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Coronary Revascularization

🎧 Coronary Revascularization — deep-dive podcast

📋 Key Information Summary

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  • Coronary revascularisation encompasses percutaneous coronary intervention (PCI) and coronary artery bypass grafting (CABG), guided by clinical presentation, anatomical complexity (SYNTAX score), left ventricular function, comorbidities, and patient preference via a Heart Team approach.
  • Drug-eluting stents (DES) are preferred over bare-metal stents (BMS) in nearly all PCI scenarios due to significantly lower rates of in-stent restenosis and target-lesion revascularisation.
  • Dual antiplatelet therapy (DAPT) duration post-PCI: ≥12 months after ACS, ≥6 months for stable CAD with DES (shortened to 1–3 months with newer-generation DES in selected cases), and 1 month only for BMS.
  • CABG remains superior to PCI for left main coronary artery (LMCA) disease with intermediate-to-high SYNTAX score (≥23), triple-vessel disease (especially SYNTAX ≥23), and patients with diabetes mellitus and multivessel disease.
  • The SYNTAX score II 2020 integrates anatomical complexity with clinical variables (age, creatinine clearance, LVEF, COPD, PVD) to generate individualised PCI vs CABG mortality predictions.
  • Chronic total occlusion (CTO) PCI has improved with antegrade dissection re-entry and retrograde techniques; procedural success rates at experienced Australian centres exceed 85%.
  • Rotational atherectomy (Rotablator®) is indicated for severely calcified lesions that prevent stent delivery or adequate expansion; available at major Australian PCI centres.
  • Stent thrombosis is a rare but life-threatening complication (<1% with newer-generation DES); emergency PCI with aspiration thrombectomy and escalation of antiplatelet therapy is the standard management.
  • In-stent restenosis is managed with drug-coated balloons (DCB) or repeat DES implantation; intravascular imaging (IVUS/OCT) is essential to guide treatment.
  • Transradial access is the default approach for PCI in Australia, associated with lower major bleeding and vascular complications compared with transfemoral access.
  • Periprocedural myocardial infarction (Type 4a MI) occurs in 5–30% of PCI cases depending on definition; troponin surveillance is mandatory post-procedure.
  • Aboriginal and Torres Strait Islander Australians have 1.7× higher rates of coronary revascularisation, present later with more severe disease, and face barriers to accessing specialist cardiac services in remote regions.
🎬 Coronary Revascularization — clinical explainer

Introduction & Australian Epidemiology

Coronary revascularisation — comprising percutaneous coronary intervention (PCI) and coronary artery bypass grafting (CABG) — is a cornerstone of management for obstructive coronary artery disease (CAD). In Australia, over 25,000 PCI procedures and approximately 10,000 CABG operations are performed annually, making revascularisation one of the most common therapeutic interventions in the health system.

The Australian Institute of Health and Welfare (AIHW) reports that ischaemic heart disease remains the leading cause of death in Australia, accounting for over 17,000 deaths in 2022. Coronary revascularisation is indicated across the spectrum of acute coronary syndromes (ACS) — ST-elevation myocardial infarction (STEMI), non-ST-elevation ACS (NSTEACS) — and chronic coronary syndromes (CCS) with refractory symptoms or high-risk anatomy despite optimal medical therapy (OMT).

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Australian Revascularisation Volumes (2022–23): Approximately 25,200 PCIs and 9,800 CABG operations were performed nationally. The PCI:CABG ratio is approximately 2.6:1, reflecting a global trend toward increasing PCI utilisation. Transradial access for PCI exceeds 80% at most Australian metropolitan centres.

Contemporary revascularisation practice in Australia is guided by the Cardiac Society of Australia and New Zealand (CSANZ) consensus statements, the European Society of Cardiology (ESC) / European Association for Cardio-Thoracic Surgery (EACTS) myocardial revascularisation guidelines, and National Heart Foundation of Australia (NHF) clinical recommendations. The multidisciplinary Heart Team — comprising interventional cardiologists, cardiac surgeons, imaging specialists, and allied health — is the recommended model for complex decision-making.

Trends in Australian practice include increasing use of newer-generation DES (everolimus- and zotarolimus-eluting), growing adoption of intravascular imaging-guided PCI (IVUS and OCT), expanding CTO programs, and an emerging role for transcatheter techniques in structural heart disease that complement traditional revascularisation.

Coronary Revascularization clinical infographic — pathophysiology, clinical clues, diagnosis, imaging, and management
Tap or click image to enlarge — Coronary Revascularization: pathophysiology, clinical clues, diagnosis, imaging, and management.
Coronary Revascularization infographic, full size

PCI Indications & Techniques

Indications for PCI

PCI is indicated across a broad clinical spectrum:

  • Primary PCI for STEMI: Emergent PCI of the culprit lesion within 120 minutes of first medical contact (FMC) is the gold standard reperfusion strategy. Door-to-balloon time target: ≤90 minutes at PCI-capable centres, ≤120 minutes for transfer patients.
  • Early invasive strategy for NSTEACS: Coronary angiography ± PCI within 24 hours for high-risk features (GRACE score >140, dynamic ECG changes, haemodynamic instability, recurrent angina). Very-high-risk features mandate immediate (<2 hours) angiography.
  • Stable chronic coronary syndromes: PCI for angina refractory to OMT, or in selected patients with significant stenosis (>90%) and demonstrable ischaemia on functional testing (FFR ≤0.80 or iFR ≤0.89). Routine PCI for stable CAD without ischaemia assessment is not recommended.
  • Left main stem (LMS) PCI: Increasingly performed for ostial/shaft LMS disease and selected distal bifurcation LMS disease with low-intermediate SYNTAX score, as an alternative to CABG.

