OBJECTIVE: The present study evaluated the doses received by companions who had shared therapeutic rooms with patients undergoing treatment with 131-iodine (131I). The results were compared with the limits established by the Brazilian radiation protection regulatory standard. MATERIALS AND METHODS: Six pairs of persons (a patient and a companion sharing a same therapeutic room) were evaluated. Still, other 23 experiments were accomplished with a phantom replacing the companion. The therapeutic 131I activities given to the patients corresponded to 3700 MBq or 5550 MBq. Powdered lithium fluoride thermoluminescent dosimeters doped with magnesium, titanium and sodium were utilized for evaluating the doses. RESULTS: The results demonstrate that a person sharing a same therapeutic room, for two days, with a patient who had been given 3700 MBq or 5550 MBq of 131I, according to radioprotection recommendations, is exposed to a mean dose of (0.51 ± 0.02) mSv for a 99% confidence level. CONCLUSION: According to the Brazilian radiation protection standards there is no impediment for a person to accompany a nuclear medicine patient who has been given 3700 MBq or 5550 MBq of 131I during the patient stay in the therapeutic room.

Keywords: Nuclear medicine, Companion, Therapeutic room, Thermoluminescent dosimeter

OBJECTIVE: To perform a survey on routine quality control tests of dose calibrators at nuclear medicine units in the city of São Paulo, SP, Brazil. To evaluate the accuracy of measurements of seven dose calibrators activities, utilizing sources of clinically significant radionuclides at the calibration laboratory of Instituto de Pesquisas Energéticas e Nucleares. MATERIALS AND METHODS: The survey on quality control of dose calibrators has been based on questionnaires answered by the nuclear medicine units. Seven dose calibrators, Ga-67, Tc-99m and Tl-201 sources and a secondary standard instrument have been utilized in the accuracy study. RESULTS: The survey results on the quality control tests of the dose calibrators showed some inappropriateness, for example, the absence of daily reproducibility tests in all of the units. The accuracy tests for the seven dose calibrators showed results within the acceptable limit in compliance with the national regulations (±10%). CONCLUSION: According to the few nuclear medicine units participating in the survey, the dose calibrators quality control is unsatisfactory. The accuracy study of seven dose calibrators has not demonstrated any performance faults, and has established the calibration of these instruments for the utilized sources.

Keywords: Nuclear medicine, Dose calibrators, Calibration, Quality control

OBJECTIVE: To assess the performance of radionuclide calibrators in 55 Brazilian nuclear medicine services in the measurement of 99Tc m radiopharmaceutical activity. Proficiency tests were applied to data sets with 63 results originated from the comparison program developed by Laboratório Nacional de Metrologia das Radiações Ionizantes of Instituto de Radioproteção e Dosimetria. MATERIALS AND METHODS: The calibrators' performance was evaluated in compliance with the acceptance criterion of ±10% accuracy required by the Brazilian standards and also the criteria established by the ISO/IEC Guide 43-1, and classified as either "acceptable" or "non-acceptable". The samples of 99Tc m utilized in the comparison were supplied by some of the participants and calibrated at Laboratório Nacional de Metrologia das Radiações Ionizantes for determining the activity reference value. RESULTS: The present study utilizing 99Tc m has shown that 82.5% of the calibrators were considered as acceptable according to the Brazilian standards, while by the criteria established by ISO/IEC 43-1, 81.0% were considered as acceptable. On the other hand, radionuclide calibrators with Geiger-Müller detectors presented unsatisfactory performance when compared with calibrators with ionization chambers. CONCLUSION: The performance evaluation based on the ISO/IEC 43-1 criteria, which are applied to analytical laboratories, in spite of being more restrictive, has demonstrated to be quite consistent with the accuracy criterion established by the Brazilian standard.

Keywords: Proficiency test, Radionuclide calibrator, Nuclear medicine, 99Tc m

OBJECTIVE: To develop an atlas of myocardial perfusion scintigraphy and evaluating its applicability in computer-aided detection of myocardial perfusion defects in patients with ischemic heart disease. MATERIALS AND METHODS: The atlas was created with rest-stress myocardial perfusion scintigraphic images of 20 patients of both genders with low probability of coronary artery disease and considered as normal by two experienced observers. Techniques of image registration and mathematical operations on images were utilized for obtaining template images depicting mean myocardial uptake and standard deviation for each gender and physiological condition. RESULTS: Myocardial perfusion scintigraphy images of one male and one female patient were aligned with the corresponding atlas template image, and voxels with myocardial uptake rates two standard deviations below the mean voxel value of the respective region in the atlas template image were highlighted on the tomographic sections and confirmed as perfusion defects by both observers. CONCLUSION: The present study demonstrated the creation of an atlas of myocardial perfusion scintigraphy with promising results of this tool as an aid in the detection of myocardial perfusion defects. However, further prospective validation with a more representative sample is recommended.

