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Dementia
IS NOT a
specific
disease.

Dementia is a
GROUP OF SYMPTOMS
affecting intellectual and
social abilities severely
enough to interfere with
daily functioning.

Memory loss generally
occurs in dementia, but
memory loss alone
does not imply you
have dementia.

DEMENTIA

Alzheimer's disease is
the most common
cause of a progressive
dementia.

There are many
causes of dementia
symptoms.
PROGRESSSIVE BRAIN
DETERIORATION

Dementia

Normal
Aging

Mild
Cognitive
Decline
(MCD)
Normal
cognitive decline
associated with
age:
*Structural
changes –size,
weight and
neurons
*Varying
degrees of
cortical atrophy
*Memory and
speed of
processing
decline

Normal
Cognitive
Decline

Dementia
Mild
Cognitive
Decline
(MCD)
Transitional Phase-increased
probability of developing dementia
AGE-INCREASES PROBABILITY!
Amnestic type: memory impairment
(without the generalized deficits)
Non-amnestic: other domain is
affected

Dementia

Normal
Aging

Mild
Cognitive
Decline
(MCD)
Dementia

Normal
Cognitive
Decline

Mild
Cognitive
Decline
(MCD)

Behavioural Syndrome
with cognitive and
emotional symptoms
that affect everyday
life.
Memory impairment +
Other cognitive
impairments
More than 50 known
causes
Generally Progressive
Develops due to brain disease
Chronic and progressive in nature
Consciousness remaining intact
Deterioration of higher order cognitive functioning
Disturbances in social behaviour, emotional control and
motivation
The essential feature of any dementia is the development of multiple cognitive deficits that
include:
• memory impairment
and at least one of the following cognitive disturbances:

•
•
•
•

aphasia (language disturbance),
apraxia (impaired ability to carry out motor activities despite intact motor function),
agnosia (failure to recognize or identify objects despite intact sensory function), and
executive dysfunction (difficulty in planning, organizing, sequencing, abstracting).

The deficits must also be sufficiently severe and must represent a decline from a previously higher level of
functioning.
The diagnosis of dementia may be accompanied by subtypes and specifiers such as
• Early (before the age of 65) or Late Onset (after 65)
• With Behavioral Disturbance (e.g., wandering, striking out during care);
• With Delirium (if delirium is superimposed on dementia);
• With Delusions (if delusions are most prominent feature);
• With Depressed Mood (if depressed mood is most prominent feature); and
• Uncomplicated (if none of the aforementioned predominates the clinical presentation).
Changes in
mood and
personality

Withdrawal
from work or
social activities

Decreased or
poor judgment

Memory loss
that disrupts
daily
functioning

Challenges in
planning or
solving
problems

WARNING
SIGNS

Misplacing
things and
losing the
ability to
retrace steps

New problems
with words in
speaking or
writing

Difficulty
completing
familiar tasks
at home, at
work or at
leisure

Confusion with
time or place

Trouble
understanding
visual images
and spatial
relationships
CLINICAL DEMENTIA RATING SCALE
NONE
(O)

QUESTIONNABLE (0.5)

MILD
(1)

MODERATE (2)

SEVERE (3)

MEMORY

OK

CONSISTENT
FORGETFULNES
S

MEMORY LOSS
FOR RECENT
EVENTS

ONLY HIGH
LEARNING
MATERIAL
RETAINED

ONLY
FRAGMENTS
REMAIN

ORIENTATI-ON

FULLY

DIFFICULTY
WITH TIME

GEOGRAPHIC

TIME AND
PLACE

ONLY PERSON

JUDGEME-NT
AND PROBLEM
SOLVING

GOOD

SLIGHT
IMPAIRMENT

SOCIAL
JUDGMENT
OK,
DIFFICULTIES
WITH
SIMILARITIES
AND
DIFFERENCES

ISSUES WITH
SOCIAL
JUDGEMENT
SEVERELY
IMPAIRED
PROBLEM
SOLVING

UNABLE TO
MAKE
JUDGEMENTS
NONE
0

QUESTIONABLE
0.5

MILD
1

MODERA-TE
2

SEVERE
3

COMMUNITY
AFFAIRS

Independent to
work, shop
and have
social life

Slight
impairment

Unable to be
independent
but still
engaged

Well at home
but not outside

No
responsibilities
in or out the
home

HOME &
HOBBIES

Maintained

Slight
impairment

Complicated
hobbies or
chores
abandoned

Only simple
chores
maintained.
Low interest

No function

PERSONAL
CARE

Fully capable

Fully capable

Needs
prompting

Need
assistance

Help with
personal care
& incontinence
CORTICAL
• ALZHEIMER’S DISEASE
• Genetic hypothesis: chromosomes 1, 14, 21
• Neuropathology: cortical atrophy, amyloid plaques and
neurofibrillary tangles
• General cognitive decline with severe memory impairment

