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How to make a good peripheral neuropathy referral

Please see the 'How to make a good Neurology referral' page for general rules on the minimum dataset.

Neuropathies can be categorised into the mian groups below. Identifying the likely category helps ensure you include the most important details when contacting UHB.

Small fibre neuropathy

  • Purely sensory: numbness, pain and tingling
  • Slow or no progression
  • Examination and nerve conduction studies can be normal
  • Currently no evidence that any treatment can reverse or slow progression
  • Can do a skin biopsy to confirm the diagnosis but doesn't change management, so don't offer this as standard
  • Treat neuropathic pain and monitor HbA1c, B12 and immunglobulins annually
  • Neurology input or follow-up not needed

Metabolic neuropathy

  • Predominantly sensory and mostly spinothalamic (pain and temperature)
  • Slowly progressive (years) or triggered by chemotherapy. Exception is nitrous oxide induced/functional B12 deficiency
  • Nerve conduction studies show axonal sensory-motor neuropathy
  • Need to test and monitor HbA1c, B12 levels and immunoglobulin profile. Treat B vitamin deficiency (B1, B6 and B12) and diabetes if present
  • May need to see a neurologist if the problem is due to critical/functional B12 deficiency

Diabetic neuropathy

  • Patients with suspected diabetic neuropathy do not need to be referred to the Neurology clinic
  • Please ensure bloods for neuropathy screen have been done to include:
    • HbA1C
    • B12
    • Folate
    • TFTs
    • Vasculitis screen
    • Anti-neuronal antibodies
    • HIV
    • Hep B and C
    • Syphilis serology
    • FBC
    • UEs
    • LFTs
  • If results are normal/negative, the preferrence is to not suggest anything further other than symptomatic management
  • You could request nerve conduction studies directly from the Neurophysiology department via your local secondary care provider, but this would likely not change management

Inflammatory neuropathy

  • Usually motor and sensory including large fibre/posterior column involvement (joint position sense). It can be just motor (multi-focal motor neuropathy) or just sensory (neuronopathy)
  • Usually start with distal paraesthesia (tingling in hands and feet)
  • Rapidly progressive:
    • A few days (Guillain Barre syndrome, GBS)
    • Up to three months (chronic inflammatory demyelinating polyradiculoneuropathy, CIDP)
  • Need to contact the Neurology team urgently. GBS will likely need to go to ED
  • Nerve conduction studies will be abnormal. May show 'demyelinating neuropathy'

Vasculitic neuropathy

  • Usually 'patchy' and 'stepwise' onset with big nerves being picked off overnight
  • Most commonly seen in the context of established systemic vasculitis (inflammation of the blood vessels)
  • Can be a painful, rapidly progressive, 'length dependent neuropathy' (starting in the feet and working up to the knees and then affecting the hands)
  • Often needs urgent treatment - contact the patients usual team (renal/rheumatology) or the Neurology team urgently

Inherited neuropathy

  • Evident from childhood. Ask about early development:
    • Were you walking at about 12 months?
    • Were you good at sports?
  • Pes cavus: a high lateral arch of the foot and 'hammer toes'
  • May be a family history; not all inherited neuropathies are dominantly inherited
  • Nerve conductions studies will be abnormal. The commonest type, Charcot Marie Tooth disease type 1 (CMT1) is demyelinating
  • Should be referred to neurology – please include details of any relatives that are already diagnosed and any known genetic mutations

Motor neurone disease

  • Purely motor, no sensory loss (beware patients who also have a diabetic neuropathy)
  • Prominent wasting and fasciculations – look at the anatomical snuffbox and the tongue
  • Note if there is not weakness or wasting and the patient can both see and feel the fasciculations themself it could be benign fasciculation syndrome – the patient would still need nerve conductions studies but should be reassured
  • The nerve conduction studies (actually the electromyogram; EMG) should be abnormal. Rarely they need to be repeated after three to six months if the clinical suspiscion is high
  • All patients should also have an MRI scan of their neck unless contraindicated
  • Contact neurology urgently and we will fast-track the nerve conductions studies and OPD appointment if they confirm the diagnosis

Last reviewed: 26 January 2026