Home > Interventional radiology >Peripheral arterial disease

Peripheral Arterial Disease Treatment in Mumbai

Peripheral arterial disease (PAD)  narrowing or blockage of the arteries supplying blood to the legs and feet from atherosclerotic plaque , is a serious, progressive vascular condition that affects an estimated 40 million Indians. Mild PAD causes leg pain on walking (intermittent claudication) that limits activity and quality of life.

Severe PAD  critical limb-threatening ischaemia (CLTI)  causes rest pain, tissue loss, non-healing wounds, and threatened limb amputation. India's rising rates of Type 2 diabetes, hypertension, dyslipidaemia, and tobacco use drive an epidemic of PAD that results in enormous preventable morbidity from amputation.

At Shree Hospitals Ghatkopar East, our Interventional Radiology team treats peripheral arterial disease with catheter-based peripheral angioplasty, drug-eluting balloons, and stenting  restoring arterial blood flow to ischaemic limbs through minimally invasive procedures that achieve limb salvage and symptom relief without major vascular surgery in the majority of patients.

(24×7 Emergency Care)

(24×7 Emergency Care)

Our approach in managing Peripheral Arterial Disease

Our PAD management programme at Shree Hospitals integrates vascular risk factor modification, accurate arterial imaging, catheter-based revascularisation for appropriate disease patterns, wound care for ischaemic tissue loss, and long-term surveillance to maintain arterial patency. Limb salvage  preventing amputation  is the primary goal in critical limb-threatening ischaemia; improving walking distance and quality of life is the primary goal in claudication.

Step 1 — Ankle-Brachial Index and Non-Invasive Assessment

The ankle-brachial index (ABI)  the ratio of systolic blood pressure measured at the ankle to that measured at the brachial artery  is the primary non-invasive screening test for PAD. An ABI below 0.9 diagnoses PAD with 95% sensitivity and specificity. An ABI of 0.7–0.9 indicates mild-to-moderate PAD. An ABI below 0.4 indicates severe PAD consistent with critical limb ischaemia. ABI above 1.4 in diabetic patients suggests arterial calcification making the vessels non-compressible  toe-brachial index (TBI, below 0.7 is abnormal) or toe pressure measurement is used in this population. Duplex ultrasound of the iliac, femoral, popliteal, and tibial arteries at Shree Hospitals characterises plaque morphology, stenosis severity, and flow velocities  providing the first-line vascular mapping that determines whether CT angiography (CTA) or magnetic resonance angiography (MRA) is required for pre-procedural planning.

Step 2 — CT Angiography and Arterial Disease Mapping

CTA of the aortoiliac, femoral, popliteal, and infrapopliteal tibial arteries provides the complete roadmap for revascularisation planning. At Shree Hospitals, CTA with 3D reconstruction maps the level, length, and morphology of each stenosis or occlusion, identifies collateral pathways, and determines the optimal catheter access site, the appropriate balloon and stent dimensions, and whether the disease pattern is best suited for angioplasty alone, drug-eluting balloon (DEB), primary stenting, or atherectomy. TASC II classification of iliac and femoral artery disease guides the choice between endovascular and surgical revascularisation , TASC A and B lesions are optimally managed endovascularly; TASC C and D complex long-segment occlusions may require surgical bypass in appropriate operative candidates. CTA simultaneously assesses coronary and carotid disease burden , PAD is a powerful predictor of concurrent atherosclerotic cardiovascular disease, and many PAD patients have unrecognised significant CAD.

Step 3 — Peripheral Angioplasty and Stenting

Peripheral angioplasty (percutaneous transluminal angioplasty, PTA) at Shree Hospitals is performed through a 4–6 French sheath inserted via the femoral, popliteal, or radial artery under local anaesthesia. Angiographic roadmap imaging identifies the target lesion; a guidewire is advanced across the stenosis or occlusion, and a balloon catheter is inflated to restore vessel lumen. Drug-eluting balloons (DEB)  coated with paclitaxel that elutes into the vessel wall during balloon inflation, inhibiting neointimal hyperplasia  are used for femoropopliteal lesions to reduce the 30–40% restenosis rate seen with conventional balloon alone. Stenting is used for flow-limiting dissection after balloon dilatation, elastic recoil, aortoiliac occlusive disease (TASC A–B iliac lesions: primary stenting is the standard), and in cases where angioplasty alone is insufficient. Self-expanding nitinol stents are preferred in the femoropopliteal segment due to their ability to conform to the repeated bending forces of the knee.

