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Reproducibility of left and right ventricular mass measurements with cardiac CT
Background Cardiac CT provides volumetric data that enables characterization of the myocardium. Objective We evaluated intraobserver, interobserver, and interstudy reproducibility of left ventricular (LV) and right ventricular (RV) mass quantification with cardiac CT. Methods Thirty-eight patients w...
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Published in: | Journal of cardiovascular computed tomography 2011-09, Vol.5 (5), p.317-324 |
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creator | Schwarz, Florian, MD Takx, Richard, BS Schoepf, U. Joseph, MD Lee, Yeong Shyan, MB, BCh, FRCR Ruzsics, Balazs, MD, PhD Gassner, Eva Maria, MD Chiaramida, Salvatore, MD Henzler, Thomas, MD |
description | Background Cardiac CT provides volumetric data that enables characterization of the myocardium. Objective We evaluated intraobserver, interobserver, and interstudy reproducibility of left ventricular (LV) and right ventricular (RV) mass quantification with cardiac CT. Methods Thirty-eight patients who underwent cardiac CT twice within 365 days were included in this analysis. Functional reconstructions in 10% steps throughout the R-R interval and axial 1.5-mm sections were used. Semiautomatic contour detection was used to trace epicardial and endocardial borders in all cardiac phases for calculation of LV and RV ejection fraction, end-diastolic volume, end-systolic volume, cardiac output, stroke volume, and ventricular mass. For each study 2 observers measured LV and RV mass twice. Results LV mass parameters derived from semiautomatic contour detection algorithm had excellent intraobserver ( r = 1.00), interobserver ( r = 0.99), and interstudy ( r = 0.99) reproducibility ( P < 0.0001). Average end-diastolic LV mass was 146.2 ± 42.9 g at the first CT study and 146.8 ± 44.4 g at the second study. For measuring RV mass, reproducibility was good on all levels ( r = 0.78, r = 0.78, and r = 0.68, respectively, with an average end-diastolic mass of 25.7 ± 5.8 g at the first study and 24.4 ± 4.8 g at the second study. Conclusion Quantification of LV mass at cardiac CT with the threshold-based, region-growing semiautomatic segmentation analysis software evaluated here is highly observer independent and reproducible. This largely holds true for the estimation of RV mass as well; however, further improvements are needed to optimize reproducibility for RV mass quantification. |
doi_str_mv | 10.1016/j.jcct.2011.08.004 |
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Joseph, MD ; Lee, Yeong Shyan, MB, BCh, FRCR ; Ruzsics, Balazs, MD, PhD ; Gassner, Eva Maria, MD ; Chiaramida, Salvatore, MD ; Henzler, Thomas, MD</creator><creatorcontrib>Schwarz, Florian, MD ; Takx, Richard, BS ; Schoepf, U. Joseph, MD ; Lee, Yeong Shyan, MB, BCh, FRCR ; Ruzsics, Balazs, MD, PhD ; Gassner, Eva Maria, MD ; Chiaramida, Salvatore, MD ; Henzler, Thomas, MD</creatorcontrib><description>Background Cardiac CT provides volumetric data that enables characterization of the myocardium. Objective We evaluated intraobserver, interobserver, and interstudy reproducibility of left ventricular (LV) and right ventricular (RV) mass quantification with cardiac CT. Methods Thirty-eight patients who underwent cardiac CT twice within 365 days were included in this analysis. Functional reconstructions in 10% steps throughout the R-R interval and axial 1.5-mm sections were used. Semiautomatic contour detection was used to trace epicardial and endocardial borders in all cardiac phases for calculation of LV and RV ejection fraction, end-diastolic volume, end-systolic volume, cardiac output, stroke volume, and ventricular mass. For each study 2 observers measured LV and RV mass twice. Results LV mass parameters derived from semiautomatic contour detection algorithm had excellent intraobserver ( r = 1.00), interobserver ( r = 0.99), and interstudy ( r = 0.99) reproducibility ( P < 0.0001). Average end-diastolic LV mass was 146.2 ± 42.9 g at the first CT study and 146.8 ± 44.4 g at the second study. For measuring RV mass, reproducibility was good on all levels ( r = 0.78, r = 0.78, and r = 0.68, respectively, with an average end-diastolic mass of 25.7 ± 5.8 g at the first study and 24.4 ± 4.8 g at the second study. Conclusion Quantification of LV mass at cardiac CT with the threshold-based, region-growing semiautomatic segmentation analysis software evaluated here is highly observer independent and reproducible. This largely holds true for the estimation of RV mass as well; however, further improvements are needed to optimize reproducibility for RV mass quantification.