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. Author manuscript; available in PMC: 2022 Sep 5.
Published in final edited form as: Health Phys. 2015 Nov;109(5):427–439. doi: 10.1097/HP.0000000000000350

Table 4.

Incidence, latency, and duration of FN with bacteriology post-PBI/BM5.

Exposure Treatment Incidence of FN (% of NHP) First Day of FN # of Days Incidence of Infection (% of Cultured NHP)
Gram+ Gram−
10.0 Gy Control (n=15) 47% 15.9 ± 2.8 1.1 ± 0.1 29% 0%

Neupogen® on
day 1 (n=7)
14% (n=1) 4 1 0% 0%

Neupogen® on day 3 (n=8) 13% (n=1) 12 1 0% 0%

11.0 Gy Control (n=22) 32% 16.1 ± 2.8 2.1 ± 0.5 57% 0%

Neupogen® on day 1 (n=5) 0% NA NA NA NA

Neupogen® on day 3 (n=8) 25% 8.0 ± 1.0 1.5 ± 0.5 50% 0%

Neupogen® on day 5 (n=8) 0% NA NA NA NA

Rhesus macaques were exposed to 10.0 or 11.0 Gy PBI/BM5 utilizing 6 MV LINAC-derived photons. Animals were administered control article (5% dextrose in water) or Neupogen® beginning at the indicated times post-irradiation, through the third consecutive day an ANC ≥ 1,000 cells μL−1 was observed post-nadir. FN was defined as ANC < 500 cells μL−1 with rectal body temperature ≥ 103.0 °F (39.4 °C), and blood cultures were collected on days when FN was observed. The time values displayed are means ± sem.