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Educational draft · awaiting clinical reviewUse Rapid for revision, not patient-care decisions. Check current national and local guidance and the BNF or BNFC before acting.

Diabetic foot infection

Infectious diseases, microbiology and sexual health · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
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Limb-threatening infection or ischaemia

Sepsis, rapidly progressive necrosis, deep abscess, compartment pressure, wet gangrene or infection with critical limb ischaemia threatens life and limb.

Action: Use ABCDE, start the local severe diabetic-foot intravenous regimen after useful cultures, keep the patient non-weight-bearing and obtain immediate surgical, vascular, podiatry, microbiology and diabetes-team assessment for drainage, debridement or revascularisation.

Synopsis

Diagnose diabetic foot infection clinically, grade limb and systemic threat, obtain deep microbiology and coordinate debridement, perfusion restoration, offloading and antimicrobial treatment.

  • Diabetic foot infection is a clinical diagnosis: purulence or at least two local inflammatory features must be attributed to infection, not culture alone.
  • Do not give antibiotics to an uninfected ulcer; colonisation is expected and treatment does not promote healing.
  • Remove dressings, inspect between toes and examine depth, undermining, necrosis, fluctuance, deformity, sensation and perfusion.
  • Grade infection as mild, moderate or severe because extent, depth and systemic features determine setting, spectrum and urgency.
  • After cleaning and debridement, obtain deep tissue or curettage for culture; avoid using a superficial swab when a better sample is feasible.
  • Plain radiography is the initial bone study; MRI is the preferred advanced imaging test when osteomyelitis remains uncertain.
  • Antibiotics are only one component: drainage, debridement, offloading, perfusion restoration, glucose management and wound care determine outcome.
  • For a mild infection, NICE lists flucloxacillin 500 mg to 1 g four times daily for seven days as a first-choice adult regimen, with review and culture adjustment.

Key red flags

Hypotension, confusion, tachypnoea, lactate rise or oliguria indicates severe infection with organ dysfunction.

Crepitus, bullae, anaesthesia, necrosis or disproportionate pain suggests necrotising soft-tissue infection.

Fluctuance, purulent tracking or pain with passive movement suggests a deep abscess or compartment infection.

Cool skin, absent pulses, rest pain, gangrene or delayed capillary return indicates limb-threatening ischaemia.

Visible or probe-detectable bone, chronic deep ulcer or persistent inflammatory drainage raises osteomyelitis probability.

Neuropathy can remove pain, so an apparently comfortable patient may still have extensive infection.

Moderate deep disease

Erythema extending more widely, lymphangitis, abscess, gangrene or involvement of tendon, muscle, joint or bone requires urgent multidisciplinary assessment.

Severe systemic disease

Temperature disturbance, tachycardia, tachypnoea, hypotension, confusion or metabolic deterioration makes infection severe and usually requires admission.

Ischaemic phenotype

Cool pale or cyanosed skin, absent pulses, dependent rubor, rest pain, tissue loss or gangrene suggests inadequate perfusion and poor healing capacity.

Neuropathic masking

Loss of protective sensation can make deep infection painless; callus, deformity and an unexpectedly deep ulcer are important danger clues.

Investigation priorities

01
Cleaned and debrided wound examinationFirst step

Define ulcer size, depth, undermining, exposed structures, drainage and viable versus necrotic tissue.

Management branches

ASSESSRemove dressings and grade threat

A person with diabetes has a new ulcer, drainage, redness, swelling or unexplained metabolic deterioration.

  1. Use ABCDE when systemically unwell, remove all dressings and inspect both feet, interdigital spaces, footwear and the entire affected limb.
  2. Clean and debride enough to assess ulcer depth, purulence, necrosis, fluctuance, exposed tendon or bone, sensation and deformity.
  3. Assess pulses, temperature, capillary return and Doppler signals and classify both infection severity and ischaemic urgency.
  4. Refer immediately through the diabetic-foot multidisciplinary pathway when moderate, severe, deep, ischaemic or rapidly progressive disease is present.

Key medicines

Flucloxacillin for mild infectionGive 500 mg to 1 g orally four times daily for seven days for mild diabetic foot infection, with further duration only after clinical review.Clarify immediate penicillin allergy, review liver and renal function and culture history, and escalate anatomy rather than merely prolonging treatment when deep disease is suspected.
Clarithromycin allergy alternativeGive 500 mg orally twice daily for seven days when penicillin allergy makes flucloxacillin unsuitable and local guidance supports macrolide activity.Review QT prolongation, hepatic dysfunction and interactions including statins, warfarin and colchicine; local resistance or previous cultures may require another agent.
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Sources and review status3 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.

  • NICE NG19 Diabetic foot problems prevention and management
  • NICE NG253 Suspected sepsis in people aged 16 or over
  • NICE BNF Diabetic foot infections treatment summary

Editorial contact: Doctor’s Passport editorial team. Source-check date is separate from clinical approval. Report a content problem · Content changes

Authoring stateRapid draftClinical stateAwaiting reviewJurisdictionUnited Kingdom