OBJECTIVE: Evaluation of equipment conditions and dosimetry in computed tomography services utilizing protocols for head, abdomen, and lumbar spine in adult patients (in three different units) and pediatric patients up to 18 months of age (in one of the units evaluated). MATERIALS AND METHODS: Computed tomography dose index and multiple-scan average dose were estimated in studies of adult patients with three different units. Additionally, entrance surface doses as well as absorbed dose were estimated in head studies for both adult and pediatric patients in a single computed tomography unit. RESULTS: Mechanical quality control tests were performed, demonstrating that computed tomography units comply with the equipment-use specifications established by the current standards. Dosimetry results have demonstrated that the multiple-scan average dose values were in excess of up to 109.0% the reference levels, presenting considerable variation amongst the computed tomography units evaluated in the present study. Absorbed doses obtained with pediatric protocols are lower than those with adult patients, presenting a reduction of up to 51.0% in the thyroid gland. CONCLUSION: The present study has analyzed the operational conditions of three computed tomography units, establishing which parameters should be set for the deployment of a quality control program in the institutions where this study was developed.

Keywords: Computed tomography equipment, Quality control, Dosimetry, Dose reduction

OBJECTIVE: The present study was aimed at evaluating the frequency of radiographic assessment of paranasal sinuses in pediatric patients in hospitals of Belo Horizonte, MG, Brazil. Additionally, aspects regarding radiation protection conditions and radiographic parameters were evaluated, and entrance air kerma and organ doses were estimated. MATERIALS AND METHODS: Patients' data and parameters of radiographic technique employed in the assessment of children in the age range between 1 and 16 years were collected in five examination rooms of four hospitals in Belo Horizonte, also taking into consideration the radiation protection aspects. Entrance air kerma calculation was based on the x-ray tubes output, and organ doses were estimated with the PCXMC software. RESULTS: Mean entrance air kerma values found in the five rooms were, respectively, 1398 µGy, 829 µGy, 877 µGy, 1168 µGy and 3886 µGy for patients with ages between 1 and 5 years. CONCLUSION: Most frequently, mento-naso and fronto-naso views are requested in conjunction in the majority of hospitals, which increases the radiation dose to the patients. It may be concluded that the risks for patients can be reduced by means of the utilization of an appropriate x-ray field, non-utilization of antiscattering grids, selection of high voltages and lower exposure times.

Keywords: Pediatric radiology, Patient dose, Organ dose

OBJECTIVE: To present the solidly established traceability structure for ionometric standards and for thermoluminescent dosimetry system that ensures reliability of the Dosimetry Quality Assurance Program and is aimed to certify the highest level of accuracy of the measurements. MATERIALS AND METHODS: Thermoluminescent powder dosimeters (DTL 937) placed into plastic capsules and packed in specific kits for each intended application were mailed to the participant centers. RESULTS: The results of the intercomparisons performed between "Laboratório de Ciências Radiológicas da Universidade do Estado do Rio de Janeiro" and EQUAL-ESTRO for the beam of 60Co gamma rays, expressed for (1sigma), and the results of the dose absorbed measurements obtained with the chambers of the Program EQUAL and the chambers of the Dosimetry Quality Assurance Program were lower than 0.5%. CONCLUSION: Based on these results we concluded that the Dosimetry Quality Assurance Program reached the desired level of reliability to allow its implementation.

Keywords: Quality assurance, Radiotherapy, Dosimetric intercomparison, Thermoluminescent dosimetry, TLD

OBJECTIVE: To compare radiological techniques used in Brazil and in Australia, and to evaluate radiation doses of the most common x-ray procedures. MATERIALS AND METHODS: The entrance skin dose (ESD) and the effective dose (ED) were obtained with the software DoseCal. In both countries the study was conducted in large public hospitals. Four distinct procedures were evaluated: chest, abdomen, pelvis and thoracic spine in three views (anterior-posterior, posterior-anterior and lateral) In Australia, all x-ray equipment are digital and linked with PACS whereas in Brazil conventional equipment is used. RESULTS: The mean values of ESD and ED were consistently higher in Brazil, except for chest x-rays. The higher differences were seen in pelvis (26 fold higher in Brazil) and thoracic spine (43 fold higher in Brazil) radiographs. CONCLUSION: All Australian hospitals have quality assurance programs (QAP) implemented on a permanent basis, the most advanced digital equipment and count with an effective medical physics service. These factors are determinant for high quality images, low rejection rates and low doses imparted to patients when compared to Brazilian standards. Theses results reinforce the need of implementation of quality assurance programs in Brazil. However, when analyzing the results of ESD for chest x-rays, we concluded that low doses can also be achieved in Brazil with the use of appropriate x-ray techniques.

