Patterns of electronic portal use among vulnerable patients in a nationwide practice-based research network: From the OCHIN Practice-based Research Network (PBRN)

Lorraine S. Wallace, Heather Angier, Nathalie Huguet, James A. Gaudino, Alex Krist, Marla Dearing, Marie Killerby, Miguel Marino, Jennifer Devoe

Research output: Contribution to journalArticle

23 Scopus citations

Abstract

Background: Underserved patient populations experience barriers to accessing and engaging within the complex health care system. Electronic patient portals have been proposed as a potential new way to improve access and engagement. We studied patient portal use for 12 consecutive months (365 days) among a large, nationally distributed, underserved patient population within the OCHIN (originally created as the Oregon Community Health Information Network and renamed OCHIN as other states joined) practice-based research network (PBRN). Methods: We retrospectively assessed adoption and use of Epic's MyChart patient portal in the first 12 months after MyChart was made available to the OCHIN PBRN. We examined electronic health record data from 36,549 patients aged ≥18 years who were offered a MyChart access code between May 1, 2012, and April 30, 2013, across the OCHIN PBRN in 13 states. Results: Overall, 29% of patients offered an access code logged into their MyChart account. Superusers (minimum of 2 logins per month over a 12-month period) accounted for 6% of users overall. Men, nonwhite patients, Hispanic patients, Spanish-speaking patients, and those with the lowest incomes were significantly less likely to activate. Publicly insured and uninsured patients were also less likely to log in to their MyChart account, but once activated they were more likely than privately insured patients to use MyChart functions. Conclusions: Our findings suggest that, compared with others, certain patient groups may be less interested in using patient portals or may have experienced significant barriers that prevented use. Making portal access available is a first step. Additional studies need to specifically identify health system-, clinic-, and patient-level barriers and facilitators to portal adoption and use.

Original languageEnglish (US)
Pages (from-to)592-603
Number of pages12
JournalJournal of the American Board of Family Medicine
Volume29
Issue number5
DOIs
Publication statusPublished - Sep 1 2016

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Keywords

  • Ambulatory Care Facilities
  • Electronic Health Records
  • Hispanic Americans
  • Information Services
  • Medical Assistance
  • Medically Uninsured
  • Oregon
  • Poverty
  • Practice-based Research
  • Retrospective Studies
  • Vulnerable Populations

ASJC Scopus subject areas

  • Public Health, Environmental and Occupational Health
  • Family Practice

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