One-liner#
Systematic evaluation of memory loss and cognitive decline in older adults—distinguishing normal aging from mild cognitive impairment (MCI) and dementia, identifying reversible causes, and providing diagnosis, prognosis, and care planning for patients and families.
Quick nav#
- Red flags / send to ED
- Key history
- Focused exam
- Differential (quick pattern recognition)
- Workup
- Initial management
- Management by diagnosis
- Follow-up
- Patient instructions
- Smartphrase snippets
Red flags / send to ED#
- Acute onset confusion (hours to days) → This is delirium, not dementia → ED workup
- Rapid progression (weeks to months) → Consider Creutzfeldt-Jakob disease, malignancy, autoimmune encephalitis → Urgent neurology
- New focal neurologic deficits → ED (stroke, mass)
- Severe headache with cognitive changes → ED (hemorrhage, mass)
- Seizures → ED
- Gait disturbance + incontinence + dementia (NPH triad) → Urgent neurology/neurosurgery
Urgent (expedited outpatient):
- Cognitive decline with new gait abnormality
- Rapid decline over weeks
- Young-onset dementia (<65 years)
- Behavioral changes suggesting frontotemporal dementia
- Concern for elder abuse or self-neglect
Key history#
CRITICAL: Interview patient AND informant separately
- Patients often minimize or lack insight into deficits
- Family/caregiver provides essential collateral
- Discrepancy between patient and informant report is itself informative
Characterize the cognitive complaint:
- What specific problems are you/they noticing?
- When did it start? (months, years)
- Is it getting worse? How fast?
- Gradual progression (typical dementia) vs stepwise decline (vascular) vs fluctuating (Lewy body)
Cognitive domains affected:
- Memory: Repeating questions, forgetting appointments, losing things
- Language: Word-finding difficulty, trouble following conversations
- Executive function: Difficulty with planning, multitasking, managing finances, cooking
- Visuospatial: Getting lost in familiar places, difficulty parking, trouble with spatial tasks
- Attention: Easily distracted, can’t follow a movie or book
Functional impact (critical for staging):
- IADLs (instrumental): Managing finances, medications, driving, cooking, shopping, using phone
- BADLs (basic): Bathing, dressing, toileting, eating, transferring
- MCI: Cognitive decline but IADLs preserved
- Dementia: Cognitive decline WITH functional impairment
Behavioral and psychiatric symptoms:
- Depression (common, can mimic or coexist with dementia)
- Anxiety
- Apathy (common in dementia, often mistaken for depression)
- Agitation, irritability
- Hallucinations (visual → think Lewy body; auditory → think psychiatric)
- Delusions (paranoia, theft accusations common in Alzheimer’s)
- Sleep disturbance (REM sleep behavior disorder → Lewy body)
- Personality changes (disinhibition, apathy → frontotemporal)
Medical history (reversible causes):
- Thyroid disease
- B12 deficiency
- Depression
- Sleep apnea
- Hearing loss (contributes to cognitive decline)
- Recent surgery or hospitalization (post-operative cognitive decline)
- Head trauma
- Alcohol use
- Vascular risk factors (HTN, DM, hyperlipidemia, smoking, AF)
Medication review:
- Anticholinergics (diphenhydramine, oxybutynin, TCAs)
- Benzodiazepines
- Opioids
- Anticonvulsants
- Polypharmacy
Family history:
- Dementia (Alzheimer’s has genetic component)
- Parkinson’s disease
- Psychiatric illness
- Age of onset in affected relatives
Social history:
- Education level (affects cognitive reserve and test interpretation)
- Living situation
- Caregiver availability and stress
- Driving status
- Firearms in home
- Advance directives status
Focused exam#
Cognitive testing (essential):
MoCA (Montreal Cognitive Assessment) - Preferred screening tool:
- 30 points; takes 10-15 minutes
- More sensitive than MMSE for MCI
- Tests multiple domains: memory, visuospatial, executive, attention, language, orientation
- Score interpretation:
- 26-30: Normal
- 18-25: Mild cognitive impairment
