cardiovascular imaging Flashcards
1
Q
imaging techniques
A
- x-ray methods:
- catheter or direct puncture angiography: invasive
- radiography, fluoroscopy (non-invasive) - ultrasound - Doppler methods (non-invasive)
- CT, CT-angiography (non-invasive)
- MR, MR-angiography (non-invasive)
2
Q
radiography
A
- digital is preferred over analog
- summation images: high spatial resolution, low contrast resolution
- bi-directional (PA, lateral) CXR -> heart + great vessels are in the mediastinal shadow, well contoured by air-containing lungs
- information on: heart size, dilation + course of mediastinal vessels, calliber of pulmonary vessels, cardiac + vessel wall calcification, inserted IV lines, devices, pacemakers
- fluoroscopy: pulsation of heart + vessels
3
Q
signs of congestive heart failure
A
- cephalization of pulmonary vasculature -> pulmonary venous pressure increases
- Kerley lines: interlobular septal thickening - interstitial edema
- diffuse alveolar edema: perihilar distribution, butterfly or bat-wing pattern, coalescing fluffy opacities, air-bronchogram
- pleural effusion
- enlarged heart (+/-)
4
Q
ultrasonography
A
- fluids: hypo- or an-echoic -> blood-filled vessels + heart chambers are dark on 2D ultrasound images
- real time imaging (echocardiography)
- high resolution imaging of vessel wall & lumen: for superficial vessels, plaque analysis
- bones & air are not penetrated by US. “Acoustic window” is needed
- Doppler techniques: accurate velocity measurements - haemodynamic analysis. Color Doppler - flow map.
- 2D ultrasound images + spectrum Doppler = duplex ultrasound
5
Q
main indications of duplex sonography
A
- cerebrovascular disease (carotid stenosis, transcranial Doppler)
- obliterative arterial disease of extremities (atherosclerotic chronic disease, acute embolic occlusion)
- deep venous thrombosis of the extremities
- abdominal vessels (AAA - aneurysm of the abdominal aorta, renal artery stenosis, abdominal angina - mesenteric artery stenosis, portal HTN)
- soft tissue vascularisation (eg tumors)
- post-surgical conditions - complications
6
Q
significant arterial stenosis
A
- vessel wall irregularity
- plaques causing stenosis
- > 50% stenosis - quantification is more accurate on haemodynamic basis
- elevated end-systolic & end-diastolic peak velocity
- sign of turbulence - filling of :systolic window”
7
Q
patent deep venous trunk
A
- echo-free compressible lumen
- spontaneous flow with preserved respiratory fluctuations
- augmentable with manoeuvres
8
Q
acute thrombosis
A
- dilated non-compressible lumen
- lack of spontaneous flow
- restricted augmentation
- intraluminal echoes +/-
9
Q
chronic thrombosis
A
- difficult diagnosis
- deliniation of lumen is less clear, irregular “braid-like” collaterals
- variable spontaneous flow, restricted respiratory fluctuation, reflux augmentable
10
Q
advanced CT & MRI techniques in cardiovascular imaging
A
- spiral CT-angiography
- ECG-gated cardio-CT
- MR-angiography
- ECG-triggered cardio-MR
11
Q
vascular imaging by CT
A
- non-contrast CT: pathologic mural calcification, coronary Ca scoring
- contrasted-enhanced CT -> “conventional” technique: aorta (d >/= 1cm)
- spiral CT-angiography: single detector row spiral CT ( branches of aorta, d >/= 2-3 mm), multidetector row spiral CT (peripheral vessels, d >/= 1 mm)
12
Q
helical (spiral) CT angiography
A
- dynamic IV administration of contrast material
- scan-delay optimised for the selected circulation phase
- helical scanning with thin collimation during the first pass of contrast bolus
- post-processing of primary scan data: multiplanar and 3D reformatted images resembling DSA
13
Q
vascular imaging by CT - scanning parameters
A
- slice thickness as thin as possible (isotropic imaging): 4-16 slice CT: 1 - 1,25 mm / 16-256 slice CT: 0,5 - 1,25 mm
- multiphase examination if necessary: venous filling, vessel walls, perivascular tissues, parenchymal organs
- ECG-gating: coronary CTA, congenital anomalies, “triple rule-out” approach for acute chest pain
14
Q
vascular imaging by CT - contrast administration
A
- type: non-ionic, preferably low osmolality
- dose: MDCT: 1 - 1,5 cc/kgBW
- automatic injection: 2,5 - 5 cc/sec, second phase saline flush
- scan timing to achieve optimal “first pass” effect: empiric -> variable circulation times, bolus detecting program (bolus tracking) -> automatic detection of intravascular density elevation at arrival of contrast bolus
15
Q
MR angiography: without contrast - TOF (time-of-flight)
A
short repetition time results in the saturation of stationary tissues; signal is generated only by the unsaturated spins in the blood entering the examination plane (inflow effect)
application: intracranial arteries