Reference calibration
Reference lumen diameters are taken at face value by default. Where the reference
cross-section itself carries calcium, blooming narrows the apparent lumen, so a small
upward correction (k, default 1.05) is applied. k is a
placeholder until you calibrate it against your own scanner, kernel and analysis
software — a systematically wrong k biases the whole CCTA arm in one direction.
Diameter
Five published strategies are selectable; pre-specify one rather than choosing per case.
The default anchors to the distal lumen reference and rounds up, which is
the EAPCI consensus approach. The vessel / EEL option transposes the
ILUMIEN III–IV protocol to CT: take the outer-wall diameter at both references, use the
smaller, and round down. Rounding direction is not cosmetic — lumen understates
the vessel so it rounds up; the outer wall overstates what the artery tolerates so it
rounds down. Vessel-based sizing selects larger devices, so the strategy choice moves mean
stent diameter systematically.
Whichever strategy runs, three bounds hold: at most 1.20× the distal reference
(perforation ceiling), at least 0.95× (malapposition floor), and at most 1.10× the
proximal reference. If nothing satisfies all three, the malapposition floor is waived
first — the perforation ceiling is never waived silently — and the case is flagged for
intraprocedural confirmation.
Length
Target coverage is the lesion plus a landing zone each side (default 2 mm, absolute
minimum 1 mm). Candidates are scored with an asymmetric cost: falling
short is penalised 1.6× harder than overshooting, because geographic miss is worse than a
few millimetres of excess metal. Where no single device reaches the minimum, overlapping
stents are planned with 3 mm of overlap, capped at three devices.
Calcium
Calcium does not change the diameter — it triggers a preparation plan, because the failure
mode with heavy calcium is under-expansion, not undersizing. A CT-adapted score weights
circumferential calcium, arc ≥180°, calcified length >5 mm and calcified nodule.
Thickness is deliberately omitted: blooming makes CT calcium thickness unreliable. The
thresholds are transposed from intravascular imaging and are not externally
validated.
Several lesions
Lesions in the same vessel interact. Two separated by 10 mm or less become
one treatment unit spanning both plus the segment between — one stent
beats two stents and a fragile bridge. The merged unit inherits the outermost references,
the worst image quality, and the union of all calcium and anatomy flags. Because the distal
reference of a proximal lesion and the proximal reference of the one below it describe the
same artery, a disagreement over 0.50 mm is flagged as a measurement problem.
Within a vessel the distal lesion goes first, so no device crosses a fresh stent. Across
vessels, ordering follows prognostic priority — a convention for discussion, not evidence,
and labelled as such. The sequence can be reordered by hand and the override is recorded.
Chronic total occlusions
Crossing comes before sizing. CT-RECTOR and the CCTA J-CTO score are implemented to their
source definitions, and the crossing strategy follows the published hybrid algorithm from
cap ambiguity, occlusion length, distal vessel quality and collaterals.
Collateral suitability is not a CT measurement — enter it from angiography
or the planner will say so.
Sizing fails in the opposite direction here. Distal to an occlusion the vessel is
negatively remodelled from chronic low flow and is systematically under-measured, and it
enlarges over the months after recanalisation. The diameter shown is therefore a
floor, with the range imaging is likely to reveal shown alongside it. The
planner never upsizes on the CT number alone, and intravascular imaging is mandatory.
A donor-vessel lesion is always sequenced ahead of any CTO attempt.
Confidence
Confidence starts high and is downgraded for moderate or poor image quality, motion,
blooming or circumferential calcium, diffuse disease without a normal reference, a distal
reference under 2.5 mm, and any multi-stent plan. A lesion can carry high confidence and
still mandate verification — the two answer different questions.
What this cannot do
- It is decision support. Device selection, crossing strategy and sequencing rest with the operator; record deviations in the CRF.
- Sizing uses lumen diameters unless outer-wall measurements are supplied.
- Centreline lengths under-represent delivered length in tortuous anatomy — flagged, not corrected.
- Bifurcations are handled as provisional main-vessel strategy only.
- In-stent restenosis, bypass grafts and CTO within a graft are out of scope.
- The passcode on the locked parameters is in this file's source. It prevents casual edits, not determined ones.