Radionuclide studies Flashcards

1
Q

How does radionuclide study evaluate cardiac shunt

A
  • 1st pass radionuclide angiocardiography
    o Records passage of radioactive bolus through central circulation
    o CrVC → RA → RV → PAs → lungs → PVs → LA → LV → Ao
  • Normal dog: ↑ activity in lungs → rapidly ↓ to low level as bolus passes through pulmonary vasculature
    o Residual activity = systemic arterial blood supply to lung + thoracic wall activity
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2
Q

What radionuclide is typically used

A

Pertechnetate bolus

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3
Q

Abn w/ L to R shunt

A
  • Prolonged retention of radioactivity in the lungs
    o Recirculation of blood in pulmonary vasculature
     1st peak + 2nd peak of activity
     Delayed washout phase as bolus continuously recirculates
  • Area under curve of peak of time activity α to blood volume
    o Magnitude of shunt can be estimated from areas under 1st (A1) and 2nd (A2) peak
    o Qp/Qs = A1/A2 – A2
    o Qp/Qs >1.2 indicates L to R shunting
  • Anatomic location cannot always be determined
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4
Q

Abn w/ R to L shunt

A
  • Simultaneous activity in PA and Ao
    o Shunted radioactive blood appear early in systemic circulation → bypass pulmonary circulation
    o Small shunt may obscure Ao by high activity in the lungs
  • Injection of 99mTcmacroaggregated albumin (99mTc-MAA)
    o Large particle size → trapped in capillaries
    o Normal animals = all particles trapped in lungs
    o R → L shunt = bypass the lungs and go to systemic circulation
  • % shunt = extrapulmonary activity/ extrapulmonary + pulmonary activity
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5
Q

how does radionuclide can eval LV fct

A
  • Gated equilibrium radionuclide angiography (gated blood pool ventriculography)
    o Imaging cardiac blood pool after injected tracer has mixed with IV space
     IV injection of blood pool agent
  • 99mTc-labeled red blood cells (99mTc-RBC)
  • 99mTc-labeled serum albumin (99mTc-HAS)
    o After equilibration w blood pool → activity of given qty of blood directly related to its volume
     Image acquisition (gamma camera, scintigraphic images) synchronized w R wave from ECG = various stages of cardiac cycle obtained at specific intervals
     Changes in ventricular activity = volume changes
  • Derived functional indices from ventricular time activity
    o EF% → if MR, not indicator of myocardial function
    o Filling times
    o Peak filling rates
    o Time/rate of ventricular ejection
    o Regional wall motion
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6
Q

Advantages of LV fct eval w/ radionuclide

A

independent images from R and L side → permit to better isolate/evaluate RV

data from several hundreds of cardiac cycles → more accurate average cardiac fct

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7
Q

Disadvantages of LV fct eval w/ radionuclide

A

only 4-6 cardiac cycle can be evaluated

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8
Q

Evaluation of myocardial perfusion, ischemia and infarction w/ radionuclide

A
  • Myocardial uptake of Thalium-201 is α to myocardial blood flow
    o 85% of injected Thalium-201 removed in single pass
    o After several hours → redistributes to the heart to reflect distribution of K+ pool
  • Myocardial defect → show extent of perfusion abnormality
    o Suggest fixed abnormality (permanent scar)
    o If improve after initial scan → indicate myocardial ischemia
  • Attenuation: can happen with overlying soft tissue → false positive results
    o More likely with Technetium-99m
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9
Q

Agent used for myocardial perfusion eval

A

Thalium-201
o Similar biologic properties to K+ → K+ analog

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10
Q

Imaging agents

A
  • Radioactive Thalium-201
  • Technetium-99m markers
  • Iodine-123 labeled fatty acid
  • Iodine-123 metaiodobenzylguanidine
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11
Q

What is eval by radionuclide ventriculography

A
  • Evaluate ventricular function
    o 1st transit studies → beat to beat evaluation
     RV function
     Intracardiac shunt
    o Gated (ECG synchronized) blood pool imaging → multiple gated acquisition
     Nuclear medicine gated blood pool scan: labelling RBCs with radiopharmaceutical
     Measure amount of blood in heart during different part of cardiac cycle
     Images acquired from gamma camera (scintigraphy)
     Blood pool → analysis of amount of radioactive blood pooling in cardiac chambers at different times on cardiac cycle
     Gated → study performed in time with heart rhythm
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12
Q

Viability studies

A
  • Dysfunctional but viable myocardium → potential to recover function after reperfusion
  • Assessment of myocardial viability with scintigraphic techniques
    o Intact perfusion
     Evaluated by Thalium-201/Technetium-m99 labeled tracers
    o  membrane integrity
     Evaluated by Thalium-201
    o Intact mitochondria
     Technetium-m99 labeled tracers
    o Preserved glucose/fatty acid metabolism
     FDG and radiolabelled fatty acids (Iodine-123)
    o Contractile reserve
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