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APPROACH TO
DEMENTIA
Moderater : Asst. Prof. Dr. Bhupendra Shah
Presenter: Dr. Manoj Subedi
How big is the problem?
 The number of people living with dementia worldwide in
2015 was estimated at 47.47 million, reaching 75.63
million in 2030 and 135.46 million in 2050
 37% in High income countries vs. 63% in low income
countries
 10% of population aged >70yr
1/13/2019
3
Epidemiology and impact of dementia: WHO report, 2015
WHAT ARE WE DISCUSSING ?
 Memory and its type
 Introduction to dementia
 Types
 Assessment tool
 How to Approach
WHAT WE ARE NOT DISCUSSING ?
 Complex Pathophysiology of memory/circuits
 Detailed clinical features
 Investigations
 Treatment
 What is the capital of Nepal ?
 What journal did we discussed on 1st week of June in
morning seminar?
 How many of you, can ride a motorcycle ?
MEMORY
DEMENTIA: WHEN TO SUSPECT ?
 Dementia (Latin: dement-out of one’s mind)
 An acquired deterioration in cognitive abilities that
impairs the successful performance of activities of daily
living
 Elderly with slowly progressive memory loss over years
 Initial cues: Difficulty in managing money, shopping,
following instructions, finding words or navigating
BENIGN FORGETFULLNESS OF
ELDERLY
 Age associated memory loss
 Thought to be an extreme of normal aging
 Subtle cumulative decline in episodic memory
 Doesn't interfere with Activities of daily living
 Not a precursor of pathological aging
MILD COGNITIVE IMPAIRMENT vs.
DEMENTIA
 A measurable cognitive problem that does not seriously
disrupt daily activities is often referred to as mild
cognitive impairment (MCI)
 Search for factors that help in progression of MCI to
Dementia
 Prominent memory defecit
 Family history
 Apolipoprotein e4 allele
 Small hippocampal volume
IS IT DEPRESSION OR NOT ?
Symptom Dementia Depression
Cognition Lack of concern or denial about
symptoms
Amplification of
&preoccupation with deficits
Mood Normal most of time Subacute onset of
pervasively sad mood
Concentration and
thinking
Uncommon, impaired in late
dementia
Subacute loss of
concentration and focus
Guilt, worthlessness Uncommon Common
Eating behavior Gradual loss of weight over
months to year
Subacute changes[week] in
appetite, increase or
decrease in weight
Energy Normal energy level, but
reduced activity due to poor
initiation
Subacute decrease in
energy and increase
complaints of fatigue
Interest , Initiative Gradual loss of interest or
apathy
Subacute loss with low
mood and affect,
hopelessness
The Canadian Review of Alzheimer’s Disease and Other Dementias,
September 2009
HOW SEVERE IS YOUR DEMENTIA?
ABBREVIATED MENTAL TEST
SCORE(AMTS)
Score 8 or less at the time of testing indicate cognitive impairment and requires
further evaluation
MINI MENTAL STATE EXAMINATION
MMSE LIMITATIONS
 Age and Education
 Only screening, rather then diagnostic
 Visual and auditory impairment
 Not able to differentiate type of dementia
OTHER TOOLS
 Montreal Cognitive Assessment [ MOCA]
 ADAS-cog
 ADCS-ADL scale
 NPI
 CRD-SB
COGNITIVE TEST IN ILLETERATE
 Literacy Independent Cognitive Assessment(LICA)
 Montreal Cognitive Assessment [ MOCA]
