Mild Cognitive Impairment in Parkinson's Disease: Impact on Caregiver Outcomes

作者：Szeto Jennifer Y Y; Mowszowski Loren; Gilat Moran; Walton Courtney C; Naismith Sharon L; Lewis Simon J G^*

来源：Journal of Parkinson's Disease, 2016, 6(3): 589-596.

DOI：10.3233/JPD-160823

• Mild cognitive impairment
• Parkinson's disease
• caregiver burden
• quality of life
• caregiver outcomes

Background: Recent attempts to standardise the definition of Mild Cognitive Impairment (MCI) in Parkinson's disease (PD) by the Movement Disorder Society Task Force has led to a greater understanding of this entity but to date, there has been a paucity of research regarding the impact of PD-MCI on caregiver outcomes.
Objective: The aim of this study was to utilise the newly established PD-MCI diagnostic criteria to investigate caregiver outcomes in relation to four specific aspects: (1) caregiver burden, (2) quality of life (QoL), (3) caregiving experience, and (4) psychological distress.
Methods: This study included a total of 166 patient-caregiver dyads. Caregiver outcomes including quality of life, caregiver burden, mood disturbances, and caregiver experience were compared between caregivers of PD patients classified as having normal cognition (PD-NC) and PD-MCI.
Results: Despite the two groups being matched on demographic and clinical features, caregivers of PD-MCI patients reported a lower level of QoL with regard to physical health and more interruptions with usual activities. On the other hand, a higher impact on finances was reported in caregivers of PD-NC patients, relative to caregivers of PD-MCI patients.
Conclusions: This study has shown that even at earlier stages of cognitive impairment, PD-MCI caregivers already experience elevated levels of distress in the role of providing care to their care-recipients. These findings highlight the need to include management of caregiver distress and associated sequelae alongside the management of PD-MCI patients, early on in the disease course.

• 出版日期2016