Geriatrics

Every syndrome, assessment tool, prescribing principle, classification system, functional measure, ethical framework, and management strategy in geriatric medicine in one place.

01 Physiology of Aging

Aging produces predictable physiological changes across every organ system. These changes reduce physiological reserve and narrow the margin between baseline function and clinical decompensation. Understanding normal aging is essential to distinguishing disease from senescence and to anticipating how older adults respond differently to illness, medications, and surgery.

Cardiovascular Changes

The aged heart demonstrates increased left ventricular wall thickness (up to 30% increase by age 80), decreased diastolic compliance, and reduced maximal heart rate (estimated max HR = 220 − age). Arterial stiffening raises systolic blood pressure while diastolic pressure may decrease after age 60, widening pulse pressure. Cardiac output at rest is generally maintained, but maximal cardiac output declines ~1% per year after age 30. Baroreceptor sensitivity diminishes, predisposing to orthostatic hypotension (present in 20–30% of community-dwelling elders ≥65). The conduction system accumulates fibrosis and fat, increasing the prevalence of atrial fibrillation (10% by age 80) and sick sinus syndrome.

Pulmonary Changes

Chest wall compliance decreases (costal cartilage calcification, kyphosis), while lung compliance increases (loss of elastic recoil). FEV1 declines ~30 mL/year after age 30. Residual volume (RV) increases; vital capacity (VC) decreases. FRC and closing capacity converge, leading to airway closure during tidal breathing (particularly in the supine position), which creates ventilation-perfusion mismatch and reduces PaO2. Expected PaO2 ≈ 104 − (0.27 × age) mmHg. Mucociliary clearance slows, and the cough reflex weakens, increasing aspiration pneumonia risk.

Renal Changes

Renal mass decreases ~25–30% by age 80, primarily from cortical nephron loss. GFR declines approximately 1 mL/min/1.73 m² per year after age 40, even without hypertension or diabetes. Serum creatinine may remain normal despite reduced GFR because of decreased muscle mass (reduced creatinine production). The Cockcroft-Gault equation [(140 − age) × weight / (72 × Cr) × 0.85 if female] or CKD-EPI is essential for dosing adjustments. Tubular concentrating ability declines, reducing the ability to conserve sodium and water — older adults are more susceptible to dehydration and hyponatremia.

Neurological Changes

Brain weight declines ~5% per decade after age 40. Cerebral blood flow decreases ~20% by age 80. Processing speed slows, and short-term memory mildly declines, but crystallized intelligence (vocabulary, general knowledge) is preserved. Deep tendon reflexes may diminish; ankle jerks may be absent. Vibratory sensation in the feet decreases. Sleep architecture shifts: total sleep time decreases, sleep latency increases, Stage N3 (slow-wave sleep) decreases, and nighttime awakenings increase.

Lateral view of the brain showing frontal, parietal, temporal, and occipital lobes
Figure 1 — Brain Lobes. The aging brain loses volume primarily in the frontal and temporal lobes. Hippocampal atrophy correlates with memory decline and is an early feature of Alzheimer disease. Source: Wikimedia Commons. Licensed under CC BY-SA 3.0.

Musculoskeletal Changes

Muscle mass declines ~3–8% per decade after age 30 (sarcopenia). Type II (fast-twitch) muscle fibers are preferentially lost, reducing power and increasing fall risk. Bone mineral density peaks at age 25–30 and then declines ~0.5–1% per year; in postmenopausal women, loss accelerates to 2–3% per year for the first 5–10 years. Joint cartilage thins, and intervertebral discs lose water content, contributing to height loss (~1 cm per decade after age 40).

Hepatic & GI Changes

Hepatic blood flow decreases ~40–45% by age 65, reducing first-pass metabolism. Phase I metabolism (CYP450 oxidation) declines, while Phase II (conjugation) is relatively preserved. Gastric acid production may decrease (achlorhydria in ~30% of those >80). Colonic transit time increases, contributing to constipation (reported in 30–50% of community-dwelling elders).

Immune System — Immunosenescence

Thymic involution begins in puberty; by age 60–70, the thymus is largely replaced by fat. Naïve T-cell production declines, and the T-cell repertoire narrows. Vaccine response is attenuated — influenza vaccine efficacy drops from 70–90% in young adults to 30–40% in those ≥65 (hence high-dose and adjuvanted formulations). Chronic low-grade inflammation ("inflammaging") contributes to atherosclerosis, sarcopenia, and frailty.

Normal aging reduces reserve but does not cause disease. New-onset incontinence, falls, confusion, or functional decline should never be attributed to "just old age" — each warrants a thorough workup.

02 Comprehensive Geriatric Assessment

The Comprehensive Geriatric Assessment (CGA) is the cornerstone of geriatric medicine — a multidimensional, interdisciplinary diagnostic process to determine an older person's medical, psychological, social, and functional capabilities and to develop a coordinated care plan. Randomized trials show CGA improves survival, function, and rates of living at home versus usual care (meta-analysis: NNT ~12 to prevent one death or institutional placement at 12 months).

CGA Domains

DomainAssessment ToolsKey Elements
Functional statusKatz ADL, Lawton IADL, Barthel IndexBathing, dressing, toileting, transfers, continence, feeding; shopping, cooking, finances, medications, transportation
CognitionMMSE, MoCA, Mini-Cog, Clock DrawMemory, orientation, executive function, language, visuospatial
MoodGDS-15, PHQ-9, Cornell ScaleDepression, anxiety, apathy, suicidal ideation
Mobility & balanceTimed Up and Go (TUG), Berg Balance Scale, 4-Stage Balance, gait speedFall risk, assistive device use, lower-extremity strength
NutritionMNA (Mini Nutritional Assessment), BMI, albumin, prealbuminWeight loss, appetite, dentition, dysphagia screening
PolypharmacyBeers criteria, STOPP/START, medication reconciliationNumber of medications, high-risk drugs, adherence, OTC/supplements
SocialSocial history, caregiver assessmentLiving situation, caregiver burden (Zarit), financial resources, social isolation
SensoryWhisper test, Snellen chart, otoscopyVision (cataracts, macular degeneration), hearing (presbycusis)
Advance care planningAdvance directive reviewHealthcare proxy, POLST, code status, goals of care
The CGA identifies problems missed by standard medical evaluation in 50–75% of cases. The five "geriatric giants" first described by Bernard Isaacs: immobility, instability (falls), incontinence, intellectual impairment (dementia/delirium), and iatrogenesis (polypharmacy/ADRs).

Screening Tools at a Glance

ToolTimeCut-offUse
Mini-Cog3 min≤2 of 5 (3-word recall + clock) = positiveRapid dementia screen
MoCA10 min<26/30 = cognitive impairmentDetects MCI (more sensitive than MMSE)
MMSE7–10 min<24/30 = dementia likelyClassic cognitive screen; ceiling effect
GDS-155 min≥5 = depression likelyYes/no format; avoids somatic symptoms
TUG1 min≥12 sec = high fall riskRise from chair, walk 3 m, turn, return, sit
Gait speed1 min<0.8 m/s = mobility limitationSingle best predictor of disability and mortality in elders
Gait speed has been called the "sixth vital sign" in geriatrics. Gait speed <0.8 m/s predicts falls, disability, hospitalization, and death. Gait speed <0.6 m/s predicts inability to cross a street in one traffic-light cycle.

03 Key Terminology & Abbreviations

Geriatric medicine relies on specific terminology for syndromes, functional measures, prescribing frameworks, and care settings. Mastering these terms is essential for communicating across the multidisciplinary team.

AbbreviationMeaning
CGAComprehensive geriatric assessment
ADL / IADLActivities of daily living / instrumental ADLs
MMSE / MoCAMini-Mental State Examination / Montreal Cognitive Assessment
GDSGeriatric Depression Scale
CDRClinical Dementia Rating
CAMConfusion Assessment Method (delirium)
TUGTimed Up and Go test
BBSBerg Balance Scale
MNAMini Nutritional Assessment
FRAXFracture Risk Assessment Tool
DXADual-energy X-ray absorptiometry
AGSAmerican Geriatrics Society
STOPP/STARTScreening Tool of Older Persons' Prescriptions / Screening Tool to Alert to Right Treatment
ACBAnticholinergic Cognitive Burden scale
POLST / MOLSTPhysician Orders for Life-Sustaining Treatment / Medical Orders for LST
SNFSkilled nursing facility
ALFAssisted living facility
FIMFunctional Independence Measure
LCDLocal Coverage Determination (hospice eligibility)
ACPAdvance care planning
HCPHealthcare proxy
DNR / DNIDo not resuscitate / do not intubate
BPSDBehavioral and psychological symptoms of dementia
PIMPotentially inappropriate medication
ADRAdverse drug reaction
CFSClinical Frailty Scale
ACS-NSQIPAmerican College of Surgeons National Surgical Quality Improvement Program

04 Dementia — Alzheimer Disease

Alzheimer disease (AD) accounts for 60–80% of all dementias. Prevalence doubles every 5 years after age 65 (1% at 65, 3% at 70, 6% at 75, 12% at 80, >30% at 85). It is characterized pathologically by extracellular amyloid-beta plaques and intraneuronal neurofibrillary tangles (hyperphosphorylated tau), beginning in the entorhinal cortex and hippocampus before spreading to neocortical areas.

Clinical Presentation

The earliest feature is episodic memory impairment (inability to learn and retain new information) — patients repeat questions and misplace items. Language difficulty (word-finding), visuospatial dysfunction (getting lost in familiar places), and executive dysfunction (impaired planning, judgment) follow. Progression is insidious over 8–12 years. Anosognosia (lack of awareness of deficits) is common and increases with severity.

Diagnosis

Diagnosis is clinical, supported by neuropsychological testing, structural imaging (MRI showing hippocampal & medial temporal lobe atrophy), and biomarkers. CSF biomarkers: decreased Aβ42 and elevated phospho-tau and total tau. Amyloid PET (florbetapir, flutemetamol) positive. FDG-PET shows temporoparietal hypometabolism. Labs to exclude reversible causes: TSH, B12, folate, CBC, CMP, RPR/VDRL, HIV (in appropriate populations).

Pharmacological Management

DrugClassDoseStageKey Points
Donepezil (Aricept)AChE inhibitor5 mg daily × 4–6 wk, then 10 mg daily; 23 mg daily for moderate-severeMild-moderate-severeGI side effects (nausea, diarrhea); bradycardia risk; vivid dreams
Rivastigmine (Exelon)AChE inhibitorPatch: 4.6 mg/24h → 9.5 mg/24h → 13.3 mg/24hMild-moderatePatch preferred (less GI effects); also approved for Parkinson dementia
Galantamine (Razadyne)AChE inhibitor4 mg BID → 8 mg BID → 12 mg BIDMild-moderateAlso modulates nicotinic receptors
Memantine (Namenda)NMDA antagonist5 mg daily → 10 mg BID (target 20 mg/day)Moderate-severeCan combine with AChE inhibitor; renal dose adjustment at CrCl <30
Memantine/donepezil (Namzaric)Combination28 mg/10 mg dailyModerate-severeConvenience; take at bedtime
Cholinesterase inhibitors provide modest symptomatic benefit (average 2–4 point improvement on ADAS-Cog over 6 months) but do not alter disease progression. They should be continued as long as the patient derives clinical benefit. Abrupt withdrawal can cause rapid cognitive decline that may not recover upon re-initiation.

Non-Pharmacological Management

Structured daily routines, cognitive stimulation therapy, physical exercise (150 min/week moderate aerobic activity associated with slowed decline), caregiver education and support, adult day programs, and environmental safety modifications (remove throw rugs, install grab bars, door alarms for wandering). Music therapy and reminiscence therapy can reduce agitation.

NIA-AA DIAGNOSTIC CRITERIA FOR AD (2011)

Probable AD dementia: (1) Insidious onset; (2) Clear history of worsening cognition; (3) Initial and most prominent deficits in one of: amnestic presentation (most common), nonamnestic (language, visuospatial, or executive); (4) No evidence of other dementia etiology. Biomarker support: Positive amyloid (CSF Aβ42 low or amyloid PET positive) + positive neurodegeneration markers (CSF tau elevated, FDG-PET temporoparietal hypometabolism, MRI hippocampal atrophy).