CLUES FOR THE LOCATION
CORTICAL VS SUBCORTICAL
DEMENTIA
 CORTICAL DEMENTIA
 Symptoms: changes in memory, Language deficits,
perceptual deficits, praxis disturbances, lack of
extrapyramidal features
 Affected area: Temporal cortex, parietal cortex, frontal
lobe cortex
 Examples: AD,DLB,FTD, Vascular dementia
CORTICAL VS SUBCORTICAL
DEMENTIA
 SUBCORTICAL DEMENTIA
 Symptoms: Behavioral change, impaired mood and
affect, motor slowing, executive dysfunction,
extrapyramidal findings
 Affected areas: Thalamus, Straitum, Midbrain and
straitofrontal projections
 Examples: PDD, NPH, HD, CJD, Chronic meningitis
• Episodic memory initiallyMemory
• Language, Visuospatial and Praxis
• Judgment
• Problem solving abilities
Mental faculties
• Depression, apathy and anxiety
• Delusion, hallucinations
• Agitation, insomnia sleep disturbances
• Sleep disturbances, disinhibition
Neuropsychiatric
and social deficits
IMPACT OF DEMENTIA
ETIOLOGY
Reversible
• Hypothyroidism
• Thiamine
deficiency
• Vitamin B12
deficiency
• NPH
• SDH
• Chronic
infection
• Brain tumor
• Drug
intoxication
• Autoimmune
encephalopathy
Irreversible/
Degenerative
• Alzheimer’s
disease
• Frontotemporal
dementia
• Huntington’s
dementia
• Dementia with
Lewy body
• Vascular
• Leukoencephalo
pathies
• Parkinson's
Psychiatric
• Depression
• Schizophrenia
• Conversion
reaction
HOW TO PROCEED
 Clinical history and Symptom analysis
 Physical and neurological examination
 Cognitive and Neuropsychiatric examination
 Laboratory tests
3 QUESTIONS TO BE IN MIND?
1. What is the best fit for clinical diagnosis?
2. What component of dementia syndrome is treatable or
reversible?
3. Can the physician help to alleviate the burden on
caregiver?
HISTORY
 Onset, Duration and temporal of progression
 Acute or subacute onset of confusion: delirium
 Infection, Intoxication or Metabolic derangement]
ALZHEIMERS DISEASE
 Elderly with slowly progressive memory loss over years
 Initial cues:
 Difficulty in managing money,
 Shopping, following instructions,
 Finding words
 Navigating
FRONTOTEMPORAL DEMENTIA
 Personality change, disinhibition and weight gain
because of compulsive eating
 Prominent apathy, compulsivity, loss of empathy for
others, loss of speech fluency
 Relative sparing of memory and Visuospatial abilities
DEMENTIA OF LEWY BODY
 Early visual hallucinations
 Parkinsonism
 Proneness to delirium
 Rapid eye movement behavior disorder-RBD
 Capgras syndrome
VASCULAR DEMENTIA
 History of stroke
 Irregular stepwise progression
 Look for HTN, AF, PVD, DM
LABORATORY TESTS
 CBC
 TSH
 Vitamin B12
 Electrolytes
 CT/MRI
 CXR
 LP
 LFT
 RFT
 HIV,VDRL or RPR
 Apolipoprotein E
 EEG,PTH, Adrenal function, urine heavy metals,
Angiogram, PET, SPECT, Autoantibody
 Brain Biopsy
SEARCH FOR REVERSIBLE CAUSES
 Alcohol-malnutrition and thiamine deficiency
 B12 deficiency: veganism, bowel irradiation, h/o gastric
surgery
 Occupation: Battery or chemical factory-heavy metal
intoxication
 Search for depression related cognitive impairment
IMAGING
MRI FINDING IN FTD
CLINICAL VINGETTES
 Case 1:
 A 55 yr male, non smoker, alcohol consumer for last
year[30unit/day], without any prior co morbidities
presented with the complaints of irrelevant behavior and
slurred speech for 6 months
 No FND
 MMSE: 19/30
 CT Head: diffuse brain atrophy
ANY CLUE
?
 Case 2
 26 yr male, non smoker, non alcohol consumer w/o prior
co morbidities presented with abnormal, purposeless
body movement of UL and LL for year 3 year, and
irrelevant behavior for 6 months
 All metabolic parameter-Normal
 MMSE: 21/30
 CT –normal
 MRI
WHAT DID YOU SEE ?
TAKE HOME MESSAGE
 Dementia is decline in cognitive function with impairment
of daily activities
 Memory and its type
 Mild cognitive impairment and depression should be
differentiated
 MMSE as a screening tool
 Different imaging finding
REFERENCES
 Harrisons principle of medicine, 19th edition
 Dementia: Clinical review, BMJ,2009
 Epidemiology and impact of dementia: WHO report,
2015
 The Canadian Review of Alzheimer’s Disease and Other
Dementias, September 2009
 Dementia: role of MRI, Alzheimer Centre and Image
Analysis Centre,2012

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Approach to Dementia

  • 1. APPROACH TO DEMENTIA Moderater : Asst. Prof. Dr. Bhupendra Shah Presenter: Dr. Manoj Subedi
  • 2.
  • 3. How big is the problem?  The number of people living with dementia worldwide in 2015 was estimated at 47.47 million, reaching 75.63 million in 2030 and 135.46 million in 2050  37% in High income countries vs. 63% in low income countries  10% of population aged >70yr 1/13/2019 3 Epidemiology and impact of dementia: WHO report, 2015
  • 4. WHAT ARE WE DISCUSSING ?  Memory and its type  Introduction to dementia  Types  Assessment tool  How to Approach
  • 5. WHAT WE ARE NOT DISCUSSING ?  Complex Pathophysiology of memory/circuits  Detailed clinical features  Investigations  Treatment
  • 6.  What is the capital of Nepal ?  What journal did we discussed on 1st week of June in morning seminar?  How many of you, can ride a motorcycle ?
