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Use of quality indicators to evaluate the care of patients with localized prostate carcinoma

dc.contributor.authorMiller, David C.en_US
dc.contributor.authorLitwin, Mark S.en_US
dc.contributor.authorSanda, Martin G.en_US
dc.contributor.authorMontie, James E.en_US
dc.contributor.authorDunn, Rodney L.en_US
dc.contributor.authorResh, Jenniferen_US
dc.contributor.authorSandler, Howard M.en_US
dc.contributor.authorWei, John T.en_US
dc.date.accessioned2006-04-19T13:31:04Z
dc.date.available2006-04-19T13:31:04Z
dc.date.issued2003-03-15en_US
dc.identifier.citationMiller, David C.; Litwin, Mark S.; Sanda, Martin G.; Montie, James E.; Dunn, Rodney L.; Resh, Jennifer; Sandler, Howard; Wei, John T. (2003)."Use of quality indicators to evaluate the care of patients with localized prostate carcinoma." Cancer 97(6): 1428-1435. <http://hdl.handle.net/2027.42/34367>en_US
dc.identifier.issn0008-543Xen_US
dc.identifier.issn1097-0142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/34367
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=12627506&dopt=citationen_US
dc.description.abstractBACKGROUND The goal of quality assurance in health care is to preserve and improve patient care. Recently, RAND developed a set of evidence-based candidate indicators for evaluating the quality of care for patients with localized prostate carcinoma; however, the feasibility and sensitivity of these indicators have not been tested in a clinical setting. The objectives of this study were to evaluate the feasibility of measuring these quality indicators and to determine their sensitivity to change in practice patterns over time. METHODS One hundred sixty-eight men who presented in either 1995 or in 2000 and were treated for localized prostate carcinoma were selected randomly from the University of Michigan tumor registry. A combination of electronic data base review and explicit chart review was used to assess the feasibility of measuring compliance for each indicator. For each indicator in which assessment was feasible, compliance with the RAND indicators was determined for patients in both years. Multivariate regression analysis was used to adjust for potential confounding effects of disease stage, tumor grade, prostate specific antigen (PSA) level, patient age, and therapy. RESULTS Based on review of available clinical data, measurement of compliance was feasible for 19 of 22 RAND candidate quality indicators (86%). For five indicators, significant differences in documentation (compliance) were detected between 1995 and 2000 ( P < 0.05). Treatment received and higher PSA levels were associated independently with documentation of compliance for several indicators ( P < 0.05). CONCLUSIONS Measurement of the majority of the RAND quality indicators for the treatment of patients with localized prostate carcinoma was feasible, and improvements in several indicators were observed between 1995 and 2000. Demonstration of such variation, even within a single institution, suggests that the indicators are sufficiently sensitive to detect differences in practice patterns. Cancer 2003;97:1428–35. © 2003 American Cancer Society. DOI 10.1002/cncr.11216en_US
dc.format.extent129748 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherLife and Medical Sciencesen_US
dc.subject.otherCancer Research, Oncology and Pathologyen_US
dc.titleUse of quality indicators to evaluate the care of patients with localized prostate carcinomaen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Urology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Urology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Urology, University of Michigan, Ann Arbor, Michigan ; James E. Montie is an investigator for Astra Zeneca and UroCor.en_US
dc.contributor.affiliationumDepartment of Urology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Urology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Radiation Oncology, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationumDepartment of Urology, University of Michigan, Ann Arbor, Michigan ; The Veterans Affairs Center for Practice Management and Outcomes Research, Ann Arbor Veterans Affairs Medical Center, Ann Arbor, Michigan ; Fax: (734) 936-9127 ; Department of Urology, Taubman Health Care Center, University of Michigan Health System, 1500 East Medical Center Drive, Ann Arbor, MI 48109-0330en_US
dc.contributor.affiliationotherDepartments of Urology and Health Services, University of California-Los Angeles, Los Angeles, Californiaen_US
dc.identifier.pmid12627506en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/34367/1/11216_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/cncr.11216en_US
dc.identifier.sourceCanceren_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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