cardiovascular imaging Flashcards

1
Q

imaging techniques

A
  1. x-ray methods:
    - catheter or direct puncture angiography: invasive
    - radiography, fluoroscopy (non-invasive)
  2. ultrasound - Doppler methods (non-invasive)
  3. CT, CT-angiography (non-invasive)
  4. MR, MR-angiography (non-invasive)
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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
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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 (+/-)
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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
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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
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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”
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7
Q

patent deep venous trunk

A
  • echo-free compressible lumen
  • spontaneous flow with preserved respiratory fluctuations
  • augmentable with manoeuvres
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8
Q

acute thrombosis

A
  • dilated non-compressible lumen
  • lack of spontaneous flow
  • restricted augmentation
  • intraluminal echoes +/-
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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
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10
Q

advanced CT & MRI techniques in cardiovascular imaging

A
  • spiral CT-angiography
  • ECG-gated cardio-CT
  • MR-angiography
  • ECG-triggered cardio-MR
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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)
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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
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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
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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
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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

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16
Q

MR angiography: without contrast - PC (phase contrast)

A

flow (depending on its direction and velocity) changes the phase of precessing spins

  • flow direction determination
  • flow velocity determination

application: haemodynamic analysis

17
Q

MR angiography: with contrast material (CE-MRA)

A

sequences based on the marked T1 shortening effect of paramagnetic Gd

  • dynamic IV administration of contrast material (Gd)
  • scan-delay optimised for the selected circulation phase
  • T1 weighted 3D gradient echo fast sequence during the first pass of contrast material
18
Q

CE-MRA post-processing

A

a. 2D reformatted images:
- multiplanar (MPR)
- curved (analog the course of vessels)

b. 3D reformatted images:
- maximun intensity projection (MIP)
- volume rendering (VR)
- shaded surface display (SSD)

c. semi-automatic analysis programs:
- automatic segmentation, “bone-removal”
- stenosis quantification based on diameter and/or cross-sectional area reduction measurement
- aneurysm sizing for stent-graft implantation

19
Q

CE-MRA evaluation

A
  1. primary slices: these contain all the information provided by the study. Any further processing may result in data loss
  2. MIP (maximum intensity projection): DSA-like demonstration of global vascular anatomy. “slab MIP” -> target volume, stenosis analysis
  3. MPR (multiplanar reconstruction), CR: stenosis, plaque analysis
  4. 3D volume rendering (VR), SSD: demonstration of complex anatomy of vessels / bones / parenchymal organs
20
Q

CT/MRA main indications: emergency conditions

A
  • acute chest pain: acute aortic syndrome, acute pulmonary embolism, acute coronary syndrome
  • acute abdominal pain: rupture or pending rupture of AAA, mesenterial ishcemia
  • subarachnoid bleeding: aneurysm of the circle of Willis, vascular malformation
  • traumatic injury of great vessels
  • massive bleeding with haemodynamic instability: tracheo-bronchial, gastrointestinal, genito-urinary
21
Q

thoracoabdominal aorta - aneurysms

A

PRIMARY ASSESSMENT:

  • diameter, length
  • anatomy of proximal and distal necks
  • origin of branches
  • intraluminal thrombus
  • vessel wall thickness, periaortic tissues (inflammation?)
  • signs of imminent rupture

FOLLOW UP:

  • growth
  • d > 5,5 - 6 cm is indication for intervention
  • postoperative follow-up: anastomoses, signs of pseudoaneurysm formation, early complications, late complications (aorto-duodenal fistula)
22
Q

aortic dissection - acute

A
  • type: Stanford A or B?
  • possible dissection variant
  • intramural hematoma
  • penetrating ulcer, circumscribed dissection
  • anatomy of true + false lumen, diameter
  • side branches (supraaortic, renal, splanchnic, iliac)
  • origin from true or false lumen
  • dissection affecting the aortic branch
  • signs of stenosis, thrombosis, hypoperfusion
23
Q

aortic dissection - chronic

A
  • progression of secondary aneurysm
  • signs of imminent rupture
  • side branches
24
Q

planning and follow-up of endovascular interventions

A
  1. sizing before stent-graft implantation:
    - accurate diameters of proximal and distal vessel segments
    - distance from proximal and distal branches, bifurcations
  2. post-intervention follow-up:
    - endoleak?
    * type (source)
    * degree, progression
25
Q

endovascular interventions: indications

A
  • atherosclerotic obliterative arterial disease
  • cerebrovascular disease
  • renovascular hypertension
  • mesenteric ischemia
  • limb ischemia
  • (ischemic heart disease)
26
Q

renal arteries - pathology

A
  1. renovascular hypertension:
    - clinical suspicion of RAS with equivocal examination results (clinical data, US, nuclear medicine)
    - after catheter angiography: complex anatomy
    - AAA +/- RAS?
    - assessment of the arterial supply of transplanted kidney
    - post-operative / stent follow-up
  2. renal artery aneurysm
  3. renal artery anomalies: lower polar artery causing ureteral stenosis?
27
Q

extremity arteries - pathology

A
  1. obliterative disease:
    - for the selection of optimal treatment choice: CTA or MRA, instead of DSA -> able to map the whole extremity arterial tree
    - special MRA technique with table stepping
    - only MDCT enables the imaging of long segments (whole extremity) with reasonable contrast amount & x-ray exposure
  2. femoro-popliteal aneurysms
  3. popliteal entrapment syndrome
  4. vascular injuries associated to pelvic and long bone fractures
28
Q

indications of CTA - MRA: pulmonary circulation

A
  1. acute pulmonary embolism:
    - direct visualization of emboli filling the lumen completely or partially
    - peripheral branches down to subsegmental level are adequately assessed
    - IV contrast administration
    - feasible in critically ill, non-cooperative patients as well
    - DDX: ptx, pneumonia, tumor, etc
  2. chronic pulmonary thrombo-embolic disease:
    - clinical signs of pulmonary arterial HTN
    - known embolic episode in clinical history