This document provides an overview of dementia, including its definition, diagnosis, causes, and approach to evaluation and management. It defines dementia as acquired cognitive impairment that interferes with daily life. The diagnostic criteria from the DSM-V are outlined. Common causes of dementia like Alzheimer's disease, vascular dementia, and Lewy body dementia are reviewed. The document discusses taking a history, performing a physical and neurological exam, cognitive testing, and medical investigations to diagnose the underlying cause of dementia.
The world’s population is ageing rapidly, and with it is coming to a significant increase in the number of
older people with dementia. This increase presents major challenges for the provision of healthcare
generally and for dementia care in particular, for as more people have dementia, there will be more
people exhibiting behavioural and psychological symptoms of dementia (BPSD).
BPSD exact a high price from both the patient and the caregiver in terms of the distress and disability
they cause if left untreated. BPSD is recognisable, understandable and treatable. The recognition and
appropriate management of BPSD are important factors in improving our care of dementia patients
and their caregivers,
The association of neuropsychiatric disorders with cerebrovascular disease has been recognized by clinicians for over 100 years. Disease of the vascular system contribute greatly to the sum total of psychiatric disability, chiefly in the elderly population, mainly as a result of stroke, cerebrovascular accidents & subarachnoid haemorrhage.
The world’s population is ageing rapidly, and with it is coming to a significant increase in the number of
older people with dementia. This increase presents major challenges for the provision of healthcare
generally and for dementia care in particular, for as more people have dementia, there will be more
people exhibiting behavioural and psychological symptoms of dementia (BPSD).
BPSD exact a high price from both the patient and the caregiver in terms of the distress and disability
they cause if left untreated. BPSD is recognisable, understandable and treatable. The recognition and
appropriate management of BPSD are important factors in improving our care of dementia patients
and their caregivers,
The association of neuropsychiatric disorders with cerebrovascular disease has been recognized by clinicians for over 100 years. Disease of the vascular system contribute greatly to the sum total of psychiatric disability, chiefly in the elderly population, mainly as a result of stroke, cerebrovascular accidents & subarachnoid haemorrhage.
Presentation made by Drs. Charles Driscoll and Ms. Angela Taylor at the live webinar hosted by AlzPossible on the 29th of May, 2014. See recording at http://www.alzpossible.org/wordpress-3.1.4/wordpress/webinars-2/dementia-with-lewy-bodies/
Delirium, also referred to as "acute confusional state" or "acute brain syndrome," is a condition of severe confusion and rapid changes in brain function.
Presentation delivered by Dr. Carol Manning at the live webinar hosted by AlzPossible at www.alzpossible.org on the 17th of March, 2014.
www.alzpossible.org
Aging is associated with cognitive decline, and older subjects can have demonstrable cognitive impairment without crossing the threshold for dementia.
This condition has been termed “mild cognitive impairment” (MCI), and these patients have an increased risk of developing dementia, especially Alzheimer disease (AD).
Studies conducted in referral clinics have shown that patients with MCI progress to AD at a rate of 10% to 15% per year, and 80% of these patients have converted to AD after approximately 6 years of follow-up.
The identification and classification of MCI can be a major challenge.
This PPT contains all the important guidelines that are needed to manage a patient of Dementia. It involves diagnosis, psychosocial treatment, non-pharmacological management and pharmacological management. This PPT is prepared from NICE, APA and SIGN guidelines.
topic on dementia covering all aspects regarding classification,pathophysiology and treatment .Difference between MCI and DEMENTIA .best for post graduates ,house officers and medical students
Presentation made by Drs. Charles Driscoll and Ms. Angela Taylor at the live webinar hosted by AlzPossible on the 29th of May, 2014. See recording at http://www.alzpossible.org/wordpress-3.1.4/wordpress/webinars-2/dementia-with-lewy-bodies/
Delirium, also referred to as "acute confusional state" or "acute brain syndrome," is a condition of severe confusion and rapid changes in brain function.
