OBJECTIVE: To evaluate, by means of magnetic resonance imaging, the standardized field borders in radiotherapy for malignant neoplasm of uterine cervix, and to determine the role of this method in the reduction of possible planning errors related to the conventional technique. MATERIALS AND METHODS: Magnetic resonance imaging studies for planning of treatment of 51 patients with uterine cervix cancer were retrospectively analyzed. The parameters assessed were the anterior and posterior field borders on sagittal section. RESULTS: The anterior field border was inappropriate in 20 (39.2%) patients and geographic miss was observed in 37.3% of cases in the posterior border. The inappropriateness of both field borders did not correlate with clinical parameters such as patients' age, tumor staging, histological type and degree. CONCLUSION: The evaluation of standardized field borders with the use of magnetic resonance imaging has demonstrated high indices of inappropriateness of the lateral field borders, as well as the relevant role of magnetic resonance imaging in the radiotherapy planning for patients with uterine cervix cancer with a view to reduce the occurrence of geographic miss of the target volume.

Keywords: Uterine cervix cancer, Radiotherapy planning, Magnetic resonance imaging, Geographic miss, Tumor volume

OBJECTIVE: The present study was aimed at developing a thermoluminescent dosimetric system capable of assessing the doses delivered to the rectum of patients submitted to high-dose-rate brachytherapy for uterine cervix cancer. MATERIALS AND METHODS: LiF:Mg,Ti,Na powder was the thermoluminescent material utilized for evaluating the rectal dose. The powder was divided into small portions (34 mg) which were accommodated in a capillary tube. This tube was placed into a rectal probe that was introduced into the patient's rectum. RESULTS: The doses delivered to the rectum of six patients submitted to high-dose-rate brachytherapy for uterine cervix cancer evaluated by means of thermoluminescent dosimeters presented a good agreement with the planned values based on two orthogonal (anteroposterior and lateral) radiographic images of the patients. CONCLUSION: The thermoluminescent dosimetric system developed in the present study is simple and easy to be utilized as compared to other rectal dosimetry methods. The system has shown to be effective in the evaluation of rectal doses in patients submitted to high-dose-rate brachytherapy for uterine cervix cancer.

Keywords: Rectum, Brachytherapy, HDR, Thermoluminescent dosimetry, Uterine cervix cancer

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 calculate spectra of cobalt-60 beam at water depth and correction factors for absorbed dose measurements obtained with lithium fluoride thermoluminescent dosimeters using Monte Carlo simulation. MATERIALS AND METHODS: The simulations of secondary spectra of clinical cobalt-60 sources were performed with the PENELOPE Monte Carlo code at different water depths. Experimental measurements of deep doses were obtained with thermoluminescent dosimeters and ionization chamber under reference conditions for radiotherapy. Correction factors for the thermoluminescent dosimeters detectors were obtained through the ratio between the relative energy absorption for the low energy spectrum and the total spectrum. RESULTS: Deep spectral analysis has demonstrated the presence of secondary low-energy spectra responsible for a significant portion of the dose deposition. Discrepancies of 3.2% were observed among the doses measured with ionization chamber and thermoluminescent dosimeters. The adoption of correction factors has allowed a reduction in the discrepancy among absorbed doses to a maximum of 0.3%. CONCLUSION: Simulated spectra allow the calculation of correction factors for reading of thermoluminescent dosimeters utilized in the measurement of deep doses, contributing for the reduction of uncertainties associated with quality control of clinical beams in radiotherapy.

Keywords: Monte Carlo simulation, Radiotherapy, Spectrometry, Quality control, Thermoluminescent dosimetry, TLD

OBJECTIVE: The present study evaluates the dose distribution received by physicians involved in hemodynamic procedures of coronary angiography and coronariography. The influence of some factors such as pulsed or continuous fluoroscopy mode and vein and/or artery access site was investigated. MATERIALS AND METHODS: Measurements have been performed with LiF:Mg,Ti thermoluminescent dosimeters placed on seven different sites of the practitioners' bodies: hands, left knee, neck, forehead and chest, under and over the lead apron. Radiation doses for each procedure were evaluated in physicians who had performed 60 coronariography and 30 angioplasty procedures. The thermoluminescent dosimeters were calibrated in the operational quantity personal dose equivalent, Hp(d), at depths of 0.07, 3 and 10 mm. RESULTS: The results of the present study demonstrate the significant role played by thyroid protectors and lead aprons for reducing radiation doses received by practitioners. Occupational doses in continuous mode fluoroscopy through brachial access were higher than with pulsed mode fluoroscopy through femoral access. CONCLUSION: The present study has demonstrated the necessity of implementing additional protective measures as well as a mechanism of training in radiation protection for physicians involved in interventional cardiological procedures.

