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Quantitative analysis of factors influencing late lumen loss and restenosis after directional coronary atherectomy

dc.contributor.authorPopma, Jeffrey J.en_US
dc.contributor.authorDe Cesare, Nicoletta B.en_US
dc.contributor.authorPinkerton, Cass A.en_US
dc.contributor.authorKereiakes, Dean J.en_US
dc.contributor.authorWhitlow, Patrick L.en_US
dc.contributor.authorKing, III, Spencer B.en_US
dc.contributor.authorTopol, Eric J.en_US
dc.contributor.authorHolmes, David R.en_US
dc.contributor.authorLeon, Martin B.en_US
dc.contributor.authorEllis, Stephen G.en_US
dc.date.accessioned2006-04-10T15:52:44Z
dc.date.available2006-04-10T15:52:44Z
dc.date.issued1993-03-01en_US
dc.identifier.citationPopma, Jeffrey J., De Cesare, Nicoletta B., Pinkerton, Cass A., Kereiakes, Dean J., Whitlow, Patrick, King, III, Spencer B., Topol, Eric J., Holmes, David R., Leon, Martin B., Ellis, Stephen G. (1993/03/01)."Quantitative analysis of factors influencing late lumen loss and restenosis after directional coronary atherectomy." The American Journal of Cardiology 71(7): 552-557. <http://hdl.handle.net/2027.42/30957>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6T10-4C70BXR-1SF/2/bfe29c8cd3987ada7ebe419df7f16fe9en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30957
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=8438740&dopt=citationen_US
dc.description.abstractAlthough encouraging initial results have been demonstrated after directional atherectomy, the mechanisms and predictors of late lumen loss and restenosis after this procedure have not been evaluated. To examine these issues, clinical and angiographic follow-up were obtained in 262 (96%) and 212 (77%) of 274 patients undergoing successful directional coronary atherectomy. Symptom recurrence developed in 87 (33%) patients and angiographic restenosis was found in 93 (44%). Restenosis was highest in restenotic lesions in saphenous vein grafts (78% [95% confidence interval (CI): 56 to 100%]) and lowest in new-onset lesions in the left anterior descending (27% [95% CI: 15 to 39%]) and circumflex (14% [95% CI: 0 to 43%]) coronary arteries. Residual lumen diameter immediately after atherectomy was smaller in re-stenotic lesions (p = 0.002) and in lesions &gt;=10 mm in length (p = 0.02). Late lumen loss was associated with the minimal lumen diameter immediately after atherectomy (p =10 mm in length (p = 0.018), saphenous vein graft lesion location (p = 0.025) and male gender (p = 0.045) were independent predictors for restenosis. It is concluded that restenosis after directional atherectomy is related both to factors resulting in a suboptimal initial result and to factors contributing to excessive late lumen loss. These results may have implications for lesion selection in patients undergoing directional coronary atherectomy.en_US
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dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleQuantitative analysis of factors influencing late lumen loss and restenosis after directional coronary atherectomyen_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 (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA; University of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA.en_US
dc.contributor.affiliationumUniversity of Michigan, Ann Arbor, Michigan, USA; St. Vincent's Hospital, Indianapolis, Indiana, USA; Christ Hospital, Cincinnati, Ohio, USA; Cleveland Clinic, Cleveland, Ohio, USA; Emory University, Atlanta, Georgia, USA; Mayo Clinic, Rochester, Minnesota, USA; Department of Internal Medicine (Cardiology Division) of the Washington Hospital Center, Washington, D.C., USA.en_US
dc.identifier.pmid8438740en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30957/1/0000629.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0002-9149(93)90510-Jen_US
dc.identifier.sourceThe American Journal of Cardiologyen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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