Presentation delivered by Dr. Carol Manning at the live webinar hosted by AlzPossible at www.alzpossible.org on the 17th of March, 2014.
www.alzpossible.org
Aging is associated with cognitive decline, and older subjects can have demonstrable cognitive impairment without crossing the threshold for dementia.
This condition has been termed “mild cognitive impairment” (MCI), and these patients have an increased risk of developing dementia, especially Alzheimer disease (AD).
Studies conducted in referral clinics have shown that patients with MCI progress to AD at a rate of 10% to 15% per year, and 80% of these patients have converted to AD after approximately 6 years of follow-up.
The identification and classification of MCI can be a major challenge.
This PPT contains all the important guidelines that are needed to manage a patient of Dementia. It involves diagnosis, psychosocial treatment, non-pharmacological management and pharmacological management. This PPT is prepared from NICE, APA and SIGN guidelines.
topic on dementia covering all aspects regarding classification,pathophysiology and treatment .Difference between MCI and DEMENTIA .best for post graduates ,house officers and medical students
Scrub typhus is a growing and emerging disease grossly under-diagnosed due to its non-specific clinical presentation, limited awareness, and low index of suspicion
consider as a differential diagnosis in acute febrile illness with thrombocytopenia, renal impairment, LFT abnormalities, altered sensorium,encephalitis, pneumonitis, or ARDS
WEIL FELIX test very Specific
Early diagnosis and treatment are imperative to reduce the mortality and the complications associated with the disease
In today's society, leanness is often equated with beauty, success, fitness, and self-control. Obesity, on the other hand, is considered as undesirable as leanness is desirable, for reasons that are often more related to cosmetic concerns than to actual or potential medical complications.
Understand the relation of psychiatry and some common cause of organic brain diseases.
Identify common organic causes of psychiatric presentations
Differentiate dementia and delirium
Principle management of dementia
Identify neuro cognitive domains, differences between major and minor neurocognitive disorders
Palestine last event orientationfvgnh .pptxRaedMohamed3
An EFL lesson about the current events in Palestine. It is intended to be for intermediate students who wish to increase their listening skills through a short lesson in power point.
The French Revolution, which began in 1789, was a period of radical social and political upheaval in France. It marked the decline of absolute monarchies, the rise of secular and democratic republics, and the eventual rise of Napoleon Bonaparte. This revolutionary period is crucial in understanding the transition from feudalism to modernity in Europe.
For more information, visit-www.vavaclasses.com
2024.06.01 Introducing a competency framework for languag learning materials ...Sandy Millin
http://sandymillin.wordpress.com/iateflwebinar2024
Published classroom materials form the basis of syllabuses, drive teacher professional development, and have a potentially huge influence on learners, teachers and education systems. All teachers also create their own materials, whether a few sentences on a blackboard, a highly-structured fully-realised online course, or anything in between. Despite this, the knowledge and skills needed to create effective language learning materials are rarely part of teacher training, and are mostly learnt by trial and error.
Knowledge and skills frameworks, generally called competency frameworks, for ELT teachers, trainers and managers have existed for a few years now. However, until I created one for my MA dissertation, there wasn’t one drawing together what we need to know and do to be able to effectively produce language learning materials.
This webinar will introduce you to my framework, highlighting the key competencies I identified from my research. It will also show how anybody involved in language teaching (any language, not just English!), teacher training, managing schools or developing language learning materials can benefit from using the framework.
Embracing GenAI - A Strategic ImperativePeter Windle
Artificial Intelligence (AI) technologies such as Generative AI, Image Generators and Large Language Models have had a dramatic impact on teaching, learning and assessment over the past 18 months. The most immediate threat AI posed was to Academic Integrity with Higher Education Institutes (HEIs) focusing their efforts on combating the use of GenAI in assessment. Guidelines were developed for staff and students, policies put in place too. Innovative educators have forged paths in the use of Generative AI for teaching, learning and assessments leading to pockets of transformation springing up across HEIs, often with little or no top-down guidance, support or direction.
