Next‐of‐kin’s conceptions of medical technology in palliative homecare

Berit Munck, Anna Sandgren, Bengt Fridlund and Jan Mårtensson

Journal of Clinical Nursing, 2012, vol. 21, issue 13-14, 1868-1877

Abstract: Aims and objectives. Describe next‐of‐kin’s conceptions of medical technology in palliative homecare. Background. Next‐of‐kin to palliative patients are in an exposed position with increasing responsibility. The more involved they are in the care, the greater caregiver burden they describe. Medical technology has become increasingly common in palliative homecare, and previous research suggests that the devices transform the homes to a hospital ward, thus shifting responsibility from the personnel to the next‐of‐kin. Design. An explorative descriptive design with a phenomenographic approach was chosen to describe qualitatively different conceptions of the phenomenon medical technology. Method. Interviews with 15 next‐of‐kin to patients in palliative homecare were analysed in a seven‐step process where 10 conceptions emerged in five description categories. Results. Medical technology in palliative homecare required next‐of‐kin’s responsibility in monitoring or providing practical help. It also implied uncertainty among the next‐of‐kin because of worries about its safety or because of an improper handling. The technology trespassed on daily life because it restricted and affected the private sphere. Medical technology enabled comfort as it implied security and was a prerequisite for the patient to be cared for at home. It also required an adjustment to comprehend and manage the medical technology. Conclusions. Medical technology resulted in an increased caregiver burden and uncertainty among the next‐of‐kin. Although it meant restrictions and affected their social life, they had great confidence in its possibilities. Relevance to clinical practice. It is important to limit the amount of personnel and materials in the home to avoid trespassing on the family’s daily life. Medical personnel also have to be sensitive to what next‐of‐kin have the strength to do and not use them as informal caregivers.

Date: 2012
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Persistent link: https://EconPapers.repec.org/RePEc:wly:jocnur:v:21:y:2012:i:13-14:p:1868-1877

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