The European intercomparison of in-vivo monitoring laboratories: the EIVIC-2020 project.

The EIVIC project was launched in 2020, and the main goal was the organisation of a European intercomparison of in-vivo monitoring laboratories dealing with direct measurements of gamma-emitting radionuclides incorporated into the body of exposed workers. This project was organised jointly by members of EURADOS Working Group 7 on internal dosimetry (WG7), the Federal Office for Radiation Protection (BfS, Germany) and the Radioprotection and Nuclear Safety Institute (IRSN, France). The objective was to assess the implementation of individual-monitoring requirements in EU Member States on the basis of in-vivo measurements and to gain insight into the performance of in-vivo measurements using whole-body counters. In this context, a total of 41 in-vivo monitoring laboratories from 21 countries, together with JRC (EC) and IAEA participated. The results were submitted in terms of activity (Bq) of the radionuclides identified inside phantoms that were circulated to all participants. The measured data were compared with reference activity values to evaluate the corresponding bias according to the standards ISO 28218 and ISO 13528. In general, the results of the different exercises are good, and most facilities are in conformity with the criteria for the bias and z-scores in the ISO standards. Furthermore, information about technical and organisational characteristics of the participating laboratories was collected to test if they had a significant influence on the reported results.

Uncertainty induced by chest wall thickness assessment methods on lung activity estimation for plutonium and americium: a large population-based study.

In vivo lung counting aims at assessing the retained activity in the lungs. The calibration factor relating the measured counts to the worker's specific retained lung activity can be obtained by several means and strongly depends on the chest wall thickness. Here we compare, for 374 male nuclear workers, the activity assessed with a reference protocol, where the material equivalent chest wall thickness is known from ultrasound measurements, with two other protocols. The counting system is an array of four germanium detectors.It is found that non site-specific equations for the assessment of the chest wall thickness induce large biases in the assessment of activity. For plutonium isotopes or (241)Am the proportion of workers for whom the retained activity is within ± 10% of the reference one is smaller than 10%.The use of site-specific equations raises this proportion to 20% and 58% for plutonium and (241)Am, respectively.Finally, for the studied population, when site-specific equations are used for the chest wall thickness, the standard uncertainties for the lung activity are 42% and 12.5%, for plutonium and (241)Am, respectively. Due to the relatively large size of the studied population, these values are a relatively robust estimate of the uncertainties due to the assessment of the chest wall thickness for the current practice at this site.

Analysis of the time reversal operator for a scatterer undergoing small displacements.

The method of the time reversal operator decomposition is usually employed to detect and characterize static targets using the invariants of the time reversal operator. This paper presents a theoretical and experimental investigation into the impact of small displacements of the target on these invariants. To find these invariants, the time reversal operator is built from the multistatic response matrix and then diagonalized. Two methods of recording the multistatic response matrix while the target is moving are studied: Acquisition either element by element or column by column. It is demonstrated that the target displacement generates new significant eigenvalues. Using a perturbation theory, the analytical expressions of the eigenvalues of the time-reversal operator for both acquisition methods are derived. We show that the distribution of the new eigenvalues strongly depends on these two methods. It is also found that for the column by column acquisition, the second eigenvector is simply linked to the scatterer displacements. At last, the implications on the Maximum Likelihood and Multiple Signal Classification detection are also discussed. The theoretical results are in good agreement with numerical and 3.4 MHz ultrasonic experiments.

Patient-specific biokinetics and hybrid 2D/3D approach integration in OEDIPE software: Application to radioiodine therapy.

BACKGROUND: The progression of targeted radionuclide therapy requires the development of dosimetry software accounting for patient-specific biokinetics. New functionalities were thus developed in the OEDIPE software, to deal with multiple 3D images or multiple planar images and a SPECT image. MATERIEL & METHOD: Methods were implemented to recover patient biokinetics in volumes of interest. If several 3D SPECT images are available, they are registered to a reference CT scan. When several planar images and a single SPECT are available, the planar images are registered to the SPECT and counts of the planar images converted to activity. To validate these developments, six SPECT/CT and planar images of a Jaszczak phantom containing I-131 were acquired at different dates. Cumulated activity was estimated in each sphere using the SPECT/CT images only or the planar series associated to one SPECT/CT. Biokinetics and doses in lesions and in the lungs of a patient treated with I-131 for differentiated thyroid cancer were then estimated using four planar images and a SPECT/CT scan. Whole-body retention data were used to compare the biokinetics obtained from the planar and SPECT data. RESULTS: Activities and cumulated activities estimated using OEDIPE in the phantom spheres agreed well with the reference values for both approaches. Results obtained for the patient compared well with those derived from whole-body retention data. CONCLUSION: The implemented features allow automatic evaluation of patient-specific biokinetics from different series of patient images, enabling patient-specific dosimetry without the need for external software to estimate the cumulated activities in different VOIs.

Novel transforaminal approach allows surgical decompression of an atlantoaxial band in dogs: a cadaveric study and clinical cases.

OBJECTIVES: To describe a novel transforaminal approach for surgical excision of the atlantoaxial (AA) band and examine its feasibility, safety, and mechanical advantages in an ex vivo study and clinical cases. SAMPLES: 26 canine cadavers and 2 canine patients with AA bands. PROCEDURES: The transforaminal approach via the first intervertebral foramen was designed to avoid damaging the dorsal AA ligament (DAAL) and dorsal laminas to maintain joint stability. The cadaveric study started on December 2020 and lasted 3 months. The ligamentum flavum (LF) was removed using a novel approach; then, gross examination was conducted to verify the potential damage to the spinal cord and associated structures and the adequacy of LF removal. Subsequently, the ex vivo tension test of the DAAL was conducted to establish whether the approach induced mechanical damage to the ligaments. Finally, 2 dogs diagnosed with an AA band were surgically treated with the transforaminal approach. RESULTS: In the cadaveric study, postsurgical evaluation verified the subtotal removal of LF without damage to the dura mater. There were no significant differences in the mechanical properties of the DAAL, including the ultimate strength (P = .645) and displacement (P = .855), between the surgical and intact groups during the ex vivo tension test. In clinical cases, clinical signs and neurologic grades improved until the final follow-up. CLINICAL RELEVANCE: The described surgical procedure using a transforaminal approach appears to sufficiently permit the removal of an AA band while reducing damage to the DAAL and spinal cord. Our study highlights the feasibility of the transforaminal approach.

Using radial distribution functions to calculate cellular cross-absorbed dose forßemitters: comparison with reference methods and application for18F-FDG cell labeling.

To further improve the understanding ofin vitrobiological effects of incorporated radionuclides, it is essential to accurately determine cellular absorbed doses. In the case ofßemitters, the cross-dose is a major contribution, and can involve up to millions of cells. Realistic and efficient computational models are needed for that purpose. Conventionally, distances between each cell are calculated and the related dose contributions are cumulated to get the total cross-dose (standard method). In this work, we developed a novel approach for the calculation of the cross-absorbed dose, based on the use of the radial distribution function (rdf)) that describes the spatial properties of the cellular model considered. The dynamic molecular tool LAMMPS was used to create 3D cellular models and computerdfsfor various conditions of cell density, volume size, and configuration type (lattice and randomized geometry). The novel method is suitable for any radionuclide of nuclear medicine. Here, the model was applied for the labeling of cells with18F-FDG used for PET imaging, and first validated by comparison with other reference methods. MeanScrossvalues calculated with the novel approach versus the standard method agreed very well (relative differences less that 0.1%). Implementation of therdf-based approach with LAMMPS allowed to achieved results considerably faster than with the standard method, the computing time decreasing from hours to seconds for 106cells. Therdf-based approach was also faster and easier to accommodate more complex cellular models than the standard and other published methods. Finally, a comparative study of the meanScrossfor different types of configuration was carried out, as a function of the cell density and the volume size, allowing to better understand the impact of the configuration on the cross-absorbed dose.

