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GCC Nursing Guide — Peripheral Vascular Disease & Vascular Nursing
Vascular GCC Context ABI / Fontaine / Rutherford Updated Apr 2026
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PAD — Pathophysiology

Peripheral Arterial Disease (PAD) results from systemic atherosclerosis causing progressive narrowing of peripheral arteries, most commonly in the lower limbs. Reduced blood supply leads to limb ischaemia.

Mechanism Cascade

  1. Lipid deposition & endothelial injury → atherosclerotic plaque formation
  2. Progressive plaque growth → arterial stenosis
  3. Reduced perfusion pressure distal to stenosis → claudication on exertion
  4. Critical stenosis / occlusion → rest pain, tissue loss, gangrene
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PAD is a marker of systemic atherosclerosis. Patients have high concurrent risk of MI and stroke — cardiovascular risk management is mandatory alongside limb management.

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Fontaine Classification

Stage I
Asymptomatic
Haemodynamically significant disease but no symptoms. Detected incidentally or by ABI screening.
Stage IIa
Intermittent Claudication — Mild
Pain on walking >200 metres. Relieved fully by rest within minutes.
Stage IIb
Intermittent Claudication — Severe
Pain on walking <200 metres. Functionally limiting claudication.
Stage III
Ischaemic Rest Pain
Pain at rest, worse at night, relieved by hanging foot dependent. ABI typically <0.4.
Stage IV
Tissue Loss / Gangrene
Ulceration, necrosis, or gangrene. Critical limb ischaemia — limb salvage emergency.
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Rutherford Classification

Rutherford complements Fontaine with more granular clinical grading. Used widely in vascular surgery literature and trials.

Category Clinical Description Fontaine Equivalent Notes
0AsymptomaticStage INormal treadmill test
1Mild claudicationStage IIaCompletes treadmill test; AP >50 mmHg after exercise
2Moderate claudicationStage IIa/IIbBetween categories 1 and 3
3Severe claudicationStage IIbCannot complete treadmill; AP <50 mmHg after exercise
4Ischaemic rest painStage IIIResting ankle pressure <40 mmHg
5Minor tissue lossStage IVNon-healing ulcer, focal gangrene; ankle pressure <60 mmHg
6Major tissue lossStage IVExtending beyond transmetatarsal level — limb not salvageable
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Ankle-Brachial Index (ABI) — Measurement Technique

Equipment & Patient Preparation

  • Handheld Doppler probe (8 MHz), sphygmomanometer, BP cuffs
  • Patient supine, resting ≥10 minutes before measurement
  • Warm room — cold causes peripheral vasoconstriction, falsely low readings

Step-by-Step Technique

  1. Measure brachial BP bilaterally using Doppler. Record highest brachial systolic pressure.
  2. Apply ankle cuff just above malleolus. Locate dorsalis pedis (DP) pulse with Doppler.
  3. Inflate cuff until signal disappears; slowly deflate; record systolic at signal return.
  4. Repeat for posterior tibial (PT) pulse at same ankle.
  5. Repeat steps 2–4 on opposite ankle.
  6. ABI = highest ankle pressure (DP or PT) ÷ highest brachial pressure. Calculate for each limb.

ABI Interpretation

> 1.3
Calcified / Non-Compressible Vessels
Falsely elevated. Common in diabetes, CKD, elderly. Use TBI instead.
0.91–1.30
Normal
No significant PAD. Reassess if symptoms develop.
0.70–0.90
Mild PAD
Claudication likely. Risk factor management, supervised exercise programme.
0.40–0.69
Moderate PAD
Significant claudication. Vascular surgery referral. Further imaging likely needed.
< 0.40
Severe / Critical Limb Ischaemia
Rest pain or tissue loss. Urgent vascular surgery referral. Limb-threatening.
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Compression CONTRAINDICATED if ABI <0.8. Always perform ABI before applying compression bandaging. ABI 0.5–0.8: use modified reduced compression only with vascular specialist input.

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Critical Limb Ischaemia (CLI)

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CLI = Limb Salvage Emergency. Requires urgent vascular surgery review within hours.