05 Vascular, Lewy Body & Frontotemporal Dementias

Vascular Dementia (VaD)

Second most common cause (~15–20% of dementias). Caused by cerebrovascular disease — large-vessel strokes, small-vessel ischemia (lacunar infarcts, white matter disease), or hemorrhagic events. Classic features: stepwise decline (sudden worsening with new vascular events), executive dysfunction prominent (planning, organization, processing speed impaired more than memory), focal neurological signs (gait abnormality, pseudobulbar affect, urinary urgency). Imaging shows multi-infarct pattern or extensive white matter hyperintensities (Fazekas grade 2–3). Management: secondary stroke prevention (antihypertensives, statins, antiplatelets), control vascular risk factors. AChE inhibitors have limited evidence but are sometimes used.

Dementia with Lewy Bodies (DLB)

Third most common dementia (~5–10%). Core features (2 of 4 = probable DLB): (1) Fluctuating cognition with pronounced variations in attention and alertness; (2) Recurrent visual hallucinations (typically well-formed, detailed — people, animals); (3) REM sleep behavior disorder (acting out dreams, may precede cognitive symptoms by years); (4) Spontaneous parkinsonism (bradykinesia, rigidity, rest tremor). Supportive features: severe neuroleptic sensitivity (can cause NMS or severe EPS), postural instability, repeated falls, autonomic dysfunction.

EMERGENCY — NEUROLEPTIC SENSITIVITY IN DLB

Patients with DLB are at extreme risk for severe, potentially fatal reactions to antipsychotics — including marked worsening of parkinsonism, NMS-like syndrome, and death. Avoid first-generation antipsychotics (haloperidol). If absolutely necessary for severe psychosis or agitation, use low-dose quetiapine (12.5–25 mg) or pimavanserin (34 mg daily, FDA-approved for Parkinson disease psychosis). Monitor closely.

Frontotemporal Dementia (FTD)

Onset typically age 45–65 (younger than AD). Three clinical variants: (1) Behavioral variant FTD (bvFTD) — the most common; early personality change, disinhibition, apathy, loss of empathy, compulsive behaviors, dietary changes (sweet-food craving), executive dysfunction with relative preservation of memory and visuospatial skills; (2) Semantic variant PPA — loss of word and object meaning, fluent but empty speech; (3) Nonfluent/agrammatic variant PPA — effortful, halting speech with grammatical errors. Imaging: frontal and/or temporal atrophy. Pick bodies (intraneuronal tau inclusions) in some cases. No disease-modifying treatment; SSRIs for behavioral symptoms; AChE inhibitors are NOT effective and may worsen behavior.

Key differentiator: AD typically presents with memory loss first, while bvFTD presents with personality and behavioral changes first, with relative sparing of memory in early stages. FTD onset is typically 10–20 years earlier than AD.

06 Delirium

Delirium is an acute, fluctuating disturbance in attention and awareness, with additional cognitive disturbance (memory, orientation, language, visuospatial, perception), that develops over hours to days and is caused by a medical condition, substance, or medication. It occurs in 10–30% of hospitalized older adults and up to 50–80% of ICU patients. It is independently associated with increased mortality (3-fold), prolonged hospitalization, increased institutionalization, and accelerated cognitive decline.

MEDICAL EMERGENCY — DELIRIUM

Delirium is a medical emergency signaling acute brain failure. Every new case of delirium demands an urgent search for the underlying cause. Common etiologies (mnemonic DELIRIUM): Drugs (anticholinergics, benzodiazepines, opioids, steroids); Electrolyte abnormalities (Na, Ca, glucose); Lack of drugs (withdrawal from alcohol, benzodiazepines); Infection (UTI, pneumonia, skin/soft tissue); Reduced sensory input (missing glasses/hearing aids); Intracranial pathology (stroke, SDH, meningitis); Urinary/fecal retention; Myocardial/pulmonary (MI, PE, hypoxia).

Confusion Assessment Method (CAM)

The CAM is the most widely used bedside delirium screening tool (sensitivity 94%, specificity 89%). Diagnosis requires both of:

(1) Acute onset and fluctuating course — Is there evidence of an acute change in mental status from baseline? Does the abnormal behavior fluctuate during the day?

(2) Inattention — Does the patient have difficulty focusing attention (e.g., easily distracted, difficulty keeping track of what is being said)?

Plus one or more of:

(3) Disorganized thinking — Rambling or irrelevant conversation, illogical flow of ideas, unpredictable switching between subjects.

(4) Altered level of consciousness — Anything other than "alert" (vigilant, lethargic, stuporous, comatose).

Delirium Subtypes

SubtypePrevalenceFeaturesPrognosis
Hyperactive~25%Agitation, restlessness, hallucinations, pulling at lines/tubes, combativenessBetter recognized; generally better prognosis
Hypoactive~50%Lethargy, withdrawal, decreased responsiveness, apathy, reduced movementOften missed (mistaken for depression or fatigue); worse prognosis
Mixed~25%Features of both; fluctuates between hyperactive and hypoactive statesIntermediate prognosis
Hypoactive delirium is the most common subtype but is frequently unrecognized because the "quiet, sleepy" patient does not draw clinical attention. It carries the worst prognosis. Always screen actively using CAM, especially in post-operative elderly patients.

Prevention — HELP Protocol

The Hospital Elder Life Program (HELP) reduces delirium incidence by ~40% (NNT = 6). Key components: (1) Frequent reorientation (calendar, clock, familiar objects); (2) Non-pharmacologic sleep protocol (warm milk, massage, noise reduction, avoid nighttime vitals); (3) Early mobilization; (4) Vision and hearing aids provided; (5) Hydration and nutrition; (6) Avoid deliriogenic medications (benzodiazepines, anticholinergics, meperidine).

Delirium Workup

Systematic evaluation for every new case: (1) Medications review — recent additions, dose changes, or discontinuations (especially opioids, benzodiazepines, anticholinergics, steroids, fluoroquinolones); (2) Infection — CBC, UA with culture, CXR, blood cultures if febrile; (3) Metabolic — BMP (Na, Ca, glucose, BUN/Cr), hepatic panel, TSH; (4) Cardiac/pulmonary — ECG, troponin (if indicated), pulse oximetry, ABG if hypoxic; (5) Urinary/fecal — assess for retention (bladder scan) and impaction; (6) CNS — CT head (if focal signs, on anticoagulation, or history of fall/trauma); lumbar puncture if meningitis suspected; (7) Substance — alcohol level, urine drug screen if appropriate.

Management

First line: Treat the underlying cause. Non-pharmacological interventions (reorientation, de-escalation, family presence, minimize tethers). Pharmacological (only for severe agitation with risk of harm): Haloperidol 0.5–1 mg PO/IM q4h PRN (avoid IV — QTc risk); alternative: olanzapine 2.5–5 mg PO/IM. Avoid benzodiazepines (worsen delirium) except in alcohol/benzodiazepine withdrawal and DLB/Parkinson patients (avoid antipsychotics). Dexmedetomidine for ICU delirium.

Delirium vs Dementia vs Depression

FeatureDeliriumDementiaDepression
OnsetAcute (hours to days)Insidious (months to years)Weeks to months
CourseFluctuatingProgressiveDiurnal variation (worse AM)
AttentionImpaired (core feature)Intact until late stagesIntact but may lack effort
ConsciousnessAltered (clouded)Clear until lateClear
HallucinationsCommon (visual)Less common (except DLB)Rare
ReversibilityUsually reversibleIrreversible (mostly)Treatable
PsychomotorHyper- or hypoactiveNormal until lateRetarded (or agitated)

07 Depression & Behavioral Disturbances

Late-Life Depression

Major depression affects 1–5% of community-dwelling elders but 10–15% of hospitalized elderly and up to 25–50% of nursing home residents. Late-life depression often presents differently than in younger adults: somatic complaints predominate (fatigue, pain, GI symptoms, weight loss), cognitive dysfunction is prominent ("pseudodementia" — depressive cognitive impairment that improves with treatment), and patients may deny feeling "sad" but endorse hopelessness, worthlessness, or loss of interest. Suicide risk is highest in white men ≥85 years (rate 4× the national average).

Geriatric Depression Scale (GDS-15)

ScoreInterpretation
0–4Normal, no depression
5–8Mild depression
9–11Moderate depression
12–15Severe depression

Treatment: SSRIs are first-line (sertraline 25–50 mg starting dose, target 100–200 mg; escitalopram 5 mg starting, target 10–20 mg). Avoid TCAs in elderly (anticholinergic burden, orthostatic hypotension, cardiac conduction delays). Mirtazapine (7.5–30 mg at bedtime) is useful when insomnia and weight loss are prominent. Bupropion (100–300 mg/day) avoids sexual side effects and sedation; avoid if seizure risk. SNRIs (duloxetine 30–60 mg, venlafaxine 75–225 mg) are helpful with comorbid chronic pain. Start low, go slow — but titrate to adequate dose. Response may take 6–12 weeks in elderly (longer than younger adults).

Behavioral & Psychological Symptoms of Dementia (BPSD)

BPSD affect up to 90% of dementia patients at some point. Includes agitation, aggression, wandering, sundowning, sleep-wake cycle disruption, psychosis (delusions, hallucinations), apathy, and disinhibition.

Management approach: (1) Rule out underlying cause (pain [use PAINAD scale in nonverbal patients], infection, constipation, urinary retention, medication side effect); (2) Non-pharmacological interventions first (music therapy, aromatherapy, structured activities, reduce environmental stimulation, caregiver training — DICE approach: Describe, Investigate, Create, Evaluate); (3) Pharmacological only if non-pharmacological fails and patient is danger to self/others.

FDA BLACK BOX WARNING — ANTIPSYCHOTICS IN DEMENTIA

All antipsychotics (typical and atypical) carry an FDA black box warning for increased mortality in elderly patients with dementia-related psychosis (1.6–1.7× increased risk of death, primarily from cardiovascular events and infections). Use only when benefits clearly outweigh risks, with informed consent, and frequent reassessment for discontinuation.

08 Falls Assessment & Prevention

Falls are the leading cause of injury, injury-related death, and emergency department visits in adults ≥65. One-third of community-dwelling elders and two-thirds of nursing home residents fall each year. Of those who fall, 20–30% suffer moderate to severe injury (hip fractures, subdural hematomas, lacerations). Fall-related costs in the US exceed $50 billion annually.

Risk Factors for Falls

IntrinsicExtrinsicSituational
Gait/balance impairmentThrow rugs, clutterRushing to the bathroom
Lower-extremity weaknessPoor lightingReaching overhead
Visual impairmentLack of grab bars/handrailsClimbing on chairs/ladders
Orthostatic hypotensionSlippery surfacesCarrying heavy objects
Cognitive impairmentIll-fitting shoesAlcohol use
Medications (sedatives, antihypertensives, ≥4 meds)Stairs without railingsUnfamiliar environments
Peripheral neuropathyUneven surfacesAcute illness
Arthritis, foot disordersRestraints (increase fall risk)Post-prandial hypotension

Falls Assessment Tools

TestMethodInterpretation
Timed Up and Go (TUG)Rise from armchair, walk 3 meters, turn, walk back, sit<10 sec = normal; 10–12 sec = borderline; ≥12 sec = high fall risk; ≥20 sec = significant mobility impairment
Berg Balance Scale (BBS)14-item test of static and dynamic balance (0–56 points)<45 = increased fall risk; <36 = nearly 100% fall risk
30-Second Chair StandNumber of sit-to-stand repetitions in 30 secondsBelow age-sex norms = weakness
4-Stage Balance TestFeet together → semi-tandem → tandem → single-leg stand (10 sec each)Inability to hold tandem for 10 sec = increased fall risk
Morse Fall Scale (hospital)6-item scale: history of falls, secondary diagnosis, ambulatory aid, IV/heparin lock, gait, mental status0–24 = low risk; 25–50 = moderate; ≥51 = high risk

Multifactorial Fall Prevention

Exercise programs are the single most effective intervention (NNT ~10 to prevent 1 fall). Tai Chi reduces falls by 20–40%. The Otago Exercise Programme (strength + balance exercises, 3×/week + walking 2×/week) reduces falls by 35%. Additional interventions: medication review (withdraw sedatives, reduce antihypertensives if orthostatic), home safety assessment, vision correction, vitamin D supplementation (≥800 IU/day if deficient), management of orthostatic hypotension, footwear assessment, and physical therapy referral.

AGS/BGS guidelines (2022) recommend asking all patients ≥65 about falls annually. A single fall with gait/balance problem, or ≥2 falls in the past year, should trigger a multifactorial fall risk assessment.

