Synopsis
Recognise Takayasu arteritis in young people with inflammatory and pulse-deficit phenotypes, confirm arterial-wall disease with whole-aorta imaging, separate active inflammation from fixed stenosis, and coordinate immunosuppression, revascularisation and pregnancy care.
- Suspect Takayasu arteritis in a person usually younger than fifty with unexplained inflammation, limb claudication, bruits, absent pulses, inter-arm pressure difference, renovascular hypertension or cerebral symptoms.
- Measure blood pressure in both arms and, when upper-limb disease makes values unreliable, use an unaffected limb or validated lower-limb strategy with vascular advice.
- Examine carotid, subclavian, aortic, renal and limb territories, heart murmurs and end-organ perfusion; normal peripheral oxygen saturation does not assess arterial supply.
- Use MRA or CTA of the entire aorta and major branches for diagnosis and anatomical mapping; ultrasound helps accessible arteries and FDG-PET can support activity assessment.
- Inflammatory markers support but neither prove nor exclude active disease, particularly during glucocorticoid or IL-6 blockade.
- Obtain tissue only when surgery or another diagnosis provides a safe opportunity; large-artery biopsy is not a routine confirmatory route.
- Start high-dose glucocorticoid for active disease and add a conventional steroid-sparing agent early because relapse during steroid monotherapy is common.
- Use biologic therapy, commonly TNF inhibition or tocilizumab, for refractory or relapsing disease under specialist off-label and commissioning pathways.
- Perform elective angioplasty or bypass when inflammation is controlled where possible because active wall disease increases restenosis and procedural complications.
- Treat critical cerebral, coronary, mesenteric, renal or limb ischaemia immediately; threatened tissue overrides the preference to wait for inflammatory remission.
Key red flags
Focal neurological deficit, transient retinal loss or cerebral hypoperfusion symptoms require emergency stroke and vascular imaging.
Chest pain, troponin rise, new heart failure or aortic regurgitant murmur suggests coronary ostial or aortic-root disease.
Severe abdominal pain or lactate rise may reflect mesenteric ischaemia and needs urgent surgical review.
Marked inter-arm pressure difference, absent pulses or limb rest pain indicates critical stenosis rather than constitutional inflammation alone.
Pregnancy with uncontrolled renovascular hypertension, aortic disease or active inflammation requires high-risk maternal cardiovascular care.
Dizziness, syncope, retinal symptoms, TIA or stroke with carotid or vertebral bruits indicates threatened cerebral flow.
Chest pain, heart failure, aortic regurgitation or unequal pulses may indicate coronary ostial, root, aneurysmal or dissecting disease.
Investigation priorities
Map pulse, pressure, bruit and perfusion abnormalities and establish a clinical baseline.
Management branches
A young person has inflammatory symptoms with pulse, pressure, bruit or organ-ischaemic findings.
- Perform four-limb pressures, pulses, bruits, cardiac and neurological examination and obtain inflammation, renal and organ baseline tests.
- Request MRA or CTA from aortic root through major branches and add ultrasound, PET or coronary and pulmonary imaging for the phenotype.
- Discuss imaging in a large-vessel vasculitis service and record active wall features, fixed damage and immediately threatened territory separately.