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Myocardial Imaging by CT & CT Myocardial Perfusion (CTP)
1. Overview: CT as a Myocardial Imaging Tool
Cardiac CT is fundamentally a 3D volume technique — any imaging plane can be reconstructed, giving it an advantage over echocardiography and nuclear medicine in anatomical flexibility. When applied to the myocardium specifically, cardiac CT can assess:
- Myocardial structure and tissue — wall thickness, masses, thrombus, aneurysm
- Ventricular function — ejection fraction, wall motion, volumes (LV + RV)
- Myocardial perfusion — stress CT myocardial perfusion (stress CTP)
- Coronary-myocardial correlation — combining CCTA anatomy with perfusion physiology
"Stress CT myocardial perfusion may be used for evaluating myocardial perfusion for the detection of functionally significant coronary artery disease." — Grainger & Allison's Diagnostic Radiology
2. CT Imaging of Myocardial Structure & Function
2.1 Myocardial Tissue Visualisation
The myocardial tissue can be visualised in any reconstructed plane. Standard views used in practice:
| View | Best For |
|---|
| Transverse (axial) images | RV evaluation, scrolling through heart |
| Two-chamber view | LV long axis, mitral valve |
| Three-chamber view | LVOT, aortic valve, LV |
| Four-chamber view | Both ventricles and atria |
| Short-axis (SA) views | LV myocardium 17-segment model — direct correlation with echo, CMR, nuclear |
The SA view is the most important for 17-segment myocardial evaluation — it enables direct comparison with SPECT, PET, and CMR findings.
2.2 Ventricular Function by CT
For LV/RV functional analysis, data acquisition must be performed throughout the entire cardiac cycle (not just at one phase):
- Retrospective ECG gating: images reconstructed at every 5–10% of the R-R interval → allows calculation of:
- End-diastolic volume (EDV)
- End-systolic volume (ESV)
- Ejection fraction (EF)
- Stroke volume
- Regional wall motion analysis
- Radiation dose is higher with retrospective gating (12–21 mSv), but can be reduced with ECG-dose modulation
- Low-dose CT data throughout the cardiac cycle can be used if only functional data are needed (not coronary anatomy)
3. CT Myocardial Perfusion Imaging (Stress CTP)
3.1 Concept and Rationale
CTP is based on the same physiological principle as SPECT/PET perfusion imaging:
Resting myocardial perfusion is normal until luminal diameter narrowing exceeds 90–95%. With maximal coronary hyperemia (pharmacological stress), a progressive decrease in hyperemic response occurs above a threshold of ~50% diameter stenosis. — Fuster & Hurst's The Heart, 15th ed.
In CTP, iodinated contrast acts as the perfusion tracer. Under pharmacological stress (vasodilator), a flow-limiting stenosis creates a relative underperfusion in the subtended myocardial territory — visible as a region of reduced CT attenuation (HU) compared to normally perfused myocardium.
CTP is particularly appealing as an add-on to CCTA because it combines:
- Anatomy (plaque severity, stenosis %) from CCTA
- Physiology (perfusion, flow reserve) from CTP
- In a single examination with iodinated contrast
"Evolving new applications for the adjudication of the hemodynamic significance of stenosis such as CT myocardial perfusion imaging and FFR-CT are now being used in clinical practice." — Fuster & Hurst's The Heart, 15th ed.
3.2 Types of CT Myocardial Perfusion
| Type | Description |
|---|
| Static (First-Pass) CTP | Single acquisition during peak myocardial contrast enhancement at stress; quick; lower radiation; qualitative/semi-quantitative |
| Dynamic (4D) CTP | Sequential/continuous acquisitions over time; generates time-attenuation curves; allows quantification of absolute myocardial blood flow (mL/min/g) and myocardial perfusion reserve (MPR) |
4. Protocol: CT Myocardial Perfusion (CTP)
4.1 Patient Preparation
| Step | Detail |
|---|
| Caffeine restriction | Avoid for 24 hours before scan — caffeine is an adenosine receptor antagonist and directly antagonises vasodilator stress agents |
| PDE5 inhibitors | Withhold sildenafil/tadalafil for 24–48 hours |
| Fasting | 4–6 hours |
| IV access | 18G or 20G antecubital (right arm preferred) |
| ECG leads | 3–4 lead for gating and monitoring |
| Baseline HR and BP | Document before proceeding |
| Renal function | eGFR must be checked — iodinated contrast required |
| Beta-blockers | NOT given for CTP stress — vasodilators work by relative flow heterogeneity and β-blockade may interfere; HR control not as critical for perfusion as for CCTA |
| Bronchospasm history | If asthma/COPD: dobutamine preferred over adenosine/regadenoson |
4.2 Stress Agents Used in CTP
The same pharmacological stressors as nuclear perfusion imaging are used:
Vasodilators (First-line)
| Agent | Mechanism | Dose | Duration of Action | Reversal |
|---|
| Regadenoson | Selective A2A adenosine receptor agonist | 0.4 mg fixed IV bolus over 10 sec | Peak ~1 min; lasts ~2 min | IV aminophylline 50–100 mg |
| Adenosine | Non-selective adenosine receptor agonist | 140 μg/kg/min infused over 4–6 min | ~13 seconds (short acting) | Rarely needed |
| Dipyridamole | Inhibits adenosine breakdown | 0.56 mg/kg over 4 min | 20–30 min | IV aminophylline |
Regadenoson is the most commonly used vasodilator in current practice (United States) — selective A2A agonism means fewer systemic side effects and less bronchoconstriction. CT scan is initiated 10–20 seconds after regadenoson injection, during the peak hyperemic window.
