Geriatrics Flashcards

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1
Q

Confusion Assessment Method (CAM)

A

Four core features:

1) Inattention (examination: serial 7s, months backwards)
2) Acute onset and fluctuating course (history: collateral RN/family)
3) Disorganized thinking (observation: Patient making sense? “can a stone float on water?”)
4) LOC altered (observation: hypervigilant? somnolent? both?)

  • Need 1 and 2 + either 3 or 4
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2
Q

Delirium: Work-up

A

Indications for neuroimaging:
1. Focal neurological sign
2. Head trauma
3. Fever + acute change (if encephalitis is suspected)
4. No other cause identified
5. Cannot do a neuro exam (hypoactive/somnolent)

Drugs :

Too much: opioids, benzodiazepines, sedatives, anticholinergics, intoxications/recreational,

Too Little: Pain undertreated, withdrawal (EtOH, benzo, opioid, nicotine)
+/- ASA/Tylenol/EtOH levels, tox screen

Infection/Inflammation:

Vitals, focal signs/sources of infection, cultures as appropriate (blood, urine, Chest XR, +/- LP)

Metabolic :

CBC, lytes, Cr, LEs/LFT, Calcium, VBG, glucose, TSH, B12, cortisol (hypoactive)

Environment:

Sensory deprivation (windowless room, hearing/vision aids), sensory overload, isolation from
familiar surroundings, absence of orientation (clock/calendar), restraints, disruption to rest/sleep

Retention Abdominal XR, bladder scan

Structural abnormality

Neuro: ex. seizure, stroke, hemorrhage (exam, +/- neuroimaging, EEG), Cardiac: MI/CHF
(Troponin, CK, ECG +/-BNP); Resp ex. asthma/COPDe, PE (+/-CTPA), Abdo exam, Derm (rashes),
MSK examination for source of pain, etc.

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3
Q

Delirium: Management

A

ABCs, consider thiamine, naloxone, O2, glucose depending on acuity
1. Treat the underlying causes and contributors
2. Supportive care (Non-Pharmacological)

– Multi-component intervention (see Prevention: relieve sensory deprivation, re-
orient, mobilize, ensure hydration/nutrition, sleep, cognitive stimulation)5

– Pharmacological intervention not effective as treatment1,2,3
3. Safety (Non-Pharmacological +/- Pharmacological)
– Address safety/behavioural disturbances to prevent complication
– Antipsychotics only if i) danger to self/others, ii) distressing psychosis, or iii)
preventing medically necessary care
* When needed: Low dose, short duration. Haldol or atypical antipsychotic 1st line

Quetiapine-Preferred agent if parkinsonism present.
Lorazepam-Preferred for withdrawal delirium,
neuroleptic malignant syndrome, 2nd line if parkinsonism.

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4
Q

Alzheimer’s Dementia

A

Diagnosis:
– Dementia AND
– Insidious onset, gradual progression (months-years)
– Atrophy on imaging [hippocampal –> global]
– Initial and most prominent deficits in:
* Memory (aka amnestic AD, most common)
* Non-amnestic

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5
Q

Vascular Dementia

A
  • Diagnosis:
    1. Cognitive impairment (any domain, but often frontal/executive) AND
    2. Imaging evidence of cerebrovascular disease
  • Strokes
  • White matter changes
  • Microhemorrhages may be seen with severe uncontrolled hypertension
    – Note: Microhemorrhages and cognitive impairment can also be seen in Cerebral Amyloid Angiopathy (CAA)
    the underlying etiology of cognitive impairment in CAA is likely mixed amyloid and vascular pathology

+/- temporal relationship
Two main syndromes:
– post-stroke vascular dementia – “step-wise decline”
– subcortical ischemic syndrome – more common, insidious onset
* Imaging: periventricular white matter changes “moderate micro-angiopathic changes” +/- lacunar infarcts
* Clinically: frontal/executive syndrome
* Supportive findings: insidious onset, gait disturbance, “slow”