09 Gait Disorders & Assistive Devices

Common Gait Patterns in the Elderly

Gait TypeDescriptionCommon Causes
Antalgic gaitShort stance phase on affected side; limping to minimize painArthritis, hip fracture, foot pathology
Parkinsonian gaitShort shuffling steps, reduced arm swing, flexed posture, festination, difficulty initiating movement, en bloc turningParkinson disease, vascular parkinsonism, DLB
Frontal/apraxic gaitWide-based, magnetic (feet "glued to floor"), short steps, difficulty initiating gait, relatively preserved leg strength in bedNormal pressure hydrocephalus (triad: gait, incontinence, dementia), frontal lobe lesions
Cerebellar ataxic gaitWide-based, irregular steps, unsteady, difficulty with tandem gaitCerebellar stroke/degeneration, alcohol, phenytoin toxicity
Sensory ataxic gaitWide-based, high-stepping, positive Romberg sign (worsens with eyes closed)B12 deficiency (subacute combined degeneration), peripheral neuropathy, posterior column disease
Steppage gaitHigh-stepping to avoid dragging foot; foot drop with foot slapPeroneal nerve palsy, L5 radiculopathy, peripheral neuropathy
Waddling gaitTrunk sways side-to-side; Trendelenburg sign positiveProximal myopathy, bilateral hip OA

Assistive Device Selection

DeviceSupport LevelIndicationsKey Points
Standard cane~25% body weight offloadMild balance impairment, unilateral weaknessHold in contralateral hand; top should align with wrist crease
Quad cane (small/large base)~25% with greater stabilityModerate balance impairment, mild hemiparesisMore stable than standard cane; slower gait
Standard walker~50% body weightSignificant bilateral weakness or balance impairmentMust be lifted with each step; requires upper-extremity strength
Front-wheeled walker~50% with easier advancementPatients who cannot lift standard walker; parkinsonian gaitWheels allow continuous forward motion
Rollator (4-wheeled walker)~25% with seat for restEndurance limitations, need for seated restBrake locks essential; less stable than standard walker
WheelchairFull supportNon-ambulatory or severely limited enduranceProper fit critical; pressure relief cushion; consider power wheelchair if upper extremity weakness

10 Hip Fractures

Hip fractures are a geriatric emergency. Over 300,000 occur annually in the US, with 95% in patients ≥65. One-year mortality is 20–30% (higher in men: 37% vs 20% in women). Only 40–60% regain pre-fracture mobility, and 10–20% require long-term institutionalization. Median age at fracture is 80 years.

Classification

TypeLocationBlood SupplyTreatment
Femoral neck (intracapsular)Between femoral head and intertrochanteric lineDisrupted (medial femoral circumflex artery) — high AVN riskNon-displaced: internal fixation with screws. Displaced: hemiarthroplasty (≥65 yr, low-demand) or total hip arthroplasty (active, independent)
Intertrochanteric (extracapsular)Between greater and lesser trochanterPreserved — low AVN riskSliding hip screw (stable patterns) or intramedullary nail (unstable patterns)
SubtrochantericBelow lesser trochanter (within 5 cm)PreservedIntramedullary nail; consider atypical fracture (bisphosphonate-related) if lateral cortex thickening present
EMERGENCY — HIP FRACTURE MANAGEMENT

Time to surgery: Operate within 24–48 hours of presentation (delays >48 hours associated with increased mortality, pulmonary complications, and pressure injuries). Preoperative: crossmatch, ECG, CXR, CBC, BMP, coagulation studies. Hold anticoagulation per protocol. DVT prophylaxis from admission (LMWH or fondaparinux if not on therapeutic anticoagulation). Pain control: fascia iliaca block preferred over systemic opioids; acetaminophen 1 g q6h scheduled. Early mobilization post-op (day 1). Orthogeriatric co-management reduces 30-day mortality by 5–7%.

Diagram showing femoral neck, intertrochanteric, and subtrochanteric hip fracture locations
Figure 2 — Hip Fracture Classification. The three major types of hip fracture based on anatomical location: femoral neck (intracapsular), intertrochanteric (extracapsular), and subtrochanteric. Intracapsular fractures disrupt blood supply to the femoral head, increasing avascular necrosis risk. Source: Wikimedia Commons. Public domain.
Every hip fracture patient should be evaluated for osteoporosis and started on treatment before discharge (calcium, vitamin D, and anti-resorptive therapy). Only 20–30% of hip fracture patients receive osteoporosis treatment within 6 months of fracture — a critical care gap.

11 Osteoporosis

Osteoporosis is defined by the WHO as a DXA T-score ≤−2.5 at the lumbar spine, femoral neck, or total hip. Prevalence: ~25% of women and ~5% of men ≥65. Osteoporosis is responsible for >2 million fractures annually in the US (vertebral compression fractures most common, followed by hip and distal radius fractures).

WHO Diagnostic Criteria (DXA T-score)

T-scoreClassification
≥−1.0Normal
−1.0 to −2.5Osteopenia (low bone mass)
≤−2.5Osteoporosis
≤−2.5 with fragility fractureSevere (established) osteoporosis

FRAX Tool

The FRAX (Fracture Risk Assessment Tool) calculates 10-year probability of major osteoporotic fracture and hip fracture using age, sex, BMI, prior fracture, parental hip fracture, smoking, alcohol (≥3 units/day), glucocorticoids, rheumatoid arthritis, secondary osteoporosis, and femoral neck BMD. Treatment thresholds (US NOF): ≥20% 10-year risk of major osteoporotic fracture OR ≥3% 10-year risk of hip fracture.

Screening Recommendations

USPSTF: DXA screening for all women ≥65 and younger postmenopausal women with risk factors (FRAX equivalent of a 65-year-old white woman). Men: screen at ≥70 or earlier with risk factors (glucocorticoid use, low body weight, prior fracture, hypogonadism).

Pharmacological Treatment

DrugClassDoseKey Points
Alendronate (Fosamax)Oral bisphosphonate70 mg weeklyTake fasting with 8 oz water, remain upright 30 min; esophagitis risk; drug holiday after 5 years if low-risk
Risedronate (Actonel)Oral bisphosphonate35 mg weekly or 150 mg monthlySimilar to alendronate; delayed-release formulation taken after breakfast
Zoledronic acid (Reclast)IV bisphosphonate5 mg IV once yearlyPreferred if GI intolerance to oral; hydrate before infusion; acute phase reaction (flu-like) in 30%
Denosumab (Prolia)RANKL inhibitor60 mg SQ q6 monthsNo renal contraindication; rebound vertebral fractures if discontinued — must transition to bisphosphonate
Teriparatide (Forteo)PTH analog (anabolic)20 mcg SQ daily × 2 yearsFor severe osteoporosis; black box: osteosarcoma in rats (avoid if Paget or radiation history); follow with antiresorptive
Romosozumab (Evenity)Sclerostin inhibitor (anabolic)210 mg SQ monthly × 12 monthsDual action (builds and prevents resorption); black box: MI/stroke risk; avoid if recent CV event; follow with antiresorptive

All patients should receive calcium 1,000–1,200 mg/day (diet + supplement) and vitamin D 800–1,000 IU/day (target 25(OH)D ≥30 ng/mL). Weight-bearing exercise and fall prevention are essential non-pharmacological measures.

12 Sarcopenia & Frailty

Sarcopenia

Sarcopenia is the progressive, age-related loss of skeletal muscle mass and function. The EWGSOP2 (2019) definition requires: (1) Low muscle strength (grip strength <27 kg men, <16 kg women; or chair stand >15 sec for 5 rises) for probable sarcopenia; (2) Low muscle quantity (appendicular skeletal muscle mass index by DXA: <7.0 kg/m² men, <5.5 kg/m² women) to confirm; (3) Low physical performance (gait speed <0.8 m/s, SPPB ≤8, TUG ≥20 sec) indicates severe sarcopenia. Prevalence: 5–13% in 60–70 year-olds, 11–50% in those ≥80. Treatment: resistance exercise (most effective), adequate protein intake (1.0–1.2 g/kg/day, ideally 25–30 g per meal), vitamin D supplementation if deficient.

Frailty

Frailty is a clinical syndrome of decreased physiological reserve and increased vulnerability to stressors (illness, surgery, medications), leading to disproportionate adverse outcomes. Two major conceptualizations:

Fried Frailty Phenotype (Physical Frailty)

≥3 of 5 criteria = frail; 1–2 = pre-frail; 0 = robust:

#CriterionMeasurement
1Unintentional weight loss≥10 lbs (4.5 kg) or ≥5% body weight in past year
2Self-reported exhaustionCES-D scale: "everything was an effort" or "could not get going" ≥3 days/week
3Low physical activityLowest quintile of kcal/week expended (men <383 kcal/wk, women <270 kcal/wk)
4Slow walking speedLowest quintile for height (<0.65–0.76 m/s depending on sex and height)
5Weakness (grip strength)Lowest quintile adjusted for sex and BMI

Clinical Frailty Scale (Rockwood, 9-point)

ScoreCategoryDescription
1Very fitRobust, active, energetic, well-motivated, exercises regularly
2FitNo active disease symptoms but less fit than category 1
3Managing wellMedical problems well controlled; not regularly active beyond walking
4Living with very mild frailtyNot dependent but slowed down; symptoms limit activities
5Living with mild frailtyMore evident slowing; needs help with IADLs (finances, transportation, heavy housework)
6Living with moderate frailtyNeeds help with all outside activities and housekeeping; problems with stairs; may need help with bathing
7Living with severe frailtyCompletely dependent for ADLs; stable, not at high risk of dying within 6 months
8Very severely frailCompletely dependent; approaching end of life; could not recover from minor illness
9Terminally illApproaching end of life; life expectancy <6 months; not otherwise evidently frail
Frailty is a stronger predictor of surgical complications and mortality than age alone. The CFS is increasingly used for pre-operative risk stratification (CFS ≥5 associated with 2–3× increased 30-day mortality after major surgery). Frailty is potentially reversible in early stages with exercise, nutrition, and medical optimization.

13 Beers Criteria & High-Risk Medications

The AGS Beers Criteria (updated 2023) is the most widely referenced list of potentially inappropriate medications (PIMs) in older adults (≥65). Polypharmacy (≥5 medications) affects >40% of community-dwelling elders and >90% of nursing home residents. The risk of adverse drug reactions (ADRs) increases roughly linearly with the number of medications: 5 drugs = ~50% risk of drug interaction; 8+ drugs = ~100% risk.

Key Beers Criteria Categories (Selected High-Yield)

Drug/ClassConcern in ElderlyRecommendation
Benzodiazepines (all)Cognitive impairment, delirium, falls, fractures, motor vehicle accidentsAvoid for insomnia, agitation, or delirium (use for seizures, alcohol withdrawal, anesthesia only)
Non-benzo hypnotics (zolpidem, eszopiclone)Similar risks to benzodiazepines; minimal improvement in sleep latencyAvoid
Anticholinergics (1st-gen antihistamines: diphenhydramine, hydroxyzine; antispasmodics: oxybutynin, tolterodine)Confusion, constipation, urinary retention, dry mouth, blurred vision, delirium, cognitive declineAvoid; use 2nd-gen antihistamines; for OAB, use mirabegron or vibegron instead
NSAIDs (chronic use)GI bleeding (risk 2–4× increased), renal failure, fluid retention, HTN exacerbationAvoid chronic use; short course only with PPI; topical NSAIDs preferred
Sulfonylureas (glyburide, chlorpropamide)Prolonged hypoglycemia (especially glyburide — long half-life, active metabolites)Avoid glyburide; use glipizide or glimepiride if SU needed; target A1c 7.5–8.5% in frail elders
Meperidine (Demerol)Neurotoxic metabolite (normeperidine) causes seizures; poor analgesic in elderlyAvoid completely
MetoclopramideExtrapyramidal symptoms, tardive dyskinesia (risk increases with duration)Avoid unless gastroparesis; limit to ≤12 weeks
Sliding scale insulin (sole therapy)Higher risk of hypoglycemia without improved glycemic controlAvoid as sole strategy; use basal insulin with correction scale
Alpha-blockers for HTN (doxazosin, prazosin, terazosin)Orthostatic hypotension, syncope, fallsAvoid for hypertension; acceptable for BPH
Skeletal muscle relaxants (cyclobenzaprine, methocarbamol, carisoprodol)Sedation, anticholinergic effects, falls; poorly toleratedAvoid
The "prescribing cascade" occurs when a side effect of one drug is misinterpreted as a new medical condition, leading to prescription of an additional drug. Example: NSAID causes hypertension → antihypertensive added → antihypertensive causes dizziness → meclizine added. Always ask: "Is this new symptom a drug side effect?" before adding a new medication.

