Abstract

Background: Behavioral and psychological symptoms of dementia (BPSD, also known as neuropsychiatric symptoms (NPS), changed behaviors and responsive behaviors), occur in up to 90 percent of people living with dementia (PLWD). These symptoms and behaviors strongly correlate with functional and cognitive impairment and contribute to ~30% of overall dementia costs. As decisions regarding care and strategies for BPSD are generally based on professional frames of reference, this study investigates whether the perspectives of PLWD and families/care partner on BPSD terminology can inform a more nuanced conceptualization of BPSD.Methods: PLWD and families/care partners participated in one-on-one semi-structured interviews. A thematic iterative approach was used to code the data and identify common themes until theoretical saturation was reached. Themes were compared between groups. Data were analyzed deductively in relation to pre-existing terminology regarding BPSD, and inductively to discover new ideas on use of such terminology as perceived by PLWD and others.Results: Forty-one volunteers were interviewed: 21 PLWD, mean age 71 yrs, mean Mini-Mental State Examination score 25, and 20 family members/care partners. Three main themes emerged from the data: (1) descriptions of BPSD from people with lived experience compared to clinical terms, (2) viewpoints on interpreting causes, and (3) experiences of concurrent BPSD. The experiences described and terms used by PLWD and families/care partners differed from terms used in existing professional frameworks (e.g., “disinhibition” described as ‘loss of filter') and there were differences between PLWD and family members' interpretations of BPSD causes.Discussion/Conclusion: Reports from PLWD and families/carers describing their experiences of BPSD suggest a reconceptualization of BPSD terminology is needed to understand and de-stigmatize these symptoms and behaviors. For example, the term “agitated/hard to handle” would benefit by clearer, contextualized description, such as “frustrated with cognitive decline, discriminatory behavior and inadequate support systems.” In better understanding individual expressions of BPSD, families, professionals and societies will be able to respond in ways that are helpful for PLWD. An informed, integrated understanding of BPSD and improved terminology use will have the potential to improve the quality of care and support for PLWD.

Highlights

  • Behavioral and psychological symptoms of dementia (BPSD; known as neuropsychiatric symptoms (NPS), changed behaviors and responsive behaviors) are estimated to affect approximately 90 percent of people living with dementia (PLWD)

  • “BPSD”: PLWD and Carer Perspectives complementary approach to data analysis supported our research aims by allowing existing BPSD terminology to be integral to the process of deductive thematic analysis, while allowing for themes to emerge directly from the data using inductive coding

  • this grief. (The) results reported in this article include responses from questions related to specific experiences of BPSD and any other changes in behavior participants experienced or observed (see Supplementary Material 2, responses to part (a) of all numbered questions are presented here)

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Summary

Introduction

Behavioral and psychological symptoms of dementia (BPSD; known as neuropsychiatric symptoms (NPS), changed behaviors and responsive behaviors) are estimated to affect approximately 90 percent of people living with dementia (PLWD). BPSD terminology includes aggression, agitation, anxiety, apathy, depression, disinhibited behaviors, nocturnal disruption, psychotic symptoms, vocally disruptive behaviors and wandering (2) These symptoms and behaviors can cause distress for PLWD (3, 4), families and/or care partners (5) and care staff (6), and they impose a financial burden on society in relation to the cost of informal and formal support services, contributing approximately 30 percent of overall costs (7–9). Behavioral and psychological symptoms of dementia (BPSD, known as neuropsychiatric symptoms (NPS), changed behaviors and responsive behaviors), occur in up to 90 percent of people living with dementia (PLWD). These symptoms and behaviors strongly correlate with functional and cognitive impairment and contribute to ∼30% of overall dementia costs. As decisions regarding care and strategies for BPSD are generally based on professional frames of reference, this study investigates whether the perspectives of PLWD and families/care partner on BPSD terminology can inform a more nuanced conceptualization of BPSD

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