- 10-17: Moderate impairment
- <10: Severe impairment
- Add 1 point if education ≤12 years
Mini-Cog (quick screen, 3 minutes):
- 3-word recall + clock draw
- Abnormal: 0-2 words recalled OR abnormal clock
- Good for screening; if abnormal, do full MoCA
MMSE (Mini-Mental State Examination):
- 30 points; less sensitive for MCI than MoCA
- Ceiling effect in educated patients
- 24-30: Normal; 18-23: Mild; 10-17: Moderate; <10: Severe
Depression screening:
- PHQ-2/PHQ-9 or Geriatric Depression Scale (GDS)
- Depression can cause “pseudodementia” and commonly coexists with dementia
Neurologic exam:
- Gait: Shuffling (Parkinson’s, NPH), magnetic gait (NPH), ataxia
- Parkinsonism: Bradykinesia, rigidity, tremor (Lewy body, Parkinson’s dementia)
- Focal deficits: Suggest vascular or mass lesion
- Frontal release signs: Grasp, snout, palmomental (nonspecific but suggest frontal involvement)
- Reflexes: Asymmetry suggests vascular; hyperreflexia suggests myelopathy
General exam:
- Vital signs (HTN as vascular risk factor)
- Thyroid (goiter)
- Cardiovascular (AF, carotid bruits, signs of HF)
- Signs of self-neglect (hygiene, nutrition)
Differential (quick pattern recognition)#
Common/likely (outpatient)#
| Diagnosis | Keywords patients use | Key clues | Focused exam clues | Initial next step |
|---|---|---|---|---|
| Alzheimer’s disease | “Can’t remember things,” “asks the same questions,” “forgets names” | Gradual onset; memory predominant early; word-finding difficulty | Low MoCA (especially memory recall); otherwise normal neuro exam | MoCA; labs for reversible causes; consider MRI |
| Mild cognitive impairment (MCI) | “Memory isn’t what it used to be,” “have to write everything down” | Subjective and objective cognitive decline; IADLs preserved | MoCA 18-25; functional status intact | MoCA; labs; monitor for progression |
| Vascular dementia | “Got worse after the stroke,” “stepwise decline” | Vascular risk factors; stepwise progression; focal symptoms | May have focal deficits; gait abnormality | MRI brain (white matter disease, infarcts); vascular risk management |
| Depression (“pseudodementia”) | “Don’t care anymore,” “can’t concentrate,” “everything is hard” | Mood symptoms; rapid onset; patient complains more than family | PHQ-9 elevated; may perform better than expected on testing | PHQ-9; trial of antidepressant; retest cognition after treatment |
| Medication-induced | “Foggy since starting [med]” | Temporal relationship; anticholinergics, benzos, opioids | May improve with medication reduction | Medication review; reduce/stop culprits; retest |
| Sleep apnea | “Tired all the time,” “snore,” “can’t think clearly” | Snoring; daytime sleepiness; obesity | Obesity; crowded airway | STOP-BANG; sleep study; treat OSA then reassess |
| Hearing loss | “Can’t follow conversations,” “people mumble” | Difficulty in group settings; asks for repetition | Hearing impaired on exam | Audiology referral; hearing aids; reassess cognition |
| Normal aging | “Not as sharp as I used to be” | Mild forgetfulness; no functional impact; stable over time | MoCA ≥26; normal function | Reassurance; lifestyle counseling; monitor |
Can’t-miss / urgent#
| Diagnosis | Keywords patients use | Key clues | Focused exam clues | Initial next step |
|---|---|---|---|---|
| Lewy body dementia | “Sees things that aren’t there,” “acts out dreams,” “stiff” | Visual hallucinations; REM sleep behavior disorder; parkinsonism; fluctuating cognition | Parkinsonism; visual hallucinations | Neurology referral; avoid antipsychotics (severe sensitivity) |
| Frontotemporal dementia | “Personality changed,” “says inappropriate things,” “doesn’t care about anything” | Behavioral changes; disinhibition; apathy; language problems; younger onset (<65) | Frontal release signs; behavioral changes on exam | Neurology referral; MRI (frontal/temporal atrophy) |
| Normal pressure hydrocephalus | “Wet, wacky, wobbly” | Triad: gait apraxia, dementia, incontinence | Magnetic gait; cognitive impairment; incontinence | MRI brain; neurology/neurosurgery referral for LP trial |