14 STOPP/START Criteria

The STOPP/START criteria (version 3, 2023) complement the Beers list with a European evidence-based approach. STOPP (Screening Tool of Older Persons' Prescriptions) identifies PIMs to stop; START (Screening Tool to Alert to Right Treatment) identifies beneficial medications that are commonly omitted in older adults.

Selected STOPP Criteria (Medications to Discontinue)

CriterionRationale
PPI beyond 8 weeks without indication (ulcer, GERD, Barrett)C. difficile risk, hypomagnesemia, hip fracture, B12 deficiency
Long-acting benzodiazepine (diazepam, chlordiazepoxide, flurazepam)Prolonged sedation, falls, cognitive impairment
Duplicate drug classes (e.g., 2 SSRIs, 2 ACE inhibitors)No added benefit; increased side effects
Anticholinergic drugs in patients with dementiaWorsens cognitive function
Aspirin for primary prevention in ≥70 without established CVDBleeding risk exceeds benefit (ASPREE trial)
Beta-blockers with verapamil or diltiazemRisk of heart block and severe bradycardia
Theophylline as monotherapy for COPDNarrow therapeutic index; safer alternatives exist

Selected START Criteria (Medications to Consider Starting)

CriterionRationale
Statin in diabetes with major CV risk factorCardiovascular risk reduction
ACE-I/ARB in heart failure with reduced EFMortality reduction; frequently underused in elderly
Bone protection (bisphosphonate + calcium/vitamin D) if on chronic steroidsGlucocorticoid-induced osteoporosis prevention
Pneumococcal, influenza, herpes zoster vaccinesPreventable infections; frequently omitted
Topical prostaglandin for open-angle glaucomaFirst-line treatment; prevents vision loss
Beta-blocker post-MISecondary prevention of MI; mortality benefit
SSRI/SNRI for moderate-severe depressionUntreated depression increases morbidity and mortality

15 Deprescribing & Adverse Drug Reactions

Deprescribing Principles

Deprescribing is the planned, supervised process of dose reduction or stopping medications that are no longer beneficial or may be causing harm. It is not simply "stopping medications" — it requires a systematic approach:

(1) Ascertain all medications (prescription, OTC, supplements, herbals); (2) Identify potentially inappropriate medications using Beers/STOPP criteria and clinical judgment; (3) Determine whether each medication can be discontinued (consider indication, life expectancy, time-to-benefit, goals of care); (4) Plan withdrawal schedule (many drugs require gradual taper: benzodiazepines, SSRIs, beta-blockers, corticosteroids, opioids, gabapentinoids); (5) Monitor for withdrawal syndromes and disease recurrence.

Medications Requiring Gradual Taper

Drug ClassWithdrawal RiskTaper Strategy
BenzodiazepinesSeizures, insomnia, anxiety, deliriumReduce by 10–25% every 1–2 weeks; slower if long-term use
SSRIs/SNRIsDiscontinuation syndrome (dizziness, nausea, paresthesias, irritability)Reduce by 25–50% every 2–4 weeks; paroxetine and venlafaxine highest risk
OpioidsWithdrawal syndrome (sweating, diarrhea, anxiety, pain flare)Reduce by 10% every 1–2 weeks
CorticosteroidsAdrenal insufficiency if >3 weeks of useTaper by 2.5–5 mg prednisone equivalent every 3–7 days
Beta-blockersRebound tachycardia, hypertension, anginaReduce by 25–50% every 1–2 weeks
PPIsRebound acid hypersecretionStep down to H2 blocker or half dose × 2–4 weeks, then stop

Adverse Drug Reactions in the Elderly

ADRs account for 5–10% of hospital admissions in older adults and occur 2–7× more frequently than in younger adults. The most common culprits: anticoagulants (bleeding), diuretics (electrolyte disturbances, falls), NSAIDs (GI bleed, renal failure), digoxin (toxicity), hypoglycemic agents, and psychotropics. Presentation is often atypical: confusion (anticholinergics), falls (sedatives, antihypertensives), incontinence (diuretics, cholinesterase inhibitors), constipation (opioids, calcium channel blockers), anorexia (digoxin, SSRIs).

When an older patient presents with a new symptom, always ask: "Could this be a drug side effect?" The most common ADR presentations in elderly: falls, confusion, constipation, urinary retention, and bleeding.

16 Renal Dosing & Anticholinergic Burden

Renal Dosing in the Elderly

Age-related GFR decline makes renal dose adjustment critical. Key drugs requiring adjustment in CKD:

DrugNormal DoseCrCl 30–60CrCl 15–30CrCl <15
Gabapentin300–600 mg TID200–700 mg BID100–300 mg daily100–300 mg post-HD
Metformin500–1000 mg BID500 mg BID (max)Avoid (eGFR <30)Contraindicated
Enoxaparin (treatment)1 mg/kg BIDStandard dose1 mg/kg dailyAvoid; use UFH
Dabigatran150 mg BID150 mg BID75 mg BIDAvoid
Memantine10 mg BIDStandard5 mg BID5 mg BID
Allopurinol300 mg daily200 mg daily100 mg daily100 mg QOD
Pregabalin150–300 mg BID75–150 mg BID25–75 mg daily25–75 mg post-HD

Anticholinergic Cognitive Burden (ACB) Scale

The ACB scale assigns points (1–3) to medications based on anticholinergic activity. A total ACB score ≥3 is associated with increased risk of cognitive decline, delirium, falls, hospitalization, and mortality. Each 1-point increase is associated with a 26% increase in mortality risk.

ACB ScoreLevelExamples
1 (possible anticholinergic)Serum anticholinergic activity but no known clinical effectFurosemide, metoprolol, ranitidine, trazodone, alprazolam, atenolol, prednisone
2 (definite anticholinergic — clinically relevant)Evidence of clinical anticholinergic effectsAmantadine, carbamazepine, cyproheptadine, loperamide, nortriptyline, pimozide
3 (definite anticholinergic — high potency)Strong anticholinergic effects; most dangerous in elderlyOxybutynin, tolterodine, amitriptyline, paroxetine, chlorpheniramine, diphenhydramine, hydroxyzine, olanzapine, clozapine, thioridazine, doxepin (>6 mg)
A practical rule: if total ACB ≥3, systematically review each ACB-3 drug for alternatives. For OAB, switch oxybutynin to mirabegron (beta-3 agonist, no anticholinergic activity). For insomnia, replace diphenhydramine with melatonin 0.5–3 mg or low-dose trazodone 25–50 mg. For depression, switch paroxetine to sertraline or escitalopram (ACB score 0).

17 Urinary Incontinence

Urinary incontinence affects 30–50% of community-dwelling women ≥65 and 15–30% of men ≥65. Prevalence exceeds 50% in nursing home residents. Despite being common, it is frequently underreported and under-treated. It is a major contributor to social isolation, depression, skin breakdown, falls (rushing to bathroom), and institutionalization.

Types of Urinary Incontinence

TypeMechanismPresentationCommon CausesTreatment
StressUrethral sphincter weakness; loss of anatomic supportLeakage with cough, sneeze, laugh, exercise, liftingPelvic floor weakness, vaginal atrophy, post-prostatectomyPelvic floor exercises (Kegels), pessary, topical estrogen, duloxetine, surgical sling
Urge (overactive bladder)Detrusor overactivitySudden urge followed by involuntary leakage; frequency, nocturiaIdiopathic, CNS disease (stroke, dementia, Parkinson), bladder irritation (UTI, stones)Behavioral (bladder training, timed voiding), mirabegron 25–50 mg daily, vibegron 75 mg daily; avoid anticholinergics in elderly if possible
OverflowDetrusor underactivity or outlet obstructionContinuous dribbling, incomplete emptying, large PVR (>200 mL)BPH, diabetic neuropathy, anticholinergic drugs, spinal cord lesionsAlpha-blocker (tamsulosin 0.4 mg), 5-alpha reductase inhibitor, intermittent catheterization, discontinue causative meds
FunctionalPhysical or cognitive inability to reach toilet in timeNormal urinary tract; incontinence due to external factorsSevere arthritis, dementia, restraints, environmental barriersPrompted voiding, scheduled toileting, bedside commode, remove barriers
MixedCombination (usually stress + urge)Features of both typesMultiple factorsAddress predominant component first

Transient Causes — DIAPERS Mnemonic

Delirium; Infection (UTI); Atrophic vaginitis; Pharmaceuticals (diuretics, anticholinergics, alpha-blockers, sedatives); Excessive urine output (hyperglycemia, CHF, hypercalcemia); Restricted mobility; Stool impaction (fecal impaction can cause urinary retention/overflow).

Always evaluate for transient causes before assuming chronic incontinence. A post-void residual (PVR) >200 mL suggests overflow incontinence and requires evaluation for obstruction. Urinalysis is the only mandatory initial test — urodynamic studies are reserved for complex or refractory cases.

18 Pressure Injuries

Pressure injuries (formerly pressure ulcers or decubitus ulcers) affect ~2.5 million patients annually in the US. Prevalence in acute care: 5–15%; long-term care: 10–25%. They result from sustained pressure over bony prominences that exceeds capillary closing pressure (~32 mmHg), causing tissue ischemia and necrosis. Most common locations: sacrum (28–36%), heels (23–30%), ischial tuberosities (sitting), greater trochanters, lateral malleoli.

NPUAP/EPUAP Pressure Injury Staging (2016)

StageDescriptionFeatures
Stage 1Non-blanchable erythema of intact skinSkin intact; area may be painful, firm, soft, warmer or cooler than adjacent tissue. Darkly pigmented skin may not show visible blanching.
Stage 2Partial-thickness skin loss with exposed dermisWound bed is viable, pink or red, moist. May present as intact or ruptured serum-filled blister. No granulation tissue, slough, or eschar.
Stage 3Full-thickness skin lossFat visible; granulation tissue and rolled wound edges may be present. Slough and/or eschar may be visible. Undermining and tunneling may occur. Fascia, muscle, tendon, ligament, cartilage, or bone NOT exposed.
Stage 4Full-thickness skin and tissue lossExposed or palpable fascia, muscle, tendon, ligament, cartilage, or bone. Slough and/or eschar may be present. Undermining and tunneling often present. Osteomyelitis risk.
UnstageableObscured full-thickness skin and tissue lossExtent of tissue damage cannot be determined because it is covered by slough (yellow, tan, gray, green, brown) or eschar (tan, brown, black). True depth cannot be determined until slough/eschar is removed. Stable eschar on heel should NOT be removed.
Deep tissue pressure injury (DTPI)Persistent non-blanchable deep red, maroon, or purple discolorationIntact or non-intact skin with localized area of deep tissue damage. May evolve rapidly to reveal full extent of injury. Epidermal separation revealing dark wound bed or blood-filled blister.
Diagram showing the four stages of pressure injuries from Stage 1 through Stage 4
Figure 3 — Pressure Injury Staging. Cross-sectional illustration of pressure injury progression from Stage 1 (non-blanchable erythema, intact skin) through Stage 4 (full-thickness tissue loss with exposed bone/muscle). Source: Wikimedia Commons. Public domain.

Prevention — Braden Scale

The Braden Scale assesses pressure injury risk using 6 subscales (each scored 1–4, except friction/shear scored 1–3; total range 6–23):

SubscaleRangeMeasures
Sensory perception1–4Ability to respond meaningfully to pressure-related discomfort
Moisture1–4Degree of skin exposure to moisture
Activity1–4Degree of physical activity
Mobility1–4Ability to change and control body position
Nutrition1–4Usual food intake pattern
Friction and shear1–3Amount of sliding in bed/chair

Risk levels: 19–23 = no risk; 15–18 = at risk; 13–14 = moderate risk; 10–12 = high risk; ≤9 = very high risk.

Norton Scale

FactorScore Range
Physical condition1 (very bad) – 4 (good)
Mental condition1 (stuporous) – 4 (alert)
Activity1 (bedbound) – 4 (ambulant)
Mobility1 (immobile) – 4 (full)
Incontinence1 (doubly incontinent) – 4 (none)

Total score range: 5–20. Score ≤14 = at risk; ≤12 = high risk.

Management Principles

Prevention: repositioning q2h, pressure-redistribution surfaces, moisture management, nutrition optimization (protein 1.25–1.5 g/kg/day, vitamin C 500 mg BID, zinc 220 mg daily). Treatment by stage: Stage 1–2: keep moist with appropriate dressings (hydrocolloid, foam, transparent film), relieve pressure. Stage 3–4: debridement (sharp, enzymatic [collagenase], or autolytic), negative-pressure wound therapy (wound VAC), infection management, surgical consultation for closure. Osteomyelitis: suspect if bone visible or probe-to-bone positive; MRI is gold standard; treat with 6–8 weeks IV antibiotics ± surgical debridement.

