Literature DB >> 24646089

Personal health communities: a phenomenological study of a new health-care concept.

Johanna Wilhelmina Maria Aarts1, Femke Vennik2, Willianne L D M Nelen1, Martijn van der Eijk3, Bastiaan R Bloem3, Marjan J Faber4, Jan A M Kremer1.   

Abstract

CONTEXT: Fragmentation of care, complexity of diseases and the need to involve patients actively in their individual health care led to the development of the personal health community (PHC). In a PHC, patients can -regardless of the nature of their condition- invite all professionals that are involved in their health care process. Once gathered, the patient and health care team can exchange information about the patient's health and communicate through several functionalities, in a secured environment.
OBJECTIVES: Exploring the use, first experiences and potential consequences of using PHCs in health care.
DESIGN: Qualitative phenomenological study. PARTICIPANTS: Eighteen respondents, consisting of women experiencing infertility (n = 5), persons with Parkinson's disease (n = 6), a gynaecologist, a fertility doctor, a fertility nurse, three Parkinson's specialist nurses and a neurologist.
RESULTS: First experiences with PHCs showed that patients use their PHC differently, dependending on their condition and people involved. Various (potential) advantages for future health care were mentioned relating to both organizational aspects of care (e.g. continuity of care) and the human side of care (e.g. personal care). Patient involvement in care was facilitated. Disadvantages were the amount of work that it took and technological issues.
CONCLUSIONS: Using PHCs leads to promising improvements in both the organization of care and care experience, according to the participants in this study. They indicate that patients with different diseases and in different circumstances can benefit from these improvements. The PHC seem to be an online tool that can be applied in a personalized way. When (technically) well facilitated, it could stimulate active involvement of patients in their own health and health care. It warrants further research to study its effect on concrete health outcomes.
© 2014 John Wiley & Sons Ltd.

Entities:  

Keywords:  Internet; health reform; patient empowerment; patient participation; quality of care

Mesh:

Year:  2014        PMID: 24646089      PMCID: PMC5810707          DOI: 10.1111/hex.12177

Source DB:  PubMed          Journal:  Health Expect        ISSN: 1369-6513            Impact factor:   3.377


  34 in total

Review 1.  Qualitative research in health care. Analysing qualitative data.

Authors:  C Pope; S Ziebland; N Mays
Journal:  BMJ       Date:  2000-01-08

2.  The individual formerly known as patient, TIFKAP.

Authors:  J A M Kremer; M Van Der Eijk; J W M Aarts; B R Bloem
Journal:  Minerva Med       Date:  2011-12       Impact factor: 4.806

3.  Psychosocial burden of infertility and assisted reproduction.

Authors:  Lone Schmidt
Journal:  Lancet       Date:  2006-02-04       Impact factor: 79.321

4.  Electronic health records in the age of social networks and global telecommunications.

Authors:  Aviv Shachak; Alejandro R Jadad
Journal:  JAMA       Date:  2010-02-03       Impact factor: 56.272

Review 5.  The Parkinson's complex: parkinsonism is just the tip of the iceberg.

Authors:  J William Langston
Journal:  Ann Neurol       Date:  2006-04       Impact factor: 10.422

6.  Why does patient activation matter? An examination of the relationships between patient activation and health-related outcomes.

Authors:  Jessica Greene; Judith H Hibbard
Journal:  J Gen Intern Med       Date:  2012-05       Impact factor: 5.128

7.  Measuring patient-centredness, the neglected outcome in fertility care: a random multicentre validation study.

Authors:  Inge W H van Empel; Johanna W M Aarts; Ben J Cohlen; Dana A Huppelschoten; Joop S E Laven; Willianne L D M Nelen; Jan A M Kremer
Journal:  Hum Reprod       Date:  2010-08-18       Impact factor: 6.918

8.  Patients' attitudes to the summary care record and HealthSpace: qualitative study.

Authors:  Trisha Greenhalgh; Gary W Wood; Tanja Bratan; Katja Stramer; Susan Hinder
Journal:  BMJ       Date:  2008-05-29

9.  Implementation and adoption of nationwide electronic health records in secondary care in England: final qualitative results from prospective national evaluation in "early adopter" hospitals.

Authors:  Aziz Sheikh; Tony Cornford; Nicholas Barber; Anthony Avery; Amirhossein Takian; Valentina Lichtner; Dimitra Petrakaki; Sarah Crowe; Kate Marsden; Ann Robertson; Zoe Morrison; Ela Klecun; Robin Prescott; Casey Quinn; Yogini Jani; Maryam Ficociello; Katerina Voutsina; James Paton; Bernard Fernando; Ann Jacklin; Kathrin Cresswell
Journal:  BMJ       Date:  2011-10-17

10.  Introduction of shared electronic records: multi-site case study using diffusion of innovation theory.

Authors:  Trisha Greenhalgh; Katja Stramer; Tanja Bratan; Emma Byrne; Yara Mohammad; Jill Russell
Journal:  BMJ       Date:  2008-10-23
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  3 in total

1.  Improving maternity care using a personal health record: study protocol for a stepped-wedge, randomised, controlled trial.

Authors:  Carola J M Groenen; Marjan J Faber; Jan A M Kremer; Frank P H A Vandenbussche; Noortje T L van Duijnhoven
Journal:  Trials       Date:  2016-04-16       Impact factor: 2.279

2.  Do online communities change power processes in healthcare? Using case studies to examine the use of online health communities by patients with Parkinson's disease.

Authors:  Laura M Visser; Inge L Bleijenbergh; Yvonne W M Benschop; Allard C R Van Riel; Bastiaan R Bloem
Journal:  BMJ Open       Date:  2016-11-07       Impact factor: 2.692

Review 3.  A Viewpoint on Wearable Technology-Enabled Measurement of Wellbeing and Health-Related Quality of Life in Parkinson's Disease.

Authors:  Janet M T van Uem; Tom Isaacs; Alan Lewin; Eros Bresolin; Dina Salkovic; Alberto J Espay; Helen Matthews; Walter Maetzler
Journal:  J Parkinsons Dis       Date:  2016-03-10       Impact factor: 5.568

  3 in total

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