Dementia diagnosis and_treatment

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Dementia: Diagnosis and Treatment Debra L. Bynum, MD Division of Geriatric Medicine November 2003

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Transcript of Dementia diagnosis and_treatment

Page 1: Dementia diagnosis and_treatment

Dementia: Diagnosis and Treatment

Debra L. Bynum, MD

Division of Geriatric Medicine

November 2003

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Case …

Mr. Jones is a 72 y/o gentleman brought to you by his daughter for progressive memory loss. He denies any problems. She reports that he was an accountant, and is now unable to keep his own check book straight. He has also had difficulty with getting lost while driving to the store. His wife died 2 years ago, and he was diagnosed with depression at that time. In addition, he has HTN and DM. His father was diagnosed with alzheimer’s disease at the age of 85. On exam, his BP is 170/90; he is oriented, scores 26/30 on the MMSE (0/3 recall and difficulty with the intersecting pentagon); he is unable to do the clockface.

A few months later, his MMSE is 24/30; on exam he has some mild cogwheel rigidity and a slight shuffling gate, but no tremor. His daughter reports that he has been having vivid visual hallucinations and paranoid thought…

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Questions

1. What are some limitations to the MMSE? 2. Is there any association between HTN and

dementia in the elderly? 3. What are the risk factors for dementia? 4. Would apo E testing be of benefit in this case? 5. What type of dementia might Mr. Jones have? 6. What medications should be avoided with this type

of dementia?

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Outline

1. Risk factors and definition of dementia 2. Types of Dementias 3. MMSE and testing 4. Treatment options

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Risk factors for dementia

Age (risk of AD 1% age 70-74, 2% age 75-79, 8.4% for those over age 85)

Family hx (10-30% risk of AD in patients with first degree relative with dementia); also cross with parkinson’s with dementia

Head trauma Depression (?early marker for dementia) Low educational attainment? ?hyperlipidemia ?diabetes

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Risk factors for AD…

Gender (confounding in literature – women more likely to live longer, be older….)

Down’s syndrome ?estrogen (probably not) ?NSAIDS (probably not)

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Cognitive decline with aging

Mild changes in memory and rate of information processing

Not progressive Does not interfere with daily function

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DSM Criteria

1. Memory impairment 2. At least one of the following:

– Aphasia– Apraxia– Agnosia– Disturbance in executive functioning

3. Disturbance in 1 and 2 interferes with daily function

4. Does not occur exclusively during delirium

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Activities of Daily Living

ADLs: bathing, toileting, transfer, dressing, eating

IADLs (executive functioning):– Maintaining household– Shopping– Transportation– Finances

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Diagnosis of Dementia

Delirium: acute, clouding of sensorium, fluctuations in level of consciousness, difficulty with attention and concentration

Depression: more likely to complain of memory loss than in those with dementia

Delirium and depression both markers for future dementia

5% people over age 65 and 35-50 % over 85 have dementia, pretest probability of dementia in older person with memory loss at least 60%

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Alzheimer’s Disease

60-80% of cases of dementia in older patients Memory loss, personality changes, global cognitive

dysfunction and functional impairments Visual spatial disturbances (early finding) Apraxia Language disturbances Personality changes Delusions/hallucinations (usually later in course)

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Alzheimer’s Disease

Depression occurs in 1/3 Delusions and hallucinations in 1/3 Extracellular deposition of amyloid-beta

protein, intracellular neurofibrillary tangles, and loss of neurons

Diagnosis at autopsy

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Alzheimer’s Disease

Onset usually near age 65; older age, more likely diagnosis

Absence of focal neurological signs (but significant overlap in the elderly with hx of CVAs…)

Aphasia, apraxia, agnosia Family hx Normal/nonspecific EEG Personality changes

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Vascular dementia

Onset of cognitive deficits associated with a stroke (but often no clear hx of CVA, more multiple small, undiagnosed CVAs)

Abrupt onset of sxs with stepwise deterioration Findings on neurological examination Infarcts on cerebral imaging (do not over read ct and

mri scans….) In reality, significant overlap between alzheimer’s and

vascular dementias; 90 y/o likely to have both based purely on demographics; treatment likely targets both…

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Dementia with Parkinson’s

30% with PD may develop dementia; Risk Factors:– Age over 70– Depression– Confusion/psychosis on levodopa– Facial masking upon presentation

Hallucinations and delusions– May be exacerbated by treatment

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Dementia with Lewy Bodies

Cortical Lewy Bodies on path Overlap with AD and PD Fluctuations in mental status (may appear delirious) Early delusions and hallucinations Mild extrapyramidal signs Neuroleptic hypersensitivity!!! Unexplained falls or transient changes in

consciousness

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Progressive Supranuclear Palsy

Uncommon Vertical supranuclear palsy with downward

gaze abnormalities Postural instability Falls (especially with stairs) “surprised look” Difficulty with spilling food/drink

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Frontal Lobe Dementia

Impairment of executive function– Initiation– Goal setting– planning

Disinhibited behavior Cognitive testing may be normal/minimally abnormal;

memory loss not prominent early feature 5-10% cases of dementia Onset usually 45-65

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Frontal Lobe Dementia…

Focal atrophy of frontal and/or anterior temporal lobes

Frontal lobe degeneration of the non-AD type (lack of distinctive histopath findings seen with AD or Pick’s)

May be autosomal dominant (inherited form known as frontotemporal dementia)