This Gasta posits a strategic approach to integrating AI into HEIs to prepare staff, students and the curriculum for an evolving world and workplace. We will highlight the advantages of working with these technologies beyond the realm of teaching, learning and assessment by considering prompt engineering skills, industry impact, curriculum changes, and the need for staff upskilling. In contrast, not engaging strategically with Generative AI poses risks, including falling behind peers, missed opportunities and failing to ensure our graduates remain employable. The rapid evolution of AI technologies necessitates a proactive and strategic approach if we are to remain relevant.
Macroeconomics- Movie Location
This will be used as part of your Personal Professional Portfolio once graded.
Objective:
Prepare a presentation or a paper using research, basic comparative analysis, data organization and application of economic information. You will make an informed assessment of an economic climate outside of the United States to accomplish an entertainment industry objective.
Unit 8 - Information and Communication Technology (Paper I).pdfThiyagu K
This slides describes the basic concepts of ICT, basics of Email, Emerging Technology and Digital Initiatives in Education. This presentations aligns with the UGC Paper I syllabus.
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Synthetic fiber production is a fascinating and complex field that blends chemistry, engineering, and environmental science. By understanding these aspects, students can gain a comprehensive view of synthetic fiber production, its impact on society and the environment, and the potential for future innovations. Synthetic fibers play a crucial role in modern society, impacting various aspects of daily life, industry, and the environment. ynthetic fibers are integral to modern life, offering a range of benefits from cost-effectiveness and versatility to innovative applications and performance characteristics. While they pose environmental challenges, ongoing research and development aim to create more sustainable and eco-friendly alternatives. Understanding the importance of synthetic fibers helps in appreciating their role in the economy, industry, and daily life, while also emphasizing the need for sustainable practices and innovation.
Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
Francesca Gottschalk - How can education support child empowerment.pptxEduSkills OECD
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2. DEMENTIA- “OUT OF ONE’S MIND”
DEMENTIA- the disease with acquired deterioration in cognitive/
intellectual abilities, without impairment of consciousness, that
impairs the successful performance of activities of daily living.
Cognitive impairment represents a decline from previous level of
functioning.
Episodic memory, the ability to recall events specific in time &
place, is the cognitive function most commonly lost.
In addition to memory, dementia may erode language, visuospatial,
praxis, calculation, judgement & problem solving abilities.
3. MAJOR NEUROCOGNITIVE DISORDER
DSM- V (DIAGNOSTIC AND STATISTICAL MANUAL)
A. Evidence of significant cognitive decline from a previous level of
performance in one or more area of cognitive domains ( complex
attention, executive function, learning and memory, language,
perceptual-motor or social cognition) based on :
1. Concern of the individual , a knowledgeable informant or the
clinician that there has been a significant decline in cognitive
function; and
2. Substantial impairment in cognitive performance, preferably
documented by standardized neuropsychological testing or , in its
absence , another quantified clinical assessment.
B. The cognitive deficits interfere with independence in everyday
activities.
C. The cognitive deficits do not occur exclusively in the context of a
delirium.
D. The cognitive deficits are not better explained by another mental
disorder (e.g., major depressive disorder, schizophrenia).
4. EPIDEMIOLOGY
~ 5 to 8 % of persons age 65
to 70 years
~ 10 % of persons age >70
years
20-40% of persons age>85
years
• Alzheimer's disease is most
common cause of dementia
50-75%
• Vascular dementia is second
most frequent cause.
• Dementia with lewy bodies is
also common in 15- 30% of
patients.
7. o Symptoms-major changes in
memory, language & perceptual
deficits, apraxia .Lack of
extrapyramidal features
o Areas affected-temporal cortex
(medial), parietal cortex, and
frontal lobe cortex
o Examples-Alzheimer’s Ds
Dementia with Lewy Bodies
Frontotemporal Dementia
Vascular Dementia
o Symptoms-behavioral changes,
impaired affect and mood, motor
slowing, executive dysfunction,
less severe changes in
memory.extra pyramidal features
o Areas affected- thalamus,
striatum, midbrain, striatofrontal
projections
o Examples - Parkinson’s disease,
progressive supranuclear palsy,
NPH, Huntington’s disease,
Creutzfeldt-Jakob disease, vit.