  • 8. DEMENTIA: WHEN TO SUSPECT ?  Dementia (Latin: dement-out of one’s mind)  An acquired deterioration in cognitive abilities that impairs the successful performance of activities of daily living  Elderly with slowly progressive memory loss over years  Initial cues: Difficulty in managing money, shopping, following instructions, finding words or navigating
  • 9. BENIGN FORGETFULLNESS OF ELDERLY  Age associated memory loss  Thought to be an extreme of normal aging  Subtle cumulative decline in episodic memory  Doesn't interfere with Activities of daily living  Not a precursor of pathological aging
  • 10. MILD COGNITIVE IMPAIRMENT vs. DEMENTIA  A measurable cognitive problem that does not seriously disrupt daily activities is often referred to as mild cognitive impairment (MCI)  Search for factors that help in progression of MCI to Dementia  Prominent memory defecit  Family history  Apolipoprotein e4 allele  Small hippocampal volume
  • 11. IS IT DEPRESSION OR NOT ? Symptom Dementia Depression Cognition Lack of concern or denial about symptoms Amplification of &preoccupation with deficits Mood Normal most of time Subacute onset of pervasively sad mood Concentration and thinking Uncommon, impaired in late dementia Subacute loss of concentration and focus Guilt, worthlessness Uncommon Common Eating behavior Gradual loss of weight over months to year Subacute changes[week] in appetite, increase or decrease in weight Energy Normal energy level, but reduced activity due to poor initiation Subacute decrease in energy and increase complaints of fatigue Interest , Initiative Gradual loss of interest or apathy Subacute loss with low mood and affect, hopelessness The Canadian Review of Alzheimer’s Disease and Other Dementias, September 2009 HOW SEVERE IS YOUR DEMENTIA?
  • 12. ABBREVIATED MENTAL TEST SCORE(AMTS) Score 8 or less at the time of testing indicate cognitive impairment and requires further evaluation
  • 13. MINI MENTAL STATE EXAMINATION
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  • 15. MMSE LIMITATIONS  Age and Education  Only screening, rather then diagnostic  Visual and auditory impairment  Not able to differentiate type of dementia
  • 16. OTHER TOOLS  Montreal Cognitive Assessment [ MOCA]  ADAS-cog  ADCS-ADL scale  NPI  CRD-SB
  • 17. COGNITIVE TEST IN ILLETERATE  Literacy Independent Cognitive Assessment(LICA)  Montreal Cognitive Assessment [ MOCA]
  • 18. CLUES FOR THE LOCATION
  • 19. CORTICAL VS SUBCORTICAL DEMENTIA  CORTICAL DEMENTIA  Symptoms: changes in memory, Language deficits, perceptual deficits, praxis disturbances, lack of extrapyramidal features  Affected area: Temporal cortex, parietal cortex, frontal lobe cortex  Examples: AD,DLB,FTD, Vascular dementia
  • 20. CORTICAL VS SUBCORTICAL DEMENTIA  SUBCORTICAL DEMENTIA  Symptoms: Behavioral change, impaired mood and affect, motor slowing, executive dysfunction, extrapyramidal findings  Affected areas: Thalamus, Straitum, Midbrain and straitofrontal projections  Examples: PDD, NPH, HD, CJD, Chronic meningitis
  • 21. • Episodic memory initiallyMemory • Language, Visuospatial and Praxis • Judgment • Problem solving abilities Mental faculties • Depression, apathy and anxiety • Delusion, hallucinations • Agitation, insomnia sleep disturbances • Sleep disturbances, disinhibition Neuropsychiatric and social deficits IMPACT OF DEMENTIA
  • 23. Reversible • Hypothyroidism • Thiamine deficiency • Vitamin B12 deficiency • NPH • SDH • Chronic infection • Brain tumor • Drug intoxication • Autoimmune encephalopathy Irreversible/ Degenerative • Alzheimer’s disease • Frontotemporal dementia • Huntington’s dementia • Dementia with Lewy body • Vascular • Leukoencephalo pathies • Parkinson's Psychiatric • Depression • Schizophrenia • Conversion reaction
  • 24. HOW TO PROCEED  Clinical history and Symptom analysis  Physical and neurological examination  Cognitive and Neuropsychiatric examination  Laboratory tests
  • 25. 3 QUESTIONS TO BE IN MIND? 1. What is the best fit for clinical diagnosis? 2. What component of dementia syndrome is treatable or reversible? 3. Can the physician help to alleviate the burden on caregiver?
