Peripheral Arterial Disease
Peripheral arterial disease (PAD) is a manifestation of systemic atherosclerosis in which lower-limb arterial flow cannot meet demand, causing intermittent claudication or, when tissue perfusion is inadequate at rest, chronic limb-threatening ischaemia.
Definition
Peripheral arterial disease is atherosclerotic narrowing or occlusion of arteries supplying the limbs, most often the legs. It ranges from asymptomatic disease and intermittent claudication to chronic limb-threatening ischaemia with rest pain, ulceration or gangrene.
Epidemiology
PAD is more common with increasing age, smoking, diabetes, hypertension, dyslipidaemia, chronic kidney disease and other atherosclerotic disease. It is a marker of systemic cardiovascular risk, so myocardial infarction and stroke prevention are central to care even when leg symptoms are mild.
Pathophysiology
Atherosclerotic plaque reduces arterial lumen and flow reserve. Exercise raises muscle demand beyond the available supply, producing claudication. Further loss of perfusion causes rest pain, poor wound healing, ulceration and gangrene. Diabetes and chronic kidney disease can cause arterial calcification and make ABPI falsely high or non-diagnostic.
First principles
Claudication is a supply-demand problem
Atherosclerotic narrowing limits the maximum blood flow available to exercising muscle. Resting demand may still be met, but walking increases demand beyond supply and produces reproducible muscle pain that settles with rest. The distance is often consistent enough to be a useful clinical clue, but symptoms and walking ability vary with terrain, pace and comorbidity.1,2,3
Tissue loss means resting perfusion is failing
When perfusion becomes inadequate even at rest, the person may develop chronic limb-threatening ischaemia (CLTI), previously described in NICE guidance as critical limb ischaemia. Rest pain, non-healing ulceration or gangrene needs urgent vascular assessment because the goals shift from symptom control to pain relief, wound preservation, limb salvage and safe revascularisation.1,2
PAD is a systemic cardiovascular-risk marker
Atherosclerosis in the leg commonly coexists with coronary and cerebrovascular disease. Treating the leg symptom alone is not enough: smoking cessation, antiplatelet treatment where indicated, lipid modification, blood-pressure and diabetes management, exercise and shared risk-factor care reduce future cardiovascular harm.1,4,3
Severity and urgency are clinical, not ABPI-only decisions
History, foot examination, pulses, Doppler signals, tissue loss, pain and function determine severity. ABPI supports diagnosis, but a normal or raised ABPI does not exclude PAD in diabetes because arterial calcification can make vessels incompressible. A sudden deterioration is acute limb ischaemia, not simply progression of stable PAD, and requires the emergency vascular pathway.1,5,6
Presentation
Intermittent claudication is exertional leg-muscle pain, usually in the calf, thigh or buttock, that is reproducible and relieved by rest. Advanced disease causes forefoot rest pain, non-healing ulcers or gangrene. Sudden pain, pallor, coldness, sensory loss or weakness suggests acute limb ischaemia and needs a separate emergency pathway.1,2,6,3
Cardinal features
- Exertional calf, thigh or buttock pain relieved by rest
- Reduced or absent femoral, popliteal or foot pulses
- Cool, shiny skin with hair loss or brittle nails
- Dependent rubor or prolonged capillary refill
- Forefoot rest pain, often worse when the leg is elevated at night and eased by dependency
- Painful non-healing ulceration or gangrene at a distal pressure point
Red flags
- Rest pain, ulceration or gangrene: urgent vascular referral for possible CLTI
- Rapidly worsening pain, pallor, coldness, paraesthesia or weakness: suspect acute limb ischaemia
- Spreading infection in an ischaemic foot or systemic illness: urgent multidisciplinary assessment
- A non-healing foot wound in diabetes, even if ABPI is normal or raised
- Disabling symptoms despite risk-factor treatment and supervised exercise
- New chest pain, transient neurological symptoms or stroke symptoms indicating associated cardiovascular disease
Investigations
Clinical vascular assessment and ABPI
Take a structured history of exertional distance, rest pain, tissue loss and acute change. Examine both limbs and feet, palpate femoral, popliteal and pedal pulses, and measure ABPI at rest with a Doppler where possible. Calculate the highest ankle pressure divided by the highest arm pressure for each leg.
Expected finding: An ABPI below 0.9 supports PAD. A normal or raised result does not exclude PAD in diabetes or incompressible arteries; interpret alongside symptoms, examination and Doppler signals.
1,2,6Duplex ultrasound when revascularisation is being considered
Offer duplex ultrasound as first-line anatomical imaging when revascularisation is being considered. It localises stenosis or occlusion and assesses flow without ionising radiation.
Expected finding: Flow-limiting stenosis or occlusion with altered velocities and distal run-off that helps plan intervention.
1,2Contrast-enhanced MRA or CTA for treatment planning
If further imaging is needed after duplex, offer contrast-enhanced MRA. Offer CTA when MRA is contraindicated or not tolerated, considering renal function, contrast risk and the need for detailed arterial anatomy.
Expected finding: The level, length and distribution of disease, distal run-off and anatomy relevant to angioplasty or bypass.
1Cardiovascular and tissue-risk assessment
Assess smoking, blood pressure, diabetes, lipids, renal function, cardiovascular symptoms, mobility, nutrition, wound status and infection. In CLTI, document pain, tissue loss, infection and function so a vascular multidisciplinary team can plan limb salvage or palliation.
Expected finding: Modifiable cardiovascular risks, tissue loss or infection requiring parallel medical, wound, podiatry, diabetes, pain or vascular management.