Deficiency, thyroid ds, metabolic,
dementia pugilistica
CORTICAL VS. SUBCORTICAL DEMENTIA
CORTICAL SUBCORTICAL
8. MIXED
Both cortical and sub-cortical area involved.
Example: vascular dementia, Dementia with Lewy
bodies, Corticobasal degeneration, Neurosyphilis
9. REVERSIBLE DEMENTIA
D = Delirium
E = Emotions (Depression) & Endocrine Disease
M= Metabolic Disturbances
E = Eye & Ear Impairments
N = Nutritional Disorders, NPH
T = Tumors, Toxicity, Trauma to Head(SDH)
I = Infectious Disorders
A= Alcohol, Arteriosclerosis
11. DIAGNOSTIC APPROACH
COGNITIVE IMPAIRMENT ?
DETERIORATION FROM A
PREVIOUSLY HIGHER LEVEL ?
CONSCIOUSNESS ALTERED?
MULTIPLE COGNITIVE FUNCTIONS
INVOLVED ?
DEMENTIA
YES
YES
YES
NO
NO
YES
NO
MENTAL
RETARDATION
DELIRIUM
APHASIA
AMNESTIC , etc
SERIOUS INTERFERRENCE
WITH DAILY ACTIVITIES??
YES
NO
MILD COGNITIVE
IMPAIRMENT(MCI)
12. HOW TO DIAGNOSE A CASE OF DEMENTIA
Focussed History
Symptoms analysis
Focussed physical examination
Cognitive and neuropsychiatric examination
Laboratory evaluation
13. FOCUSSED HISTORY
Chronology of the problem
- Mode of onset – acute(Delirium) vs gradual
- Progression -slow (AD)
-stepwise (Vascular dementia)
-rapid (CJD,FTD)
-progression with fluctuations(DLB)
- Duration of symptoms
15. COGNITIVE IMPAIREMENT
o Memory impairment
(Episodic; Immediate,recent or
remote; Anterograde vs
retrograde amnesia)
o Aphasia
(impairment of naming,
comprehension or fluency)
o Apraxia
(impaired ability to carry out
learned motor activities despite
intact motor function)
o Agnosia
(failure to recognize or identify
objects despite intact sensory
function)
o Impairment in executive
functioning
(disturbances in planning,
organizing, sequencing, and
abstracting, problem solving)
o Impaired visuo-spatial
functioning
(interference with dressing,
eating or even walking, failure
to solve simple problems or copy
geometric figures or clock
reading)
16. Each of the cognitive deficits results in a significant impairment in
functioning that represents a decline from a previous level of
functioning.
Difficulties with job performance if the patient is still working.
Difficulties in driving, shopping & housekeeping.
Difficulties in social functioning
disengagement from usual activities & interests,
trouble maintaining social relationships & social roles, and
difficulty performing activities of daily living.
FUNCTIONAL IMPAIRMENT
18. Apathy, disinhibition, compulsivity, loss of empathy for others
& overeating suggests FTD.
Agitation, aggressive behavior, uncooperative behavior, and
wandering.
Agitation, particularly worsening in the evening hours, is
common.
These symptoms account for substantial caregiving burden and
are often the trigger for moves to higher levels of care.
BEHAVIOURAL DISTURBANCES
19. 10% Dementia pts in early course have Major Depression.
50% Alzheimer’s pts have depressive symptoms.
Depressive symptoms, emotional lability, & irritability may be
related to psychological reactions to the awareness of losing one's
memory & anticipation of increasing functional impairment.
Suicidal ideation and behavior may also occur – esp in mildly
impaired.
MOOD CHANGES
20. ~ 60% of pts encounter anxiety
Manifest as fear of being alone, patients will search for their
caregivers so as not to be alone.