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Pick’s Disease

Subtype of frontal lobe dementia Pick bodies (silver staining intracytoplasmic

inclusions in neocortex and hippocampus) Language abnormalities

– Logorrhea (abundant unfocused speech)– Echolalia (spontaneous repetition of

words/phrases)– Palilalia (compulsive repetition of phrases)

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Primary Progressive Aphasia

Patients slowly develop nonfluent, anomic aphasia with hesitant, effortful speech

Repetition, reading, writing also impaired; comprehension initially preserved

Slow progression, initially memory preserved but 75% eventually develop nonlanguage deficits; most patients eventually become mute

Average age of onset 60

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“Reversible” Causes of Dementia

?10% of all patients with dementia; in reality, only 2-3% at most will truly have a reversible cause of dementia

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“Modifiable” Causes of Dementia

Medications Alcohol Metabolic (b12, thyroid, hyponatremia,

hypercalcemia, hepatic and renal dysfunction)

Depression? (likely marker though…) CNS neoplasms, chronic subdural NPH

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Normal Pressure Hydrocephalus

Triad:– Gait disturbance– Urinary incontinence– Cognitive dysfunction

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NPH

Diagnosis: initially on neuroimaging Miller Fisher test: objective gait assessment

before and after removal of 30 cc CSF Radioisotope diffusion studies of CSF

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Creutzfeldt-Jacob Disease

Rapid onset and deterioration Motor deficits Seizures Slowing and periodic complexes on EEG Myotonic activity

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Other infections and dementia

Syphilis HIV

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MMSE

24/30 suggestive of dementia (sens 87%, spec 82%)

Not sensitive for MCI Spuriously low in people with low educational

level, low SES, poor language skills, illiteracy, impaired vision

Not sensitive in people with higher educational background

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Additional evaluation

Clockface Short assessments with good validity: 3 item recall

and clockface Neurological exam (focality, frontal release signs

such as grasp, jawjerk; apraxia, cogwheeling, eye movements)

Lab testing and neuroimaging Apolipoprotein E epsilon 4 allele: probably not

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Prognosis

Previous estimate of median survival after onset of dementia have ranged from 5-10 years

Length bias: failing to consider people with rapidly progressive illness who died before they could be included in the study

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Prognosis…

NEJM, april 2001 Data from Canadian Study of Health and

Aging, estimate adjusted for length bias, with random sample of 10,263 people over age 65 screened for cognitive impairment; for those with dementia, ascertained date of onset and conducted followup for 5 years

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Prognosis…

821 subjects (396 with probably AD) Unadjusted median survival 3.3 years Median survival 3.1 years for those with

probable AD

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Treatment of AD…

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Tacrine

Cholinesterase inhibitor 1 systematic review with 5 RCTs, 1434 people, 1-39

weeks No difference in overall clinical improvement Some clinically insignificant improvement in cognition Significant risk of LFT abnormalities: NO ON USE

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Donepezil

Aricept Cholinesterse inhibitor Easy titration (start 5/day, then 10) Side effects: GI (nausea, diarrhea) Associated with improved cognitive function;

main effect seems to be lessening of rate of decline, delayed time to needing nursing home/more intensive care

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Other agents…

Rivastigmine Galantamine Cholinesterase inhibitors ?more side effects, more titration required Future directions:

– Prevention of delirium in at risk patients (cholinergic theory of delirium)

– Behavioral effects in those with severe dementia– Treatment of Lewy Body dementia– Treatment of mixed Vascular/AD dementia

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Comments about cholinesterase inhibitor studies…

Highly selected patients (mild-mod dementia) ?QOL improvements… Not known: severe dementia and mild CI

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Memantine

NEJM april 2003 Moderate to severe AD (MMSE 3-14) N-methyl D aspartate (NMDA) receptor antagonist;

theory that overstimulation of NMDA receptor be glutamate leads to progressive damage in neurodegenerative diseases

28 week, double blinded, placebo controlled study; 126 in each group; 67% female, mean age 76, mean MMSE 7.9

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Memantine…

Found less decline in ADL scores, less decline in MMSE (-.5 instead of –1.2)

Problem: significant drop outs (overall 28% dropout rate) in both groups; data analyzed did not account for drop outs, followed those “at risk”

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Selegiline

Unclear benefit Less than 10mg day, selective MAO B

inhibitor Small studies, not very conclusive

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Vitamin E (alpha tocopherol)

NEJM 1997: selegiline, vit E, both , placebo for tx of AD

Double blind, placebo controlled, RCT with mod AD; 341 patients

Primary outcome: time to death, institutionalization, loss of ADLS, severe dementia

Baseline MMSE higher in placebo group No difference in outcomes; adjusted for MMSE

differences at baseline and found delay in time to NH from 670 days with vit E to 440 days with placebo)

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Ginkgo Biloba

1 systematic review of 9 double blind RCTs with AD, vascular, or mixed dementia

Heterogeneity, short durations High withdrawal rates; best studies have

shown no sig change in clinician’s global impression scores

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Other treatments

NO good evidence to support estrogens or NSAIDS

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Other treatments…

Behavioural/agitation:– Nonpharm strategies– Low dose newer antipsychotics (.5 risperidone, olanzepine);

Olanzepine has higher anticholinergic profile, but may benefit/not worsen tremor/rigidity of Parkinson’s

– Reasons for NH placement: Agitation Incontinence Falls Caregiver stress

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MMSE tips…

No on serial sevens (months backwards, name backwards… assessment of attention)

Assess literacy prior Assess for dominant hand prior to handing paper

over Do not over lead… 3 item repetition, repeat all 3 then have patients

repeat; 3 stage command, repeat all 3 parts of command and then have patient do…