Diagnostic Criteria (all three):

  • Ischaemic rest pain (Fontaine III / Rutherford 4)
  • ABI <0.4 (or ankle pressure <50 mmHg)
  • Tissue loss: ulceration, necrosis, or gangrene (Fontaine IV)

Nursing Priorities in CLI

  • Do NOT elevate limb — worsens ischaemia (keep dependent or flat)
  • Protect limb from pressure/trauma — use heel protectors, bed cradle
  • Avoid heat pads / electric blankets — burn risk on insensate limb
  • Analgesia — rest pain is severe; opiates often required
  • Urgent duplex / CTA imaging and vascular surgical referral

Acute Limb Ischaemia — 6 Ps

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SURGICAL EMERGENCY. Window for limb salvage is 4–6 hours from symptom onset before irreversible muscle death.

P
Pain
Sudden, severe, unrelenting
P
Pallor
White / mottled skin
P
Paraesthesia
Tingling / numbness
P
Pulselessness
Absent peripheral pulses
P
Poikilothermia
Cold limb vs contralateral
P
Paralysis
Late sign — poor prognosis

Paralysis + paraesthesia = neuromuscular involvement = irreversible damage imminent. Escalate immediately and activate vascular surgical team.

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ABI Calculator & PAD Severity Classifier

Enter Systolic Blood Pressures (mmHg)

Highest brachial value will be used as the denominator for both ABI calculations.

Right Ankle Pressures
Left Ankle Pressures
Right ABI
Left ABI
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Vascular Imaging Modalities

Duplex Ultrasound
First-LineNo RadiationNo Contrast

Combines B-mode imaging with colour flow Doppler. Quantifies stenosis percentage and peak systolic velocity (PSV) ratio. PSV ratio >2.0 = >50% stenosis; >4.0 = >75% stenosis.

Used for: graft surveillance, access site assessment, DVT diagnosis, vein mapping before bypass surgery.

CT Angiography (CTA)
IV ContrastRadiationRapid

Excellent spatial resolution. Gold standard for pre-procedural planning and runoff assessment. Multi-planar reconstruction shows anatomy from aorta to foot.

Nursing consideration: Nephrotoxic contrast — check eGFR, hold metformin 48 h peri-procedure, ensure IV hydration. Post-scan: monitor for contrast reactions, urine output.

MR Angiography (MRA)
No RadiationRenal Safe

Uses gadolinium contrast (nephrosystem-safe alternative) or non-contrast techniques. Good for patients with contrast allergy or renal impairment. Slightly lower spatial resolution than CTA. Longer scan time; not suitable for claustrophobic patients or metallic implants.

Digital Subtraction Angiography (DSA)
InvasiveRadiationGold StandardTherapeutic

Catheter-based imaging. Gold standard for arterial imaging and the only modality enabling simultaneous intervention (angioplasty, stenting, thrombolysis).

Access: femoral (commonest), radial, or brachial. Post-procedure nursing care essential — access site monitoring, limb perfusion checks.

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Physiological Tests & Pressure Studies

Toe-Brachial Index (TBI)

Used when ABI is falsely elevated (>1.3) due to calcified, non-compressible vessels — common in diabetes and CKD. Digital arteries rarely calcify.

Normal TBI: ≥0.70. TBI <0.70 indicates PAD. TBI <0.15 = critical ischaemia.

Uses photoplethysmography (PPG) probe on toe and standard arm cuff.

Transcutaneous Oxygen Tension (TcPO2)

Measures oxygen diffusion through skin surface — surrogate for tissue perfusion. Applied over wound area and dorsum of foot.

TcPO2 >40 mmHg: wound healing expected.
TcPO2 30–40 mmHg: healing uncertain.
TcPO2 <30 mmHg: healing unlikely without revascularisation.

Segmental Pressures & Pulse Volume Recordings (PVR)

Multiple cuffs applied at thigh, above knee, below knee, ankle. Pressure gradients >20–30 mmHg between adjacent segments indicate significant stenosis at that level.

PVR: waveform analysis of volume changes — normal triphasic waveform becomes biphasic then monophasic as PAD severity increases.

Post-Procedure Vascular Monitoring

Access Site Monitoring (Post-DSA / Post-PTA)

1
Check access site every 15 min × 4, then 30 min × 2, then hourly — for haematoma, bruising, swelling, active bleeding.
2
Femoral access: apply manual pressure or compression device for 20–30 min. Patient remains supine, affected leg straight for 2–4 hours.
3
Radial access: TR Band inflated per protocol; deflate gradually over 2 hours using air-removal technique; assess for patent haemostasis.
4
Closure device used (Angioseal, Perclose): document clearly. No compression device needed but earlier mobilisation has different haematoma risk profile.

