Author:
Harrop Emily,Byrne Anthony,Nelson Annmarie
Abstract
Abstract
Background
Family carers play an essential role in providing end-of-life care to their relatives but have been found to experience uncertainty and a lack of confidence in fulfilling their caregiving roles, prompting recent calls for educational or information based resources to be developed for carers.
Methods
We carried out four focus groups with Clinical Nurse Specialists, healthcare assistants, former and current carers at a hospice in the UK, to explore the information and support needs of family carers.
Results
Our findings support previous research by highlighting a number of care situations where carers experience uncertainty and could seemingly benefit from greater information or instruction. Three main themes were identified which reflected carer experiences and needs in relation to potential information giving or educational interventions. These have been described as the knowledge and competence of carers; the preparedness of carers and low levels of carer identification with, and confidence in their roles as ‘carers’, which influences help seeking behaviours; and in turn how potential supportive interventions might be received by carers.
Conclusions
Family carers experience multiple needs for information and education, but meeting these needs remains a challenge. Our results suggest three domains which could underpin this type of intervention: developing knowledge and competence; facilitating preparedness; supporting role recognition and confidence building. We recommend an integrated information giving approach which addresses these domains by combining a resource pack for carers with a more explicit acknowledging role for health professionals. Together these could provide key information and also build confidence amongst family carers to ask for further support and advice as needed.
Publisher
Springer Science and Business Media LLC
Reference25 articles.
1. Bee PE, Barnes P, Luker KA: A systematic review of informal caregivers’ needs in providing home-based end-of-life care to people with cancer. J Clin Nurs. 2009, 18: 1379-1393. 10.1111/j.1365-2702.2008.02405.x.
2. Jansma FF, Schure LM, Meyboom de Jong B: Support requirements for caregivers of patients with palliative cancer. Patient Counsell Health Educ. 2004, 58: 182-186.
3. National Institute for Clinical Excellence: Improving supportive and palliative care for adults with cancer. 2004, London: National Institute for Clinical Excellence (NICE)
4. Harding R, Higginson I: Working with ambivalence: informal caregivers at the end of life. Support Care Canc. 2001, 9: 642-645. 10.1007/s005200100286.
5. Harding R, Leam C, Pearce A, Taylor E, Higginson IJ: A Multi-Professional short term group intervention for informal caregivers of patients using a home palliative care service. J Palliat Care. 2002, 18: 275-281.
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