  • 26. HISTORY  Onset, Duration and temporal of progression  Acute or subacute onset of confusion: delirium  Infection, Intoxication or Metabolic derangement]
  • 27. ALZHEIMERS DISEASE  Elderly with slowly progressive memory loss over years  Initial cues:  Difficulty in managing money,  Shopping, following instructions,  Finding words  Navigating
  • 28. FRONTOTEMPORAL DEMENTIA  Personality change, disinhibition and weight gain because of compulsive eating  Prominent apathy, compulsivity, loss of empathy for others, loss of speech fluency  Relative sparing of memory and Visuospatial abilities
  • 29. DEMENTIA OF LEWY BODY  Early visual hallucinations  Parkinsonism  Proneness to delirium  Rapid eye movement behavior disorder-RBD  Capgras syndrome
  • 30. VASCULAR DEMENTIA  History of stroke  Irregular stepwise progression  Look for HTN, AF, PVD, DM
  • 31. LABORATORY TESTS  CBC  TSH  Vitamin B12  Electrolytes  CT/MRI  CXR  LP  LFT  RFT  HIV,VDRL or RPR  Apolipoprotein E  EEG,PTH, Adrenal function, urine heavy metals, Angiogram, PET, SPECT, Autoantibody  Brain Biopsy
  • 32. SEARCH FOR REVERSIBLE CAUSES  Alcohol-malnutrition and thiamine deficiency  B12 deficiency: veganism, bowel irradiation, h/o gastric surgery  Occupation: Battery or chemical factory-heavy metal intoxication  Search for depression related cognitive impairment
  • 35. CLINICAL VINGETTES  Case 1:  A 55 yr male, non smoker, alcohol consumer for last year[30unit/day], without any prior co morbidities presented with the complaints of irrelevant behavior and slurred speech for 6 months  No FND  MMSE: 19/30  CT Head: diffuse brain atrophy
  • 37.  Case 2  26 yr male, non smoker, non alcohol consumer w/o prior co morbidities presented with abnormal, purposeless body movement of UL and LL for year 3 year, and irrelevant behavior for 6 months  All metabolic parameter-Normal  MMSE: 21/30  CT –normal  MRI
  • 38. WHAT DID YOU SEE ?
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  • 40. TAKE HOME MESSAGE  Dementia is decline in cognitive function with impairment of daily activities  Memory and its type  Mild cognitive impairment and depression should be differentiated  MMSE as a screening tool  Different imaging finding
  • 41. REFERENCES  Harrisons principle of medicine, 19th edition  Dementia: Clinical review, BMJ,2009  Epidemiology and impact of dementia: WHO report, 2015  The Canadian Review of Alzheimer’s Disease and Other Dementias, September 2009  Dementia: role of MRI, Alzheimer Centre and Image Analysis Centre,2012

Notes de l'éditeur

  1. The Abbreviated mental test score (AMTS) was introduced by Hodkinson in 1972[1] to rapidly assess elderly patients for the possibility of dementia. The following questions are put to the patient. Each question correctly answered scores one point. A score of 7-8 or less suggests cognitive impairment at the time of testing, although further and more formal tests are necessary to confirm a diagnosis of dementia, delirium or other causes of cognitive impairment
  2. originally introduced by Folstein et al. in 1975, in order to differentiate organic from functional psychiatric patients it is affected by demographic factors; age and education exert the greatest effect lack of sensitivity to mild cognitive impairment and its failure to adequately discriminate patients with mild Alzheimer's disease from normal patients
  3. Using a cut-off score of below 24, the MMSE is 87% sensitive and 82% specific in detecting dementia and de-irium among inpatients on a general medical ward
  4. Neuropsychiatry inventory
  5. In respect to a diagnosis of dementia in literate subjects,theLICA-S(cut-offpoint70)hadasensitivityof92% and specificity of 91%
  6. Capgras syndrome, the delusion that a familiar person has been replaced by an impostor
  7. A history of mood disorders, the recent death of a loved one, or depressive signs, such as insomnia or weight loss, raise the possibility of depression-related cognitive impairments.
  8. Fazekas 0: None or a single punctate WMH lesion Fazekas 1: Multiple punctate lesions Fazekas 2: Beginning confluency of lesions (bridging) Fazekas 3: Large confluent lesions