• This involves the selective injection of contrast medium into the right and left coronary arteries and the left ventricle (while recording the resultant moving images) • A percutaneous femoral arterial catheterization is the usual approach (an alternative percutaneous route is the radial artery) at least 3 shaped catheters are required – one for each coronary artery and one for the left ventricle) low osmolality contrast media is used with rapid filming at 25+ frames/s images are acquired in multiple orientations with very short exposures (5–10 ms) to freeze cardiac motion • The severity and length of a stenosis the presence of a complete occlusion (± collateral vessels) the number of affected vessels the vessel diameter and stenosis configuration Significant (>50% diameter reduction) accessible stenoses in 1 or 2 vessels (with a diameter > 2mm) are treated by angioplasty or stenting Left main coronary artery disease or significant disease affecting all 3 coronary arteries is usually best treated with a CABG • Poor ventricular function is associated with an increased risk, but a greater potential benefit (the prognosis is related to the degree of ventricular dysfunction) • High-risk patients with unstable angina or non-ST elevation myocardial infarction may benefit from early angioplasty or stenting • Demonstration of the effects of IHD on ventricular function A large infarct will appear hypoechoic, whereas fibrotic scar tissue is stiffer than normal myocardium and appears hyperechoic • Detecting structural complications such as a VSD, papillary muscle dysfunction (causing mitral regurgitation) and ventricular thrombus • Demonstrating the origins of the main coronary arteries (especially with transoesophageal echocardiography) demonstrating any anomalous origins and coronary artery aneurysms (e.g. Kawasaki’s disease) • This detects reversible wall motion abnormalities (indicating reversible ischaemia) using the same stimulants as for CT or MR stress imaging • It enables risk stratification for patients with known or suspected IHD (a normal study indicates a very good prognosis) • It enables preoperative risk assessment (this determines myocardial viability) • It is more sensitive for detecting ischaemia than a conventional ECG-based exercise test the endpoint of the test is the appearance of new wall motion abnormalities (chronic ischaemia causes diffuse dysfunction, an acute myocardial infarction causes more localized changes) • Factors affecting the accuracy of the technique: the threshold for defining a significant stenosis whether there is single or multivessel disease whether an adequate stress is achieved (especially for exercise-based protocols) the presence of other disease processes which affect myocardial function (such as cardiomyopathy, microvascular disease, or hypertrophy) Complications of cardiac angiography* ACC/AHA guidelines for coronary angiography* • Severe resting left ventricular dysfunction (LVEF <35%) • MDCTA can detect significant (>50%) stenoses with a 90% sensitivity and specificity (if there is not significant calcification) it can reliably demonstrate normal coronary arteries and detect stenoses with a high positive (90%) and negative (95%) predictive value it allows reliable identification of patients who do not need coronary angiography in addition (in up to 10% of cases) MDCT can detect significant non-cardiac diagnoses (e.g. pneumonia or pneumothorax) • Images are obtained at end diastole there are limitations related to heavy arterial calcification and imaging vessels < 2mm in diameter accurate imaging requires a slow enough heart rate (<70 beats/min) and good breath holding (at least 10s) • Evaluation of aortic and other vascular disease as well as some structural cardiac abnormalities (such as pericardial constriction, tumours and thrombus) • Evaluation of arterial and venous great vessel anatomy • Evaluation of cardiac dimensions (there are limitations imposed by the need for iodinated contrast medium and the radiation exposure) • Assessment of myocardial viability and perfusion – images can be analysed in a similar manner to that with MR perfusion imaging • Assessment of resting myocardial perfusion, which can be used to evaluate the size of an acute myocardial infarction and recovery following reperfusion • It is able to accurately determine CABG patency and may be able to determine the patency of the infarct-related artery after coronary