Stent Selection: DES vs BMS

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DES are the default stent in contemporary PCI. BMS are reserved for rare clinical scenarios where prolonged DAPT is contraindicated (e.g., planned major surgery within 1–3 months, active non-cardiac bleeding, high bleeding risk with inability to tolerate >1 month DAPT). Even in high-bleeding-risk patients, newer-generation DES with short DAPT (1–3 months) are preferred.
Feature Drug-Eluting Stent (DES) Bare-Metal Stent (BMS)
In-stent restenosis rate 3–8% (newer-generation) 20–30%
Stent thrombosis rate 0.5–1.0% per year (early DES: higher) 1–2% per year
Minimum DAPT duration 3–6 months (6–12 months post-ACS) 1 month
Preferred platform Thin-strut cobalt-chromium or platinum-chromium Stainless steel
Australian PBS listing Commonwealth-funded under Prostheses List Commonwealth-funded under Prostheses List

Contemporary DES Platforms Available in Australia

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XIENCE (Abbott)
Everolimus-eluting · Cobalt-chromium · Thin strut (81 μm)
Drug dose Everolimus 100 μg/cm²
Polymer Fluorinated copolymer (biocompatible, durable)
Evidence EXAMINATION, COMPARE, SORT OUT trials — low stent thrombosis <0.5%/yr
Prostheses List ✔ MBS/Prostheses Listed
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Resolute Onyx (Medtronic)
Zotarolimus-eluting · Cobalt-chromium · 81 μm strut
Drug dose Zotarolimus 1.6 μg/mm
Polymer BioLinx polymer (hydrophilic outer, hydrophobic inner)
Evidence TWENTE, RESOLUTE All Comers — safe short DAPT (1–3 months) in selected patients
Prostheses List ✔ MBS/Prostheses Listed
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SYNERGY (Boston Scientific)
Everolimus-eluting · Platinum-chromium · 74 μm strut · Bioabsorbable polymer
Drug dose Everolimus abluminal coating
Polymer PLGA (bioabsorbed within 4 months — polymer-free long-term)
Evidence EVOLVE II, BIO-RESORT — excellent short DAPT data, reduced late stent thrombosis risk
Prostheses List ✔ MBS/Prostheses Listed

Bifurcation Lesion PCI

Bifurcation lesions account for approximately 15–20% of all PCI. The provisional single-stent strategy (main vessel stenting with provisional side-branch intervention) is the default approach and is supported by the DKCRUSH-V, Nordic-Baltic Bifurcation Study IV, and BBC ONE trial data.

  • Provisional stenting (preferred): Stent the main vessel first; only stent the side branch if there >70% residual stenosis, reduced TIMI flow, or dissection after main vessel stenting. Final kissing balloon inflation (FKBI) is recommended if side-branch intervention is performed.
  • Planned two-stent techniques: Reserved for true bifurcations with large side branches (≥2.5 mm) with significant disease extending >5 mm into the side branch. Culotte, T-stent, and DK-crush techniques are available. DK-crush has the best evidence for LMS bifurcation (DKCRUSH-V: lower 3-year target-lesion failure vs provisional).
  • Intravascular imaging: IVUS or OCT is strongly recommended for bifurcation PCI to optimise stent expansion, detect geographic miss, and confirm side-branch ostial coverage.

Chronic Total Occlusion (CTO) Interventions

CTOs are found in 15–30% of patients undergoing coronary angiography but account for only 5–10% of PCI attempts, reflecting technical complexity. Indications for CTO PCI include refractory angina despite OMT, heart failure with viable myocardium in the CTO territory, and patient preference after informed discussion of risks and benefits.

Australian CTO programs: Major tertiary centres in Sydney, Melbourne, Brisbane, Adelaide, and Perth have established dedicated CTO programs. Procedural success rates at experienced Australian centres are 80–90%, comparable to international benchmarks. Referral to a high-volume CTO operator (>50 CTO PCIs/year) is recommended.
1
Antegrade Wire Escalation (AWE)
First-line approach: sequential use of polymer-jacketed guidewires from soft (Fielder XT) to stiff (Confianza Pro 12) through the occluded segment. Suitable for short (<20 mm), non-calcified, tapered-stump CTOs.
2
Antegrade Dissection Re-entry (ADR)
Controlled subintimal tracking with re-entry into the true lumen distally. Devices: Stingray® re-entry system, CrossBoss™ catheter. Used when AWE fails or for long occlusions (>20 mm).
3
Retrograde Approach
Access via collateral channels (septal or epicardial) to approach the occlusion from the distal cap. Wire externalisation through the antegrade guide catheter for stenting. Essential for CTO with blunt proximal cap, proximal cap ambiguity, or failed antegrade. Requires experienced operator and dual guide catheter setup.