Keywords: Entrance skin dose, Radiodiagnosis, Effective dose, Dosimetry

We analyzed the dose area product (DAP) of 12 patients submitted to videofluoroscopic swallowing studies. The aim of this study was to establish, in a preliminary manner, the values of radiation exposure for patients submitted to this type of examination. A Diamentor equipment was used to register the cumulative radiation doses emitted by the x-ray tubes. Two different rooms with identical radiological equipment were used to collect the data. The protocol used was rigorously the same and the same experienced professional performed the examinations. DAP's values for the three phases (oral, pharyngeal and esophagogastric) of the videofluoroscopic swallowing study were, for the room A (7 patients), 4,101 cGy.cm², DAP/min. = 577 cGy.cm²/min., and for the room B (5 patients), 804 cGy.cm², DAP/min = 119 cGy.cm²/min. These different results were obtained from patients of the same height and weight, using the same examination time (around 7 minutes) for all patients. We concluded that the data showing doses five times lower in room B are more reliable that those obtained for room A and that DAP and DAP/min. are good elements to inform patient doses imparted by videofluoroscopic swallowing examination. We believe that the high dose differences observed between the two groups are due to lack of calibration of the x-ray equipment, since unfortunately "quality assurance programs" are not routinely implemented.

Keywords: Dosimetry, Videofluoroscopy, Dose area product (DAP), Swallowing

OBJECTIVE: The aim of this work is to discuss the effects of the main parameters that influence image quality and the entrance skin dose. MATERIALS AND METHODS: The pediatric chest radiographs of three different Institutions were evaluated. Tests on all x-ray equipment were performed. The skin entrance dose was assessed using thermoluminescent dosimeters. RESULTS: Only one of all x-ray equipments tested was in good operation condition. The average skin entrance dose was: (0.222 ± 0.088) mGy for children under 1 year, (0.28 ± 0.11) mGy for 1.1 to 4 years, (0.26 ± 0.13) mGy for 4.1 to 6 years, (0.23 ± 0.13) mGy for 6.1 to 10 years and (0.26 ± 0.25) mGy for older than 10 years. CONCLUSION: The results showed that the average skin entrance doses are higher than the European Community Commission reference levels and other values reported in the literature. We recommend the implantation of quality assurance programs to reduce skin entrance doses and for obtaining good quality images.

Keywords: Pediatric radiology, Skin dose, Reference levels

The authors report a case of a patient with an extensive angiosarcoma of the scalp that was submitted only to radiotherapy with a combination of orthovoltage roentgentherapy and high-dose rate brachytherapy, using a mould. The clinical and technical features as well as the therapeutic outcome are presented, and the usefulness and peculiarities of high-dose rate brachytherapy for this particular indication is discussed. A comparative analysis of the difficulties and limitations of employing low-dose rate brachytherapy is also presented. The authors concluded that high-dose rate brachytherapy might be an useful, practical and safe option to treat neoplastic lesions of the scalp, and an alternative treatment to electrontherapy.

Keywords: High-dose rate brachytherapy, Mould, Scalp angiosarcoma

High dose rate brachytherapy has been increasingly recognized in most countries, and radiotherapy services using this equipment are encouraged to have a very efficient quality assurance program to ensure protection for patients, workers and other personnel involved. The objective of this paper was to determine the types of tests for high dose rate equipment required by official protocols (TG40, TG56 and ARCAL XXX) and to compare them with the types of tests utilized by some radiotherapy services. We concluded that: a) the protocol TG56 is more extensive and complete than the other official protocols (TG40 and ARCAL XXX); b) the protocols used by the services evaluated on this study were based on the protocol TG56, and were concordant with the other official protocols. In these protocols annual tests were frequently replaced by tests performed quarterly or twice a year. This study established the types of test used and their frequency of utilization, and permitted the design of an optimized protocol that may help in the implementation of basic and indispensable tests in order to ensure patient adequate treatment and safety to personnel involved, and consequently improve high dose rate brachytherapy quality assurance

Keywords: Dosimetry. Brachytherapy. High dose rate brachytherapy (HDR). Quality control

Human mistakes are an important source of errors in radiotherapy and may occur at every step of the radiotherapeutic planning and treatment. To reduce this level of uncertainties, several specialized organizations have recommended a comprehensive quality assurance program. In Brazil, the requirement for these programs has been strongly stressed, and most radiotherapy services have pursued this goal regarding radiation units and dosimetry equipment, as well as the verification of the calculations of the patient's dose and the revision of the plan charts. As a contribution to the improvement of quality control, we present some recommendations to avoid failure of treatment due to error in the delivered dose, such as redundant check of the manual or computer calculations, weekly check of the total dose for each patient, and prevention of inadvertent access to any safety system of the equipment by any staff member that is only supposed to operate the machine. Moreover, the use of a computerized treatment record and verification system should be considered in order to eliminate errors due to incorrect selection of the treatment parameters, in a daily basis. We report four radioactive incidents with patient injuries occurred throughout the world and some gross errors of dose.

Keywords: Radiotherapy. Treatment. Dose errors. Quality assurance.

OBJECTIVE: The present study proposes the evaluation of the depth-dose profiles and the spatial distribution of radiation dose for ocular proton beam radiotherapy protocols, based on computer simulations in nuclear codes and an eye model discretized into voxels. MATERIALS AND METHODS: The employed computational tools were Geant4 (GEometry ANd Tracking) Toolkit and SISCODES (Sistema Computacional para Dosimetria em Radioterapia - Computer System for Dosimetry in Radiotherapy). Geant4 is a toolkit for simulating the passage of particles through the matter, based on Monte Carlo method. Computer simulations of proton therapy were performed based on preexisting facilities. RESULTS: Simulation data were integrated into SISCODES on the eye's model generating spatial dose distributions. Dose depth profiles reproducing the pure and modulated Bragg peaks are presented. Relevant aspects of proton beam radiotherapy planning are considered such as material absorber, modulation, collimator dimensions, incident proton energy and isodose generation. CONCLUSION: The conclusion is that proton therapy when properly modulated and directed can reproduce the ideal conditions for the dose deposition in the treatment of ocular tumors.

Keywords: Proton therapy; Geant4; SISCODES; Ocular radiotherapy; Protons.

Objective: The present paper describes a procedure for conversion of computed tomography or magnetic resonance images into a three-dimensional voxel model for dosimetry purposes. Such model is a personalized representation of the patient that can be utilized in nuclear particle transport simulations by means of the MCNP (Monte Carlo N-Particle) code, reproducing the stochastic process of nuclear particles interaction with human tissues. Materials and Methods: The developed computational system – SISCODES – is a tool designed for 3D planning of radiotherapy or radiological procedures. Based on tomographic images of the patient, the treatment plan is modeled and simulated. Then, the absorbed doses are shown by means of isodose curves superimposed on the model. The SISCODES couples the threedimensional model with the MCNP5 code, simulating the protocol of exposure to ionizing radiation. Results: The SISCODES has been utilized by the NRI/CNPq in the creation of anthropomorphic and anthropometric voxel models which are coupled with the MCNP code for modeling brachytherapy and teletherapy applied to lung, pelvis, spine, head and neck tumors, among others. The current SISCODES modules are presented together with examples of cases of radiotherapy planning. Conclusion: The SISCODES provides a fast method to create personalized voxel models of any patient which can be used in stochastic simulations. The combination of the MCNP simulation with a personalized model of the patient increases the dosimetry accuracy in radiotherapy.

Keywords: SISCODES; Radiotherapy; Dosimetry; Absorbed dose; Teletherapy; Brachytherapy.

Objective: The present paper addresses the dosimetric evaluation of carbon ion radiotherapy as compared with proton therapy. Materials and Methods: Computer simulations were undertaken with the Geant4 (GEometry ANd Tracking) code. An eye model discretized into voxels and implemented in the Siscodes system (computer system for dosimetry in radiation therapy) was utilized to generate and superimpose depth dose profiles and isodose curves. Different values for beam energy were adopted in the simulations of carbon ion beams, while in the simulation with proton beams irradiation line devices were included with different absorbing material thicknesses. Results: The simulations outputs were processed and integrated into the Siscodes to generate the spatial dose distribution in the eye model, considering changes in the beam entrance position. The dose rates were normalized as a function of the maximum dose for a beam at a specific entrance position, incident particle energy and number of incident carbon ions and protons. Conclusion: The described benefits together with the presented results contribute to the development of clinical applications and researches on carbon ion and proton therapy.

