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Geriatric Medicine

Falls, delirium, dementia, polypharmacy, frailty, continence, and comprehensive geriatric assessment.

21 topics · 31 linked questions

Falls and Fall Prevention

Falls are the most common cause of injury-related death in people over 75 in the UK, requiring a multifactorial risk assessment and individualised intervention programme.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • One in three adults over 65 falls each year; one in two over 80
  • Falls are the most common cause of injury-related death in people >75 in the UK
  • NICE CG161 recommends multifactorial falls risk assessment for all older people presenting with a fall or at risk of falling
  • Key assessable risk factors: gait and balance, muscle weakness, postural hypotension, polypharmacy, visual impairment, cognitive impairment, environmental hazards
  • Strength and balance training (e.g. Otago Exercise Programme) reduces falls by 30-40% in community-dwelling older adults
  • Medication review: reduce or stop high-risk medications (benzodiazepines, antihypertensives, sedatives, anticholinergics)
  • Lying and standing blood pressure must be measured in all falls assessments (postural drop ≥20mmHg systolic)
  • Hip protectors reduce hip fracture risk in nursing home residents who are at high risk of falls

Overview

Key Facts

Falls in older people are rarely due to a single cause. A comprehensive multifactorial assessment is essential to identify and address modifiable risk factors.

Epidemiology

  • One in three people >65 falls each year; increases to one in two >80
  • Falls cause >250,000 fractures per year in the UK
  • Approximately 30% of falls result in injury; 5% result in fracture
  • Hip fracture: approximately 66,000 per year in the UK; 30-day mortality ~8%
  • Annual NHS cost of falls in older people: approximately £2.3 billion

Aetiology

Falls are usually multifactorial:

  • Intrinsic factors: muscle weakness, gait/balance problems, visual impairment, cognitive impairment, postural hypotension, syncope, peripheral neuropathy, arthritis, vestibular dysfunction
  • Extrinsic factors: environmental hazards (loose carpets, poor lighting, uneven surfaces), inappropriate footwear
  • Medications: sedatives, antihypertensives, anticholinergics, opioids, polypharmacy (≥4 medications)

Pathophysiology

  • Age-related decline in muscle mass (sarcopenia), proprioception, vestibular function, and visual acuity
  • Postural hypotension: impaired baroreceptor reflex sensitivity
  • Cognitive impairment: reduced hazard awareness and reaction time
  • Osteoporosis: does not cause falls but increases fracture risk from falls

Clinical Presentation

History

  • Circumstances of fall (where, when, what doing)
  • Preceding symptoms (dizziness, palpitations, blackout, trip/slip)
  • Frequency of falls
  • Fear of falling (major contributor to reduced mobility and further falls)
  • Medication history
  • Functional history (ADLs, mobility aids, living situation)

Examination

  • Gait and balance assessment (Timed Up and Go test, Berg Balance Scale)
  • Lying and standing BP (postural hypotension)
  • Cardiovascular examination (murmurs, arrhythmias)
  • Visual acuity
  • Neurological examination (power, sensation, cerebellar signs)
  • Musculoskeletal assessment (joint range, deformity)
  • Cognitive assessment (AMT, 4AT for delirium)
  • Footwear assessment

Red Flags

  • Loss of consciousness (syncope vs mechanical fall)
  • Head injury (subdural haematoma risk, especially if anticoagulated)
  • Focal neurological signs (stroke)
  • New-onset heart failure or arrhythmia
  • Long lie (>1 hour on the floor - risk of rhabdomyolysis, hypothermia, pressure injury)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Mechanical fall (trip/slip)Clear environmental cause, no LOCEnvironmental assessment
Syncope (vasovagal, cardiac, orthostatic)LOC, presyncope symptomsLying/standing BP, ECG, echo
Stroke/TIAFocal neurological deficitCT head, neuro examination
EpilepsyWitnessed seizure, tongue biting, incontinenceEEG, MRI brain
Vestibular disorder (BPPV, labyrinthitis)Vertigo, nystagmusDix-Hallpike, HINTS
Cauda equina/myelopathyLower limb weakness, urinary symptomsMRI spine

Diagnosis / Investigation

Bedside

  • Lying and standing BP (1 and 3 minutes standing): postural drop ≥20mmHg systolic or ≥10mmHg diastolic
  • ECG: arrhythmia, heart block, QT prolongation
  • Timed Up and Go (TUG): >12 seconds suggests increased falls risk
  • 4AT: screening for delirium
  • Urinalysis (UTI as precipitant)
  • Blood glucose

Bloods

  • FBC (anaemia), U&Es (dehydration, AKI from long lie), calcium (hypercalcaemia)
  • TFTs, vitamin D, B12/folate
  • CK (rhabdomyolysis if long lie)
  • HbA1c (diabetes)
  • Bone profile (if fracture suspected)

Imaging

  • X-ray: if fracture suspected (hip, wrist, spine)
  • CT head: if head injury, anticoagulated, or neurological signs
  • DEXA scan: fracture risk assessment
  • Echocardiography: if murmur or suspected cardiac cause

Special Tests

  • 24-hour ECG (Holter): if arrhythmia suspected
  • Tilt table test: for suspected vasovagal syncope
  • Home hazard assessment by occupational therapist
  • Visual acuity testing
  • FRAX/QFracture: 10-year fracture risk assessment

Management

Non-pharmacological

  • Strength and balance training: Otago Exercise Programme or equivalent (30-40% fall reduction)
    • ≥3 sessions/week for ≥12 weeks (NICE CG161)
  • Home hazard assessment and modification (occupational therapy): grab rails, improved lighting, remove loose rugs
  • Footwear advice: well-fitting, low-heeled, non-slip soles
  • Visual correction: cataract surgery if indicated; avoid bifocal/varifocal glasses when walking
  • Assistive devices: walking frame, stick, personal alarm
  • Education: falls prevention awareness, strategies to get up after a fall

Pharmacological

  • Medication review: reduce/stop high-risk medications
    • Stop/reduce: benzodiazepines, Z-drugs, sedating antihistamines, anticholinergics, opioids
    • Review: antihypertensives (reduce if postural hypotension), diuretics, alpha-blockers
  • Vitamin D supplementation: 800-1,000 IU daily (especially if deficient or housebound)
  • Treat postural hypotension: reduce offending drugs; consider fludrocortisone 50-200mcg OD or midodrine 2.5-10mg TDS if persistent
  • Osteoporosis treatment: alendronate 70mg weekly, risedronate, denosumab (to reduce fracture risk from falls)

Surgical/Interventional

  • Cataract surgery: if visual impairment contributing to falls (reduces falls risk by 34%)
  • Cardiac pacemaker: if falls due to bradycardia, carotid sinus hypersensitivity, or complete heart block
  • Hip protectors: reduce hip fracture risk in care home residents

Referral Criteria

  • All older people presenting with a fall: multifactorial falls risk assessment
  • Recurrent falls (≥2 in 12 months): falls prevention service
  • Unexplained falls with LOC: cardiology/syncope assessment
  • Injurious falls in care home: community falls team
  • Osteoporosis identified: fracture liaison service

Prognosis

  • Multicomponent interventions reduce falls rate by 30-40% in community-dwelling older adults
  • Fear of falling affects 50% of fallers; contributes to activity restriction and further decline
  • Hip fracture: 30-day mortality ~8%; 1-year mortality ~30%
  • Long lie (>1 hour): associated with 50% mortality at 6 months
  • Falls are the leading cause of injury-related death in older adults
  • Most falls are preventable with appropriate multifactorial intervention

Other Relevant Information

NICE CG161 Multifactorial Falls Assessment Components

ComponentAssessment
Falls historyFrequency, circumstances, injuries
Gait and balanceTUG, Berg Balance Scale
Muscle strengthSit-to-stand, grip strength
Postural hypotensionLying/standing BP
Medication reviewIdentify high-risk drugs
Visual acuitySnellen chart
Cognitive assessment4AT, AMT, MMSE
CardiovascularECG, heart rate, murmurs
ContinenceUrgency, frequency, nocturia
Feet and footwearFoot problems, appropriate shoes
Environmental hazardsHome assessment

Timed Up and Go (TUG) Test

TimeInterpretation
<12 secondsNormal
12-20 secondsModerately impaired; increased fall risk
>20 secondsSignificantly impaired; high fall risk

NICE Guidelines / CKS

Balance and Mobility Assessment

Balance and mobility assessment is a core component of falls evaluation and geriatric assessment, using validated tools to identify gait and balance impairments and guide targeted interventions.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Gait and balance impairment is the single strongest predictor of future falls in older adults
  • Timed Up and Go (TUG): stand from chair, walk 3m, turn, return, sit down; >12 seconds suggests increased fall risk
  • Berg Balance Scale (BBS): 14 items scored 0-4 (max 56); <45 indicates increased fall risk
  • 30-second Chair Stand Test: functional lower limb strength; <8 stands is below normal for >65
  • Tinetti Performance-Oriented Mobility Assessment (POMA): gait (12 points) + balance (16 points); <19 = high fall risk
  • Short Physical Performance Battery (SPPB): combines balance, gait speed, and chair stands (0-12); <10 = increased disability risk
  • Gait speed <0.8 m/s is associated with increased mortality and frailty
  • Dual-task testing (walking while performing cognitive task) identifies those at highest fall risk

Overview

Key Facts

Balance and mobility assessment should be performed for all older adults at risk of falls or presenting with mobility difficulties. It informs targeted exercise prescriptions and intervention planning.

Epidemiology

  • Gait speed declines approximately 1-2% per year after age 60
  • Balance impairment is present in approximately 30% of people >65
  • Gait and balance disorders are the second most common cause of falls (after environmental hazards)
  • Reduced mobility is strongly associated with institutionalisation and death

Aetiology

Balance and mobility impairment in older adults is usually multifactorial:

  • Musculoskeletal: sarcopenia, arthritis, deconditioning
  • Neurological: stroke, Parkinson's disease, peripheral neuropathy, cerebellar disease, normal pressure hydrocephalus
  • Sensory: visual impairment, vestibular dysfunction, proprioceptive loss
  • Cardiovascular: postural hypotension, cardiac failure
  • Medications: sedatives, anticholinergics, opioids
  • Psychological: fear of falling, depression

Pathophysiology

  • Balance requires integration of visual, vestibular, and proprioceptive inputs in the central nervous system
  • Age-related changes: reduced muscle mass and strength, slower reaction times, decreased proprioception, reduced visual acuity
  • Sarcopenia: loss of muscle mass and function → reduced power generation for postural correction
  • Neurodegeneration: affects basal ganglia (gait initiation), cerebellum (coordination), and corticospinal tracts (motor control)

Clinical Presentation

History

  • Mobility baseline (independent, walks with aid, wheelchair)
  • Recent changes in mobility
  • Fear of falling
  • Functional capacity (ADLs, IADLs)
  • Near-misses and actual falls
  • Exercise tolerance

Examination

  • Observation of gait: speed, stride length, base width, arm swing, turning, step height
  • Romberg test: proprioceptive/vestibular assessment (eyes closed → increased sway)
  • Tandem stance/tandem walk: cerebellar assessment
  • Functional reach test: forward reach while maintaining balance (normal >25cm)
  • Chair stand test: functional lower limb strength
  • Joint examination: hip, knee, ankle range of motion and pain
  • Neurological examination: tone, power, reflexes, sensation (especially vibration sense/proprioception), coordination

Red Flags

  • Sudden-onset gait disturbance (stroke, spinal cord compression)
  • Gait with urinary incontinence and cognitive decline (normal pressure hydrocephalus)
  • Progressive bilateral weakness (myelopathy, polyneuropathy)
  • Festinant gait with freezing (Parkinson's disease)
  • Wide-based ataxic gait (cerebellar lesion)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Parkinson's diseaseShuffling gait, festination, freezing, tremorClinical, DaTSCAN
Peripheral neuropathyStocking sensory loss, high-stepping gaitNerve conduction studies
Normal pressure hydrocephalusGait apraxia, incontinence, dementiaCT/MRI brain, LP
Cerebellar diseaseWide-based ataxic gait, dysdiadochokinesisMRI brain
Cervical myelopathySpastic gait, upper limb signs, Lhermitte'sMRI spine
Vestibular disorderVertigo, nystagmus, veering gaitDix-Hallpike, HINTS
OsteoarthritisPain on weight-bearing, antalgic gaitX-ray, clinical

Diagnosis / Investigation

Bedside

  • Timed Up and Go (TUG): >12 seconds increased fall risk; >20 seconds high risk
  • 30-second Chair Stand Test: number of full stands in 30 seconds
  • 4-metre gait speed: <0.8 m/s = slow; <0.6 m/s = significantly impaired
  • Berg Balance Scale: if available (scored 0-56)
  • SPPB (Short Physical Performance Battery): balance + gait speed + chair stands (0-12)
  • Romberg test
  • Functional reach test
  • Observation of transfers and walking (with and without walking aid)

Bloods

  • Vitamin D (deficiency common and correctable)
  • B12 and folate (peripheral neuropathy)
  • TFTs (hypothyroid myopathy)
  • HbA1c (diabetic neuropathy)
  • CK (myopathy)

Imaging

  • MRI brain: if NPH, cerebellar disease, or stroke suspected
  • MRI spine: if myelopathy suspected
  • X-ray joints: if arthritic contribution

Special Tests

  • Nerve conduction studies: peripheral neuropathy
  • Vestibular function tests: if vestibular cause suspected
  • Comprehensive geriatric assessment (CGA): holistic assessment

Management

Non-pharmacological

  • Targeted exercise programme: based on assessment findings
    • Strength training (resistance exercises for major muscle groups)
    • Balance training (tandem stance, single-leg stance, Tai Chi)
    • Otago Exercise Programme: proven to reduce falls by 35%
  • Physiotherapy: individualised programme based on specific deficits
  • Occupational therapy: functional assessment, home modifications, assistive devices
  • Walking aids: correct selection and fitting (frame, stick, rollator)
  • Footwear: well-fitting shoes with good grip
  • Falls prevention groups: community-based exercise classes

Pharmacological

  • Vitamin D 800-1,000 IU daily: if deficient (improves muscle function)
  • Address underlying causes: levodopa for Parkinson's, B12 replacement, thyroid replacement
  • Medication review: reduce/stop drugs impairing balance

Surgical/Interventional

  • Joint replacement: if severe arthritis limiting mobility
  • VP shunt: for confirmed normal pressure hydrocephalus
  • Cataract surgery: if visual impairment contributing

Referral Criteria

  • Significant gait/balance impairment: physiotherapy and/or falls prevention service
  • Suspected neurological cause: neurology referral
  • Complex mobility issues in older adults: geriatric medicine referral (CGA)
  • Progressive mobility decline: investigate and refer early

Prognosis

  • Exercise interventions: reduce falls by 30-40% and improve balance, strength, and confidence
  • Gait speed <0.8 m/s: associated with increased mortality and disability
  • Fear of falling: responds to exercise-based interventions and CBT
  • Untreated mobility impairment leads to progressive disability, social isolation, and institutionalisation
  • Early identification and intervention can maintain independence and reduce falls-related morbidity and mortality

Other Relevant Information

Balance and Mobility Assessment Tools Summary

TestWhat It MeasuresCut-off for Fall Risk
Timed Up and Go (TUG)Functional mobility>12 seconds
Berg Balance ScaleStatic and dynamic balance (0-56)<45
30-second Chair StandLower limb strength<8 stands
Gait speed (4m)Walking speed<0.8 m/s
SPPBComposite physical performance (0-12)<10
Tinetti POMAGait and balance (0-28)<19 = high risk
Functional ReachStanding balance<25cm

Gait Speed as a Vital Sign

Gait SpeedInterpretation
>1.0 m/sNormal; good prognosis
0.8-1.0 m/sMild impairment
0.6-0.8 m/sModerate impairment; increased fall risk
<0.6 m/sSevere impairment; frailty indicator

NICE Guidelines / CKS

Frailty

Frailty is a state of increased vulnerability to poor resolution of homeostasis after a stressor event, identified using validated tools and managed through comprehensive geriatric assessment.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Frailty affects approximately 10% of people >65 and 25-50% of people >85 in the UK
  • Fried's frailty phenotype: ≥3 of - unintentional weight loss, exhaustion, low physical activity, slow walking speed, weak grip strength
  • Clinical Frailty Scale (CFS): 9-point scale widely used in UK clinical practice; CFS ≥5 indicates mild frailty
  • Electronic Frailty Index (eFI): uses primary care data to automatically screen for frailty (GP contract requirement)
  • Comprehensive Geriatric Assessment (CGA) is the gold standard management approach; reduces mortality and institutionalisation (meta-analysis evidence)
  • Frailty is potentially reversible in early stages with exercise, nutrition, and medication optimisation
  • Frailty and acute illness: frail patients are at higher risk of delirium, falls, prolonged hospital stay, and death
  • NICE NG56: all people ≥65 should be assessed for frailty using a validated tool at GP encounters

Overview

Key Facts

Frailty is a distinct clinical syndrome, not an inevitable consequence of ageing. Early identification allows intervention to prevent or slow decline.