Distal Limb Perfusion Assessment

1
Doppler assessment of DP and PT pulses: compare signal quality pre- and post-procedure. Loss of signal = urgent escalation.
2
Assess: skin colour, capillary refill time (<2 sec normal), skin temperature, sensation, movement — 6 Ps screening.
3
Document baseline limb observations before procedure to enable accurate comparison post-procedure.
4
Monitor urine output and creatinine 24–48 h post-contrast for contrast-induced nephropathy (CIN).
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Retroperitoneal haematoma: Flank/back pain + hypotension after femoral access = retroperitoneal bleed. Urgent CT and surgical review.

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Endovascular Procedures

Percutaneous Transluminal Angioplasty (PTA)

Balloon catheter passed across stenosis under fluoroscopic guidance; inflated to dilate vessel. Can be performed as day case or overnight stay. Less invasive, faster recovery, suitable for high-risk surgical patients.

Post-PTA Nursing Care

  • Access site: femoral = 20–30 min manual pressure; radial = TR Band protocol
  • Limb perfusion checks every 15 min × 4 (as above)
  • Antiplatelet medications: dual antiplatelet (aspirin + clopidogrel) typically continued — confirm with prescribing team; do not omit
  • Contrast nephropathy monitoring: urine output, creatinine at 24 h
  • Discharge education: signs of re-stenosis (return of claudication), wound care, medication compliance
Stenting

Metal stent deployed after PTA to maintain vessel patency. Balloon-expandable (precise placement) or self-expanding (flexible). Drug-eluting stents reduce re-stenosis rate in femoropopliteal segment.

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Bypass Surgery

Femoral-Popliteal Bypass

Conduit (autologous vein — great saphenous preferred — or PTFE graft) tunnelled from femoral to popliteal artery. Above-knee or below-knee depending on disease distribution.

Aortobifemoral Bypass

For aorto-iliac occlusive disease. Prosthetic graft from infrarenal aorta to both femoral arteries. Major surgery — high-risk patient population (concurrent cardiac / respiratory disease).

Post-Bypass Nursing Care

  • Graft surveillance: Duplex ultrasound at 6 weeks, 3 months, 6 months, annually — detect stenosis before graft occlusion
  • Limb perfusion checks: Doppler pulses post-op, colour, warmth, sensation, movement every 1–4 h per unit protocol
  • Groin wound care: High-risk infection site — observe for haematoma, lymphocoele, infection signs; keep dry, aseptic technique
  • Antiplatelet therapy compliance — essential for graft patency
  • Fluid balance: maintain adequate hydration to support renal perfusion
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Graft thrombosis: Sudden loss of previously present Doppler signal + return of ischaemia symptoms = immediate surgical escalation. 4–6 hour window.

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Aortic Aneurysm (AAA) Nursing

Size-Based Surveillance
AAA <3.0 cmIncidental — GP follow-up
3.0–4.4 cmUltrasound surveillance yearly
4.5–5.4 cm3-monthly surveillance, refer vascular
≥ 5.5 cmRepair indicated (EVAR or open)
Symptomatic / rupturedEmergency repair

Lower threshold for women (≥5.0 cm) and rapidly expanding (>1 cm/year).

EVAR — Endovascular Aortic Repair

Stent-graft deployed via femoral access under X-ray guidance. Excludes aneurysm sac from aortic circulation. Lower perioperative mortality vs open surgery — suitable for high-risk patients.

Post-EVAR Nursing

  • Monitor for contrast-induced nephropathy (CTA used intra-procedure)
  • Bilateral groin access site checks
  • Distal limb perfusion (graft limb occlusion risk)
  • Annual CT surveillance for endoleak (blood flow outside stent into sac) — types I, II, III, IV
Open AAA Repair
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Ruptured AAA = highest-risk surgical emergency. Mortality >50% even with emergency surgery.

