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[A Study of uncertainty factors in cross calibration of dosimeter for diagnostic X-rays].

Although patient exposure has been increasing in recent years, few institutions have dosimeters and are able to ascertain patients' exposure dose. Internationally, however, it is necessary to adopt safety levels for patient exposure doses, and guidance levels have been introduced. Therefore, the need for measurement in areas of x-ray diagnosis has been increasing. As a result, several societies concerned with radiation dose have been endeavoring to establish a calibration system of radiation measurement and a dosimeter calibration system, which are the basics of radiation protection. Ten regional centers for standardization of doses in x-ray diagnosis were established and have begun trials relating to dosimeter cross calibration. Our institution, as one of these centers, has instituted a trial. In this study, the cross-calibration field, the reliability of the cross-calibration skill of our regional center, and the standard uncertainty of cross calibration were investigated. As a consequence of the investigation, it was determined that our cross-calibration field follows the protocol of the Japanese Society of Radiological Technology, the difference between calibration factor/cross calibration factor obtained by JQA and our regional center is within 2.5%, and the expanded uncertainty of our cross calibration is about 7.2% (k=2).

Calibration↗

Reflectance-based calibration of SeaWiFS. II. Conversion to radiance.

For instruments that carry onboard solar diffusers to orbit, such as the Sea-Viewing Wide Field-of-View Sensor (SeaWiFS), it is possible to convert the instrument's reflectance measurements to radiance measurements by knowledge of the solar irradiance. This process, which generally requires the application of a solar irradiance model, is described. The application of the irradiance model is separate from the measurements by the instrument and from the instrument's reflectance calibration. In addition, SeaWiFS was calibrated twice before launch for radiance response by use of radiance sources with calibrations traceable to the National Institute of Standards and Technology. With the inclusion of the at-launch diffuser-based radiance calibration, SeaWiFS has three possible radiance calibrations forthe start of on-orbit operations. The combination of these three into a single calibration requires changes of 4% or less for the current at-launch radiance calibration of the instrument. Finally, this process requires changes of 4% or less for the reflectance calibration coefficients to provide consistency among the radiance calibration, the reflectance calibration, and the solar irradiance.

Journal Article↗

Practical calibration correction method for the maintenance of an on-line near-infrared monitoring system for molten polymers.

The present study has investigated a practical calibration correction method for an on-line monitoring system for molten polymers using a near-infrared (NIR) spectrometer. A partial least squares (PLS) calibration model for the ethylene (C2) content in melt polypropylene (PP) was developed for the investigation of changes in the performance of the on-line system before and after maintenance necessitated by the relocation. The predicted values for the C2 content from the spectra measured after maintenance by using the calibration model developed from the spectra collected before maintenance showed that there were some differences between the spectra obtained by the NIR spectrometer system before and after maintenance. The loadings from factor analysis suggested that the main cause for the differences in the system performance before and after maintenance was wavenumber shifts in the NIR spectra of PP in the melt state. Six popular standardization or calibration transfer methods (direct standardization (DS), piecewise direct standardization (PDS), additive correction (AD), multiplicative correction (MP), slope and bias (SB), and difference spectrum with interpolation (DSI)) were evaluated for the calibration correction of the on-line NIR monitoring system. However, the results of the evaluation showed that these standardization methods need more than two samples to obtain the high accuracy for the nonlinearity contained in the spectra set. From the standpoint of practical calibration in a real plant, the acceptable number of samples for the calibration is one or two. Moreover, recalibration using transferred spectra is not preferable because of the traceability for a calibration model. As a practical solution for a calibration correction in a real plant, a method considering wavenumber shift and path-length correction has been proposed in this study. The predicted results for the C2 content in the melt-state PP from the spectra measured after maintenance by using the proposed method have shown that the proposed method is useful for calibration correction in a real plant in spite of using only one sample.

Journal Article↗

Calibration of pesticide leaching models: critical review and guidance for reporting.

Calibration of pesticide leaching models may be undertaken to evaluate the ability of models to simulate experimental data, to assist in their parameterisation where values for input parameters are difficult to determine experimentally, to determine values for specific model inputs (e.g. sorption and degradation parameters) and to allow extrapolations to be carried out. Although calibration of leaching models is a critical phase in the assessment of pesticide exposure, lack of guidance means that calibration procedures default to the modeller. This may result in different calibration and extrapolation results for different individuals depending on the procedures used, and thus may influence decisions regarding the placement of crop-protection products on the market. A number of issues are discussed in this paper including data requirements and assessment of data quality, the selection of a model and parameters for performing calibration, the use of automated calibration techniques as opposed to more traditional trial-and-error approaches, difficulties in the comparison of simulated and measured data, differences in calibration procedures, and the assessment of parameter values derived by calibration. Guidelines for the reporting of calibration activities within the scope of pesticide registration are proposed.