| Subdural hematoma | “Hit head,” “getting worse” | History of fall/trauma (may be minor); anticoagulation | Focal deficits; altered mental status | CT head |
| B12 deficiency | “Numb feet,” “unsteady” | Neuropathy; macrocytic anemia; vegan diet; metformin use | Decreased vibration sense; ataxia | B12 level; treat if low |
| Hypothyroidism | “Tired,” “cold,” “constipated,” “slow” | Fatigue; weight gain; cold intolerance | Bradycardia; dry skin; delayed reflexes | TSH |
| Brain tumor/metastases | “Headaches,” “seizures,” “rapid change” | Rapid progression; headache; focal symptoms; cancer history | Focal deficits; papilledema | MRI brain with contrast |
| Creutzfeldt-Jakob disease | “Rapid decline,” “jerking movements” | Very rapid progression (weeks-months); myoclonus; ataxia | Myoclonus; ataxia; rapid cognitive decline | Urgent neurology; MRI; CSF |
Workup#
Initial workup (all patients with cognitive complaint):
| Test | Rationale |
|---|---|
| MoCA or MMSE | Objective cognitive assessment |
| Depression screen (PHQ-9 or GDS) | Depression mimics and coexists with dementia |
| TSH | Hypothyroidism is reversible |
| Vitamin B12 | Deficiency is reversible; common in elderly |
| CBC | Anemia; macrocytosis (B12) |
| CMP | Metabolic abnormalities; renal/liver function |
Second-tier testing (based on clinical suspicion):
| Test | When to order |
|---|---|
| MRI brain without contrast | Recommended for most new dementia diagnoses; rules out mass, NPH, vascular disease, atrophy pattern |
| RPR or VDRL | If risk factors for syphilis (rare but treatable) |
| HIV | If risk factors |
| Folate | If macrocytic anemia or poor nutrition |
| Vitamin D | Deficiency associated with cognitive decline |
| Ammonia | If liver disease |
| Heavy metals | If occupational exposure |
| Sleep study | If OSA suspected |
| Lumbar puncture | If NPH suspected (therapeutic trial); if rapid progression or atypical features |
| EEG | If seizures suspected; CJD |
| PET scan (amyloid or FDG) | Specialist-ordered for atypical cases |
When NOT to order extensive workup:
- Classic Alzheimer’s presentation in elderly patient with gradual progression
- Known dementia with stable course (unless new symptoms)
- Very advanced dementia where results won’t change management
Neuroimaging guidance:
- MRI preferred over CT (better for white matter disease, atrophy patterns, small infarcts)
- CT acceptable if MRI contraindicated or unavailable
- Contrast not routinely needed unless mass suspected
Initial management#
After diagnosis:
- Disclose diagnosis with sensitivity (patient and family together, unless patient prefers otherwise)
- Assess and document decision-making capacity
- Discuss prognosis (general trajectory, not specific timeline)
- Address safety concerns (driving, firearms, wandering, finances)
- Identify caregiver and assess caregiver burden
- Discuss advance care planning
- Connect with resources (Alzheimer’s Association, support groups)
Safety assessment (every visit):
- Driving:
- Dementia is a progressive condition that eventually impairs driving
- Refer for formal driving evaluation if any concern (occupational therapy driving assessment)
- Many states require physician reporting of dementia diagnosis to DMV
- Have direct conversation with patient and family; document discussion
- Consider: getting lost, accidents/near-misses, family concerns, MoCA <20
- Firearms: Recommend removal from home
- Wandering risk: Door alarms, ID bracelet, GPS tracker
- Financial exploitation: Assess for signs; consider POA
- Medication management: Assess ability; consider pill boxes, supervision
- Home safety: Fall risks, stove safety, supervision needs
Anosognosia (lack of insight):
- Common in dementia; patient may deny or minimize problems
- Family report often more accurate than patient report
- Does not mean patient is being dishonest
- Complicates safety discussions (patient may resist giving up driving, etc.)