Keywords: Scintigraphy, SPECT, Myocardium, Nuclear medicine, Computer-assisted image processing, Computer-assisted diagnosis

The main objective of this study is to implement an impartial and efficient inspection method for a correct and secure use of ionizing radiation in nuclear medicine. The radiological protection model was tested in 113 nuclear medicine services (NMS) all over Brazil, following a biannual analysis schedule (1996, 1998, 2000 and 2002). In the analytical process, we adopted the methodology of assigning different importance levels to each of 82 features, based on the risk factors established by the "Comissão Nacional de Energia Nuclear" (CNEN) and on the International Atomic Energy Agency (IAEA) recommendations. A feature was considered a radioprotection fault when in nonconformity with the rules mentioned above, and was imparted a grade. The sum of those grades, classified the NMS in one of the three different ranges, as follows: operating without restriction - 100 points and below; operating with restriction - between 100 and 300 points; temporary shutdown - above 300 points. Permission for the second group to carry on operation should be attached to a defined and restricted period of time (6 to 12 months), considered enough for the NMS to solve the problems and submit to a new evaluation. The NMS's classified in the third group are supposed to go back into operation only after compliance with all the pending radioprotection requirements. Until the next regular evaluation, a multiplication factor 2n was applied to the recalcitrant NMS's, where n is the number of unwilling occurrences. The previous establishment of those items of radioprotection, with their respective grades, excluded subjective and personal values in the judgement and technical evaluation of the institutions.

Keywords: Nuclear medicine, Radiation protection, Rules, Inspection

OBJECTIVE: The aim of this work was to establish a working standard for intercomparison and calibration of dose calibrators used in most of nuclear medicine facilities for the determination of the activity of radionuclides administered to patients in specific examinations or therapeutic procedures. MATERIALS AND METHODS: A commercial dose calibrator, a set of standard radioactive sources, and syringes, vials and ampoules with radionuclide solutions used in nuclear medicine were utilized in this work. RESULTS: The commercial dose calibrator was calibrated for radionuclide solutions used in nuclear medicine. Simple instrument tests, such as linearity response and variation response with the source volume at a constant source activity concentration were performed. CONCLUSION: This instrument may be used as a reference system for intercomparison and calibration of other activity meters, as a method of quality control of dose calibrators utilized in nuclear medicine facilities.

Keywords: Nuclear medicine, Dose calibrator, Working standard, Intercomparison, Calibration, Quality control

Clinical examination alone is not sufficient to precisely evaluate lymph node involvement in head and neck cancer. The results of computed tomography of the neck and lymphoscintigraphy were evaluated in 21 patients with carcinoma of the mouth and oropharynx staged N0. Nine patients were treated by homolateral and 12 by bilateral neck dissection. Sensitivity and specificity of computed tomography were 16% and 73% for homolateral side and 0% and 90% for contralateral side, respectively. Lymphatic drainage was observed in 76.2% of the cases. No-migration was associated with cases involving the retromolar region and tonsillar fossa, where injection of the 99mTc-Dextran 500 is more difficult. Bilateral migration occurred only in carcinomas of the floor of the mouth, with involvement of the midline. From these results it was concluded that computed tomography was less efficient than clinical examination. Nevertheless, it must be considered that conventional computed tomography was used. We are currently undertaking similar studies with helical computed tomography. Lymphoscintigraphy showed promising results, and the same method to evaluate sentinel lymph nodes in patients with carcinoma of the mouth is being used.

Keywords: Scintigraphy, Nuclear medicine, Computed tomography

Objective: The present study was aimed at determining the acceptability of a national or regional phantoms bank to be deployed in Brazil for shared use in quality control activities by nuclear medicine centers. Materials and Methods: The authors analyzed the answers to a questionnaire applied to medical physicists and radioprotection supervisors in Brazilian nuclear medicine centers. Initially, the questionnaire was validated by professionals in the city of Aracaju, SE, which is located in the Northeast region. The present study sample was geographically distributed as follows: the Northeast region, with answers from 13 professionals of nuclear medicine centers; the North region, with 2 professionals; the South region, with 7 professionals; the Southeast region, with 43 professionals; and the Midwest region, with 2 professionals. Results: According to the data analyzed, 82% of the respondents consider that the implementation of a phantoms bank would be a suitable alternative for improving nuclear medicine quality control. The interest in sharing the bank was reported by 87% of the respondents. Conclusion: The present study demonstrated the motivation for a shared use of a future phantoms bank.

Keywords: Nuclear medicine; Quality control; Phantom.

Objective: To validate the proposal for development of a virtual collaborative environment for training of nuclear medicine personnel. Materials and Methods: Organizational assumptions, constraints and functionalities that should be offered to the professionals in this field were raised early in the development of the environment. The prototype was developed in the Moodle environment, including data storage and interaction functionalities. A pilot interaction study was developed with a sample of specialists in nuclear medicine. Users’ opinions collected by means of semi-structured questionnaire were submitted to quantitative and content analysis. Results: The proposal of a collaborative environment was validated by a community of nuclear medicine professionals and considered as an aid in the training in this field. Suggestions for improvements and new functionalities were made. There is a need to establish a program for education of moderators specifically for this environment, considering the different interaction characteristics as the online and conventional teaching methods are compared. Conclusion: The collaborative environment will allow the exchange of experiences and case discussions among professionals from institutions located in different regions all over the country, enhancing the collaboration among them. Thus, the environment can contribute in the early and continued education of nuclear medicine professionals.

Keywords: Collaborative environment; Nuclear medicine; Medical education; Distance education.

OBJECTIVE: To determine correction factors for the variation in volume of radiopharmaceuticals in containers of different geometries, comparing the influence of such factors on the determination of ^99mTc and ¹²³I activity with two types of calibrators – one with ionization chamber and another with Geiger-Müller (G-M) detector –; and to evaluate calibrators performance in the measurement of ^99mTc and ¹²³I activities. MATERIALS AND METHODS: Eight calibrators, 10R glass vials, 3 and 5 mL plastic syringes and ^99mTc and ¹²³I solutions were utilized. The correction factors were determined with basis on practical measurements of the variation in the calibrators' response according to the volume of radionuclide solution in the glass vials. The performance was evaluated according to the acceptance criterion of ±10% accuracy required by the Brazilian standard. RESULTS: The variation of the calibrators' response according to the variation in radionuclide volume was reasonably greater in the calibrator with G-M detector. It was also greater for ¹²³I than for ^99mTc. CONCLUSION: The results confirm that the calibrators' response depends on the radionuclide volume contained in the vials. Such dependence is more critical for the calibrators equipped with G-M detector and for ¹²³I as compared with ^99mTc.

Keywords: Radionuclides calibrator; Nuclear medicine; Activity; Tc-99m; I-123.

OBJECTIVE: To investigate the outpatient access to nuclear medicine procedures by means of the Brazilian Unified Health System (SUS), analyzing the correspondence between data provided by this system and those from Comissão Nacional de Energia Nuclear (CNEN) (National Commission of Nuclear Energy). MATERIALS AND METHODS: Data provided by Datasus regarding number of scintillation chambers, outpatient procedures performed from 2008 to 2012, administrative responsibility for such procedures, type of service providers and outsourced services were retrieved and evaluated. Also, such data were compared with those from institutions certified by CNEN. RESULTS: The present study demonstrated that the system still lacks maturity in terms of correct data input, particularly regarding equipment available. It was possible to list the most common procedures and check the growth of the specialty along the study period. Private centers are responsible for most of the procedures covered and reimbursed by SUS. However, many healthcare facilities are not certified by CNEN. CONCLUSION: Datasus provides relevant data for analysis as done in the present study, although some issues still require attention. The present study has quantitatively depicted the Brazilian reality regarding access to nuclear medicine procedures offered by/for SUS.

Keywords: SUS; Nuclear medicine; Gamma camera.

OBJECTIVE: This article presents a way to obtain estimates of dose in patients submitted to radiotherapy with basis on the analysis of regions of interest on nuclear medicine images. MATERIALS AND METHODS: A software called DoRadIo (Dosimetria das Radiações Ionizantes [Ionizing Radiation Dosimetry]) was developed to receive information about source organs and target organs, generating graphical and numerical results. The nuclear medicine images utilized in the present study were obtained from catalogs provided by medical physicists. The simulations were performed with computational exposure models consisting of voxel phantoms coupled with the Monte Carlo EGSnrc code. The software was developed with the Microsoft Visual Studio 2010 Service Pack and the project template Windows Presentation Foundation for C# programming language. RESULTS: With the mentioned tools, the authors obtained the file for optimization of Monte Carlo simulations using the EGSnrc; organization and compaction of dosimetry results with all radioactive sources; selection of regions of interest; evaluation of grayscale intensity in regions of interest; the file of weighted sources; and, finally, all the charts and numerical results. CONCLUSION: The user interface may be adapted for use in clinical nuclear medicine as a computer-aided tool to estimate the administered activity.