Keywords: Interventional radiology, Fluoroscopy, Hemodynamic procedures, Radiation protection, Thermoluminescent dosimetry

Energy and angular dependences of different thermoluminescent materials were studied with the objective to verify which type of detector would be the most appropriate for beta monitoring of workers. Three types of CaSO4:Dy + teflon pellets were studied. The energy dependence was evaluated using standard beta radiation sources (147Pm, 204Tl and 90Sr+90Y). For the angular dependence study, the pellets were exposed to beta radiation of the 90Sr+90Y source, varying the incidence angle between 0° and 90°. In relation to the studied characteristics, the CaSO4:Dy + 10% C dosimeters were the most adequate for use in beta monitoring of workers.

Keywords: Thermoluminescent dosimetry, Beta radiation, Angular dependence, Energetic dependence

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 assess the rate of geographic miss on conventional radiotherapy planning of patients with cervical cancer, using magnetic resonance imaging. MATERIALS AND METHODS: Thirty-two patients with squamous cell carcinoma of the uterine cervix were studied. Magnetic resonance imaging of the pelvis was performed after clinical staging. Magnetic resonance imaging findings were compared with the classic fields described for the "box" technique. Target volume within less than 1 cm margins of the fields' limits was considered as geographic miss. RESULTS: Classical radiation field limits were inadequate in 24 cases (75%), all in the anterior (46%) or posterior (40%) border of the lateral fields. CONCLUSION: Magnetic resonance detected a high probability of geographic miss on conventional radiotherapy planning in this population, both in initial and advanced stages of the disease.

Keywords: Uterine cervix cancer, Radiotherapy, Magnetic resonance imaging

OBJECTIVE: To evaluate the precision of the absorbed radiation doses in bone marrow transplant therapy during whole body irradiation. MATERIALS AND METHODS: Two-hundred CaSO4:Dy + teflon tablets were calibrated in air and in "phantom". These tablets were randomly selected and divided in groups of five in the patients' body. The dosimetric readings were obtained using a Harshaw 4000A reader. Nine patients had their entire bodies irradiated in parallel and opposite laterals in a cobalt-60 Alcion II model, with a dose rate of 0.80 Gy/min at 80.5 cm, {(10 × 10) cm² field}. The dosimetry of this unit was performed using a Victoreen 500 dosimeter. For the determination of the mean dose at each point evaluated, the individual values of the tablets calibrated in air or "phantom" were used, resulting in a build up of 2 mm to superficialize the dose at a distance of 300 cm. RESULTS: In 70% of the patients a variation of less than 5% in the dose was obtained. In 30% of the patients this variation was less than 10%, when values obtained were compared to the values calculated at each point. A mean absorption of 14% was seen in the head, and an increase of 2% of the administered dose was seen in the lungs. In patients with latero-lateral distance greater than 35 cm the variation between the calculated doses and the measured doses reached 30% of the desired dose, without the use of compensation filters. CONCLUSION: The measured values of the absorbed doses at the various anatomic points compared to the desired doses (theoretic) presented a tolerance of ± 10%, considering the existent anatomical differences and when using the individual calibration factors of the tablets.

Keywords: Whole body irradiation, Dosimetry, Thermoluminescent dosimeters, Doses, Bone marrow transplantation

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

The use of high-dose rate brachytherapy for cancer treatment is increasing and the number of patients treated in Brazil is high, considering the number of existing equipments. However, the small number of equipments is a limiting factor that bring on a lot of pressure on the working routine. For this reason, a reevaluation of emergency procedures is not carried out in most centers. This paper describes the most frequent emergency situations and suggests a code of practice when errors do not allow the return of the radiation source to the shield and result in undesirable radiation exposure to the patient and staff in remote centers for brachytherapy. We suggest training, additional caution measures and quality control in order to minimize undesirable doses.

Keywords: HDR. Brachytherapy. Remote afterloading. Radiology emergency. Quality control. Code of practice.

