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1.
J Med Internet Res ; 11(4): e44, 2009 Oct 27.
Article in English | MEDLINE | ID: mdl-19861298

ABSTRACT

BACKGROUND: Electronic personal health records (PHRs) are increasingly recognized and used as a tool to address various challenges stemming from the scattered and incompatible personal health information that exists in the contemporary US health care system. Although activity around PHR development and deployment has increased in recent years, little has been reported regarding the use and utility of PHRs among low-income and/or elderly populations. OBJECTIVE: The aim was to assess the use and utility of PHRs in a low-income, elderly population. METHODS: We deployed a Web-based, institution-neutral PHR system, the Personal Health Information Management System (PHIMS), in a federally funded housing facility for low-income and elderly residents. We assessed use and user satisfaction through system logs, questionnaire surveys, and user group meetings. RESULTS: Over the 33-month study period, 70 residents participated; this number was reduced to 44 by the end of the study. Although the PHIMS was available for free and personal assistance and computers with Internet connection were provided without any cost to residents, only 13% (44/330) of the eligible residents used the system, and system usage was limited. Almost one half of the users (47%, 33/70) used the PHIMS only on a single day. Use was also highly correlated with the availability of in-person assistance; 77% of user activities occurred while the assistance was available. Residents' ability to use the PHR system was limited by poor computer and Internet skills, technophobia, low health literacy, and limited physical/cognitive abilities. Among the 44 PHIMS users, 14 (32%) responded to the questionnaire. In this selected subgroup of survey participants, the majority (82%, 9/11) used the PHIMS three times or more and reported that it improved the quality of overall health care they received. CONCLUSIONS: Our findings suggest that those who can benefit the most from a PHR system may be the least able to use it. Disparities in access to and use of computers, the Internet, and PHRs may exacerbate health care inequality in the future.


Subject(s)
Electronic Health Records/statistics & numerical data , Poverty , Adult , Aged , Aged, 80 and over , Delivery of Health Care/standards , Delivery of Health Care/statistics & numerical data , Education, Nursing, Graduate , Female , Health Services for the Aged/statistics & numerical data , Humans , Internet , Male , Medical Records Systems, Computerized/statistics & numerical data , Middle Aged , Patient Participation/statistics & numerical data , Young Adult
2.
AMIA Annu Symp Proc ; : 409-13, 2007 Oct 11.
Article in English | MEDLINE | ID: mdl-18693868

ABSTRACT

Personal Health Records (PHRs) are increasingly recognized as a strategy to improve patient-provider communication, availability of health information, and quality of care, by making the delivery of care more patient-centered. However, not much is known about the effects of self-managing personal health information (PeHI), patients' perception of PeHI and patient workflow around PeHI management. We studied PHR use in a low-income, elderly and/or disabled population for 18 months, and describe how the PHR was used through an analysis of database access server log data. Some patients may not keep their PHR up-to-date because they don't value, can't access, or don't understand certain categories of their health information. Understanding of usage patterns can guide the development and maintenance of more usable and pragmatic PHR systems.


Subject(s)
Disabled Persons , Medical Records Systems, Computerized/statistics & numerical data , Medical Records/statistics & numerical data , Adult , Aged , Female , Humans , Internet , Male , Middle Aged , Patient Access to Records , Self Care , Washington
3.
AMIA Annu Symp Proc ; : 156-60, 2006.
Article in English | MEDLINE | ID: mdl-17238322

ABSTRACT

Personal health information management (PHIM) refers to activities that support consumers' access, integration, organization, and use of their personal health information. We investigated PHIM in the health consumer population using a focus group and participatory design. In collaboration with health consumers, we identified PHIM activities and explored the design of new supportive technology. Our findings describe prominent PHIM activities such as monitoring and assessing health, as well as health-related decision making, planning, and action. We describe design principles our participants used during the participatory design of a PHIM tool. These include individual control, sharing, integration, security and flexibility. These findings provide new insights into emerging ideas in consumer health informatics research and technology design. Understanding health consumers' PHIM needs is an important step in creating technology to support these needs.


Subject(s)
Access to Information , Community Participation , Information Management , Medical Informatics , Medical Records , Consumer Behavior , Focus Groups , Humans , Information Services
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