The Needs of Caregivers for Persons with Parkinson’s Disease

Authors

  • Jidarat Hwanmeerot Faculty of Nursing, Chiang Mai University
  • Mayulee Somrarnyart Faculty of Nursing, Chiang Mai University
  • Chomphoonut Srirat Faculty of Nursing, Chiang Mai University

Keywords:

Caregivers’ needs, Caregivers of persons with Parkinson’s disease, Parkinson’s disease

Abstract

Parkinson’s disease is a chronic and incurable illness. The symptoms get worse throughout the duration of the disease. As a result, patients’ ability to take care of themselves decreases, and they require continuous assistance from their caregivers who, therefore, are important persons in caring for Parkinson’s disease patients. The purpose of this descriptive study was to explore the needs of caregivers of persons with Parkinson’s disease. The participants were caregivers of persons with Parkinson’s disease who were treated by neurologists from four hospitals. The 214 caregivers were purposively selected to be participants. Data collection instruments included: 1) a personal record form for caregivers, 2) a personal record form for persons with Parkinson’s disease, and 3) an interview form on caregivers’ needs. Data were analyzed using descriptive statistics.

          The results showed that:

  1. The overall needs of caregivers of persons with Parkinson’s disease were at a moderate level (= 2.13, S.D. = 0.91). For the specific aspects of caregiver needs, four aspects (information, physical, psychological, and legal and/or financial) were at a moderate level, and three aspects (spiritual, respite, and household management) were at a mild level. 
  2. The needs of caregivers were different related to the level of disease severity. Caregivers’ needs were at a mild level when disease severity was at level 1, and caregivers’ needs were a moderate level when disease severity was at level 2, 3, 4, and 5.
  3. The needs of caregivers were different relative to the personal characteristics of caregivers. The personal characteristics of caregivers which were related to different needs were: age, education, occupation, comorbidities, family income, relationship with patients, and duration of patient care.

          Nurses should plan and advise caregivers regarding information, physical, psychological, and legal and/or financial needs by considering disease severity and the personal characteristics of caregivers, to provide appropriate care relative to patients’ conditions and to meet the needs of caregivers, which will increase the efficiency of care.

References

Balzer-Geldsetzer, M., Ferreira, J., Odin, P., Bloem, B. R., Meissner, W. G., Lorenzl, S., … Schrag, A. (2018). Study protocol: Care of late-stage parkinsonism (CLaSP): A longitudinal cohort study. BMC Neurology, 18(1), 1-8.

Baudry, A. S., Anota, A., Bonnetain, F., Mariette, C., & Christophe, V. (2019). Psychometric validation of the French version of the supportive care needs survey for partners and caregivers of cancer patients. European Journal of Cancer Care, 28(1), 1-12.

Boonsin, S., & Panidchakul, K. (2016). Factors related to need of caregivers in stroke patients. Journal of Boromarajonani Collage of Nursing Bangkok, 32(2), 68-80. (in Thai)

Cui, J., Song, L. J., Zhou, L. J., Meng, H., & Zhao, J. J. (2014). Needs of family caregivers of advanced cancer patients: A survey in Shanghai of China. European Journal of Cancer Care, 23(4), 562-569.

Gadudom, P., Apinyalungkorn, K., Janjaroen, K., & Wae, N. (2018). Family roles to increase quality of life of older persons in a changing situation. The Southern College Network Journal of Nursing and Public Health, 5(3), 300-310. (in Thai)

Habermann, B., & Shin, J. Y. (2017). Preferences and concerns for care needs in advanced Parkinson’s disease: A qualitative study of couples. Journal of Clinical Nursing, 26(11-12), 1650-1656.

Hatano, T., Kubo, S. I., Shimo, Y., Nishioka, K., & Hattori, N. (2009). Unmet needs of patients with Parkinson’s disease: Interview survey of patients and caregivers. Journal of Internal Medical Research, 37(3), 717-726.

Hermanowicz, N., & Edwards, K. (2015). Parkinson's disease psychosis: Symptoms, management, and economic burden. The American Journal of Managed Care, 21(10), 199-206.

Hoehn, M. M., & Yahr, M. D. (1967). Parkinsonism: Onset, progression and mortality. Neurology, 17(5), 427-442.

Krejice, R. V., & Morgan, D. W. (1970). Determining sample size for research activities. Educational and Psychological Measurement, 30(3), 607-610.

Leiknes, I., Lien, U., & Severinsson, E. (2015). The relationship among caregiver burden, demographic variables, and the clinical characteristics of patients with Parkinson’s disease a systematic review of studies using various caregiver burden instruments. Open Journal of Nursing, 5(10), 855-877.

Phuaksawat, P., Nakkhun, N., & Rotchanarak, W. (2016). Situation, problems, and health care needs for home-bound and bed-bound chronically ill patients in Surat Thani municipal community. Nursing Journal of the Ministry of Public Health, 26(2), 54-64. (in Thai)

Puangkam, A., Suwansri, D., Yamsri, T., Saengrueang-eak, M., & Towannang, R. (2020). The impact of patient and caregivers: Relevant factors and needs of relatives who care for chronic end-stage illness at home. Medical Journal of Srisaket Surin Buriram Hospitals, 35(2), 303-316. (in Thai)

Shin, J., Ko, H., Lee, J. W., Kim, K., & Song, Y. M. (2019). Influence of time lapse after cancer diagnosis on the association between unmet needs and quality of life in family caregivers of Korean cancer patients. European Journal of Cancer Care, 28(5), 1-7.

Sihapark, S. (2014). The effects and caregiving burdens of older persons in long term care based on Thai culture. Khon Kaen: Boromarajonani College of Nursing, Khon Kaen. (in Thai)

Soleimani, M. A., Bastani, F., Negarandeh, R., & Greysen, R. (2016). Perceptions of people living with Parkinson's disease: A qualitative study in Iran. British Journal of Community Nursing, 21(4), 188-195.

Surakan, P., & Jongudomkan, D. (2019). The family caregiver’s role in providing care for chronically the ill family members: A synthesis of qualitative research theses. Journal of the Office of DPC 7 Khon Kaen, 26(2), 83-92. (in Thai)

Tandee, P., Somausorn, S., & Sumngern, C. (2016). Factor related to the need of elderly caregivers in caring for family members with cancer. Journal of Boromarajonani College of Nursing, Bangkok, 32(2), 48-55. (in Thai)

Tatangelo, G., McCabe, M., Macleod, A., & You, E. (2018). "I just don't focus on my needs." the unmet health needs of partner and offspring caregivers of people with dementia: A qualitative study. International Journal of Nursing Studies, 77(1), 8-14.

Wingate, L. A., & Lacky, R. N. (1989). A description of the needs of no institutionalized cancer patients and their primary caregiver. Cancer Nursing, 12(4), 216-225.

Downloads

Published

2022-06-30

How to Cite

Hwanmeerot, J., Somrarnyart, M., & Srirat, C. (2022). The Needs of Caregivers for Persons with Parkinson’s Disease. Nursing Journal CMU, 49(2), 326–339. Retrieved from https://he02.tci-thaijo.org/index.php/cmunursing/article/view/255781

Issue

Section

Research Article