Rotational Atherectomy

Rotational atherectomy (RA) using the Rotablator® system (Boston Scientific) is indicated for severely calcified coronary lesions that cannot be crossed by a balloon or where adequate stent expansion is unlikely without lesion preparation. The diamond-coated burr ablates calcific plaque into microparticles (<5 μm) that are cleared by the reticuloendothelial system.

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Key safety principle — "Peck and Go": RA runs should be brief (15–20 seconds), with burr speeds maintained at 135,000–180,000 rpm. Aggressive burring, slow speeds (<135,000 rpm), or prolonged runs increase the risk of no-reflow, perforation, and burr entrapment. Burr-to-artery ratio should not exceed 0.6–0.7.
Parameter Detail
Burr sizes available 1.25 mm, 1.50 mm, 1.75 mm, 2.00 mm, 2.15 mm, 2.25 mm, 2.50 mm
Starting burr 1.25 mm (burr-to-artery ratio ~0.4–0.5)
Burr speed 135,000–180,000 rpm
Rotaglide® solution Heparinised saline + nitroglycerin + verapamil + Rotaglide (reduces friction and spasm)
Contraindications Saphenous vein graft lesions, thrombus-laden lesions, severe LV dysfunction (EF <25%) — relative, dissection, severe angulation (>60°)
Complications No-reflow (2–6%), perforation (<1%), burr entrapment (rare), slow flow, spasm
Australian availability All major public and private PCI-capable centres

Intravascular Imaging-Guided PCI

The ILUMIEN IV (OCT-guided) and RENOVATE-COMPLEX-PCI (IVUS-guided) trials demonstrated that intravascular imaging-guided PCI improves clinical outcomes compared with angiography-guided PCI, particularly in complex lesions (LMCA, long lesions, bifurcations, calcified lesions). CSANZ recommends IVUS or OCT use during complex PCI where available.

  • IVUS: Provides cross-sectional vessel imaging with plaque characterisation, measurement of vessel diameter and lesion length, assessment of stent expansion and apposition. Useful for LMS assessment and calcified lesions.
  • OCT: Higher resolution (10–20 μm vs 100–200 μm for IVUS), superior for assessing stent strut coverage, dissection flaps, and thrombus. Requires contrast flush. Limited by vessel diameter >3.0 mm for adequate imaging.
  • FFR/iFR physiology: Fractional flow reserve (FFR ≤0.80) and instantaneous wave-free ratio (iFR ≤0.89) are the standard invasive physiology assessments. FAME 3 confirmed FFR-guided PCI is superior to angiography-guided PCI in multivessel disease. iFR does not require adenosine, improving patient comfort and reducing procedural time.

CABG Indications

CABG remains the revascularisation strategy of choice for several high-risk anatomical and clinical scenarios. Contemporary CABG in Australia is performed with a strong emphasis on arterial grafting — particularly left internal mammary artery (LIMA) to the left anterior descending (LAD) artery — and increasing use of bilateral internal mammary arteries (BIMA) and radial artery grafts.

Class I Indications for CABG

LIMA-to-LAD grafting is the single most impactful element of CABG, with 90–95% 10-year patency and documented survival benefit. All CABG candidates with LAD disease should receive a LIMA graft.
  • Left main coronary artery (LMCA) disease: CABG is indicated for significant LMCA stenosis (≥50%) regardless of symptoms. PCI is a reasonable alternative for LMCA disease with SYNTAX score 0–22 and for intermediate SYNTAX (23–32) in selected patients; CABG is preferred for SYNTAX ≥33.
  • Triple-vessel disease (3VD): CABG is the preferred revascularisation strategy, particularly with SYNTAX ≥23. The SYNTAX trial 10-year data demonstrated CABG superiority over PCI with first-generation DES for 3VD (mortality: CABG 22% vs PCI 29%, p=0.006 for SYNTAX ≥23).
  • Diabetes with multivessel disease: The FREEDOM trial (2012) demonstrated CABG superiority over PCI in diabetic patients with multivessel disease (composite of death, MI, stroke at 5 years: 18.7% CABG vs 26.6% PCI, p=0.005). CABG is Class I recommended for DM with 2- or 3-vessel disease.
  • Ischaemic cardiomyopathy with viable myocardium: CABG improves survival in patients with LVEF ≤35% and viable myocardium in ≥4 dysfunctional segments (STICH trial, STICHES 10-year follow-up). Requires viability assessment (PET, dobutamine echo, or cardiac MRI with late gadolinium enhancement).
  • Failed PCI or anatomy unsuitable for PCI: Diffuse disease, heavy calcification precluding stent delivery, or failed CTO PCI with ongoing ischaemia.

SYNTAX Score Application

The SYNTAX score is an angiographic grading system that quantifies coronary artery disease complexity based on the number, location, and characteristics of lesions. It is calculated from 12 coronary segments and incorporates lesion dominance, bifurcations, CTOs, calcification, thrombus, and diffuse disease.

