Patient Access to Medical Information: A Multi-Perspecitive Study

dc.contributor.advisorParrish, Danielle E.
dc.contributor.committeeMemberAchenbaum, W. Andrew
dc.contributor.committeeMemberSittig, Dean F.
dc.creatorGiardina, Traber Davis
dc.date.accessioned2018-12-04T22:13:32Z
dc.date.available2018-12-04T22:13:32Z
dc.date.createdMay 2014
dc.date.issued2014-05
dc.date.submittedMay 2014
dc.date.updated2018-12-04T22:13:33Z
dc.description.abstractRecent U.S health care policy emphasizes increased patient access to medical information to empower patients and improve quality of care. However, little is known about what access should consist of, how these systems will impact patients and physicians, and whether their use leads to better outcomes. Furthermore, the discrepancy between the 85 percent of Americans who use the internet and the 10 percent who access a patient portal is striking, suggesting a need to better understand barriers and facilitators concerning the use of patient portals. This three article dissertation builds upon existing research by: 1) providing a systematic review of the literature to determine the impact of patient-accessible records on quality of care; 2) identifying physician perceptions of patients’ access to test results; and 3) exploring patients’ experiences using portal-based test result notification. Despite a lack of evidence in the literature, psychological harm to patients is a major concern for both physicians and patients, especially as it relates to the release of sensitive test results. As portals continue to evolve, it is important to address both patient and physician concerns to facilitate acceptance and use, and to ensure that patients understand the medical information they are accessing. These findings suggest important considerations for health professionals, including medical social workers, who may be able to leverage this technology to engage patients in their care.
dc.description.departmentSocial Work, Graduate College of
dc.format.digitalOriginborn digital
dc.format.mimetypeapplication/pdf
dc.identifier.citationPortions of this document appear in: Davis Giardina, Traber, Shailaja Menon, Danielle E. Parrish, Dean F. Sittig, and Hardeep Singh. "Patient access to medical records and healthcare outcomes: a systematic review." Journal of the American Medical Informatics Association 21, no. 4 (2013): 737-741.
dc.identifier.citationPortions of this document appear in: Davis Giardina, Traber, Shailaja Menon, Danielle E. Parrish, Dean F. Sittig, and Hardeep Singh. "Patient access to medical records and healthcare outcomes: a systematic review." Journal of the American Medical Informatics Association 21, no. 4 (2013): 737-741.
dc.identifier.urihttp://hdl.handle.net/10657/3648
dc.language.isoeng
dc.rightsThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. UH Libraries has secured permission to reproduce any and all previously published materials contained in the work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
dc.subjectPatient access
dc.subjectRecords
dc.subjectPatient portal
dc.subjectPersonal health record
dc.subjectTest result notification
dc.titlePatient Access to Medical Information: A Multi-Perspecitive Study
dc.type.dcmiText
dc.type.genreThesis
thesis.degree.collegeGraduate College of Social Work
thesis.degree.departmentSocial Work, Graduate College of
thesis.degree.disciplineSocial Work
thesis.degree.grantorUniversity of Houston
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy

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