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.

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