Literature DB >> 24923652

Perceived healthcare provider reactions to patient and caregiver use of online health communities.

Douglas J Rupert1, Rebecca R Moultrie2, Jennifer Gard Read2, Jacqueline B Amoozegar3, Alexandra S Bornkessel2, Amie C O'Donoghue4, Helen W Sullivan4.   

Abstract

OBJECTIVE: Many Internet users seek health information through online health communities (OHCs) and other social media. Yet few studies assess how individuals use peer-generated health information, and many healthcare providers (HCPs) believe OHCs interfere with patient-provider relationships. This study explored how individuals use OHC content in clinical discussions and how HCPs react to it.
METHODS: We conducted in-person and virtual focus groups with patients/caregivers who visited OHCs (n=89). A trained moderator asked about reasons for membership, sharing OHC content with providers, HCP reactions, and preferred roles for HCPs. Two researchers independently coded verbatim transcripts (NVivo 9.2) and conducted thematic response analysis.
RESULTS: Participants described OHCs as supplementing information from HCPs, whom they perceived as too busy for detailed discussions. Almost all participants shared OHC content with HCPs, although only half cited OHCs as the source. Most HCPs reacted negatively to OHC content, making participants feel disempowered. Despite these reactions, participants continued to use OHCs, and most desired HCP feedback on the accuracy of OHC content.
CONCLUSIONS: Individuals do not use OHCs to circumvent HCPs but instead to gather more in-depth information. PRACTICE IMPLICATIONS: HCPs should discuss OHC content with patients to help them avoid misinformation and make more informed decisions.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Online communities; Patient–provider communication; Shared decision making; Social media

Mesh:

Year:  2014        PMID: 24923652      PMCID: PMC7325560          DOI: 10.1016/j.pec.2014.05.015

Source DB:  PubMed          Journal:  Patient Educ Couns        ISSN: 0738-3991


  22 in total

1.  The patient-doctor relationship and online social networks: results of a national survey.

Authors:  Eric G Campbell; Karen Donelan; Catherine DesRoches; Anthony Roman; Dragana Bolcic-Jankovic
Journal:  J Gen Intern Med       Date:  2012-04       Impact factor: 5.128

2.  Health-related message boards/chat rooms on the Web: discussion content and implications for pharmaceutical sponsorships.

Authors:  Wendy Macias; Liza Stavchansky Lewis; Tenikka L Smith
Journal:  J Health Commun       Date:  2005 Apr-May

3.  Shared decision-making in the medical encounter: what does it mean? (or it takes at least two to tango).

Authors:  C Charles; A Gafni; T Whelan
Journal:  Soc Sci Med       Date:  1997-03       Impact factor: 4.634

4.  Apomediation and the significance of online social networking.

Authors:  Dan O'Connor
Journal:  Am J Bioeth       Date:  2009       Impact factor: 11.229

5.  Preliminary benefits of information therapy.

Authors:  Nikki Keene; Amy Chesser; Traci A Hart; Philip Twumasi-Ankrah; Douglas D Bradham
Journal:  J Prim Care Community Health       Date:  2011-01-01

6.  The patient-doctor relationship and online social networks: results of a national survey.

Authors:  Gabriel T Bosslet; Alexia M Torke; Susan E Hickman; Colin L Terry; Paul R Helft
Journal:  J Gen Intern Med       Date:  2011-06-25       Impact factor: 5.128

7.  Australian mental health consumers' priorities for research: qualitative findings from the SCOPE for Research project.

Authors:  Michelle A Banfield; Lisa J Barney; Kathleen M Griffiths; Helen M Christensen
Journal:  Health Expect       Date:  2012-01-04       Impact factor: 3.377

Review 8.  Shared decision making: examining key elements and barriers to adoption into routine clinical practice.

Authors:  France Légaré; Holly O Witteman
Journal:  Health Aff (Millwood)       Date:  2013-02       Impact factor: 6.301

9.  Experiences and attitudes of Dutch rheumatologists and oncologists with regard to their patients' health-related Internet use.

