Acute radiation syndrome (ARS) in the human population is primarily divided in 4
different categories. Below 2 Gy, some individuals may experience some symptoms,
such as emesis, however these individuals will not require immediate medical
intervention for survival. Over doses of 2 Gy, individuals will experience and
expire from myelosuppression (hematopoietic syndrome). The LD50/60
without medical intervention is ∼3.5 Gy, however with medical
intervention it shifts upwards to ∼7 Gy. Only two medications have been
FDA approved for the hematopoietic syndrome, Neupogen® and
Neulasta®. Individuals exposed with a dose of 10 Gy and
above will expire from gastrointestinal (GI) syndrome within 7-14 days post
irradiation, although some individuals can have symptoms of GI syndrome with as
low as 6 Gy. Individuals exposed to doses >20 Gy, although some can show
symptoms as low as 10 Gy, will expire within days from cardiovascular and/or
central nervous system syndromes. Since not all individuals can undergo an
invasive procedure such as hematopoietic stem cell transplantation, only a small
percentage falling between a dose range that cannot adequately benefit from
cytokine therapy and antibiotic treatments, will be candidates for such
treatments. Sources for the information include (DiCarlo et al., 2011, Sullivan et
al., 2013, CDC, 2015).