Nuclear Cardiology Flashcards
role of left ventricular perfusion imaging
evaluate blood flow to myocardium
Questions to ask yourself during perfusion study
- is perfusion abnormality reversible during rest or fixed during stress/rest?
- size of perfusion abnormality
- severity: mild/subendocardial, moderate, or severe/transmural
- which coronary artery territory?
- associated abnormalities such as right ventricular uptake, ischemic dilation, wall motion abnormalities?
types of stress in perfusion imaging
physical (treadmill)
pharmacologic/adrenergic (dobutamine)
pharmacologic/vasodilatory (dipyridamole/adenosine)
indications for myocardial perfusion imaging
- evaluation of acute chest pain (evaluate ambiguous cases; chest pain with negative EKG/troponins)
- evaluation of hemodynamic significant coronary stenosis
- risk stratification after MI
- preoperative risk for noncardiac surgery
- viability prior to revascularization therapy
- evaluation of myocardial revascularization status pose CABG
high risk patients after MI
- significant peri-infarct ischemia
- defect in different vascular territory (multivessel disease)
- significant lung uptake
- left ventricular aneurysm
- low ejection fraction < 40%
hibernating myocardium
hypoperfused myocardium that is viable; meaning could be revascularizaed and isn’t scar tissue
viability imaging
rest–redistribution thallium-201 perfusion imaging or F-18 FDG PET. F-18 FDG PET is the gold standard for evaluation of myocardial viability, although unlike thallium FDG-PET does not evaluate perfusion.
static SPECT images from pure pefusion exams
Tc-99m sestamibi, rubidium-82 PET, or N-13 ammonia PET cannot distinguish between scar/hibernating scar tissue
Thallium 201
cyclotron produced radionuclide with half life 73 hrs
decays by electron capture; emits characteristic xray 69-81 keV
how does thallium work physiologically
acts like potassium analog and crosses into cells via ATP dependent Na K pump
thallium in the heart
myocardial uptake directly proportional to myocardial perfusion
50% stenosis»_space; perfusion defect with maximal exercise
undergoes redistribution with simultaneous cellular washout; ischemic myocardium washes out more slowly than normal myocardium
scar tissue will have persistent defect
Technetium 99m sestamibi (Cardiolite); physiologic activity and redistribution?
enters myocardium via passive diffusion, binding to mitochondrial proteins ;
myocardial uptake proportional to perfusion
does not undergo redistribution; stays in the myocardium
rubidium 82 is generated from? half life? physiology? type of stress test?
PET perfusion agent generated from strontium 82
half life 76 seconds so high doses can be administered; used as pharmacologic stress
acts as potassium analog, like thallium
nitrogen 13 ammonia production? half life? physiology?type of stress test?
PET perfusion agent
cyclotron produced; must be produced on site due to short half-life
10 min half life
pharmacologic stress
F18 FDG agent? viability?
positron emitting PET viability agent
half life 110 min; can’t be used for perfusion
can be used with sestabmibi perfusion study to evaluate viability; differentiate between hibernating myocardium