Authors:  Cornelia F van Uden-Kraan; Constance H C Drossaert; Erik Taal; Wim M Smit; Erwin R Seydel; Mart A F J van de Laar
Journal:  Clin Rheumatol       Date:  2010-04-11       Impact factor: 2.980

10.  Online focus groups as a tool to collect data in hard-to-include populations: examples from paediatric oncology.

Authors:  Kiek Tates; Marieke Zwaanswijk; Roel Otten; Sandra van Dulmen; Peter M Hoogerbrugge; Willem A Kamps; Jozien M Bensing
Journal:  BMC Med Res Methodol       Date:  2009-03-03       Impact factor: 4.615

View more
  23 in total

1.  Are We Ready to Treat Our Diabetes Patients Using Social Media? Yes, We Are.

Authors:  Goran Petrovski; Marija Zivkovic
Journal:  J Diabetes Sci Technol       Date:  2018-08-22

2.  Future Challenges and Opportunities in Online Prescription Drug Promotion Research Comment on "Trouble Spots in Online Direct-to-Consumer Prescription Drug Promotion: A Content Analysis of FDA Warning Letters".

Authors:  Brian G Southwell; Douglas J Rupert
Journal:  Int J Health Policy Manag       Date:  2016-01-16

3.  Online health information seeking, low atrial fibrillation-related quality of life, and high perceived efficacy in patient-physician interactions in older adults with atrial fibrillation.

Authors:  Jordy Mehawej; Ajay Mishra; Jane S Saczynski; Molly E Waring; Darleen Lessard; Hawa O Abu; Vincent La; Mayra Tisminetzky; Khanh-Van Tran; Essa Hariri; Andreas Filippaios; Tenes Paul; Apurv Soni; Weijia Wang; Eric Y Ding; Benita A Bamgbade; Joanne Mathew; Catarina Kiefe; Robert J Goldberg; David D McManus
Journal:  Cardiovasc Digit Health J       Date:  2022-03-11

4.  Online health information seeking by adults hospitalized for acute coronary syndromes: Who looks for information, and who discusses it with healthcare providers?

Authors:  Molly E Waring; David D McManus; Daniel J Amante; Chad E Darling; Catarina I Kiefe
Journal:  Patient Educ Couns       Date:  2018-06-30

5.  Patient and family social media use surrounding a novel treatment for a rare genetic disease: a qualitative interview study.

Authors:  Alexander A Iyer; Julie R Barzilay; Holly K Tabor
Journal:  Genet Med       Date:  2020-06-30       Impact factor: 8.822

6.  Virtual Versus In-Person Focus Groups: Comparison of Costs, Recruitment, and Participant Logistics.

Authors:  Douglas J Rupert; Jon A Poehlman; Jennifer J Hayes; Sarah E Ray; Rebecca R Moultrie
Journal:  J Med Internet Res       Date:  2017-03-22       Impact factor: 5.428

Review 7.  Patients' perceived needs of osteoarthritis health information: A systematic scoping review.

Authors:  Louisa Chou; Lisa Ellis; Michelle Papandony; K L Maheeka D Seneviwickrama; Flavia M Cicuttini; Kaye Sullivan; Andrew J Teichtahl; Yuanyuan Wang; Andrew M Briggs; Anita E Wluka
Journal:  PLoS One       Date:  2018-04-16       Impact factor: 3.240

Review 8.  Social media use in healthcare: A systematic review of effects on patients and on their relationship with healthcare professionals.

Authors:  Edin Smailhodzic; Wyanda Hooijsma; Albert Boonstra; David J Langley
Journal:  BMC Health Serv Res       Date:  2016-08-26       Impact factor: 2.655

9.  Impact of Social Processes in Online Health Communities on Patient Empowerment in Relationship With the Physician: Emergence of Functional and Dysfunctional Empowerment.

Authors:  Gregor Petrič; Sara Atanasova; Tanja Kamin
Journal:  J Med Internet Res       Date:  2017-03-13       Impact factor: 5.428

Review 10.  Analysis of Content Shared in Online Cancer Communities: Systematic Review.

Authors:  Mies C van Eenbergen; Lonneke V van de Poll-Franse; Emiel Krahmer; Suzan Verberne; Floortje Mols
Journal:  JMIR Cancer       Date:  2018-04-03
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.