Epidemiology

  • Prevalence: ~10% of people >65; ~25-50% >85
  • Pre-frailty (intermediate state): ~40% of people >65
  • More common in women, lower socioeconomic groups, and those with multimorbidity
  • Frail individuals have 2-3× higher risk of falls, hospitalisation, disability, and death

Aetiology

  • Biological ageing: sarcopenia, immune dysregulation, neuroendocrine decline
  • Multimorbidity: cumulative effect of multiple chronic conditions
  • Polypharmacy: drug side effects and interactions
  • Social factors: isolation, poverty, malnutrition
  • Psychological: depression, cognitive decline

Pathophysiology

  • Sarcopenia: age-related loss of muscle mass and function (central to frailty)
  • Chronic inflammation: elevated IL-6, TNF-α, CRP ("inflammageing")
  • Neuroendocrine dysregulation: reduced IGF-1, DHEA-S, testosterone
  • Immune senescence: impaired response to infection and vaccination
Dysregulated stress response
reduced physiological reserve
disproportionate decline after minor stressor (e.g. UTI
delirium
falls
hip fracture
death)

Clinical Presentation

Frailty Syndromes

  • Falls
  • Delirium
  • Immobility
  • Incontinence
  • Susceptibility to medication side effects

Fried's Frailty Phenotype (≥3 of 5)

  • Unintentional weight loss (>4.5 kg in past year)
  • Self-reported exhaustion
  • Low physical activity
  • Slow walking speed (<0.8 m/s)
  • Weak grip strength (below age/sex norms)

Clinical Frailty Scale

  • 1-3: Well/managing well
  • 4: Vulnerable (not dependent but slowing)
  • 5: Mildly frail (needs help with IADLs)
  • 6: Moderately frail (needs help with ADLs and IADLs)
  • 7: Severely frail (completely dependent, approaching end of life)
  • 8: Very severely frail (completely dependent, bed-bound)
  • 9: Terminally ill

Red Flags

  • Rapid functional decline
  • Unintentional weight loss >5% in 6 months
  • Recurrent hospital admissions ("revolving door")
  • New delirium or confusion
  • Polypharmacy (≥10 medications)
  • Social crisis (carer breakdown, self-neglect)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
DepressionLow mood, anhedonia, fatiguePHQ-9, GAD-7
HypothyroidismFatigue, weight gain, cold intoleranceTFTs
Heart failureDyspnoea, oedema, fatigueBNP, echocardiography
MalignancyWeight loss, fatigue, painBloods, imaging
AnaemiaFatigue, pallor, dyspnoeaFBC, haematinics
DementiaCognitive decline, functional impairmentCognitive assessment, MRI

Diagnosis / Investigation

Bedside

  • Clinical Frailty Scale: quick bedside assessment
  • Functional assessment (ADLs, IADLs)
  • Nutritional screening (MUST score)
  • Cognitive screening (4AT, AMT, MoCA)
  • Mood assessment (GDS-15)
  • Gait speed and grip strength

Bloods

  • FBC, U&Es, LFTs, TFTs
  • Vitamin D, B12, folate, ferritin
  • HbA1c, albumin (nutritional marker)
  • CRP (chronic inflammation)

Imaging

  • As directed by CGA findings (not routine for frailty itself)
  • CXR if respiratory symptoms
  • DEXA if osteoporosis risk

Special Tests

  • Electronic Frailty Index (eFI): automated from GP electronic health records
  • Comprehensive Geriatric Assessment (CGA): holistic multidomain assessment
  • FRAX/QFracture: fracture risk
  • Medication review using STOPP/START criteria

Management

Non-pharmacological

  • Comprehensive Geriatric Assessment (CGA): multidimensional assessment by MDT (geriatrician, physiotherapist, OT, dietitian, social worker, pharmacist)
  • Exercise: resistance training + balance exercises (most effective single intervention)
    • ≥150 minutes/week moderate activity; strength exercises ≥2 days/week
  • Nutrition: adequate protein intake (1.0-1.2 g/kg/day); high-calorie supplements if malnourished (Fortisip, Ensure)
  • Social support: address isolation, befriending, day centres
  • Advance care planning: discuss preferences for future care
  • Falls prevention: as per NICE CG161

Pharmacological

  • Medication optimisation: deprescribing using STOPP/START criteria
    • Stop: unnecessary PPIs, long-term benzodiazepines, anticholinergics, duplicate drugs
    • Consider stopping statins if life expectancy <1 year
  • Vitamin D supplementation: 800-1,000 IU daily
  • Treat underlying conditions: anaemia, hypothyroidism, depression, heart failure
  • Vaccination: annual influenza, pneumococcal, COVID-19, shingles

Surgical/Interventional

  • Frailty assessment should inform surgical decision-making (CFS used in perioperative risk assessment)
  • Prehabilitation before elective surgery in frail patients
  • Rockwood CFS ≥5 associated with increased surgical complications and mortality

Referral Criteria

  • Moderate-severe frailty (CFS ≥6): geriatric medicine assessment
  • Complex multimorbidity: MDT CGA
  • Recurrent admissions: community geriatrics/integrated care team
  • Carer strain: social services, carer support
  • Approaching end of life: palliative care referral

Prognosis

  • Pre-frailty is reversible in approximately 40% with exercise and nutrition
  • Mild frailty may stabilise or improve with intervention
  • Moderate-severe frailty: progressive in most; focus shifts to maintaining quality of life
  • CGA in hospital reduces mortality (OR 0.76) and increases likelihood of being alive and at home at 12 months
  • Frail older adults have 2-3× mortality compared to non-frail age-matched individuals
  • Frailty index predicts mortality better than age or individual comorbidities
  • Quality of life and patient-centred goals should guide management in advanced frailty

Other Relevant Information

Clinical Frailty Scale (Rockwood)

ScoreCategoryDescription
1Very fitRobust, active, energetic
2WellNo active disease, less fit than category 1
3Managing wellMedical problems well controlled
4VulnerableNot dependent but symptoms limit activities
5Mildly frailNeeds help with IADLs (finances, transport, housework)
6Moderately frailNeeds help with ADLs and IADLs
7Severely frailCompletely dependent; approaching end of life
8Very severely frailCompletely dependent; cannot recover from minor illness
9Terminally illLife expectancy <6 months

Comprehensive Geriatric Assessment Domains

DomainAssessment
MedicalProblem list, medication review, comorbidities
FunctionalADLs, IADLs, mobility, falls
CognitiveMMSE, MoCA, 4AT (delirium)
PsychologicalDepression (GDS), anxiety
NutritionalMUST, weight, dietary intake
SocialLiving situation, carers, isolation, finances
EnvironmentalHome safety, aids and adaptations

NICE Guidelines / CKS

Comprehensive Geriatric Assessment

Comprehensive Geriatric Assessment (CGA) is a multidimensional, interdisciplinary diagnostic process to determine the medical, psychological, functional, and social capabilities of a frail older person to develop a coordinated care plan.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • CGA is the gold standard for assessment and management of frail older people in hospital and community settings
  • Meta-analysis evidence (Ellis et al. 2011, 2017): CGA increases the likelihood of being alive and in own home at 12 months (NNT = 13)
  • CGA reduces mortality (OR 0.76), institutionalisation, functional decline, and length of stay
  • Multidomain assessment: medical, functional, cognitive, psychological, nutritional, social, environmental
  • MDT approach: geriatrician, nurse, physiotherapist, occupational therapist, dietitian, speech therapist, social worker, pharmacist
  • CGA should be delivered in a dedicated geriatric unit where possible (associated with best outcomes)
  • Goal-setting is a key component: patient-centred goals guide the management plan
  • CGA is process-driven (not just a one-off assessment) with regular review and adaptation

Overview

Key Facts

CGA is one of the most evidence-based interventions in medicine for improving outcomes in frail older adults. It is both an assessment tool and a management framework.

Epidemiology

  • Approximately 30-50% of hospital inpatients >65 would benefit from CGA
  • Acute frailty units using CGA have improved outcomes compared to standard care
  • CGA is recommended by NICE for all frail older people admitted to hospital

Aetiology

CGA addresses the multifactorial nature of illness and decline in older adults, recognising that a single disease model is inadequate.

Pathophysiology

  • Frail older adults have reduced physiological reserve
  • Acute illness causes disproportionate functional decline
  • Multiple interacting problems (medical, cognitive, psychological, social) require a holistic approach
  • CGA identifies these interactions and creates an integrated management plan

Clinical Presentation

Indications for CGA

  • Frail older adults (CFS ≥5)
  • Multiple comorbidities
  • Functional decline
  • Recurrent admissions
  • Complex discharge planning
  • Cognitive impairment with comorbidities
  • Falls and mobility problems
  • Polypharmacy

CGA Process

  1. Multidomain assessment by MDT
  2. Problem identification across all domains
  3. Goal-setting with patient and family
  4. Creation of integrated care plan
  5. Implementation
  6. Regular review and adaptation

Red Flags Triggering CGA

  • Functional decline not explained by acute illness alone
  • Delirium
  • Recurrent falls
  • New incontinence
  • Significant weight loss
  • Carer breakdown
  • Discharge to higher level of care being considered

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Single-organ diseaseTypical presentation, no complexityStandard investigation
Multimorbidity without frailtyMultiple conditions but good functionCGA not necessarily needed
Frailty syndromesFalls, delirium, immobility, incontinenceCGA indicated
End of lifeProgressive decline despite treatmentPalliative approach within CGA

Diagnosis / Investigation

Bedside

  • Medical: comprehensive medical history, medication reconciliation
  • Functional: ADLs (Barthel Index), IADLs (Lawton Scale), mobility (TUG, gait speed)
  • Cognitive: 4AT (delirium), AMT-10, MoCA/ACE-III (dementia)
  • Psychological: GDS-15 (depression), GAD-7 (anxiety)
  • Nutritional: MUST score, weight, BMI, dietary history
  • Social: living situation, carers, social support, advance care planning
  • Environmental: home safety assessment

Bloods

  • FBC, U&Es, LFTs, TFTs, calcium, vitamin D, B12, folate, ferritin
  • HbA1c, albumin, CRP
  • Medication levels where appropriate

Imaging

  • As directed by CGA findings

Special Tests

  • Medication review (STOPP/START)
  • Swallow assessment if dysphagia
  • Continence assessment
  • Tissue viability assessment
  • Carer strain assessment

Management

Non-pharmacological

  • Personalised care plan based on CGA findings and patient goals
  • Rehabilitation: physiotherapy (strength, balance), OT (functional goals, ADLs)
  • Cognitive stimulation: for dementia/delirium prevention
  • Nutritional optimisation: dietitian input, supplementation
  • Social prescribing: address isolation, community activities
  • Discharge planning: start from admission; MDT assessment of safe discharge
  • Follow-up: community geriatric teams, GP care plan

Pharmacological

  • Medication optimisation: STOPP/START criteria, deprescribing
  • Treat identified conditions: heart failure, infection, depression, pain
  • Preventive measures: vitamin D, vaccination, bone protection

Surgical/Interventional

  • CGA informs surgical risk assessment in older adults
  • Proactive geriatric liaison in surgical patients (hip fracture, emergency surgery)
  • Perioperative CGA reduces post-operative complications

Referral Criteria

  • All frail older adults admitted to hospital
  • Complex community patients with functional decline
  • Pre-operative assessment for frail surgical patients
  • Recurrent admissions
  • Complex discharge planning

Prognosis

  • CGA in hospital: NNT 13 to prevent one death or institutional placement at 12 months
  • CGA reduces mortality: OR 0.76 (95% CI 0.64-0.90)
  • CGA reduces institutionalisation: OR 0.80
  • Outcomes best when delivered by a dedicated geriatric MDT on a specialist unit
  • CGA in the community also improves outcomes (reduces hospital admissions)
  • Goal attainment is associated with improved patient satisfaction and quality of life

Other Relevant Information

CGA Domains and Assessment Tools

DomainKey Tools
MedicalProblem list, medication review (STOPP/START), comorbidity index (Charlson)
FunctionalBarthel Index, Lawton IADL Scale, TUG, gait speed
Cognitive4AT, AMT-10, MoCA, ACE-III
PsychologicalGDS-15 (depression), CAM (delirium)
NutritionalMUST, MNA
SocialSocial history, carer assessment
EnvironmentalHome hazard assessment, community resources

Evidence for CGA

StudyFinding
Ellis et al. (2011, 2017)CGA improves survival and likelihood of remaining at home
Stuck et al. (1993)CGA reduces functional decline
Baztan et al. (2009)Acute geriatric units reduce mortality and LOS
POPS studyProactive geriatric care in surgery improves outcomes

NICE Guidelines / CKS

Delirium

Delirium is an acute, fluctuating disturbance of consciousness and cognition caused by an underlying medical condition, affecting up to 30% of hospitalised older adults and associated with increased mortality.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Delirium affects up to 30% of hospitalised older adults and 50-80% of ICU patients
  • 4AT is the recommended rapid screening tool (NICE NG103, Sign 157); score ≥4 suggests delirium
  • Three subtypes: hyperactive (agitation), hypoactive (most common, worst prognosis, often missed), mixed
  • Always reversible in principle - identify and treat the underlying cause; use the mnemonic PINCH ME (Pain, Infection, Nutrition, Constipation, Hydration, Medication, Environment)
  • Avoid antipsychotics unless patient is at risk of harm; if essential, use haloperidol 0.5-1mg (avoid in Lewy body/Parkinson's - use lorazepam 0.5-1mg)
  • Predisposing factors: age >65, dementia, severe illness, hip fracture, visual/hearing impairment
  • Precipitating factors: infection (UTI, pneumonia), drugs (opioids, anticholinergics, benzodiazepines), pain, constipation, urinary retention, metabolic disturbance
  • Delirium is associated with increased mortality (30-40% at 1 year), prolonged hospital stay, and accelerated cognitive decline

Overview

Key Facts

Delirium is a medical emergency requiring urgent identification and treatment of the underlying cause. Prevention is more effective than treatment.

Epidemiology

  • Affects 20-30% of medical inpatients >65; up to 50% post-operatively
  • Hypoactive delirium accounts for 50-70% and is frequently unrecognised
  • Incidence increases with age, frailty, and cognitive impairment

Aetiology

PINCH ME mnemonic:

  • Pain
  • Infection (UTI, pneumonia, cellulitis)
  • Nutrition (dehydration, electrolyte disturbance)
  • Constipation / urinary retention
  • Hydration (dehydration, fluid overload)
  • Medication (opioids, anticholinergics, benzodiazepines, steroids, drug/alcohol withdrawal)
  • Environment (unfamiliar surroundings, sleep deprivation, immobility)

Pathophysiology

  • Multifactorial model: predisposing vulnerability + precipitating insult
Neuroinflammation: systemic inflammation
microglial activation
neurotransmitter imbalance
  • Cholinergic deficiency and dopaminergic excess are central to the pathophysiology
  • Disruption of the ascending reticular activating system
  • Blood-brain barrier dysfunction during acute illness

Clinical Presentation

Core Features

  • Acute onset (hours to days)
  • Fluctuating course (lucid intervals)
  • Inattention (key feature - cannot sustain attention)
  • Altered level of consciousness
  • Cognitive disturbance (disorientation, memory impairment)
  • Perceptual disturbance (hallucinations, illusions)
  • Psychomotor disturbance (agitation or withdrawal)
  • Sleep-wake cycle disturbance

Subtypes

  • Hyperactive: agitation, restlessness, hallucinations, aggression (25%)
  • Hypoactive: withdrawal, drowsiness, reduced movement, quiet confusion (50-70%) - worst prognosis, often missed
  • Mixed: alternating between hyperactive and hypoactive (25%)

Red Flags

  • Sudden onset confusion in previously well/stable patient
  • New agitation or aggression in a patient with dementia
  • Reduced consciousness level (GCS drop)
  • Fever with confusion (sepsis)
  • Head injury with confusion (intracranial pathology)
  • Post-operative confusion (common; always investigate)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
DementiaChronic, gradual onset, no fluctuation in alertnessCognitive assessment, collateral history
DepressionLow mood, anhedonia, psychomotor retardationPHQ-9, psychiatric assessment
Psychosis (functional)Younger, clear sensorium, organised delusionsPsychiatric assessment
Non-convulsive status epilepticusSubtle motor signs, unexplained altered consciousnessEEG
StrokeFocal neurological deficit, sudden onsetCT head
HypoglycaemiaDiaphoresis, tremor, rapid response to glucoseCBG

Diagnosis / Investigation

Bedside

  • 4AT screening tool: ≥4 = probable delirium (alertness, AMT4, attention, acute change)
  • Observations: temperature, HR, BP, O2 sats, RR, blood glucose
  • Urinalysis (UTI)
  • ECG
  • Pain assessment
  • Medication chart review

Bloods

  • FBC, CRP (infection)
  • U&Es (dehydration, AKI, electrolyte disturbance)
  • LFTs, calcium, magnesium, phosphate
  • Blood glucose, HbA1c
  • TFTs
  • Blood cultures (if pyrexial)
  • B12, folate (if nutritional deficiency suspected)

Imaging

  • CXR (pneumonia)
  • CT head: if head injury, focal neurology, no clear cause identified, anticoagulated
  • CT abdomen/pelvis: if intra-abdominal cause suspected

Special Tests

  • MSU (urine culture)
  • Confusion Assessment Method (CAM): research gold standard
  • EEG: if non-convulsive status suspected (diffuse slowing in delirium)
  • Lumbar puncture: if meningitis/encephalitis suspected

Management

Non-pharmacological (FIRST LINE)

  • Identify and treat underlying cause (treat infection, stop offending drugs, correct dehydration, relieve pain/constipation/retention)
  • Reorientation: clocks, calendars, familiar objects, consistent staff
  • Ensure sensory aids (glasses, hearing aids)
  • Promote sleep-wake cycle: natural light, reduce nocturnal interventions
  • Mobilise early: avoid unnecessary catheterisation and restraint
  • Involve family/carers
  • Avoid unnecessary ward moves
  • Delirium prevention: NICE CG103 recommends multicomponent intervention for all at-risk patients

Pharmacological

  • Only if patient at risk of harm to self or others, and non-pharmacological measures have failed
  • Haloperidol 0.5mg PO/IM (start low, max 2mg/24h in elderly); avoid in Parkinson's/Lewy body dementia
  • Lorazepam 0.5-1mg PO/IM: preferred in Parkinson's/Lewy body, alcohol withdrawal, seizure risk
  • Olanzapine 2.5-5mg: alternative if haloperidol contraindicated
  • Review and stop offending medications: opioids, anticholinergics, benzodiazepines, steroids
  • Treat underlying causes: antibiotics for infection, IV fluids for dehydration, analgesia for pain

Surgical/Interventional

  • Address surgical causes: urinary retention (catheterise), constipation (enemas), fracture fixation

Referral Criteria

  • Persistent delirium (>2 weeks): consider psychiatric/geriatric review
  • Delirium superimposed on dementia: specialist assessment
  • Complex cases: liaison psychiatry

Prognosis

  • In-hospital mortality: 10-26% (2× higher than non-delirious patients)
  • 1-year mortality: 30-40% (delirium is an independent predictor of death)
  • Mean excess hospital stay: 7-10 days
  • 30-50% develop dementia within 2-3 years of a delirium episode
  • Full recovery in approximately 50%; persistent cognitive impairment in many
  • Hypoactive delirium has worst prognosis (often undiagnosed)
  • Prevention reduces delirium incidence by 30-40% (multicomponent interventions)

Other Relevant Information

4AT Rapid Clinical Test for Delirium

ItemScore
Alertness (normal = 0; abnormal = 4)0 or 4
AMT4 (age, DOB, place, year - all correct = 0; 1 error = 1; ≥2 errors or untestable = 2)0, 1, or 2
Attention (months backwards - 7+ correct = 0; <7 or refuses = 1; untestable = 2)0, 1, or 2
Acute change or fluctuating course (no = 0; yes = 4)0 or 4
Total ≥4: possible delirium ± cognitive impairment
Total 1-3: possible cognitive impairment
Total 0: delirium or cognitive impairment unlikely

PINCH ME - Causes of Delirium

LetterCause
PPain
IInfection
NNutrition
CConstipation
HHydration
MMedication
EEnvironment

NICE Guidelines / CKS

Dementia

Dementia is a progressive syndrome of cognitive decline affecting approximately 900,000 people in the UK, with Alzheimer's disease being the most common cause, requiring early diagnosis, acetylcholinesterase inhibitors, and comprehensive support.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Dementia affects approximately 900,000 people in the UK; projected to exceed 1 million by 2025
  • Alzheimer's disease (62%), vascular dementia (17%), mixed (10%), Lewy body (4%), frontotemporal (2%)
  • NICE NG97: refer to memory assessment service; assess with validated cognitive tools (ACE-III, MoCA)
  • Acetylcholinesterase inhibitors: first-line for mild-moderate Alzheimer's - donepezil 5-10mg OD, rivastigmine, galantamine
  • Memantine 10-20mg OD: for moderate-severe Alzheimer's or if AChEIs not tolerated (NMDA receptor antagonist)
  • Lewy body dementia: visual hallucinations, parkinsonism, fluctuating cognition, REM sleep behaviour disorder; avoid antipsychotics (severe sensitivity reactions)
  • Vascular dementia: stepwise decline, vascular risk factors, focal neurological signs; manage cardiovascular risk factors
  • Diagnosis requires impairment in ≥2 cognitive domains (memory, language, visuospatial, executive, behaviour) sufficient to affect daily function

Overview

Key Facts

Dementia is not a normal part of ageing. Early diagnosis enables access to treatment, support, and future planning including advance care planning.