Caregiver support:
- Assess caregiver stress and burnout
- Provide education about disease progression
- Connect with support groups and respite care
- Screen caregiver for depression
Management by diagnosis#
Alzheimer’s disease#
Education:
- Alzheimer’s is a progressive brain disease affecting memory and thinking
- Medications may help symptoms but don’t cure or stop progression
- Planning ahead while the patient can participate is important
- Average survival after diagnosis is 4-8 years, but varies widely
Treatment - Cholinesterase inhibitors (mild-moderate AD):
| Drug | Dose | Contraindications | Monitoring | Cost | Notes |
|---|---|---|---|---|---|
| Donepezil | 5 mg daily x 4-6 weeks, then 10 mg daily; 23 mg daily for moderate-severe | Sick sinus syndrome; AV block (without pacemaker) | GI side effects; bradycardia; vivid dreams | $ | Once daily; can give at bedtime if GI upset; most commonly used |
| Rivastigmine | 1.5 mg BID, titrate to 6 mg BID; or patch 4.6 mg/24h → 9.5 mg/24h → 13.3 mg/24h | Same as donepezil | GI side effects; weight loss | $ (oral), $$ (patch) | Patch has fewer GI side effects |
| Galantamine | 4 mg BID, titrate to 12 mg BID; or ER 8 mg daily → 24 mg daily | Same as donepezil; severe renal/hepatic impairment | GI side effects | $ |
Treatment - NMDA receptor antagonist (moderate-severe AD):
| Drug | Dose | Contraindications | Monitoring | Cost | Notes |
|---|---|---|---|---|---|
| Memantine | 5 mg daily, increase by 5 mg weekly to 10 mg BID; or ER 7 mg daily → 28 mg daily | Severe renal impairment (reduce dose if CrCl 5-29) | Confusion, dizziness, headache | $ | Can combine with cholinesterase inhibitor; modest benefit |
Combination therapy: Donepezil + memantine commonly used in moderate-severe AD.
Realistic expectations:
- Cholinesterase inhibitors: Modest symptomatic benefit; may slow decline by ~6 months
- Not disease-modifying; benefit diminishes over time
- ~50% of patients show no measurable response
- Consider discontinuation in severe dementia or if no perceived benefit
New disease-modifying therapies (specialist-initiated):
- Lecanemab, aducanumab: Anti-amyloid monoclonal antibodies
- Require amyloid PET or CSF confirmation
- Modest benefit with significant risks (ARIA—brain edema/hemorrhage)
- Specialist (neurologist/geriatrician) should initiate and monitor
- Not appropriate for all patients; shared decision-making essential
Non-pharmacologic (equally important):
- Cognitive stimulation (puzzles, social engagement, music)
- Physical exercise (reduces behavioral symptoms, may slow decline)
- Structured routine
- Caregiver education and support
Follow-up: Every 3-6 months; assess cognition, function, behavior, caregiver status.
Mild cognitive impairment (MCI)#
Education:
- MCI means memory or thinking problems beyond normal aging, but you can still do daily activities
- Some people with MCI stay stable, some improve, and some progress to dementia
- About 10-15% of people with MCI progress to dementia each year
- Lifestyle factors may help slow progression
Management:
- No FDA-approved medications for MCI
- Cholinesterase inhibitors NOT recommended (no proven benefit, side effects)
- Focus on modifiable risk factors:
- Cardiovascular risk management (BP, cholesterol, diabetes, smoking)
- Physical exercise (strongest evidence)
- Cognitive engagement
- Social activity
- Treat depression if present
- Treat sleep apnea if present
- Hearing aids if hearing impaired
- Mediterranean diet
Monitoring:
- Repeat cognitive testing every 6-12 months
- Monitor for functional decline (signals conversion to dementia)
- Reassess driving safety
Follow-up: Every 6-12 months with repeat MoCA.
Vascular dementia#
Education:
- Vascular dementia is caused by reduced blood flow to the brain, often from small strokes
- Controlling vascular risk factors is the most important treatment
- Progression can sometimes be slowed with good risk factor control
Treatment:
- Vascular risk factor management (primary intervention):
- Blood pressure control (target <130/80 if tolerated)
- Statin therapy
- Diabetes management
- Smoking cessation
- Antiplatelet therapy (aspirin 81 mg) if ischemic strokes
- Anticoagulation if AF
- Cholinesterase inhibitors: May have modest benefit; often tried
- Memantine: May have modest benefit in moderate-severe
Follow-up: Every 3-6 months; monitor vascular risk factors and cognition.