</description><identifier>ISSN: 1934-5925</identifier><identifier>EISSN: 1876-861X</identifier><identifier>DOI: 10.1016/j.jcct.2011.08.004</identifier><identifier>PMID: 21875827</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Algorithms ; Cardiac CT ; Cardiac Output ; Cardiovascular ; Female ; Heart Ventricles - diagnostic imaging ; Heart Ventricles - physiopathology ; Humans ; Hypertrophy, Left Ventricular - diagnostic imaging ; Hypertrophy, Left Ventricular - physiopathology ; Hypertrophy, Right Ventricular - diagnostic imaging ; Hypertrophy, Right Ventricular - physiopathology ; Linear Models ; Male ; Middle Aged ; Observer Variation ; Organ Size ; Predictive Value of Tests ; Radiographic Image Interpretation, Computer-Assisted ; Reproducibility of Results ; Retrospective Studies ; Semiautomatic software ; Software ; Stroke Volume ; Tomography, X-Ray Computed ; Ventricular Function, Left ; Ventricular Function, Right ; Ventricular mass ; Ventricular volumetric parameters</subject><ispartof>Journal of cardiovascular computed tomography, 2011-09, Vol.5 (5), p.317-324</ispartof><rights>Society of Cardiovascular Computed Tomography</rights><rights>2011 Society of Cardiovascular Computed Tomography</rights><rights>Copyright © 2011 Society of Cardiovascular Computed Tomography. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-f807729cb10ba6ae9d45afd5cf3451ba63b7c192100e12b1cac99ca0b7f67f8d3</citedby><cites>FETCH-LOGICAL-c410t-f807729cb10ba6ae9d45afd5cf3451ba63b7c192100e12b1cac99ca0b7f67f8d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21875827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Schwarz, Florian, MD</creatorcontrib><creatorcontrib>Takx, Richard, BS</creatorcontrib><creatorcontrib>Schoepf, U. Joseph, MD</creatorcontrib><creatorcontrib>Lee, Yeong Shyan, MB, BCh, FRCR</creatorcontrib><creatorcontrib>Ruzsics, Balazs, MD, PhD</creatorcontrib><creatorcontrib>Gassner, Eva Maria, MD</creatorcontrib><creatorcontrib>Chiaramida, Salvatore, MD</creatorcontrib><creatorcontrib>Henzler, Thomas, MD</creatorcontrib><title>Reproducibility of left and right ventricular mass measurements with cardiac CT</title><title>Journal of cardiovascular computed tomography</title><addtitle>J Cardiovasc Comput Tomogr</addtitle><description>Background Cardiac CT provides volumetric data that enables characterization of the myocardium. Objective We evaluated intraobserver, interobserver, and interstudy reproducibility of left ventricular (LV) and right ventricular (RV) mass quantification with cardiac CT. Methods Thirty-eight patients who underwent cardiac CT twice within 365 days were included in this analysis. Functional reconstructions in 10% steps throughout the R-R interval and axial 1.5-mm sections were used. Semiautomatic contour detection was used to trace epicardial and endocardial borders in all cardiac phases for calculation of LV and RV ejection fraction, end-diastolic volume, end-systolic volume, cardiac output, stroke volume, and ventricular mass. For each study 2 observers measured LV and RV mass twice. Results LV mass parameters derived from semiautomatic contour detection algorithm had excellent intraobserver ( r = 1.00), interobserver ( r = 0.99), and interstudy ( r = 0.99) reproducibility ( P < 0.0001). Average end-diastolic LV mass was 146.2 ± 42.9 g at the first CT study and 146.8 ± 44.4 g at the second study. For measuring RV mass, reproducibility was good on all levels ( r = 0.78, r = 0.78, and r = 0.68, respectively, with an average end-diastolic mass of 25.7 ± 5.8 g at the first study and 24.4 ± 4.8 g at the second study. Conclusion Quantification of LV mass at cardiac CT with the threshold-based, region-growing semiautomatic segmentation analysis software evaluated here is highly observer independent and reproducible. This largely holds true for the estimation of RV mass as well; however, further improvements are needed to optimize reproducibility for RV mass quantification.