$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1401620$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Molloy, Thomas J.</creatorcontrib><creatorcontrib>Okin, Peter M.</creatorcontrib><creatorcontrib>Devereux, Richard B.</creatorcontrib><creatorcontrib>Kligfield, Paul</creatorcontrib><title>Electrocardiographic detection of left ventricular hypertrophy by the simple QRS voltage-duration product</title><title>Journal of the American College of Cardiology</title><addtitle>J Am Coll Cardiol</addtitle><description>Objectives. The object of this study was to assess the hypothesis that the product of QRS voltage and duration, as an approximation of the time-voltage integral of the QRS complex, can improve the electrocardiographic (ECG) identification of left ventricular hypertrophy.
Background. Electrocardiographic identification of left ventricular hypertrophy has been limited by the poor sensitivity of standard voitage criteria. However, increases in left ventricular mass can be more closely related to increases in the time-voltage integral of the summed left ventricular dipole than to changes in voltage or QRS duration alone.
Methods. Antemortem ECGs were compared with left ventricular mass at autopsy in 220 patients. There were 95 patients with left ventricular hypertrophy, defined by left ventricular mass index 118 g/m2in men and 104 g/m2in women. The voltage-duration product was calculated as the product of QRS duration and Cornell voltage (Cornell product) and the 12-lead sum of QRS voltage (12-lead product).
Results. At partitions with a matched specificity of 95%, each voltage-duration product significantly improved sensitivity for the detection of left ventricular hypertrophy when compared with simple voltage criteria alone (Cornell product 51 % [48 of 95] vs. Cornell voltage 36% [34 of 95], p < 0.005 and 12-lead product 45% [43 of 95] vs. 12-lead voltage 31% [30 of 95], p < 0.001). Sensitivity of both the Cornell product and 12-lead product was significantly greater than that found for QRS duration alone (28%, 27 of 95, p< 0.005) and the Romhilt-Estes point score (27%, 28 of 95, p < 0.005), and compared favorably with the sensitivity of hie complex Cornell multivariate score (44%, 42 of 95, p = NS). Comparison of receiver operating characteristic curves demonstrated that improved performance of the voltage-duration products for the detection of left ventricular hypertrophy was independent of test partition selection. In addition, test performance of the voltage-duration products was not significantly affected by the presence or absence of a bundle branch block.
Conclusions. These data suggest that the simple product of either Cornell or 12-lead voltage and QRS duration can identify left ventricular hypertrophy more accurately than can voltage or QRS duration criteria alone and may approach or exceed the performance of more complex multiple regression analyses.</description><subject>Biological and medical sciences</subject><subject>Bundle-Branch Block - diagnosis</subject><subject>Bundle-Branch Block - epidemiology</subject><subject>Bundle-Branch Block - pathology</subject><subject>Cardiac dysrhythmias</subject><subject>Cardiology. Vascular system</subject><subject>Chi-Square Distribution</subject><subject>Electrocardiography - methods</subject><subject>Electrocardiography - statistics & numerical data</subject><subject>Female</subject><subject>Heart</subject><subject>Heart Ventricles - pathology</subject><subject>Humans</subject><subject>Hypertrophy, Left Ventricular - diagnosis</subject><subject>Hypertrophy, Left Ventricular - epidemiology</subject><subject>Hypertrophy, Left Ventricular - pathology</subject><subject>Least-Squares Analysis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Organ Size</subject><subject>ROC Curve</subject><issn>0735-1097</issn><issn>1558-3597</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1992</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtrVDEYhoModVr9BwpZiOji1FzPZSNIaa1QkHqB7kIuXzqRzDnHJGdg_r2ZztDuXIRAvud9v_Ag9IaSc0po-4l0XDaUDN2HgX0cCO_a5u4ZWlEp-4bLoXuOVo_IS3Sa8x9CSNvT4QSdUFEbGFmhcBnBljRZnVyY7pOe18FiB6W-hmnEk8cRfMFbGEsKdok64fVuhlQz83qHzQ6XNeAcNnMEfPvjJ95Oseh7aNyS9EPFnCa32PIKvfA6Znh9vM_Q76vLXxfXzc33r98uvtw0VvRdaSj31klqBYAVAnrfEu4ldC0TprVc9j0wENQY41rmmegkN5QYUY_mg-n5GXp_6K17_y6Qi9qEbCFGPcK0ZNVxRgbKhgqKA2jTlHMCr-YUNjrtFCVqb1jt9am9PjUw9WBY3dXY22P_YjbgnkIHpXX-7jjX2erokx5tyI-YEKKXLa3Y5wMG1cU2QFLZBhgtuJCqe-Wm8P9__AOD0Jmo</recordid><startdate>19921101</startdate><enddate>19921101</enddate><creator>Molloy, Thomas J.</creator><creator>Okin, Peter M.</creator><creator>Devereux, Richard B.</creator><creator>Kligfield, Paul</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>6I.