Step 4 — Below-the-Knee (BTK) Angioplasty for Critical Limb Ischaemia

Critical limb-threatening ischaemia in India most commonly involves the tibial arteries  the peroneal, anterior tibial, and posterior tibial arteries below the knee  particularly in diabetic patients with distal small-vessel disease. BTK angioplasty at Shree Hospitals restores direct arterial flow to the foot through technically demanding interventions on 2–4mm tibial arteries using dedicated coronary-technique equipment: 0.014-inch guidewires, 2–4mm diameter long balloon catheters, and drug-coated balloons for the tibial bed. The angiosome concept guides BTK revascularisation  targeting the specific tibial artery that directly perfuses the tissue area of ischaemia or wound  to maximise wound healing after revascularisation. Successful BTK angioplasty in CLTI achieves limb salvage in 70–80% of patients at 1 year.

Step 5 — Medical Optimisation and Long-Term Vascular Surveillance

Revascularisation without concurrent medical management of the atherosclerotic risk factors that caused PAD produces early restenosis and inadequate limb salvage outcomes. At Shree Hospitals, every PAD patient is discharged on a structured medical regimen: antiplatelet therapy (aspirin 75–100mg daily; clopidogrel 75mg daily after endovascular intervention, typically for 1–6 months depending on device used); high-intensity statin (atorvastatin 40–80mg) targeting LDL below 70 mg/dL — statin therapy independently reduces cardiovascular events and improves walking distance in PAD; smoking cessation support (tobacco smoking is the most powerful PAD risk factor); blood pressure control below 130/80 mmHg; and blood glucose optimisation in diabetics. Post-procedure duplex surveillance at 1, 3, 6, and 12 months identifies restenosis early  when it can be retreated with repeat angioplasty before recurrence of limb-threatening ischaemia. Supervised exercise rehabilitation  structured walking programmes with a physiotherapist  improves claudication walking distance by 100–150% in patients with stable claudication.

How to Identify Peripheral Arterial Disease?

The classic symptom of PAD is intermittent claudication  a reproducible, cramp-like pain, ache, or heaviness in the calf, thigh, or buttock muscles that comes on with walking and is promptly relieved by 2–5 minutes of standing rest. The characteristic pattern  walk, stop, rest, walk again  is so typical that a careful history establishes the diagnosis before any investigation is performed.

Claudication pain reflects demand-supply mismatch: at rest, the reduced blood flow through narrowed arteries is adequate for resting muscle oxygen demand; with walking, oxygen demand increases and the diseased arteries cannot meet it, causing ischaemic muscle pain.

The location of claudication localises the disease level: buttock and hip claudication suggests aortoiliac disease; calf claudication suggests femoral or popliteal disease; foot claudication suggests tibial disease.

Critical limb-threatening ischaemia (CLTI)  the severe end of PAD  produces rest pain: constant burning pain in the foot and toes at rest, often worst at night when the horizontal position removes the gravitational assist that helps blood reach the foot. Patients classically sleep with the foot hanging over the bed edge to reduce pain  the dependent position using gravity to maintain distal perfusion when arterial pressure is insufficient to perfuse the foot lying flat.

Tissue loss in CLTI presents as non-healing foot wounds and ulcers, ischaemic gangrene (dry gangrene of the toes in pure PAD; wet infectious gangrene in diabetic CLTI), and skin changes pallor on elevation and dependent rubor (redness on dependency) reflecting the compensatory vasodilation of maximally dilated peripheral arterioles in ischaemic tissue.

Important FAQs: Peripheral Arterial Disease

What causes PAD and can it be prevented?

