• Journal of the Korean Society of Radiology
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• v.14 no.3
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• pp.289-294
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• 2020

In order to control the quality of X-ray images and patient exposure, it is necessary to document the output dose(air absorption dose(mGy)) output from the X-ray unit from the measurement. The purpose of this study is to find an equation that can calculate the output dose from the measurement of the output dose and output factor(Of) of the X-ray Unit. The output dose and output factors of the X-beam irradiated from the X-ray unit were measured using an XR multi-detector. The output dose calculation formula was obtained by fitting the measured output dose divided by the tube current-exposure time product(mAs) and the set tube voltage with Allometric1. The final output dose calculation formula was obtained by multiplying this formula with the output factor. It is considered that the obtained final output dose calculation formula will be useful for all tube voltages, tube currents, exposure times, field sizes, and distances.

• The Journal of the Korea Contents Association
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• v.10 no.2
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• pp.258-267
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• 2010

This interest in radiation exposure makes increasing doctor's awareness and knowledge of radiation dose in patients during X-ray test important in reducing patient's uneasiness. However, very few facilities are equipped with measurement instruments. Therefore, an intensive study to find out patient dose using computational method has been initiated. This study used special features of the bit system and NDD-M and directly measured the output dose of diagnostic X-ray instruments used in Korea to create tables. Two different methods were found to be adequate when applied to cases when X-ray outputs were both known and unknown, and comparative experiments with real measurement doses were carried out. Presented methods were found to provide more accurate results compared to the bit system and NDD-M. Therefore, patient dose during clinical trials were found to be more easily acceptable to medical personnel in the radiation field in terms of radiation exposure and reduction of medical X ray dose.

• 대한방사선치료학회:학술대회논문집
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• 1998.03a
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• pp.18-19
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• 1998

• Progress in Medical Physics
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• v.5 no.1
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• pp.87-99
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• 1994

Purpose : The determination of electron beam output factor was investigated from individual applicator for various energy of ML-15MDX linear accelerator. The output factor of electron beam was extended from square to rectangular field in individual applicator size through with a least-square fit to a polynomial expression. Materials : In this experiments. the measurement of output was obtained from 2${\times}$cm$^2$ to 20${\times}$20cm$^2$ of field size in different applicator size for 4 to 15 MaV electron beam energy. The output factor was defined as the ratio of maximum dose output on the central axis of the field of individual applicator size to that of a given field size. Applicator factors were derived from comparing with the output dose of reference field size 10${\times}$10cm$^2$. The thickness of block was specially designed as 10mm in thickness of Lipowitz metal for field shaping in all electron energy. Two types of output curves are included as output factors versus side of square fields and that of variable side length for X and Y in one-dimensional to compare the expected values to that of experiments. Results : Expected output factors of rectangular which was derived from that of square fields in individual applicator size from 2${\times}$2cm$^2$ to 20${\times}$20cm$^2$ in different electron energy was very closed to that of experimental measurements within 2% uncertainty. However 1D method showed a 3% discrepancy in small rectangular field for low energy electron beam. Conclusion : Emperical non-linear polynomial regressions of square root and 1D method were performed to determin the output factor in various field size and electron energy. The expected output of electron beam of square root method for square field and 1D method for rectangular field were very closed to that of measurement in all selected electron beam energy.

• Progress in Medical Physics
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• v.12 no.2
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• pp.141-146
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• 2001

It is well known that assurance of the radiation therapy needs for an accuracy of $\pm$ 5 % in the delivery of an absorbed dose to target volume. Therefore, the dose evaluation of brachytherapy source and/or linear accelerate beam must be a stability with accuracy. In an advanced country, they recommended to use the radioactive check source for reference air ionization chamber for a stable response of radiation field chamber. In this experiments, the radioactive source Sr-90 and PR-05 air ionization chamber were used for standard source and reference ion chamber. The response of reference ion chamber showed as an 1.000$\pm$ 0.010 uncertainty for 10 years long and the evaliuation f dose discrepancy of clinical field ion chamber showed as 0.997 $\pm$0.011 in a $^{60}$ Co brachytherapy soruce. In our experiments, we can assuarance the long halflife standard source is reliable to preserve the calibration factor of reference chamber in stability.

• Progress in Medical Physics
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• v.22 no.2
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• pp.92-98
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• 2011

This study is to keep the accuracy and stability of the output dose evaluations for linear accelerator photon beams by using the air ionization chambers (TM31010, 0.125 cc, PTW) through the Task Group 51 protocol. The absorbed dose to water calibration factor $N_{dw}{^{Co-60}}$ was delivered from the air kerma calibration factor $N_k$ which was provided from manufacture through SSDL calibration for determination of output factor. The ionization chamber of TM31010 series was reviewed the calibration factor and other parameters for reduce the uncertainty within ${\pm}2%$ discrepancy and we found the supplied $N_{dw}{^{Co-60}}$ which was derived from Nk has shown a -2.8% uncertainty compare to that of PSDL. The authors provided the program to perform the output dosimetry with TG-51 protocol as it is composed same screen of TG-51 worksheets. The evaluated dose by determination of output factor delivered to postal TLD block for comparison the output dose to that of MDACC (RPC) in postal monitoring program. The results have shown the $1.001{\pm}0.013$ for 6 MV and $0.997{\pm}0.012$ discrepancy for 15 MV X rays for 5 years followed. This study shows the evaluated outputs for linear accelerate photon beams are very close to that of international output monitor with small discrepancy of ${\pm}1.3%$ with high reliability and showing the gradually stability after 2010.