Post-Operative Monitoring

  • Level 2/3 care (HDU/ICU) post-op
  • Bowel ischaemia: diarrhoea, bloody stool, raised lactate — mesenteric ischaemia risk
  • Renal function: suprarenal cross-clamp → AKI risk
  • Spinal cord ischaemia: check lower limb movement/sensation post-op
  • Graft infection: delayed complication — fever, back pain, sepsis months–years later
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Arterial vs Venous vs Neuropathic Ulcer Comparison

Arterial Ulcer
LocationDistal: toes, heel, dorsum foot, pressure points (lateral malleolus)
AppearancePunched-out, well-defined edges, pale / necrotic base, minimal granulation
ExudateMinimal / dry
PainSevere, constant, worse on elevation — relief hanging foot dependent
Surrounding skinPale, cold, hairless, shiny atrophic skin; delayed cap refill
PulsesAbsent or markedly diminished
ABITypically <0.6
ManagementRevascularisation priority. NO compression. Keep flat / dependent.
Venous Ulcer
LocationMedial gaiter area (above medial malleolus)
AppearanceShallow, irregular edges, red / granulating base
ExudateHigh exudate — copious, serous
PainAching, relieved by elevation (reduces venous hypertension)
Surrounding skinHaemosiderin staining (brown discolouration), lipodermatosclerosis, varicosities, oedema
PulsesUsually present
ABIUsually normal (≥0.8)
ManagementCompression therapy (4-layer or equivalent) if ABI ≥0.8. Leg elevation. Treat underlying venous insufficiency.
Neuropathic Ulcer
LocationPlantar aspect: metatarsal heads, heel (pressure points)
AppearanceDeep, callous surrounding, punched-out, may track to tendon / bone
ExudateVariable
PainOften painless — loss of protective sensation (LOPS)
Surrounding skinWarm foot (intact circulation), callous, dry skin, hammer toes, Charcot changes
PulsesPresent (unless combined neuro-ischaemic)
ABIMay be falsely elevated (calcified vessels)
ManagementOffloading (total contact cast gold standard), glycaemic control, debridement, infection management.
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Compression Therapy in Venous Leg Ulcers

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CONTRAINDICATED in arterial disease. ALWAYS measure ABI before applying any compression. ABI <0.8 = do NOT compress.

Four-Layer Bandage System (Charing Cross / Smith & Nephew)

1
Layer 1 — Wool: orthopaedic wool (e.g. Softban). Applied from toes to below knee. Padding, moisture absorption, ankle bony prominence protection.
2
Layer 2 — Crepe: light conforming crepe bandage. Smooth wool layer, provide initial compression, retain layer 1.
3
Layer 3 — Light compression: elastic bandage (e.g. Litepress / Elset). Graduated compression building from ankle upward.
4
Layer 4 — Cohesive compression: elastic cohesive bandage (e.g. Coban). Provides sustained 40 mmHg compression at ankle. Reduces venous hypertension.

Target: 40 mmHg at ankle, reducing to 17 mmHg at knee (graduated compression). Change weekly or as clinically indicated. Use reduced compression systems (e.g. 2-layer) if ABI 0.5–0.8 with vascular input.

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Debridement in Vascular Disease

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Ischaemic tissue debridement: Conservative approach — avoid aggressive debridement in non-infected dry gangrene where blood supply is insufficient for healing.

Debridement Principles by Tissue Type

Dry eschar / dry gangreneConservative — keep dry; protect; await revascularisation
Wet / infected gangreneUrgent surgical debridement — spreading infection / sepsis risk
Sloughy venous ulcerAutolytic (hydrogel) or sharp debridement; adequate blood supply present
Neuropathic ulcer with callousSharp debridement of callous — improves pressure distribution and healing

Referral Pathways

  • Critical limb ischaemia / CLI: Same-day vascular surgery referral
  • PAD with non-healing arterial ulcer: Urgent vascular outpatient referral
  • Chronic venous leg ulcer: Community wound clinic / leg ulcer service
  • Diabetic foot ulcer: Multidisciplinary diabetic foot team (vascular, podiatry, orthopaedics, endocrinology)
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Cardiovascular Risk Factor Modification

Smoking Cessation
Most Impactful Intervention

Smoking is the single greatest modifiable risk factor for PAD. Cessation reduces progression of disease, improves claudication distance, and reduces cardiovascular mortality. Patients who continue smoking after bypass have significantly reduced graft patency.

GCC context: Shisha (water pipe) smoking is highly prevalent. Shisha significantly increases PAD risk — equivalent or greater vascular toxicity than cigarettes due to session duration and toxic gas volume. Patients often do not consider shisha as "smoking." Always ask specifically about shisha use.

Diabetes Management

Diabetes is the strongest risk factor for PAD in the GCC region. HbA1c target: <53 mmol/mol (7%) for most patients with PAD. Poorly controlled diabetes combined with PAD carries the highest amputation risk.