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6
Q

Dementia with Lewy Bodies (DLB)

A
  • Diagnosis:
    – Dementia and 2 of:
  • Fluctuating cognition
  • Recurrent visual hallucinations
  • Parkinsonism (bradykinesia, rest tremor,
    rigidity)
  • REM sleep behaviour disorder

“1 year rule” to distinguish DLB and Parkinson’s
disease dementia (PDD)
– if dementia precedes or begins within 1 year of
onset of parkinsonism, then DLB

May also have 1 clinical feature
and 1 biomarker, including:
-Low dopamine uptake in basal ganglia
-Abnormal iodine-MIBG myocardial
scintigraphy
-Polysomnographic confirmation of REM
sleep without atonia
Supportive but non-diagnostic
features:
Sensitivity to antipsychotics, postural
instability, repeated falls, severe
autonomic dysfunction (constipation,
urinary incontinence, orthostasis,
syncope), hyposmia, hallucinations or
delusions, apathy/anxiety/depression

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7
Q

Behavioural Variant

Frontotemporal Dementia (bvFTD)

A
  • Diagnosis:
    – Dementia and 3 of
  • Disinhibition
  • Apathy
  • Loss of empathy
  • Perseveration
  • Hyperorality
  • Executive dysfunction
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8
Q

Mixed Dementia

A
  • Diagnosis:
    – Dementia
    – Any combination of syndromes
    – Most common:
  • Alzheimer’s clinical syndrome AND
  • Imaging findings consistent with vascular dementia
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9
Q

Rapidly Progressive Dementia

A

Evolving “more rapidly than expected for dementia syndrome” i.e. <1-2 years from first symptom
to dementia
* Causes:
– Degenerative (MOST COMMON): Prion disease (CJD) relatively common cause of RPD (up to 59% of cases),other neurodegenerative (up to 22%)*

– Inflammatory (Hashimoto’s encephalitis, NMDA-Encepahlitis), Vascular, Toxic, Metabolic, Neoplastic,
Infectious

Work-up:
– History and Physical Exam
– Investigations (consider the following):
* Labs lytes, ext lytes, liver panel, Cr, B12, TSH, ESR, CRP, ANA, ANCA, SPEP, anti-TPO, anti Tg, syphilis, lyme, HIV
* LP: CSF for cell count, protein, glucose, c+s, serologies, paraneoplastic panel (consult neuro)
* Neuroimaging: MRI indicated, consider MRV/ vessel wall imaging
* Other imaging as indicated (ex. paraneoplastic syndrome)
* Brain Biopsy: Indicated if there dx unclear and indentifiable focus on imaging

  • Management: consider thiamine if poor nutritional status or alcohol, manage according to
    etiology
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10
Q

Principles of Dementia Management

A
  1. Track progression/response to therapy
    * Repeat subjective and objective assessments of cognition and function
  2. Non-pharmacological and Pharmacological management
  3. Screen for and manage complications
    * Geriatric review of systems: dysphagia, malnutrition, weight loss, incontinence, falls
    * Behavioral and psychological symptoms of dementia
    * Caregiver burnout
    * Monitor for safety concerns: Stove on, water running, getting lost/wandering,
    driving, firearms, power tools
  4. Future planning
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11
Q

Pharmacotherapy for Alzheimer’s Dementia

A
  • ChEIs (Donepezil, Galantamine, Rivastigmine)
    – Trial is recommended for most patients with AD.
    – Modest improvements in cognition, function, global assessment &
    behaviour
    – Side Effects: GI intolerance (anorexia), urinary incontinence, wild or
    vivid dreams, bradycardia
    – Avoid if pts have conduction defects (except RBBB), bradycardia, or
    unexplained syncope. Use with caution in asthma, COPD, seizures, GI
    bleeds, urinary incontinence
    – When to discontinue: Intolerable side effects, lack of benefit, end- stage dementia (as no ongoing benefit), consider if significant cognitive
    decline not explained by other precipitant
  • HOW to discontinue – taper by 50% every 4 weeks and monitor for clinical
    worsening
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12
Q