Low
SYNTAX Score 0–22
Low anatomical complexity. PCI and CABG have equivalent outcomes for most endpoints. Patient preference and comorbidity profile guide the decision.
Setting: Heart Team discussion — either PCI or CABG acceptable
Intermediate
SYNTAX Score 23–32
Intermediate complexity. CABG generally preferred, especially for 3VD. PCI may be considered for selected patients (favourable lesion morphology, patient preference, high surgical risk). SYNTAX II 2020 should be applied.
Setting: Heart Team — CABG preferred, PCI considered case-by-case
High
SYNTAX Score ≥33
High anatomical complexity. CABG is clearly superior. PCI should generally be avoided unless the patient is inoperable or has prohibitive surgical risk. Multiple bifurcations, CTOs, and diffuse disease typical.
Setting: CABG strongly recommended; PCI only if surgically inoperable

Graft Strategy in CABG

Graft Conduit Target 10-Year Patency Comment
Left internal mammary artery (LIMA) LAD (preferred) 90–95% Gold standard; survival benefit established
Right internal mammary artery (RIMA) RCA / circumflex 85–90% BIMA recommended in selected patients <70 yr; slightly higher sternal wound infection risk (diabetes caution)
Radial artery (RA) Circumflex / diagonal 85–90% ART trial: RA graft may be superior to SVG; Allen test pre-operatively mandatory
Saphenous vein graft (SVG) Any coronary target 50–60% Most commonly used conduit for non-LAD targets; attrition from intimal hyperplasia and atherosclerosis

Off-Pump vs On-Pump CABG

On-pump CABG with cardiopulmonary bypass remains the standard technique. Off-pump CABG (OPCAB) avoids cardiopulmonary bypass and may benefit patients with heavily atheromatous aorta, severe renal impairment, or high neurological risk. However, the ROOBY and CORONARY trials showed no long-term mortality benefit for OPCAB, with a signal toward lower graft patency. Australian practice: on-pump is the default; OPCAB at surgeon discretion for selected cases.

PCI vs CABG Decision-Making

The Heart Team Approach

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Heart Team is mandatory for complex CAD decision-making. ESC/EACTS guidelines (2018, updated 2024) mandate that all patients with left main or multivessel disease be discussed by a Heart Team comprising at least one interventional cardiologist and one cardiac surgeon. The patient must be an active participant in the shared decision-making process.

The Heart Team meeting should include:

  • Interventional cardiologist — review of coronary anatomy, SYNTAX score, feasibility of complete revascularisation by PCI
  • Cardiac surgeon — operative risk assessment (EuroSCORE II, STS score), conduit availability, technical feasibility of CABG
  • Non-invasive cardiologist or imaging specialist — LV function, viability assessment, functional testing results
  • The patient — informed discussion of risks, benefits, alternatives, recovery time, and personal preferences

SYNTAX Score II 2020

The SYNTAX Score II 2020 refines the original anatomical SYNTAX score by incorporating clinical variables to generate individualised predictions of 4-year and 10-year mortality for PCI vs CABG. Variables include:

  • Anatomical SYNTAX score
  • Age
  • Creatinine clearance (Cockcroft-Gault)
  • Left ventricular ejection fraction (LVEF)
  • Chronic obstructive pulmonary disease (COPD)
  • Peripheral vascular disease (PVD)
  • Sex
  • Diabetes mellitus
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Syntaxscore.org calculator: The SYNTAX II 2020 web calculator (syntaxscore.org) is freely available and should be used at Heart Team meetings to generate individualised treatment recommendations. A predicted PCI mortality greater than predicted CABG mortality favours surgery.

Key Trial Evidence: PCI vs CABG

Trial Population Key Finding Follow-Up
SYNTAX (2009, 2019) 3VD ± LMS CABG superior to PCI (first-gen DES) for 3VD with SYNTAX ≥23; equivalent for LMS with low SYNTAX 10 years
FREEDOM (2012) DM + MVD CABG superior to PCI (5-yr composite: 18.7% vs 26.6%) 5 years (7.5 yr extended)
EXCEL (2019) LMS (SYNTAX ≤32) PCI non-inferior to CABG for primary composite at 5 years; stroke lower with PCI; revascularisation higher with PCI 5 years
NOBLE (2020) LMS PCI not non-inferior to CABG for MACCE at 5 years (29% vs 19%) 5 years
STICH / STICHES (2016) LVEF ≤35% + CAD CABG + OMT superior to OMT alone for 10-year survival (HR 0.84) 10 years
ISCHEMIA (2020) Stable CAD, moderate-severe ischaemia Initial invasive strategy did not reduce death/MI vs OMT; revascularisation improved angina-related quality of life 3.2 years median
FAME 3 (2022) 3VD (FFR-guided PCI vs CABG) FFR-guided PCI not non-inferior to CABG for 1-year MACCE (10.6% vs 6.9%) 1 year

Surgical Risk Assessment

Surgical risk stratification is essential for the Heart Team. Two validated scoring systems are used in Australian practice:

  • EuroSCORE II: Predicts in-hospital mortality for cardiac surgery. Variables include age, sex, renal function, cardiac status, recent MI, pulmonary disease, neurological disease, extracardiac arteriopathy, active endocarditis, critical preoperative state, diabetes on insulin, NYHA class, CCS class 4 angina, LV function, pulmonary hypertension, urgency, weight of intervention, and thoracic aorta surgery.
  • STS Risk Score (Society of Thoracic Surgeons): Predicts operative mortality and morbidity for isolated CABG. Widely used in Australian cardiac surgery units. An STS predicted mortality >5% identifies high-risk patients.
  • Frailty assessment: Gait speed, grip strength, cognitive function (Montreal Cognitive Assessment), and nutritional status. Frailty is an independent predictor of poor post-CABG outcomes and should be incorporated into decision-making.