GCC context: Type 2 diabetes prevalence among the highest globally (UAE, Saudi Arabia, Kuwait). High sedentary lifestyle, high-calorie traditional diets, genetic predisposition contribute.

Metformin: hold 48 h before and after iodinated contrast procedures due to CIN + lactic acidosis risk.

Hypertension & Dyslipidaemia

BP target in PAD: <130/80 mmHg. ACE inhibitors / ARBs preferred (cardiovascular protective, reduce amputation risk). Avoid beta-blockers in severe claudication (may worsen symptoms) unless strong cardiac indication.

Statins: Mandatory for ALL PAD patients regardless of cholesterol level. Statins improve claudication, slow progression, and reduce cardiovascular events. High-intensity statin (atorvastatin 40–80 mg) recommended.

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Supervised Exercise Therapy

First-line therapy for intermittent claudication (Fontaine IIa/IIb). Improves claudication distance, quality of life, and cardiovascular fitness.

Frequency3 times per week minimum
Duration30–45 minutes per session
ModeTreadmill walking until near-maximal claudication pain, then rest, repeat
Duration of programmeMinimum 12 weeks (optimal benefit)
OutcomeDoubles claudication distance on average
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Mechanism: Promotes collateral vessel formation, improves endothelial function, skeletal muscle metabolism adaptation, and reduces inflammatory markers.

Antiplatelet Therapy in PAD

  • Symptomatic PAD: antiplatelet therapy reduces MACE (MI, stroke, vascular death)
  • Single antiplatelet: aspirin 75–100 mg daily OR clopidogrel 75 mg daily (clopidogrel preferred per CAPRIE trial)
  • Post-endovascular intervention: dual antiplatelet (aspirin + clopidogrel) typically for 1–3 months
  • Vorapaxar or rivaroxaban + aspirin for high-risk symptomatic PAD (specialist decision)
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Foot Care Education in PAD

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In PAD + diabetes: minor foot injuries can rapidly progress to limb-threatening ulceration. Prevention education is critical.

Daily Foot Care Instructions (Patient Education)

  1. Daily inspection: examine entire foot including between toes and sole — use mirror or ask carer. Look for blisters, cuts, redness, swelling.
  2. Washing: warm (not hot) water — test temperature with elbow first. Dry thoroughly, especially between toes.
  3. Footwear: properly fitted, extra-depth shoes; never walk barefoot; no tight socks with elastic tops; inspect shoes before putting on (foreign bodies).
  4. Avoid extremes: no heat pads, hot water bottles, or sitting close to fires — neuropathic + ischaemic feet cannot feel burns.
  5. Nail care: cut straight across; never cut corns or callouses yourself — attend podiatry. Do not use corn-removal plasters (caustic in ischaemic tissue).
  6. Moisturise: apply emollient to dry skin but NOT between toes (maceration risk).
  7. Report immediately: any new wound, redness, swelling, discolouration, or pain — do not wait for routine appointment.
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GCC Context — Rising PAD Epidemic

Epidemiology in the Gulf

PAD prevalence is rising rapidly in GCC countries, driven by the high burden of type 2 diabetes, hypertension, dyslipidaemia, and tobacco use (cigarettes and shisha). UAE, Saudi Arabia, and Kuwait have some of the highest diabetes-related amputation rates in the world.

Diabetic Foot + PAD — Highest Risk

The combination of peripheral neuropathy and PAD creates the highest amputation risk. Sensory loss (no warning pain) + ischaemia (poor healing) = rapid progression from minor trauma to amputation. Multidisciplinary diabetic foot team is essential — vascular surgery, podiatry, endocrinology, orthopaedics, wound care nursing.

Cultural & Behavioural Factors

Sedentary lifestyle: traditional sitting posture, limited physical activity, air-conditioned environments. Dietary patterns: high refined carbohydrate, sugary beverages.

Language barriers: ensure patient education materials available in Arabic. Family-centred decision-making: involve family in education sessions where culturally appropriate.