Epidemiology

  • ~900,000 people in the UK; ~70,000 people <65 (young-onset dementia)
  • Prevalence doubles every 5 years after age 65
  • Leading cause of death in England and Wales
  • Annual NHS cost: approximately £26 billion

Aetiology

  • Alzheimer's disease: amyloid plaques (Aβ42) and neurofibrillary tangles (hyperphosphorylated tau)
  • Vascular dementia: cerebrovascular disease (multi-infarct, small vessel disease, strategic infarct)
  • Lewy body dementia: α-synuclein Lewy bodies in cortex and brainstem
  • Frontotemporal dementia: tau or TDP-43 protein aggregates; frontal/temporal atrophy
  • Risk factors: age, family history, APOE ε4 allele (Alzheimer's), hypertension, diabetes, obesity, smoking, depression, low education

Pathophysiology

Alzheimer's
amyloid cascade hypothesis - Aβ42 aggregation
neuritic plaques
tau hyperphosphorylation
neurofibrillary tangles
synaptic loss
neuronal death; cholinergic deficit (basis for AChEI treatment)
  • Vascular: white matter ischaemia, lacunar infarcts, strategic infarcts (thalamus, angular gyrus)
  • Lewy body: Lewy body deposition in cortex → cholinergic and dopaminergic disruption
  • Frontotemporal: frontal/temporal neuronal loss → personality change, language impairment

Clinical Presentation

Alzheimer's Disease

  • Insidious onset, gradual progression
  • Early: short-term memory loss (episodic memory), word-finding difficulty
  • Moderate: disorientation, impaired ADLs, behavioural changes
  • Severe: loss of speech, immobility, incontinence

Vascular Dementia

  • Stepwise decline (episodes of deterioration)
  • Focal neurological signs
  • Emotional lability
  • Preservation of personality (early)

Lewy Body Dementia

  • Visual hallucinations (detailed, recurrent)
  • Fluctuating cognition (marked fluctuations in alertness and attention)
  • Parkinsonism (rigidity, bradykinesia, but tremor less prominent)
  • REM sleep behaviour disorder (acts out dreams)
  • Autonomic dysfunction, falls

Frontotemporal Dementia

  • Behavioural variant: personality change, disinhibition, apathy, loss of empathy
  • Semantic: loss of word meaning
  • Progressive non-fluent aphasia: effortful speech, grammatical errors
  • Memory relatively preserved early

Red Flags

  • Rapid cognitive decline (weeks-months): consider CJD, autoimmune encephalitis, tumour
  • Young onset (<65): genetic causes, metabolic
  • Focal neurological signs: stroke, space-occupying lesion
  • Gait disturbance + incontinence + dementia: normal pressure hydrocephalus (potentially reversible)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
DeliriumAcute onset, fluctuating, inattention4AT, treat underlying cause
Depression (pseudodementia)Low mood, anhedonia, subjective cognitive complaintsPHQ-9, trial of antidepressant
Normal pressure hydrocephalusGait apraxia, incontinence, dementia (Hakim's triad)CT/MRI (ventriculomegaly), LP
HypothyroidismFatigue, cognitive slowing, weight gainTFTs
B12 deficiencyPeripheral neuropathy, macrocytic anaemiaB12 level
Subdural haematomaHistory of fall/trauma, fluctuating consciousnessCT head

Diagnosis / Investigation

Bedside

  • Cognitive assessment: ACE-III (88 or below abnormal), MoCA (≤25 abnormal), MMSE, 6-CIT
  • Collateral history from carer/family (essential)
  • Functional assessment (ADLs, IADLs)
  • Behavioural assessment
  • Depression screening (GDS-15)

Bloods

  • Dementia screening bloods (to exclude reversible causes): FBC, U&Es, LFTs, calcium, TFTs, B12, folate, HbA1c
  • Syphilis serology (if indicated)
  • HIV (if risk factors)

Imaging

  • MRI brain (preferred): hippocampal atrophy (Alzheimer's), vascular changes (WMH, infarcts), frontotemporal atrophy
  • CT head: alternative if MRI contraindicated
  • FDG-PET or SPECT: if diagnostic uncertainty (e.g. differentiating Alzheimer's from FTD)
  • DaTSCAN (FP-CIT SPECT): abnormal in Lewy body dementia (reduced dopamine transporter uptake)

Special Tests

  • CSF: Aβ42 (low) and tau/p-tau (elevated) in Alzheimer's (specialist use)
  • Amyloid PET: emerging diagnostic tool
  • Genetic testing: familial Alzheimer's (APP, PSEN1, PSEN2), FTD (MAPT, GRN, C9orf72)
  • EEG: CJD (periodic sharp wave complexes), non-convulsive status

Management

Non-pharmacological

  • Cognitive stimulation therapy (CST): NICE-recommended; group-based; improves cognition and QoL
  • Reminiscence therapy: using past experiences to stimulate memory
  • Physical exercise: regular aerobic and resistance exercise
  • Occupational therapy: strategies for maintaining independence
  • Carer support: education, respite care, support groups (Alzheimer's Society)
  • Environmental modifications: clear signage, good lighting, memory aids
  • Advance care planning: discuss early while capacity present
  • Lasting Power of Attorney: encourage early discussion

Pharmacological

  • Mild-moderate Alzheimer's disease:
    • Donepezil 5mg OD → increase to 10mg after 4-6 weeks (AChEI)
    • Alternatives: rivastigmine (patches 4.6-13.3mg/24h), galantamine 8-24mg MR OD
  • Moderate-severe Alzheimer's:
    • Memantine 5mg OD → titrate to 20mg OD over 4 weeks (NMDA antagonist)
    • Can use in combination with AChEI
  • Lewy body dementia: AChEIs (rivastigmine preferred); avoid antipsychotics (neuroleptic sensitivity)
  • Vascular dementia: no specific pharmacological treatment; optimise cardiovascular risk factors
  • FTD: no disease-modifying treatment; SSRIs for behavioural symptoms (trazodone for agitation)
  • BPSD (behavioural and psychological symptoms):
    • First-line: non-pharmacological approaches
    • If severe/distressing: risperidone 250mcg-1mg OD (only antipsychotic licensed for BPSD; short course, regular review)

Surgical/Interventional

  • VP shunt for normal pressure hydrocephalus (potentially reversible dementia)

Referral Criteria

  • Suspected dementia: memory assessment service/memory clinic
  • Young-onset (<65): specialist neurology/neuropsychiatry
  • Diagnostic uncertainty: specialist neuroimaging, CSF biomarkers
  • Complex BPSD: old age psychiatry
  • Carer strain: social services, Alzheimer's Society

Prognosis

  • Alzheimer's disease: mean survival 8-10 years from diagnosis; progressive
  • Vascular dementia: variable; depends on cardiovascular management; median survival 5 years
  • Lewy body dementia: median survival 5-8 years; high risk of falls and aspiration
  • Frontotemporal dementia: median survival 6-8 years (behavioural variant); 3-5 years (motor neurone disease variant)
  • AChEIs: modest but significant improvement in cognition, function, and behaviour (delay decline by ~6-12 months)
  • Dementia is a terminal illness; palliative care approach in advanced stages
  • Leading cause of death in England and Wales

Other Relevant Information

Comparison of Dementia Subtypes

FeatureAlzheimer'sVascularLewy BodyFrontotemporal
OnsetInsidiousStepwise/suddenInsidious, fluctuatingInsidious
MemoryEarly, prominentVariableVariableLate
HallucinationsLateUncommonEarly, visualUncommon
MotorLateFocal signsParkinsonismLate (MND variant early)
ImagingHippocampal atrophyWMH, infarctsRelatively preservedFrontal/temporal atrophy
TreatmentAChEI, memantineCVD risk managementAChEI (rivastigmine)Symptomatic only

Cognitive Assessment Tools

ToolScore RangeCut-offTime
MMSE0-30≤24 abnormal10 min
MoCA0-30≤25 abnormal10 min
ACE-III0-100≤88 abnormal15 min
6-CIT0-28≥8 significant impairment5 min

NICE Guidelines / CKS

Polypharmacy and Deprescribing

Polypharmacy is the concurrent use of multiple medications, commonly defined as 5 or more regular drugs, with deprescribing being the planned, supervised withdrawal of inappropriate medications to improve outcomes.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Polypharmacy (≥5 medications) affects approximately 50% of people >65 and >70% of care home residents in the UK
  • Appropriate polypharmacy is necessary for multimorbidity; problematic polypharmacy occurs when the risks outweigh benefits
  • Adverse drug reactions (ADRs) account for 6-7% of hospital admissions in older adults
  • STOPP/START criteria (v2, 2015): evidence-based screening tool for potentially inappropriate medications (STOPP) and potential prescribing omissions (START)
  • Beers Criteria: American Geriatrics Society list of potentially inappropriate medications in older adults
  • Anticholinergic burden: cumulative effect of anticholinergic drugs increases falls, delirium, and cognitive impairment risk
  • NICE NG56: recommends structured medication review for all people with multimorbidity, especially those on ≥10 medications
  • Deprescribing should be gradual, patient-centred, and monitored for withdrawal effects

Overview

Key Facts

Medication review and deprescribing are essential components of managing older adults with multimorbidity. The goal is to optimise medications, reduce harm, and improve quality of life.

Epidemiology

  • 50% of >65s take ≥5 medications; 20% take ≥10
  • ADRs cause 6-7% of hospital admissions in older adults (preventable in ~50%)
  • Falls related to polypharmacy: 1.5-2× increased risk
  • Care home residents: average 7-8 regular medications

Aetiology

  • Multimorbidity: multiple conditions requiring multiple treatments
Prescribing cascades
drug side effect treated with another drug (e.g. NSAID
hypertension
antihypertensive)
  • Failure to review: medications continued beyond indicated duration
  • Multiple prescribers: lack of coordination between specialists and GP
  • Patient expectations: reluctance to stop medications

Pathophysiology

  • Pharmacokinetic changes with ageing: reduced hepatic metabolism (CYP450), reduced renal clearance (GFR declines ~1ml/min/year after 40), increased body fat (lipophilic drug accumulation), reduced plasma albumin (increased free drug)
  • Pharmacodynamic changes: increased sensitivity to CNS depressants, reduced baroreceptor sensitivity (postural hypotension), reduced homeostatic reserve
  • Drug-drug interactions: exponential increase with number of drugs
  • Anticholinergic burden: cumulative anticholinergic effect → dry mouth, constipation, urinary retention, confusion, falls

Clinical Presentation

Indicators of Problematic Polypharmacy

  • ≥10 regular medications (hyperpolypharmacy)
  • Recurrent falls
  • Adverse drug reactions
  • Poor medication adherence
  • Drug-drug interactions
  • Drugs prescribed without clear indication
  • Drugs continued beyond recommended duration
  • Prescribing cascades

Common ADRs in Older Adults

  • Falls (sedatives, antihypertensives, anticholinergics)
  • GI bleeding (NSAIDs, anticoagulants, SSRIs)
  • Delirium (opioids, anticholinergics, benzodiazepines)
  • Hypoglycaemia (sulfonylureas, insulin)
  • Renal impairment (NSAIDs, ACEi, diuretics)
  • Electrolyte disturbance (diuretics, PPIs)

Red Flags

  • New symptom that could be an ADR (always consider "could this be a drug side effect?")
  • Anticholinergic burden score ≥3
  • Falling while on high-risk medications
  • Delirium in a patient on multiple CNS-active drugs
  • Renal function decline on nephrotoxic drugs

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
ADR causing symptomsTemporal relationship to drug initiationMedication review, drug levels
Disease progressionWorsening of known conditionClinical assessment
Drug-drug interactionSymptoms after adding new drugInteraction check
Non-adherenceTreatment failure, erratic drug levelsMedication history, adherence tools
Drug withdrawalSymptoms after stopping medicationClinical history

Diagnosis / Investigation

Bedside

  • Comprehensive medication review (include OTC, herbal, supplements)
  • Medication reconciliation (compare different drug lists)
  • Adherence assessment (ask patient, pill count, dosette box review)
  • Lying and standing BP (postural hypotension from drugs)

Bloods

  • U&Es (renal function for dose adjustment)
  • LFTs (hepatic function)
  • Drug levels where appropriate (digoxin, lithium, phenytoin, aminoglycosides)
  • HbA1c (diabetes management review)

Imaging

  • Not routine for polypharmacy itself

Special Tests

  • STOPP/START screening: systematic review using criteria
  • Anticholinergic Burden Calculator: score anticholinergic load
  • Beers Criteria: alternative screening tool
  • NO TEARS tool: Need, Open questions, Tests/monitoring, Evidence, ADRs, Risk, Simplification
  • GFR estimation (CKD-EPI) for dose adjustment

Management

Non-pharmacological

  • Structured medication review (NICE NG56): at least annually; more frequently if on ≥10 drugs, after hospital discharge, or after ADR
  • Patient involvement: shared decision-making; discuss goals, preferences, and life expectancy
  • Simplify regimens: reduce dose frequency, use combination preparations
  • Use compliance aids: dosette boxes, blister packs (consider with pharmacy)

Pharmacological (Deprescribing)

  • Apply STOPP/START criteria:
    • STOPP examples: PPI >8 weeks without clear indication; benzodiazepines >4 weeks; anticholinergics in dementia; long-acting sulfonylureas in >65
    • START examples: statin in diabetes with CVD risk; ACEi in heart failure; calcium + vitamin D in osteoporosis
  • Deprescribing approach:
    1. Identify potentially inappropriate medications
    2. Assess risk of withdrawal vs continuation
    3. Prioritise which to stop first (highest risk of harm)
    4. Reduce gradually (especially benzodiazepines, opioids, antidepressants, beta-blockers, corticosteroids)
    5. Monitor for withdrawal or disease relapse
  • High-priority for deprescribing: PPIs, benzodiazepines/Z-drugs, anticholinergics, opioids for non-cancer pain, statins (if limited life expectancy)

Surgical/Interventional

  • Not applicable

Referral Criteria

  • Complex polypharmacy: clinical pharmacist review, geriatric medicine
  • Suspected ADR causing hospital admission: medicines optimisation team
  • Specialist medications: liaise with relevant specialist before stopping

Prognosis

  • Medication review and deprescribing reduces inappropriate prescribing, ADRs, and falls
  • Structured reviews can reduce number of medications by 2-3 in care home residents
  • 50% of ADR-related admissions are preventable
  • Deprescribing is safe when done gradually with monitoring
  • No consistent evidence of increased mortality from appropriate deprescribing
  • Patient satisfaction and quality of life often improve after deprescribing

Other Relevant Information

Selected STOPP Criteria (v2)

DrugStop If
PPI>8 weeks at full dose without clear indication
Benzodiazepine>4 weeks (fall risk, dependence)
NSAID>3 months; with CKD, HF, peptic ulcer
AnticholinergicIn patients with dementia or delirium
Long-acting sulfonylurea (glibenclamide)In >65 (hypoglycaemia risk)
Loop diureticFor ankle oedema without heart failure
Duplicate drugsTwo drugs from same class

Selected START Criteria (v2)

DrugStart If
StatinIn diabetes with ≥1 CVD risk factor
ACEi/ARBIn heart failure with reduced EF
Inhaled corticosteroidIn moderate-severe asthma/COPD
Calcium + vitamin DIn known osteoporosis
MetforminFirst-line in type 2 diabetes
AnticoagulantIn atrial fibrillation with CHA2DS2-VASc ≥2

NICE Guidelines / CKS

Urinary Incontinence in the Elderly

Urinary incontinence affects approximately 30-50% of older adults, with stress, urge, overflow, and functional subtypes requiring targeted investigation and management including behavioural therapies and pharmacotherapy.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Urinary incontinence affects 30-50% of community-dwelling older adults and >50% of care home residents
  • Types: stress (weak pelvic floor), urge/overactive bladder (most common in elderly), overflow (retention), functional (mobility/cognition), mixed
  • NICE NG123: behavioural therapies (bladder training, pelvic floor exercises) are first-line for all types
  • Antimuscarinics for urgency/OAB: oxybutynin 2.5-5mg BD-TDS (avoid in elderly due to cognitive effects) - prefer solifenacin 5-10mg OD or tolterodine 2-4mg MR OD
  • Mirabegron 50mg OD (β3 agonist): alternative to antimuscarinics with fewer cognitive side effects (preferred in elderly)
  • Always exclude: UTI, urinary retention, constipation, diabetes, medication causes (diuretics, anticholinergics) before diagnosis
  • Post-void residual >100ml suggests overflow incontinence (retention with overflow)
  • Incontinence causes significant psychosocial impact: depression, social isolation, falls, skin breakdown, carer burden

Overview

Key Facts

Urinary incontinence is common but not inevitable in ageing. It is often under-reported and under-treated. Many cases are modifiable with appropriate assessment and intervention.

Epidemiology

  • Prevalence: 30-50% community-dwelling >65; >50% in care homes
  • More common in women (stress incontinence) but urge incontinence is equally common in both sexes in old age
  • Only 25-50% of affected individuals seek help

Aetiology

  • Stress incontinence: pelvic floor weakness (multiparity, menopause, obesity, pelvic surgery)
  • Urge incontinence (OAB): detrusor overactivity (idiopathic, neurological: stroke, Parkinson's, MS)
  • Overflow: urinary retention (BPH, anticholinergics, faecal impaction, diabetic neuropathy, spinal cord disease)
  • Functional: mobility impairment, cognitive impairment, environmental barriers
  • Transient causes (mnemonic DIAPERS): Delirium, Infection, Atrophic vaginitis, Pharmaceuticals, Excess fluid, Restricted mobility, Stool impaction

Pathophysiology

  • Stress: intrinsic sphincter deficiency and/or urethral hypermobility
  • Urge: uninhibited detrusor contractions; age-related reduction in bladder capacity and detrusor compliance
Overflow
detrusor underactivity or bladder outlet obstruction
chronic retention
overflow
  • Functional: unable to reach toilet in time due to physical or cognitive barriers

Clinical Presentation

Stress Incontinence

  • Leakage with coughing, sneezing, laughing, lifting
  • Small volumes
  • No urgency

Urge Incontinence (OAB)

  • Sudden compelling desire to void that is difficult to defer
  • Leakage with urgency (before reaching toilet)
  • Frequency (>8 voids/day), nocturia

Overflow Incontinence

  • Constant dribbling
  • Sensation of incomplete emptying
  • Weak stream, straining
  • Palpable bladder

Functional Incontinence

  • Normal urinary system but unable to reach toilet
  • Associated with immobility, dementia, environmental barriers

Red Flags

  • Haematuria (malignancy, stones)
  • Pelvic mass on examination
  • Acute urinary retention
  • New neurological symptoms (cauda equina)
  • Recurrent UTIs
  • Significant post-void residual

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
UTIDysuria, frequency, feverMSU, urinalysis
BPH/prostate cancerLUTS, poor stream, nocturia (men)DRE, PSA, USS
Bladder cancerPainless haematuriaCystoscopy, CT urogram
Diabetes mellitus/insipidusPolyuria, polydipsiaBlood glucose, osmolality
Faecal impactionConstipation, overflow incontinenceAbdominal examination, AXR
Neurological (cauda equina, MS)Saddle anaesthesia, neurological signsMRI, neurological assessment

Diagnosis / Investigation

Bedside

  • Bladder diary (3 days minimum): frequency, volumes, leakage episodes
  • Urinalysis (UTI, haematuria, glycosuria)
  • Post-void residual volume (bladder scanner; >100ml abnormal)
  • Abdominal examination (palpable bladder, faecal loading)
  • DRE (men: prostate; both: faecal impaction)
  • Pelvic examination (women: prolapse, atrophic vaginitis)
  • Cough stress test (observed leakage on coughing)

Bloods

  • U&Es (renal function, especially if retention)
  • Blood glucose/HbA1c (diabetes)
  • Calcium (hypercalcaemia → polyuria)
  • PSA (if prostate pathology suspected)

Imaging

  • Renal USS: if retention, raised creatinine, or recurrent UTIs
  • Abdominal X-ray: faecal loading

Special Tests

  • Urodynamics: if diagnosis unclear, before surgery, or mixed incontinence
  • Cystoscopy: if haematuria, recurrent UTIs, suspected bladder pathology
  • Uroflowmetry (men: voiding assessment)

Management

Non-pharmacological

  • Bladder training (urge incontinence): scheduled voiding with gradual increase in intervals; aim for 3-4 hourly (minimum 6 weeks - NICE first-line)
  • Pelvic floor muscle training (stress incontinence): 8 contractions × 3/day for ≥3 months (supervised by physiotherapist)
  • Prompted voiding/timed toileting: for cognitively impaired patients
  • Lifestyle modifications: reduce caffeine, manage fluid intake (1.5-2L/day), weight loss if obese
  • Containment products: pads, sheaths (not a substitute for assessment)

