Back to Search
Start Over
Analysis of Long-Term Quality Control Data for a 137Cs Dosimetry Calibration Source.
- Source :
-
Health physics [Health Phys] 2021 Feb 01; Vol. 120 (2), pp. 227-242. - Publication Year :
- 2021
-
Abstract
- Abstract: Strict quality assurance programs are required for many radiological applications, but these seldom exist for verifying dosimetry calibration sources. After initial characterization of a dosimetry calibration facility, quality control procedures are recommended to ensure the early detection of any changes or malfunctions. These also result in refined knowledge about average dose rate and experimental variations in dose delivery. This paper describes the implementation of a phase I quality control protocol for a 137Cs dosimetry calibration source and includes an analysis of the resulting data collected over a 24-mo period. During this time, substantial data was collected to establish trial control limits. Air kerma rate measurements were obtained using an ion chamber and were adjusted for decay, corrected for ambient temperature, pressure and humidity, and then analyzed using quality control charts. Three variations of rational subgrouping methods were used in order to find assignable causes of error, and Nelson's Rules were followed to detect any non-random statistical variations. Measurements were subgrouped according to same-day measurements in order to detect positional errors as well as atmospheric correction errors. Additionally, measurements were subgrouped according to analogous experimental setups in order to detect failure in equipment or incorrect settings. Both were analyzed using the X-bar and R chart method. Similarly, individuals and moving ranges charts were used to carefully examine each position in order to observe any situational errors that may occur which include timing, positional, or interference errors. Each method was successful in identifying unique out-of-control data points that occurred during the phase I application of forming control limits. Over the 24-mo period, enough data points were deemed in-control to establish reliable trial limits. Future experiments will include the phase II application of gaining more reliable measurements in order to fine-tune the limits, as well as performing a designed experiment, where variables are purposefully changed in order to test the variation of the data.<br />Competing Interests: The authors declare no conflicts of interest.<br /> (Copyright © 2020 Health Physics Society.)
Details
- Language :
- English
- ISSN :
- 1538-5159
- Volume :
- 120
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Health physics
- Publication Type :
- Academic Journal
- Accession number :
- 33315651
- Full Text :
- https://doi.org/10.1097/HP.0000000000001355