Some patients exhibit “catastrophic reactions” when confronted with
their cognitive limitations or when facing changes in routine or
environment.
ANXIETY
21. Disinhibition
Impulsivity
Making inappropriate jokes
Being overly familiar with
strangers
Disregarding social norms
Loss of judgement & reasoning
Inappropriate sexual remarks or
behaviors
PERSONALITY CHANGES
22. o Delusions are common, usually with common themes of theft,
infidelity or misidentification in late stages of AD.
o In late stages, 10% of AD patients develop Capgras’
syndrome, the delusion that a caregiver has been replaced by
an impostor.
o Visual hallucinations & Capgras’ syndrome are early features
in DLB.
PSYCHOSIS
23. SLEEP DISTURBANCES
REM sleep behavior disorder(RBD) is common in DLB.
ADVANCING DEMENTIA
ALTERED SLEEP-WAKE
CYCLES
DISRUPTED AND FRAGMENTED SLEEP in ~50%
24. H/o movement disorders ( myoclonus in CJD)
H/o seizures may indicate strokes or neoplasm but can also
occur in AD(particularly early age of onset AD)
H/o gait disturbance is common in vascular dementia,
PD/DLB & NPH.
H/o recurrent head trauma could indicate chronic SDH,
chronic traumatic encephalopathy(dementia pugulistica or
punch-drunk syndrome), intracranial hypotension or NPH.
H/o alcohol abuse causing malnutrition & thiamine
deficiency which causes Wernicke’s encephalopathy
(confusion,ataxia & diplopia) & irreversible Korsakoff’s
syndrome(unable to recall new information,confabulation).
H/o veganism, bowel irradiaton, gastric surgery, chronic
antihistamine therapy predispose to B12 deficiency(SACD).
OTHER IMPORTANT POINTS IN HISTORY
25. Past H/o HTN & DM important in vascular dementia.
H/o high risk sexual behaviors & IV drug abuse can lead to CNS
infection esp HIV or syphilis.
Occupational History for heavy metal intoxication.
H/o chronic drug intake esp. sedatives & analgesics.
Family History for HD & familial forms of AD, FTD, DLB or prion
disorders.
26. ALZHEIMER’S DISEASE(AD) – Patients usually begin with memory
symptoms but other early symptoms include difficulty with managing
money, driving, shopping, following instructions, finding words or
navigation.
FRONTOTEMPORAL DEMENTIA(FTD) – Suggested by personality
change, disinhibition and weight gain or compulsive eating. Other
suggestive points may include prominent apathy, loss of empathy for
others, loss of executive function or progressive abnormalities in
speech. There is relative sparing of memory or visuospatial abilities.
DEMENTIA WITH LEWY BODIES(DLB) – Suggested by early visual
hallucinations, parkinsonism, proneness to delirium, REM sleep
behaviour disorder(RBD) or Capgras syndrome.
VASCULAR DEMENTIA – History of sudden stroke with irregular
stepwise progression.
CREUTZFELDT- JAKOB DISEASE – Rapid progression of dementia in
association with motor rigidity and myoclonus.
28. Alzheimer’s Disease – Initially neurological examination is
normal. Motor system involvement occurs later in course.
Frontotemporal Dementia – Patients develop axial rigidity,
supranuclear gaze palsy or a motor neuron disease.
Dementia with Lewy bodies – Initial symptoms may include
new onset of a parkinsonian syndrome but it often starts with
visual hallucinations or dementia.
Progressive supranuclear palsy(PSP) is a/w unexplained falls,
axial rigidity, dysphagia & supranuclear vertical gaze deficits.
Corticobasal syndrome(CBS) features asymmetric rigidity,
dystonia, myoclonus, apraxia of one limb, alien limb
phenomenon(limb exhibits unintended motor actions such as
grasping, groping, drifting or undoing), pyramidal signs,
nonfluent aphasia, executive dysfunction or a behavioural
disorder.
