Factors related to feelings of burden among caregivers looking after impaired elderly in Japan under the Long-Term Care insurance system
Autor: | Hiroko Miura, Teruko Ueda, Masakazu Washio, Keigo Kumamoto, Yumiko Arai, Kei Kudo |
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Rok vydání: | 2004 |
Předmět: |
Adult
Male Gerontology medicine.medical_specialty Activities of daily living National Health Programs Frail Elderly media_common.quotation_subject Behavioral Symptoms Insurance Long-Term Care Cost of Illness Japan Alzheimer Disease Respite care Activities of Daily Living Humans Medicine Dementia Long-term care insurance Psychiatry Aged media_common Aged 80 and over business.industry General Neuroscience General Medicine Caregiver burden Middle Aged Community Health Nursing medicine.disease Psychiatry and Mental health Long-term care Cross-Sectional Studies Mood Caregivers Neurology Feeling Female Neurology (clinical) Respite Care business |
Zdroj: | Psychiatry and Clinical Neurosciences. 58:396-402 |
ISSN: | 1440-1819 1323-1316 |
DOI: | 10.1111/j.1440-1819.2004.01274.x |
Popis: | Since the 1970s, the burden of caregiving has been the subject of rather intense study, a trend that will continue with the rapid graying of populations worldwide. Since the Long-Term Care insurance system began in 2000, few cross-sectional studies have attempted to identify factors related to the feelings of burden among caregivers looking after the impaired elderly in Japan. In the present report, among 46 pairs of caregivers and impaired elderly, the elderly receiving regular nurses' visits in Kyoto Prefecture, Japan were assessed for problems with activities of daily living, the severity of dementia, the presence of behavioral disturbance, and cognitive impairment. The caregivers were asked to complete questionnaires in relation to their feelings of burden and caregiving situation. The results indicated that caregivers of impaired elderly with behavioral disturbances were more likely to feel a 'heavier burden.' Those temporarily relieved of caregiving three or more hours a day were less likely to experience 'heavier' caregiver burden than those who were not. Moreover, caregivers who found it 'inconvenient' to use care services tended to be more likely to feel a 'heavier' caregiver burden than those who did not. Recourse to respite services, which are ideally positioned to help, proved inconvenient because of their advance reservation system. More ready access to respite services in emergencies could do much to reduce caregiver burden. |
Databáze: | OpenAIRE |
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