Minority Health Archive

Variation in Use of Internet-Based Patient Portals by Parents of Children With Chronic Disease

Byczkowski, T. L. and Munafo, J. K. and Britto, M. T. (2011) Variation in Use of Internet-Based Patient Portals by Parents of Children With Chronic Disease. Archives of Pediatrics and Adolescent Medicine, 165 (5). pp. 405-411. ISSN 1072-4710

Full text not available from this repository.

Abstract

OBJECTIVES: To assess the use of Internet-based portals among families of children with chronic diseases and to describe characteristics of portal registrants and users. DESIGN: Retrospective observational study. SETTING: Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, using data from September 1, 2003, through February 29, 2008. Patients/ PARTICIPANTS: Parents of children with diabetes mellitus, juvenile idiopathic arthritis, or cystic fibrosis. INTERVENTIONS: Parents of children with a chronic disease were given the opportunity to access health-related information for their children via an Internet-based portal. OUTCOME MEASURES: Percentage of families who obtained a portal account (registered), used the portal for the first time within 3 months and again 3 to 6 months after registration, number of times logged in, and session length. RESULTS: Of 1900 families, 27.9% obtained a portal account. Of those, 47.8% used the portal within 3 months of registration and 15.9% continued to use the portal 3 to 6 months after registration. Families of African American patients and of patients insured by Medicaid were less likely to obtain a portal account. More outpatient visits and having private health insurance coverage were associated with increased portal registration and use. CONCLUSIONS: Understanding the feasibility of portal use by parents is an important first step to using portals for improving self-management, patient-provider interactions, and outcomes for children with chronic diseases. Subsequent studies should address parent perceptions of the value portals add to the management of the chronic disease of their child and ways to increase that value. Barriers to using portals among racial minorities and publicly insured families should also be studied to address disparities.


Export/Citation:EndNote | BibTeX | Dublin Core | ASCII (Chicago style) | HTML Citation | OpenURL | Reference Manager
Social Networking:

Item Type: Article
Additional Information: This article is available at the publisher’s Web site. Access to the full text is subject to the publisher’s access restrictions.
Uncontrolled Keywords: disparities, racial minorities, Internet-based portals, children with chronic diseases
Subjects: Health > Disparities
Health > Prenatal & Pediatric Health
Health > Public Health > Chronic Illness & Diseases
Related URLs:
Depositing User: Users 141 not found.
Date Deposited: 28 Jul 2011 10:38
Last Modified: 28 Jul 2011 10:38
Link to this item (URI): http://health-equity.pitt.edu/id/eprint/2883

Actions (login required)

View Item