29. Hemiparesis or other focal neurological deficits suggest vascular
dementia or brain tumour.
Dementia with myelopathy and peripheral neuropathy suggests
Vitamin B12 deficiency.
Peripheral neuropathy may also indicate another vitamin
deficiency, heavy metal intoxication, thyroid dysfunction, Lyme
ds or vasculitis.
Dry, cool skin, hair loss and bradycardia suggest
hypothyroidism.
In the elderly, Hearing impairment or visual loss may produce
confusion and disorientation misinterpreted as dementia.
30. COGNITIVE & NEUROPSYCHIATRIC EXAMINATION
Folstein Mini-Mental Status Examination (MMSE)
Earliest deficits on cognitive testing:-
AD- Episopic memory loss
FTD- Deficits in executive control or language function
PDD/DLB- Deficits in visuospatial function
Vascular dementia-Mixture of executive comtrol & visuospatial
deficits, with prominent psychomotor slowing
32. INVESTIGATIONS
ASSESSMENTS RATIONALE
Labs: Complete blood count, serum
electrolytes, renal and thyroid function
and vitamin B12 level
Rule out correctable or contributory causes of
dementia
Imaging: Computed tomography without
contrast or magnetic resonance
imaging(MRI)
Rule out infarcts, primary & metastatic neoplasms,
subdural hematomas, NPH, diffuse white matter ds
or regional pattern of atrophy.
PET and SPECT Temporal-parietal hypoperfusion or hypometabolism
in AD & frontotemporal deficits in FTD.
Amyloid Imaging, Pittsburgh Compound-
B(PiB) & 18F-AV-45(florbetapir)
Radioligands for detecting brain amyloid a/w
amyloid angiopathy or neuritic plaques of AD
Lumbar Puncture Indicated when CNS infection or inflammation are
possibilities. Presence of low AB42 & mildly elevated
CSF tau is highly suggestive of AD.
EEG Can suggest CJD(repetitive bursts of diffuse high
amplitude sharp waves or periodic complexes) or
underlying nonconvulsive seizure disorder.
Brain Biopsy Only to diagnose vasculitis, potentially treatable
neoplasms or unusual infections.
33. TREATMENT
Major goals are to treat reversible causes. e.g. thyroid replacement for
hypothyroidism, vitamin therapy for thiamine & B12 deficiency,
antimicrobials for infections, ventricular shunting for NPH, appropriate
treatment for CNS neoplasms etc.
Symptomatic treatment in irreversible causes.
Drugs used in Alzheimer’s Ds are cholinesterase inhibitors(donepezil,
rivastigmine, galantamine); NMDA receptors blockers(memantine).
SSRIs are commonly used for depressive symptoms(e.g. escitalopram)
Seizures can be treated with levetiracetam.
Antipsychotics such as quetiapine can be used for patients with
agitation, aggression & psychosis but all antipsychotics should be used
with caution due to their untoward side effects.
37. ALZHEIMER’S DISEASE (AD)
About 70% of all cases of dementia in elderly
Incidence increases with age
Occurs in up to 20-40% of persons >85 years old
Risk factors include old age, family history, female sex, ApoE4 allele,
HTN,DM,elevated homocysteine & cholesterol levels, decreased folic
acid level, low intake of fruits, vegetables, low levels of exercise.
Characterized by:
Progressive loss of cortical neurons
Formation of neuritic plaques (beta-amyloid is major component)
and intraneuronal neurofibrillary tangles (hyperphosphorylated tau
protein is major constituent)
Decrease in cortical levels of neurotransmitters esp. Ach & nicotinic
cholinergic receptors.
39. NORMAL BRAIN CELLS
Once the message is sent, then
enzymes lock onto the messenger
chemicals and take them out of
circulation so a new message can be
sent
41. Alzheimer’s drugs provide
FAKE messenger chemicals
that distract the enzymes.
They attach to the Fake ACh
& the message can get thru
(Cholinesterase inhibitors)
WHAT DO ALZHEIMER’S DRUGS DO?