Patient Preferences and Shared Decision-Making

Patient-centred care requires that revascularisation decisions incorporate individual values and preferences:

  • Recovery time: PCI typically allows return to normal activity within 1–2 weeks; CABG requires 6–12 weeks for sternal healing and full recovery.
  • Stroke risk: CABG carries a 1–2% perioperative stroke risk (higher in elderly, aortic atherosclerosis); PCI stroke risk is <0.5%.
  • Repeat revascularisation: PCI has higher rates of repeat revascularisation (5–15% at 5 years) vs CABG (2–5%).
  • DAPT commitment: PCI mandates prolonged DAPT; CABG does not require DAPT post-operatively (unless recent ACS or LIMA graft concern).
  • Angina relief: CABG provides more complete and durable angina relief, especially with multivessel disease.
🖼️ Coronary Revascularization — visual summary
Coronary Revascularization visual summary infographic

Complications & Management

Stent Thrombosis

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Stent thrombosis is a medical emergency. Presents as STEMI or cardiogenic shock with angiographic confirmation of thrombus within a previously stented segment. Mortality is 20–45% depending on timing and presentation. Emergent re-angiography with aspiration thrombectomy, intravascular imaging, and optimisation of antiplatelet therapy are essential.
Classification Timing Incidence (newer DES) Common Causes
Acute (<24 hours) 0–24 hours post-PCI 0.5–1.0% Inadequate stent expansion, dissection, no-reflow, clopidogrel non-response
Subacute (1–30 days) 1–30 days post-PCI 0.5–2.0% Premature DAPT cessation, clopidogrel resistance, malapposition
Late (1–12 months) 1–12 months post-PCI 0.2–0.5% Delayed endothelialisation, chronic malapposition, neoatherosclerosis
Very late (>12 months) >12 months post-PCI 0.2–0.4%/yr Neoatherosclerosis, stent malapposition, uncovered struts, polymer hypersensitivity

Management of stent thrombosis:

  1. Emergency coronary angiography with aspiration thrombectomy (Export® catheter)
  2. Intravascular imaging (IVUS or OCT) to identify the mechanism — underexpansion, malapposition, geographic miss, edge dissection, neoatherosclerosis
  3. Treat the underlying cause: high-pressure balloon dilatation, additional stenting for dissection or geographic miss
  4. GP IIb/IIIa inhibitor (abciximab or eptifibatide) if not already administered
  5. Confirm or escalate antiplatelet therapy: switch from clopidogrel to ticagrelor (Brilinta®) 90 mg BD or prasugrel (Effient®) 10 mg OD (if not already on these agents)
  6. Check platelet function testing (VerifyNow® P2Y12 assay) if clopidogrel resistance suspected — available at major Australian centres
  7. Extended DAPT consideration: ≥12 months (or lifelong) if stent thrombosis occurred despite DAPT

In-Stent Restenosis (ISR)

In-stent restenosis is the recurrence of significant luminal narrowing (>50%) within a stented segment. Presentation ranges from asymptomatic (detected on routine surveillance) to ACS. ISR rates with newer-generation DES are 3–8%, compared with 20–30% for BMS.

1
Intravascular Imaging Assessment
IVUS or OCT is essential to determine the ISR mechanism: neointimal hyperplasia (most common for DES-ISR), stent underexpansion, stent malapposition (late acquired), or neoatherosclerosis with rupture.
2
Drug-Coated Balloon (DCB) Angioplasty
Paclitaxel-coated balloons (SeQuent Please®, Pantera Lux®) are the first-line treatment for DES-ISR. Deliver anti-proliferative drug without adding a new stent layer. Require adequate predilatation (TIMI 3 flow, no flow-limiting dissection). RIBS V and ISAR-DESIRE 3 trials support DCB use.
3
Repeat DES Implantation
For focal ISR or DCB failure, implantation of a DES of a different drug/polymer platform (heterogeneous DES strategy) reduces recurrence. For diffuse ISR, DES implantation is preferred over DCB alone based on RIBS V data.
4
Drug-Eluting Stent (BMS-ISR Only)
For BMS-ISR, DES implantation is superior to DCB (ISAR-DESIRE 3, RIBS V). Repeat stenting with newer-generation DES is the standard approach.

Periprocedural Myocardial Infarction (Type 4a MI)

Type 4a MI is defined as an elevation of cardiac troponin (>5× 99th percentile upper reference limit [URL]) within 48 hours of PCI, with either (a) symptoms of myocardial ischaemia, (b) new ischaemic ECG changes, (c) angiographic loss of patency of a major coronary artery, or (d) imaging evidence of new loss of viable myocardium. The incidence ranges from 5–30% depending on the definition used and the complexity of the lesion.

  • Prevention: Adequate pre-treatment with DAPT, intravascular imaging to avoid geographic miss, careful side-branch protection during bifurcation PCI, distal protection devices for SVG interventions, and avoidance of slow/no-reflow with appropriate lesion preparation.
  • Post-PCI troponin surveillance: All patients should have serial high-sensitivity troponin (hs-cTn) measured at 6–12 hours post-PCI. Routine post-PCI troponin elevation (1–5× URL) is common and generally benign; elevation >5× URL with clinical correlate requires further investigation.
  • Management: Angiographic re-look if troponin rise is significant with ECG or haemodynamic changes. Treat the cause (side-branch occlusion, distal embolisation, no-reflow). GP IIb/IIIa inhibitors and intracoronary vasodilators (nitroprusside, adenosine, verapamil) for no-reflow.

Vascular Access Complications

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Transradial access (TRA) is the default approach for PCI in Australia. Meta-analyses (MATRIX, RIVAL) demonstrate TRA reduces major bleeding by 40–60% and all-cause mortality by 20–30% compared with transfemoral access (TFA) for ACS. TFA is reserved for specific scenarios (large-bore devices, chronic total occlusion requiring dual access, haemodynamic support devices).
Complication Access Site Incidence Management
Radial artery occlusion (RAO) Radial 1–10% (usually asymptomatic) Patency haemostasis (TR Band®), adequate anticoagulation (ACT >250s), ipsilateral ulnar artery compression post-procedure. Usually recanalises spontaneously.
Radial artery spasm Radial 5–15% Intra-arterial vasodilators (nitroglycerin 200 μg + verapamil 2.5 mg ± lidocaine 20 mg). Hydrophilic-coated sheaths reduce spasm.
Haematoma (large) Femoral > radial TFA: 2–6%; TRA: <1% Prolonged compression, reversal of anticoagulation, surgical evacuation if expanding or compartment syndrome suspected.
Retroperitoneal haemorrhage Femoral 0.5–1.0% CT abdomen/pelvis, fluid resuscitation, blood transfusion, reversal of anticoagulation. Embolisation or surgical repair if ongoing bleeding.
Pseudoaneurysm Femoral 0.5–2.0% Ultrasound-guided thrombin injection (first-line). Surgical repair if >3 cm, expanding, infected, or failed thrombin injection.
Arteriovenous fistula Femoral 0.1–0.5% Usually self-limiting. Ultrasound-guided compression or surgical repair if persistent (>4 weeks) or symptomatic.
Compartment syndrome Radial or femoral <0.1% Surgical emergency — fasciotomy. Continuous monitoring of limb perfusion is mandatory after large haematoma.

Periprocedural Antiplatelet and Anticoagulation Strategy

Optimal pharmacotherapy is critical to minimise both ischaemic and bleeding complications:

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Aspirin
Aspro-Protect® · Alka-Seltzer® · Antiplatelet (COX-1 inhibitor)
Loading dose 300 mg PO (pre-procedure) if not already on aspirin
Maintenance dose 100 mg PO OD — lifelong post-revascularisation
Renal adjustment None required
PBS status ✔ PBS General Benefit
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Ticagrelor
Brilinta® · AstraZeneca · P2Y12 inhibitor
Loading dose 180 mg PO (pre-PCI or at diagnosis of ACS)
Maintenance dose 90 mg PO BD for 12 months post-ACS; may de-escalate to 60 mg BD after 12 months if continued
Renal adjustment No dose adjustment
Key side effects Dyspnoea (10–15%), bleeding, ventricular pauses (first week)
PBS status ✔ PBS General Benefit (for ACS)
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Clopidogrel
Plavix® · Iscover® · Generic · P2Y12 inhibitor (thienopyridine)
Loading dose 300–600 mg PO (600 mg preferred for faster onset ~2 hours)
Maintenance dose 75 mg PO OD
Key limitation CYP2C19 poor metabolisers (2–15% of Caucasians, 15–20% of East Asians) have reduced drug activation — higher ischaemic risk
PBS status ✔ PBS General Benefit
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Prasugrel
Effient® · Eli Lilly · P2Y12 inhibitor (thienopyridine)
Loading dose 60 mg PO (for PCI in ACS)
Maintenance dose 10 mg PO OD (5 mg OD if body weight <60 kg)
Contraindications History of stroke/TIA (increased intracranial bleeding), age ≥75 years (relative), weight <60 kg (relative)
Advantage No CYP2C19 variability — more predictable platelet inhibition than clopidogrel
PBS status ⚠ PBS Authority Required (ACS with PCI)
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Unfractionated Heparin (UFH)
Heparin sodium · Anticoagulant (antithrombin III activator)
Dose during PCI 70–100 units/kg IV bolus (adjust to ACT 250–350 seconds; 200–250 with GP IIb/IIIa inhibitors)
Reversal Protamine sulfate 1 mg per 100 units heparin (max 50 mg IV)
PBS status ✔ PBS General Benefit

DAPT Duration Recommendations

Clinical Scenario Minimum DAPT Preferred P2Y12 Agent Notes
STEMI / ACS post-PCI (any stent) 12 months Ticagrelor 90 mg BD or prasugrel 10 mg OD Clopidogrel only if high bleeding risk or contraindication to ticagrelor/prasugrel
Stable CAD, DES, low bleeding risk 6 months Clopidogrel 75 mg OD or ticagrelor 60 mg BD May extend to 12 months if high ischaemic risk
Stable CAD, DES, high bleeding risk 1–3 months Clopidogrel 75 mg OD Newer-generation DES (SYNERGY, Onyx) allow short DAPT; guided by DAPT score and PRECISE-DAPT score
BMS implantation (rare) 1 month Clopidogrel 75 mg OD BMS rarely used; consider only if DAPT absolutely contraindicated >1 month
LMS / complex PCI (SYNTAX ≥23) 12 months (consider longer) Ticagrelor or prasugrel preferred Consider extended DAPT (up to 36 months) if high ischaemic / low bleeding risk

Special Populations

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Pregnancy

PCI in pregnancy: PCI can be performed during pregnancy for STEMI or high-risk ACS. Femoral access preferred (avoid foetal radiation from radial approach close to uterus, though radial is feasible with abdominal shielding). Minimise fluoroscopy time; use lead shielding on abdomen. IVUS/OCT preferred over prolonged fluoroscopy.
Stent choice: BMS historically preferred due to shorter DAPT duration; however, newer-generation DES with short DAPT (1–3 months) may be used if indicated. Aspirin 75–100 mg is considered safe in pregnancy (Category A).
Antiplatelet agents: Clopidogrel — limited human data, no evidence of teratogenicity (Category B1). Ticagrelor and prasugrel — no safety data in pregnancy (Category B3); avoid if possible. Heparin (UFH or enoxaparin) — safe; does not cross the placenta.
CABG in pregnancy: Extremely rare; associated with significant maternal and foetal morbidity. Reserved for life-threatening LMCA disease or failed PCI. Performed with cardiopulmonary bypass with normothermia and high flow rates to maintain placental perfusion. Foetal monitoring mandatory.
Multidisciplinary team (cardiologist, obstetrician, cardiac surgeon, neonatologist, anaesthetist) essential for all cases of coronary revascularisation in pregnancy.
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Paediatrics

Kawasaki disease: Coronary artery aneurysms occur in 25% of untreated children; 5% with IVIG treatment. Giant aneurysms (>8 mm) carry long-term risk of MI. PCI or CABG may be required in adolescence/young adulthood for coronary stenosis secondary to aneurysm thrombosis.
Congenital coronary anomalies: Anomalous left coronary artery from the pulmonary artery (ALCAPA) requires surgical reimplantation. Post-arterial switch operation coronary stenosis may require PCI.
Heart transplant vasculopathy: Cardiac allograft vasculopathy (CAV) is a leading cause of late graft failure. PCI for focal stenoses; CABG is rarely performed due to diffuse nature of disease. DES preferred.
Paediatric coronary intervention requires specialised paediatric cardiology and cardiac surgery expertise. Refer to tertiary paediatric cardiac centres (e.g., Royal Children's Hospital Melbourne, Children's Hospital Westmead, Queensland Children's Hospital).
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Elderly (≥75 years)

Increased procedural risk: Older patients have higher rates of calcified disease, tortuous vessels, reduced renal function, frailty, and bleeding risk. Transradial access is strongly preferred. Contrast minimisation strategies essential (pre/post-hydration, low-osmolar contrast, staged procedures for multivessel disease).
Prasugrel caution: Contraindicated or used at reduced dose (5 mg OD) in patients ≥75 years due to increased intracranial bleeding risk (TRITON-TIMI 38). Ticagrelor or clopidogrel preferred in this age group.
CABG vs PCI: CABG perioperative risk is higher in the elderly (EuroSCORE II typically elevated). However, CABG still offers superior long-term outcomes for complex multivessel disease. Patient-centred discussion regarding frailty, cognitive status, goals of care, and recovery expectations is essential.
DAPT duration: High bleeding risk is more common; consider shortened DAPT (1–3 months with newer-generation DES) guided by PRECISE-DAPT score. Proton pump inhibitor (PPI) co-prescription (pantoprazole 40 mg OD) is strongly recommended.
Assess frailty (Clinical Frailty Scale), cognitive function (MoCA), polypharmacy, and social support before revascularisation. Goals-of-care discussion is mandatory.
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Renal Impairment

Contrast-induced acute kidney injury (CI-AKI): Risk is highest with eGFR <30 mL/min/1.73 m². Pre-hydration with isotonic saline (1 mL/kg/hr for 6–12 hours pre-procedure) is standard. Use low- or iso-osmolar contrast; minimise contrast volume (<100 mL ideal, <3.7 × eGFR threshold). N-acetylcysteine has no proven benefit (ACT trial).
Stent choice: DES preferred regardless of renal function. Haemodialysis patients have higher rates of in-stent restenosis and stent thrombosis — intravascular imaging-guided PCI is recommended.
Antiplatelet dosing: Ticagrelor, clopidogrel, and aspirin — no dose adjustment. Prasugrel — no dose adjustment but caution in dialysis patients (limited data). Bivalirudin — no dose adjustment if eGFR >30; reduce infusion rate for eGFR <30 (avoid if on dialysis).
CABG considerations: Patients with CKD (especially eGFR <30 or on dialysis) have significantly higher perioperative mortality with CABG. Off-pump CABG may reduce acute kidney injury risk. Heart Team decision should weigh the benefits of more complete revascularisation against surgical risk.
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Hepatic Impairment

Bleeding risk: Chronic liver disease (Child-Pugh B/C) is associated with coagulopathy, thrombocytopenia, and portal hypertensive gastropathy — all increase bleeding risk with PCI. Transradial access mandatory. DAPT with PPI cover essential.
Antiplatelet metabolism: Clopidogrel and prasugrel are hepatically metabolised — use with caution in severe hepatic impairment (Child-Pugh C). Ticagrelor is also hepatically metabolised and is contraindicated in severe hepatic impairment.
CABG: Liver disease significantly increases perioperative CABG mortality. Child-Pugh C and MELD score >15 are associated with prohibitive surgical risk. Conservative management or PCI may be preferred.
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Immunocompromised

HIV-positive patients: Accelerated atherosclerosis is a recognised complication of chronic HIV infection and antiretroviral therapy (particularly protease inhibitors). PCI outcomes are comparable to the general population. Drug interactions: ritonavir inhibits CYP3A4 — avoid ticagrelor (contraindicated with strong CYP3A4 inhibitors); clopidogrel is safe. Check interactions with antiretroviral regimen before prescribing P2Y12 inhibitors.
Transplant recipients: Immunosuppressive agents (tacrolimus, cyclosporine) may interact with antiplatelet agents. Cardiac allograft vasculopathy in heart transplant patients is managed with PCI (DES preferred) and maximisation of immunosuppression (everolimus has anti-proliferative properties that may slow CAV progression).
Post-PCI infection risk: Standard infection prevention applies. There is no increased risk of stent infection from immunosuppression alone. Antibiotic prophylaxis is not routinely recommended for PCI.

Aboriginal and Torres Strait Islander Health Considerations

Aboriginal and Torres Strait Islander Health

Aboriginal and Torres Strait Islander Australians experience cardiovascular disease at 1.4 times the rate of non-Indigenous Australians and have significantly higher rates of coronary revascularisation, particularly at younger ages. The AIHW reports that Indigenous Australians are hospitalised for coronary revascularisation at 1.7 times the rate of non-Indigenous Australians, with the disparity greatest in remote and very remote areas.

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Later presentation and more severe disease: Aboriginal and Torres Strait Islander patients are more likely to present with STEMI and cardiogenic shock, have higher rates of multivessel disease and diabetes, and are less likely to receive timely access to primary PCI and cardiac catheterisation. Closing this gap requires targeted strategies addressing systemic, geographic, and cultural barriers.
Geographic barriers
Approximately 38% of Aboriginal and Torres Strait Islander people live in remote or very remote areas where PCI-capable centres are absent. Transfer times for primary PCI can exceed 2–6 hours by road or air. Systems for prehospital ECG transmission, telemedicine-guided thrombolysis, and rapid retrieval (Royal Flying Doctor Service, state aeromedical retrieval) are critical to reducing time to reperfusion. Statewide STEMI networks (e.g., NSW Stemi Pathway, Victorian Cardiac Networks) have improved access but further investment is needed in remote NT, WA, and QLD.
Cultural safety
Cultural safety in cardiac catheterisation and surgical settings is essential. This includes availability of Aboriginal and Torres Strait Islander health workers and liaison officers, culturally appropriate informed consent processes (in language where required), recognition of family and community decision-making models, and awareness of sorry business and cultural obligations. The National Agreement on Closing the Gap emphasises Indigenous-led, culturally responsive healthcare.
Comorbidity burden
Aboriginal and Torres Strait Islander patients undergoing revascularisation have significantly higher rates of type 2 diabetes (40–50% vs 15–20%), chronic kidney disease (eGFR <60 in 30–40%), rheumatic heart disease, and smoking (40% prevalence). These comorbidities increase procedural risk, affect stent and graft patency, and necessitate more intensive post-procedural management. Contrast-induced AKI prevention strategies are particularly important given the high CKD prevalence.
Medication adherence & access
DAPT adherence post-PCI is critical. In remote communities, pharmacy access may be limited (e.g., remote NT communities may have a visiting pharmacist or health centre dispensary). Closing the Gap PBS co-payment (CTG scripts) reduces out-of-pocket costs for PBS-listed medications, improving access to aspirin, clopidogrel, ticagrelor, and statins. Medication adherence programs through Aboriginal Community Controlled Health Organisations (ACCHOs) and Remote Area Health Corps should be leveraged. Home Medicines Review (HMR, MBS item 900) is available and should be utilised post-discharge.
Cardiac rehabilitation
Participation in cardiac rehabilitation post-revascularisation is significantly lower among Aboriginal and Torres Strait Islander patients compared with non-Indigenous Australians (20–30% vs 40–50%). Culturally adapted cardiac rehab programs (e.g., Indigenous-specific programs run through ACCHOs, Yarning Circles, community-based exercise groups) have been shown to improve attendance and outcomes. Telehealth cardiac rehab is increasingly available in remote areas and should be offered as a standard option.
Follow-up & secondary prevention
Post-revascularisation follow-up requires coordination between metropolitan specialist centres and primary healthcare services in the patient's home community. The RHDAustralia and NHF recommend structured transition-of-care pathways including: discharge medication reconciliation, GP follow-up within 2 weeks, specialist review at 4–6 weeks (telehealth or in-person), lipid profile and HbA1c monitoring, and ongoing smoking cessation support. Aboriginal health workers and chronic disease coordinators within ACCHOs play a vital role in maintaining continuity of care.
📊 Coronary Revascularization — slide deck

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📚 References

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