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ABI Interpretation — Exam Reference Table

ABI Value Interpretation Fontaine Stage Compression? Action
> 1.3Calcified vessels (non-compressible)N/AUse TBIOrder TBI; likely PAD in diabetics
0.91–1.30NormalISafeRisk factor management; reassess if symptoms
0.70–0.90Mild PADIIaSafeSupervised exercise; antiplatelet; statin
0.50–0.69Moderate PADIIbCaution / ReducedVascular referral; imaging; consider endovascular
0.40–0.49Moderate-Severe PADIIICONTRAINDICATEDUrgent vascular referral
< 0.40Critical Limb IschaemiaIII–IVCONTRAINDICATEDSame-day vascular surgery — limb salvage emergency

Exam tip: The cut-off for compression contraindication is ABI <0.8, NOT <0.4. ABI 0.8–1.0 with symptoms = mild PAD; compression with monitoring is acceptable. ABI <0.8 = do NOT compress.

Acute Limb Ischaemia — 6 Ps Quick Reference

P
Pain
Sudden severe
P
Pallor
White / mottled
P
Paraesthesia
Tingling / numb
P
Pulselessness
No Doppler signal
P
Poikilothermia
Cold limb
P
Paralysis
Late — poor prognosis
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Exam tip: Paralysis and paraesthesia are the most clinically significant Ps — indicate neurological involvement. Irreversible muscle damage begins at 4–6 hours.

Fontaine Classification Quick Reference

Stage IAsymptomatic — detectable by ABI only
Stage IIaClaudication >200 m
Stage IIbClaudication <200 m
Stage IIIRest pain (dependent positioning relieves)
Stage IVTissue loss / ulceration / gangrene
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DHA / DOH / SCFHS / QCHP High-Yield PAD Questions

Most Frequently Tested Concepts

Q: What is the ABI cut-off below which compression is contraindicated?

A: ABI <0.8 — do NOT apply compression bandaging without vascular specialist input.

Q: How is ABI calculated?

A: Highest ankle pressure (DP or PT) divided by highest brachial pressure. One ABI per limb.

Q: ABI is 1.4 in a diabetic patient. What do you do?

A: ABI >1.3 = calcified vessels (non-compressible). Order Toe-Brachial Index (TBI) instead.

Q: What is the most impactful intervention in PAD management?

A: Smoking cessation — slows disease progression, improves symptoms, reduces cardiovascular mortality.

Q: Patient presents with sudden cold, pale, pulseless leg. What condition is this?

A: Acute limb ischaemia. Surgical emergency. Activate vascular surgery immediately — 4–6 hour window.

Q: What position should you place the leg in critical limb ischaemia?

A: Flat or dependent (hanging down) — do NOT elevate. Elevation reduces perfusion pressure, worsening ischaemia.

Q: Which ulcer type is painful with minimal exudate at the toes?

A: Arterial ulcer. Venous ulcers are high exudate, medial gaiter area. Neuropathic ulcers are painless plantar.

Q: Are statins indicated in PAD if cholesterol is normal?

A: YES — statins are mandatory for ALL PAD patients regardless of cholesterol level (pleiotropic vascular protective effects).

Q: What surveillance is required after EVAR?

A: Annual CT imaging for endoleak detection (types I–IV). Endoleak = blood flow outside stent-graft but within the aneurysm sac.

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Key Drug Summary — PAD Pharmacology

Drug Class Example Indication in PAD Key Nursing Point
AntiplateletClopidogrel 75 mg od / Aspirin 75 mg odAll symptomatic PAD, post-interventionDo NOT omit peri-procedurally without vascular team instruction; monitor for bleeding
Statin (high-intensity)Atorvastatin 40–80 mg nocteALL PAD patients — mandatoryMyopathy monitoring; liver function baseline; check for drug interactions
ACE Inhibitor / ARBRamipril, PerindoprilHypertension in PAD; cardiovascular protectionMonitor renal function and potassium; hold before contrast procedures in AKI risk
AnticoagulantHeparin IV / LMWHAcute limb ischaemia; post-bypass; DVTMonitor activated clotting time (intra-procedure); APTT for heparin infusion; bleeding precautions
ThrombolyticAlteplase (rt-PA), UrokinaseCatheter-directed thrombolysis in acute ischaemiaStrict monitoring for bleeding — neurological, GI, access site; contraindications: recent surgery/stroke
CilostazolCilostazol 100 mg bdIntermittent claudication (second-line)Contraindicated in heart failure; improves walking distance; headache common side effect
ProstanoidIloprost IV infusionCritical limb ischaemia not amenable to revascularisationSpecialist use; hypotension, flushing — careful rate titration; inpatient administration