Dobutamine (Alternative)
- Used in asthma, COPD with bronchospasm, or recent caffeine ingestion
- Protocol: stepwise increments from 5 μg/kg/min up to 40 μg/kg/min, ± atropine if target HR not achieved
- Less ideal because it achieves lower peak coronary blood flow than vasodilators
Contraindications to Vasodilators
- Second- or third-degree AV block
- Sick sinus syndrome (without functioning pacemaker)
- Severe asthma / active bronchospasm
- Systolic BP <90 mmHg
- Caffeine within 12–24 hours
4.3 Scanner Parameters — Static (First-Pass) CTP Protocol
| Parameter | Value |
|---|
| Scanner | ≥64-slice MDCT; dual-source or wide-volume (256/320-row) preferred |
| Scan mode | Prospective ECG triggering (step-and-shoot) |
| Acquisition timing | During peak myocardial contrast enhancement at stress (bolus tracking in LV cavity — trigger at ~250–300 HU) |
| Tube voltage | 100 kVp (standard); 80 kVp in thin patients (increases iodine conspicuity) |
| Tube current | Weight-adapted; 200–400 mAs |
| Slice thickness | 0.5–0.75 mm collimation; reconstructed at 3 mm for perfusion analysis |
| Contrast volume | 60–80 mL iodinated contrast (350–400 mgI/mL) |
| Injection rate | 5–6 mL/sec followed by 30–40 mL saline chaser |
| Cardiac phase | Mid-diastole (75% R-R) — phase of least motion |
| Breath-hold | Full inspiration single breath-hold |
| Radiation dose | ~3–5 mSv for static CTP; significantly higher for dynamic CTP |
Typical complete CTP study sequence:
- Non-contrast scan → CAC scoring (Agatston score baseline)
- Stress CTP acquisition → during pharmacological hyperemia
- Rest CCTA → coronary anatomy 10–15 minutes later (after stress agent wears off and HR stabilises)
- (Optional) Rest CTP → for comparison with stress to define reversibility
4.4 Scanner Parameters — Dynamic (4D) CTP Protocol
| Parameter | Value |
|---|
| Scan mode | Shuttle mode (table oscillates) or wide-volume axial (320-row CT covers entire heart in single rotation) |
| Temporal sampling | Every 1–3 cardiac cycles over ~30–60 seconds |
| Coverage | Entire LV myocardium (z-coverage ≥12 cm needed; wide-volume CT ideal) |
| Contrast volume | 50–70 mL at 5–6 mL/sec |
| Output | Time-attenuation curves (TAC) per myocardial segment |
| Quantification | Myocardial blood flow (MBF in mL/min/g), myocardial blood volume (MBV), myocardial perfusion reserve (MPR = stress MBF / rest MBF) |
| Radiation dose | Higher — 8–15 mSv due to repeated acquisitions |
Dynamic CTP provides absolute quantification of myocardial blood flow — analogous to PET perfusion imaging. This overcomes the limitation of "balanced ischemia" seen in multivessel CAD with relative perfusion methods (where all territories appear equally underperfused and the defect is missed).
5. Image Interpretation in CTP
5.1 Normal vs. Abnormal
- Normal perfusion: uniform myocardial enhancement throughout all segments; attenuation values homogeneous
- Perfusion defect: region of reduced CT attenuation (appears darker/hypodense) compared to surrounding normally perfused myocardium
5.2 Defect Classification
| Defect Type | Stress | Rest | Interpretation |
|---|
| Reversible (ischemia) | Present (hypodense) | Absent / fills in | Flow-limiting stenosis; viable ischemic myocardium |
| Fixed (scar/infarct) | Present | Present | Prior myocardial infarction; scar tissue |
| Mixed | Present (large) | Present (smaller core) | Ischemia surrounding a scar (peri-infarct ischemia) |
5.3 Quantitative Thresholds (Dynamic CTP)
| Parameter | Normal | Abnormal (Ischemia) |
|---|
| Myocardial Blood Flow (MBF) — stress | >2.0 mL/min/g | <1.5–2.0 mL/min/g |
| Myocardial Perfusion Reserve (MPR) | ≥2.0–2.5 | <2.0 |
| Myocardial Blood Volume (MBV) | Preserved | Reduced in dense scar |
5.4 17-Segment Model
The standard AHA 17-segment model is used for localization:
| Coronary Territory | LV Segments |
|---|
| LAD | Anterior wall, anteroseptum, apex (segments 1, 2, 7, 8, 13, 14, 17) |
| RCA | Inferior wall, inferoseptum (segments 3, 4, 9, 10, 15) |
| LCx | Lateral wall, inferolateral (segments 5, 6, 11, 12, 16) |
6. Combined CCTA + CTP (One-Stop Cardiac CT)
The most powerful application is the hybrid CCTA + CTP protocol in a single session:
Step 1: Non-contrast scan → CAC Score
Step 2: Pharmacological stress → Stress CTP (functionally significant stenosis?)