• Progress in Medical Physics
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• v.18 no.1
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• pp.13-19
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• 2007

The purpose of study Is to Investigate whether glass rod detector (GRD) would be suitable for dosimeter of radiotherapy units. A GRD Is used for the measurement of the ou4put factors and x-axis beam profiles from Gamma Knife. The output factors measured with GRD from the 14, 8 and 4mm collimators relative to the 18mm collimator are $0.980{\pm}0.013,\;0.949{\pm}0.013\;and\;0.872{\pm}0.012$, respectively. The output factors obtained with a GRD are within 1.0% In good agreement with the values recommended by the manufacture. The full width at half maximum (FWHM) of x-axis beam profiles measured with GRD are 5.9mm at a 4mm collimator.

• Journal of radiological science and technology
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• v.27 no.4
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• pp.37-41
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• 2004

Purpose : Raise ability cultivation in presence at a sicked business by performance management estimation of device through measurement. Also Learn a technology that measure exact tube voltage, exposure time, output dose. And it is to grasp photofluorography X-ray generator existing circumstances using at hospital. Material & Method : Investigated Photofluorography X-ray generator(inside, outside each 10) of 10 university hospitals using tube voltage, exposure time, output dose measuring instrument. Result : Photofluorography device that tube voltage correctness is incongruent by examination PAE decision came out 3, and at exposure time correctness examination 2 incongruent, Also 3 that calculate coefficient of variation about exposure in repeatability examination of exposure were incongruent. Inappropriate photofluorography device is 5 outside hospital(mobile unit) and the thing in hospital was 3 in 3 kind of efficiency test. It appeared high that photofluorography device outside hospital is more incongruent than thing in hospital. Conclusion : May ready situation that can offer patient medical service of good quality by radiation exposure reduction, image quality administration, retake decrease etc. by keeping performance of Photofluorography device. Therefore, is considered that need on-time efficiency test.

• Progress in Medical Physics
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• v.20 no.4
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• pp.308-316
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• 2009

To achieve the accurate evaluation of given absorbed dose from output dose of linear accelerator photon beam through investigate the characteristics of LiF:Mg,Cu,P TLD powder. This experimental TL phosphor is performed with a commercial LiF:Mg,Cu,P powder (Supplied by PTW) and TL reader (LTM, France). The TLD was exposed to 6 MV X rays of linear accelerator photon beam with range 15 to 800 cGy in blind dose at two hospitals. The dose evaluation of TLD was through the experimental algorithms which were dose dependency, dose rate dependency, fading and powder weight dependency. The glow curve has shown the three peaks which are 110, 183 and 232 degrees of heating temperature and the main dosimetric peak showed highest TL response at 232 high temperature. In this experiments, the LiF:Mg,Cu,P phosphor has shown the 2.5 eV of electron trap energy with a second order. This experiments guided the dose evaluation accuracy is within 1% +2.58% of discrepancy. The TLD powder of LiF:Mg,Cu,P was analyzed to dosimetric characterists of electron captured energy and order by glow shape, and dose-TL response curve guided the accuracy within 1.0+2.58% of output dose discrepancy.

• Proceedings of the Korean Society of Medical Physics Conference
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• 2003.09a
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• pp.66-66
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• 2003

목적 : 선량측정의 정확성을 향상시키기 위하여 물 흡수선량 표준에 토대를 두고 있는 표준측정법, AAPM TG-51과 IAEA TRS-398, 이 발표되어 선량측정의 파라다임이 변화하고 있다. 본 연구에서는 이들 대표적인 표준측정법에 대하여 사용자 편의성을 고려하여 웹에 기반한 선량교정 프로그램을 개발하고자 한다. 대상 및 방법 : 미국의학물리학회 AAPM TG-51과 국제원자력기구 IAEA TRS-398 표준측정법에 선량교정 프로그램은 Microsoft IIS 6.0 웹서버와 .NET 플렛폼상에서 Visual Studio. NET 도구를 사용하여 개발하였다. 개발언어로는 C# 언어를 사용하였고 각 표준측정법에 대한 선량교정 작업서는 ASP. NET 페이지로 작성하였다. 웹페이지와 산량 교정 모듈을 분리하여서 개발 후 유지보수가 쉽게 설계하였다. 또한 기준점에서의 선량 계상에 사용하는 모든 물리적인 파라미터와 데이터는 데이터베이스에 저장하였다. 이로써 향후 수식체계의 변화 또는 물리적인 데이터의 변화로 인한 프로그램 수정이 최소화하도록 하였다. 결과 : 이들 표준측정법은 모두 물 흡수선량 교정인수에 토대를 두고 있으나 측정 조건 및 물리적인 자료 에 있어 약간의 차이를 보이고 있다. 그러므로 각 표준측정법간의 유사점 및 차이점을 비교 분석하기가 용이하였다. 그리고 개발된 프로그램을 이용하여 표준측정법에서 제시된 선량교정 작업서에 따라 선량 교정을 수행한 교정 결과 데이터를 XML 파일 형식으로 저장하여 이전의 측정 자료를 관리할 수 있게 하였다. 이 과거 측정 자료를 사용하여 출력 선량 교정의 변화 및 기타 중요한 물리적인 데이터 값의 변화를 분석할 수 있다. 결론 : 두 표준측정법에 대한 선량교정 프로그램은 사용자가 선호하는 표준측정법을 선택할 수 있고, 웹에 토대를 두고 있어 프로그램으로 전국 방사선종양학과의 방사선치료기기의 출력 및 물리적인 변화에 대한 자료를 비교 분석하기 용이하고 수작업으로 인해 발생할 수 있는 실수 및 오차를 줄일 수 있다. 또한 개발된 프로그램의 활용을 통하여 국내 실정에 적합한 물 흡수선량 표준에 기반한 표준측정법 개발에 토대를 마련하는데 있어 기여할 것으로 사료된다.