Pharmacological

  • Urge incontinence/OAB:
    • First-line: bladder training + antimuscarinic or mirabegron
    • Solifenacin 5-10mg OD or tolterodine 2-4mg MR OD (preferred over oxybutynin in elderly)
    • Mirabegron 50mg OD (β3 agonist): preferred in elderly (no anticholinergic cognitive effects)
    • Avoid oxybutynin in frail elderly/dementia (crosses BBB → cognitive impairment)
  • Stress incontinence: duloxetine 40-80mg BD (limited evidence; SNRI; not first-line)
  • Overflow (retention in men): tamsulosin 400mcg OD (alpha-blocker); finasteride 5mg OD (if prostate >30g)
  • Atrophic vaginitis: topical vaginal oestrogen (estriol 0.01% cream)
  • Nocturia: desmopressin 50-100mcg sublingual ON (caution: hyponatraemia; monitor Na+ at 3 days and 1 week)

Surgical/Interventional

  • Stress incontinence: colposuspension, autologous fascial sling (mesh procedures under moratorium in UK)
  • Urge incontinence (refractory): intravesical botulinum toxin A (100 units); sacral nerve stimulation; posterior tibial nerve stimulation
  • Overflow (retention): intermittent self-catheterisation (preferred) or long-term catheter if not possible; TURP for BPH

Referral Criteria

  • Haematuria: 2-week wait urology
  • Recurrent UTIs or significant residual: urology
  • Failed conservative/pharmacological treatment: continence service/urology
  • Neurological symptoms: neurology/urology
  • Prolapse: urogynaecology

Prognosis

  • Bladder training: effective in 50-70% of women with urge incontinence
  • Pelvic floor exercises: cure/improvement in 50-70% with stress incontinence (adherence is key)
  • Antimuscarinics: reduce urgency episodes by 1-2/day
  • Mirabegron: similar efficacy to antimuscarinics with better tolerability
  • Botulinum toxin: 70% improvement; lasts 6-9 months; repeat injections needed
  • Incontinence significantly impacts quality of life but is treatable in most cases
  • Many older adults do not seek help; proactive assessment is important

Other Relevant Information

Types of Urinary Incontinence Summary

TypeMechanismKey FeatureFirst-line Treatment
StressPelvic floor weaknessLeaks with cough/exertionPelvic floor exercises
Urge (OAB)Detrusor overactivityUrgency, frequency, nocturiaBladder training ± antimuscarinic/mirabegron
OverflowRetention with overflowDribbling, palpable bladderCatheterisation, alpha-blocker
FunctionalMobility/cognitive impairmentCannot reach toiletPrompted voiding, adaptations
MixedStress + urgeCombined featuresTreat predominant type first

DIAPERS - Transient Causes of Incontinence

LetterCause
DDelirium
IInfection (UTI)
AAtrophic vaginitis
PPharmaceuticals
EExcess fluid/diuretics
RRestricted mobility
SStool impaction

NICE Guidelines / CKS

Constipation in the Elderly

Constipation affects up to 50% of older adults and care home residents, requiring identification of reversible causes and a stepwise approach to laxative therapy, with particular attention to medication-related and secondary causes.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Constipation affects 20-30% of community-dwelling older adults and up to 50% of care home residents
  • Rome IV criteria: <3 spontaneous bowel movements per week with straining, hard stools, or incomplete evacuation
  • Common causes in elderly: medications (opioids, anticholinergics, calcium, iron), immobility, dehydration, low fibre, hypothyroidism, hypercalcaemia, colorectal cancer
  • NICE CG99: first-line laxatives include macrogol (Movicol) and osmotic or stimulant laxatives
  • Opioid-induced constipation: co-prescribe laxatives prophylactically (senna + docusate); consider naloxegol 25mg OD if standard laxatives fail
  • Faecal impaction can cause overflow diarrhoea (often misdiagnosed), delirium, urinary retention, and incontinence
  • Always exclude colorectal cancer in patients with new-onset constipation over 60 (change in bowel habit >4 weeks + rectal bleeding → 2-week wait)
  • Bristol Stool Chart types 1-2 indicate constipation; aim for type 3-4

Overview

Key Facts

Constipation in older adults is often multifactorial and requires a systematic approach to identify and address reversible causes before escalating laxative therapy.

Epidemiology

  • 20-30% of community-dwelling >65; up to 50% in care homes
  • More common in women and with increasing age
  • A common reason for GP consultation and A&E attendance

Aetiology

  • Medications: opioids (most common drug cause), anticholinergics, calcium supplements, iron, antipsychotics, tricyclic antidepressants
  • Lifestyle: low fibre diet, inadequate fluid intake, immobility
  • Metabolic/endocrine: hypothyroidism, hypercalcaemia, diabetes (autonomic neuropathy)
  • Neurological: Parkinson's disease, stroke, spinal cord disease, MS
  • Structural: colorectal cancer, diverticular stricture, pelvic organ prolapse, anal fissure
  • Functional: slow-transit constipation, pelvic floor dyssynergia

Pathophysiology

  • Slow-transit constipation: reduced colonic motility (fewer high-amplitude propagating contractions)
  • Pelvic floor dyssynergia: paradoxical contraction of puborectalis during defaecation
  • Opioid-induced: μ-receptor activation in GI tract → reduced peristalsis, increased water absorption, increased sphincter tone
  • Immobility: reduced colonic motility and gravitational assist

Clinical Presentation

Symptoms

  • Infrequent bowel movements (<3/week)
  • Straining at stool
  • Hard, lumpy stools (Bristol 1-2)
  • Sensation of incomplete evacuation
  • Abdominal bloating and discomfort
  • Digital manoeuvres to assist evacuation

Complications

  • Faecal impaction (with overflow diarrhoea - often misdiagnosed as diarrhoea)
  • Delirium
  • Urinary retention and incontinence
  • Rectal prolapse
  • Stercoral ulceration and perforation (rare, serious)
  • Volvulus
  • Haemorrhoids and anal fissure

Red Flags

  • New-onset constipation in >60 (consider malignancy)
  • Change in bowel habit with rectal bleeding
  • Weight loss
  • Palpable abdominal or rectal mass
  • Iron deficiency anaemia
  • Absolute constipation with vomiting and abdominal distension (obstruction)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Colorectal cancerChange in bowel habit, weight loss, rectal bleedingFIT, colonoscopy
HypothyroidismFatigue, weight gain, cold intoleranceTFTs
HypercalcaemiaPolyuria, confusion, bone painCalcium, PTH
Bowel obstructionAbsolute constipation, vomiting, distensionAXR, CT abdomen
Irritable bowel syndromeAbdominal pain relieved by defaecation, bloatingClinical criteria (Rome IV)
Diverticular diseaseLIF pain, altered bowel habitCT, colonoscopy

Diagnosis / Investigation

Bedside

  • Abdominal examination: distension, palpable faecal loading
  • Digital rectal examination: faecal impaction, rectal mass, anal tone, prolapse
  • Bristol Stool Chart: record stool consistency
  • Medication review

Bloods

  • TFTs (hypothyroidism)
  • Calcium (hypercalcaemia)
  • FBC (iron deficiency anaemia → malignancy)
  • U&Es (dehydration)
  • Blood glucose/HbA1c (diabetic autonomic neuropathy)

Imaging

  • AXR: faecal loading (not routine; useful if impaction/obstruction suspected)
  • CT abdomen: if malignancy or obstruction suspected

Special Tests

  • FIT (faecal immunochemical test): if colorectal cancer suspected (>60 with change in bowel habit)
  • Colonoscopy: if red flags for malignancy
  • Transit study (Sitzmarks): if slow-transit constipation suspected (specialist)
  • Anorectal manometry and defaecating proctogram: if pelvic floor dyssynergia suspected (specialist)

Management

Non-pharmacological

  • Lifestyle measures: increase dietary fibre gradually (25-30g/day), adequate fluid intake (1.5-2L/day), regular physical activity
  • Toileting routine: regular time after meals (utilise gastrocolic reflex), adequate time, correct positioning (feet elevated on footstool)
  • Medication review: stop/change offending medications where possible

Pharmacological

  • Step 1 - Bulk-forming: ispaghula husk (Fybogel) 1 sachet BD (requires adequate fluid intake; avoid if immobile/fluid-restricted)
  • Step 2 - Osmotic: macrogol (Movicol) 1-3 sachets daily (NICE first-line for most patients); lactulose 15-30ml BD (alternative)
  • Step 3 - Stimulant: senna 15-30mg ON; bisacodyl 5-10mg ON
  • Combination: often needed; senna + docusate (softener + stimulant)
  • Faecal impaction: high-dose macrogol (Movicol 8 sachets/day for up to 3 days) for soft impaction; glycerine suppositories or phosphate enema for rectal loading; manual evacuation under sedation if necessary
  • Opioid-induced constipation: prophylactic senna + docusate; if refractory: naloxegol 25mg OD (peripherally acting μ-opioid receptor antagonist) or methylnaltrexone 12mg SC
  • Prucalopride 1mg OD (5-HT4 agonist): for chronic constipation when two laxatives have failed (specialist initiation)
  • Linaclotide 290mcg OD: for IBS-C if standard laxatives fail

Surgical/Interventional

  • Manual evacuation: for hard faecal impaction in rectum
  • Transanal irrigation: for neurogenic bowel
  • Surgery: very rarely needed; subtotal colectomy for refractory slow-transit constipation (specialist)

Referral Criteria

  • Red flags for malignancy: 2-week wait (NICE NG12)
  • Failed two laxatives over adequate trial: specialist referral
  • Suspected pelvic floor dyssynergia: specialist investigation
  • Recurrent faecal impaction: continence service/geriatric assessment

Prognosis

  • Lifestyle measures + appropriate laxatives effective in majority of cases
  • Macrogol: preferred first-line; well-tolerated; effective for both treatment and prevention
  • Faecal impaction: recurrence common without ongoing bowel management
  • Chronic constipation impairs quality of life and is associated with increased healthcare utilisation
  • Opioid-induced constipation does not resolve with tolerance (unlike nausea); always needs proactive management

Other Relevant Information

Bristol Stool Chart

TypeDescriptionInterpretation
1Separate hard lumpsSevere constipation
2Sausage-shaped but lumpyConstipation
3Like a sausage with cracksNormal
4Like a sausage, smooth and softNormal (ideal)
5Soft blobs with clear edgesTending towards diarrhoea
6Fluffy pieces, mushyDiarrhoea
7Watery, no solid piecesSevere diarrhoea

Stepwise Approach to Laxatives

StepAgentExample
1Bulk-formingIspaghula husk (Fybogel)
2OsmoticMacrogol (Movicol), lactulose
3StimulantSenna, bisacodyl
4CombinationSenna + docusate
5SpecialistPrucalopride, naloxegol (opioid-induced)

NICE Guidelines / CKS

Malnutrition and Sarcopenia

Malnutrition affects approximately 3 million people in the UK and sarcopenia affects 10-30% of community-dwelling older adults, both contributing significantly to frailty, falls, and mortality.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Malnutrition affects approximately 3 million people in the UK; >30% of hospital admissions in older adults are malnourished
  • MUST (Malnutrition Universal Screening Tool): should be used on all hospital admissions and care home residents (NICE CG32)
  • Sarcopenia (EWGSOP2 definition): low muscle strength + low muscle quantity/quality ± low physical performance
  • Prevalence: sarcopenia affects 10-30% of community-dwelling >60; up to 50% in hospitalised older adults
  • Protein intake: older adults need 1.0-1.2 g/kg/day (higher than younger adults); 1.2-1.5 g/kg/day if acutely ill
  • Resistance exercise is the most effective intervention for sarcopenia; combined with adequate protein
  • Oral nutritional supplements (ONS): Fortisip/Ensure; improve nutritional status and reduce mortality in malnourished patients
  • Refeeding syndrome: risk in severely malnourished patients when refeeding; monitor phosphate, potassium, magnesium

Overview

Key Facts

Malnutrition and sarcopenia are interrelated conditions that significantly worsen outcomes in older adults. Both are modifiable with appropriate nutrition and exercise.

Epidemiology

  • Malnutrition: ~3 million affected in the UK; 30% of hospital admissions
  • Sarcopenia: 10-30% of community-dwelling >60; increases with age
  • Both contribute to frailty, falls, functional decline, and mortality
  • Malnutrition costs the NHS approximately £20 billion/year

Aetiology

  • Malnutrition causes: reduced intake (poor dentition, dysphagia, depression, dementia, poverty), increased requirements (acute illness, infection, cancer), impaired absorption (malabsorption syndromes)
  • Sarcopenia causes: ageing (primary), inactivity, malnutrition, chronic disease (secondary)
  • Risk factors: hospitalisation, social isolation, polypharmacy, chronic disease

Pathophysiology

Malnutrition
negative energy and protein balance
loss of fat and muscle mass
impaired immune function, wound healing, and organ function
  • Sarcopenia: multifactorial muscle loss - reduced protein synthesis, increased proteolysis (ubiquitin-proteasome pathway), mitochondrial dysfunction, hormonal changes (reduced testosterone, GH, IGF-1), chronic inflammation (IL-6, TNF-α), neuronal loss (motor unit remodelling)

Clinical Presentation

Malnutrition

  • Unintentional weight loss (>5% in 3 months or >10% in 6 months)
  • BMI <18.5 kg/m² (or <20 in elderly)
  • Loose clothing, visible wasting
  • Fatigue, weakness
  • Poor wound healing
  • Increased susceptibility to infection
  • Oedema (hypoalbuminaemia)

Sarcopenia

  • Reduced grip strength
  • Slow gait speed (<0.8 m/s)
  • Difficulty rising from chair, climbing stairs
  • Falls and fractures
  • Functional decline

Red Flags

  • Unintentional weight loss >5% in 3 months (consider malignancy)
  • Dysphagia (oesophageal/oropharyngeal pathology)
  • BMI <16 (severe malnutrition; refeeding risk)
  • Progressive muscle weakness (consider myopathy, myositis, MND)
  • Malabsorption symptoms (steatorrhoea, deficiency states)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Malignancy (cachexia)Unintentional weight loss, fatigue, known cancerCT, tumour markers
HyperthyroidismWeight loss despite good appetite, tremor, tachycardiaTFTs
DepressionReduced appetite, low mood, anhedoniaPHQ-9
Coeliac diseaseDiarrhoea, bloating, iron/folate deficiencytTG antibodies, duodenal biopsy
Inflammatory myopathyProximal weakness, elevated CK, rash (dermatomyositis)CK, EMG, MRI, biopsy
Heart failureCardiac cachexia, dyspnoea, oedemaBNP, echocardiography

Diagnosis / Investigation

Bedside

  • MUST screening: BMI + unplanned weight loss + acute disease effect → risk score (0 = low, 1 = medium, ≥2 = high)
  • Weight, height, BMI
  • Grip strength (dynamometer): cut-offs for sarcopenia - <27kg men, <16kg women
  • Gait speed (<0.8 m/s abnormal)
  • Chair stand test (5 stands)
  • Nutritional intake assessment (food diary)
  • Oral health assessment (dentition, oral candida)
  • Swallowing screen

Bloods

  • Albumin (indicator of inflammation/acute phase, not purely nutritional)
  • Pre-albumin (shorter half-life; better nutritional marker)
  • FBC, ferritin, B12, folate (micronutrient deficiencies)
  • Vitamin D, calcium, magnesium, zinc
  • U&Es, phosphate (refeeding risk)
  • TFTs, CRP

Imaging

  • DEXA (whole body): gold standard for muscle mass measurement (appendicular skeletal muscle mass index)
  • Bioelectrical impedance analysis (BIA): alternative for muscle mass estimation
  • CT/MRI: can assess muscle cross-sectional area (research/specialist)

Special Tests

  • SARC-F questionnaire: screening tool for sarcopenia (5 questions)
  • Swallow assessment (SALT) if dysphagia suspected
  • Malabsorption screen: faecal elastase, tTG antibodies

Management

Non-pharmacological

  • Dietary optimisation: energy-dense, protein-rich diet; fortified foods; little and often
    • Protein: 1.0-1.2 g/kg/day (healthy older); 1.2-1.5 g/kg/day (malnourished/acutely ill)
    • Distribute protein across all meals (25-30g per meal for optimal muscle protein synthesis)
  • Oral nutritional supplements (ONS): Fortisip Compact Protein, Ensure, Complan; 300-600 kcal/day supplementation
  • Resistance exercise: most effective single intervention for sarcopenia
    • Progressive resistance training 2-3 times/week
    • Combined with aerobic and balance exercise
  • Mealtime support: assisted feeding, protected mealtimes, social dining
  • Treat underlying causes: dental treatment, manage dysphagia (SALT, modified diet), treat depression, review medications affecting appetite

Pharmacological

  • Micronutrient supplementation: vitamin D 800-1,000 IU daily (if deficient), iron, B12, folate as indicated
  • Appetite stimulants: limited evidence; megestrol acetate (palliative setting only - thrombosis risk)
  • Refeeding syndrome prevention: start feeding slowly (10 kcal/kg/day), supplement thiamine 200-300mg IV before feeding, monitor K+, PO4³⁻, Mg²⁺ daily for first week

Surgical/Interventional

  • Nasogastric (NG) feeding: short-term if oral intake inadequate
  • PEG (percutaneous endoscopic gastrostomy): if long-term enteral feeding needed (>4 weeks)
  • Parenteral nutrition (TPN): if gut not functioning (intestinal failure)

Referral Criteria

  • MUST score ≥2: dietitian referral
  • Dysphagia: SALT referral
  • Severe malnutrition (BMI <16): nutrition support team
  • Suspected sarcopenia with functional decline: geriatric assessment
  • Suspected malabsorption: gastroenterology

Prognosis

  • Malnutrition increases hospital mortality by 2-3×; prolongs LOS by 30%; increases readmission
  • ONS in malnourished patients reduces mortality (NNT ~24) and complications
  • Sarcopenia is independently associated with 2× mortality and 3× fall risk
  • Resistance exercise + protein: can reverse sarcopenia in early stages
  • Refeeding syndrome: can be fatal if unrecognised (cardiac arrhythmias, respiratory failure)
  • Both conditions are modifiable with appropriate intervention

Other Relevant Information

MUST (Malnutrition Universal Screening Tool)

StepAssessmentScore
1BMI >20 = 0; 18.5-20 = 1; <18.5 = 20-2
2Unplanned weight loss in 3-6 months: <5% = 0; 5-10% = 1; >10% = 20-2
3Acute disease effect (no intake >5 days)Add 2
Total0 = low risk; 1 = medium; ≥2 = high

EWGSOP2 Sarcopenia Criteria (2019)

ComponentMeasureCut-off
Low muscle strengthGrip strength<27kg (M), <16kg (F)
Low muscle quantityDEXA (ASMI) or BIA<7.0 kg/m² (M), <5.5 kg/m² (F)
Low physical performanceGait speed<0.8 m/s
Probable sarcopeniaLow strength
Confirmed sarcopeniaLow strength + low quantity
Severe sarcopeniaLow strength + low quantity + low performance

NICE Guidelines / CKS

Osteoporosis and Fragility Fractures

Osteoporosis is a systemic skeletal disease characterised by low bone density and microarchitectural deterioration, causing approximately 500,000 fragility fractures per year in the UK.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Osteoporosis affects approximately 3 million people in the UK; causes ~500,000 fragility fractures/year
  • Defined by DEXA T-score ≤ -2.5 at hip or spine; osteopenia: T-score -1.0 to -2.5
  • FRAX/QFracture: 10-year fracture risk assessment tools; guide treatment decisions (NICE CG146/TA464)
  • First-line treatment: oral bisphosphonates - alendronate 70mg weekly or risedronate 35mg weekly
  • Fragility fracture = fracture from standing height or less; hip, spine, and wrist most common
  • Vitamin D (800-1,000 IU daily) + calcium (1,000mg total daily intake): recommended with bisphosphonate therapy
  • Denosumab 60mg SC 6-monthly: if bisphosphonates contraindicated/not tolerated (FREEDOM trial)
  • Fracture Liaison Service (FLS): secondary fracture prevention; all fragility fracture patients should be assessed

Overview

Key Facts

Osteoporosis is often called the 'silent disease' as it is typically asymptomatic until a fracture occurs. Secondary fracture prevention is critical as the risk of further fracture is highest in the first 2 years.

