TABLE 4

Comparison of Dose Estimates of Methods 2–4 Against Conventional Method 1 Dose Estimates for Patients Grouped by Prior Treatments and Abnormal Renal Function

Patient groupConventional, method 1Blood only, method 2Camera only, method 348-h camera only, method 4
PT+ and AF− (n = 26)12 ± 9 cGy/GBq12 ± 9 cGy/GBq, P = 0.6313 ± 8 cGy/GBq, *P = 0.0313 ± 11 cGy/GBq, P = 0.76
PT− and AF− (n = 22)22 ± 17 cGy/GBq21 ± 16 cGy/GBq, P = 0.2223 ± 17 cGy/GBq, P = 0.2514 ± 12 cGy/GBq, *P = 0.002
PT− and AF+ (n = 17)29 ± 9 cGy/GBq30 ± 10 cGy/GBq, P = 0.5427 ± 11 cGy/GBq, P = 0.1720 ± 13 cGy/GBq, *P = 0.0008
PT+ and AF+ (n = 6)34 ± 13 cGy/GBq35 ± 11 cGy/GBq, P = 0.5130 ± 14 cGy/GBq, P = 0.1129 ± 29 cGy/GBq, P = 0.52
  • * P < 0.05 vs. method 1.

  • PT+ = patients who had prior 131I treatment; AF− = patients with normal renal function; PT− = patients who did not have prior 131I treatment; AF+ = patients with abnormal renal function.