Pharmacotherapy for Alzheimer’s Dementia

A

NMDA RA (Memantine)

– DOMINO-AD trial: memantine had benefit vs. placebo in moderate-
severe dementia (defined as MMSE 5-13), but no additional benefit

when combined with cholinesterase inhibitors
– Canadian guidelines say combination is rational, but not enough
evidence to recommend for or against
* DOMINO-AD trial (2012) no benefit to combination therapy
* Recent network meta-analysis concluded memantine + donepezil superior to
monotherapy and placebo.

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13
Q

Pharmacotherapy for Vascular Dementia

A
  • Optimization of vascular risk factors (nonpharm & pharm)
  • ChEIs (& memantine)
    – 2020 Canadian Consensus Recommendations suggest that ChEIs and
    memantine “may be considered” given diagnostic uncertainty and lack of other options
    – Indicated in mixed AD & vascular dementia
  • ASA is not indicated with white matter changes only,
    considered if micro-infarcts detected

-Glantamine

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14
Q

Pharmacotherapy for Dementia with Lewy Bodies
(DLB) & Parkinson’s Disease Dementia (PDD)

A
  • ChEIs
    – Good evidence cognition, global assessment, and
    behavioural disturbance, hallucinations
    – 1st trials used rivastigmine, but donepezil is better
    tolerated
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15
Q

Behavioural & Psychological
Symptoms of Dementia (BPSD)

A

Clusters of symptoms:
– Psychosis: delusions, hallucinations, suspiciousness
– Aggression: verbal, physical, defensive, resistance to care
– Agitation: restlessness, anxiety, vocalization, repetitive actions,
pacing, wandering, hoarding
– Depression: sadness, guilt, hopelessness, irritability, suicidality
– Mania: irritability, euphoria, pressured speech, sexual
disinhibition
– Apathy: amotivation, withdrawn

Recent network meta-analysis3 demonstrated non-medication treatments (e.g. outdoor therapy, music and massage, massage and touch) were as or more efficacious than medications.

Pharmacologic:
* Some symptoms respond more to Rx than others
* Empiric pain control, Tylenol 1 g PO TID often
suffices1
* Risperidone2 approved by Health Canada (max 1
mg/d) only if all three conditions met: pure AD, non-
pharm Rx ineffective, and risk to self/others or
distressing psychotic symptoms
– Re-evaluate and taper q3months

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16
Q

Pharmacotherapy for Frontotemporal Dementia (FTD)

A

-No role for ChEIs
* NO medication has been shown to help the cognitive decline
in FTD
* Trazodone or SSRIs for behaviours (cautiously), often
paradoxical worsening to antipsychotics
* Androgen Deprivation Therapy for sexual disinhibition

17
Q

Depression Treatment

A

Pharmacologic treatment:
– First line: sertraline, duloxetine
– Second line: citalopram, escitalopram (QT prolongation)
– Other appropriate therapies: venlafaxine, mirtazapine, buproprion
vortioxetine
– Longer trial of therapy for effect (10-12 weeks)
– Third (or fourth) line: Tricyclic antidepressants (generally try to avoid)
– Avoid: paroxetine, fluoxetine (anticholinergic), MOA-i
* Monitor for hyponatremia in first 2 weeks
* Augment if partial response (eg add another antidepressant,
lithium, or aripiprazole)

Chief complaint may be somatic or cognitive, but need to ask
about mood symptoms
– More complexity (eg, other chronic conditions like dementia or
comorbidities causing poor concentration, low energy, low
appetite, or even depression itself)
– “Pseudodementia” is the cognitive symptoms of depression
(decreased frontal activity)
– Attempt suicide less, but higher completion rate

