PROJECTION: Worlds dementia population is expected to triple by 2050

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DEMENTIA C L I S K C O N S U LTA N T P H Y S I C I A N I N A C U T E M E D I C I N E A N D G E R I AT R I C M E D I C I N E, B A R N E T H O S P I TA L, R O YA L F R E E N H S F O U N D AT I O N T R U S T A N D H E R T F O R D S H I R E C O M M U N I T Y N H S T R U S T

MENU Epidemiology of dementia Continum of Alzheimers dementia AD Pathological features of AD Clinical features Differential diagnosis Investigations Cognitive testing Management including Resources available and update in the clinical use of established therapies The future perhaps: agents in development Biomarkers Prevention of AD; is this achievable or a pipedream?

Alzheimers dementia Neurodegenerative disorder marked by cognitive and behavioural impairment that significantly interferes with social and occupational functioning. Incurable with long preclinical period and progressive course

PROJECTION: Worlds dementia population is expected to triple by 2050

COSTS

AD PREVALENCE

THE CONTINUM OF AD

Risk factors for AD

AD overview

PATHOLOGICAL FEATURES OF AD

Plaque deposition and AD pathology

Clinical signs and symptoms MILD AD Memory loss Confusion about the location of familiar places Taking longer to accomplish normal daily tasks Trouble handling money and paying bills Compromised judgement often leading to bad decisions Loss of spontaneity and sense of initiative Mood and personality changes; increased anxiety MODERATE AD Increasing memory loss and confusion Shortened attention span Problems recognising friends and family members Difficulty with language; problems with reading, writing, working with numbers Difficulty organising thoughts and thinking logically Inability to learn new things or to cope with new unexpected situations Restlessness, agitation, anxiety, tearfulness, wandering Repetitive statements or movement; occasional muscle twitches, Hallucinations, delusions, suspiciousness or paranoia, irritability Loss of impulse control Perceptual motor problems such as trouble getting out of a chair or setting the table

Clinical signs and symptoms (severe) Cannot recognise family or loved ones Completely independent for all ADLS Vanishing sense of self Weight loss Seizures, skin infections, difficulty swallowing Groaning, moaning, grunting Increased sleeping Lack of bladder and bowel control Death usually from aspiration pneumonia frequently

Other signs and symptoms Language disorders; anosmic, aphasia or anomia Visuospatial and executive functions impairment Less commonly right parietal lobe syndrome, spastic paraparesis.

Distinguishing AD from MCI

Physical examination Complete physical examination Mental status examination Attention and concentration Recent and remote memory Language Praxis (ability to perform skilled motor task without nonverbal prompting) Executive function Visiospatial function

Assessing language

Declining ability to function

RACHEL.

Mood and emotional changes

WHAT TESTS WOULD YOU ORDER FOR RACHEL?

Determining the level of impairment

Cognitive impairment

Differential diagnosis

Differential diagnosis

Workup and what next..

Cognitive testing

AD 8

Biomarker testing

Neuroimaging in AD

Hippocampal volume assessment

MRI IMAGING

MRI

MANAGEMENT: CHOLINESTERASE INHIBITORS

FDA APPROVED DRUGS FOR AD

Cognitive benefit of donepezil

Cognitive benefit of donepezil

Cognitive benefit of donepezil

Rivastigmine

Cognitive effects of rivastigmine

Galantamine

Memantine

Side effects of cholinesterase inhibitors

Caide score for predicting risk of dementia

Antihypertensives and AD

OBSTACLES TO RECOGNISING DEMENTIA

DETECTING COGNITIVE IMPAIRMENT IN PRIMARY CARE

DETECTING COGNITIVE IMPAIRMENT IN PRIMARY CARE

Conclusions