Epidemiology

  • ~3 million people affected in the UK
  • ~500,000 fragility fractures/year: hip (~66,000), vertebral (~120,000), wrist (~70,000)
  • 1 in 2 women and 1 in 5 men >50 will have a fragility fracture
  • Annual cost to NHS: ~£4.4 billion

Aetiology

  • Primary: postmenopausal (oestrogen deficiency) and age-related
  • Secondary causes: corticosteroid use (≥5mg prednisolone >3 months), rheumatoid arthritis, hyperparathyroidism, hyperthyroidism, hypogonadism, coeliac disease, CKD, eating disorders, alcohol excess, smoking, early menopause (<45)

Pathophysiology

  • Bone remodelling imbalance: osteoclast resorption > osteoblast formation
  • Oestrogen deficiency: accelerated bone loss at menopause (2-3% per year for 5-10 years)
  • RANK-RANKL-OPG pathway: RANKL activates osteoclasts; denosumab is a RANKL inhibitor
  • Corticosteroid-induced: reduced osteoblast function, increased osteoclast activity, reduced calcium absorption, increased renal calcium excretion
Trabecular bone affected first
vertebral crush fractures; cortical bone loss
hip fractures

Clinical Presentation

Typical Presentation

  • Often asymptomatic until fracture occurs
  • Fragility fracture (from standing height or less)
  • Loss of height (vertebral fractures)
  • Kyphosis (dowager's hump)
  • Back pain (vertebral fracture)

Common Fracture Sites

  • Hip (neck of femur)
  • Vertebral (thoracic and lumbar)
  • Distal radius (Colles' fracture)
  • Proximal humerus
  • Pelvis

Red Flags

  • Fragility fracture (triggers investigation and treatment)
  • Height loss >4cm (vertebral fractures)
  • Sudden severe back pain (acute vertebral fracture)
  • Multiple fractures or fracture at unusual site (<50 or atypical location)
  • Long-term corticosteroid use without bone protection

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
OsteomalaciaBone pain, proximal myopathy, low vitamin DVitamin D, ALP, calcium
MyelomaBone pain, anaemia, renal impairment, hypercalcaemiaSerum/urine electrophoresis, BJP
Bone metastasesFocal bone pain, known primary cancerBone scan, CT, ALP
Paget's diseaseBone pain, deformity, raised ALPALP, X-ray, bone scan
HyperparathyroidismHypercalcaemia, stones, bones, moans, groansCalcium, PTH

Diagnosis / Investigation

Bedside

  • Height measurement (compare to historical; loss >4cm suggests vertebral fractures)
  • BMI
  • FRAX or QFracture risk assessment

Bloods

  • Calcium, phosphate, ALP (bone profile)
  • Vitamin D (25-hydroxyvitamin D)
  • PTH (if calcium abnormal)
  • TFTs, LFTs, U&Es
  • FBC, ESR, CRP
  • Testosterone (men), oestradiol (premenopausal women)
  • Myeloma screen (serum protein electrophoresis) if suspicious
  • Coeliac serology (tTG) if suspected

Imaging

  • DEXA scan: gold standard for bone density measurement
    • T-score ≤ -2.5 = osteoporosis
    • T-score -1.0 to -2.5 = osteopenia
    • T-score > -1.0 = normal
  • Spinal X-ray (thoracic/lumbar): vertebral fracture assessment
  • VFA (vertebral fracture assessment): DEXA-based; alternative to X-ray

Special Tests

  • FRAX tool: 10-year probability of major osteoporotic fracture and hip fracture
  • Bone turnover markers (CTX, P1NP): specialist use for monitoring treatment

Management

Non-pharmacological

  • Weight-bearing and resistance exercise
  • Falls prevention (as per NICE CG161)
  • Smoking cessation
  • Reduce alcohol (<14 units/week)
  • Dietary calcium (aim 1,000mg total daily intake including supplements if needed)

Pharmacological

  • First-line: alendronate 70mg weekly (take on empty stomach, remain upright 30 minutes)
    • Alternative: risedronate 35mg weekly
  • Vitamin D: 800-1,000 IU daily (colecalciferol)
  • Calcium supplementation: only if dietary intake insufficient (Adcal D3, Calcichew D3)
  • If bisphosphonates contraindicated/not tolerated:
    • Denosumab 60mg SC 6-monthly (RANKL inhibitor; FREEDOM trial; must not miss doses - rebound vertebral fractures)
    • Raloxifene 60mg OD (SERM; for postmenopausal vertebral fracture prevention)
  • Severe osteoporosis/multiple fractures:
    • Teriparatide 20mcg SC daily (PTH analogue; anabolic; max 2 years; NICE TA161)
    • Romosozumab 210mg SC monthly (anti-sclerostin; 12 months then switch to anti-resorptive)
  • Corticosteroid-induced osteoporosis: start bone protection if prednisolone ≥7.5mg daily for ≥3 months (or lower dose with other risk factors)

Surgical/Interventional

  • Vertebroplasty/kyphoplasty: for acute painful vertebral fractures not responding to conservative management
  • Fracture fixation: for hip and other fragility fractures

Referral Criteria

  • Fragility fracture: Fracture Liaison Service (FLS)
  • FRAX above treatment threshold: initiate treatment in primary care
  • Bisphosphonate intolerance/contraindication: metabolic bone specialist
  • Atypical femoral fracture or ONJ (bisphosphonate complications): specialist review
  • Pre-menopausal osteoporosis or young men: metabolic bone/endocrine referral

Prognosis

  • Alendronate: reduces hip fracture by 40% and vertebral fracture by 50% over 3 years
  • Denosumab: reduces hip fracture by 40%, vertebral by 68% (FREEDOM trial)
  • Teriparatide: reduces vertebral fracture by 65%
  • Hip fracture: 30-day mortality ~8%; 1-year mortality ~30%
  • Risk of second fracture is highest in first 1-2 years ("imminent fracture risk")
  • Treatment should be reviewed at 5 years (alendronate) or 3 years (zoledronate) - consider drug holiday in low-risk patients

Other Relevant Information

FRAX Risk Factors

Risk Factor
Age
Sex
BMI
Previous fragility fracture
Parental hip fracture
Current smoking
Alcohol ≥3 units/day
Glucocorticoid use
Rheumatoid arthritis
Secondary osteoporosis cause
Femoral neck BMD (if available)

Osteoporosis Treatment Summary

DrugDoseRouteKey Points
Alendronate70mg weeklyOralFirst-line; empty stomach, upright 30 min
Risedronate35mg weeklyOralAlternative bisphosphonate
Zoledronate5mg yearlyIVIf oral not tolerated
Denosumab60mg 6-monthlySCRANKL inhibitor; no missed doses
Teriparatide20mcg dailySCAnabolic; severe osteoporosis; max 2 years
Romosozumab210mg monthlySCAnti-sclerostin; 12 months

NICE Guidelines / CKS

Hip Fracture

Hip fracture is a common and serious injury in older adults with approximately 66,000 cases per year in the UK, requiring surgery within 36 hours and comprehensive orthogeriatric care to reduce mortality.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Hip fracture affects approximately 66,000 people/year in the UK; predominantly older women with osteoporosis
  • 30-day mortality: approximately 8%; 1-year mortality: approximately 30%
  • NICE NG124: surgery within 36 hours of admission (improves outcomes and reduces mortality)
  • Intracapsular fractures: hemiarthroplasty (displaced) or cannulated screws (undisplaced) in fit patients; total hip replacement if independently mobile and cognitively intact
  • Extracapsular fractures: dynamic hip screw (DHS) for intertrochanteric; intramedullary nail for subtrochanteric/reverse oblique
  • Orthogeriatric care (shared care with geriatrician from admission): reduces mortality by 30% and LOS
  • Best Practice Tariff (BPT) standards: surgery <36h, orthogeriatric assessment <72h, bone protection, falls assessment, physio from day 1
  • All patients should receive bone protection and falls prevention - secondary fracture prevention is critical

Overview

Key Facts

Hip fracture is one of the most common reasons for emergency hospital admission in older adults and is associated with significant morbidity and mortality. Rapid surgery and comprehensive geriatric care are essential.

Epidemiology

  • ~66,000 hip fractures/year in the UK
  • Mean age: 83 years; 75% are women
  • 30-day mortality: ~8%; 1-year mortality: ~30%
  • Only 50% regain pre-fracture level of independence
  • Annual cost: ~£2 billion

Aetiology

  • Low-energy fall (standing height) in the context of osteoporosis (most common scenario)
  • Risk factors: age, female sex, osteoporosis, falls risk factors, previous fracture, low BMI, smoking, alcohol, dementia
  • High-energy trauma in younger patients (road traffic collision)

Pathophysiology

  • Intracapsular (subcapital/transcervical - within joint capsule): disrupts blood supply to femoral head (retinacular vessels) → risk of avascular necrosis (AVN) and non-union
    • Garden classification: I-II (undisplaced); III-IV (displaced)
  • Extracapsular (intertrochanteric/subtrochanteric - outside capsule): blood supply intact; lower AVN risk; heals well with fixation
  • Subtrochanteric: higher mechanical forces; may be associated with bisphosphonate use (atypical fracture)

Clinical Presentation

Typical Presentation

  • Older adult after a fall (usually low-energy)
  • Pain in hip/groin (may be referred to knee)
  • Unable to weight-bear
  • Shortened and externally rotated leg (displaced fracture)
  • Pain on axial loading and log-roll

Occult Hip Fracture

  • Pain on weight-bearing but X-ray appears normal
  • May be ambulant
  • Requires MRI (gold standard) or CT if MRI not available

Red Flags

  • Pathological fracture (minimal/no trauma, known malignancy)
  • Bilateral fractures or fracture in young patient (metabolic bone disease, malignancy)
  • Neurovascular compromise (rare)
  • Signs of long lie: pressure injury, rhabdomyolysis, hypothermia, dehydration

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Pubic ramus fractureGroin pain, can weight-bear (usually), tenderness over pubic ramusPelvic X-ray
Peri-prosthetic fracturePrevious hip replacement, fallX-ray
Soft tissue injuryPain but normal imaging, can weight-bearClinical, imaging if needed
Pathological fractureMinimal trauma, bone lesion on X-rayX-ray, CT, biopsy
Septic arthritisFever, hot swollen joint, unable to move hipAspiration, blood cultures

Diagnosis / Investigation

Bedside

  • Hip examination: shortened, externally rotated limb, pain on log-roll
  • Observations: HR, BP, temperature
  • ECG (pre-operative)
  • Cognitive screen (4AT for delirium; AMT for baseline cognition)
  • Lying/standing BP if possible
  • Fluid and nutritional assessment

Bloods

  • FBC, U&Es, LFTs, bone profile, clotting
  • Group and save/crossmatch
  • CRP (baseline)
  • CK if long lie (rhabdomyolysis)
  • Vitamin D

Imaging

  • AP pelvis + lateral hip X-ray: first-line imaging
  • MRI hip: gold standard for occult fracture (X-ray normal but clinical suspicion)
  • CT hip: alternative if MRI not available or contraindicated
  • CXR: pre-operative assessment

Special Tests

  • NHFD (National Hip Fracture Database): all patients entered
  • Pre-operative anaesthetic assessment
  • Echocardiography if significant murmur or cardiac history

Management

Non-pharmacological

Fast-track pathway
A&E
hip fracture pathway
orthopaedic ward
  • Pain management: femoral nerve block (best practice) + regular analgesia (paracetamol 1g QDS, avoid/minimise opioids)
  • Surgery within 36 hours (NICE NG124; BPT standard)
  • Early mobilisation: physiotherapy from day 1 post-op; aim weight-bearing as tolerated
  • Orthogeriatric review within 72 hours: CGA approach
  • Delirium prevention: multicomponent intervention
  • Thromboprophylaxis: LMWH (enoxaparin 40mg SC OD) for 28 days post-op (unless contraindicated)

Pharmacological

  • Analgesia: paracetamol 1g QDS + nerve block; opioids PRN (reduced dose in elderly; monitor for delirium)
    • Fascia iliaca block (FIB): effective regional anaesthesia
  • Bone protection: start before discharge
    • Alendronate 70mg weekly + vitamin D 800-1,000 IU daily + calcium (if dietary intake low)
    • Or denosumab/zoledronate if oral bisphosphonate not appropriate
  • Falls prevention: as per CGA

Surgical/Interventional

  • Intracapsular undisplaced (Garden I-II): cannulated screws (internal fixation) - preserves native hip
  • Intracapsular displaced (Garden III-IV):
    • Hemiarthroplasty (cemented): standard for most elderly patients
    • Total hip replacement: for patients who were independently mobile outdoors, cognitively intact, and medically fit (NICE NG124)
  • Extracapsular intertrochanteric: dynamic hip screw (DHS)
  • Extracapsular subtrochanteric/reverse oblique: intramedullary nail (IM nail)

Referral Criteria

  • All hip fractures: orthopaedic + orthogeriatric input
  • Post-discharge: Fracture Liaison Service for bone protection
  • Falls prevention service
  • Community rehabilitation (physiotherapy, OT)

Prognosis

  • 30-day mortality: ~8%
  • 1-year mortality: ~30% (higher in men, frail, dementia, medical comorbidities)
  • Surgery <36 hours: reduces 30-day mortality and morbidity
  • Orthogeriatric care: reduces mortality by ~30%
  • Only 50% regain pre-fracture mobility level; 25% require long-term care
  • Hip fracture doubles the risk of a second hip fracture
  • Alendronate post-hip fracture: reduces further fractures by 40-50%

Other Relevant Information

Hip Fracture Classification and Surgical Management

Fracture TypeClassificationSurgery
Intracapsular undisplacedGarden I-IICannulated screws
Intracapsular displacedGarden III-IVHemiarthroplasty or THR
IntertrochantericAO/OTA 31-A1/A2Dynamic hip screw (DHS)
SubtrochantericAO/OTA 32Intramedullary nail

NICE NG124 Best Practice Tariff Standards

StandardTarget
Surgery within 36 hoursYes
Orthogeriatric assessment within 72 hoursYes
Nursing assessment within 6 hoursYes
Bone protection assessmentBefore discharge
Falls assessmentBefore discharge
Physiotherapy from day 1Yes
NHFD data entryMandatory

NICE Guidelines / CKS

Vertebral Fractures

Vertebral fractures are the most common osteoporotic fracture, yet only one-third are clinically diagnosed, causing significant pain, kyphosis, and functional decline in older adults.

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Key Facts

  • Vertebral fractures are the most common osteoporotic fracture; approximately 120,000/year in the UK
  • Only one-third are clinically diagnosed (two-thirds are incidental or unrecognised)
  • Height loss >4cm or kyphosis should prompt investigation for vertebral fractures
  • Thoracolumbar junction (T11-L1) is the most common site
  • Vertebral fracture assessment (VFA) via DEXA or spinal X-ray: identifies compression fractures
  • Management: analgesia, early mobilisation, physiotherapy, bone protection (alendronate 70mg weekly)
  • Vertebroplasty/kyphoplasty: for acute painful fractures not responding to conservative treatment (evidence equivocal; NICE IPG12)
  • One vertebral fracture increases the risk of further vertebral fracture by 5× ("vertebral fracture cascade")

Overview

Key Facts

Vertebral fractures are under-diagnosed and under-treated, yet they are a major cause of pain, disability, and further fracture risk in older adults.

Epidemiology

  • ~120,000 vertebral fractures/year in the UK
  • Only ~33% clinically diagnosed (most are incidental findings)
  • Female:male ratio 2:1
  • Prevalence increases with age: 20% of women >70, 35% of women >80

Aetiology

  • Osteoporosis (primary cause in older adults)
  • Minimal or no trauma (spontaneous in severe osteoporosis)
  • Secondary causes: corticosteroids, malignancy (myeloma, metastases), Paget's disease
  • High-energy trauma in younger patients (RTCs, falls from height)

Pathophysiology

  • Vertebral body compression due to reduced bone strength
  • Anterior wedge fracture (most common): anterior height loss → kyphosis
  • Biconcave fracture: central height loss
  • Crush fracture: uniform height loss (severe)
  • Thoracolumbar junction most vulnerable (transition from fixed thoracic to mobile lumbar spine)
  • One fracture increases stress on adjacent vertebrae → fracture cascade

Clinical Presentation

Acute Vertebral Fracture

  • Sudden onset back pain (thoracic or lumbar)
  • Pain worse with movement, relieved by rest
  • Localised tenderness over spinous process
  • Paravertebral muscle spasm

Chronic/Incidental

  • Height loss (>2cm since last measurement or >4cm from recalled height)
  • Progressive thoracic kyphosis (dowager's hump)
  • Reduced rib-pelvis distance
  • Chronic back pain
  • Protuberant abdomen
  • Reduced respiratory function (multiple thoracic fractures)

Red Flags

  • Neurological deficit (cord compression - rare in osteoporotic fractures but consider malignancy)
  • Severe pain not controlled with standard analgesia
  • Known malignancy (pathological fracture)
  • Fever (infection/discitis)
  • Age <50 without major trauma (consider secondary causes)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Metastatic spinal diseaseKnown cancer, night pain, neurological signsMRI, bone scan
MyelomaBone pain, anaemia, renal impairmentSPEP, BJP, FBC
Paget's diseaseBone pain, enlarged bone, raised ALPALP, X-ray
Disc prolapseRadicular pain, dermatomal distributionMRI
Spinal stenosisClaudicant leg pain, relieved by flexionMRI
Discitis/osteomyelitisFever, severe pain, raised CRPMRI, blood cultures

Diagnosis / Investigation

Bedside

  • Height measurement (compare with previous records)
  • Spinal examination (tenderness, kyphosis, range of motion)
  • Neurological examination of lower limbs

Bloods

  • Bone profile (calcium, phosphate, ALP)
  • Vitamin D
  • FBC, ESR, CRP (exclude infection, myeloma)
  • Serum protein electrophoresis (myeloma screen)
  • TFTs, U&Es, LFTs
  • PTH (if calcium abnormal)

Imaging

  • Spinal X-ray (thoracic and lumbar AP + lateral): first-line; assess vertebral body height
  • VFA (vertebral fracture assessment) via DEXA: alternative screening
  • MRI spine: if neurological signs, suspected malignancy, or infection; differentiates acute from chronic fractures (bone marrow oedema)
  • DEXA scan: bone density assessment
  • CT: if MRI contraindicated; detailed bony anatomy

Special Tests

  • FRAX/QFracture: 10-year fracture risk
  • Genant classification: grading vertebral fracture severity (mild 20-25%, moderate 25-40%, severe >40% height loss)

Management

Non-pharmacological

  • Analgesia: paracetamol 1g QDS, short-course opioids if needed (minimise), topical heat
  • Early mobilisation: bed rest should be avoided; physiotherapy for posture, core strengthening
  • Spinal extension exercises: improve kyphosis and reduce fracture risk (evidence from PROVES trial)
  • Thoracolumbar orthosis (brace): short-term for comfort; not routinely recommended
  • Falls prevention: as per NICE CG161

Pharmacological

  • Bone protection (all patients with vertebral fragility fracture):
    • Alendronate 70mg weekly + vitamin D 800-1,000 IU daily (first-line)
    • Denosumab 60mg SC 6-monthly (if bisphosphonate contraindicated)
    • Teriparatide 20mcg SC daily: for severe osteoporosis with multiple vertebral fractures (NICE TA161)
  • Pain management: paracetamol, codeine/tramadol short-term, consider calcitonin nasal spray 200 IU daily for acute fracture pain (limited evidence)

Surgical/Interventional

  • Vertebroplasty: percutaneous injection of bone cement into fractured vertebral body (pain relief)
  • Kyphoplasty: balloon inflation then cement injection (aims to restore height)
    • Consider for painful fractures not responding to 6 weeks of conservative treatment (NICE IPG12)
    • Evidence equivocal (VERTOS-II showed benefit vs sham; INVEST/FREE trials mixed)

Referral Criteria

  • All vertebral fragility fractures: Fracture Liaison Service
  • Severe pain not responding to conservative measures: spine MDT
  • Neurological deficit: emergency MRI and neurosurgical/orthopaedic review
  • Multiple fractures or severe osteoporosis: metabolic bone specialist
  • Suspected malignancy: urgent investigation

Prognosis

  • One vertebral fracture increases risk of further fracture by 5× (fracture cascade)
  • 20-25% of patients with one vertebral fracture will have another within 1 year
  • Alendronate: reduces vertebral fracture risk by 50%
  • Teriparatide: reduces vertebral fracture risk by 65%
  • Kyphosis and multiple fractures impair respiratory function and quality of life
  • Most acute pain resolves within 6-12 weeks
  • Chronic pain in 30-40% of patients
  • Vertebral fractures are independently associated with increased mortality

Other Relevant Information

Genant Classification of Vertebral Fracture Severity

GradeHeight LossDescription
0NoneNormal vertebra
1 (Mild)20-25%Wedge, biconcave, or crush deformity
2 (Moderate)25-40%More pronounced deformity
3 (Severe)>40%Marked deformity

Types of Vertebral Fracture

TypeDescriptionFeature
WedgeAnterior height lossMost common; causes kyphosis
BiconcaveCentral height loss"Codfish" vertebra
CrushUniform height lossSevere; entire body collapsed

NICE Guidelines / CKS

Parkinson Disease in the Elderly

Parkinson's disease is a progressive neurodegenerative disorder affecting approximately 150,000 people in the UK, characterised by bradykinesia, rigidity, and rest tremor, managed with levodopa as the mainstay of treatment.

