None listed
Conditions
Brief summary
This research project aims to obtain information to better diagnose delirium, which commonly affects older adults. Delirium is often poorly diagnosed and result in many negative consequences for the affected person. This research project will aim to first determine how many people living in the three participating residential aged care facilities are diagnosed to suffer from delirium on one selected day. It will then examine some people with delirium more closely and compared them with people suffering with dementia but not delirium.
Interventions
This study aims to better understand cognitive fluctuation in older people living in residential age care and how it relates to diagnosis of delirium and dementia. The study will first estimate the prevalence of delirium in older adults in three rural residential care facilities (Study 1). It will then compare the occurrence and characteristics of cognitive fluctuations in people with delirium with people with dementia but no delirium (Study 2). Consent will be obtained for both Study 1 and Study 2 at the outset. Study 1 includes collection of data routinely collected by the residential aged facility for all older adults who have consented or for whom there is appropriate proxy consent. Following this, on a selected day 4AT will be administered. 4AT is an evidence-based bedside tool for rapid delirium screening that takes about 2 minutes to administer, Study 2 will prospectively identify participants who may have delirium from the group of participants who have previously consented or have proxy consent. Following screening with 4AT a participant with delirium and a participant with dementia but no delirium will be assessed for arousal levels using Modified Richmond Agitation Sedation Scale (mRASS) every hour. mRASS is an observational instrument derived from the Richmond Agitation Sedation Scale that measures the states of arousal, from unarousable (-5) to combative (+4). If arousal level allows for attention assessment, then participants' attention will be assessed hourly (where permitting) using DelApp. Hourly assessments will occur over two consecutive days from 9 am to 6 pm to minimise impact on sleep.
Sponsors
Eligibility
Inclusion criteria
1. Permanently placed older adults aged 65 years and over residing in one of the three residential aged care facilities of the study site.
Exclusion criteria
1. Coma 2. Unable to consent or no proxy consent available.