SUBCORTICAL
• Huntington’s Disease
• Genetic: ITI5 on chromosome 4. Abnormal repetitions
• Neuropathology: deterioration of the caudate nucleus, globus
pallidus, putamen and striatum
• Motor functioning and frontal functioning affected
Neurofibrillary
&
Tangles
AMYLOID
PLAQUES
NEUROANATOMY OF ALZHEIMER’S
DISEASE…
NEUROANATOMY OF HUNTINGTON’S
DISEASE…
STATIC
• Heavy Metal Poisoning
• The whole system is affected, including the brain
• Cognitive decline and behavioural changes that can be stopped
by ending the exposure or with detox treatment

PROGRESSIVE
•
•
•
•

Vascular Dementia
Blood supply is affected (multi-infarcts)
Damage to multiple areas of the brain
Cognitive decline + hallucinations/delusions , personality
changes
REVERSIBLE
•
•
•
•

Severe Anemia
Memory loss (holes).
Cognitive decline similar to AD
Lack of vitamin B12 that can be reverted with treatment

IRREVERSIBLE
• Parkinson’s Dementia
• Motor symptoms of tremor, rigidity, and slowness of
movement.
• Loss of dopamine from the substantia nigra
personality
/ mood

behavior

navigation

memory

language

thought
PSYCHOLOGICAL AND BEHAVIOURAL DISTURBANCES

Depression
• Reaction to early cognitive
decline
• Less prevalent in severe
dementia due to impaired
awareness
• Vascular dementia more
susceptible
• Early Onset-Dementia as a
predictor of severity

Psychotic

Disturbances
• Approximately 50% will
display disturbances
• DELUSIONS- 1/3 will display
persecutory delusions not
attributed to memory
impairment
• Moderate Level
• HALLUCINATIONS- less
frequent
• More significant relationship
with cognitive decline
• Associated with a rapid
decline at a more severe
stage

Behavioural
Problems
• Agitation, irritability,
fatigue, tiredness, apathy,
psychomotor behaviours,
anxiety and sadness.
• AD patients with co-morbid
psychotic symptoms more
likely to display severe
aggression and behaviour
problems
• Pre-morbid communication
emulated
• RISK FACTORS:
• Genetics, personality
variables, location of
deterioration
• Social implications on self
and caregiver
Shultz (2004) defines the role of
caregiving as:
“… the provision of extraordinary care,
exceeding the bounds
of what is normative or usual in family
relationships. Caregiving
typically involves a significant
expenditure of time, energy, and
money over potentially long periods of
time; it involves tasks that
may be unpleasant and uncomfortable
and are psychologically
stressful and physically exhausting”

(259).
“Stigma is an attribute, behaviour, or reputation which is socially
discrediting in a particular way: it causes an individual to be
mentally classified by others in an undesirable, rejected
stereotype rather than in an accepted , normal one” (Goffman,
1963, as cited in Batsch, & Mittelman, 2012).
CAREGIVER &
PATIENT
COUNSELLING FOR
ACCEPTANCE

COMBATING
STIGMA
INVOLVE MEDIA,
GOVERNMENT,O
THER
STRUCTURAL
SERVICES

RAISE AWARENESS
–CAMPAIGNS,
EDUCATIONAL
PROGRAMS
-2011, 5.5 million
individuals living
with HIV in S.A

Challenges when
screening for
HAD:language, culture,
inadequate resources.,
inappropriate tools,
untrained staff.

Risk Factors: lower CD4
count, older age, lower
levels of education,
depression, substance
abuse .
Prevalence: 25.4% of
adults living with HIV met
the criteria for HAD.

