Your browser doesn't support javascript.
loading
The Danish landscape of providing support for caregivers of people with potentially life-threatening disease: A cross-sectional study among representatives of health services in Danish municipalities and hospitals.
Dieperink, Karin B; Møller, Jens-Jakob K; Mikkelsen, Tina B; Nissen, Nina Konstantin; La Cour, Karen; Rottmann, Nina.
Affiliation
  • Dieperink KB; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
  • Møller JK; Department of Oncology, Odense University Hospital, Denmark.
  • Mikkelsen TB; Family focused healthcare Research (FaCe), University of Southern Denmark, Nyborg, Denmark.
  • Nissen NK; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
  • La Cour K; REHPA, The Danish Knowledge Centre for Rehabilitation and Palliative Care, Odense University Hospital, Nyborg, Denmark.
  • Rottmann N; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
Scand J Public Health ; : 14034948231159464, 2023 Apr 06.
Article in En | MEDLINE | ID: mdl-37026179
ABSTRACT

AIMS:

(a) To investigate support for caregivers of people diagnosed with stroke, cancer, chronic obstructive pulmonary disease (COPD), dementia, or heart disease provided across healthcare settings in Denmark; (b) to assess differences in caregiver support across diagnoses and settings.

METHODS:

A cross-sectional nationwide survey among professionals representing healthcare settings at municipalities (n = 479) and hospital wards and outpatient clinics (n = 425). The survey assessed identification of caregivers and support initiatives.

RESULTS:

The response rate was 81% for municipalities and 49% for hospitals. Identification of caregivers was frequent in dementia care (81% and 100%) and less frequent in COPD care (58% and 64%) in municipalities and hospitals, respectively. Caregiver support differed significantly across diagnoses within municipalities (p = 0.009) and hospitals (p < 0.001). Systematic identification of vulnerable caregivers was <25% for all diagnoses except dementia. The most common support initiatives involving caregivers were primarily aimed at the ill person and included guidance about the disease and consequences for everyday life and lifestyle changes. Caregivers were least involved in support initiatives addressing physical training, work retention, sexuality, or cohabitation.

CONCLUSIONS:

Disparities and significant differences across diagnoses exist in the identification of caregivers and the provision of support initiatives. Support initiatives involving caregivers primarily targeted patients. Future studies should investigate how caregivers' needs can be met across different diagnoses and healthcare settings and investigate potential changes in caregivers' needs during disease trajectories. In clinical practice, identification of vulnerable caregivers should be a major focus, and disease-specific clinical guidelines may be required to ensure sufficient support for caregivers.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Guideline / Observational_studies / Prevalence_studies / Qualitative_research Language: En Journal: Scand J Public Health Journal subject: MEDICINA SOCIAL / SAUDE PUBLICA Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Guideline / Observational_studies / Prevalence_studies / Qualitative_research Language: En Journal: Scand J Public Health Journal subject: MEDICINA SOCIAL / SAUDE PUBLICA Year: 2023 Document type: Article Affiliation country: