LAUSR

Abstract Purpose The purpose of this study was to experimentally validate UF‐RIPSA, a rapid in‐clinic peak skin dose mapping algorithm developed at the University of Florida using optically stimulated luminescent dosimeters (OSLDs) and tissue‐equivalent phantoms. Methods The OSLDs used in this study were InLightTM Nanodot dosimeters by Landauer, Inc. The OSLDs were exposed to nine different beam qualities while either free‐in‐air or on the surface of a tissue equivalent phantom. The irradiation of the OSLDs was then modeled using Monte Carlo techniques to derive correction factors between free‐in‐air exposures and more complex irradiation geometries. A grid of OSLDs on the surface of a tissue equivalent phantom was irradiated with two fluoroscopic x ray fields generated by the Siemens Artis zee bi‐plane fluoroscopic unit. The location of each OSLD within the grid was noted and its dose reading compared with UF‐RIPSA results. Results With the use of Monte Carlo correction factors, the OSLD's response under complex irradiation geometries can be predicted from its free‐in‐air response. The predicted values had a percent error of −8.7% to +3.2% with a predicted value that was on average 5% below the measured value. Agreement within 9% was observed between the values of the OSLDs and RIPSA when irradiated directly on the phantom and within 14% when the beam first traverses the tabletop and pad. Conclusions The UF‐RIPSA only computes dose values to areas of irradiated skin determined to be directly within the x ray field since the algorithm is based upon ray tracing of the reported reference air kerma value, with subsequent corrections for air‐to‐tissue dose conversion, x ray backscatter, and table/pad attenuation. The UF‐RIPSA algorithm thus does not include the dose contribution of scatter radiation from adjacent fields. Despite this limitation, UF‐RIPSA is shown to be fairly robust when computing skin dose to patients undergoing fluoroscopically guided interventions.