There are many aspects of PD that can intensify the caregiver burden (e.g., impaired movement, sleep disorders, pain, cognitive impairment, etc.).1-4
Attentional deficits may have a negative impact on the ability of people with PD to perform basic everyday tasks, including physical and social activities.1 Consequently, caregivers may take on these responsibilities, further increasing the burden of care and reducing quality of life (which may already be considerably affected).1
Researchers are hoping to determine the effects of caring for a person with PD on the cognitive function of the caregiver, as well as the potential impact that any such impairment might have on both parties.1
References:
1.Lawson RA, Yarnall AJ, Johnston F, et al. Cognitive impairment in Parkinson’s disease: impact on quality of life of carers. Int J Geriatr Psychiatry 2017; 32 (12): 1362–1370.
2.Martinez-Martin P, Skorvanek M, Henriksen T, et al. Impact of advanced Parkinson’s disease on caregivers: an international real-world study. J Neurol 2023; 270 (4): 2162–2173.
3.Lim SY, Tan AH, Fox SH, et al. Integrating patient concerns into Parkinson’s disease management. Curr Neurol Neurosci Rep 2017; 17 (1): 3.
4.Martinez-Martin P, Rodriguez-Blazquez C, Forjaz MJ. Quality of life and burden in caregivers for patients with Parkinson’s disease: concepts, assessment and related factors. Expert Rev Pharmacoecon Outcomes Res 2012; 12 (2): 221–230.
