Zz. If exposed to neutrons, s whole body count should be rade to estimate the amount of radionuclides produced. possible. marrow biological lymphocytes should be obtained whits cose estimate, (HLA platelet still available, th e tissue should be set up AS svun as possible, before ¢ty Ding and storage results of the lymphopenia for later mixed typing will be useful for t-: eznsfusions and the {xrst five days, fluid and electrolyte identification of a possible bone marrow donor. crea te 4. In the early staves, the balance must be monitored closely acc restored by the appropriate 3. Reverse isolation ak intravenous or oral solution. techniques to prevent ingress of pathogens to the irraciation individuals are gene:ally believed to have been effective in preventing infections in patients unugergotng treativent for leukemia and subsequent bone marrow transplantation, procedure in the event of a potentlily his would probably be a useful fatal irradiation acecicent. I1£ possible, the inuiviaual should be av 7 {tted to a mouern laminar air-flow roon with a complete regimen of skin Ster{illzation, non-absorbable antibiotics for sterilization ot tract. 2 git, rion injucyree Ss flora is desirable, i and the .astroinutestinal this is not feasible, meascres should be initiated to prevent commensal and pathogenic such diet, and infections. this can be lRecuction in the vastrointestinal accomplished with oral, non~absorbable broad-spectrum antibiotics such as nveaycin and antifungal agents such as aystatin. Platelet transfusions, preferably fresh, shuvid be given when the in 6. 4 . Aas J ‘ platelet count approaches 25,00G and reneated to maintain levels above this. fe the patient should teffactor, to randur donor clatelets, Che a” sf ULa-mactcned platelets frou unrelated SUNGOTS May Decome necessary. ¢ ee Ally-wenver transfusion shoula not tx ? ©bone warrow trans;lantation has bwe:, = Ught sensitize the patient to the administered until ex¢luded antirens Lecause of a possibie ~107- FET : u A the posstbilicy such transfusions dotuot. 2 TAT 2 become uw % - toms If sterile st matching of granulocyte, and TPT REE lymphocyte The bune periphe val blood lymphocytes for later analysis of for hurian direct 1s ae ae to 4 . aot, et Oetr Bate ro of promptly as I pepw ceo preparations studies hem pete Tt Op geek ee Uy togene tic leukocyte cultures. of done as be sets in, qusue ing laburatuory including a complete hematologic ew: luation should phy tohemaglufinin stimulated wy bE GUTY examination, and ETERS ryfag THR Ranta, SEARS VTA Tou -- ar physical « moa ’ Medical history, ua ce See PYRE te caeiadate SF amaPe “P 3. OR REESe ee Sry eee a Som ee