42. CLINICAL MANIFESTATIONS
Begin with memory impairment language
visuospatial skills
Anosognosia - unaware of difficulties
Cognitive decline-driving, shopping, house-keeping, job difficulties
Language impaired- naming, comprehension then
- fluency
Apraxia – learned seq. motor task can’t perform
Visuospatial deficits
Late stages- Delusions, capgras’ syndrome,loss of judgement & reasoning,
disinhibition, disrupted sleep-wake patterns.
End stage - rigid, mute, incontinent & bed-ridden, hyperactive DTRs,
myoclonic jerks.
Death resuls from malnutrition,. Secondary infections, pulmonary emboli,
heart ds or, most commonly, aspiration.
43. AD DIAGNOSIS
Neuroimaging- CT/MRI shows posterior predominant cortical
atrophy & atrophy of medial temporal memory structures
(entorhinal cortex & hippocampus).
PET – Hypometabolism in posterior temporal-parietal cortex. It
can also detect presence of fibrillar amyloid in the brain.
EEG- Normal or non-specific slowing
Lumbar Puncture- CSF shows low AB42 & mildly elevated tau.
Treatment- Cholinesterase inhibitors (donepezil, rivastigmine,
galantamine) & NMDA glutamate receptor blockers(memantine).
44.
45.
46. The Changing Brain in
Alzheimer’s Disease
No one knows what causes AD to begin,
but we do know a lot about what happens
in the brain once AD takes hold.
Pet Scan of
Normal Brain
Pet Scan of Alzheimer’s
Disease Brain
AD and the Brain
Slide 19
47. VASCULAR DEMENTIA
Multi-infarct dementia- recurrent strokes
-step wise progression
-H/o HTN,DM,CAD
MRI- multiple areas of infarction
Diffuse white matter disease (Binswanger’s ds, leukoaraiosis)
-lacunar infarction, microangiopathy
-dementia may be insidious in onset & progress slowly
-confusion, personality changes, psychosis , emotional lability
-pyramidal signs & cerebellar signs + ,
-gait disorder, urinary incontinence, dysarthria
-MRI- B/L T2 signal hyperintensities in subcortical white matter
48.
49. FRONTOTEMPORAL DEMENTIA
Often begins with marked behavioral disturbances, unlike AD
Behavioral variant FTD-Apathy,disinhibition,compulsivity,loss of
empathy & overeating, deficits in executive control
Semantic variant PPA- Inability to decode word,object,person-
specific & emotion meaning.
Nonfluent/agrammatic variant PPA- Prominent motor speech
impairment.
Memory & visuo spatial skills spared.
May be accompanied by motor neuron disease.
MRI- Focal atrophy of frontal, insular and/or temporal cortex
Disease is subtyped according to protein composition of neuronal &
glial inclusions, which contain-
tau,
TDP-43 or
FUS
50. FTLD spectrum containing tau deposition includes Pick’ s disease,
Progressive supranuclear palsy syndrome(PSP-S) & Corticobasal
Syndrome(CBS).
PSP-S(Steele-Richardson-Olszewski syndrome)- It involves degeneration
of brainstem,basal ganglia,limbic structures & selected area of cortex. It
is characterized by falls, personality changes, supranuclear vertical
gaze palsy, axial dystonia with hypererect posture,dysarthria,dysphagia
& symmetric axial rigidity.
Corticobasal syndrome(CBS) is dementia movement disorder a/w
atrophy in perirolandic cortex & basal ganglia. Patients present with
asymmetric rigidity, dystonia, myoclonus, apraxia of one limb, alien limb
phenomenon(limb exhibits unintended motor actions such as grasping,
groping, drifting or undoing), pyramidal signs, nonfluent aphasia,
executive dysfunction or a behavioural disorder.
Treatment of FTD is symptomatic. SSRIs can be used.
51. PARKINSON’S DISEASE DEMENTIA AND
DEMENTIA WITH LEWY BODIES
When dementia occurs after an established diagnosis of Parkinson’s
Disease, the term used is Parkinson’s Disease Dementia(PDD).
