Abstract

Accurate radiation dose estimates are critical for determining eligibility for therapies by timely triaging of exposed individuals after large-scale radiation events. However, the universal assessment of a large population subjected to a nuclear spill incident or detonation is not feasible. Even with high-throughput dosimetry analysis, test volumes far exceed the capacities of first responders to measure radiation exposures directly, or to acquire and process samples for follow-on biodosimetry testing. To significantly reduce data acquisition and processing requirements for triaging of treatment-eligible exposures in population-scale radiation incidents. Physical radiation plumes modelled nuclear detonation scenarios of simulated exposures at 22 US locations. Models assumed only location of the epicenter and historical, prevailing wind directions/speeds. The spatial boundaries of graduated radiation exposures were determined by targeted, multistep geostatistical analysis of small population samples. Initially, locations proximate to these sites were randomly sampled (generally 0.1% of population). Empirical Bayesian kriging established radiation dose contour levels circumscribing these sites. Densification of each plume identified critical locations for additional sampling. After repeated kriging and densification, overlapping grids between each pair of contours of successive plumes were compared based on their diagonal Bray-Curtis distances and root-mean-square deviations, which provided criteria (<10% difference) to discontinue sampling. We modeled 30 scenarios, including 22 urban/high-density and 2 rural/low-density scenarios under various weather conditions. Multiple (3-10) rounds of sampling and kriging were required for the dosimetry maps to converge, requiring between 58 and 347 samples for different scenarios. On average, 70±10% of locations where populations are expected to receive an exposure ≥2Gy were identified. Under sub-optimal sampling conditions, the number of iterations and samples were increased, and accuracy was reduced. Geostatistical mapping limits the number of required dose assessments, the time required, and radiation exposure to first responders. Geostatistical analysis will expedite triaging of acute radiation exposure in population-scale nuclear events.

Highlights

  • In a large-scale nuclear event or accident, many will be exposed to varying levels of radiation, some of whom would require immediate treatment

  • We simulated the analysis of 28 population-scale, 10 megaton yield nuclear detonation scenarios with dosimetry data for radiation exposures corresponding to HPAC-derived dose estimates

  • There are exceptions where equivalent accuracy is obtained with fewer overall points (e.g. Buffalo NY; Table 1) which implies that the spatial distribution of initial set of random samples can influence the accuracy of the converged plume

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Summary

Introduction

In a large-scale nuclear event or accident, many will be exposed to varying levels of radiation, some of whom would require immediate treatment. Absolute lymphocyte depletion is a strong indicator of absorbed dose, but requires repeated sampling of a patient over several hours to days after exposure [12] For this reason, management of acute radiation exposures has often relied upon physical dosimetry as a surrogate for biological exposures. One approach to alleviating the need to individually triage the entire population would be to survey radiation levels at a subset of locations and derive a radiation map by geostatistical analysis This survey may involve either location-based physical dosimetry, where high-risk individuals are identified based on their proximity to fixed radiation detectors or by geospatially targeted biodosimetry. Accurate radiation dose estimates are critical for determining eligibility for therapies by timely triaging of exposed individuals after large-scale radiation events. Even with high-throughput dosimetry analysis, test volumes far exceed the capacities of first responders to measure radiation exposures directly, or to acquire and process samples for follow-on biodosimetry testing

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