Objective: To evaluate the possible repercussions of the previous cesarean scar at uterine arteries Doppler velocimetry between the 26th and 32nd gestational weeks. Materials and Methods: Prospective cross-sectional study including 45 women between 11 and 14 weeks of gestation, divided into three groups: 17 pregnant women with uterine scar resulting from a previous elective cesarean section (group A); 14 with uterine scar resulting from a previous cesarean section performed during labor (group B); and 14 pregnant women with a single previous vaginal delivery (group C). Uterine arteries Doppler velocimetry was performed with transabdominal approach. Means, medians and standard deviation (SD) were calculated for each group in the study. The groups comparison regarding pulsatility index was performed with the non-parametric Kruskal-Wallis test. Results: In group A, the pulsatility index ranged from 0.60 to 1.60 (mean: 0.90; SD: 0.29), in group B, from 0.53 to 1.43 (mean: 0.87; SD: 0.24), and in group C, from 0.65 to 1.65 (mean: 1.01; SD: 0.37); with p = 0.6329. Conclusion: No repercussion of previous cesarean scar was observed at uterine arteries Doppler velocimetry performed in the period between the 26th and 32nd gestational weeks.

Keywords: Pregnancy; Uterine scar; Previous cesarean section; Uterine arteries Doppler velocimetry.

OBJECTIVE: To evaluate the level of ambient radiation in a PET/CT center. MATERIALS AND METHODS: Previously selected and calibrated TLD-100H thermoluminescent dosimeters were utilized to measure room radiation levels. During 32 days, the detectors were placed in several strategically selected points inside the PET/CT center and in adjacent buildings. After the exposure period the dosimeters were collected and processed to determine the radiation level. RESULTS: In none of the points selected for measurements the values exceeded the radiation dose threshold for controlled area (5 mSv/year) or free area (0.5 mSv/year) as recommended by the Brazilian regulations. CONCLUSION: In the present study the authors demonstrated that the whole shielding system is appropriate and, consequently, the workers are exposed to doses below the threshold established by Brazilian standards, provided the radiation protection standards are followed.

Keywords: Dosimetry; Thermoluminescence dosimetry; PET/CT.

OBJECTIVE: To estimate the entrance surface air kerma (K_a,e) and air kerma in the region of radiosensitive organs in radiographs of pediatric paranasal sinuses. MATERIALS AND METHODS: Patient data and irradiation parameters were collected in examinations of the paranasal sinuses in children from 0 to 15 years of age at two children's hospitals in the city of Recife, PE, Brazil. We estimated the K_a,e using the X-ray tube outputs and selected parameters. To estimate the air kerma values in the regions of the eyes and thyroid, we used thermoluminescent dosimeters. RESULTS: The K_a,e values ranged from 0.065 to 1.446 mGy in cavum radiographs, from 0.104 to 7.298 mGy in Caldwell views, and from 0.113 to 7.824 mGy in Waters views. Air kerma values in the region of the eyes ranged from 0.001 to 0.968 mGy in cavum radiographs and from 0.011 to 0.422 mGy in Caldwell and Waters views . In the thyroid region, air kerma values ranged from 0.005 to 0.932 mGy in cavum radiographs and from 0.002 to 0.972 mGy in Caldwell and Waters views. CONCLUSION: The radiation levels used at the institutions under study were higher than those recommended in international protocols. We recommend that interventions be initiated in order to reduce patient exposure to radiation and therefore the risks associated with radiological examination of the paranasal sinuses.

Keywords: Radiometry; Radiography; Paranasal sinuses; Pediatrics; Thermoluminescent dosimetry..

OBJECTIVE: To evaluate the safety and efficacy of using highly compressible calibrated microspheres in uterine artery embolization (UAE) for the treatment of uterine fibroids. MATERIALS AND METHODS: This was a prospective multicenter study. Thirty-two women with symptomatic uterine fibroids were selected for UAE between January 2019 and March 2020. The participants completed the Uterine Fibroid Symptom and Quality of Life (UFS-QOL) questionnaire, underwent contrast-enhanced pelvic magnetic resonance imaging (MRI), and were submitted to anti-Müllerian hormone measurement, subsequently undergoing UAE with Embosoft microspheres. After six months, the patients again completed the UFS-QOL questionnaire and underwent pelvic MRI. RESULTS: The most common symptoms were abnormal uterine bleeding (in 81.3% of the cases), pelvic pain (in 81.3%), and compression (in 46.9%). Of the 32 patients evaluated, 12 (37.5%) had anemia due to abnormal uterine bleeding. Thirty patients completed the study. Among those patients, we observed median reductions of 21.4% in uterine volume and 15.9% in dominant fibroid volume. We identified no adverse events that could be attributed to the material itself, although there were events attributed to the UAE procedure in general. CONCLUSION: For the treatment of uterine fibroids, UAE using Embosoft microspheres shows satisfactory results, providing reductions in uterine and dominant fibroid volumes, with a low rate of adverse events, and improving patient quality of life, as well as demonstrating safety and efficacy.

Keywords: Leiomyoma; Uterine artery; Uterine artery embolization; Microspheres.