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dc.creatorHeitman, Elizabethen
dc.date.accessioned2015-05-05T19:03:12Zen
dc.date.available2015-05-05T19:03:12Zen
dc.date.created1996en
dc.date.issued1996en
dc.identifier10.1017/S0266462300010953en
dc.identifier.bibliographicCitationInternational Journal of Technology Assessment in Health Care. 1996 Fall; 12(4): 657-672.en
dc.identifier.issn0266-4623en
dc.identifier.urihttp://worldcatlibraries.org/registry/gateway?version=1.0&url_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&atitle=The+Public's+Role+in+the+Evaluation+of+Health+Care+Technology:+The+conflict+over+Ect&title=International+Journal+of+Technology+Assessment+in+Health+Care.++&volume=12&issue=4&pages=657-672&date=1996&au=Heitman,+Elizabethen
dc.identifier.urihttp://dx.doi.org/10.1017/S0266462300010953en
dc.identifier.urihttp://hdl.handle.net/10822/754344en
dc.description.abstractThe use of electroconvulsive therapy (ECT), controversial since its inception, offers an instructive case study on the challenge of addressing patients' perspectives in the evaluation of health care technology. Despite widespread professional acceptance of ECT, groups of former psychiatric patients have worked through the U.S. legal system to restrict and even ban ECT in the treatment of mental illness. This unusual lay participation in the regulation of health care illustrates how differing conceptions of evidence can affect the evaluation of technology. ECT provides a powerful example of the value of a more complex definition of the significant outcomes of treatment and the growing practice of outcomes assessment, especially as such research is used to shape health policy.en
dc.formatArticleen
dc.languageenen
dc.sourceBRL:MEDKIE/97282227en
dc.subjectBrainen
dc.subjectBrain Pathologyen
dc.subjectConsenten
dc.subjectElectroconvulsive Therapyen
dc.subjectEvaluationen
dc.subjectGovernmenten
dc.subjectHealthen
dc.subjectHealth Careen
dc.subjectHuman Experimentationen
dc.subjectInformed Consenten
dc.subjectIllnessen
dc.subjectMental Illnessen
dc.subjectPatient Careen
dc.subjectPatient Participationen
dc.subjectPatientsen
dc.subjectPatients' Rightsen
dc.subjectPhysiciansen
dc.subjectPolitical Activityen
dc.subjectPsychiatryen
dc.subjectPublic Opinionen
dc.subjectRegulationen
dc.subjectResearchen
dc.subjectRightsen
dc.subjectRisks and Benefitsen
dc.subjectSelection for Treatmenten
dc.subjectState Governmenten
dc.subjectTechnical Expertiseen
dc.subjectTechnologyen
dc.subjectTechnology Assessmenten
dc.subjectTreatment Outcomeen
dc.titleThe Public's Role in the Evaluation of Health Care Technology: The Conflict Over ECTen
dc.provenanceDigital citation created by the National Reference Center for Bioethics Literature at Georgetown University for the BIOETHICSLINE database, part of the Kennedy Institute of Ethics' Bioethics Information Retrieval Project funded by the United States National Library of Medicine.en
dc.provenanceDigital citation migrated from OpenText LiveLink Discovery Server database named NBIO hosted by the Bioethics Research Library to the DSpace collection BioethicsLine hosted by Georgetown University.en


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