Step 3: Wait 10–15 min → Rest CCTA (anatomy: which vessel, stenosis degree, plaque type?)
Clinical decision pathway:
- CCTA stenosis <50% → low likelihood of hemodynamic significance → no CTP needed
- CCTA stenosis 50–70% (intermediate) → CTP determines if functionally significant
- CTP positive + CCTA significant stenosis → refer for ICA / revascularization
- CTP negative despite stenosis on CCTA → medical management (hemodynamically insignificant)
"In analogy to CMR, CCT can also be used to study myocardial perfusion under stress conditions; in particular, the combination with morphological depiction of the plaque and plaque stenosis severity at coronary CT angiography, this is potentially a very appealing application." — Grainger & Allison's Diagnostic Radiology
7. Diagnostic Accuracy of Stress CTP
| Comparison | Sensitivity | Specificity | Notes |
|---|
| CTP alone vs. ICA | ~85–90% | ~80–85% | Single-center data |
| CTP + CCTA hybrid vs. ICA (FFR gold standard) | ~90% | ~87% | Superior to CCTA alone for functional stenosis |
| vs. SPECT | Similar or superior sensitivity; better spatial resolution | CTP detects smaller subendocardial defects | Less soft-tissue attenuation artifact |
| vs. CMR perfusion | Comparable accuracy | CMR superior in soft tissue contrast; CTP allows simultaneous coronary anatomy | |
Limitation note: CTP remains an emerging technology compared to SPECT and CMR perfusion — Harrison's Principles of Internal Medicine (22nd ed.) notes it is still evolving in widespread clinical application. The main downsides are higher radiation dose (especially dynamic protocols) and contrast requirements.
8. Imaging Markers of Myocardial Viability on CT
| Finding | Appearance | Significance |
|---|
| Myocardial wall thinning | <5.5 mm wall thickness on CT | Scar / non-viable myocardium |
| Subendocardial hypoenhancement | Dark inner rim on contrast CT | Microvascular obstruction or infarct |
| Transmural hypoenhancement | Full thickness dark zone | Transmural infarct |
| LV aneurysm | Bulging, thin, akinetic wall segment | Late complication of MI |
| LV thrombus | Low-density filling defect in cavity | Requires delayed imaging to confirm |
| Fixed perfusion defect on CTP | Hypodense at both stress and rest | Prior infarction / scar |
9. Radiation Dose Comparison
| CT Technique | Approximate Dose |
|---|
| CAC scoring | 1–3 mSv |
| CCTA (prospective) | 1–5 mSv |
| CCTA (retrospective) | 12–21 mSv |
| Static stress CTP + rest CCTA | 5–10 mSv |
| Dynamic (4D) stress CTP | 8–15 mSv |
| Full combined study (CAC + stress CTP + rest CCTA) | 8–15 mSv |
Dose reduction strategies applicable to CTP:
- Prospective ECG triggering for rest CCTA component
- 100 kVp or 80 kVp tube voltage
- Weight-based tube current modulation
- Iterative reconstruction algorithms
- Stress-only CTP protocol if rest images not needed
10. Clinical Indications Summary
| Indication | Recommended CT Technique |
|---|
| Symptomatic patient, intermediate pretest probability | CCTA ± CTP |
| CCTA shows 50–70% stenosis (intermediate) | Add stress CTP or CT-FFR |
| Post-ACS, need viability assessment | Late-phase contrast CT or CMR preferred |
| Pre-TAVI / structural intervention | Functional CT (retrospective gating for EF + anatomy) |
| Known CAD, need functional assessment | Stress CTP or SPECT/PET |
| Asymptomatic, risk stratification only | CAC scoring (no CTP needed) |
| Suspected balanced ischemia (multivessel) | Dynamic CTP (absolute MBF quantification) or PET |
11. Limitations of CT Myocardial Perfusion
| Limitation | Detail |
|---|
| Radiation dose | Higher than SPECT for dynamic protocols; limits repeated scanning |
| Contrast requirement | Not usable in CKD (eGFR <30), contrast allergy |
| Blooming artifact from calcification | High CAC scores degrade both CCTA and CTP quality |
| Beam-hardening artifacts | Can mimic or mask perfusion defects, especially inferior wall |
| No absolute quantification with static CTP | Static protocol is qualitative/semi-quantitative only |
| Emerging technology | Less validated outcomes data than SPECT/PET; not yet universally adopted |
| Temporal resolution | Lower than CMR for first-pass dynamics |
Sources:
- Fuster and Hurst's The Heart, 15th Edition
- Grainger & Allison's Diagnostic Radiology
- Goldman-Cecil Medicine, International Edition
- Harrison's Principles of Internal Medicine, 22nd Edition