18
Q

Hypertension in Older Adults

A

Age ≥75 is a criterion for intensive management (targeting SBP ≤ 120
mmHg)
* Exclusion criteria for SPRINT trial:
– T2DM, previous stroke, eGFR < 20, protein >1g/day
– Orthostatic hypotension with SBP < 110mmHg
– Dementia, prognosis <3 year, institutionalized
* Frailty not part of management algorithm, but meta-analysis finds no
benefit of even SBP < 140mmHg in frail persons2
– Diabetes Canada suggests “individualized target” for those who are
functionally dependent, frail, or experience orthostasis

19
Q

DM in older adults

A

Avoid sulfonylureas (eg, glyburide) due to hypoglycemia risk
* Generally: metformin, then DPP-4 inhibitors or GLP-1 (however known side
effects of weight loss), then SGLT2 (may be at higher risk of dehydration)
then long-acting insulin
* A1c targets should scale based on functional status
– Functionally independent, A1c ≤ 7.0%
– Functionally dependent, A1c 7.1 - 8.0%
– Frail and/or dementia, A1c 7.1 - 8.5%
– End of life: avoid symptomatic hyperglycemia and hypoglycemia, BG checks
not indicated
– If below target, de-intensify therapy

Avoid intensification of antihypertensives and diabetes regimens
among patients over age 65 during hospitalization

20
Q

Vaccinations in Older Adults

A

Tdap: one booster per lifetime
– Td (tetanus, diphtheria): every 10 years
– Influenza: annually for age >65 years (high dose approved and
covered for those >65 in Ontario)
– Pneumococcal: Prevnar + Pneumovax (8 wks later) 65 years
– Zoster: recombinant subunit adjuvant vaccine (Shingrix), as of
October 2020; 2 doses 2-6mo apart
– COVID 19 mRNA vaccination – fall booster recommended

21
Q

Normal Aging: Neuro

A

Cognition:
– Age-related changes occur typically after age >70 and should not affect function
– Executive Function:
* Processing and Performance Speed: decrease rxn time, finger tapping, timed tests
* Attention span: difficulty with multi-tasking

– Memory:
* decrease in short term memory (recall) and free recall of events (“tip of the tongue” experience)
*decrease in episodic long-term memory
– Semantic memory/fund of knowledge, procedural memory preserved
– Registration preserved

22
Q

Incontinence Management

A
  • Sympathetic Nervous System (STORES!)
    – alpha adrenergic è constricts internal sphincter
    – beta adrenergic è relaxes detrusor
  • Parasympathetic Nervous System (PEES!)
    – cholinergic è contracts detrusor
  • Non-Pharmacological First line treatment for all types:
    – LIFESTYLE modifications: limit fluids, caffeine and EtOH; weight loss; treat constipation; bladder
    training (cog intact), pelvic floor muscle training (cog intact), prompted/timed voiding (cog impaired),
    functional intervention training, or pessary (stress)
  • Stress:
  • Pessary for prolapse, no pharmacotherapy, surgical options
  • Effective, but trials do not represent older adult population. Health Canada warning re: mid urethral
    sling due to complications.
  • Urge:
  • Beta-agonist (Mirabegron): s.e. headache, tachycardia afib, HTN, nasopharyngitis effectiveness low
    (<1/3), ++ side effects (on BEERs List to avoid)
  • Antimuscarinic: s.e. anticholinergic sedation, confusion, dizziness, urinary retention, constipation,
  • On Beer’s List. Fesoterodine most studied, more favorable cognitive profile, oxybutynin worst
  • Botox into detrusor
23
Q

CONSTIPATION RED FLAGS:

A

CONSTIPATION RED FLAGS:

Family history of colon cancer
Hematochezia
Anemia
Weight loss ≥ 5 kg in previous 6 months
Positive result of fecal occult blood test
Persistent constipation unresponsive to
treatment
Acute onset of constipation