-International HIV

Dementia Scale
(IHDS)

Consequences: In
addition to HIV,
cognitive
impairments such as
poor concentration,
attention and
executive functioning

Sample of 65 nonadherent HIV
patients
8O% screened
positive for HAD
FREQUENTLY
ENGAGE IN
MENTALLY
STIMULATING
ACTIVITIES

REGULAR
PHYSICAL
ACTIVITY

NUTRITION
AL DIETS,
MODERATELOW
ALCOHOL
INTAKE

ENGAGE IN
SOCIAL
ACTIVITIES

TAKING
CARE OF
MENTAL
HEALTH
• Nerve growth factor (NGF)
• No fewer than 10 drugs
• Cognitive training
• Reality orientation
• Reminiscence therapy
• Cognitive rehabilitation

• Psychodynamic Therapy
• Support groups

•Public education
•Training professionals
•Developing programs
•Integrating services
SHAAKERA SUBJEE AND SHAREEKA  ANGAMIA-DEMENTIA PRESENTATION
SHAAKERA SUBJEE AND SHAREEKA  ANGAMIA-DEMENTIA PRESENTATION
SHAAKERA SUBJEE AND SHAREEKA  ANGAMIA-DEMENTIA PRESENTATION
SHAAKERA SUBJEE AND SHAREEKA  ANGAMIA-DEMENTIA PRESENTATION

