DTPA | MAG-3 | |
Excretion | Filtration 90% extracted from blood by 4 hours |
Tubular excretion (95%) and filtration (5%) |
Renal function estimate | GFR May underestimate, since some DTPA is bound to plasma proteins |
ERPF |
Response to captopril in RAS | Decreased activity (since GFR goes down) | Increased activity (since GFR and hence tubular secretion goes down) |
Parenchymal visualization | Poor due to short nephrographic phase. Even worse in patients with obstruction or renal impairment, since filtration is impaired | Good |
Dose-limiting organ | Bladder | Bladder |
Dose | 370-740 MBq (10-20 mCi) | 370-740 MBq (10-20 mCi) |
The difference in excretion is important in understanding post-ACE inhibitor images. In patients with renal artery stenosis, captopril causes a decrease in GFR. If DTPA is used, there is diminished initial uptake of radiotracer with or without prolonged parenchymal transit. The latter is manifested by a delay in time to peak activity and excretion.
Since the drop in GFR doesn't affect MAG-3 uptake, there is adequate initial uptake and secretion. However, the drop in GFR results in decreased urine production and flow and decreased washout of MAG-3, resulting in cortical retention.
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