Lewy body dementia#
Education:
- Lewy body dementia causes memory problems, visual hallucinations, and movement symptoms
- Symptoms can fluctuate day to day
- Some medications can make symptoms much worse—always check before starting new medications
CRITICAL - Medication sensitivity:
- Avoid typical antipsychotics (haloperidol)—can cause severe parkinsonism, neuroleptic malignant syndrome
- Avoid most atypical antipsychotics—use only quetiapine or clozapine if absolutely necessary
- Avoid anticholinergics—worsen cognition
Treatment:
| Drug | Dose | Contraindications | Monitoring | Cost | Notes |
|---|---|---|---|---|---|
| Donepezil | 5-10 mg daily | Cardiac conduction disease | GI effects; bradycardia | $ | May help cognition AND hallucinations |
| Rivastigmine | Titrate as for AD | Same | Same | $ | Also effective |
| Quetiapine | 12.5-50 mg at bedtime | Use with extreme caution | Sedation; parkinsonism | $ | ONLY if hallucinations distressing; start very low |
| Carbidopa-levodopa | Neurology to initiate | $ | For parkinsonism; may worsen hallucinations |
Referral: Neurology for diagnosis confirmation and management.
Follow-up: Every 3 months given complexity; close monitoring for medication effects.
Frontotemporal dementia#
Education:
- FTD affects the front part of the brain, causing personality and behavior changes
- Memory is often preserved early, unlike Alzheimer’s
- There are no FDA-approved medications; treatment focuses on managing symptoms
- Progression is variable; average survival 6-8 years from symptom onset
Management:
- No disease-modifying treatment
- Cholinesterase inhibitors NOT recommended (may worsen behavior)
- SSRIs for behavioral symptoms (disinhibition, compulsions, depression)
- Trazodone for agitation, sleep
- Avoid antipsychotics if possible
- Behavioral strategies and caregiver education
- Speech therapy for language variants
Referral: Neurology for diagnosis and management.
Follow-up: Every 3-6 months; focus on behavioral management and caregiver support.
Depression with cognitive symptoms (“pseudodementia”)#
Education:
- Depression can cause memory and concentration problems that look like dementia
- Treating the depression often improves thinking
- Sometimes depression and dementia occur together
Treatment:
| Drug | Dose | Contraindications | Monitoring | Cost | Notes |
|---|---|---|---|---|---|
| Sertraline | 25-50 mg daily, max 200 mg | MAOIs | Mood; GI effects | $ | Good first-line in elderly |
| Escitalopram | 5-10 mg daily, max 20 mg | MAOIs; QTc prolongation | QTc; mood | $ | Well-tolerated |
| Mirtazapine | 7.5-15 mg at bedtime | Weight; sedation | $ | Good if poor appetite, insomnia | |
| Duloxetine | 30-60 mg daily | Severe renal/hepatic impairment | BP; mood | $ | Good if comorbid pain |
Avoid in elderly: TCAs (anticholinergic), paroxetine (anticholinergic)
Follow-up: 4-6 weeks to assess mood response; repeat cognitive testing after depression treated (wait 3+ months).
Normal pressure hydrocephalus (NPH)#
Education:
- NPH is caused by fluid buildup in the brain that can be treated
- The classic symptoms are walking problems, memory problems, and bladder control problems
- A procedure to drain fluid can help determine if surgery would work
Recognition: Triad of gait apraxia (magnetic gait), dementia, urinary incontinence
Management:
- MRI brain (enlarged ventricles out of proportion to atrophy)
- Neurology/neurosurgery referral
- Large-volume lumbar puncture (30-50 mL) as diagnostic/therapeutic trial
- If improvement after LP: Consider VP shunt placement
Follow-up: Per neurosurgery; gait often improves most, cognition variable.
Follow-up#
Frequency:
- MCI: Every 6-12 months
- Mild dementia: Every 3-6 months
- Moderate-severe dementia: Every 3 months or as needed
What to reassess:
- Cognitive status (repeat MoCA annually or if change noted)
- Functional status (ADLs, IADLs)
- Behavioral symptoms
- Safety (driving, wandering, firearms, finances)
- Medication tolerance and adherence
- Caregiver burden and health
- Advance care planning status
Advance care planning:
- Discuss early while patient can participate
- Healthcare proxy/POA
- Living will/advance directive
- Goals of care (hospitalization, feeding tubes, CPR)
- Revisit as disease progresses
Patient instructions#
For patient (early stage) and family/caregiver:
- Memory and thinking problems can have many causes. We’re doing tests to find out what’s causing yours and whether it can be treated.