 PAD is caused by atherosclerosis , progressive build-up of lipid-rich plaques within the arterial wall that narrow the vessel lumen and reduce blood flow. The risk factors for peripheral atherosclerosis are identical to those for coronary artery disease: tobacco smoking (the most powerful independent PAD risk factor ,smokers have a 2–4 times higher PAD risk than non-smokers), Type 2 diabetes (doubles PAD risk and causes the most severe distal tibial disease), hypertension, dyslipidaemia, chronic kidney disease, and advancing age. In India, the combination of high tobacco use, rising T2DM prevalence, hypertension, and low statin use creates a particularly high-risk population. Prevention requires addressing all modifiable risk factors: smoking cessation, blood glucose optimisation, statin initiation for LDL reduction, antiplatelet therapy, and blood pressure control. Once PAD is diagnosed, these risk factor interventions are disease-modifying , they slow progression and reduce major cardiovascular events (heart attack, stroke, cardiovascular death) that are the primary cause of mortality in PAD patients.

Is angioplasty permanent or will the artery block again?

 Peripheral angioplasty is not permanently guaranteed ,restenosis (re-narrowing of the treated artery) occurs in a proportion of patients at rates that depend on artery location, lesion length, calcification severity, diabetic status, and whether drug-coated technology was used. Iliac arteries have the best long-term patency after stenting (85–90% at 5 years) because of their large calibre and favourable anatomy. SFA drug-eluting balloon angioplasty achieves freedom from restenosis of 60–75% at 2 years. BTK tibial angioplasty patency is lower — 50–60% at 1 year , but in CLTI, the wound-healing benefit occurs within 3–6 months of revascularisation, so durable long-term patency is less critical than immediate adequate flow for wound healing. Restenosis when it occurs can typically be re-treated with repeat angioplasty , and many patients undergo 2–3 procedures over a 5–10 year period to maintain arterial patency, which is entirely acceptable compared with the alternative of progressive limb loss.

Is peripheral angioplasty safe for elderly and diabetic patients?

 Peripheral angioplasty has an excellent safety profile compared with surgical bypass , it avoids general anaesthesia, major incisions, graft harvest, and the prolonged hospital stay and recovery of vascular surgery. This makes it particularly well-suited for the elderly, frail, and multi-comorbid patients who constitute the majority of CLTI patients in India. The primary procedural risks are: access site haematoma (managed with pressure), contrast nephropathy in patients with impaired renal function (managed with pre-hydration, iso-osmolar contrast, and dose limitation), and rare distal embolization. Diabetic patients with calcified tibial arteries are technically challenging to treat , calcified vessels require higher balloon inflation pressures, are more prone to recoil, and have worse long-term outcomes than non-calcified vessels , but remain amenable to angioplasty in experienced hands. The limb salvage benefit of successful tibial revascularisation in a diabetic CLTI patient outweighs these procedural risks substantially.

What is the difference between PAD and DVT — both cause leg symptoms?

 PAD and DVT produce different types of leg symptoms through completely different mechanisms. PAD is an arterial disease  the arteries carrying oxygenated blood to the muscles and tissues are narrowed by atherosclerosis, causing ischaemia (inadequate oxygen delivery). PAD causes leg pain on walking (claudication) or at rest in severe cases, absent foot pulses, and pale/cold feet. DVT is a venous disease  a blood clot forms in the deep veins of the leg, impairing venous outflow. DVT causes leg swelling, warmth, redness, and a deep aching pain that is constant rather than effort-related  the affected leg is swollen and often warm, in contrast to the cold pale foot of severe PAD. ABI is normal in DVT; duplex ultrasound shows venous non-compressibility and absence of flow. The conditions require completely different treatments: angioplasty/stenting for PAD, anticoagulation for DVT.

Can I avoid amputation if I have a gangrenous toe from PAD?

Yes — in many cases. Dry gangrene of a toe from PAD does not necessarily lead to below-knee amputation if arterial blood flow can be restored to the foot. The principle of "revascularise before you amputate" is central to modern limb salvage practice. At Shree Hospitals, every patient presenting with gangrenous toes, ischaemic foot ulcers, or rest pain from PAD undergoes urgent CTA and consideration for emergency or semi-urgent peripheral angioplasty to restore arterial inflow. Successful revascularisation that restores a straight-line arterial flow to the foot allows minor amputation  removal of the gangrenous toe or toes at the digital or metatarsal level  with primary wound healing, preserving the foot structure and bipedal ambulation. The alternative  allowing gangrene to progress to wet infectious gangrene in the absence of revascularisation  leads to emergency below-knee amputation that is entirely preventable in a significant proportion of patients with timely intervention.

