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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.

Neuropathic pain

Palliative and end-of-life care · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

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Neuropathic pain with neurological compromise

New burning or radicular pain with weakness, gait change, saddle sensory loss, sphincter dysfunction, cranial neuropathy or rapidly ascending deficit may indicate cord, cauda equina, plexus or brain compression.

Action: Perform urgent structured neurological examination, protect an unstable spine when relevant and activate the appropriate MRI, acute oncology, spinal or neurological pathway. Start emergency disease-specific treatment when indicated while providing analgesia; do not wait for an adjuvant trial to declare failure.

Synopsis

Diagnose pain caused by a somatosensory lesion, identify urgent compressive and treatment-related causes, combine cause-directed care with a cautious adjuvant trial, and judge success by function and tolerability rather than complete symptom abolition.

  • Diagnose neuropathic pain only when characteristic symptoms and sensory signs fit a plausible lesion or disease of the somatosensory system.
  • First-line examination maps light touch, pinprick, temperature, allodynia, reflexes, power and gait and checks urgently for cord, root or plexus compromise.
  • Treat the cause when possible: decompression, radiotherapy, diabetes control, vitamin replacement, antiviral treatment or modification of a neurotoxic medicine may preserve function.
  • NICE initial non-trigeminal options are amitriptyline, duloxetine, gabapentin or pregabalin, selected by comorbidity, interactions, renal function, misuse risk and patient preference.
  • Start one medicine low, titrate gradually, set a functional goal and allow an adequate trial at a tolerated dose before switching.
  • If the first option fails or is not tolerated, offer one of the remaining choices rather than layering multiple sedatives immediately.
  • Capsaicin cream is an option for localised neuropathic pain when oral medicines are unsuitable or not wanted; high-concentration patch use is specialist.
  • Tramadol should be considered only as short-term rescue in this pathway, not routine long-term treatment, because of dependence, seizure and serotonin risks.
  • There is no single gold-standard medicine. The benchmark is improved sleep or function with tolerable harm, reviewed alongside cause and rehabilitation.

Key red flags

Back or radicular pain with new motor, sensory, gait or bladder or bowel change requires emergency MSCC or cauda-equina assessment.

Rapidly progressive, asymmetric or proximal neuropathy may indicate plexopathy, vasculitis, infection, leptomeningeal disease or treatment toxicity needing specialist investigation.

A hot, swollen, colour-changing limb with allodynia after procedure requires evaluation for infection, thrombosis and complex regional pain syndrome.

New confusion, falls or respiratory slowing after gabapentinoid addition to an opioid is medication toxicity until reviewed.

Gabapentin and pregabalin require renal adjustment and gradual withdrawal; abrupt cessation after sustained use can cause severe symptoms or seizures.

Active suicidal thinking, marked mood change, misuse or escalating unsanctioned doses requires same-day mental-health and medicine-safety assessment.

Compressive emergency

Pain with new weakness, gait decline, saddle loss or sphincter dysfunction requires urgent structural imaging and specialist care.

Investigation priorities

01
First-line neurological pain historyFirst stepFirst line

Map distribution, positive and negative symptoms, onset, progression, triggers, functional loss and temporal relation to cancer or treatment.

Management branches

Initial treatmentChoose one adjuvant by patient risk

Non-trigeminal neuropathic pain is diagnosed and no neurological emergency requires immediate intervention.

  1. Identify and treat the cause, define a sleep or function goal and review renal, hepatic, cardiac, falls, mood, interaction and misuse risks.
  2. Choose amitriptyline, duloxetine, gabapentin or pregabalin, start at a tolerable dose and provide titration, driving and withdrawal information.
  3. Review after each increase and after an adequate trial; continue for meaningful benefit, taper and switch for failure or harm and avoid abrupt gabapentinoid cessation.

Key medicines

Amitriptyline for neuropathic painStart 10 mg orally at night, or 10 to 25 mg in a younger robust adult, and titrate slowly every one to two weeks according to response and the BNF, usually not exceeding 75 mg nightly for pain.Avoid or use specialist caution with arrhythmia, glaucoma, urinary retention, severe constipation, cognitive impairment, falls and overdose risk; sedation and postural hypotension are common.
Duloxetine for neuropathic painA common regimen is 60 mg orally once daily, with 30 mg once daily initially when tolerability is a concern before increasing under the BNF and local pathway.Review liver disease, renal impairment, blood pressure, hyponatraemia, bleeding and serotonergic interactions; nausea and withdrawal occur, so taper rather than stop abruptly.
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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.

  • NICE CG173 neuropathic pain recommendationsInitial medicine choices, switching, topical treatment, rescue tramadol and review.
  • BNF neuropathic pain summaryUK medicine selection, titration and safety information.
  • BNF pregabalin monographRenal adjustment, dosing, adverse effects, dependence and interactions.
  • NICE NG234 spinal metastases and MSCCEmergency recognition, MRI and treatment for cord or cauda-equina compression.

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