When dementia precede or co-emerge with parkinsonism, it is referred to
as Dementia with Lewy Bodies(DLB).
DLB is characterized by visual hallucinations,parkinsonism,fluctuating
alertness, falls, capgras syndrome & REM sleep behavior disorder(RBD).
Better memory but severe visuospatial deficit.
Patients sensitive to adverse effects of neuroleptics
Lewy bodies are found in brainstem, substantia nigra, limbic system and
cortex.
Lewy bodies are intraneuronal cytoplasmic inclusions containing alpha-
synuclein.
Cholinesterase inhibitors provide significant benefit.
52. NORMAL PRESSURE HYDROCEPHALUS
Triad
1. Dementia: typically subcortical with executive impairment
2. Gait instability(ataxic or apractic)
3. Urinary incontinence
Walk with “feet stuck to floor”.
Symptoms progress over weeks to months.
It is a communicating hydrocephalus with a patent aqueduct of
sylvius. LP opening pressure falls in high normal range.
Cause is obstruction to normal CSF flow over cerebral convexities &
delayed resorption into venous system.
CT shows enlarged lateral ventricles with little or no cortical
atrophy, although sylvian fissures may appear propped open(so
called “boxcarring”), which can be mistaken for perisylvian atrophy.
53.
54. CRUETZFELDT-JAKOB DISEASE(CJD)
Rapidly progressive prion disorder a/w dementia, focal cortical
signs, rigidity & myoclonus.
90% has myoclonus vs 10% in AD
Death <1 year after first symptom appear.
EEG- diffuse slowing and abnormal periodic complexes.
MRI- Cortical ribboning & basal ganglia hyperintensities on
FLAIR MRI.
CSF- detect specific amino acid sequence (PrPSc)
55.
56.
57. CASE 1
70 yr old female present with progressive memory loss for past 1
yr. She also complaints of difficulty in naming objects and driving
car and house keeping. for the past 1 month she has difficulty in
dressing ,eating and gets agitated easily and wanders around at
night.
MMSE – 15/30
Neurological exam- normal
Vision & hearing- normal
58. CASE 2
76 yr old male presented in neuro opd with c/o progressive memory
loss, emotional lability, gait disturbance for past 5 months
h/o of 3 episodes of cerebrovascular accidents +
recent attack 7 months back
h/o HTN,DM,CAD+
O/E- incresed tone in all limbs,power 3+ in RT.UL &LL. 4+ in LT
side, B/L extensor plantar
59. CASE 3
55 YR old woman presented with 2yr history of progressive
alteration in social behavior. The pt had h/o social disinhibition,
abusive language, euphoria. there are complaints of excessive food
intake and weight gain for past 1 yr and pt was taken to
psychiatrist once.
o/e- vitals stable..neurological exam –WNL
MMSE-18/30
60. CASE 4
82 yr old male came to opd with c/o progressive decline in memory
for the past 6-8 months. He also complaints of having decreased
sleep and occasional nightmares. He occasional sees his deceased
wife at times.
o/e- vitals stable ,rigidity of limbs+
- gait- slow stepping gait, bradykinesia+
MMSE- 21/30
WHAT IS THE DIAGNOSIS?
61. CASE 5
65 YR old male presented to neuro opd with c/o gait disturbance for
past 1 yr. On history taking his son complained his father is
having memory loss for past 6 months and it is progressing.
The pt also c/o of urinary incontinence+
Neurolog exam- no focal deficits
MMSE- 23/30
62. CASE 6
50 YR old woman was admitted with c/o progressive memory loss
and gait problem ,slurred speech within one month; The pt also
had behavioral problem – insomnia, agitation,aggression duration
of 3 weeks.the pt also c/o abnormal jerky hand movements for past
1 month
o/e- limb & gait ataxia +, reflexes-exagg.
- tone increased all limbs, plantar b/l extensor
- no focal weakness
MMSE- 16/30