19 Malnutrition & Failure to Thrive

Malnutrition in the Elderly

Malnutrition affects 5–10% of community-dwelling elders, 30–60% of hospitalized elders, and 35–85% of nursing home residents. Causes include decreased appetite (anorexia of aging), dental problems, dysphagia, depression, dementia, medications (causing nausea, altered taste), social isolation, and poverty. Malnutrition increases mortality (2–3×), hospital length of stay, infection risk, pressure injury risk, and impairs wound healing.

Screening — Mini Nutritional Assessment (MNA)

The MNA-Short Form (MNA-SF) is a validated 6-item screening tool (max 14 points): ≥12 = normal nutritional status; 8–11 = at risk of malnutrition; 0–7 = malnourished. Items: food intake decline, weight loss, mobility, acute disease/stress, neuropsychological problems, BMI (or calf circumference if BMI unavailable).

Laboratory Markers

MarkerHalf-lifeNormalClinical Significance
Albumin~20 days3.5–5.0 g/dLReflects chronic nutritional status AND inflammation (negative acute phase reactant); <3.0 associated with poor surgical outcomes
Prealbumin (transthyretin)2–3 days20–40 mg/dLBetter indicator of recent nutritional change; goal >15 mg/dL during repletion
Transferrin8–10 days200–360 mg/dLIntermediate marker; affected by iron status
Total lymphocyte countN/A>1,500/mm³<800 = severe immune compromise from malnutrition

Failure to Thrive (FTT)

Geriatric failure to thrive is a syndrome of weight loss (>5% in 1 month or >10% in 6 months), decreased appetite, poor nutrition, inactivity, dehydration, depression, and cognitive impairment — leading to progressive functional decline. It represents the convergence of multiple geriatric syndromes. Workup: exclude reversible causes (depression, thyroid disease, malignancy, medication effects, dental disease, dysphagia, social factors). Management is multidisciplinary: treat underlying causes, dietary supplements (oral nutritional supplements add 200–600 kcal/day), appetite stimulants (mirtazapine 7.5–15 mg, megestrol acetate 160–800 mg/day [risk of DVT, adrenal suppression — use cautiously]), physical therapy, and social services.

Unintentional weight loss >5% in 6–12 months in an older adult is always pathological and demands investigation. The mnemonic MEALS ON WHEELS: Medications, Emotional problems (depression), Anorexia/Alcoholism, Late-life paranoia, Swallowing problems, Oral/dental problems, No money, Wandering/dementia, Hyperthyroidism/Hypoadrenalism, Enteric problems, Eating problems (functional), Low-salt/low-cholesterol diets (restrictive), Shopping/social problems.

20 Constipation, Sleep Disorders & Dizziness

Constipation

Affects 30–50% of community-dwelling elders and up to 74% of nursing home residents. Defined as <3 bowel movements per week, straining, hard stools, or sense of incomplete evacuation. Causes: low fiber/fluid intake, immobility, medications (opioids, calcium channel blockers, anticholinergics, iron, aluminum antacids), hypothyroidism, hypercalcemia, colorectal cancer, and neurological disorders (Parkinson disease, spinal cord lesions).

Management ladder: (1) Increase fiber (25–30 g/day) and fluids (1.5–2 L/day); (2) Osmotic laxative: polyethylene glycol (MiraLAX) 17 g daily (safest long-term choice); (3) Stimulant laxative: senna 8.6–17.2 mg at bedtime (safe for chronic use despite old myths); (4) For opioid-induced: methylnaltrexone 8–12 mg SQ or naloxegol 25 mg PO daily. Avoid chronic use of mineral oil (aspiration risk, lipoid pneumonia) and phosphate enemas in CKD (hyperphosphatemia, cardiac arrest).

Sleep Disorders in the Elderly

Sleep complaints affect >50% of older adults. Normal age-related changes: decreased total sleep time (6–7 hours), increased sleep latency, more nighttime awakenings, decreased slow-wave sleep (Stage N3), and advanced sleep phase (earlier bedtime and wake time). Pathological sleep disorders: insomnia, obstructive sleep apnea (OSA; prevalence 20–60% in elderly), restless legs syndrome (RLS; 10–35%), REM sleep behavior disorder (screen for prodromal synucleinopathy), and periodic limb movement disorder.

Insomnia management: First-line: sleep hygiene (consistent bed/wake times, dark/cool/quiet room, avoid screens, limit caffeine after noon, avoid daytime naps >30 min) and CBT-I (cognitive behavioral therapy for insomnia — most effective long-term intervention). Pharmacological (short-term only if non-pharmacological fails): melatonin 0.5–3 mg, suvorexant 10 mg (dual orexin receptor antagonist), low-dose trazodone 25–50 mg. Avoid: benzodiazepines, zolpidem, diphenhydramine (Beers criteria).

Dizziness & Vertigo

Dizziness is reported by 30% of people ≥65 and 50% of those ≥85. Four categories: (1) Vertigo (illusion of movement — BPPV, vestibular neuritis, Meniere disease); (2) Presyncope (lightheadedness — orthostatic hypotension, cardiac arrhythmia, vasovagal); (3) Disequilibrium (unsteadiness — peripheral neuropathy, cerebellar disease, musculoskeletal problems); (4) Non-specific dizziness (multifactorial, anxiety, medications).

BPPV is the most common cause of vertigo in elderly (~50% of cases). Diagnosed by the Dix-Hallpike maneuver (positive = latent-onset, fatigable, upbeating/torsional nystagmus). Treated with the Epley maneuver (canalith repositioning; 80% effective in single session). Meclizine suppresses symptoms but delays central compensation — use only for acute severe episodes (≤3 days).

21 ADLs, IADLs & Functional Scales

Katz Index of Independence in ADLs

Assesses 6 basic activities of daily living. Each activity is scored as independent (1) or dependent (0). Total score: 6 = full independence; 4 = moderate impairment; ≤2 = severe functional impairment.

ADLIndependentDependent
BathingBathes self completely or needs help with only one body partNeeds help bathing more than one body part or getting in/out of tub
DressingGets clothes and dresses self completely; may need help with shoesNeeds help dressing or needs to be completely dressed
ToiletingGoes to toilet, cleans self, arranges clothesNeeds help going to toilet, cleaning, or uses bedpan/commode
TransferringMoves in/out of bed and chair independently (may use cane/walker)Needs help moving in/out of bed or chair or is bedbound
ContinenceControls bladder and bowel completelyPartially or totally incontinent
FeedingGets food to mouth independently (food prep may be by others)Needs partial or total help with feeding or uses parenteral feeding
ADL hierarchy: bathing is typically lost first, followed by dressing, toileting, transferring, continence, and feeding (lost last). Recovery occurs in reverse order. Bathing dependence is often the trigger for requiring home health aide or nursing home placement.

Lawton Instrumental ADL Scale

Assesses 8 more complex activities that allow independent community living. Each scored 0 (low function, dependent) or 1 (high function, independent). Total: 0 (completely dependent) to 8 (completely independent).

IADLExamples of Assessment
Using telephoneLooks up numbers, dials independently vs. cannot use telephone
ShoppingShops independently for all needs vs. needs accompaniment or unable
Food preparationPlans and prepares adequate meals vs. needs meals prepared
HousekeepingMaintains house alone or with occasional help vs. needs help with all tasks
LaundryDoes personal laundry completely vs. all laundry done by others
TransportationDrives or arranges travel independently vs. does not travel at all
MedicationsTakes medications correctly and independently vs. unable to manage
FinancesManages financial matters independently vs. unable to handle money

Functional Independence Measure (FIM)

The FIM is an 18-item scale used in rehabilitation settings. Each item scored 1 (total assistance) to 7 (complete independence). Total score range: 18–126. Two subscales: motor FIM (13 items, max 91): self-care, sphincter control, transfers, locomotion; cognitive FIM (5 items, max 35): comprehension, expression, social interaction, problem-solving, memory. FIM score determines rehabilitation intensity needed and is used for Medicare reimbursement in inpatient rehabilitation facilities.

FIM LevelScoreDescription
Complete independence7All tasks performed safely, without modification, in reasonable time
Modified independence6Task requires assistive device, extra time, or safety concerns
Supervision/setup5No physical assistance but standby, cueing, or coaxing needed
Minimal assistance4Subject performs ≥75% of task
Moderate assistance3Subject performs 50–74% of task
Maximal assistance2Subject performs 25–49% of task
Total assistance1Subject performs <25% of task

22 Rehabilitation Goals & Settings

Levels of Post-Acute Care

SettingRequirementsTherapy IntensityTypical Stay
Inpatient Rehabilitation Facility (IRF)Can tolerate 3 hours of therapy/day, 5–7 days/week; requires physician supervision; must have realistic functional goalsHigh (PT, OT, SLP as needed)12–16 days average
Skilled Nursing Facility (SNF)Requires skilled nursing or therapy services; Medicare covers days 1–20 at 100% (after qualifying 3-day hospitalization); days 21–100 with copayModerate (1–2 hours/day)20–35 days average
Long-Term Acute Care Hospital (LTACH)Average LOS ≥25 days; patients with complex medical needs (ventilator weaning, complex wounds, IV antibiotics)Variable≥25 days
Home HealthHomebound status; requires skilled services (nursing, PT, OT, SLP); physician-ordered plan of careIntermittent (2–5 visits/week)60-day episodes
Outpatient rehabilitationMedically stable; can travel to facilityVariable (2–5 times/week)Weeks to months

Medicare Requirements for SNF Coverage

The "3-day rule": patient must have a qualifying inpatient hospital stay of ≥3 consecutive midnights (observation status does NOT count) within 30 days of SNF admission. Medicare Part A covers: days 1–20 fully; days 21–100 with daily copay ($204.50/day in 2024); days 101+ not covered. Patient must require daily skilled services (skilled nursing care, PT, OT, or SLP).

A common pitfall: patients placed on "observation status" (outpatient) rather than "inpatient" status may not meet the 3-day rule for SNF coverage. The NOTICE Act requires hospitals to inform patients of their observation status. Medicare Advantage plans may waive the 3-day rule.

Short Physical Performance Battery (SPPB)

The SPPB is a composite measure of lower-extremity function used in geriatric rehabilitation research and clinical practice. Three timed tests, each scored 0–4 (total 0–12):

ComponentScoring (0–4)
Balance (side-by-side, semi-tandem, tandem × 10 sec each)0 = unable; 1 = side-by-side only; 2 = semi-tandem; 3 = tandem 3–9 sec; 4 = tandem ≥10 sec
Gait speed (4-meter walk)0 = unable; 1 = >8.70 sec; 2 = 6.21–8.70; 3 = 4.82–6.20; 4 = <4.82 sec
Chair stands (×5)0 = unable; 1 = >16.70 sec; 2 = 13.70–16.69; 3 = 11.20–13.69; 4 = <11.19 sec

Interpretation: 0–3 = severe limitation (disability, high mortality); 4–6 = moderate limitation; 7–9 = mild limitation; 10–12 = minimal limitation. A 1-point change is clinically meaningful. SPPB ≤9 is used as a diagnostic criterion for severe sarcopenia.

23 Elder Abuse — Types & Screening

Elder abuse affects an estimated 10% of community-dwelling older adults (≥60) annually, though only 1 in 14 cases is reported. It is associated with 300% increased risk of death within 3 years. Types of elder abuse:

TypePrevalenceIndicators
Physical abuse~2%Unexplained bruises (in various stages of healing), fractures, burns (especially in patterns), welts; injuries inconsistent with stated history; fear of caregiver
Neglect (most common)~5%Poor hygiene, malnutrition, dehydration, untreated medical conditions, pressure injuries, soiled clothing, unsafe living conditions
Emotional/psychological abuse~5%Withdrawal, fearfulness, depression, anxiety, agitation; caregiver belittling, threatening, isolating the elder
Financial exploitation~5%Unexplained changes in financial situation, missing belongings, unpaid bills despite adequate resources, new "best friends," sudden changes in will/power of attorney
Sexual abuse~0.6%Genital bruising, STIs in unexpected populations, torn undergarments, behavioral changes
Self-neglect~10%Inability or unwillingness to meet own basic needs (food, hygiene, medical care, safe living environment); hoarding
AbandonmentRareDesertion by caregiver; "granny dumping" at ED

Risk Factors

Victim: cognitive impairment, functional dependence, social isolation, prior history of family violence. Perpetrator: caregiver stress/burnout, substance abuse, mental illness, financial dependence on the elder, history of violence.

