Journal of Movement Disorders (Sep 2017)

Patients and Their Caregivers’ Burdens for Parkinson’s Disease in Korea

  • Jong Sam Baik,
  • Joong-Seok Kim,
  • Seong-Beom Koh,
  • Jin Whan Cho,
  • Phil Hyu Lee,
  • Hyeo-Il Ma,
  • Yun Joong Kim,
  • Tae-Beom Ahn,
  • Sang Jin Kim,
  • Yong Duk Kim,
  • Seong-min Choi,
  • Ho-Won Lee,
  • Hee Tae Kim

DOI
https://doi.org/10.14802/jmd.17053
Journal volume & issue
Vol. 10, no. 3
pp. 109 – 115

Abstract

Read online

Objective Many patients with Parkinson’s disease (PD) suffer from motor and non-motor symptoms. According to these variable symptoms of PD, patients or caregivers have a poorer quality of life than patients with other neurodegenerative diseases. Since the difficulties are varied for all patients, prioritizing their difficulties differs among all cases. The goal of this study was to investigate the burdens of PD among the caregivers as well as patients and to identify areas requiring aid from the government. Methods We surveyed the awareness and perceptions of PD in patients and caregivers of PD by a face-to-face questionnaire. The questionnaire was divided into three sections: symptoms of PD (part A), desire for policies (part B), and difficulties faced by their caregivers (part C). Part A comprised 8 questions, Part B had 2 questions, and Part C had 3 questions. Results In total, 853 subjects (702 patients and 151 caregivers) were enrolled in this study. The major difficulties experienced by PD patients were physical (67%), psychiatric (60%) and socio-economic (52%). Assessing the physical difficulties, more than half the patients experienced severe difficulties (29% very severe, 39% severe). Psychiatric difficulties were assessed as severe (35%) and very severe (21%) among the patients. Severe difficulties were also experienced socio-economically, at 52% in patients and 49% in caregivers, especially among patients in their fifties (58%) and those with their spouse (65%) as caregivers. The topmost need was the introduction of new technology for treatment of PD (62%), followed by relief of costs for treatment (38%) and a family support system (31%). The majority (91%) of the patients were diagnosed with PD within two years after onset of symptoms. Conclusion We know that the difficulties of PD and the needs for government assistance are different between patients and caregivers. These results emphasize that perceiving the difficulties and needs of patients and caregivers early can help to prevent and ameliorate the burden of disease.

Keywords