Keywords: Nuclear medicine; Biokinetic distribution; Dosimetric evaluations; Administered activity.

OBJECTIVE: The present study was aimed at evaluating the viability of replacing ¹⁸F with ^99mTc in dose calibrator linearity testing. MATERIALS AND METHODS: The test was performed with sources of ^99mTc (62 GBq) and ¹⁸F (12 GBq) whose activities were measured up to values lower than 1 MBq. Ratios and deviations between experimental and theoretical ^99mTc and ¹⁸F sources activities were calculated and subsequently compared. RESULTS: Mean deviations between experimental and theoretical ^99mTc and ¹⁸F sources activities were 0.56 (± 1.79)% and 0.92 (± 1.19)%, respectively. The mean ratio between activities indicated by the device for the ^99mTc source as measured with the equipment pre-calibrated to measure ^99mTc and ¹⁸F was 3.42 (± 0.06), and for the ¹⁸F source this ratio was 3.39 (± 0.05), values considered constant over the measurement time. CONCLUSION: The results of the linearity test using ^99mTc were compatible with those obtained with the ¹⁸F source, indicating the viability of utilizing both radioisotopes in dose calibrator linearity testing. Such information in association with the high potential of radiation exposure and costs involved in ¹⁸F acquisition suggest ^99mTc as the element of choice to perform dose calibrator linearity tests in centers that use ¹⁸F, without any detriment to the procedure as well as to the quality of the nuclear medicine service.

Keywords: Nuclear medicine; Dose calibrator; Linearity test; Nuclear instrumentation.

OBJECTIVE: The present study is aimed at contributing to identify the most appropriate OSEM parameters to generate myocardial perfusion imaging reconstructions with the best diagnostic quality, correlating them with patients' body mass index. MATERIALS AND METHODS: The present study included 28 adult patients submitted to myocardial perfusion imaging in a public hospital. The OSEM method was utilized in the images reconstruction with six different combinations of iterations and subsets numbers. The images were analyzed by nuclear cardiology specialists taking their diagnostic value into consideration and indicating the most appropriate images in terms of diagnostic quality. RESULTS: An overall scoring analysis demonstrated that the combination of four iterations and four subsets has generated the most appropriate images in terms of diagnostic quality for all the classes of body mass index; however, the role played by the combination of six iterations and four subsets is highlighted in relation to the higher body mass index classes. CONCLUSION: The use of optimized parameters seems to play a relevant role in the generation of images with better diagnostic quality, ensuring the diagnosis and consequential appropriate and effective treatment for the patient.

Keywords: Nuclear cardiology; Myocardial perfusion imaging; Iterative methods; Image reconstruction; Nuclear medicine.

OBJECTIVE: To evaluate the maximum and mean standardized uptake values, together with the metabolic tumor value and the total lesion glycolysis, at the primary tumor site, as determined by ¹⁸F-fluorodeoxyglucose positron-emission tomography/computed tomography (¹⁸F-FDG-PET/CT), performed before and after neoadjuvant chemoradiotherapy (nCRT), as predictors of residual disease (RD) in patients with esophageal cancer. MATERIALS AND METHODS: The standardized uptake values and the volumetric parameters (metabolic tumor value and total lesion glycolysis) were determined by ¹⁸F-FDG-PET/CT to identify RD in 39 patients before and after nCRT for esophageal carcinoma. We used receiver operating characteristic curves to analyze the diagnostic performance of ¹⁸F-FDG-PET/CT parameters in the definition of RD. The standard of reference was histopathological analysis of the surgical specimen. RESULTS: Eighteen patients (46%) presented RD after nCRT. Statistically significant areas under the curve (approximately 0.72) for predicting RD were obtained for all four of the variables evaluated after nCRT. Considering the presence of visually detectable uptake (higher than the background level) at the primary tumor site after nCRT as a positive result, we achieved a sensitivity of 94% and a specificity of 48% for the detection of RD. CONCLUSION: The use of ¹⁸F-FDG-PET/CT can facilitate the detection of RD after nCRT in patients with esophageal cancer.

Keywords: Esophageal neoplasms; Neoadjuvant therapy; Positron-emission tomography; Nuclear medicine.