Swipe om te navigeren naar een ander artikel
Our aim was to assess the perceived emotional burden and quality of life (QOL) in a sample of Greek primary caregivers of patients with multiple sclerosis (MS).
Twenty-two male and 13 female primary caregivers (mean age 47.3 ± 12.4 years), and an equal number of patients with MS, completed the Greek validated version of the hospital anxiety and depression scale (HADS) and the Greek validated version of EuroQOL (EQ-5D). Thirty-five age-, gender-, and education-matched healthy controls were used for comparison.
Caregivers experienced higher degree of anxiety than depression. The mean score of the HADS-A subscale was 9.5 ± 4 (range 3–15), and the mean score of the HADS-D subscale was 7.1 ± 3.1 (range 2–14). The mean scores of caregivers on both HADS-A and HADS-D were significantly higher than the controls’ (P < 0.0001). Twenty-two caregivers were diagnosed with manifesting anxiety, whereas 12 of them also presented depression. Highly educated caregivers were more prone to manifest increased levels of anxiety and depression. The increased psychological distress was further supported by the responses in the anxiety/depression dimension on the EQ-5D: 27 reported a moderate level of anxiety/depression and three indicated an extreme degree. The caregivers reported a mean EQ-VAS value of 61.9 ± 13.8 (range 40–100), with 10 caregivers rating their health status a score of 50 or lower; the controls scored significantly higher (90.3 ± 7.1; P < 0.0001).
The sample of caregivers we studied was psychologically burdened to a significant degree, a fact that obviously deteriorates their QOL. Appropriate psychopharmacological interventions are warranted to reduce caregivers’ burden.
Log in om toegang te krijgen
Met onderstaand(e) abonnement(en) heeft u direct toegang:
Morimoto, T., Schreiner, A. S., & Asano, H. (2003). Caregiver burden and health-related quality of life among Japanese stroke caregivers. Age Aging, 32(2), 218–223. CrossRef
Kurtzke, J. F. (1983). Rating neurologic impairment in multiple sclerosis: An expanded disability status scale (EDSS). Neurology, 33(11), 1444–1452. PubMed
Aronson, K. J. (1997). Quality of life among persons with multiple sclerosis and their caregivers. Neurology, 48, 74–80. PubMed
Figved, N., Myhr, K. M., Larsen, J. P., & Aarsland, D. (2007). Caregiver burden in multiple sclerosis: The impact of neuropsychiatric symptoms. Journal of Neurology, Neurosurgery and Psychiatry, 78(10), 1097–1102. CrossRef
Waldron-Perrine, B., Rapport, L. J., Ryan, K. A., & Harper, K. T. (2009). Predictors of life satisfaction among caregivers of individuals with multiple sclerosis. Clinical Neuropsychology, 23(3), 462–478. CrossRef
McMillan, S. C. (1996). Quality of life of primary caregivers of hospice patients with cancer. Cancer Practice, 4, 191–198. PubMed
- Quality of life and emotional burden of primary caregivers: a case–control study of multiple sclerosis patients in Greece
Andreas A. Argyriou
Amalia A. Ifanti
- Springer Netherlands