Keywords: Carbon ion therapy; Proton therapy; Geant4; Siscodes.

OBJECTIVE: The present paper is aimed at presenting a comparative dosimetric study of prostate brachytherapy with I-125 and Pd-103 seeds. MATERIALS AND METHODS: A protocol for both implants with 148 seeds was simulated on a heterogeneous three-dimensional pelvic phantom by means of the SISCODES/MCNP5 codes. Dose-volume histograms on prostate, rectum and bladder, dose indexes D₁₀, D₃₀, D₉₀, D_0.5cc, D_2cc and D_7cc, and representations of the spatial dose distribution were evaluated. RESULTS: For a D₉₀ index equivalent to the prescription dose, the initial activity of each I-125 seed was calculated as 0.42 mCi and of Pd-103 as 0.94 mCi. The maximum dose on the uretra was 90% and 108% of the prescription dose for I-125 and Pd-103, respectively. The D_2cc for I-125 was 30 Gy on the rectum and 127 Gy on the bladder; for Pd-103 was 29 Gy on the rectum and 189 Gy on the bladder. The D₁₀ on the pubic bone was 144 Gy for I-125 and 66 Gy for Pd-103. CONCLUSION: The results indicate that Pd-103 and I-125 implants could deposit the prescribed dose on the target volume. Among the findings of the present study, there is an excessive radiation exposure of the pelvic bones, particularly with the I-125 protocol.

Keywords: Radiotherapy; Dosimetry; Prostate cancer; Brachytherapy; SISCODES; MCNP.

OBJECTIVE: Aiming at contributing to the knowledge on doses in computed tomography (CT), this study has the objective of determining dosimetric quantities associated with pediatric abdominal CT scans, comparing the data with diagnostic reference levels (DRL). MATERIALS AND METHODS: The study was developed with a Toshiba Asteion single-slice CT scanner and a GE BrightSpeed multi-slice CT unit in two hospitals. Measurements were performed with a pencil-type ionization chamber and a 16 cm-diameter polymethylmethacrylate trunk phantom. RESULTS: No significant difference was observed in the values for weighted air kerma index (C_W), but the differences were relevant in values for volumetric air kerma index (C_VOL), air kerma-length product (P_KL,CT) and effective dose. CONCLUSION: Only the C_W values were lower than the DRL, suggesting that dose optimization might not be necessary. However, P_KL,CT and effective dose values stressed that there still is room for reducing pediatric radiation doses. The present study emphasizes the importance of determining all dosimetric quantities associated with CT scans.

Keywords: Pediatric computed tomography scans; Dosimetric quantities; Weighted dose index; Volumetric air kerma index; Air kermalength product.

OBJECTIVE: In the present study, the authors investigated the in vitro behavior of radio-resistant breast adenocarcinoma (MDA-MB-231) cells line and radiosensitive peripheral blood mononuclear cells (PBMC), as a function of different radiation doses, dose rates and post-irradiation time kinetics, with a view to the interest of clinical radiotherapy. MATERIALS AND METHODS: The cells were irradiated with Co-60, at 2 and 10 Gy and two different exposure rates, 339.56 cGy.min^-1 and the other corresponding to one fourth of the standard dose rates, present over a 10-year period of cobalt therapy. Post-irradiation sampling was performed at pre-established kinetics of 24, 48 and 72 hours. The optical density response in viability assay was evaluated and a morphological analysis was performed. RESULTS: Radiosensitive PBMC showed decrease in viability at 2 Gy, and a more significant decrease at 10 Gy for both dose rates. MDA-MB-231 cells presented viability decrease only at higher dose and dose rate. The results showed MDA-MB-231 clone expansion at low dose rate after 48-72 hours post-radiation. CONCLUSION: Low dose rate shows a possible potential clinical impact involving decrease in management of radio-resistant and radiosensitive tumor cell lines in cobalt therapy for breast cancer.

Keywords: Radiation; MDA-MB-231; PBMC; LET; Dose; Dose rate.