thrombolysis • Multiphase reconstruction provides cine images of ventricular and valve movement Radiation dose from cardiac imaging studies compared with other imaging studies* • ‘Black blood’ imaging: the myocardium and vascular wall appear bright and the blood dark this is useful for high-definition anatomical imaging of the heart and vessels but is rather slow to perform • A 180° inverting pulse is applied to the whole imaging volume followed by a slice selective 180° ‘de-inversion’ pulse: the net result is inverted spins outside of the imaged slice but the spins within the imaged slice are unchanged (they have experienced both inversion and de-inversion) the time at which this is applied is the time at which the longitudinal magnetization of blood has reached zero from the initial inversion – therefore blood flowing into the slice will generate no signal (‘black blood’) there may be variable signal from slow or in-plane blood flow (producing artefacts) • ‘White blood’ imaging: blood produces a higher SI than that seen with spin-echo sequences • This is because only one radiofrequency pulse is used and there is less time for the blood to move out of the imaging plane between slice selection and image acquisition (turbulent blood flow will produce areas of signal loss) • The gradient-echo sequence can be repeated more rapidly with a reduced RF flip angle, allowing the acquisition of cine loops this also allows quantification of ventricular stroke volumes (comparing end-systolic and end-diastolic volumes) • This allows quantification of flow velocities • Positive velocity encoding: if a gradient is applied in the direction of blood flow for a finite time and then turned off, the relationship of phase will change in relation to the two ends of the gradient (the protons at the stronger end of the gradient precess at a faster rate during its application than those at the weaker end) • Negative velocity encoding: when the gradient is turned off, the rate of precession becomes constant again in the slice, but the phase relationship has changed and the phase signature remains when the gradient is reversed and applied for the same period of time as the original gradient, the phase signature of still material is cancelled, but flowing blood moving during the gradients to a different phase territory retains a phase change proportional to its velocity
Ischaemic heart disease
CONVENTIONAL CORONARY ANGIOGRAPHY AND ECHOCARDIOGRAPHY
CONVENTIONAL CORONARY ANGIOGRAPHY
Technique
Considerations during coronary angiography
ECHOCARDIOGRAPHY
Indications
Stress echocardiography
Vascular
Haematoma
False aneurysm
Arteriovenous fistula
Mycotic aneurysm
Retroperitoneal haematoma
Acute occlusion
Arterial dissection
Cardiac
Arrhythmias (catheter manipulation)
Myocardial infarction
Coronary dissection
Systemic embolus (including stroke)
Myocardial perforation
Contrast medium
Heart failure (reduced with low-osmolality contrast agent)
Arrhythmias (sinus bradycardia, sinus arrest, ventricular fibrillation in 0.1-1.0%)
ECG changes (wide QRS, long QT, ST changes, change in QRS axis)
Hypotension (reduced with low-osmolality contrast agent)
Allergic/idiosyncratic (reduced with non-ionic contrast agent)
Renal impairment (possibly reduced with low-osmolality contrast agent)
• High-risk treadmill score (score ≥ 11)
• Severe exercise left ventricular dysfunction (exercise LVEF <35%)
• Stress-induced large perfusion defect (particularly if anterior)
• Stress-induced moderate size multiple perfusion defects
• Large, fixed perfused defect with left ventricular dilatation or increased lung uptake (201TI)
• Stress-induced moderate size perfusion defect with left ventricular dilatation or increased lung uptake (201TI)
• Echocardiographic wall motion abnormality (involving more than two segments) developing at a low dose of dobutamine or at a low heart rate
• Stress echocardiography evidence of extensive ischaemia
CT IMAGING IN ISCHAEMIC HEART DISEASE
CARDIAC CT AND CT ANGIOGRAPHY (CTA)
CORONARY CTA
OTHER CARDIAC CT INDICATIONS
Procedure
Effective dose (mSv)
Yearly background radiation
3.6
Chest radiograph
0.032–0.1
Skull examination
0.15
Lumbar spine series
3
Bone scintigram
4.4
Coronary arteriogram
2–6
EBCT calcium scoring
0.5–1
Coronary MDCTA
6–8 (constant tube current)
MR IMAGING IN ISCHAEMIC HEART DISEASE
CARDIAC MRI (CMR) AND MR ANGIOGRAPHY (MRA)
Types of imaging
Spin-echo imaging
Gradient-echo imaging
Phase shift velocity mapping