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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.

Axial spondyloarthritis and ankylosing spondylitis

Rheumatology · UK scope · Sources checked 27 Aug 2026 · Clinical review pending

RapidFull
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Escalate

Urgently assess new neurological deficit, sphincter disturbance or severe spinal pain after minor trauma because an ankylosed spine fractures readily and injuries may be unstable. Acute painful red eye with photophobia needs same-day ophthalmology for possible anterior uveitis.

Synopsis

Recognise axial spondyloarthritis before radiographic damage, use the recommended imaging sequence, combine exercise and anti-inflammatory treatment, and escalate persistent active disease through specialist biologic pathways.

  • Consider axial spondyloarthritis when chronic back pain begins before age forty-five, especially with night waking, buttock pain and improvement with movement rather than rest.
  • Ask about uveitis, psoriasis, inflammatory bowel disease, enthesitis, dactylitis, peripheral arthritis and first-degree family history.
  • Normal CRP, negative HLA-B27 and normal radiographs do not exclude axial spondyloarthritis.
  • Follow the NICE imaging sequence: sacroiliac radiography when appropriate, followed by a protocolled MRI if suspicion remains and radiographs are nondiagnostic.
  • Structured exercise and physiotherapy addressing spinal mobility, posture, strength, aerobic fitness and breathing are central long-term treatments.
  • An NSAID trial may improve pain and stiffness when gastrointestinal, renal and cardiovascular risk permits; review effectiveness and toxicity rather than prescribing indefinitely by default.
  • For persistently active disease after appropriate non-pharmacological and conventional care, TNF, IL-17 or JAK inhibition may be selected under the applicable NICE approval; no class is generally superior for musculoskeletal efficacy. Choose jointly for licence and eligibility, prior response, comorbidity and extra-musculoskeletal disease. Prefer a monoclonal TNF inhibitor for recurrent or moderate-to-severe uveitis; in active inflammatory bowel disease prefer monoclonal TNF or JAK inhibition and do not start an IL-17 inhibitor.
  • Protect the ankylosed spine after trauma: maintain alignment, obtain urgent CT and add MRI after CT for a neurological abnormality potentially due to cord injury; image the rest of the spine when a new fracture is identified.

Key red flags

Acute uveitis

Unilateral eye pain, photophobia, redness and blurred vision requires same-day ophthalmic assessment to prevent sight-threatening complications.

Unstable spinal injury

New severe focal pain, deformity or neurological change after minor trauma in an ankylosed spine requires emergency immobilisation, imaging and spinal review.

Investigation priorities

01
Sacroiliac-joint radiographyFirst step

Identify definite structural sacroiliitis and alternative bony pathology in the NICE diagnostic sequence.

Management branches

Suspected axial SpAUse clinical features and staged imaging

Chronic back pain begins before forty-five with inflammatory or extra-articular features.

  1. Document onset, night symptoms, movement response, buttock pain, family history and psoriasis, uveitis, bowel, entheseal and peripheral-joint features.
  2. Refer according to NICE criteria, obtain HLA-B27 and markers when useful, and follow sacroiliac radiography then protocolled MRI when needed.
  3. Retain specialist follow-up or reassessment when early imaging is negative but the phenotype remains convincing rather than converting the diagnosis to mechanical pain automatically.

Key medicines

NaproxenCommon adult anti-inflammatory dosing is 250–500 mg orally twice daily with food, using the lowest effective dose for the shortest necessary period.Assess ulcer or bleeding, renal, heart-failure, blood-pressure, cardiovascular, anticoagulant and interaction risks and add gastroprotection when indicated. Avoid systemic NSAIDs from 20 weeks of pregnancy unless essential; use the lowest dose for the shortest time and consider fetal monitoring after several days. They are contraindicated after 28 weeks.
AdalimumabThe usual adult regimen for axial spondyloarthritis is 40 mg subcutaneously every other week under specialist prescribing and product information.Do not start during active serious infection and stop for a new serious infection; screen for tuberculosis and hepatitis and update immunisation first. Avoid live vaccines during treatment, and seek an alternative in demyelinating disease. Adalimumab is contraindicated in NYHA III or IV heart failure. If continued through pregnancy, document exposure and the BSR plan to defer infant live vaccines until 6 months.
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Sources and review status9 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 NG65 spondyloarthritisRecognition, referral, imaging and management.
  • NICE TA383 TNF inhibitors for axial SpASpecialist TNF-inhibitor treatment criteria.
  • NICE NG41 spinal injuryUrgent imaging and spinal precautions after trauma.
  • BSR 2025 axial spondyloarthritis guidelineCurrent targeted-treatment sequencing and extra-musculoskeletal class selection.
  • Adalimumab UK product informationAxial-SpA dose, contraindications, infection and vaccine precautions.
  • Naproxen UK product informationAdult dosing and gastrointestinal, renal and cardiovascular safety.
  • MHRA NSAID pregnancy safetyRestrictions from 20 weeks and contraindication after 28 weeks of pregnancy.
  • BOASt spine trauma assessmentAlignment, CT, MRI and whole-spine assessment in ankylosed-spine trauma.
  • BSR pregnancy prescribing guideline
Anti-TNF use in pregnancy and exposure-specific infant vaccination.

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