- Some causes of memory problems can be improved with treatment (like thyroid problems, vitamin deficiencies, or depression).
- If you have Alzheimer’s disease or another type of dementia, medications may help with symptoms, but there is no cure yet.
- Staying physically active, socially engaged, and mentally stimulated may help maintain function.
- It’s important to plan ahead while you can make decisions. This includes choosing someone to make medical and financial decisions if needed, and discussing your wishes for future care.
- Safety is important. We’ll talk about driving, managing medications, and home safety.
- Caregivers need support too. The Alzheimer’s Association (1-800-272-3900, alz.org) has resources for patients and families.
- Keep a list of all medications and bring it to every appointment. Some medications can worsen memory—always check before starting something new.
- Call us if you notice sudden changes in thinking or behavior, new symptoms like weakness or trouble walking, or if you’re struggling to manage at home.
Smartphrase snippets#
.COGNITIVEEVAL
Cognitive evaluation in [age]-year-old. Chief complaint: [memory loss / family concern / functional decline]. Duration [X months/years]. Progression: [gradual / stepwise / rapid]. Domains affected: [memory / language / executive / visuospatial]. Functional status: IADLs [intact / impaired - specify]; BADLs [intact / impaired]. Behavioral symptoms: [none / depression / anxiety / hallucinations / agitation]. MoCA score: [X]/30. PHQ-9: [X]. Neurologic exam: [normal / findings]. Labs: [pending / results]. Assessment: [MCI / probable Alzheimer’s / vascular dementia / other]. Plan: [Labs / imaging / referral / medication / safety assessment / advance care planning discussion]. Follow-up in [X weeks/months].
.DEMENTIADIAGNOSIS
Diagnosis of [Alzheimer’s disease / vascular dementia / mixed dementia] discussed with patient and [family member]. Explained that this is a progressive condition affecting memory and thinking. Discussed that medications may help symptoms but do not cure or stop progression. Reviewed safety concerns: [driving / firearms / wandering / finances / medication management]. Advance care planning discussed; [patient has / will complete] healthcare proxy and advance directive. Caregiver [name] present; provided Alzheimer’s Association resources. Started [donepezil 5 mg daily / other]. Follow-up in [4-6 weeks] to assess tolerance, then [3-6 months] ongoing.
.MCIFOLLOW
MCI follow-up. Patient reports [stable / worsening] symptoms. Functional status: IADLs remain [intact / specify changes]. MoCA today: [X]/30 (previous [X]). No new safety concerns. Reinforced lifestyle recommendations: exercise, cognitive engagement, social activity, cardiovascular risk management. Not starting cholinesterase inhibitor at this time (not indicated for MCI). Will repeat cognitive testing in [6-12 months]. Return sooner if functional decline or new symptoms.
Related pages#
- Dementia (problem) — ongoing management of diagnosed dementia
- Delirium — acute confusion vs chronic decline
- Depression — pseudodementia vs dementia
- Falls (geriatric) — cognitive impairment increases fall risk
- Polypharmacy — medication-induced cognitive impairment
- Frailty (problem) — cognitive frailty and functional decline
Coding/billing notes#
- G31.84: Mild cognitive impairment
- G30.9: Alzheimer’s disease, unspecified
- G30.0: Alzheimer’s disease with early onset (<65)
- G30.1: Alzheimer’s disease with late onset (≥65)
- F01.50: Vascular dementia without behavioral disturbance
- F01.51: Vascular dementia with behavioral disturbance
- G31.83: Lewy body dementia
- G31.09: Frontotemporal dementia
- G91.2: Normal pressure hydrocephalus
- F32.9: Major depressive disorder (if depression causing cognitive symptoms)
- R41.81: Age-related cognitive decline (normal aging)
Annual Wellness Visit cognitive assessment:
- Required component of Medicare AWV
- Document structured assessment performed
- Can use any validated tool (Mini-Cog, MoCA, etc.)
Advance care planning billing:
- 99497: First 30 minutes of ACP discussion
- 99498: Each additional 30 minutes
- Document time spent and topics discussed