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Key Facts

  • Parkinson's disease affects approximately 150,000 people in the UK; prevalence increases with age (1-2% >65)
  • Cardinal features: bradykinesia (must be present) + at least one of: rest tremor, rigidity
  • Levodopa (co-careldopa/co-beneldopa) is the most effective symptomatic treatment; start when symptoms affect quality of life
  • NICE NG71: do not delay levodopa to prevent motor complications; refer to specialist before starting treatment
  • Non-motor symptoms are common and disabling: depression, constipation, REM sleep behaviour disorder, anosmia, cognitive impairment, orthostatic hypotension
  • Never abruptly stop Parkinson's medications (risk of neuroleptic malignant-like syndrome / parkinsonism-hyperpyrexia)
  • Avoid dopamine-blocking drugs: metoclopramide, haloperidol, prochlorperazine (worsen Parkinson's); use domperidone for nausea
  • Falls are common in Parkinson's disease: multifactorial (postural instability, freezing, orthostatic hypotension, cognitive impairment)

Overview

Key Facts

Parkinson's disease is the second most common neurodegenerative disease after Alzheimer's. Management is complex, requiring specialist input and multidisciplinary care.

Epidemiology

  • ~150,000 affected in the UK; ~18,000 new diagnoses/year
  • Prevalence: 1-2% of >65; mean age of onset: 65 years
  • Male:female ratio 1.5:1
  • Young-onset Parkinson's: <50 years (~5-10%)

Aetiology

  • Idiopathic (most common)
  • Loss of dopaminergic neurons in the substantia nigra pars compacta
  • Lewy bodies: α-synuclein protein aggregates (hallmark pathology)
  • Genetic: LRRK2, SNCA, Parkin, PINK1, GBA mutations (5-10% familial)
  • Risk factors: age, male sex, pesticide exposure, head trauma, family history
  • Protective: smoking (paradoxical), caffeine (epidemiological association)

Pathophysiology

Progressive loss of dopaminergic neurons in substantia nigra
striatal dopamine depletion
loss of inhibition of indirect pathway and loss of excitation of direct pathway
excessive inhibitory output from GPi
thalamic suppression
hypokinesia
  • Symptoms appear when >60-80% of striatal dopamine is lost
Lewy body pathology spreads via Braak staging: enteric/olfactory
brainstem
midbrain
cortex (explains non-motor symptoms preceding motor symptoms)

Clinical Presentation

Motor Features

  • Bradykinesia (essential for diagnosis): slowness of movement, progressive fatiguing/decrement on repetitive movements, reduced amplitude
  • Rest tremor (70%): 4-6 Hz, "pill-rolling", worse at rest, suppressed by action, unilateral onset
  • Rigidity: lead-pipe ± cogwheeling (superimposed tremor); increased tone throughout range of movement
  • Postural instability (late feature): retropulsion, falls
  • Gait: shuffling, reduced stride length, reduced arm swing, festination, freezing of gait

Non-Motor Features

  • Anosmia (often earliest symptom)
  • REM sleep behaviour disorder (may precede motor symptoms by years)
  • Constipation (common, may be prodromal)
  • Depression and anxiety (40-50%)
  • Cognitive impairment/dementia (80% develop PDD eventually)
  • Orthostatic hypotension
  • Urinary urgency/frequency
  • Pain (musculoskeletal, dystonic, central)

Red Flags (Suggest Atypical Parkinsonism)

  • Symmetrical onset
  • Early falls (PSP)
  • Poor/no response to levodopa
  • Early severe autonomic failure (MSA)
  • Cerebellar signs (MSA-C)
  • Vertical gaze palsy (PSP)
  • Rapid progression
  • Early dementia (DLB)
  • Alien limb phenomenon (CBD)

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Essential tremorAction/postural tremor, bilateral, family history, improves with alcoholClinical, trial of propranolol
Drug-induced parkinsonismSymmetrical, no rest tremor; dopamine blockersMedication history
Vascular parkinsonismLower body predominant, stepwise progression, vascular risk factorsMRI brain
Progressive supranuclear palsy (PSP)Early falls, vertical gaze palsy, poor levodopa responseClinical, MRI (midbrain atrophy)
Multiple system atrophy (MSA)Early autonomic failure, cerebellar signs, poor levodopa responseClinical, MRI (hot cross bun sign)
Lewy body dementiaEarly dementia, visual hallucinations, fluctuating cognitionDaTSCAN, clinical

Diagnosis / Investigation

Bedside

  • Neurological examination: bradykinesia testing (finger tapping, hand movements, toe tapping), tremor assessment, rigidity, gait, postural reflexes
  • Lying/standing BP (orthostatic hypotension)
  • Cognitive assessment (MoCA - screens executive function well)
  • Anosmia testing (UPSIT)

Bloods

  • Routine bloods to exclude secondary causes (TFTs, copper studies if Wilson's suspected in <40)

Imaging

  • MRI brain: not diagnostic of PD but excludes structural causes, vascular parkinsonism, NPH
  • DaTSCAN (FP-CIT SPECT): confirms dopaminergic deficit; differentiates PD from essential tremor or drug-induced parkinsonism (NICE NG71 - only if diagnosis uncertain)
  • PET imaging: research

Special Tests

  • Levodopa challenge: improvement confirms dopaminergic responsiveness (not diagnostic of PD specifically)
  • MIBG cardiac scintigraphy: reduced uptake in PD/DLB (differentiates from MSA); not widely used in UK
  • Genetic testing: if young-onset (<50) or strong family history

Management

Non-pharmacological

  • MDT approach: Parkinson's nurse specialist, physiotherapy, OT, SALT, psychology
  • Exercise: regular aerobic and resistance exercise (improves motor function, balance, mood)
  • Physiotherapy: gait training, balance, cueing strategies for freezing
  • SALT: swallowing assessment (aspiration risk in advanced disease), speech therapy (LSVT LOUD)
  • OT: home adaptations, maintaining independence
  • Patient education and support: Parkinson's UK

Pharmacological

  • Levodopa (most effective; first-line in most elderly patients):
    • Co-careldopa (Sinemet) or co-beneldopa (Madopar): start 50/12.5 TDS → titrate to effect
    • Modified-release preparations for nocturnal symptoms or fluctuations
Dopamine agonists
ropinirole 0.25mg TDS
up to 8mg TDS; pramipexole 88mcg TDS
up to 1.1mg TDS; rotigotine patch 2-16mg/24h
  • Beware impulse control disorders (gambling, hypersexuality, compulsive shopping - affects 15-20%)
  • MAO-B inhibitors: rasagiline 1mg OD, selegiline 5-10mg OD, safinamide 50-100mg OD (adjunct)
  • COMT inhibitors: entacapone 200mg with each levodopa dose, opicapone 50mg OD (adjunct to levodopa)
  • Motor fluctuations (wearing off/dyskinesia):
    • Add COMT inhibitor, MAO-B inhibitor, or dopamine agonist
    • Adjust levodopa dose/frequency
    • Amantadine 100mg BD-TDS for dyskinesia
  • Advanced therapies: apomorphine SC infusion, levodopa-carbidopa intestinal gel (LCIG/Duodopa), deep brain stimulation (DBS)
  • Non-motor management: treat depression (SSRIs, SNRIs), orthostatic hypotension (midodrine, fludrocortisone), constipation (macrogol), dementia (rivastigmine - only AChEI licensed for PDD)

Surgical/Interventional

  • Deep brain stimulation (DBS): subthalamic nucleus or GPi; for motor fluctuations/dyskinesias despite optimised medication; improves motor function by ~50%
  • Focused ultrasound thalamotomy: emerging for tremor-predominant PD

Referral Criteria

  • All suspected PD: refer to specialist (neurologist or geriatrician with PD interest) before starting treatment (NICE NG71)
  • Complex motor fluctuations: specialist review
  • Advanced therapies: specialist PD centre
  • Cognitive decline: dementia assessment
  • Falls: falls prevention service + PD specialist review

Prognosis

  • Life expectancy: reduced by approximately 2-5 years compared to age-matched population
  • Motor complications (wearing off, dyskinesia): develop in 50% within 5 years of levodopa
  • Dementia: develops in ~80% of patients over 20-year course
  • Falls: affect >60% of PD patients; leading cause of hospital admission
  • Aspiration pneumonia: leading cause of death in advanced PD
  • Quality of life significantly impacted by non-motor symptoms
  • Individual prognosis varies widely; tremor-predominant has better prognosis than postural instability-gait difficulty (PIGD) phenotype

Other Relevant Information

Hoehn and Yahr Staging

StageDescription
1Unilateral involvement only
2Bilateral involvement, no balance impairment
3Bilateral, mild-moderate disability; impaired postural reflexes
4Severely disabled; able to walk/stand unassisted
5Wheelchair-bound or bedridden unless aided

Drugs to Avoid in Parkinson's Disease

DrugReason
MetoclopramideD2 antagonist; worsens PD
HaloperidolD2 antagonist
ProchlorperazineD2 antagonist
ChlorpromazineD2 antagonist
Use domperidoneDoes not cross BBB; safe antiemetic

NICE Guidelines / CKS

Pressure Ulcers

Pressure ulcers are localised injuries to the skin and underlying tissue, usually over a bony prominence, caused by sustained pressure, affecting approximately 700,000 people per year in the UK and largely preventable.

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Key Facts

  • Pressure ulcers affect approximately 700,000 people/year in the UK; cost NHS £3.8 billion annually
  • Most are preventable: regular repositioning, pressure-relieving devices, nutrition, skin assessment
  • NICE CG179: recommends risk assessment with validated tool (Waterlow, Braden) on admission and ongoing
  • Grading (EPUAP/NPUAP): Category 1 (non-blanchable erythema) to Category 4 (full-thickness tissue loss including bone/tendon)
  • Common sites: sacrum, heels, ischial tuberosities, greater trochanters, occiput
  • Risk factors: immobility, malnutrition, incontinence, reduced sensation, cognitive impairment, acute illness
  • 2-hourly repositioning is standard practice; pressure-relieving mattress for all at-risk patients
  • SSKIN bundle: Surface (pressure-relieving), Skin inspection, Keep moving, Incontinence management, Nutrition

Overview

Key Facts

Pressure ulcers are a significant cause of morbidity, pain, and reduced quality of life. Prevention is far more effective and cost-effective than treatment.

Epidemiology

  • ~700,000 affected per year in UK
  • Prevalence: 4-10% of hospital patients; up to 30% in care homes
  • Annual NHS cost: ~£3.8 billion (accounts for 4% of total NHS expenditure)
  • Category 2 and above are reportable as clinical incidents

Aetiology

Sustained pressure over bony prominence
exceeds capillary closing pressure (~32mmHg)
tissue ischaemia
necrosis
  • Shear forces: layers of tissue slide against each other (e.g. sliding down in bed)
  • Friction: skin dragged across surface
  • Moisture: maceration from incontinence or perspiration

Pathophysiology

Pressure > capillary closing pressure
microvascular occlusion
tissue hypoxia
ischaemia-reperfusion injury
cellular death
ulceration
  • Necrosis occurs from deep tissues outward ("iceberg" phenomenon - visible damage often underestimates deep tissue injury)
  • Reperfusion injury on release of pressure: reactive hyperaemia (blanching normal; non-blanchable = tissue damage)
  • Biofilm formation in chronic wounds impairs healing

Clinical Presentation

Category Classification (EPUAP/NPUAP)

  • Category 1: Non-blanchable erythema of intact skin
  • Category 2: Partial-thickness skin loss (dermis exposed); shallow open ulcer or blister
  • Category 3: Full-thickness skin loss (subcutaneous fat visible; bone/tendon NOT visible)
  • Category 4: Full-thickness tissue loss (bone, tendon, or muscle exposed)
  • Unstageable: obscured by slough or eschar (cannot assess depth)
  • Deep tissue injury: purple/maroon localised area; intact skin with underlying damage

Common Sites

  • Sacrum (most common)
  • Heels
  • Ischial tuberosities (wheelchair users)
  • Greater trochanters
  • Occiput (ICU patients)
  • Malleoli

Red Flags

  • Signs of infection: increasing pain, warmth, erythema, purulent exudate, fever, rising CRP
  • Osteomyelitis (deep-probing bone)
  • Cellulitis spreading from ulcer
  • Rapid deterioration in wound
  • Sepsis from infected pressure ulcer

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Venous leg ulcerLower leg, gaiter area, lipodermatosclerosisABPI, duplex USS
Arterial ulcerPainful, punched-out, peripheral, absent pulsesABPI (<0.5), angiography
Diabetic foot ulcerNeuropathic distribution, callus, diabetic historyMonofilament testing, glucose
Malignant ulcer (Marjolin's)Non-healing, rolled edges, long-standing woundBiopsy
Moisture-associated dermatitisRed, macerated skin in skin folds, perianalClinical assessment

Diagnosis / Investigation

Bedside

  • Risk assessment: Waterlow score (≥10 at risk) or Braden scale (≤18 at risk)
  • Skin assessment: colour, temperature, moisture, integrity (especially over bony prominences)
  • Wound assessment: size (measure length/width/depth), category, bed tissue type (granulation, slough, eschar, necrotic), exudate, odour, edges, surrounding skin
  • Nutritional assessment (MUST score)
  • Mobility assessment
  • Continence assessment

Bloods

  • FBC, CRP (infection markers)
  • Albumin (nutritional status/healing capacity)
  • HbA1c (diabetic control)
  • Blood cultures (if sepsis suspected)

Imaging

  • X-ray/MRI: if osteomyelitis suspected (probe-to-bone test positive)

Special Tests

  • Wound swab (only if clinical signs of infection - not routine)
  • Tissue biopsy: if non-healing/malignant change suspected
  • ABPI: if arterial component suspected

Management

Non-pharmacological

  • Prevention (SSKIN bundle):
    • Surface: pressure-relieving mattress/cushion (alternating pressure, static foam)
    • Skin inspection: at least daily; document findings
    • Keep moving: reposition every 2 hours (30° tilt); encourage mobilisation
    • Incontinence: manage promptly; barrier cream
    • Nutrition: optimise diet; refer to dietitian if malnourished
  • Wound management:
    • Debridement of necrotic tissue (autolytic, sharp, or larval)
    • Appropriate dressings: maintain moist wound environment (foam, hydrocolloid, alginate depending on exudate)
    • Offloading devices (heel elevation, heel-specific devices)
  • Patient education: repositioning techniques, skin care

Pharmacological

  • Analgesia: paracetamol; topical lidocaine for dressing changes
  • Antibiotics: only if clinical signs of infection (cellulitis, purulent discharge, systemic sepsis)
    • Flucloxacillin 500mg-1g QDS (or clarithromycin if penicillin-allergic)
    • Broad-spectrum if severe/deep infection: co-amoxiclav, piperacillin-tazobactam
  • Nutritional supplementation: protein-rich ONS, vitamin C, zinc (limited evidence but commonly supplemented)

Surgical/Interventional

  • Surgical debridement: for extensive necrosis/eschar
  • Negative pressure wound therapy (VAC): for large/deep wounds; promotes granulation
  • Reconstructive surgery: flap reconstruction for large Category 3-4 ulcers (in selected patients)

Referral Criteria

  • Category 3 or 4: tissue viability specialist nurse
  • Suspected osteomyelitis: orthopaedic/surgical review
  • Non-healing wound: tissue viability team, wound biopsy
  • All pressure ulcers: clinical incident reporting (Datix)

Prognosis

  • Category 1-2: usually heal with appropriate care (weeks)
  • Category 3-4: prolonged healing (months); may never fully heal in frail patients
  • Mortality: patients who develop pressure ulcers in hospital have 4× mortality (associated with severity of illness)
  • Osteomyelitis complicates up to 20% of Category 4 ulcers (difficult to treat)
  • Prevention is far more effective than treatment
  • Recurrence rate is high if underlying risk factors not addressed

Other Relevant Information

EPUAP/NPUAP Pressure Ulcer Categories

CategoryDescription
1Non-blanchable erythema, intact skin
2Partial-thickness skin loss (dermis exposed); blister
3Full-thickness skin loss (subcutaneous visible); bone/tendon not visible
4Full-thickness tissue loss (bone/tendon exposed)
UnstageableObscured by slough/eschar
Deep tissue injuryPurple/maroon area, intact skin; underlying damage

Waterlow Score Risk Categories

ScoreRisk
10-14At risk
15-19High risk
≥20Very high risk

NICE Guidelines / CKS

End of Life Care in the Elderly

End of life care for older adults requires recognition of dying, symptom management, personalised care planning, and support for patients and families, guided by principles of comfort, dignity, and individual choice.

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Key Facts

  • ~500,000 people die each year in England; >80% of deaths are in people >65
  • Recognising dying is a clinical skill; use validated tools and clinical judgement (e.g., the Surprise Question: 'Would I be surprised if this patient died in the next 12 months?')
  • NICE NG31 (Care of Dying Adults): individualised care plan within hours of recognising dying
  • Anticipatory prescribing: prescribe PRN medications for pain (morphine), agitation (midazolam), secretions (hyoscine butylbromide/glycopyrronium), nausea (haloperidol/cyclizine)
  • Preferred place of death: approximately 70% of people prefer to die at home; only ~25% do; ~46% die in hospital
  • Syringe driver (CSCI): continuous subcutaneous infusion for patients unable to take oral medication; mix medications as per local compatibility chart
  • Clinically assisted hydration: assess individually; not routinely started or continued in last days of life if not providing benefit
  • Communication: honest, compassionate conversations with patient and family about prognosis, treatment limitations, and goals of care

Overview

Key Facts

Good end of life care is a core competency for all doctors. It requires clinical skill in recognising dying, managing symptoms, and communicating sensitively with patients and families.