Screening & Reporting

Screen with the Elder Abuse Suspicion Index (EASI) (6 yes/no questions, ≥1 positive answer warrants further investigation) or the Vulnerability to Abuse Screening Scale (VASS). All 50 US states have mandatory reporting laws for suspected elder abuse — healthcare professionals must report to Adult Protective Services (APS) even without proof. In most states, reporters are immune from liability for good-faith reports. Patient consent is NOT required to file a report.

MANDATORY REPORTING

Healthcare providers are mandatory reporters of suspected elder abuse in all 50 US states. You do NOT need proof — reasonable suspicion is sufficient. Report to Adult Protective Services (APS) or local law enforcement. Document findings objectively in the medical record (body maps for injuries, photographs with consent, verbatim quotes). If the patient is in immediate danger, involve security and social work. Do NOT confront the suspected abuser before ensuring patient safety.

24 Capacity, Guardianship & Advance Directives

Decision-Making Capacity Assessment

Capacity is a clinical determination (made by the treating physician); competency is a legal determination (made by a court). Capacity is decision-specific and may fluctuate. The four components of capacity (all must be present):

ComponentAssessment Question
Understanding"Can you tell me what the doctor has told you about your condition and the proposed treatment?"
Appreciation"How do you think this condition and treatment will affect you personally?"
Reasoning"How did you arrive at your decision? What factors did you consider?"
Expressing a choice"What is your decision about the proposed treatment?" (Must be able to clearly communicate a consistent choice)
Having dementia does not automatically mean lacking capacity. A patient with mild-moderate dementia may retain capacity for simple decisions (choosing what to eat) while lacking capacity for complex ones (financial decisions, surgical consent). Capacity must be assessed for each specific decision.

Guardianship & Conservatorship

Guardianship (of the person) grants authority over personal and healthcare decisions. Conservatorship (of the estate) grants authority over financial decisions. Both require court proceedings and a finding of incapacity. They are measures of last resort — less restrictive alternatives should be explored first (healthcare proxy, power of attorney, representative payee, supported decision-making).

Advance Directives

DocumentPurposeKey Features
Living willWritten instructions about future medical care preferencesTypically addresses end-of-life scenarios (terminal illness, permanent unconsciousness); limited in scope (cannot anticipate every situation); requires capacity at time of execution
Durable power of attorney for healthcare (healthcare proxy)Designates a surrogate decision-maker for healthcare decisionsActivated when patient loses capacity; proxy makes decisions based on patient's known wishes (substituted judgment) or best interests; most flexible advance directive
POLST / MOLSTPhysician Orders for Life-Sustaining TreatmentActionable medical orders (not just wishes); signed by physician and patient/surrogate; addresses CPR, intubation, antibiotics, artificial nutrition; portable across care settings; intended for patients with serious illness or frailty; bright pink form in most states
DNR / DNI orderSpecifies no CPR and/or no intubationMedical order written by physician; requires informed consent or surrogate consent; applies in current care setting; separate out-of-hospital DNR may be needed for community
Every patient ≥65 should be asked about advance directives at annual wellness visits. The POLST is for patients with serious illness or limited life expectancy — it is NOT a replacement for the broader advance directive/healthcare proxy, which every adult should have regardless of health status.

25 Goals of Care & Hospice Eligibility

Goals of Care Conversations

Goals of care discussions should occur at key transitions: new serious diagnosis, significant functional decline, hospitalization, or when prognosis is <1–2 years. The REMAP framework: Reframe (why the medical situation has changed); Expect emotion (respond with empathy); Map out patient values ("What matters most to you? What are you hoping for? What are you afraid of?"); Align with values; Plan next steps. Document goals clearly: full treatment, limited interventions (e.g., hospitalize but no ICU/intubation), or comfort-focused care.

Hospice Eligibility — General Criteria

Medicare Hospice Benefit requires: (1) Two physicians certify prognosis of ≤6 months if disease follows expected course; (2) Patient (or surrogate) chooses comfort over curative treatment; (3) Covered services: nursing, home health aide, medications for comfort, DME, counseling, spiritual care, respite care (up to 5 days), bereavement support for 13 months after death.

Disease-Specific LCD Guidelines for Hospice

DiseaseKey Eligibility Indicators
DementiaFAST Stage 7c (loss of ambulation, meaningful speech ≤6 words, incontinence) PLUS one or more in past 12 months: aspiration pneumonia, pyelonephritis, septicemia, multiple Stage 3–4 pressure injuries, recurrent fevers, inability to maintain sufficient intake with 10% weight loss in 6 months or albumin <2.5
Heart diseaseNYHA Class IV despite optimal treatment; EF ≤20%; refractory angina or arrhythmia; optimal medical therapy already in place; history of cardiac arrest or syncope; concomitant HIV, renal failure, or other comorbidities
Pulmonary diseaseFEV1 <30% predicted; resting O2 sat ≤88% on supplemental O2; cor pulmonale; unintentional weight loss >10% in 6 months; resting tachycardia >100; recurrent hospitalizations for exacerbations
CancerMetastatic or locally advanced with poor prognosis; declining functional status (PPS ≤50%); declining despite treatment or patient declines further treatment
Liver diseasePT >5 sec over control or INR >1.5; albumin <2.5; ascites refractory to treatment; hepatic encephalopathy; hepatorenal syndrome
Renal diseaseNot seeking or discontinuing dialysis; CrCl <10 mL/min (<15 for diabetics); serum Cr >8.0 (>6.0 for diabetics); uremia symptoms with declining status
Stroke/comaComatose with poor prognosis on day 3; persistent vegetative state; Karnofsky ≤40% or PPS ≤40%
Hospice is NOT "giving up" — it is a shift in care goals toward comfort and quality of life. Patients may revoke hospice at any time and return to curative treatment. Hospice patients actually live an average of 29 days longer than matched non-hospice patients with similar conditions (Connor et al., JPSM 2007).

26 Comfort Care & Symptom Management

Pain Management at End of Life

Pain affects 50–80% of patients at end of life. The WHO analgesic ladder (adapted for elderly): Step 1: non-opioids (acetaminophen 325–500 mg q6h, max 2 g/day in frail elderly; topical lidocaine, NSAIDs short-term); Step 2: weak opioids (tramadol 25–50 mg q6h — use cautiously due to seizure and serotonin syndrome risk); Step 3: strong opioids (morphine 2.5–5 mg PO q4h PRN initially, or oxycodone 2.5–5 mg q4–6h; hydromorphone 0.5–1 mg PO q4h for renal impairment). Adjuvants at any step: gabapentin, pregabalin (neuropathic pain); dexamethasone (bone metastases, visceral pain); lidocaine patch (localized pain).

Dyspnea Management

Opioids are first-line for dyspnea at end of life (morphine 2–5 mg PO q4h or 1–2 mg IV q2–4h). Supplemental oxygen only if hypoxic AND symptomatic benefit — a fan directed at the face can be equally effective for the sensation of breathlessness. Benzodiazepines (lorazepam 0.5–1 mg q4–6h) for anxiety-related dyspnea. Nebulized normal saline may help with secretions.

Terminal Secretions ("Death Rattle")

Occurs in 25–50% of dying patients. Caused by pooling of secretions in the hypopharynx. More distressing to family than patient (patient is typically unconscious). Treatment: reposition (lateral with head elevated), gentle oral suctioning (avoid deep suctioning), anticholinergic agents: glycopyrrolate 0.2 mg IV/SQ q4–6h (preferred — does not cross BBB), hyoscine (scopolamine) patch 1.5 mg/72h, or atropine 1% ophthalmic drops 1–2 drops SL q4h.

Nausea & Vomiting

Ondansetron 4 mg IV/PO q6–8h; haloperidol 0.5–1 mg PO/IV q6–8h (useful for opioid-induced and bowel obstruction nausea); prochlorperazine 5–10 mg PO/IV q6h. For bowel obstruction with no surgical option: octreotide 100–300 mcg SQ TID reduces GI secretions; dexamethasone 4–8 mg IV/SQ for partial obstruction.

Delirium at End of Life

Terminal delirium affects up to 88% of dying patients. First: address reversible causes if consistent with goals (medications, urinary retention, fecal impaction, pain). Haloperidol 0.5–2 mg PO/IM/IV q4–6h PRN for agitation. For refractory terminal agitation: palliative sedation with midazolam infusion (0.5–1 mg/hr IV) or phenobarbital (loading 200 mg IV, then 50–100 mg q4–6h) — a last resort for intractable symptoms near death.

Opioids used appropriately for pain and dyspnea at end of life do NOT hasten death (principle of double effect). Withholding opioids from a dying patient in pain is unethical. The goal is comfort, not sedation — titrate to effect.

Signs of Imminent Death

The following signs indicate death is likely within hours to days: (1) Progressive decrease in consciousness; (2) Mottling of extremities (livedo reticularis); (3) Cool, cyanotic extremities; (4) Decreased or absent urine output; (5) Cheyne-Stokes or agonal breathing; (6) Terminal secretions (death rattle); (7) Loss of ability to swallow; (8) Mandibular breathing (jaw movement with each breath). Educate family about these expected changes. Discontinue unnecessary medications, monitoring, and interventions. Focus on mouth care, positioning, skin care, and emotional/spiritual support.

Medications to Discontinue at End of Life

Statins, antihypertensives (unless symptomatic hypertension), diabetes medications (unless symptomatic hyperglycemia), osteoporosis medications, vitamins/supplements, anticoagulants (unless active DVT/PE causing symptoms), screening medications (aspirin for primary prevention). Continue: analgesics, anticonvulsants (prevent seizures), anxiolytics, anti-secretory agents, antiemetics, and medications providing immediate symptom relief.

27 Prognostication, Caregiver Support & Grief

Prognostication Tools

ToolPopulationKey Features
Palliative Performance Scale (PPS)All patients with serious illness11-level scale (0–100% in 10% increments); assesses ambulation, activity, self-care, intake, consciousness. PPS ≤50% associated with median survival ~6 months; PPS ≤20% associated with days to weeks
Karnofsky Performance Status (KPS)Cancer patients0–100 scale; KPS ≤40 = disabled, needs specialized care; KPS ≤20 = very sick, hospitalization needed
ePrognosis (eprognosis.ucsf.edu)Community-dwelling elderlyOnline calculators for mortality risk at 1–10 years based on demographics, function, comorbidities
FAST (Functional Assessment Staging)Alzheimer dementiaStage 7c or beyond = hospice-eligible (see Section 25); 7 stages with substages
Surprise QuestionAll patients"Would I be surprised if this patient died in the next 12 months?" If no, consider palliative care referral. Sensitivity ~70%, specificity ~70%.

Caregiver Support

Caregivers of older adults (especially those with dementia) experience high rates of depression (40–70%), anxiety, social isolation, and physical illness. The Zarit Burden Interview (ZBI) is a 22-item tool (0–88 points): 0–20 = little or no burden; 21–40 = mild to moderate; 41–60 = moderate to severe; 61–88 = severe burden. Interventions: respite care (Medicare hospice benefit includes up to 5 days of inpatient respite), support groups (Alzheimer's Association 24/7 helpline: 800-272-3900), psychoeducation, caregiver training in behavioral management techniques, family counseling, adult day programs.

Grief & Bereavement

Normal grief: sadness, yearning, preoccupation with the deceased, sleep disturbance, appetite changes; typically diminishes over 6–12 months with fluctuating intensity ("waves of grief"). Prolonged grief disorder (DSM-5-TR): persistent, pervasive grief lasting ≥12 months in adults (6 months in children) after bereavement, with intense yearning/longing, preoccupation with the deceased, and clinically significant distress or impairment. Affects ~10% of bereaved individuals. Treatment: grief-focused CBT, support groups. Anticipatory grief: grief that occurs before death (during prolonged illness); can facilitate post-death adjustment. Medicare hospice benefit provides 13 months of bereavement support for families.

28 Common Bedside Procedures

Joint Injections & Aspirations

Corticosteroid injections for osteoarthritis in elderly: triamcinolone 40 mg (large joints: knee, shoulder) or 10–20 mg (small joints). Limit to 3–4 injections per joint per year. Contraindications: overlying cellulitis, prosthetic joint (refer to orthopedics), coagulopathy. Hyaluronic acid injections (viscosupplementation) for knee OA: modest evidence; may benefit patients who cannot tolerate NSAIDs or are not surgical candidates.