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Algorithms</subject><subject>Cardiac CT</subject><subject>Cardiac Output</subject><subject>Cardiovascular</subject><subject>Female</subject><subject>Heart Ventricles - diagnostic imaging</subject><subject>Heart Ventricles - physiopathology</subject><subject>Humans</subject><subject>Hypertrophy, Left Ventricular - diagnostic imaging</subject><subject>Hypertrophy, Left Ventricular - physiopathology</subject><subject>Hypertrophy, Right Ventricular - diagnostic imaging</subject><subject>Hypertrophy, Right Ventricular - physiopathology</subject><subject>Linear Models</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Observer Variation</subject><subject>Organ Size</subject><subject>Predictive Value of Tests</subject><subject>Radiographic Image Interpretation, Computer-Assisted</subject><subject>Reproducibility of Results</subject><subject>Retrospective Studies</subject><subject>Semiautomatic software</subject><subject>Software</subject><subject>Stroke Volume</subject><subject>Tomography, X-Ray Computed</subject><subject>Ventricular Function, Left</subject><subject>Ventricular Function, Right</subject><subject>Ventricular mass</subject><subject>Ventricular volumetric parameters</subject><issn>1934-5925</issn><issn>1876-861X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kUuLFTEQRhtRnHH0D7iQ7Fx1W5V-JSCCXHzBwICO4C6kK9VO2n6MSffI_femuaMLF64SivN9JKey7DlCgYDNq6EYiNZCAmIBqgCoHmTnqNomVw1-e5juuqzyWsv6LHsS4wBQtwjqcXYmE1Ur2Z5nV5_5NixuI9_50a9HsfRi5H4VdnYi-O83q7jjeQ2ettEGMdkYxcQ2boGnNI_il19vBNngvCVxuH6aPertGPnZ_XmRfX3_7vrwMb-8-vDp8PYypwphzXsFbSs1dQidbSxrV9W2dzX1ZVVjGpVdS6glAjDKDsmS1mSha_um7ZUrL7KXp970-p8bx9VMPhKPo5152aJRupSqLEEnUp5ICkuMgXtzG_xkw9EgmN2jGczu0eweDSiTPKbQi_v6rZvY_Y38EZeA1yeA0yfvPAcTyfNM7HzgVOYW___-N__EafSzJzv-4CPHYdnCnPQZNFEaMF_2Te6LxCSkRCXL32pMmdw</recordid><startdate>20110901</startdate><enddate>20110901</enddate><creator>Schwarz, Florian, MD</creator><creator>Takx, Richard, BS</creator><creator>Schoepf, U. Joseph, MD</creator><creator>Lee, Yeong Shyan, MB, BCh, FRCR</creator><creator>Ruzsics, Balazs, MD, PhD</creator><creator>Gassner, Eva Maria, MD</creator><creator>Chiaramida, Salvatore, MD</creator><creator>Henzler, Thomas, MD</creator><general>Elsevier Inc</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>20110901</creationdate><title>Reproducibility of left and right ventricular mass measurements with cardiac CT</title><author>Schwarz, Florian, MD ; Takx, Richard, BS ; Schoepf, U. Joseph, MD ; Lee, Yeong Shyan, MB, BCh, FRCR ; Ruzsics, Balazs, MD, PhD ; Gassner, Eva Maria, MD ; Chiaramida, Salvatore, MD ; Henzler, Thomas, MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-f807729cb10ba6ae9d45afd5cf3451ba63b7c192100e12b1cac99ca0b7f67f8d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Algorithms</topic><topic>Cardiac CT</topic><topic>Cardiac Output</topic><topic>Cardiovascular</topic><topic>Female</topic><topic>Heart Ventricles - diagnostic imaging</topic><topic>Heart Ventricles - physiopathology</topic><topic>Humans</topic><topic>Hypertrophy, Left Ventricular - diagnostic imaging</topic><topic>Hypertrophy, Left Ventricular - physiopathology</topic><topic>Hypertrophy, Right Ventricular - diagnostic imaging</topic><topic>Hypertrophy, Right Ventricular - physiopathology</topic><topic>Linear Models</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Observer Variation</topic><topic>Organ Size</topic><topic>Predictive Value of Tests</topic><topic>Radiographic Image Interpretation, Computer-Assisted</topic><topic>Reproducibility of Results</topic><topic>Retrospective Studies</topic><topic>Semiautomatic software</topic><topic>Software</topic><topic>Stroke Volume</topic><topic>Tomography, X-Ray Computed</topic><topic>Ventricular