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Necrotising soft-tissue infection

Essential points for quick revision.

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Suspected necrotising infection goes directly to source control

Fascial and muscle infection can advance beyond visible skin, thrombose microvessels and release toxins, producing shock, coagulopathy and multiorgan failure while laboratory scores or early imaging remain non-diagnostic.

Action: Activate sepsis, anaesthetic, intensive-care, microbiology and surgical pathways together; draw cultures if this causes no delay, start broad-spectrum parenteral antibiotics immediately, and proceed to NCEPOD-1 exploration and radical debridement without waiting for CT, transfer, physiological normalisation or a high LRINEC score.

Synopsis

Recognise limb necrotising fasciitis or myositis before late cutaneous necrosis, resuscitate sepsis while mobilising theatre, excise all infected zones immediately, obtain correctly labelled deep samples, and plan early re-look, reconstruction or consultant-led amputation.

  • Necrotising infection is a clinical and operative diagnosis. Pain beyond erythema, rapid change, systemic toxicity and high-risk host features outweigh a low score or reassuring early skin.
  • Do not use LRINEC to rule disease out; normal sodium, white count or CRP early in the course cannot make a dangerous examination safe.
  • Start sepsis resuscitation and broad-spectrum intravenous antibiotics without delay, but never let ICU stabilisation, CT or inter-hospital transfer postpone immediate surgical exploration.

Key red flags

Pain or exquisite tenderness extending beyond erythema, rapid progression, wooden induration, sensory change, dusky skin, bullae, crepitus or shock requires immediate senior surgical review even without fever.

Investigation priorities

01
First-line operative explorationFirst stepFirst line

Confirm fascial or muscle necrosis and remove its source immediately.

Management branches

RecognitionMobilise theatre while resuscitating

Rapid deep pain, spreading tissue change or toxicity makes necrotising infection clinically plausible.

  1. Call the responsible surgical consultant, anaesthesia, intensive care and microbiology and book immediate NCEPOD-1 exploration.
  2. Apply the sepsis pathway, draw cultures if non-delaying and start local broad-spectrum intravenous therapy immediately.

Key medicines

Immediate broad-spectrum parenteral antibioticsGive the current trust necrotising-infection regimen at full protocol adult doses immediately after cultures when cultures cause no delay; include Gram-positive, Gram-negative and anaerobic cover and add toxin-suppressing therapy when microbiology recommends it.
Balanced isotonic crystalloid for sepsis hypoperfusionGive 250 mL intravenously over 10–15 minutes, reassess circulation and pulmonary tolerance after each bolus and repeat as required up to 1,000 mL before mandatory senior review of further fluid, vasopressor and critical-care needs.
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Sources and review status4 sources · checked 27 Aug 2026 · clinical review pending
Sources

Sources and review status

National guidance is shown before implementation-dependent detail. Typical adult dose examples remain subject to patient factors, contraindications and the live BNF or specialist protocol. Source check completed 27 Aug 2026; clinical approval remains outstanding.

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom