Coronary angiography
What it is
- Invasive contrast imaging of the coronary arteries, the reference standard for coronary anatomy
- Access: radial (default in Australia) > femoral
- Radial: lower bleeding, lower mortality in ACS (MATRIX/RIVAL), earlier ambulation. Femoral for large-bore devices, IABP, structural work
- Standard views: LAO/RAO with cranial/caudal angulation to open bifurcations
- "Spider" view (LAO caudal) - left main bifurcation
- Left ventriculography (RAO 30) for EF and MR if echo inadequate
What it does and does not tell you
- Gives a luminogram - the silhouette of the lumen, not the vessel wall
- Glagov positive remodelling means a plaque can be large with a preserved lumen -> angiographically "normal"
- Anatomical, not physiological - a 50-70% stenosis by eye may or may not cause ischaemia
- -> physiological assessment (FFR/iFR) or intravascular imaging closes the gap
Visual grading and INOCA
- Inter-observer variability in visual stenosis grading is substantial (~20% absolute)
- Roughly 1 in 3 intermediate lesions judged significant by eye are not significant on FFR (and vice versa)
- INOCA / ANOCA - ischaemia or angina with non-obstructive coronaries in up to 50% of women and 30% of men undergoing angiography for angina
Coronary dominance
- Right dominant ~85% (PDA from RCA), left dominant ~8%, co-dominant ~7%
- SA nodal artery: RCA 60%; AV nodal artery: RCA 90% -> inferior MI causes AV block
Lesion characteristics that matter
- Left main disease - highest risk; historically surgical
- Proximal LAD - large territory
- Bifurcation, calcification, tortuosity, chronic total occlusion (CTO) - raise procedural complexity
- Thrombus grade, plaque rupture vs erosion
- SYNTAX score - anatomical complexity; guides PCI vs CABG in multivessel and left main disease
Physiological assessment - FFR and non-hyperaemic indices
- FFR = pressure distal to the lesion / aortic pressure, at maximal hyperaemia (IV or IC adenosine)
- FFR <=0.80 = haemodynamically significant (a pressure drop of more than 20% across the lesion)
- FAME/FAME-2: FFR-guided PCI reduces stents, events and cost vs angiography alone
- Unreliable where microvascular disease blunts hyperaemia - severe LVH, recent MI, ostial lesions, severe AS
- iFR / RFR / dPR (non-hyperaemic indices) - cutoff <=0.89, no adenosine needed; non-inferior to FFR (DEFINE-FLAIR, iFR-SWEDEHEART)
- CFR (coronary flow reserve) <2.0 and IMR (index of microcirculatory resistance) >25 -> microvascular dysfunction
- Acetylcholine provocation -> epicardial spasm (vasospastic angina) vs microvascular spasm
TIMI flow grade
| Grade | Flow |
|---|---|
| 0 | No antegrade flow beyond the occlusion |
| 1 | Faint antegrade flow, incomplete distal filling |
| 2 | Complete distal filling but delayed |
| 3 | Normal flow, complete prompt distal filling |
- TIMI 3 flow post-PCI is the procedural goal and predicts outcome
- TIMI myocardial blush grade 0-3 - tissue-level (microvascular) reperfusion; TIMI 3 epicardial flow with blush 0 = no-reflow**
Intravascular imaging
| IVUS | OCT | |
|---|---|---|
| Modality | Ultrasound | Near-infrared light |
| Penetration | Deeper - good for left main, ostia, vessel wall | Shallow |
| Resolution | ~100 um | ~10 um - best for thrombus, dissection, stent apposition, plaque erosion |
| Contrast needed | No | Yes (caution in CKD) |
- Imaging-guided PCI reduces target-lesion failure and stent thrombosis vs angiography alone in complex lesions (ILUMIEN IV, OCTOBER, RENOVATE-COMPLEX-PCI) - now a guideline recommendation for complex PCI
- Essential in MINOCA work-up: identifies plaque erosion, SCAD, spontaneous thrombus
Reporting conventions
- Stenosis by diameter (%), vessel, segment; Gensini / SYNTAX scores
- Collateral flow - Rentrop grade 0-3
Indications
A. Indications
- STEMI - primary PCI (target door-to-balloon <90 min)
- NSTEACS - invasive strategy, timing by risk (<2 h if very high risk: haemodynamic instability, refractory angina, life-threatening arrhythmia, mechanical complication; <24 h if high risk: GRACE >140, dynamic ST/T changes, rise/fall in troponin)
- Stable angina - refractory to medical therapy, high-risk non-invasive test, or high-risk anatomy on CTCA
- Pre-operative assessment for valve surgery
- Unexplained ventricular arrhythmia, new cardiomyopathy of uncertain cause, out-of-hospital cardiac arrest
- MINOCA work-up
- Note: ISCHEMIA showed no mortality benefit from routine revascularisation over optimal medical therapy in stable moderate-severe ischaemia without left main disease - symptoms are the main driver in stable disease
Preparation
B. Preparation
- Consent for angiography and possible PCI; explain radiation and contrast
- Renal function, hydration in CKD (isotonic saline pre/post; minimise contrast volume)
- Metformin - withhold on the day and for 48 h after if eGFR <30 or contrast nephropathy risk
- Continue aspirin; antiplatelet loading per protocol; anticoagulant management per access and indication
- Allergy history (contrast, shellfish myth - iodine allergy is not a thing; prior contrast reaction matters)
Revascularisation decision
C. Revascularisation decision
- Heart Team for left main, multivessel, complex anatomy, diabetes
- CABG favoured: left main with high SYNTAX, three-vessel disease especially with diabetes (FREEDOM), LV dysfunction (STICH)
- PCI favoured: single/two-vessel, low SYNTAX, high surgical risk, ACS culprit
- Complete vs culprit-only revascularisation in STEMI: staged complete revascularisation is superior (COMPLETE)
Post-procedure
D. Post-procedure
- Access site observation; radial band, femoral compression
- DAPT duration per indication and bleeding risk
- Renal function at 48-72 h if at risk
- Statin, GDMT, cardiac rehabilitation
- Driving: 2 days after elective PCI (private) - Austroads; longer if ACS
Complications
| Rate | |
|---|---|
| Death (diagnostic) | ~0.1% |
| MI, stroke | ~0.1-0.2% each |
| Access site (haematoma, pseudoaneurysm, AV fistula, radial occlusion) | 1-5% (femoral > radial) |
| Contrast-associated AKI | 1-5%, higher with CKD + diabetes |
| Arrhythmia (VF on injection) | <1% |
| Coronary dissection / perforation | ~0.2% |
| Cholesterol embolisation | Rare - livedo, blue toe, eosinophilia, renal failure |
| Retroperitoneal haemorrhage (femoral) | ~0.5% - unexplained hypotension post-femoral access |
| Contrast anaphylactoid reaction | <1% |
- Radiation - operator and patient dose; skin injury in prolonged CTO cases
- No-reflow - microvascular obstruction despite a patent epicardial vessel
- Stent thrombosis (acute, subacute, late, very late) vs in-stent restenosis (neointimal hyperplasia, months-years, presents as recurrent angina not ACS)
Relationship to non-invasive testing
- CTCA - excellent negative predictive value; first-line for low-intermediate pre-test probability stable chest pain. Adds FFR-CT and plaque characterisation. Poor with heavy calcification, stents, high/irregular heart rate
- Functional imaging (stress echo, MPI, stress CMR) - detects ischaemia; better for intermediate lesions and known CAD
- Invasive angiography - reserved for high pre-test probability, ACS, or when revascularisation is intended
The conceptual sequence
1. Does this patient have coronary disease? -> CTCA
2. Is the lesion causing ischaemia? -> FFR/iFR or functional imaging
3. Will revascularising it help? -> symptoms, territory at risk, LV function, ISCHEMIA/COMPLETE data
4. PCI or CABG? -> SYNTAX, diabetes, LV function, Heart Team
- Treating an angiographic stenosis without establishing ischaemia is the classic error - the "oculostenotic reflex"
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