Abstract
Introduction: This study examined the level of agreement between caregiver and Parkinson's disease (PD) patient reports of neuropsychiatric problems.
Method: Forty-three patients and 43 informants who knew the patient well (caregivers) participated in the study. Caregivers rated patients’ behaviour, as well as their own stress, using the Neuropsychiatric Inventory (NPI). Information from patients was obtained using commonly used scales (Beck Depression Inventory, Apathy Scale, Unified Parkinson's Disease Rating Scale and the Hamilton Anxiety Depression Scale). Both the patients and the caregivers also completed the Frontal Systems Behavior Scale, which assesses behaviours associated with apathy, disinhibition and executive dysfunction.
Results: The level of agreement between these self and caregiver reports was low, with only 45.8% agreement for depression, 45.0% for apathy, 28.6% for hallucinations, 26.9% for sleep problems and 6.7% for anxiety.
Conclusions: Given this low level of agreement between self and other report, these two methods of assessment cannot be considered interchangeable.
Acknowledgements
This project has been supported by grants from the Canterbury Medical Research Foundation. Audrey McKinlay was sponsored by a scholarship from the Foundation for Science Research and Technology and by a Claude McCarthy Fellowship.