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SHAAKERA SUBJEE AND SHAREEKA ANGAMIA-DEMENTIA PRESENTATION

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  • 6. Dementia IS NOT a specific disease. Dementia is a GROUP OF SYMPTOMS affecting intellectual and social abilities severely enough to interfere with daily functioning. Memory loss generally occurs in dementia, but memory loss alone does not imply you have dementia. DEMENTIA Alzheimer's disease is the most common cause of a progressive dementia. There are many causes of dementia symptoms.
  • 8. Normal cognitive decline associated with age: *Structural changes –size, weight and neurons *Varying degrees of cortical atrophy *Memory and speed of processing decline Normal Cognitive Decline Dementia Mild Cognitive Decline (MCD)
  • 9. Transitional Phase-increased probability of developing dementia AGE-INCREASES PROBABILITY! Amnestic type: memory impairment (without the generalized deficits) Non-amnestic: other domain is affected Dementia Normal Aging Mild Cognitive Decline (MCD)
  • 10. Dementia Normal Cognitive Decline Mild Cognitive Decline (MCD) Behavioural Syndrome with cognitive and emotional symptoms that affect everyday life. Memory impairment + Other cognitive impairments More than 50 known causes Generally Progressive
  • 11. Develops due to brain disease Chronic and progressive in nature Consciousness remaining intact Deterioration of higher order cognitive functioning Disturbances in social behaviour, emotional control and motivation
  • 12. The essential feature of any dementia is the development of multiple cognitive deficits that include: • memory impairment and at least one of the following cognitive disturbances: • • • • aphasia (language disturbance), apraxia (impaired ability to carry out motor activities despite intact motor function), agnosia (failure to recognize or identify objects despite intact sensory function), and executive dysfunction (difficulty in planning, organizing, sequencing, abstracting). The deficits must also be sufficiently severe and must represent a decline from a previously higher level of functioning. The diagnosis of dementia may be accompanied by subtypes and specifiers such as • Early (before the age of 65) or Late Onset (after 65) • With Behavioral Disturbance (e.g., wandering, striking out during care); • With Delirium (if delirium is superimposed on dementia); • With Delusions (if delusions are most prominent feature); • With Depressed Mood (if depressed mood is most prominent feature); and • Uncomplicated (if none of the aforementioned predominates the clinical presentation).
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  • 15. Changes in mood and personality Withdrawal from work or social activities Decreased or poor judgment Memory loss that disrupts daily functioning Challenges in planning or solving problems WARNING SIGNS Misplacing things and losing the ability to retrace steps New problems with words in speaking or writing Difficulty completing familiar tasks at home, at work or at leisure Confusion with time or place Trouble understanding visual images and spatial relationships
  • 16. CLINICAL DEMENTIA RATING SCALE NONE (O) QUESTIONNABLE (0.5) MILD (1) MODERATE (2) SEVERE (3) MEMORY OK CONSISTENT FORGETFULNES S MEMORY LOSS FOR RECENT EVENTS ONLY HIGH LEARNING MATERIAL RETAINED ONLY FRAGMENTS REMAIN ORIENTATI-ON FULLY DIFFICULTY WITH TIME GEOGRAPHIC TIME AND PLACE ONLY PERSON JUDGEME-NT AND PROBLEM SOLVING GOOD SLIGHT IMPAIRMENT SOCIAL JUDGMENT OK, DIFFICULTIES WITH SIMILARITIES AND DIFFERENCES ISSUES WITH SOCIAL JUDGEMENT SEVERELY IMPAIRED PROBLEM SOLVING UNABLE TO MAKE JUDGEMENTS
  • 17. NONE 0 QUESTIONABLE 0.5 MILD 1 MODERA-TE 2 SEVERE 3 COMMUNITY AFFAIRS Independent to work, shop and have social life Slight impairment Unable to be independent but still engaged Well at home but not outside No responsibilities in or out the home HOME & HOBBIES Maintained Slight impairment Complicated hobbies or chores abandoned Only simple chores maintained. Low interest No function PERSONAL CARE Fully capable Fully capable Needs prompting Need assistance Help with personal care & incontinence
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  • 19. CORTICAL • ALZHEIMER’S DISEASE • Genetic hypothesis: chromosomes 1, 14, 21 • Neuropathology: cortical atrophy, amyloid plaques and neurofibrillary tangles • General cognitive decline with severe memory impairment SUBCORTICAL • Huntington’s Disease • Genetic: ITI5 on chromosome 4. Abnormal repetitions • Neuropathology: deterioration of the caudate nucleus, globus pallidus, putamen and striatum • Motor functioning and frontal functioning affected
  • 23. STATIC • Heavy Metal Poisoning • The whole system is affected, including the brain • Cognitive decline and behavioural changes that can be stopped by ending the exposure or with detox treatment PROGRESSIVE • • • • Vascular Dementia Blood supply is affected (multi-infarcts) Damage to multiple areas of the brain Cognitive decline + hallucinations/delusions , personality changes
  • 24. REVERSIBLE • • • • Severe Anemia Memory loss (holes). Cognitive decline similar to AD Lack of vitamin B12 that can be reverted with treatment IRREVERSIBLE • Parkinson’s Dementia • Motor symptoms of tremor, rigidity, and slowness of movement. • Loss of dopamine from the substantia nigra
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  • 27. PSYCHOLOGICAL AND BEHAVIOURAL DISTURBANCES Depression • Reaction to early cognitive decline • Less prevalent in severe dementia due to impaired awareness • Vascular dementia more susceptible • Early Onset-Dementia as a predictor of severity Psychotic Disturbances • Approximately 50% will display disturbances • DELUSIONS- 1/3 will display persecutory delusions not attributed to memory impairment • Moderate Level • HALLUCINATIONS- less frequent • More significant relationship with cognitive decline • Associated with a rapid decline at a more severe stage Behavioural Problems • Agitation, irritability, fatigue, tiredness, apathy, psychomotor behaviours, anxiety and sadness. • AD patients with co-morbid psychotic symptoms more likely to display severe aggression and behaviour problems • Pre-morbid communication emulated • RISK FACTORS: • Genetics, personality variables, location of deterioration • Social implications on self and caregiver
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  • 32. Shultz (2004) defines the role of caregiving as: “… the provision of extraordinary care, exceeding the bounds of what is normative or usual in family relationships. Caregiving typically involves a significant expenditure of time, energy, and money over potentially long periods of time; it involves tasks that may be unpleasant and uncomfortable and are psychologically stressful and physically exhausting” (259).
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  • 38. “Stigma is an attribute, behaviour, or reputation which is socially discrediting in a particular way: it causes an individual to be mentally classified by others in an undesirable, rejected stereotype rather than in an accepted , normal one” (Goffman, 1963, as cited in Batsch, & Mittelman, 2012).
  • 39. CAREGIVER & PATIENT COUNSELLING FOR ACCEPTANCE COMBATING STIGMA INVOLVE MEDIA, GOVERNMENT,O THER STRUCTURAL SERVICES RAISE AWARENESS –CAMPAIGNS, EDUCATIONAL PROGRAMS
  • 40.
  • 41. -2011, 5.5 million individuals living with HIV in S.A Challenges when screening for HAD:language, culture, inadequate resources., inappropriate tools, untrained staff. Risk Factors: lower CD4 count, older age, lower levels of education, depression, substance abuse . Prevalence: 25.4% of adults living with HIV met the criteria for HAD. -International HIV Dementia Scale (IHDS) Consequences: In addition to HIV, cognitive impairments such as poor concentration, attention and executive functioning Sample of 65 nonadherent HIV patients 8O% screened positive for HAD
  • 43. • Nerve growth factor (NGF) • No fewer than 10 drugs • Cognitive training • Reality orientation • Reminiscence therapy • Cognitive rehabilitation • Psychodynamic Therapy • Support groups •Public education •Training professionals •Developing programs •Integrating services