dc.creator | Heitman, Elizabeth | en |
dc.date.accessioned | 2015-05-05T19:03:12Z | en |
dc.date.available | 2015-05-05T19:03:12Z | en |
dc.date.created | 1996 | en |
dc.date.issued | 1996 | en |
dc.identifier | 10.1017/S0266462300010953 | en |
dc.identifier.bibliographicCitation | International Journal of Technology Assessment in Health Care. 1996
Fall; 12(4): 657-672. | en |
dc.identifier.issn | 0266-4623 | en |
dc.identifier.uri | http://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,+Elizabeth | en |
dc.identifier.uri | http://dx.doi.org/10.1017/S0266462300010953 | en |
dc.identifier.uri | http://hdl.handle.net/10822/754344 | en |
dc.description.abstract | The 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.format | Article | en |
dc.language | en | en |
dc.source | BRL:MEDKIE/97282227 | en |
dc.subject | Brain | en |
dc.subject | Brain Pathology | en |
dc.subject | Consent | en |
dc.subject | Electroconvulsive Therapy | en |
dc.subject | Evaluation | en |
dc.subject | Government | en |
dc.subject | Health | en |
dc.subject | Health Care | en |
dc.subject | Human Experimentation | en |
dc.subject | Informed Consent | en |
dc.subject | Illness | en |
dc.subject | Mental Illness | en |
dc.subject | Patient Care | en |
dc.subject | Patient Participation | en |
dc.subject | Patients | en |
dc.subject | Patients' Rights | en |
dc.subject | Physicians | en |
dc.subject | Political Activity | en |
dc.subject | Psychiatry | en |
dc.subject | Public Opinion | en |
dc.subject | Regulation | en |
dc.subject | Research | en |
dc.subject | Rights | en |
dc.subject | Risks and Benefits | en |
dc.subject | Selection for Treatment | en |
dc.subject | State Government | en |
dc.subject | Technical Expertise | en |
dc.subject | Technology | en |
dc.subject | Technology Assessment | en |
dc.subject | Treatment Outcome | en |
dc.title | The Public's Role in the Evaluation of Health Care Technology: The Conflict Over ECT | en |
dc.provenance | Digital 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.provenance | Digital 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 |