Calibration↗

Method for improved accuracy in endogenous urea recovery marker calibrations for microdialysis in tumors.

INTRODUCTION: Urea has been proposed as an endogenous recovery marker for microdialysis for absolute concentration calculations of analytes in microdialysis samples. Previously we demonstrated a linear relationship between urea concentrations in a rat mammary carcinoma and that in plasma, validating its use as a recovery marker for that particular tumor. In this paper, we have extended the validation to two other tumor lines, thereby providing confidence that the calibration is constant across tumor types. To improve the accuracy in the determination of the plasma/tumor urea relationship from no net flux calibrations, we extended the range of the calibration by adding exogenous urea to tumor bearing animals. This method enabled more accurate calculations of absolute recovery from plasma and dialysate urea concentrations. We confirm that by using this method the calibration is valid across three different tumor lines. The existence of a common calibration between tumors provides rationale for using plasma urea as a recovery marker for clinical trials. The existence of a common calibration between tumor types bypasses the need to perform time consuming calibrations for each patient. This makes the procedure much more practical for clinical studies. METHODS: The no net flux technique was used to determine the plasma vs. tumor urea relationship for the R3230Ac mammary carcinoma, 9 L glioma, and a fibrosarcoma (FSa), grown in Fischer 344 rats. Plasma urea was stably increased beyond the normally occurring concentration for some of the data points by subcutaneous bolus administration to extend the range of data for the no net flux calibration. RESULTS: Urea recovery was unaffected by plasma urea concentration and was consistent with other reported values. The relationship between plasma and tumor urea was fit by a line, and linear regressions of the data with the extended plasma urea range had better R2 values than we reported previously. Statistical comparison of the regressions suggests that within reasonable uncertainty limits, they are the same for the different tumor types. DISCUSSION: Increasing the plasma urea concentration range for no net flux calibrations of urea as an endogenous recovery marker in tumors resulted in more accurate determination of the plasma/tumor urea relationship. A single linear regression may describe the relationship between plasma and tumor urea concentration across tumor lines for a given set of microdialysis parameters.

Animals↗

[Hiatus calibration decreases postoperative dysphagia after laparoscopic fundoplication: case-report study].

STUDY AIM: The risk of dysphagia after antireflux surgery seems to be increased with laparoscopy compared with open surgery. Calibration of the hiatus is usually done by the surgeon's finger during open surgery. The aim of this study was to assess the results of laparoscopic calibration with a Fogarty balloon catheter. PATIENTS AND METHODS: Between 1999 and 2001, 21 patients had a laparoscopic Toupet 240 degrees fundoplication with hiatus calibration using a 4 ml-inflated 8G Fogarty balloon catheter. These patients were compared with a group of 21 patients without hiatus calibration, matched for age, sex, preoperative dysphagia and esophageal dysmotility. Judgment criteria was early and/or late postoperative dysphagia (> 3 months). RESULTS: Median follow-up was 13 months. The rate of early dysphagia with and without calibration were 66% and 48% respectively (NS). Median duration of early dysphagia with and without calibration were 25 and 43 days respectively (p = 0.05). No patient with calibration had late dysphagia. One patient (5%) without calibration had unexplained late dysphagia for 2 years. He had preoperative esophageal dysmotility without oesophagitis. CONCLUSION: Hiatus calibration with a Fogarty balloon catheter decreased early postoperative dysphagia duration after Toupet laparoscopic fundoplication. This easily reproducible technical point standardizes the hiatus closure and should be recommended.

Adult↗

Volume calibration alone may be misleading.

