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Engineering Improvements in Endovascular Devices

dc.contributor.authorWilliams, David M.en_US
dc.date.accessioned2010-06-01T18:39:32Z
dc.date.available2010-06-01T18:39:32Z
dc.date.issued2006-11en_US
dc.identifier.citationWILLIAMS, DAVID M . (2006). "Engineering Improvements in Endovascular Devices." Annals of the New York Academy of Sciences 1085(1 The Abdominal Aortic Aneurysm: Genetics, Pathophysiology, and Molecular Biology ): 213-223. <http://hdl.handle.net/2027.42/71859>en_US
dc.identifier.issn0077-8923en_US
dc.identifier.issn1749-6632en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/71859
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=17182938&dopt=citationen_US
dc.description.abstractAdvances in endovascular treatment of vascular disease have focused on basic and translational research of vascular disease and endovascular devices. Clinical trials serve to establish the safety and efficacy of engineering advances that incorporate this research. Recent position statements by the Food and Drug Administration (FDA) emphasize that research into conducting these trials in a timely and cost-effective manner (critical path research) is as important to patient care as the engineering advances themselves. This article reviews the recent FDA documents discussing critical path research, highlighting those topics that the FDA emphasizes. Several directions of translational research in which engineering advances may contribute to enhanced device design and improved patient care are reviewed.en_US
dc.format.extent320164 bytes
dc.format.extent3109 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.publisherBlackwell Publishing Incen_US
dc.rights2006 New York Academy of Sciencesen_US
dc.subject.otherCritical Path Researchen_US
dc.subject.otherEndograftsen_US
dc.subject.otherFood and Drug Administration (FDA)en_US
dc.titleEngineering Improvements in Endovascular Devicesen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelScience (General)en_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumRadiology Department, University of Michigan Hospitals, Ann Arbor, Michigan, USAen_US
dc.identifier.pmid17182938en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/71859/1/annals.1383.021.pdf
dc.identifier.doi10.1196/annals.1383.021en_US
dc.identifier.sourceAnnals of the New York Academy of Sciencesen_US
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dc.identifier.citedreference2. Office of Device Evaluation Annual Report Fiscal Year 2004. March 2005. U.S. Department of Health and Human Services, Washington, D.C. Accessed October 20, 2006: http://www.fda.gov/cdrh/annual/fy2004/ode/part3.htmlen_US
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dc.identifier.citedreference4. Innovation or Stagnation Critical Path Opportunities List. U.S. Department of Health and Human Services, Food and Drug Administration, Washington, D.C. March 2006. Accessed October 20, 2006: http://www.fda.gov/oc/initiatives/criticalpath/reports/opp_list.pdfen_US
dc.identifier.citedreference5. FDA's Science Forum Centennial Home Page. U.S. Department of Health and Human Services, Food and Drug Administration, Washington, D.C. Accessed October 20, 2006: http://www.fda.gov/scienceforum/en_US
dc.identifier.citedreference6. What is MEMS Technology. MEMS and Nanotechnology Clearinghouse. Accessed October 20, 2006: http://www.memsnet.org/mems/what-is.htmlen_US
dc.identifier.citedreferenceJ.L. Cronenwett & J.D. Birkmeyer, Eds.: 8, 122, 142. AHA Press. Chicago. http://www.dartmouthatlas.org/atlases/atlas_series.shtm. ( accessed May 3, 2006 ).en_US
dc.identifier.citedreferencePoh, M., M. Boyer, A. Solan, et al. 2005. Blood vessels engineered from human cells. Lancet. 365: 2122 2124.en_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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