Patient Experiences With Full Electronic Access to Health Records and Clinical Notes Through the My HealtheVet Personal Health Record Pilot: Qualitative Study

被引:182
作者
Woods, Susan S. [1 ,2 ]
Schwartz, Erin [1 ]
Tuepker, Anais [1 ]
Press, Nancy A. [3 ,4 ]
Nazi, Kim M. [5 ]
Turvey, Carolyn L. [6 ]
Nichol, Paul [7 ]
机构
[1] Portland VA Med Ctr, Portland, OR 97239 USA
[2] Oregon Hlth & Sci Univ, Dept Med Informat & Clin Epidemiol, Portland, OR 97201 USA
[3] Oregon Hlth & Sci Univ, Sch Nursing, Portland, OR 97201 USA
[4] Oregon Hlth & Sci Univ, Sch Med, Portland, OR 97201 USA
[5] Vet Hlth Adm, Vet & Consumers Hlth Informat Off, Off Informat & Analyt, Washington, DC USA
[6] Iowa City VA Hlth Care Syst, Ctr Comprehens Access & Delivery Res & Evaluat, Iowa City, IA USA
[7] VA Puget Sound Hlth Care Syst, Seattle, WA USA
关键词
personal health records; eHealth; patient access to records; veterans; patient participation; MEDICAL-RECORD; INVITING PATIENTS; GENERAL-PRACTICE; DOCTORS NOTES; CARE RECORD; COMMUNICATION; EXPECTATIONS; INFORMATION; ATTITUDES; TRIAL;
D O I
10.2196/jmir.2356
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Full sharing of the electronic health record with patients has been identified as an important opportunity to engage patients in their health and health care. The My HealtheVet Pilot, the initial personal health record of the US Department of Veterans Affairs, allowed patients and their delegates to view and download content in their electronic health record, including clinical notes, laboratory tests, and imaging reports. Objective: A qualitative study with purposeful sampling sought to examine patients' views and experiences with reading their health records, including their clinical notes, online. Methods: Five focus group sessions were conducted with patients and family members who enrolled in the My HealtheVet Pilot at the Portland Veterans Administration Medical Center, Oregon. A total of 30 patients enrolled in the My HealtheVet Pilot, and 6 family members who had accessed and viewed their electronic health records participated in the sessions. Results: Four themes characterized patient experiences with reading the full complement of their health information. Patients felt that seeing their records positively affected communication with providers and the health system, enhanced knowledge of their health and improved self-care, and allowed for greater participation in the quality of their care such as follow-up of abnormal test results or decision-making on when to seek care. While some patients felt that seeing previously undisclosed information, derogatory language, or inconsistencies in their notes caused challenges, they overwhelmingly felt that having more, rather than less, of their health record information provided benefits. Conclusions: Patients and their delegates had predominantly positive experiences with health record transparency and the open sharing of notes and test results. Viewing their records appears to empower patients and enhance their contributions to care, calling into question common provider concerns about the effect of full record access on patient well-being. While shared records may or may not impact overall clinic workload, it is likely to change providers' work, necessitating new types of skills to communicate and partner with patients.
引用
收藏
页码:182 / 191
页数:10
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