Construction of the temporal invariants of the time-reversal operator.

This paper proposes a method to construct the temporal Green's function from a scatterer to an array of transducers in a waveguide using free-space back propagation of the eigenvectors of the time-reversal operator (TRO). The monostatic Green's function is obtained as an eigenvector of the TRO which is known with an arbitrary phase; thus the impulse response cannot be obtained by a simple inverse Fourier transform. Assuming that the monochromatic fields obtained by the back propagation of the eigenvectors are in phase at the focal point, the phase correction is determined. Simulations and laboratory experiments are presented.

Characterization of an elastic target in a shallow water waveguide by decomposition of the time-reversal operator.

This paper reports the results of an investigation into extracting of the backscattered frequency signature of a target in a waveguide. Retrieving the target signature is difficult because it is blurred by waveguide reflections and modal interference. It is shown that the decomposition of the time-reversal operator method provides a solution to this problem. Using a modal theory, this paper shows that the first singular value associated with a target is proportional to the backscattering form function. It is linked to the waveguide geometry through a factor that weakly depends on frequency as long as the target is far from the boundaries. Using the same approach, the second singular value is shown to be proportional to the second derivative of the angular form function which is a relevant parameter for target identification. Within this framework the coupling between two targets is considered. Small scale experimental studies are performed in the 3.5 MHz frequency range for 3 mm spheres in a 28 mm deep and 570 mm long waveguide and confirm the theoretical results.

Analysis of a computational problem involving complex voxel geometries.

This communication briefly summarises the results obtained from the 'International comparison on MC modeling for in vivo measurement of Americium in a knee phantom' organised within the EU Coordination Action CONRAD (Coordinated Network for Radiation Dosimetry) as a joint initiative of EURADOS working groups 6 (computational dosimetry) and 7 (internal dosimetry). Monte Carlo simulations using the knee voxel phantom proved to be a viable approach to provide the calibration factor needed for in vivo measurements.

Internal dosimetry: towards harmonisation and coordination of research.

The CONRAD Project is a Coordinated Network for Radiation Dosimetry funded by the European Commission 6th Framework Programme. The activities developed within CONRAD Work Package 5 ('Coordination of Research on Internal Dosimetry') have contributed to improve the harmonisation and reliability in the assessment of internal doses. The tasks carried out included a study of uncertainties and the refinement of the IDEAS Guidelines associated with the evaluation of doses after intakes of radionuclides. The implementation and quality assurance of new biokinetic models for dose assessment and the first attempt to develop a generic dosimetric model for DTPA therapy are important WP5 achievements. Applications of voxel phantoms and Monte Carlo simulations for the assessment of intakes from in vivo measurements were also considered. A Nuclear Emergency Monitoring Network (EUREMON) has been established for the interpretation of monitoring data after accidental or deliberate releases of radionuclides. Finally, WP5 group has worked on the update of the existing IDEAS bibliographic, internal contamination and case evaluation databases. A summary of CONRAD WP5 objectives and results is presented here.

EURADOS work on internal dosimetry.

