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Patient perspectives on the linkage of health data for research: Insights from an online patient community questionnaire.

Publication ,  Journal Article
O'Brien, EC; Rodriguez, AM; Kum, H-C; Schanberg, LE; Fitz-Randolph, M; O'Brien, SM; Setoguchi, S
Published in: Int J Med Inform
July 2019

OBJECTIVE: To examine the patient perspective on the risks and benefits of linking existing data sources for research. MATERIALS AND METHODS: Between December 2015 and February 2016, we fielded a questionnaire in PatientsLikeMe, an online patient community representing over 2500 health conditions. The questionnaire was developed using subject matter expertise and patient feedback from a concept elicitation phase (N = 57 patients). The final questionnaire consisted of 37 items. RESULTS: Of n = 5741 who opened the email invitation, n = 3516 respondents completed the questionnaire (61.2%). Of these, 73.8% were women, 86.4% were Caucasian, 14.5% were 65 or older, and 44.9% had completed college or post-graduate education. Questionnaire respondents indicated that the most important benefits of sharing data were "helping my doctor make better decisions about my health" (94%) and "helping make new therapies available faster" (94%). The most important data sharing risk identified was health data being "stolen by hackers" (87%). Of 693 patients who were not comfortable with researchers accessing their de-identified data, most reported that their comfort levels would increase if they were able to learn how their data was protected (84%). In general, responders felt more comfortable when unique identifiers such as social security number (90%) and insurance ID (82%) were removed from the data for linkage and research use. DISCUSSION: The majority of patients in a US-based online community are comfortable with researchers accessing their de-identified data for research purposes. CONCLUSIONS: Developing methods to link databases minimizing the exposure of unique identifiers may improve patient comfort levels with linking data for research purposes.

Duke Scholars

Published In

Int J Med Inform

DOI

EISSN

1872-8243

Publication Date

July 2019

Volume

127

Start / End Page

9 / 17

Location

Ireland

Related Subject Headings

  • Young Adult
  • Surveys and Questionnaires
  • Middle Aged
  • Medical Informatics
  • Male
  • Information Dissemination
  • Humans
  • Health Records, Personal
  • Female
  • Feedback
 

Citation

APA
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ICMJE
MLA
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O’Brien, E. C., Rodriguez, A. M., Kum, H.-C., Schanberg, L. E., Fitz-Randolph, M., O’Brien, S. M., & Setoguchi, S. (2019). Patient perspectives on the linkage of health data for research: Insights from an online patient community questionnaire. Int J Med Inform, 127, 9–17. https://doi.org/10.1016/j.ijmedinf.2019.04.003
O’Brien, Emily C., Ana Maria Rodriguez, Hye-Chung Kum, Laura E. Schanberg, Marcy Fitz-Randolph, Sean M. O’Brien, and Soko Setoguchi. “Patient perspectives on the linkage of health data for research: Insights from an online patient community questionnaire.Int J Med Inform 127 (July 2019): 9–17. https://doi.org/10.1016/j.ijmedinf.2019.04.003.
O’Brien EC, Rodriguez AM, Kum H-C, Schanberg LE, Fitz-Randolph M, O’Brien SM, et al. Patient perspectives on the linkage of health data for research: Insights from an online patient community questionnaire. Int J Med Inform. 2019 Jul;127:9–17.
O’Brien, Emily C., et al. “Patient perspectives on the linkage of health data for research: Insights from an online patient community questionnaire.Int J Med Inform, vol. 127, July 2019, pp. 9–17. Pubmed, doi:10.1016/j.ijmedinf.2019.04.003.
O’Brien EC, Rodriguez AM, Kum H-C, Schanberg LE, Fitz-Randolph M, O’Brien SM, Setoguchi S. Patient perspectives on the linkage of health data for research: Insights from an online patient community questionnaire. Int J Med Inform. 2019 Jul;127:9–17.
Journal cover image

Published In

Int J Med Inform

DOI

EISSN

1872-8243

Publication Date

July 2019

Volume

127

Start / End Page

9 / 17

Location

Ireland

Related Subject Headings

  • Young Adult
  • Surveys and Questionnaires
  • Middle Aged
  • Medical Informatics
  • Male
  • Information Dissemination
  • Humans
  • Health Records, Personal
  • Female
  • Feedback