Function, Left</topic><topic>Ventricular Function, Right</topic><topic>Ventricular mass</topic><topic>Ventricular volumetric parameters</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schwarz, Florian, MD</creatorcontrib><creatorcontrib>Takx, Richard, BS</creatorcontrib><creatorcontrib>Schoepf, U. Joseph, MD</creatorcontrib><creatorcontrib>Lee, Yeong Shyan, MB, BCh, FRCR</creatorcontrib><creatorcontrib>Ruzsics, Balazs, MD, PhD</creatorcontrib><creatorcontrib>Gassner, Eva Maria, MD</creatorcontrib><creatorcontrib>Chiaramida, Salvatore, MD</creatorcontrib><creatorcontrib>Henzler, Thomas, MD</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>Journal of cardiovascular computed tomography</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schwarz, Florian, MD</au><au>Takx, Richard, BS</au><au>Schoepf, U. Joseph, MD</au><au>Lee, Yeong Shyan, MB, BCh, FRCR</au><au>Ruzsics, Balazs, MD, PhD</au><au>Gassner, Eva Maria, MD</au><au>Chiaramida, Salvatore, MD</au><au>Henzler, Thomas, MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reproducibility of left and right ventricular mass measurements with cardiac CT</atitle><jtitle>Journal of cardiovascular computed tomography</jtitle><addtitle>J Cardiovasc Comput Tomogr</addtitle><date>2011-09-01</date><risdate>2011</risdate><volume>5</volume><issue>5</issue><spage>317</spage><epage>324</epage><pages>317-324</pages><issn>1934-5925</issn><eissn>1876-861X</eissn><abstract>Background Cardiac CT provides volumetric data that enables characterization of the myocardium. Objective We evaluated intraobserver, interobserver, and interstudy reproducibility of left ventricular (LV) and right ventricular (RV) mass quantification with cardiac CT. Methods Thirty-eight patients who underwent cardiac CT twice within 365 days were included in this analysis. Functional reconstructions in 10% steps throughout the R-R interval and axial 1.5-mm sections were used. Semiautomatic contour detection was used to trace epicardial and endocardial borders in all cardiac phases for calculation of LV and RV ejection fraction, end-diastolic volume, end-systolic volume, cardiac output, stroke volume, and ventricular mass. For each study 2 observers measured LV and RV mass twice. Results LV mass parameters derived from semiautomatic contour detection algorithm had excellent intraobserver ( r = 1.00), interobserver ( r = 0.99), and interstudy ( r = 0.99) reproducibility ( P < 0.0001). Average end-diastolic LV mass was 146.2 ± 42.9 g at the first CT study and 146.8 ± 44.4 g at the second study. For measuring RV mass, reproducibility was good on all levels ( r = 0.78, r = 0.78, and r = 0.68, respectively, with an average end-diastolic mass of 25.7 ± 5.8 g at the first study and 24.4 ± 4.8 g at the second study. Conclusion Quantification of LV mass at cardiac CT with the threshold-based, region-growing semiautomatic segmentation analysis software evaluated here is highly observer independent and reproducible. This largely holds true for the estimation of RV mass as well; however, further improvements are needed to optimize reproducibility for RV mass quantification.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21875827</pmid><doi>10.1016/j.jcct.2011.08.004</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Algorithms Cardiac CT Cardiac Output Cardiovascular Female Heart Ventricles - diagnostic imaging Heart Ventricles - physiopathology Humans Hypertrophy, Left Ventricular - diagnostic imaging Hypertrophy, Left Ventricular - physiopathology Hypertrophy, Right Ventricular - diagnostic imaging Hypertrophy, Right Ventricular - physiopathology Linear Models Male Middle Aged Observer Variation Organ Size Predictive Value of Tests Radiographic Image Interpretation, Computer-Assisted Reproducibility of Results Retrospective Studies Semiautomatic software Software Stroke Volume Tomography, X-Ray Computed Ventricular Function, Left Ventricular Function, Right Ventricular mass Ventricular volumetric parameters |
title | Reproducibility of left and right ventricular mass measurements with cardiac CT |
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