hh.sePublikasjoner
Endre søk
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf
The desire for involvement in healthcare, anxiety and coping in patients and their partners after a myocardial infarction
Centre of Health Care Sciences Orebro University Hospital, Örebro and School of Health and Medical Sciences, Örebro University, Sweden.
Department of Cardiothoracic Surgery, Skåne University Hospital and Lund University, Sweden.
The Faculty of Health and Society, Malmö University, Sweden.
Högskolan i Halmstad, Akademin för hälsa och välfärd, Centrum för forskning om välfärd, hälsa och idrott (CVHI).ORCID-id: 0000-0003-4438-6673
2013 (engelsk)Inngår i: European Journal of Cardiovascular Nursing, ISSN 1474-5151, E-ISSN 1873-1953, Vol. 12, nr 5, s. 461-467Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Background: There is a lack of data about the information preferences of patients and their partners after a myocardial infarction. Aim: This paper explores anxiety, depression, coping and the desire to be actively involved in care in relation to age, gender and education level in myocardial infarction patients and partners. Methods: One hundred and twenty-eight patients and their partners answered the Swedish version of the Krantz Health Opinion Survey, the Hospital Anxiety and Depression Scale, and the Mastery Scale one year after the patient’s myocardial infarction. Results: More active roles in decision-making during care were desired by females, younger patients and partners, and patients and partners with higher education levels. Female partners reported more anxiety than male partners, and female patients reported more depression than male patients. No differences between groups were detected in coping; overall coping was rated high. Conclusions: Secondary prevention should consist of person-centred support to both the patients and their partners, since factors such as age, gender and education level can influence information preferences during patient care. © The European Society of Cardiology 2012.

sted, utgiver, år, opplag, sider
London: Sage Publications, 2013. Vol. 12, nr 5, s. 461-467
Emneord [en]
Myocardial infarction, information, Krantz Health Opinion Survey, anxiety, depression, gender, age, education level, coping, patient, partner
HSV kategori
Identifikatorer
URN: urn:nbn:se:hh:diva-20084DOI: 10.1177/1474515112472269ISI: 000324756300007PubMedID: 23303764Scopus ID: 2-s2.0-84884692290OAI: oai:DiVA.org:hh-20084DiVA, id: diva2:575606
Tilgjengelig fra: 2012-12-10 Laget: 2012-12-10 Sist oppdatert: 2018-01-12bibliografisk kontrollert

Open Access i DiVA

Fulltekst mangler i DiVA

Andre lenker

Forlagets fulltekstPubMedScopus

Personposter BETA

Svedberg, Petra

Søk i DiVA

Av forfatter/redaktør
Svedberg, Petra
Av organisasjonen
I samme tidsskrift
European Journal of Cardiovascular Nursing

Søk utenfor DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric

doi
pubmed
urn-nbn
Totalt: 132 treff
RefereraExporteraLink to record
Permanent link

Direct link
Referera
Referensformat
  • apa
  • harvard1
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Annet format
Fler format
Språk
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Annet språk
Fler språk
Utmatningsformat
  • html
  • text
  • asciidoc
  • rtf