European Radiation Dosimetry Group (EURADOS) Working Group 7 is a network on internal dosimetry that brings together researchers from more than 60 institutions in 21 countries. The work of the group is organised into task groups that focus on different aspects, such as development and implementation of biokinetic models (e.g. for diethylenetriamine penta-acetic acid decorporation therapy), individual monitoring and the dose assessment process, Monte Carlo simulations for internal dosimetry, uncertainties in internal dosimetry, and internal microdosimetry. Several intercomparison exercises and training courses have been organised. The IDEAS guidelines, which describe - based on the International Commission on Radiological Protection's (ICRP) biokinetic models and dose coefficients - a structured approach to the assessment of internal doses from monitoring data, are maintained and updated by the group. In addition, Technical Recommendations for Monitoring Individuals for Occupational Intakes of Radionuclides have been elaborated on behalf of the European Commission, DG-ENER (TECHREC Project, 2014-2016, coordinated by EURADOS). Quality assurance of the ICRP biokinetic models by calculation of retention and excretion functions for different scenarios has been performed and feedback was provided to ICRP. An uncertainty study of the recent caesium biokinetic model quantified the overall uncertainties, and identified the sensitive parameters of the model. A report with guidance on the application of ICRP biokinetic models and dose coefficients is being drafted at present. These and other examples of the group's activities, which complement the work of ICRP, are presented.

Potential of modern technologies for improving internal exposure monitoring.

Internal dosimetry is the science of assessing the amount and distribution of radionuclides in the body, and calculating resulting radiation doses to internal organs or tissues over specific time periods. Because the ionizing radiation energy deposited in a particular organ from radionuclides incorporated in the body cannot be measured directly, internal doses are estimated or inferred principally from in vivo or in vitro bioassay. As a matter of fact, in an effort to implement effective programmes in internal dosimetry, since internal dosimetry programmes exist, the internal dosimetry laboratories have always tried to develop new capabilities for these techniques or achieve the harmonisation in individual monitoring for occupational exposures. The primary goal of this paper is to categorise the principal trends made in recent developments in these fields regarding their potential and eligibility for the routine monitoring community and discuss the main aspects, which aims at a comprehensive assessment of these techniques. Secondly, starting from these data, their potential improvements are compared to the currently employed monitoring techniques used in routines.

Determination of new European biometric equations for the calibration of in vivo lung counting systems using the Livermore phantom.

New biometric equations used for assessing the thickness of the overlay plate to be added to the physical phantom were determined based on the Computed Tomography (CT) chest images of 33 adult males in order to improve the calibration of in vivo lung counting systems using the Livermore phantom. These equations are specific to systems composed of four germanium detectors with the measured subject in supine position. A comparison with the biometric equations used to date as reference in France was carried out and proved the usefulness of equations directly applicable to the Livermore phantom.

Automatic application of ICRP biokinetic models in voxel phantoms for in vivo counting and internal dose assessment.

As part of the improvement of calibration techniques of in vivo counting, the Laboratory of Internal Dose Assessment of the Institute of Radiological Protection and Nuclear Safety has developed a computer tool, 'OEDIPE', to model internal contamination, to simulate in vivo counting and to calculate internal dose. The first version of this software could model sources located in a single organ. As the distribution of the contamination evolves from the time of intake according to the biokinetics of the radionuclide, a new facility has been added to the software first to allow complex heterogeneous source modelling and then to automatically integrate the distribution of the contamination in the different tissues estimated by biokinetic calculation at any time since the intake. These new developments give the opportunity to study the influence of the biokinetics on the in vivo counting, leading to a better assessment of the calibration factors and the corresponding uncertainties.

Application of voxel phantoms in whole-body counting for the validation of calibration phantoms and the assessment of uncertainties.

This article is dedicated to the application of voxel phantoms in whole-body counting calibration. The first study was performed to validate this approach using IGOR, a physical phantom dedicated to fission and activation product (FAP) measurement, and a graphical user interface, developed at the IRSN internal dose assessment laboratory, called OEDIPE (French acronym for the tool for personalised internal dose assessment) associated with the Monte Carlo code MCNP. The method was validated by comparing the results of real measurements and simulations using voxel phantoms obtained from CT scan images of IGOR. To take this application further, two studies were carried out and are presented in this article. First, a comparison was made between the IGOR voxel based phantom (IGOVOX) and a voxel human body (Zubal Phantom) to confirm whether IGOR could be considered as a realistic representation of a human. Second, the errors made when considering sources homogeneously distributed in the body were assessed against real contamination by taking into account the biokinetic behaviour of the radioactive material for two modes of exposure: the ingestion of 137Cs in soluble form and the inhalation of insoluble 60Co several days after acute incorporation.

