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Variability of quantitative digital subtraction coronary angiography before and after percutaneous transluminal coronary angioplasty

dc.contributor.authorSanz, Mark L.en_US
dc.contributor.authorJohn Mancini, G. B.en_US
dc.contributor.authorLeFree, Michael T.en_US
dc.contributor.authorMickelson, Judith K.en_US
dc.contributor.authorStarling, Mark R.en_US
dc.contributor.authorVogel, Robert A.en_US
dc.contributor.authorTopol, Eric J.en_US
dc.date.accessioned2006-04-07T19:51:12Z
dc.date.available2006-04-07T19:51:12Z
dc.date.issued1987-07-01en_US
dc.identifier.citationSanz, Mark L., John Mancini, G. B., LeFree, Michael T., Mickelson, Judith K., Starling, Mark R., Vogel, Robert A., Topol, Eric J. (1987/07/01)."Variability of quantitative digital subtraction coronary angiography before and after percutaneous transluminal coronary angioplasty." The American Journal of Cardiology 60(1): 55-60. <http://hdl.handle.net/2027.42/26649>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T10-4C76CV7-12Y/2/6810bf3f831a8bc027f8eeecc697e5f9en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/26649
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=2955693&dopt=citationen_US
dc.description.abstractQuantitative coronary angiography has been proposed as a means of reducing observer variability in the interpretation of coronary angiograms, especially before and after percutaneous transluminal coronary angioplasty (PTCA). Analysis of 13 consecutively acquired biplane digital subtraction angiograms before and after PTCA was undertaken to determine intra- and interobserver variability of absolute lesion diameter, relative videodensitometric cross-sectional area, automated percent diameter stenosis and visual percent diameter stenosis using a new fully automated quantitative computer program. The reliability of single-view measurements was also assessed. Both before and after PTCA, measures of absolute diameter showed less interobserver variability than densitometry, percent automated diameter stenosis stenosis and percent visual diameter stenosis measurements (before, R = 0.95, 0.83, 0.86, 0.70; after, 0.95, 0.88, 0.81, 0.62, respectively). Relative videodensitometric cross-sectional area correlated poorly with images from the orthogonal view (r = 0.46). These data suggest that quantitative angiography reduces variability from visual estimates; of all quantitative angiographic measurements, the highest interobserver reproducibility is achieved using absolute lesion diameter both before and after PTCA, probably because no operator interaction is needed to identify a "normal" segment. Unselected, single-view quantitative arteriography is poorly reproducible using videodensitometry. Therefore, automated determination of absolute lesion diameter in at least 2 projections provides the most reproducible evaluation of coronary lesions both before and after PTCA.en_US
dc.format.extent1839756 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleVariability of quantitative digital subtraction coronary angiography before and after percutaneous transluminal coronary angioplastyen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Cardiology, Veterans Administration Medical Center and University Hospital, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Cardiology, Veterans Administration Medical Center and University Hospital, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Cardiology, Veterans Administration Medical Center and University Hospital, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Cardiology, Veterans Administration Medical Center and University Hospital, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Cardiology, Veterans Administration Medical Center and University Hospital, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Cardiology, Veterans Administration Medical Center and University Hospital, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine, Division of Cardiology, Veterans Administration Medical Center and University Hospital, University of Michigan Medical School, Ann Arbor, Michigan, USAen_US
dc.identifier.pmid2955693en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/26649/1/0000193.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-9149(87)90984-2en_US
dc.identifier.sourceThe American Journal of Cardiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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