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1.
Health Phys ; 106(5 Suppl 2): S65-70, 2014 May.
Article in English | MEDLINE | ID: mdl-24667387

ABSTRACT

Response to a large-scale radiological incident could require timely medical interventions to minimize radiation casualties. Proper medical care requires knowing the victim's radiation dose. When physical dosimetry is absent, radiation-specific chromosome aberration analysis can serve to estimate the absorbed dose in order to assist physicians in the medical management of radiation injuries. A mock exercise scenario was presented to six participating biodosimetry laboratories as one individual acutely exposed to Co under conditions suggesting whole-body exposure. The individual was not wearing a dosimeter and within 2-3 h of the incident began vomiting. The individual also had other medical symptoms indicating likelihood of a significant dose. Physicians managing the patient requested a dose estimate in order to develop a treatment plan. Participating laboratories in North and South America, Europe, and Asia were asked to evaluate more than 800 electronic images of metaphase cells from the patient to determine the dicentric yield and calculate a dose estimate with 95% confidence limits. All participants were blind to the physical dose until after submitting their estimates based on the dicentric chromosome assay (DCA). The exercise was successful since the mean biological dose estimate was 1.89 Gy whereas the actual physical dose was 2 Gy. This is well within the requirements for guidance of medical management. The exercise demonstrated that the most labor-intensive step in the entire process (visual evaluation of images) can be accelerated by taking advantage of world-wide expertise available on the Internet.


Subject(s)
Biological Assay/methods , Chromosome Aberrations/radiation effects , Chromosomes, Human/radiation effects , Internet/statistics & numerical data , Laboratories/standards , Mass Casualty Incidents/prevention & control , Radiation Injuries/diagnosis , Cells, Cultured , Chromosomes, Human/genetics , Cobalt Radioisotopes/adverse effects , Dose-Response Relationship, Radiation , Humans , Image Processing, Computer-Assisted , Lymphocytes/radiation effects , Metaphase/radiation effects , Radiation Injuries/genetics , Radiation Injuries/prevention & control , Radioactive Hazard Release/prevention & control , Radiometry
2.
Health Phys ; 100(5): 508-14, 2011 May.
Article in English | MEDLINE | ID: mdl-21451321

ABSTRACT

The NCRP Wound Model, which describes the retention of selected radionuclides at the site of a contaminated wound and their uptake into the transfer compartment, has been combined with the ICRP element-specific systemic models for those radionuclides to derive dose coefficients for intakes via contaminated wounds. These coefficients can be used to generate derived regulatory guidance (i.e., the activity in a wound that would result in an effective dose of 20 or 50 mSv, or in some cases, a organ-equivalent dose of 500 mSv) and clinical decision guidance (i.e., activity levels that would indicate the need for consideration of medical intervention to remove activity from the wound site, administration of decorporation therapy or both). Data are provided for 38 radionuclides commonly encountered in various activities such as nuclear weapons, fuel fabrication or recycling, waste disposal, medicine, research, and nuclear power. These include 3H, 14C, 32P, 35S, 59Fe, 57,58,60Co, 85,89,90Sr, 99mTc, 106Ru, 125,129,131I, 134,137Cs, 192Ir, 201Tl, 210Po, 226,228Ra, 228,230,232Th, 234,235,238U, 237Np, 238,239,240,241Pu, 241Am, 242,244Cm, and 252Cf.


Subject(s)
Radiation Dosage , Radioisotopes/pharmacokinetics , Wounds and Injuries/metabolism , Humans , Radium/pharmacokinetics , Technetium/pharmacokinetics , Thorium/pharmacokinetics
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