Biological Dosimetry Intercomparison Exercise: An Evaluation of Triage and Routine Mode Results by Robust Methods

Abstract Well-defined protocols and quality management standards are indispensable for biological dosimetry laboratories. Participation in periodic proficiency testing by interlaboratory comparisons is also required. This harmonization is essential if a cooperative network is used to respond to a mass casualty event. Here we present an international intercomparison based on dicentric chromosome analysis for dose assessment performed in the framework of the IAEA Regional Latin American RLA/9/054 Project. The exercise involved 14 laboratories, 8 from Latin America and 6 from Europe. The performance of each laboratory and the reproducibility of the exercise were evaluated using robust methods described in ISO standards. The study was based on the analysis of slides from samples irradiated with 0.75 (DI) and 2.5 Gy (DII). Laboratories were required to score the frequency of dicentrics and convert them to estimated doses, using their own dose–effect curves, after the analysis of 50 or 100 cells (triage mode) and after conventional scoring of 500 cells or 100 dicentrics. In the conntional scoring, at both doses, all reported frequencies were considered as satisfactory, and two reported doses were considered as questionable. The analysis of the data dispersion among the dicentric frequencies and among doses indicated a better reproducibility for estimated doses (15.6% for DI and 8.8% for DII) than for frequencies (24.4% for DI and 11.4% for DII), expressed by the coefficient of variation. In the two triage modes, although robust analysis classified some reported frequencies or doses as unsatisfactory or questionable, all estimated doses were in agreement with the accepted error of ±0.5 Gy. However, at the DI dose and for 50 scored cells, 5 out of the 14 reported confidence intervals that included zero dose and could be interpreted as false negatives. This improved with 100 cells, where only one confidence interval included zero dose. At the DII dose, all estimations fell within ±0.5 Gy of the reference dose interval. The results obtained in this triage exercise indicated that it is better to report doses than frequencies. Overall, in both triage and conventional scoring modes, the laboratory performances were satisfactory for mutual cooperation purposes. These data reinforce the view that collaborative networking in the case of a mass casualty event can be successful.

[1]  L Roy,et al.  International intercomparison for criticality dosimetry: the case of biological dosimetry. , 2004, Radiation protection dosimetry.

[2]  Pataje G S Prasanna,et al.  TRIAGE DOSE ASSESSMENT FOR PARTIAL-BODY EXPOSURE: DICENTRIC ANALYSIS , 2010, Health physics.

[3]  V. Durand,et al.  The cytogenetic dosimetry of recent accidental overexposure. , 2001, Cellular and molecular biology.

[4]  D. Lloyd,et al.  The role of cytogenetics in early triage of radiation casualties. , 2000, Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine.

[5]  W. J. Youden,et al.  Graphical Diagnosis of Interlaboratory Test Results , 1972 .

[6]  Ruth C. Wilkins,et al.  Interlaboratory Comparison of the Dicentric Chromosome Assay for Radiation Biodosimetry in Mass Casualty Events , 2008, Radiation research.

[7]  Ruth C Wilkins,et al.  Canadian Cytogenetic Emergency Network (CEN) for biological dosimetry following radiological/nuclear accidents , 2007, International journal of radiation biology.

[8]  Harold Hotelling,et al.  Rank Correlation and Tests of Significance Involving No Assumption of Normality , 1936 .

[9]  D. Lloyd,et al.  A collaborative exercise on cytogenetic dosimetry for simulated whole and partial body accidental irradiation. , 1987, Mutation research.

[10]  James Armitage,et al.  Medical Management of the Acute Radiation Syndrome: Recommendations of the Strategic National Stockpile Radiation Working Group , 2004, Annals of Internal Medicine.

[11]  C. Radhakrishna Rao,et al.  Some small sample tests of significance for a Poisson distribution , 1956 .

[12]  M Di Giorgio,et al.  Intercomparison in cytogenetic dosimetry among five laboratories from Latin America. , 1995, Mutation research.

[13]  David C Lloyd,et al.  WHO 1st Consultation on the Development of a Global Biodosimetry Laboratories Network for Radiation Emergencies (BioDoseNet) , 2009, Radiation research.

[14]  J. Armitage,et al.  Medical Management of the Acute Radiation Syndrome: Recommendations of the Strategic National Stockpile Radiation Working Group , 2004, Annals of Internal Medicine.

[15]  G. W. Parker,et al.  Radiation terrorism: what society needs from the radiobiology–radiation protection and radiation oncology communities , 2009, Journal of radiological protection : official journal of the Society for Radiological Protection.

[16]  Harold M. Swartz,et al.  BiodosEPR-2006 Meeting: Acute dosimetry consensus committee recommendations on biodosimetry applications in events involving uses of radiation by terrorists and radiation accidents , 2007 .