OEDIPE: a new graphical user interface for fast construction of numerical phantoms and MCNP calculations.

Although great efforts have been made to improve the physical phantoms used to calibrate in vivo measurement systems, these phantoms represent a single average counting geometry and usually contain a uniform distribution of the radionuclide over the tissue substitute. As a matter of fact, significant corrections must be made to phantom-based calibration factors in order to obtain absolute calibration efficiencies applicable to a given individual. The importance of these corrections is particularly crucial when considering in vivo measurements of low energy photons emitted by radionuclides deposited in the lung such as actinides. Thus, it was desirable to develop a method for calibrating in vivo measurement systems that is more sensitive to these types of variability. Previous works have demonstrated the possibility of such a calibration using the Monte Carlo technique. Our research programme extended such investigations to the reconstruction of numerical anthropomorphic phantoms based on personal physiological data obtained by computed tomography. New procedures based on a new graphical user interface (GUI) for development of computational phantoms for Monte Carlo calculations and data analysis are being developed to take advantage of recent progress in image-processing codes. This paper presents the principal features of this new GUI. Results of calculations and comparison with experimental data are also presented and discussed in this work.

Estimation of the uncertainty in internal dose calculation for two contamination cases.

The assessment of internal dose is subject to a large uncertainty due to the limits of measuring technique and to the assumptions made by the expert. Here, we propose an approach to report the confidence interval associated with the evaluated dose. The sources of uncertainties considered so far include the date of intake, the physico-chemical characteristics of the radioactive material, the counting error and the stochastic variability of excretion. Three successive levels of approximation are suggested, depending on the expected dose, for which increasingly realistic parameter values should be sought and applied. Finally, the results of a Monte Carlo dose calculation are presented in the form of a statistical distribution of possible dose values. This approach has been applied to two cases of uranium and caesium exposure.

Potential of modern technologies for improvement of in vivo calibration.

In the frame of IDEA project, a research programme has been carried out to study the potential of the reconstruction of numerical anthropomorphic phantoms based on personal physiological data obtained by computed tomography (CT) and Magnetic Resonance Imaging (MRI) for calibration in in vivo monitoring. As a result, new procedures have been developed taking advantage of recent progress in image processing codes that allow, after scanning and rapidly reconstructing a realistic voxel phantom, to convert the whole measurement geometry into computer file to be used on line for MCNP (Monte Carlo N-Particule code) calculations. The present paper overviews the major abilities of the OEDIPE software studies made in the frame of the IDEA project, on the examples of calibration for lung monitoring as well as whole body counting of a real patient.

Improvements in routine internal monitoring--an overview of the IDEA project.

The IDEA project aimed to improve the assessment of incorporated radionuclides through developments of advanced in vivo and bioassay monitoring techniques and making use of such enhancements for improvements in routine monitoring. Many of these findings are not new in the sense that they are being already employed in advanced laboratories or for specialised applications. The primary goal was to categorise those new developments regarding their potential and eligibility for the routine monitoring community. Attention has been given to in vivo monitoring techniques with respect to detector characteristics and measurement geometry to improve measurement efficiency with special attention to low energy gamma emitters. Calibration-specifically supported by or through methods of numerical simulation-have been carefully analysed to reduce overall measurement uncertainties and explore ways to accommodate the individual variability based on characteristic features of a given person. For bioassay measurements at low detection limits, inductively coupled plasma mass spectroscopy offers significant advantages both in accuracy, speed, and sample preparation. Specifically, the determination of U and Th in urine and the associated models have been investigated. Finally, the scientific achievements have been analysed regarding their potential to offer benefits for routine monitoring. These findings will be presented in greater detail in other papers at this conference, whereas this paper intends to give an overview and put both the scientific achievements as well as the derived benefits into perspective.