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Osteomyelitis

NICE BNF Treatment summaries Musculoskeletal system infections, antibacterial therapy

2025 Update to WikiGuidelines for the management of pyogenic osteomyelitis in adults. Published: Apr 2026.

Clinical Practice Guideline by the Pediatric Infectious Diseases Society and the Infectious Diseases Society of America: 2021 Guideline on Diagnosis and Management of Acute Hematogenous Osteomyelitis in Pediatrics

 

Osteomyelitis

Osteomyelitis is an infection of bone and bone marrow, usually caused by bacteria.

Causes and Risk Factors

Mechanisms of Infection

Osteomyelitis usually results from 3 main mechanisms:

Mechanism Associated risk factors
Haematogenous spread from systemic infection – common in children
  • Bacteraemia / sepsis
  • Underlying haemoglobinopathies (e.g. sickle cell disease)
  • Incomplete immunisation
Direct inoculation (direct introduction of organisms into the joint) – common in adults
  • Significant traumatic injuries (e.g. open fractures)
  • Orthopaedic surgeries (e.g. ORIF, joint replacement)
  • Presence of implanted devices (e.g. prosthetic joint)
Contiguous spread from adjacent infection – common in adults
  • Pressure ulcers
  • Diabetic foot ulcers / diabetic foot infections
  • Septic arthritis

Shared systemic risk factors:

  • Immunosuppression (e.g. diabetes)
  • IVDU
  • Vascular insufficiency

Causative Organisms

  • Staphylococcus aureus – most common organism overall
  • Salmonella species – increased risk in those with sickle cell disease and other haemoglobinopathies
  • Kingella kingae – in younger pre-school-aged children (esp. when epiphyseal osteomyelitis is suspected)
  • Haemophilus influenzae type b – increased risk in those with incomplete childhood immunisation

Clinical Features

[Ref]

Acute osteomyelitis Acute osteomyelitis is the hallmark of paediatric osteomyelitis, also common in older adults and immunocompromised patients who develop bacteraemia

Develops rapidly over days to weeks following the initial infection

  • Signs of inflammation (hot, swollen, red) over the affected bone
  • Systemic upset (e.g. fever, malaise)
  • Refuse to or reduced use of the affected limb
  • Inability to bear weight (if the lower limb is affected)
Chronic osteomyelitis Chronic osteomyelitis is common in adults with systemic comorbidities (e.g. diabetic, vascular insufficiency)

Develops gradually over months to years of persistent infection:

  • Vague, chronic pain over the affected site (+/- cycles of pain flares)
  • Systemic upset (e.g. fever, malaise) is uncommon
  • Non-healing ulcers / fractures
  • Persistent draining sinus tracts – pathognomonic for chronic osteomyelitis
  • Exposed bone can be seen in severe cases
  • Sequestrum (necrotic bone)

The probe-to-bone test is a clinical test for diabetic foot osteomyelitis

  • Description: insert a sterile, blunt metal probe into the wound
  • Positive test: feeling a hard, gritty structure at the bone

Vertebral osteomyelitis has a slightly different presentation:

  • Gradual onset of back pain – worsened by activity
  • Fever is not always present
  • Most commonly affects the lumbar spine
  • May cause / co-exist with epidural abscess (triad of back pain + fever + neurological deficits)

Clinical presentation also varies depending on the mechanism of infection: [Ref]

Haematogenous spread Haematogenous spread osteomyelitis is more common in children:

  • In children, the metaphysis of the long bones (e.g. femur, tibia) is most commonly affected – due to the rich vasculature of growth plates
  • In adults, the vertebral bodies are most commonly affected

Haematogenous osteomyelitis more commonly presents acutely

Non-haematogenous spread (direct inoculation / contiguous spread) Non-haematogenous spread osteomyelitis is more common in adults, and there are often adjacent sources of infection, such as:

  • Diabetic foot infection → diabetic foot osteomyelitis
  • Overlying chronic wound (e.g. pressure ulcer)

Non-haematogenous osteomyelitis more commonly presents chronically

Investigation and Diagnosis

Blood tests
  • Blood cultures (should be obtained prior to antibiotic therapy)
  • FBC
    • ↑ WCC (but WCC is often normal in children and in chronic osteomyelitis)
    • Possible anaemia and reactive thrombocytosis
  • Inflammatory markers (CRP, ESR)
    • Inflammatory markers may be raised but have low diagnostic accuracy for confirming osteomyelitis
    • Main purpose: monitoring disease progression and response to treatment
Imaging
  • 1st line: X-ray
    • Plain X-rays have poor sensitivity for detecting early osteomyelitis; 30-50% of bone loss must occur before changes are visible on X-ray
    • Purpose: exclude other underlying pathologies (e.g. fractures, bone tumours)
  • Imaging of choice: MRI [Ref]
    • MRI has high sensitivity for osteomyelitis and can detect early changes
    • Classic finding: bone marrow oedema
Biopsy A definitive diagnosis can be established through bone biopsy and bacterial culture

  • A bone biopsy should not routinely be performed in all patients
  • A patient with clinically suspected osteomyelitis, positive blood cultures and supportive radiological findings typically does NOT require a bone biopsy
  • The decision to perform a biopsy should be made case-by-case

Management

Approach:

  • Initial management: empirical antibiotics (after blood cultures)
  • Definitive management: orthopaedic assessment to determine the need for surgical debridement

Antibiotic Therapy

1st line:

  • Flucloxacillin for 6 weeks
  • Consider adding fusidic acid or rifampicin for the initial 2 weeks

Alternative:

  • If penicillin allergic: clindamycin
  • If MRSA suspected: vancomycin or teicoplanin +/- fusidic acid or rifampicin

Surgical Debridement

Indications for urgent surgical debridement
  • Sepsis, or
  • Persistent bacteraemia (despite 48-72 hours of medical therapy), or
  • Vertebral osteomyelitis with epidural extension or neurological involvement [Ref]
Indications for planned surgical debridement
  • Prosthetic joint infections
  • Osteomyelitis with an underlying pressure ulcer
  • Presence of a large abscess
  • Presence of necrotic bone [Ref]

References

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