Treatments For Peripheral Arterial Disease at Shree Hospitals

Duplex Ultrasound Vein Mapping

Duplex ultrasound at Shree Hospitals provides complete anatomical mapping of the venous reflux pattern before any treatment is planned. GSV and SSV diameter, reflux duration (above 0.5 seconds is pathological), SFJ and SPJ competence, deep venous system patency, and perforator vein incompetence are systematically assessed with the patient standing. The duplex report is the essential planning document for every varicose vein intervention  it identifies which vein is the primary reflux source, guides the choice between EVLA and RFA, determines the length of vein requiring ablation, and identifies additional tributary patterns requiring supplementary foam sclerotherapy or micro-phlebectomy. Duplex mapping also identifies the rare cases of varicose veins secondary to deep venous thrombosis or May-Thurner syndrome  where treating the superficial varicosities without addressing the underlying deep venous obstruction would be inadequate.

Endovenous Laser Ablation (EVLA)

EVLA at Shree Hospitals uses 1470nm diode laser energy delivered through a thin optical fibre inserted via a 2mm skin puncture under duplex guidance. Tumescent local anaesthesia  250–500ml of dilute lidocaine solution injected around the vein under ultrasound guidance  provides complete anaesthesia of the treatment zone and creates a thermal safety margin protecting surrounding tissues from heat spread. The laser fibre is withdrawn at a controlled rate of 1–2mm per second, delivering uniform thermal energy that permanently obliterates the GSV or SSV lumen over its entire length in a single continuous treatment. Total procedure time is 30–45 minutes per leg. No sutures, no general anaesthesia, walking immediately after. EVLA produces 95%+ GSV occlusion rates at 1 year with significantly lower rates of post-procedure bruising, pain, and nerve injury compared with earlier-wavelength laser systems.

Radiofrequency Ablation (RFA) — ClosureFast

RFA with the ClosureFast catheter is an alternative to EVLA that achieves identical efficacy using radiofrequency rather than laser energy. The ClosureFast catheter heats 7cm venous segments sequentially to 120°C with bipolar radiofrequency delivery, causing endothelial coagulation and vein wall shrinkage in 20-second treatment cycles. Advantages of RFA over EVLA include: even lower post-procedure pain and bruising scores in head-to-head comparisons, a slightly faster return-to-work time, and a shorter treatment session. Both EVLA and RFA are available at Shree Hospitals; the choice between them is made based on vein diameter, tortuosity, and patient preference after discussion with the interventional radiologist. For very large diameter or tortuous GSVs, EVLA with the 1470nm system may achieve more consistent circumferential heating.

Foam Sclerotherapy & Micro-Phlebectomy for Tributary Varicosities

After axial vein ablation, residual varicose tributaries the visible bulging clusters of varicosities on the calf and thigh are eliminated with ultrasound-guided foam sclerotherapy or micro-phlebectomy stab avulsions. Foam sclerotherapy injects a medically prepared foam of sodium tetradecyl sulphate under ultrasound guidance directly into the tributaries, causing chemical endothelial damage and permanent vein closure over 4–6 weeks. The foam is visible on ultrasound, confirming distribution within the target tributaries. Micro-phlebectomy removes larger, more superficial varicosities through 2mm stab incisions under tumescent local anaesthesia with a small hook instrument  providing immediate visible clearance and a histological specimen. Surface sclerotherapy with fine needles treats residual spider veins (telangiectases, C1 disease) as a final cosmetic step. The complete varicose vein treatment at Shree Hospitals typically requires 1–2 sessions and is performed entirely without general anaesthesia.

Peripheral Arterial Disease Specialists in Mumbai
Now at Shree Hospitals

For Appointment/Query

1800-268-4000

Tele consultation/2nd Opinion

Schedule Consultation

News & Updates

Shree Hospitals Introduces Advanced Robotic Surgery for Better Patient Care

Shree Hospitals Expands Advanced Surgical Care With Latest Medical Technology

Health Center

Shree Hospitals Welcomes Leading Neurosurgeon to Strengthen Advanced Neuro Care

Shree Hospitals Launches Advanced Healthcare

Follow Us

Shree
Hospitals

Shree
Hospitals

@shreehospitals