Urinary Catheterization

Indications for chronic indwelling catheter (Foley) in elderly: urinary retention not amenable to intermittent catheterization, Stage 3–4 sacral/perineal pressure injury with incontinence, comfort care in terminally ill patients, or acute urinary obstruction awaiting surgery. Catheter-associated UTI (CAUTI) risk increases ~5% per day of catheterization. Prevention: insert only for valid indications, remove as soon as possible, nurse-driven removal protocols, maintain closed drainage system. Avoid chronic catheter for convenience or nursing preference. Alternatives: condom catheter (male), intermittent catheterization, prompted voiding.

Paracentesis & Thoracentesis in the Elderly

Procedural considerations: higher bleeding risk with liver disease (but INR and platelet count do NOT reliably predict bleeding in cirrhosis — transfusion thresholds debated). Large-volume paracentesis (>5 L): give albumin 6–8 g per liter removed to prevent post-paracentesis circulatory dysfunction. Thoracentesis: limit to 1–1.5 L per session to reduce re-expansion pulmonary edema risk. Ultrasound guidance is standard of care for both procedures — reduces complications by 50%.

29 Pre-operative Assessment in the Elderly

Patients ≥65 account for ~40% of all surgical procedures but have 2–3× higher perioperative mortality and complications than younger patients. Standard cardiac risk assessment (Revised Cardiac Risk Index, ACC/AHA guidelines) is necessary but insufficient — geriatric-specific risks (frailty, cognitive impairment, functional dependence, polypharmacy, nutritional status) are equally important.

Geriatric-Specific Pre-operative Assessment

DomainAssessmentImpact
FrailtyClinical Frailty Scale, Fried criteria, or Edmonton Frail ScaleCFS ≥5 associated with 2–3× increased 30-day mortality, longer LOS, discharge to facility
CognitionMini-Cog or MoCA pre-operativelyPre-existing cognitive impairment is the strongest predictor of post-operative delirium (risk 3–5×)
FunctionADL/IADL assessmentFunctional dependence predicts complications and inability to return home
NutritionAlbumin, BMI, weight lossAlbumin <3.0 g/dL associated with 3–5× increased surgical complications and mortality
PolypharmacyMedication reconciliation; Beers criteria reviewIdentify medications to hold (anticoagulants, antiplatelets, metformin, SGLT2i) and continue (beta-blockers, statins, levothyroxine)
Falls riskTUG, fall historyPost-operative fall risk assessment and prevention protocols
Goals of careAdvance directive review; discuss surgical risks vs benefits in context of prognosis and valuesMay change decision to operate; ensures appropriate code status documentation

ACS-NSQIP Surgical Risk Calculator

The ACS-NSQIP (American College of Surgeons National Surgical Quality Improvement Program) calculator estimates 30-day risk of major complications, mortality, and length of stay based on procedure type and 21 patient variables. Available online at riskcalculator.facs.org. Does not directly measure frailty, so should be combined with frailty assessment for comprehensive risk stratification in elderly surgical candidates.

Post-operative Delirium Prevention

Affects 15–53% of elderly surgical patients (highest after hip fracture and cardiac surgery). Prevention: proactive geriatrics consultation (reduces delirium by 36%), multicomponent non-pharmacological protocols (similar to HELP), avoid benzodiazepines and meperidine, optimize pain control (regional anesthesia when possible, scheduled acetaminophen, low-dose opioids), early mobilization (post-op day 1), sleep promotion, reorient frequently, ensure glasses/hearing aids in place.

30 Feeding Tube Decisions & Wound Care

Feeding Tube Decisions in Advanced Dementia

Dysphagia and aspiration are nearly universal in advanced dementia. Evidence strongly shows that tube feeding in advanced dementia does NOT: prevent aspiration pneumonia, prolong survival, improve nutrition, promote wound healing, improve function, or increase comfort. Tube feeding in advanced dementia is associated with increased agitation (restraints often needed to prevent self-removal), increased aspiration (continued aspiration of oral secretions and gastric reflux), and medical complications (tube site infections, diarrhea, refeeding syndrome).

AGS POSITION STATEMENT (2014)

The American Geriatrics Society states: "Feeding tubes are NOT recommended for older adults with advanced dementia. Careful hand feeding should be offered." The Choosing Wisely campaign lists PEG tubes in advanced dementia as one of the top interventions to avoid. Careful hand feeding (small amounts, texture-modified diet, upright positioning, unhurried meals) provides comfort and human connection and is the recommended approach.

Wound Care Principles in the Elderly

Aging skin is thinner, less elastic, and heals more slowly (50% slower epithelialization by age 80). Key principles: (1) Moisture balance — wounds heal faster in a moist environment (use appropriate dressings: hydrocolloid for low exudate, foam for moderate, alginate/hydrofiber for heavy); (2) Debridement — remove necrotic tissue (autolytic with moist dressings, enzymatic with collagenase, or sharp debridement); (3) Infection control — distinguish colonization from infection (increasing pain, erythema, warmth, purulence, delayed healing indicate infection); (4) Nutrition optimization — protein 1.25–1.5 g/kg/day, vitamin C 500 mg BID, zinc 220 mg daily; (5) Offloading — pressure redistribution for pressure injuries; therapeutic footwear for diabetic foot ulcers.

Skin Tears

Very common in elderly (fragile skin, anti-coagulant use). Classification (ISTAP): Type 1 — no skin loss (linear or flap tear, flap can be repositioned); Type 2 — partial flap loss; Type 3 — total flap loss. Management: approximate skin flap if present, apply non-adherent dressing (silicone-based dressings preferred), avoid adhesive tape directly on fragile skin (use tubular gauze or paper tape). Prevention: moisturize skin BID, padded bed rails, long sleeves, gentle handling during transfers.

31 Imaging & Diagnostics in the Elderly

Neuroimaging

Brain MRI is the preferred modality for evaluating cognitive decline: hippocampal atrophy (AD), frontal/temporal atrophy (FTD), white matter hyperintensities (vascular disease), normal pressure hydrocephalus (ventricular enlargement disproportionate to sulcal enlargement). CT head (non-contrast) for acute presentations: falls with altered mental status (r/o subdural hematoma — chronic SDH is common in elderly on anticoagulants), acute stroke. FDG-PET: temporoparietal hypometabolism (AD), frontal hypometabolism (FTD), occipital hypometabolism (DLB). DaTscan (I-123 ioflupane SPECT): differentiates DLB (abnormal) from AD (normal); evaluates nigrostriatal dopaminergic integrity.

Bone Densitometry (DXA)

Gold standard for osteoporosis diagnosis. Measures BMD at lumbar spine (L1–L4), femoral neck, and total hip. T-score = number of standard deviations from peak bone mass of a young adult reference. Z-score (compared to age-matched controls) is used in premenopausal women and men <50 — Z-score ≤−2.0 = "below expected range for age." Artifactual elevation of lumbar spine BMD can occur from degenerative changes, compression fractures, and aortic calcification — in these cases, hip BMD is more reliable.

Laboratory Testing Considerations

Age-related reference range changes: BNP increases with age (normal <100 pg/mL in <75 years, <300 pg/mL in ≥75 years); PSA cutoffs may differ; ESR is elevated with age (rule of thumb: upper normal = age/2 in men, (age + 10)/2 in women). D-dimer: age-adjusted threshold (age × 10 ng/mL for patients >50) improves specificity for VTE without reducing sensitivity. TSH: some experts suggest higher target TSH range (0.5–8.0 mIU/L) in very elderly (≥85) to avoid overtreatment of subclinical hypothyroidism.

Echocardiography in the Elderly

Age-related findings that should not be over-interpreted: mild aortic sclerosis (50% of those ≥85; does not necessarily progress to stenosis), mild mitral annular calcification (MAC), basal septal hypertrophy (sigmoid septum), and mild diastolic dysfunction (Grade I is near-universal after age 70). Aortic stenosis prevalence increases dramatically with age (2–5% of those ≥75 have severe AS) and is the most common valvular disease requiring intervention in the elderly.

Cancer Screening Cessation

ScreeningReasonable to Stop WhenRationale
ColonoscopyAge ≥75 (USPSTF: individualize 76–85; stop at 85)Time-to-benefit for colon cancer screening is ~10 years; harms increase with age
MammographyLife expectancy <10 years (USPSTF: biennial 50–74; insufficient evidence ≥75)Time-to-benefit ~7–10 years; overdiagnosis increases with age
Pap smearAge ≥65 with adequate prior screening (3 normal Paps or 2 normal HPV co-tests in 10 years)Very low risk after adequate screening
PSAAge ≥70 or life expectancy <10–15 yearsOverdiagnosis and overtreatment; most prostate cancers in elderly are indolent
Lung CT (low-dose)Age ≥80 or 15 years since smoking cessationUSPSTF: screen ages 50–80 with ≥20 pack-year history and currently smoke or quit <15 years ago

32 Classification Systems (All)

This section consolidates all major classification and staging systems referenced throughout geriatric medicine.

Mini-Mental State Examination (MMSE) — Score Interpretation

ScoreSeverityClinical Correlation
27–30NormalNo significant cognitive impairment
21–26Mild cognitive impairmentMay manage ADLs; IADLs may be affected; subtle deficits
11–20Moderate cognitive impairmentRequires assistance with ADLs; behavioral symptoms common; cannot live independently
0–10Severe cognitive impairmentDependent for all ADLs; limited verbal communication; requires 24-hour supervision

Montreal Cognitive Assessment (MoCA) — Score Interpretation

ScoreInterpretation
26–30Normal
18–25Mild cognitive impairment
10–17Moderate cognitive impairment
<10Severe cognitive impairment

Note: add 1 point if education ≤12 years (maximum score remains 30). MoCA is more sensitive than MMSE for detecting mild cognitive impairment (90% vs 18% sensitivity for MCI).

Clinical Dementia Rating (CDR)

CDRStageDescription
0NormalNo cognitive impairment
0.5Questionable/very mild dementiaConsistent slight forgetfulness; partial recollection of events; "benign" forgetfulness; fully independent
1Mild dementiaModerate memory loss affecting daily activities; unable to function independently at community affairs; mild difficulty with home activities; personal care intact
2Moderate dementiaSevere memory loss; only highly learned material retained; oriented to person only; cannot make judgments; requires assistance with dressing, hygiene
3Severe dementiaOnly fragments of memory remain; oriented to person only; no pretense of independent function; requires much help with personal care; frequent incontinence

FAST (Functional Assessment Staging — Reisberg)

StageDescriptionClinical Correlation
1Normal adultNo functional decline
2Normal aged adultSubjective complaints of forgetfulness; no objective deficits
3Early dementiaDecreased job functioning; difficulty with complex tasks; denial
4Mild dementiaNeeds assistance with complex tasks (finances, shopping, planning)
5Moderate dementiaNeeds help choosing appropriate clothing; may need coaxing to bathe
6aModerately severeNeeds help dressing
6bNeeds help bathing
6cNeeds help with mechanics of toileting
6dUrinary incontinence
6eFecal incontinence
7aSevere dementiaSpeech ability limited to ~6 words per day
7bSpeech limited to single intelligible word
7cLoss of ambulation (hospice-eligible with comorbidities)
7dLoss of ability to sit without support
7eLoss of ability to smile
7fLoss of ability to hold head up

Fried Frailty Phenotype

See Section 12 for full criteria. Summary: 0 criteria = robust; 1–2 = pre-frail (intermediate risk); ≥3 = frail (poor outcomes).

Clinical Frailty Scale (Rockwood)

See Section 12 for complete 9-point enumeration.

Braden Scale

See Section 18 for full subscale enumeration. Total 6–23; ≤18 = at risk.

Norton Scale

See Section 18 for enumeration. Total 5–20; ≤14 = at risk.

NPUAP Pressure Injury Staging

See Section 18 for complete staging from Stage 1 through DTPI.

Berg Balance Scale (BBS)

14 items, each scored 0–4 (total 0–56): sitting balance, standing balance, sit-to-stand, standing with eyes closed, tandem standing, picking up object from floor, turning 360 degrees, alternating foot on step, standing on one leg, reaching forward, and more. Scores: 41–56 = low fall risk (independent); 21–40 = medium fall risk (walking with assistance); 0–20 = high fall risk (wheelchair-dependent).

Morse Fall Scale

ItemScore
History of falling (this admission or within 3 months)0 = No; 25 = Yes
Secondary diagnosis0 = No; 15 = Yes
Ambulatory aid0 = None/bed rest/nurse assist; 15 = Crutches/cane/walker; 30 = Furniture for support
IV/heparin lock0 = No; 20 = Yes
Gait0 = Normal/immobile; 10 = Weak; 20 = Impaired
Mental status0 = Oriented to own ability; 15 = Overestimates or forgets limitations

Total: 0–24 = low risk; 25–50 = moderate risk; ≥51 = high risk.