</scope><scope>AAFTH</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>19921101</creationdate><title>Electrocardiographic detection of left ventricular hypertrophy by the simple QRS voltage-duration product</title><author>Molloy, Thomas J. ; Okin, Peter M. ; Devereux, Richard B. ; Kligfield, Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c487t-13fcd51c4eec44e8f603f5e7624b6c3588e2e41bbbd62f24753b10b410ba39b83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1992</creationdate><topic>Biological and medical sciences</topic><topic>Bundle-Branch Block - diagnosis</topic><topic>Bundle-Branch Block - epidemiology</topic><topic>Bundle-Branch Block - pathology</topic><topic>Cardiac dysrhythmias</topic><topic>Cardiology. Vascular system</topic><topic>Chi-Square Distribution</topic><topic>Electrocardiography - methods</topic><topic>Electrocardiography - statistics & numerical data</topic><topic>Female</topic><topic>Heart</topic><topic>Heart Ventricles - pathology</topic><topic>Humans</topic><topic>Hypertrophy, Left Ventricular - diagnosis</topic><topic>Hypertrophy, Left Ventricular - epidemiology</topic><topic>Hypertrophy, Left Ventricular - pathology</topic><topic>Least-Squares Analysis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Organ Size</topic><topic>ROC Curve</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Molloy, Thomas J.</creatorcontrib><creatorcontrib>Okin, Peter M.</creatorcontrib><creatorcontrib>Devereux, Richard B.</creatorcontrib><creatorcontrib>Kligfield, Paul</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>Journal of the American College of Cardiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Molloy, Thomas J.</au><au>Okin, Peter M.</au><au>Devereux, Richard B.</au><au>Kligfield, Paul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Electrocardiographic detection of left ventricular hypertrophy by the simple QRS voltage-duration product</atitle><jtitle>Journal of the American College of Cardiology</jtitle><addtitle>J Am Coll Cardiol</addtitle><date>1992-11-01</date><risdate>1992</risdate><volume>20</volume><issue>5</issue><spage>1180</spage><epage>1186</epage><pages>1180-1186</pages><issn>0735-1097</issn><eissn>1558-3597</eissn><coden>JACCDI</coden><abstract>Objectives. The object of this study was to assess the hypothesis that the product of QRS voltage and duration, as an approximation of the time-voltage integral of the QRS complex, can improve the electrocardiographic (ECG) identification of left ventricular hypertrophy.
Background. Electrocardiographic identification of left ventricular hypertrophy has been limited by the poor sensitivity of standard voitage criteria. However, increases in left ventricular mass can be more closely related to increases in the time-voltage integral of the summed left ventricular dipole than to changes in voltage or QRS duration alone.
Methods. Antemortem ECGs were compared with left ventricular mass at autopsy in 220 patients. There were 95 patients with left ventricular hypertrophy, defined by left ventricular mass index 118 g/m2in men and 104 g/m2in women. The voltage-duration product was calculated as the product of QRS duration and Cornell voltage (Cornell product) and the 12-lead sum of QRS voltage (12-lead product).
Results. At partitions with a matched specificity of 95%, each voltage-duration product significantly improved sensitivity for the detection of left ventricular hypertrophy when compared with simple voltage criteria alone (Cornell product 51 % [48 of 95] vs. Cornell voltage 36% [34 of 95], p < 0.005 and 12-lead product 45% [43 of 95] vs. 12-lead voltage 31% [30 of 95], p < 0.001). Sensitivity of both the Cornell product and 12-lead product was significantly greater than that found for QRS duration alone (28%, 27 of 95, p< 0.005) and the Romhilt-Estes point score (27%, 28 of 95, p < 0.005), and compared favorably with the sensitivity of hie complex Cornell multivariate score (44%, 42 of 95, p = NS). Comparison of receiver operating characteristic curves demonstrated that improved performance of the voltage-duration products for the detection of left ventricular hypertrophy was independent of test partition selection. In addition, test performance of the voltage-duration products was not significantly affected by the presence or absence of a bundle branch block.
Conclusions. These data suggest that the simple product of either Cornell or 12-lead voltage and QRS duration can identify left ventricular hypertrophy more accurately than can voltage or QRS duration criteria alone and may approach or exceed the performance of more complex multiple regression analyses.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>1401620</pmid><doi>10.1016/0735-1097(92)90376-X</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Bundle-Branch Block - diagnosis Bundle-Branch Block - epidemiology Bundle-Branch Block - pathology Cardiac dysrhythmias Cardiology. Vascular system Chi-Square Distribution Electrocardiography - methods Electrocardiography - statistics & numerical data Female Heart Heart Ventricles - pathology Humans Hypertrophy, Left Ventricular - diagnosis Hypertrophy, Left Ventricular - epidemiology Hypertrophy, Left Ventricular - pathology Least-Squares Analysis Male Medical sciences Middle Aged Organ Size ROC Curve |
title | Electrocardiographic detection of left ventricular hypertrophy by the simple QRS voltage-duration product |
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