1,4,2Management
| Step | Detail | Source |
|---|---|---|
| Start best medical therapy and secondary cardiovascular prevention | Offer smoking-cessation support and manage blood pressure, diabetes, lipids, diet, weight and exercise. Offer antiplatelet treatment and lipid modification in line with current NICE guidance and the person's indications, comorbidities and preferences; use current BNF and local formulary information for medicine selection and doses. Do not treat PAD as a local leg problem only.1,4,3 | NICE CG147, NICE NG238 and NHS PAD treatment information |
| Offer a supervised exercise programme for intermittent claudication | Offer supervised exercise to everyone with intermittent claudication. A typical NICE-supported programme involves about 2 hours of supervised exercise each week for 3 months, encouraging walking towards maximal tolerable pain with rest intervals, provided there is no contraindication. Reinforce that regular activity is needed to maintain benefit.1,7,3 | NICE CG147 recommendations 1.5.1 and 1.5.2; NHS PAD treatment information |
| Consider revascularisation for persistent lifestyle-limiting claudication | Consider angioplasty when risk-factor advice has been reinforced, supervised exercise has not produced satisfactory improvement and imaging confirms suitability. Consider bypass when symptoms remain severe and angioplasty is unsuitable or unsuccessful, after discussion of procedural risks, durability, anatomy, vein availability and patient preference. Do not offer invasive treatment solely because an arterial narrowing appears on imaging without clinically important symptoms.1,2 | NICE CG147 recommendations 1.5.3 to 1.5.8 |
| Refer chronic limb-threatening ischaemia urgently to a vascular multidisciplinary team | Rest pain, tissue loss or gangrene requires urgent vascular assessment. The vascular multidisciplinary team should consider revascularisation, wound and infection care, analgesia, off-loading, diabetes and renal issues, functional status and patient preference. Angioplasty or bypass may be appropriate; the current NICE recommendations are under update for drug-eluting stents and drug-coated balloons in femoropopliteal CLTI, so do not hard-code a device choice into general teaching.1,5,2 | NICE CG147 and April 2026 exceptional surveillance of CG147 |
| Manage ischaemic pain, wounds and infection in parallel | Offer analgesia appropriate to severity and current medicines guidance, with specialist pain input if pain remains uncontrolled, revascularisation is inappropriate or pain persists after treatment. Protect the foot, arrange wound and podiatry care, assess for infection and avoid assuming that antibiotics or debridement alone can compensate for inadequate perfusion. Do not offer major amputation until revascularisation options have been considered by the vascular multidisciplinary team.1,2 | NICE CG147 recommendations 1.6.1 to 1.6.11 |
| Safety-net acute deterioration and arrange follow-up | Give urgent return advice for sudden or rapidly worsening pain, pallor, coldness, numbness, weakness, new tissue colour change, worsening ulceration, fever or systemic illness. These features may represent acute limb ischaemia or infected CLTI and require same-day emergency vascular assessment, not routine PAD follow-up. Continue secondary prevention and review exercise, symptoms, wounds, treatment adherence and cardiovascular risk.1,2,6,3 | NICE CG147, NICE CKS PAD and NHS PAD information |
Illustrations
Differentials
Neurogenic claudication
Pain or weakness triggered by standing/walking and relieved by sitting or spinal flexion, often with neurological or back symptoms and preserved pulses.
Chronic venous disease
Oedema, venous eczema and gaiter-area ulceration rather than distal ischaemic pain and absent pulses.
Diabetic peripheral neuropathy
Burning or numb stocking-distribution symptoms that may coexist with PAD; preserved pulses do not exclude neuropathy and neuropathy does not exclude PAD.
Musculoskeletal or arthritic pain
Pain related to joints, movement or posture rather than a reproducible vascular walking distance.
Acute limb ischaemia
Sudden pain, pallor, coldness, pulse loss, paraesthesia or weakness requiring an emergency vascular pathway.
Complications
- Chronic limb-threatening ischaemia with rest pain, ulceration or gangrene
- Infection, non-healing wounds and major amputation
- Acute limb ischaemia from plaque thrombosis or embolism
- Myocardial infarction and stroke from systemic atherosclerosis
- Reduced mobility, falls, depression and loss of independence
- Restenosis or graft failure after revascularisation
Prognosis
Intermittent claudication often remains stable or improves with cardiovascular risk reduction and supervised exercise, but symptoms can remain disabling. CLTI carries a high risk of tissue loss and amputation and needs urgent vascular MDT care. Long-term prognosis is strongly influenced by systemic cardiovascular disease, smoking and diabetes.
Guidelines
- Peripheral arterial disease: diagnosis and management (CG147) (NICE, 2012)
- April 2026 exceptional surveillance of CG147 (NICE, 2026)
References
- NICE CG147: Peripheral arterial disease: diagnosis and management (CG147 recommendations; current page reviewed 27 April 2026)Published 8 Aug 2012 | Updated 11 Dec 2020
- NICE CKS: Peripheral arterial disease (Current NICE CKS topic for assessment and management)
- NHS: Peripheral arterial disease treatment (NHS exercise, smoking, medicines and revascularisation information, reviewed 10 April 2026)Updated 10 Apr 2026
- NICE NG238: Cardiovascular disease: risk assessment and reduction, including lipid modification (NG238 recommendations)Published 14 Dec 2023
- NICE CG147: April 2026 exceptional surveillance decision (Update planned for drug-eluting stents and drug-coated balloon angioplasty in femoropopliteal CLTI)Published 27 Apr 2026
- NHS: Peripheral arterial disease diagnosis (NHS diagnosis and ABPI information, reviewed 10 April 2026)Updated 10 Apr 2026
- NICE QS52: Peripheral arterial disease quality standard (Quality statement 3: supervised exercise programmes)Published 21 Jan 2014
Evidence checked: 2026-08-03
This page is exam revision material, not medical advice, and must not be used for patient care. Always check drug doses against the BNF and current guidance. Full disclaimer.

