Oral Exam - Cardiac Flashcards

1
Q

Multiple-gated cardiac blood pool acquisition (MUGA)

A

○ Low inter- and intra observer variability (<5%)
○ High reproducibility

○ Heart must be in regular rhythm for optimal imaging
– Ejection fraction results less reliable if ≥ 30%irregular
beats

○ If background drawn over spleen or aorta, ejection
fraction (EF) spuriously high
○ If background drawn over stomach or outside body, EF
spuriously low

• Evaluate raw images (cine) for study quality
○ Counts, labeling, gating, views

• Compare qualitative estimation of left ventricular ejection fraction with quantitative calculation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

Things to evaluate on MUGA

A
○ Pericardial silhouette 
○ Chambersizes
○ Hypo/akinesis
○ Filling defects
○ Aneurysm
○ Ejection fraction
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

MUGA protocol

A

Radiopharmaceutical: 15-25 mCi (555-925 MBq) Tc-99m
pertechnetate autologous labeled RBCs IV

○ Image acquisition
– Patient supine
– ECG gating
□ 16-32 frames per R-R interval
– Planar images: LEAP/high-resolution collimator
– Matrix: 64 x 64
– Each image acquired for 300K counts or 5 min

Anterior view - anterolateral and apical LV; right atrium and right ventricle

Best septal view LAO: Angle chosen that best shows septum between right and left ventricles; septal, anterolateral, posterolateral LV

Left lateral/LPO: 45° greater than best septal LAO
□ Shows inferior, apical, anterolateral LV

  • Phase image: Shows equence of contraction of atria and ventricles
  • Amplitude image: Shows magnitude of contraction of atria and ventricles
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

Artifacts myocardial perfusion imaging

A

Motion artifact
○ Hurricane sign: Counts outside epicardial border on short axis
○ Blurred endocardial border
○ Lateral wall blurring

Scatter artifact
○ Counts scatter into inferior wall due to high bowel
activity

Reconstruction artifact
○ Photopenia in inferior wall from high bowel activity

Attenuation
○ Soft tissue attenuation causing fixed defects
○ Misregistration of attenuation correction map and
perfusion data

• Normal apical thinning
• Left ventricular hypertrophy: Fixed lateral wall defect
• Soft tissue attenuation of photons: Breast (anteriorwall),
diaphragm (inferior wall)
• Septal hypokinesis common in absence of MI, especially
after coronary artery bypass graft surgery

Myocardial hibernation: Myocardium with little/no
perfusion, but viable due to anaerobic glycolysis
○ 25% of fixed defects are viable on viability studies

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

Conclusion of MPI study

A

Conclusion
○ Positive or negative for inducible ischemia
○ Positive or negative for myocardial infarction (± peri-
infarct ischemia)
– Consider possibility of hibernating myocardium, need
for viability study
○ LV function: EF and wall motion

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

R-L shunt protocol

A

○ Tc-99m MAA
○ Use reduced MAA particle count (100,000-200,000) in
case of suspected shunt, pulmonary hypertension, pregnancy, or pediatric patient

Imagea cquisition
○ LEAP collimator
○ In addition to anterior/posterior planar images of lungs,
posterior images of kidneys and anterior/posterior of brain
– Brain images: Most sensitive indicator of right-to-left
shunt

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

R-L shunt findings

A

○ Abnormal uptake within brain and kidneys confirms
shunting of Tc-99m MAA administered intravenously

○ Tc-99m MAA should localize only in brain and kidneys
with shunt

○ Must be differentiated from extrapulmonary uptake of
free Tc-99m pertechnetate
– Free Tc-99m pertechnetate is also visualized in thyroid gland, salivary glands and gastric mucosa

  • Always scrutinize VQ scans for unexpected incidental uptake within brain or kidneys
  • If uptake in kidneys, must look for brain or thyroid/salivary uptake (kidneys can be either due to free pertech or r-L shunt)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Ddx R-L shunt

A

Intracardiac shunt:
ASD/PFO/VSD

Extracardiac shunt:
Pulmonary AVM
Anamolous systemic venous return
Hepatopulmonary syndrome

Free pertechnetate - kidneys, thyroid, SG, gastric mucosa

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

FDG PET Normal perfusion decreased FDG

A

Reverse mismatch

Ddx: Revascularization early after MI
LBBB
RV pacing
non-ischemic cardiomyopathy
diabetes
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

FDG PET for sarcoid

A

Focal patchy FDG uptake in the myocardium can indicate active inflammation

Not specific for sarcoidosis

Other causes of myocardial inflammation – giant cell, viral myocarditis, pericarditis etc.

NPO x 12 hours

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

High risk scan features

A
SSS > 13 (regardless of reversability)
SDS > 7
TID 1.22 with exercise; 1.35 with vasodilator
Fall in EF > 5% with stress
Post stress EF < 40%
Multiple vascular territories
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

LBB?

A

If the QRS complex is widened and downwardly deflected in lead V1, a left bundle branch block is present.

Can get rabbit ears in V6

Criteria:

  1. QRS duration greater than 120 milliseconds
  2. Absence of Q wave in leads I, V5 and V6
  3. Monomorphic R wave in I, V5 and V6
  4. ST and T wave displacement opposite to the major deflection of the QRS complex

RBBB = RSR’ in V1; No rabbit ears in V6

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Ventricular couplet

A

2 PVCs in a row

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Premature beats

A

PAC = narrow complex QRS; unusual usually biphasic P wave

PJC - narrow complex QRS, sometimes no P wave

PVC = wide complex QRS

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Ventricular tachycardia

A

3 PVCs in a row

A wide complex tachycardia without sinus P waves. Ddx BBB

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Wide QRS?

A

IF > 0.1 s or > half a large box

Reasons (assuming not VT or WPW):
Typical RBB
Typical LBB
Neither RBB or LBB -> IVCD

17
Q

To dx type of BBB

A

Look at I, V1, V6

RBB:
If RSR’ in VI -> RBB; Wide S wave in I and V6 (left leads)
ST-T wave opposite to last QRS deflection

LBB:
QRS predominantly negative in V1
1/V6 - no Q wave, upright R wave +/- notch
ST-T wave opposite to last QRS deflection

18
Q

Assessing rhythm

A

Watch your p’s, q’s, and 3 r’s:

Are there p waves?
Is the QRS wide or narrow?
3 R’s - RATE, REGULAR, if p waves, are they RELATED to QRS?

19
Q

SVT rhythms:

A
  1. A-fib
  2. A-flutter (regular) - typically 140-160
  3. Sinus tachycardia (regular) - unlikely if over 160 bpm
  4. AVRT (regular)

Tachycardia can cause ST depression - can create demand ischeimia not related to CAD. Even if ST depression persists after rate slows. `

20
Q

Complete AV block

A

Regular (or almost regular) atrial rate
Regular (or almost regular) ventricular rate

No relation between p waves and QRS complexes despite adequate opportunity for p waves to conduct

21
Q

Stopping chemotherapy

A

Relative drop of LVEF > 10 and absolute LVEF < 50%

22
Q

Extracardiac thallium or MIBI uptake

A

Other than ventricle should see no other mediastinal uptake

Ddx:
Thoracic malignancy
Pulmonary inflammatory process
Benign mediastinal neoplasm - ectopic parathyroid adenoma; malignancy needs to be excluded