WHO DXA T-score Classification

See Section 11 for complete classification.

Zarit Burden Interview

See Section 27 for scoring: 0–20 little/none; 21–40 mild-moderate; 41–60 moderate-severe; 61–88 severe.

AGS 2023 Updated Beers Criteria STOPP/START Criteria v3 (2023) Alzheimer's Association Clinical Resources

33 Medications Master Table

Cholinesterase Inhibitors & NMDA Antagonists

DrugMechanismDoseIndicationKey Side Effects / Pearls
Donepezil (Aricept)Reversible AChE inhibitor5 mg daily → 10 mg daily; 23 mg daily (mod-severe)AD (all stages)N/V/D, bradycardia, vivid dreams, muscle cramps; take at bedtime
Rivastigmine (Exelon)Pseudo-irreversible AChE + BuChE inhibitorPatch: 4.6 → 9.5 → 13.3 mg/24hAD (mild-mod), Parkinson dementiaGI effects less with patch; rotate application site; only AChEI approved for PD dementia
Galantamine (Razadyne)Reversible AChE inhibitor + nicotinic receptor modulator4 mg BID → 8 → 12 mg BID; ER: 8 → 16 → 24 mg dailyAD (mild-mod)GI side effects; adjust dose in hepatic/renal impairment (avoid if severe)
Memantine (Namenda)Non-competitive NMDA receptor antagonist5 mg daily → 5 mg BID → 10 mg BID (target 20 mg/day)AD (mod-severe)Dizziness, headache, constipation; reduce dose to 5 mg BID if CrCl <30; can combine with AChEI

Antidepressants in the Elderly

DrugClassDose RangeKey Features in Elderly
Sertraline (Zoloft)SSRI25–200 mg dailyFirst-line; well-tolerated; start 25 mg; GI side effects, hyponatremia (SIADH), bleeding risk with anticoagulants
Escitalopram (Lexapro)SSRI5–20 mg dailyFirst-line; clean pharmacokinetic profile; max 20 mg (was 10 mg in ≥65 per FDA, but recent data supports 20 mg with QTc monitoring)
Mirtazapine (Remeron)NaSSA7.5–45 mg at bedtimePromotes appetite and sleep; weight gain desirable in malnourished elderly; more sedating at 7.5–15 mg than at 30–45 mg
Bupropion (Wellbutrin)NDRI100–300 mg daily (SR/XL)Activating; no sexual side effects; no weight gain; lower seizure threshold — avoid if seizure history
Duloxetine (Cymbalta)SNRI30–60 mg dailyUseful for comorbid neuropathic pain; avoid if CrCl <30; discontinuation syndrome
Venlafaxine (Effexor XR)SNRI37.5–225 mg dailyDose-dependent HTN at >150 mg; worst discontinuation syndrome of all antidepressants; taper very slowly
Nortriptyline (Pamelor)TCA10–75 mg dailyLeast anticholinergic TCA; therapeutic window 50–150 ng/mL; ECG before starting (avoid if QTc >450); reserved for refractory cases

Antipsychotics in the Elderly

DrugDose RangeKey Features
Quetiapine (Seroquel)12.5–200 mg dailyLowest EPS risk; preferred in DLB/Parkinson; sedating; metabolic effects with chronic use
Risperidone (Risperdal)0.25–2 mg dailyBest evidence for BPSD agitation; dose-related EPS; stroke risk in dementia
Olanzapine (Zyprexa)2.5–10 mg dailyIM formulation for acute agitation; weight gain, metabolic syndrome; anticholinergic
Haloperidol (Haldol)0.5–2 mg PO/IM q4–6h PRNGold standard for acute delirium agitation; high EPS/akathisia risk; QTc prolongation (especially IV); AVOID in DLB/Parkinson
Pimavanserin (Nuplazid)34 mg dailySelective 5-HT2A inverse agonist; FDA-approved for Parkinson disease psychosis; no dopamine blockade; QTc prolongation

Bisphosphonates & Bone Agents

DrugMechanismDoseKey Pearls
Alendronate (Fosamax)Osteoclast inhibitor (bisphosphonate)70 mg PO weeklyEsophagitis risk; take fasting, upright 30 min; drug holiday after 5 yr if low-risk; avoid if CrCl <35
Zoledronic acid (Reclast)Osteoclast inhibitor (IV bisphosphonate)5 mg IV yearlyBest adherence; acute phase reaction; hydrate before; check Ca/VitD before; avoid if CrCl <35
Denosumab (Prolia)RANKL monoclonal antibody60 mg SQ q6 monthsNo renal restriction; MUST NOT miss doses (rebound vertebral fractures); transition to bisphosphonate if stopping
Teriparatide (Forteo)Recombinant PTH 1-34 (anabolic)20 mcg SQ daily × 2 yrFor severe osteoporosis, multiple fractures, or bisphosphonate failure; must follow with antiresorptive; osteosarcoma risk (box warning)
Romosozumab (Evenity)Sclerostin monoclonal antibody210 mg SQ monthly × 12 moGreatest BMD increase of any agent; CV black box warning; avoid if MI/stroke within 1 year
Calcitonin (Miacalcin)Inhibits osteoclast activity200 IU intranasal daily (alternate nostrils)Weakest agent; useful for acute vertebral compression fracture pain; nasal irritation; cancer risk with long-term use

OAB Medications (Non-Anticholinergic Preferred in Elderly)

DrugMechanismDosePearls
Mirabegron (Myrbetriq)Beta-3 adrenergic agonist25–50 mg dailyNO anticholinergic effects; HTN risk (monitor BP); preferred over oxybutynin in elderly
Vibegron (Gemtesa)Beta-3 adrenergic agonist75 mg dailySimilar to mirabegron; less BP effect in studies; no CYP interactions
Oxybutynin (Ditropan)Anticholinergic (M3 antagonist)5 mg BID-TID (IR); 5–30 mg daily (ER)AVOID in elderly (Beers criteria): crosses BBB, cognitive impairment, delirium, dry mouth, constipation, blurred vision

34 Abbreviations Master List

AbbreviationMeaning
ACBAnticholinergic Cognitive Burden
AChEIAcetylcholinesterase inhibitor
ACPAdvance care planning
ACS-NSQIPAmerican College of Surgeons National Surgical Quality Improvement Program
ADAlzheimer disease
ADLActivities of daily living
ADRAdverse drug reaction
AGSAmerican Geriatrics Society
ALFAssisted living facility
APSAdult Protective Services
BBSBerg Balance Scale
BMDBone mineral density
BPPVBenign paroxysmal positional vertigo
BPSDBehavioral and psychological symptoms of dementia
bvFTDBehavioral variant frontotemporal dementia
CAMConfusion Assessment Method
CAUTICatheter-associated urinary tract infection
CBT-ICognitive behavioral therapy for insomnia
CDRClinical Dementia Rating
CFSClinical Frailty Scale
CGAComprehensive geriatric assessment
DaTscanDopamine transporter SPECT scan
DLBDementia with Lewy bodies
DNR / DNIDo not resuscitate / do not intubate
DTPIDeep tissue pressure injury
DXADual-energy X-ray absorptiometry
EASIElder Abuse Suspicion Index
EWGSOPEuropean Working Group on Sarcopenia in Older People
FASTFunctional Assessment Staging Tool
FIMFunctional Independence Measure
FRAXFracture Risk Assessment Tool
FTDFrontotemporal dementia
FTTFailure to thrive
GDSGeriatric Depression Scale
HCPHealthcare proxy
HELPHospital Elder Life Program
IADLInstrumental activities of daily living
IRFInpatient rehabilitation facility
KPSKarnofsky Performance Status
LCDLocal Coverage Determination
LTACHLong-term acute care hospital
MCIMild cognitive impairment
MMSEMini-Mental State Examination
MNAMini Nutritional Assessment
MoCAMontreal Cognitive Assessment
MOLSTMedical Orders for Life-Sustaining Treatment
NIA-AANational Institute on Aging–Alzheimer's Association
NMDAN-methyl-D-aspartate
NMSNeuroleptic malignant syndrome
NPUAPNational Pressure Ulcer Advisory Panel
OABOveractive bladder
PAINADPain Assessment in Advanced Dementia
PEGPercutaneous endoscopic gastrostomy
PIMPotentially inappropriate medication
POLSTPhysician Orders for Life-Sustaining Treatment
PPAPrimary progressive aphasia
PPSPalliative Performance Scale
PVRPost-void residual
RANKLReceptor activator of nuclear factor kappa-B ligand
SDHSubdural hematoma
SNFSkilled nursing facility
SPPBShort Physical Performance Battery
STOPP/STARTScreening Tool of Older Persons' Prescriptions / Screening Tool to Alert to Right Treatment
TUGTimed Up and Go test
VASSVulnerability to Abuse Screening Scale
ZBIZarit Burden Interview

35 Risk Factors & Comorbidities

Multimorbidity in the Elderly

Approximately 67% of adults ≥65 have ≥2 chronic conditions and 36% have ≥4. The most prevalent chronic conditions in order: hypertension (70%), hyperlipidemia (55%), arthritis (50%), ischemic heart disease (30%), diabetes (27%), CKD (25%), heart failure (15%), COPD (12%), dementia (10%), cancer (various), depression (15–25%). Multimorbidity drives polypharmacy, functional decline, increased healthcare utilization, and mortality. Disease management must be prioritized based on patient values, prognosis, and treatment burden.

Key Risk Factors by Geriatric Syndrome

SyndromeMajor Risk Factors
FallsPrior falls, gait/balance impairment, medications (≥4 or psychotropics), visual impairment, orthostatic hypotension, cognitive impairment, lower-extremity weakness, neuropathy, environmental hazards, foot problems
DeliriumDementia (single strongest risk factor), age ≥80, severe illness, sensory impairment (vision/hearing), dehydration, malnutrition, polypharmacy (especially anticholinergics, benzodiazepines), urinary catheter, restraints, surgery (especially hip fracture, cardiac)
Pressure injuriesImmobility, incontinence, malnutrition (albumin <3.0), sensory impairment, diabetes, PVD, edema, age ≥75, acute illness, cognitive impairment
DementiaAge (strongest), family history (ApoE4 allele for AD), cardiovascular risk factors (HTN, DM, obesity, smoking, hyperlipidemia), low education, traumatic brain injury, depression, social isolation, hearing loss
FrailtyAge, sarcopenia, malnutrition, multimorbidity, polypharmacy, depression, social isolation, low physical activity, low income, cognitive impairment
Osteoporotic fracturePrior fracture (2× risk), age, female sex, low BMI, parental hip fracture, smoking, alcohol ≥3 units/day, glucocorticoids, rheumatoid arthritis, falls, low BMD, vitamin D deficiency, early menopause
Elder abuseCognitive impairment, functional dependence, social isolation, shared living situation, caregiver stress/substance abuse/mental illness, financial dependence of caregiver on elder

Preventive Care in the Elderly

InterventionRecommendation
Influenza vaccineAnnually; high-dose (Fluzone HD) or adjuvanted (FLUAD) for ≥65
Pneumococcal vaccinePCV20 alone OR PCV15 followed by PPSV23 (≥1 year later); for all adults ≥65
Shingles vaccineRecombinant zoster vaccine (Shingrix) 2 doses, 2–6 months apart; ≥50 years; >90% efficacy (vs 51% for live vaccine)
COVID-19 vaccineUpdated formulation annually per CDC guidance
Tdap/TdTdap once if not previously received; Td booster every 10 years
RSV vaccineSingle dose for adults ≥60 through shared clinical decision-making
Fall preventionScreen annually; multifactorial intervention for high-risk
Osteoporosis screeningDXA for all women ≥65; men ≥70 or with risk factors
AAA screeningOne-time US for men 65–75 who ever smoked
Statin therapyContinue in established CVD; initiation in primary prevention after 75 is individualized
AspirinDo NOT initiate for primary prevention in ≥60 (USPSTF 2022); continue if established CVD indication
Preventive care in the elderly should be individualized based on life expectancy, functional status, patient preferences, and time-to-benefit of the intervention. Screening tests with a time-to-benefit exceeding life expectancy (e.g., colonoscopy in a frail 90-year-old) are unlikely to provide net benefit and may cause harm.
USPSTF Recommendation Topics CDC Adult Immunization Schedule ePrognosis — Geriatric Prognostication Calculators Alzheimer's Association — Stages of Alzheimer's