Epidemiology

  • ~500,000 deaths/year in England
  • 80% in people over 65

  • Most common causes of death in elderly: dementia, heart disease, cerebrovascular disease, respiratory disease, cancer
  • Place of death: hospital ~46%, home ~25%, care home ~22%, hospice ~6%

Aetiology

End of life care is needed for patients dying from any cause, including:

  • Cancer (predictable trajectory)
  • Organ failure: heart failure, COPD, renal failure (unpredictable trajectory with acute exacerbations)
  • Frailty/dementia (gradual decline)

Pathophysiology

  • Dying is a physiological process: progressive organ failure
  • Common symptoms in the last days: pain, agitation, respiratory secretions, nausea, dyspnoea
  • Reduced consciousness is normal in the dying process
  • Cessation of eating and drinking is normal

Clinical Presentation

Recognising Dying

  • Progressive deterioration despite treatment
  • Bedbound, drowsy, minimal oral intake
  • Reduced urine output
  • Peripheral cyanosis, mottling
  • Altered breathing pattern (Cheyne-Stokes, irregular)
  • Cold peripheries
  • Changes in consciousness

Common Symptoms in Last Days

  • Pain (present in ~50%)
  • Agitation/restlessness (terminal agitation)
  • Respiratory secretions ("death rattle")
  • Nausea and vomiting
  • Dyspnoea
  • Dry mouth
  • Anxiety and distress

Red Flags

  • Reversible cause of deterioration not identified (infection, hypercalcaemia, medication toxicity)
  • Uncontrolled symptoms despite appropriate prescribing
  • Patient/family distress requiring specialist input
  • Disagreement within clinical team or between team and family

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Reversible deteriorationIdentifiable treatable causeBloods, imaging as appropriate
DeliriumAcute confusion, reversible cause4AT, investigate/treat cause
Opioid toxicityPinpoint pupils, myoclonus, reduced GCSReduce/rotate opioid
DepressionLow mood, withdrawal, hopelessnessClinical assessment

Diagnosis / Investigation

Bedside

  • Clinical assessment of dying (NICE NG31)
  • Symptom assessment (verbal or non-verbal tools if unable to communicate)
  • Review current medications (stop non-essential; ensure comfort medications prescribed)
  • Assessment of patient's wishes and preferences
  • Spiritual/religious needs assessment

Bloods

  • Generally not appropriate in last days of life unless result would change management
  • May check if reversible cause suspected (calcium, glucose)

Imaging

  • Generally not appropriate in last days of life

Special Tests

  • Review advance directives, ADRT, DNACPR, LPA
  • Holistic needs assessment of patient and family
  • Bereavement risk assessment

Management

Non-pharmacological

  • Recognise dying: communicate with patient and family
  • Individualised care plan: document within hours of recognising dying
  • Comfort measures: mouth care, positioning, pressure care, skin care
  • Environment: quiet, private, comfortable; unrestricted visiting
  • Communication: honest, compassionate; avoid false reassurance; explore fears and concerns
  • Spiritual care: chaplaincy, religious observances
  • Family support: information, reassurance, bereavement support after death
  • Stop unnecessary interventions: monitoring, routine observations, blood tests, IV fluids (unless for symptom management)

Pharmacological (Anticipatory Prescribing)

  • Pain: morphine sulphate 2.5-5mg SC PRN 1-hourly (reduce dose if opioid-naive, elderly, or renal impairment; 1-2.5mg)
  • Agitation/restlessness: midazolam 2.5-5mg SC PRN 1-hourly
  • Respiratory secretions: hyoscine butylbromide 20mg SC PRN 1-hourly or glycopyrronium 200mcg SC PRN
  • Nausea/vomiting: haloperidol 0.5-1mg SC PRN (or cyclizine 50mg SC PRN; levomepromazine 6.25mg SC PRN)
  • Syringe driver (CSCI): when regular SC doses needed; typically morphine + midazolam + hyoscine butylbromide ± haloperidol over 24 hours (check local compatibility charts)
  • Clinically assisted hydration: assess individually; not routinely started/continued if patient is dying and not distressed by thirst

Surgical/Interventional

  • Generally not appropriate in end of life care
  • Palliative procedures (e.g. drainage of symptomatic effusion, urinary catheterisation for retention) may be considered for symptom relief

Referral Criteria

  • Complex symptoms: specialist palliative care (hospice, hospital palliative care team)
  • Psychological distress (patient or family): psychology, counselling
  • Complex ethical decisions: clinical ethics team
  • Bereavement support: bereavement services

Prognosis

  • Recognising dying is a clinical judgement; prognostication is difficult but important
  • Surprise Question: "Would I be surprised if this patient died in the next 12 months?" - identifies those who may benefit from palliative approach
  • PPS (Palliative Performance Scale) and PPI (Palliative Prognostic Index): validated prognostic tools
  • Median survival once last days of life recognised: typically 1-3 days
  • Good end of life care improves quality of death for patient and bereavement outcomes for family

Other Relevant Information

Anticipatory Medications for Last Days of Life

SymptomFirst-lineDoseRoute
PainMorphine sulphate2.5-5mg PRN (1h)SC
AgitationMidazolam2.5-5mg PRN (1h)SC
Respiratory secretionsHyoscine butylbromide20mg PRN (1h)SC
Nausea/vomitingHaloperidol0.5-1mg PRN (1h)SC
DyspnoeaMorphine sulphate2.5-5mg PRN (1h)SC

NICE NG31 - Priorities for Care of the Dying Person

Priority
1. Recognise that the person may be dying
2. Communicate sensitively with the dying person and those important to them
3. Involve the dying person and those important to them in decisions
4. Explore and address the needs of families and carers
5. Develop an individualised care plan including food, drink, symptom management, psychological/spiritual support

NICE Guidelines / CKS

Advance Care Planning

Advance care planning is a voluntary process of discussion about future care between a person, their family, and healthcare professionals, enabling patients to express preferences and make legally binding advance decisions.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Advance care planning (ACP) is a voluntary process of discussion about future care preferences and goals
  • Advance Decision to Refuse Treatment (ADRT): legally binding under the Mental Capacity Act 2005; must be written, signed, and witnessed if refusing life-sustaining treatment
  • Lasting Power of Attorney (LPA) for health and welfare: legal authority to make decisions on behalf of someone who lacks capacity; must be registered with the Office of the Public Guardian
  • DNACPR (Do Not Attempt Cardiopulmonary Resuscitation): a clinical decision but should involve patient/family discussion; documented on ReSPECT form in most of England/Wales
  • ReSPECT process: recommended summary plan for emergency care and treatment; replaces standalone DNACPR forms
  • ACP discussions should be initiated early, when the patient has capacity - not left until crisis
  • NICE NG97, NG31: recommend ACP discussions for patients with dementia and at end of life
  • ACP does not include euthanasia or assisted dying (which remain illegal in England and Wales)

Overview

Key Facts

Advance care planning gives patients a voice in their future care, especially when they may lose the capacity to make or communicate decisions. It is a process, not a one-off event.

Epidemiology

  • Only ~4% of the UK population have an ADRT
  • ~10% have a registered health and welfare LPA
  • ReSPECT forms now in use across most of England and Wales
  • ACP is particularly important for: dementia, cancer, progressive neurological disease, frailty, COPD, heart failure

Aetiology

ACP is needed because:

  • Many patients lose capacity before death (dementia, stroke, delirium, ICU admission)
  • Without ACP, decisions are made by clinicians acting in patient's best interests (which may not align with patient's actual wishes)
  • Reduces unwanted hospital admissions and interventions at end of life

Pathophysiology

Not applicable (ethical/legal framework rather than pathological process). However, ACP is underpinned by the Mental Capacity Act 2005 which provides the legal basis for advance decisions and proxy decision-making.

Clinical Presentation

When to Discuss ACP

  • At diagnosis of life-limiting illness
  • When moving to care home
  • After significant deterioration or hospital admission
  • When Surprise Question answer is "No" (would not be surprised if died in 12 months)
  • At patient's request
  • During routine reviews for long-term conditions

Components of ACP

  • Patient's values, beliefs, and preferences
  • Understanding of their condition and prognosis
  • Preferred place of care and death
  • Specific treatment preferences (e.g. hospital admission, ICU, ventilation)
  • What matters most to the patient
  • Naming a spokesperson/proxy

Red Flags

  • Patient expressing strong views about future treatment without documented plan
  • Conflict between family members about patient's wishes
  • Patient with progressive illness and no ACP in place
  • Healthcare professional making decisions without exploring patient's wishes

Differential Diagnosis

DocumentLegal StatusScope
Advance statementNot legally bindingGeneral wishes and preferences
ADRTLegally binding (if valid and applicable)Specific refusal of treatment
LPA (health and welfare)Legally binding when registeredProxy decision-making
ReSPECT formClinical recommendationSummary emergency care plan
DNACPRClinical decisionCPR decision only

Diagnosis / Investigation

Bedside

  • Capacity assessment (see Capacity Assessment topic): does the patient have capacity to make this decision now?
  • Review of existing documents (ADRT, LPA, ReSPECT)
  • Discussion with patient about values, wishes, and preferences
  • Discussion with family/carers (with patient's consent)

Bloods

  • Not applicable

Imaging

  • Not applicable

Special Tests

  • Not applicable (ACP is a communication process, not a diagnostic process)

Management

Non-pharmacological

  • Initiate conversation: use open questions; explore what the patient understands about their condition
  • Discuss: values, preferences, fears, goals of care, preferred place of death
  • Document: in clinical records; create/update ADRT if requested; complete ReSPECT form
  • Review regularly: ACP is a process; preferences may change over time
  • Involve: family/carers (with consent), GP, specialist team, palliative care
  • Support: written information, time to reflect, opportunity to revisit

Key Legal Documents

  • Advance Decision to Refuse Treatment (ADRT):
    • Must be made when patient has capacity
    • Must specify the treatment being refused and circumstances
    • Must be written, signed, and witnessed if refusing life-sustaining treatment
    • Can be overridden by a more recent decision or if patient had capacity at the time
    • Cannot request treatment (only refuse it)
  • Lasting Power of Attorney (LPA) for Health and Welfare:
    • Appoints a proxy (attorney) to make decisions when patient lacks capacity
    • Must be registered with the Office of the Public Guardian
    • Attorney must act in patient's best interests
    • Can include authority for life-sustaining treatment decisions
  • ReSPECT form:
    • Recommended Summary Plan for Emergency Care and Treatment
    • Completed with patient (or those close to them if lacking capacity)
    • Includes CPR decision, clinical recommendations, patient preferences
    • Travels with the patient (home, ambulance, hospital)

Pharmacological

  • Not applicable

Surgical/Interventional

  • Not applicable

Referral Criteria

  • Complex ACP discussions: palliative care specialist
  • Disputed capacity: request formal capacity assessment
  • Disagreement between family and clinical team: mediation, clinical ethics committee
  • Legal queries about ADRT/LPA: Trust legal department

Prognosis

  • ACP improves: concordance between patient wishes and actual care received
  • Reduces: unwanted hospital admissions and interventions
  • Increases: likelihood of dying in preferred place (associated with better family bereavement outcomes)
  • Patients with documented ACP: more likely to receive appropriate level of care at end of life
  • ACP does not shorten life; it ensures care aligns with patient's values

Other Relevant Information

Comparison of ACP Documents

DocumentWho CreatesWhen ValidLegally BindingScope
Advance statementPatientAny timeNo (but must be considered)General wishes
ADRTPatient (with capacity)When patient lacks capacityYes (if valid and applicable)Refuses specific treatment
LPA (health)Patient (registered OPG)When patient lacks capacityYesProxy decision-maker
ReSPECTClinician with patientAny timeNo (clinical recommendation)Emergency care preferences

Mental Capacity Act 2005 - Key Principles

Principle
1. Assume capacity unless established otherwise
2. Help the person make their own decision
3. An unwise decision does not mean lack of capacity
4. Decisions made for those lacking capacity must be in their best interests
5. Least restrictive option

NICE Guidelines / CKS

Capacity Assessment

Mental capacity assessment under the Mental Capacity Act 2005 is a legal and clinical skill requiring assessment of whether a patient can understand, retain, weigh, and communicate a specific decision at a specific time.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Mental Capacity Act 2005 (England and Wales): legal framework for capacity assessment and best interests decisions
  • Capacity is decision-specific and time-specific: a person may have capacity for one decision but not another
  • Two-stage test: (1) Does the person have an impairment of, or disturbance in, the functioning of the mind or brain? (2) Does this impairment mean they cannot make the specific decision?
  • Four functional criteria: the person must be able to understand, retain, weigh/use, and communicate the information relevant to the decision
  • Principle 1: Assume capacity until established otherwise
  • Principle 3: An unwise decision does not equal lack of capacity
  • If a person lacks capacity, decisions must be made in their best interests (Section 4 MCA 2005)
  • IMCA (Independent Mental Capacity Advocate): must be instructed for serious medical treatment decisions or accommodation changes for unbefriended patients

Overview

Key Facts

Capacity assessment is a core clinical skill. All clinicians are responsible for assessing capacity for decisions within their scope of practice. It is a legal requirement under the Mental Capacity Act 2005.

Epidemiology

  • Approximately 2 million adults in England and Wales may lack capacity for some decisions
  • Commonly encountered in: dementia, delirium, brain injury, learning disability, severe mental illness, intoxication
  • Capacity assessments are performed daily in hospitals, GP practices, and social care settings

Aetiology

Impairment or disturbance of the mind or brain may be caused by:

  • Dementia
  • Delirium
  • Brain injury (stroke, traumatic)
  • Learning disability
  • Severe mental illness (psychosis, severe depression)
  • Intoxication (alcohol, drugs)
  • Loss of consciousness

Pathophysiology

The Mental Capacity Act 2005 does not define capacity in pathological terms but in functional terms - it assesses what a person can do with the information relevant to a specific decision, not their diagnosis.

Clinical Presentation

When to Assess Capacity

  • When there is reason to doubt capacity for a specific decision
  • Before any medical treatment or intervention
  • When a patient refuses treatment
  • When a patient is making a decision with significant consequences
  • When advance care planning
  • When considering discharge destination

Five Principles of the MCA 2005

  1. Assume capacity unless established otherwise
  2. Support decision-making: take all practicable steps to help the person make their own decision (e.g. timing, location, communication aids, interpreter)
  3. Unwise decisions are allowed: a person is not to be treated as lacking capacity merely because they make a decision others consider unwise
  4. Best interests: any act done for a person who lacks capacity must be in their best interests
  5. Least restrictive option: anything done must be the least restrictive of the person's rights and freedoms

Red Flags

  • Clinician assuming lack of capacity based on diagnosis alone (unlawful)
  • No documented capacity assessment before proceeding with treatment
  • Best interests decision made without consulting relevant people
  • Lack of capacity assumed because patient makes an unwise decision
  • Restraint used without proper legal framework (DoLS/LPS)

Differential Diagnosis

ScenarioCapacity StatusAction
Patient with capacity refuses treatmentHas capacityRespect decision (even if clinicians disagree)
Patient lacks capacity, treatment in best interestsLacks capacityProceed under best interests (MCA Section 4)
Patient lacks capacity, valid ADRT existsLacks capacityRespect ADRT (if valid and applicable)
Patient lacks capacity, LPA existsLacks capacityConsult attorney (who acts in best interests)
Unbefriended patient lacks capacity for serious decisionLacks capacityInstruct IMCA

Diagnosis / Investigation

Bedside

  • Stage 1: Is there an impairment of, or disturbance in, the functioning of the mind or brain? (e.g. dementia, delirium, brain injury, intoxication)
  • Stage 2 (if yes to Stage 1): Can the person:
    1. Understand the information relevant to the decision? (presented in simple terms, including risks and benefits)
    2. Retain the information long enough to make the decision? (even briefly is sufficient)
    3. Weigh/use the information as part of the decision-making process? (balance pros and cons)
    4. Communicate the decision? (by any means - speech, writing, signing, blinking)
  • Failure in any one of these four = lacks capacity for that decision

Bloods

  • May be needed to identify/treat reversible causes of impaired capacity (e.g. delirium workup)

Imaging

  • Not required for capacity assessment itself
  • May be relevant if investigating underlying cause

Special Tests

  • Cognitive assessment (AMT, MoCA, ACE-III) may inform but does not replace formal capacity assessment
  • Neuropsychological assessment: for complex cases

Management

Non-pharmacological

  • If person HAS capacity: respect their decision, even if it seems unwise; document assessment
  • If person LACKS capacity: make a best interests decision (Section 4 MCA)

Best Interests Decision (Section 4 MCA)

  • Consider all relevant circumstances
  • Consider whether the person will regain capacity
  • Involve the person as much as possible
  • Consider past and present wishes, feelings, beliefs, and values
  • Consult: carers, family, LPA, IMCA (if unbefriended)
  • Choose the least restrictive option
  • Document the decision-making process

Deprivation of Liberty Safeguards (DoLS) / Liberty Protection Safeguards (LPS)

  • If a person lacks capacity and is deprived of their liberty (e.g. kept in hospital/care home), DoLS/LPS authorisation is required
  • Six qualifying requirements: age (≥18), mental disorder, lack of capacity, best interests, eligibility, no refusals

Pharmacological

  • Not applicable to capacity assessment itself
  • Treat reversible causes of impaired capacity (e.g. treat delirium, correct metabolic disturbance)

Surgical/Interventional

  • Not applicable

Referral Criteria

  • Complex capacity assessments: psychiatry or neuropsychology
  • Disputed capacity: seek second opinion, consider Court of Protection
  • Serious medical treatment for unbefriended patient: instruct IMCA
  • Potential DoLS: supervisory body (local authority)

Prognosis

  • Capacity may fluctuate: reassess when there is reason to believe it may have changed
  • Capacity may be regained: e.g. after delirium resolves, intoxication clears, depression treated
  • Timely capacity assessment ensures patients' rights are protected
  • Failure to assess capacity appropriately may have legal consequences
  • Good documentation protects patients and clinicians

Other Relevant Information

Mental Capacity Act 2005 - Two-Stage Test

StageQuestion
1. DiagnosticIs there an impairment of, or disturbance in, the mind or brain?
2. FunctionalCan the person understand, retain, weigh/use, and communicate the decision?

Best Interests Checklist (Section 4 MCA)

Factor
Will the person regain capacity? Can the decision wait?
Involve the person as much as possible
Consider past and present wishes, feelings, beliefs, values
Consult family, carers, LPA, IMCA
Do not make assumptions based on age, appearance, condition, or behaviour
Least restrictive option
Document the decision and reasoning

NICE Guidelines / CKS

Elder Abuse and Safeguarding

Elder abuse affects approximately 500,000 older people in the UK at any time, requiring healthcare professionals to recognise, report, and respond to suspected abuse under safeguarding duties.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Elder abuse affects approximately 500,000 older people in the UK at any given time
  • Types of abuse: physical, psychological/emotional, financial, sexual, neglect, self-neglect, discriminatory, organisational/institutional, domestic abuse, modern slavery
  • Care Act 2014: places a duty on local authorities to make enquiries (Section 42) when an adult at risk may be experiencing abuse or neglect
  • Adult at risk (Section 42): has needs for care and support, is experiencing or at risk of abuse or neglect, AND is unable to protect themselves because of those needs
  • Healthcare professionals have a duty to report concerns about abuse to the local authority safeguarding team
  • Financial abuse is the most commonly reported type in community settings; neglect is most common in institutional settings
  • Risk factors for abuse: social isolation, dependency, dementia, mental illness, carer stress, substance misuse (carer)
  • Consent should be obtained before sharing information, but override consent if there is risk of serious harm to the person or others

Overview

Key Facts

Elder abuse is under-reported and under-recognised. All healthcare professionals have a responsibility to safeguard adults at risk.

