Cristin-resultat-ID: 1895797
Sist endret: 11. mai 2021, 13:24
NVI-rapporteringsår: 2021
Resultat
Vitenskapelig artikkel
2021

Participants’ views and experiences from setting up a shared patient portal for primary and specialist health services- a qualitative study

Bidragsytere:
  • Torunn Hatlen Nøst
  • Arild Faxvaag og
  • Aslak Steinsbekk

Tidsskrift

BMC Health Services Research
ISSN 1472-6963
e-ISSN 1472-6963
NVI-nivå 2

Om resultatet

Vitenskapelig artikkel
Publiseringsår: 2021
Publisert online: 2021
Volum: 21
Artikkelnummer: 171
Open Access

Importkilder

Scopus-ID: 2-s2.0-85101539409

Klassifisering

Vitenskapsdisipliner

Medisinske fag

Emneord

EHelse

Beskrivelse Beskrivelse

Tittel

Participants’ views and experiences from setting up a shared patient portal for primary and specialist health services- a qualitative study

Sammendrag

Background Recently, there has been an increasing focus among healthcare organisations on implementing patient portals. Previous studies have mainly focussed on the experiences of patient portal use. Few have investigated the processes of deciding what content and features to make available, in particular for shared portals across healthcare domains. The aim of the study was to investigate views on content and experiences from the configuration process among participants involved in setting up a shared patient portal for primary and specialist health services. Methods A qualitative study including 15 semi-structured interviews with persons participating in patient portal configuration was conducted from October 2019 to June 2020. Results Whether a shared patient portal for all the health services in the region should be established was not questioned by any of the informants. It was experienced as a good thing to have numerous participants present in the discussions on configuration, but it also was said to increase the complexity of the work. The informants considered a patient portal to be of great value for patient care, among other things because it would lead to improvements in patient follow-up and increased patient empowerment. Nevertheless, some informants advocated caution as they thought the patient portal possibly could lead to an increase in healthcare providers’ workloads and to anxiety and worries, as well as to inequality in access to health care among patients. The findings were categorized into the themes ‘A tool for increased patient involvement’, ‘Which information should be available for the patient’, ‘Concerns about increased workload’, ‘Too complex to use versus not interesting enough’, ‘Involving all services’ and ‘Patient involvement’. Conclusions Establishing a shared patient portal for primary and specialist health services was considered unproblematic. There was, however, variation in opinions on which content and features to include. This variation was related to concerns about increasing the workload for health care providers, causing anxiety and inequality among patients, and ensuring that the solution would be interesting enough to adopt.

Bidragsytere

Aktiv cristin-person

Torunn Hatlen Nøst

  • Tilknyttet:
    Forfatter
    ved Institutt for psykisk helse ved Norges teknisk-naturvitenskapelige universitet

Arild Faxvaag

  • Tilknyttet:
    Forfatter
    ved Institutt for nevromedisin og bevegelsesvitenskap ved Norges teknisk-naturvitenskapelige universitet
  • Tilknyttet:
    Forfatter
    ved Klinikk for ortopedi, revmatologi og hudsykdommer ved St. Olavs Hospital HF
Aktiv cristin-person

Aslak Irgens Steinsbekk

Bidragsyterens navn vises på dette resultatet som Aslak Steinsbekk
  • Tilknyttet:
    Forfatter
    ved Institutt for samfunnsmedisin og sykepleie ved Norges teknisk-naturvitenskapelige universitet
  • Tilknyttet:
    Forfatter
    ved Nasjonalt senter for e-helseforskning ved Universitetssykehuset Nord-Norge HF
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