Epidemiology

  • ~500,000 older people in the UK affected at any time
  • Prevalence in community: 2-5%; in care homes: 15-25%
  • Financial abuse most common in community; neglect most common in institutions
  • Often perpetrated by family members, carers, or paid care staff
  • Under-reporting is significant: estimated only 1 in 24 cases reported

Aetiology

  • Perpetrator factors: carer stress, mental illness, substance misuse, financial dependence on victim, history of domestic abuse
  • Victim factors: dependency, social isolation, dementia/cognitive impairment, physical disability, communication difficulties
  • Situational factors: overcrowded living, poor institutional culture, inadequate staffing, lack of training

Pathophysiology

Not a pathological process but a pattern of harmful behaviour. The impact includes:

  • Physical injury (fractures, burns, bruising)
  • Psychological harm (depression, anxiety, PTSD, withdrawal)
  • Financial loss
  • Neglect of medical needs
  • Death (in severe cases)

Clinical Presentation

Types of Abuse

  • Physical: hitting, pushing, restraint, inappropriate medication administration
  • Psychological/emotional: threats, humiliation, controlling behaviour, isolation
  • Financial: theft, fraud, coercion, misuse of benefits, pressure to change will
  • Sexual: any sexual activity without consent (including with patients who lack capacity)
  • Neglect: failure to provide adequate food, warmth, medication, hygiene, medical care
  • Self-neglect: refusal of care, hoarding, self-harm through neglect (if has needs for care and support)
  • Organisational: poor institutional practices, inadequate care, rigid routines
  • Domestic abuse: controlling/coercive behaviour by partner or family member

Warning Signs

  • Unexplained injuries (bruises in unusual locations, burns, fractures at different stages of healing)
  • Withdrawal, fearfulness, or agitation in presence of carer
  • Poor hygiene, malnutrition, pressure ulcers in a cared-for person
  • Unexplained financial transactions or sudden changes to will
  • Frequent A&E attendances
  • Inconsistent history between patient and carer
  • Patient not allowed to speak alone

Red Flags

  • Non-accidental pattern of injuries
  • Delay in seeking medical help
  • Carer preventing patient from being seen alone
  • Signs of restraint (wrist marks)
  • Genital/rectal trauma without explanation
  • Rapid unexplained weight loss
  • Withdrawal of food/drink/medication as punishment

Differential Diagnosis

DiagnosisKey FeaturesInvestigation
Accidental injuryConsistent history, mechanism matches injuryClinical assessment
CoagulopathyEasy bruising, anticoagulant useClotting screen, drug history
Osteoporosis fracturesLow-energy mechanism, known osteoporosisDEXA, bone profile
Skin fragility (senile purpura)Dorsal forearms/hands, thin skinClinical
Depression/self-neglectLow mood, social withdrawalPHQ-9, social assessment
Dermatitis/skin conditionsTypical distribution and morphologyDermatological assessment

Diagnosis / Investigation

Bedside

  • Full examination: skin (bruises, burns, pressure ulcers), nutritional status, hygiene, hydration
  • Document injuries: describe precisely (location, size, colour, stage of healing); photograph with consent
  • Speak to patient alone (essential)
  • Mental capacity assessment: for decisions about safeguarding and information sharing
  • Assessment of mood and anxiety
  • Nutritional assessment (MUST)

Bloods

  • FBC, clotting screen (exclude coagulopathy)
  • U&Es (dehydration)
  • Albumin (malnutrition)
  • Drug levels (if medication abuse suspected - over-sedation or withholding)
  • STI screening (if sexual abuse suspected)

Imaging

  • X-rays: if fractures suspected
  • Skeletal survey: rarely needed in adults (more common in child safeguarding)

Special Tests

  • Body map documentation
  • Safeguarding referral (Section 42 enquiry)
  • Police referral if criminal act suspected
  • Social work assessment
  • Carer assessment

Management

Non-pharmacological

  • Immediate safety: ensure the person is safe; separate from alleged abuser if necessary
  • Raise a safeguarding concern: contact local authority adult safeguarding team (regardless of the person's capacity)
  • Document thoroughly: clinical notes, body maps, photographs (with consent), chronology
  • Involve the patient: discuss concerns with them; obtain their views and wishes (unless doing so would increase risk)
  • Consent: seek consent to share information, but override if serious risk of harm
  • Multi-agency safeguarding: local authority leads Section 42 enquiry; involves police, social care, health, CQC
  • Protection plan: developed by safeguarding meeting; may include changes to care arrangements, legal action, monitoring
  • Support for the patient: advocacy, counselling, practical support
  • Support for carers: carer assessment, respite, education (if abuse relates to carer stress and patient wishes to remain with carer)

Pharmacological

  • Not directly applicable
  • Treat physical and psychological consequences of abuse

Surgical/Interventional

  • Not applicable

Referral Criteria

  • All suspected abuse: raise safeguarding concern with local authority
  • Immediate danger: call police (999)
  • Organisational abuse: CQC notification (registered provider)
  • Complex cases: adult safeguarding board
  • Domestic abuse: MARAC (Multi-Agency Risk Assessment Conference) if high risk

Prognosis

  • Elder abuse is associated with 2-3× increased mortality
  • Depression and anxiety are common consequences
  • Financial abuse can have devastating long-term impact
  • Early recognition and intervention can prevent escalation
  • Organisational abuse can be addressed through systemic changes
  • Many victims of elder abuse do not self-report; healthcare professional vigilance is essential

Other Relevant Information

Care Act 2014 - Section 42 Enquiry Criteria

CriterionRequirement
Adult at riskHas needs for care and support
Experiencing/at risk ofAbuse or neglect
Unable to protect themselvesBecause of their care and support needs

Types of Abuse Summary

TypeExamples
PhysicalHitting, restraint, force-feeding, inappropriate medication
PsychologicalThreats, humiliation, controlling, isolation
FinancialTheft, coercion, misuse of funds/benefits
SexualNon-consensual sexual contact/activity
NeglectFailure to provide food, warmth, medication, hygiene
Self-neglectRefusal of care, hoarding, neglecting own needs
OrganisationalPoor institutional care, rigid routines, inadequate staffing
DomesticControlling/coercive behaviour by partner/family

NICE Guidelines / CKS

Rehabilitation in Older Adults

Rehabilitation in older adults is a goal-directed, multidisciplinary process aimed at restoring function and independence after illness or injury, underpinned by comprehensive geriatric assessment.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Rehabilitation is a goal-directed process enabling a person to reach their optimal physical, psychological, and social functioning
  • MDT approach is essential: geriatrician, physiotherapist, occupational therapist, SALT, dietitian, social worker, psychologist, nursing
  • Comprehensive Geriatric Assessment (CGA) underpins all rehabilitation programmes for older adults
  • Early mobilisation (within 24 hours of admission) reduces deconditioning, delirium, VTE, pressure ulcers, and length of stay
  • Goal-setting should be patient-centred, SMART (Specific, Measurable, Achievable, Relevant, Time-bound), and regularly reviewed
  • Common rehabilitation settings: acute hospital, community rehabilitation unit, intermediate care, home-based rehabilitation
  • Functional independence is the primary outcome measure; tools include Barthel Index (0-20/100) and Functional Independence Measure (FIM)
  • Deconditioning in hospital: older adults lose 5% of muscle strength per day of bed rest; 10 days of bed rest = 10 years of muscle ageing

Overview

Key Facts

Rehabilitation is a core function of geriatric medicine. It requires active patient participation, realistic goal-setting, and coordinated multidisciplinary input.

Epidemiology

  • Approximately 30-50% of hospitalised older adults experience functional decline during admission
  • 10 days of bed rest in a healthy older adult leads to 14% loss of aerobic capacity and 10% loss of muscle strength
  • Intermediate care and rehabilitation services handle >500,000 episodes per year in England

Aetiology

Rehabilitation is needed after:

  • Acute illness (pneumonia, sepsis, AKI)
  • Surgical procedures (hip fracture, joint replacement, cardiac surgery)
  • Neurological events (stroke, head injury)
  • Prolonged immobility or deconditioning
  • Falls and fractures
  • Amputation

Pathophysiology

  • Deconditioning syndrome: bed rest → sarcopenia, reduced cardiovascular fitness, joint contractures, pressure ulcers, constipation, postural hypotension, depression, cognitive decline
  • Neuroplasticity: the brain can reorganise after injury (basis for stroke rehabilitation)
  • Motor learning: repetitive task-specific practice improves function

Clinical Presentation

Assessment

  • Pre-morbid function (what could the patient do 2 weeks before admission?)
  • Current functional ability (mobility, transfers, washing, dressing, toileting, feeding)
  • Cognition (capacity to participate, learning ability)
  • Mood (depression significantly impairs rehabilitation participation)
  • Social circumstances (home setup, carers, support)
  • Patient's own goals and priorities

Rehabilitation Potential

  • Motivation and engagement
  • Pre-morbid function
  • Cognitive ability to learn and participate
  • Medical stability
  • Adequate nutrition
  • Realistic goals achievable within timeframe

Red Flags

  • Failure to progress despite appropriate rehabilitation
  • New medical deterioration during rehabilitation
  • Persistent delirium impeding participation
  • Safeguarding concerns (e.g. unsafe home environment)
  • Worsening mood/psychological distress

Differential Diagnosis

Barrier to RehabilitationKey FeaturesIntervention
DeliriumFluctuating attention, acute onsetTreat underlying cause
DepressionLow mood, amotivation, apathyAntidepressant, psychology
PainLimiting movement and participationOptimise analgesia
Cognitive impairmentPoor carryover, inability to learnAdapted approach, repetition
Medical instabilityRecurrent infection, cardiac eventsMedical optimisation

Diagnosis / Investigation

Bedside

  • Barthel Index: ADL assessment (0-100; higher = more independent)
  • Functional Independence Measure (FIM): 18 items, motor + cognitive (18-126)
  • Timed Up and Go (TUG): functional mobility
  • Grip strength: dynamometry
  • Cognitive assessment: MoCA, ACE-III
  • Mood screening: GDS-15, PHQ-9
  • MUST: nutritional assessment
  • Home assessment (OT): evaluate equipment needs, safety

Bloods

  • FBC, U&Es, vitamin D, albumin, TFTs, B12/folate (optimise medical status)

Imaging

  • As indicated by medical conditions

Special Tests

  • COPM (Canadian Occupational Performance Measure): patient-centred goal-setting
  • EQ-5D: quality of life measure
  • Therapy assessment: detailed physiotherapy and OT assessments

Management

Non-pharmacological

  • Early mobilisation: within 24 hours of admission (unless contraindicated)
  • Physiotherapy: strength training, balance, gait re-education, endurance
  • Occupational therapy: ADL practice, home assessment, equipment provision, cognitive rehabilitation
  • SALT: swallowing rehabilitation, communication therapy
  • Dietitian: nutritional optimisation (protein 1.0-1.2 g/kg/day)
  • Psychology: managing adjustment, depression, anxiety, motivation
  • Social work: care packages, housing, benefits, carer support
  • Goal-setting: SMART goals, reviewed weekly at MDT meeting
  • Discharge planning: starts from day 1; community rehabilitation, intermediate care, home adaptations

Pharmacological

  • Optimise medical conditions: pain management, blood pressure, diabetes, heart failure
  • Vitamin D supplementation: 800-1,000 IU daily
  • Treat depression: SSRIs if indicated (may improve rehabilitation engagement)
  • Medication review: stop medications causing sedation, postural hypotension, or cognitive impairment

Surgical/Interventional

  • Joint replacement rehabilitation protocols
  • Hip fracture rehabilitation (BPT standards: physio from day 1)
  • Post-amputation rehabilitation and prosthetic fitting

Referral Criteria

  • All older adults with functional decline: rehabilitation assessment
  • Complex needs: community rehabilitation or intermediate care
  • Stroke rehabilitation: specialist stroke rehabilitation unit (NICE NG236)
  • Unable to return home: social services, intermediate care, residential assessment

Prognosis

  • Early mobilisation reduces hospital LOS by 1-2 days and reduces complications
  • Intermediate care rehabilitation: 60-70% of patients return home
  • Hip fracture rehabilitation: 50% regain pre-fracture mobility
  • Stroke rehabilitation: greatest recovery in first 3 months; continued improvement up to 12 months
  • Deconditioning is largely reversible with appropriate exercise
  • Factors predicting good outcome: good pre-morbid function, motivation, intact cognition, social support

Other Relevant Information

Barthel Index (Modified)

ActivityScore Range
Feeding0-2
Bathing0-1
Grooming0-1
Dressing0-2
Bowels0-2
Bladder0-2
Toilet use0-2
Transfers0-3
Mobility0-3
Stairs0-2
Total0-20

Rehabilitation Settings

SettingDurationSuitable For
Acute hospitalDays-weeksMedically complex
Community rehabilitation unit2-6 weeksRequires inpatient therapy
Intermediate care (bed-based)Up to 6 weeksStep-down from acute
Home-based rehabilitation2-6 weeksCan safely be at home
Day hospitalWeeks-monthsOutpatient rehabilitation

NICE Guidelines / CKS

Discharge Planning

Effective discharge planning is a structured process beginning at admission to ensure safe, timely transition from hospital to home or appropriate care setting, reducing readmissions and improving patient outcomes.

MRCP Part 1 · MRCP Part 2 · PLAB 1 · UKMLA · MRCGP AKT · MSRA

Key Facts

  • Discharge planning should begin at admission - not as an afterthought when the patient is medically fit
  • Estimated Date of Discharge (EDD) should be set within 24 hours of admission and communicated to patient/family
  • Discharge to Assess (D2A): model where patients are discharged when safe (not necessarily fully recovered) and assessed for ongoing needs in their usual environment
  • 4 D2A pathways: 0 (simple discharge), 1 (home with support), 2 (rehabilitation/reablement facility), 3 (complex assessment for long-term care)
  • Delayed discharges cost the NHS approximately £300 million/year and harm patients through deconditioning and hospital-acquired complications
  • Medication reconciliation: essential at discharge; ensure accurate medication list, patient/GP letter, compliance aids if needed
  • Communication: discharge summary to GP within 24 hours; must include diagnosis, investigations, medication changes, follow-up plan
  • Red flags for unsafe discharge: unstable medical condition, unresolved safeguarding concerns, no safe living environment, unassessed capacity for discharge decision

Overview

Key Facts

Good discharge planning reduces length of stay, readmissions, and patient harm. It requires a multidisciplinary approach and close coordination with community services.

Epidemiology

  • ~10-15% of hospital beds in England occupied by patients who are medically fit for discharge ("delayed transfers of care")
  • 20-25% of older adults are readmitted within 30 days of discharge
  • Average excess LOS for delayed discharge: 7 days
  • Delayed discharge associated with increased mortality, functional decline, and hospital-acquired infection

Aetiology

Common reasons for delayed discharge:

  • Awaiting social care assessment/package
  • Awaiting care home placement
  • Awaiting community equipment/adaptations
  • Family/patient choice
  • Awaiting further NHS care (rehabilitation)
  • Safeguarding concerns

Pathophysiology

  • Prolonged hospital stay → deconditioning, nosocomial infection, delirium, falls, pressure ulcers, loss of independence
  • Hospital environment is disorienting for older adults (unfamiliar, noisy, disrupted sleep-wake cycle)
  • Each day of unnecessary hospital stay increases mortality risk and reduces functional recovery

Clinical Presentation

Discharge Planning Process

  1. Admission: identify likely discharge needs; set EDD
  2. During stay: daily MDT review; progress against goals; update EDD
  3. Pre-discharge: medication reconciliation; discharge summary; patient/family education; arrange follow-up; community referrals
  4. Discharge day: ensure transport, medications, equipment, care package in place
  5. Post-discharge: follow-up (GP, community teams, outpatient)

Assessment for Discharge

  • Medical stability (not necessarily full recovery)
  • Functional ability (can manage at home with support?)
  • Cognitive assessment (safe to return home?)
  • Medication understanding and supply
  • Social support (carers, package of care)
  • Home environment (safe, appropriate equipment)
  • Follow-up arrangements

Red Flags for Unsafe Discharge

  • Medically unstable
  • Unresolved safeguarding concerns
  • Inadequate social support with high care needs
  • Patient unable to manage medications safely without planned support
  • No safe living environment
  • Unassessed capacity for high-risk discharge decisions

Differential Diagnosis

Discharge Pathway (D2A)DescriptionProportion
Pathway 0Simple discharge; no additional support~50%
Pathway 1Home with new/enhanced support~30%
Pathway 2Short-term bed-based rehabilitation~15%
Pathway 3Complex assessment (care home likely)~5%

Diagnosis / Investigation

Bedside

  • Functional assessment (Barthel, mobility, ADLs)
  • Cognitive screen (4AT, AMT - can patient manage at home?)
  • Medication review and reconciliation
  • Home environment review (OT home visit or telephone assessment)
  • Carer assessment

Bloods

  • Ensure stable results before discharge (U&Es, INR, glucose)
  • Arrange follow-up bloods with GP if needed

Imaging

  • Not specific to discharge; ensure pending results are followed up

Special Tests

  • Capacity assessment if patient refuses care or makes high-risk decisions about discharge
  • Falls risk assessment before discharge
  • Nutritional assessment (MUST)

Management

Non-pharmacological

  • Set EDD within 24 hours: communicate to patient, family, and MDT
  • Board/huddle rounds: daily MDT review of discharge plan
  • Criteria-led discharge: empower nursing and therapy staff to discharge when criteria met
  • Home assessment: OT virtual or in-person home visit if needed
  • Equipment provision: community equipment service (grab rails, commode, raised toilet seat, hospital bed)
  • Care package: arrange domiciliary care (personal care, medication prompts, meals)
  • Intermediate care/reablement: time-limited support to restore independence
  • Patient and family education: diagnosis, medications, when to seek help, follow-up plan
  • Discharge summary: to GP within 24 hours; clear, accurate, complete

Pharmacological

  • Medication reconciliation: review all medications; stop unnecessary drugs; document changes and reasons
  • Discharge prescription: ensure sufficient supply (minimum 14 days); compliance aids (dosette box) if needed
  • Anticoagulation: ensure INR monitoring arranged; DOAC monitoring if applicable
  • Controlled drugs: appropriate supply and documentation

Surgical/Interventional

  • Not specifically applicable

Referral Criteria

  • Complex discharge: MDT planning meeting
  • New care needs: social services referral
  • Rehabilitation needs: community rehabilitation/intermediate care
  • Palliative care: community palliative care team
  • Safeguarding: local authority
  • GP follow-up: ensure continuity of care

Prognosis

  • Effective discharge planning reduces readmission by 20-25%
  • D2A model reduces LOS and improves patient satisfaction
  • Failed discharge (return to hospital within 48 hours): approximately 5-10%; often related to inadequate planning
  • 30-day readmission rate: approximately 20% for older adults (higher in heart failure, COPD, pneumonia)
  • Patients who experience delayed discharge have 10% higher mortality at 6 months
  • Good communication between hospital and primary care reduces readmission risk

Other Relevant Information

Discharge to Assess (D2A) Pathways

PathwayDescriptionAssessment LocationServices
0Simple dischargeN/ANo new support needed
1Home with supportAt homeDomiciliary care, community therapy
2RehabilitationBed-based unitShort-term rehabilitation/reablement
3Complex assessmentBed-basedContinuing healthcare assessment

Discharge Summary Requirements

Component
Diagnosis and problems managed
Procedures and investigations (with pending results flagged)
Medication changes (and reasons)
Discharge medications (with duration)
Allergies
Follow-up plan
Outstanding actions for GP
Patient's functional status at discharge

NICE Guidelines / CKS