The use of spirometry is becoming more and more widespread in non-laboratory situations such as general practice or occupational medicine. In these non-laboratory situations, volume calibration with a 3000 ml syringe is often the only feasible method to ensure that the spirometer produces valid and reproducible data. Sophisticated equipment to calibrate forced manoeuvres with standard waveforms are not present. In this study, we assessed whether volumetric calibration is a guarantee for valid and comparable spirometric results. Two portable spirometers were tested. On 8 consecutive test days, both spirometers were calibrated with a 3000 ml syringe in accordance with the American Thoracic Society (ATS) guidelines. The comparability of the spirometric results (forced expiratory volume in 1 S, FEV1) was tested in two ways. Firstly, the spirometers were compared to each other using the results from 43 volunteers on the same 8 test days. The spirometers were presented in a randomized order and volunteers were asked to perform a series of reproducible manoeuvres in both spirometers. Paired observations were analysed, using Bland and Altman plots. Secondly, the spirometers were compared to a 'gold standard', a computer-driven syringe (CDS). Calibration with the 3000 ml syringe showed that both spirometers complied with the ATS criteria for volume calibration for diagnostic spirometry. However, paired FEV1 data obtained in subjects showed a systematic, volume-dependent difference between the two spirometers (mean difference: 289 ml, P < 0.001, systematic difference: 8.6%, P < 0.0001). This systematic difference was confirmed by the comparisons with the CDS. Volume calibration may be misleading. The results from volume calibration may meet the ATS criteria, but this is no guarantee that data from forced manoeuvres are accurate. If CDS equipment to simulate standard wave forms is not available, it is recommended that biological calibration is performed regularly and, if possible, that paired data from two (or more) different spirometers are compared.

Calibration↗

Assessment of calibration methods for estimating bone mineral densities in trauma patients with quantitative CT: an anthropomorphic phantom study.

RATIONALE AND OBJECTIVES: Osteoporosis may contribute to the increased morbidity and mortality of elderly persons involved in motor vehicle accidents. Such patients commonly undergo whole-body computed tomographic (CT) studies that may be analyzed with quantitative CT. Various quantitative CT calibration techniques were investigated for use with patients who have suffered trauma, who are typically scanned on a backboard. MATERIALS AND METHODS: Lumbar simulator phantoms were used to simulate small and large patients. Vertebral spongiosa inserts with a wide range of bone and fat compositions were placed in the phantoms, and their bone mineral densities (BMDs) were measured by using calibration lines derived from the CT numbers of a calibration standard. Four calibration techniques were tested. In three the lumbar simulator and the calibration standard were scanned simultaneously, with the standard placed beneath the backboard (method 1), on top of the backboard adjacent to the lumbar simulator (method 2), or on top of the abdomen region of the lumbar simulator (method 3). The fourth technique employed a single calibration line derived from a separate scan of the calibration standard beneath the small lumbar simulator without the backboard, with correction for patient body size. RESULTS: The best overall results were obtained with the single calibration line method. The root mean square errors of the BMD values were 2.9-18.4, 2.5-7.5, 2.5-14.9, and 0.3-2.8 mg/cm3 for methods 1, 2, 3, and 4, respectively (ranges represent variations in the errors of the measured BMDs of the inserts due to changes in scanner table height and lumbar simulator phantom size). CONCLUSION: The single calibration line method is an accurate means of measuring BMD in trauma patients.

Bone Density↗

Using item response theory to calibrate the Headache Impact Test (HIT) to the metric of traditional headache scales.

BACKGROUND: Item response theory (IRT) scoring of health status questionnaires offers many advantages. However, to ensure 'backwards comparability' and to facilitate interpretations of results, we need the ability to express the IRT score in the metrics of the traditional scales. OBJECTIVES: To develop procedures to calibrate IRT-based scores on the Headache Impact Test (HIT) into the metrics of the traditional headache scales. To assess the degree to which the calibrated HIT scores agree with the observed traditional scores and lead to the same conclusions in group comparisons. METHODS: We used telephone interview data (n = 1016) and Internet data (n = 1103) from general population surveys of recent headache sufferers. Analyses were conducted in four steps: (1) develop IRT models for all items, (2) for each IRT score level, calculate the expected score on each of the traditional scales (calibration), (3) adjust this calibrated score for measurement error in the IRT score, (4) for each of the traditional scales, assess agreement between calibrated HIT scores and observed scores using intraclass correlation (ICC) and evaluate the agreement of mean scores and the relative validity (RV) in discriminating among groups differing in migraine diagnosis, headache severity, and change in impact over time. RESULTS: For the traditional categorical questionnaire items (the Migraine Specific Questionnaire (MSQ) and the Headache Disability Inventory (HDI)) the calibrated HIT agreed with the observed traditional scores: ICC's were between 0.80 and 0.94. In RV analyses the maximum mean difference between the observed and expected scores was 1.7 points on a 0-100 scale for comparisons at one point in time. Analyses of change over time and analyses calibrating scores from the fixed-form HIT-6 to the metric of other questionnaires were also satisfactory although less precise. Analysis of non-standard questionnaire items (e.g. On how many days in the past 3 months did you have a headache, from the HIMQ and the MIDAS) required special IRT models. Agreement was less good: ICC's were between 0.56 and 0.61 and the maximum mean differences were 2.9 (on a 0-270 scale) and 3.8 (on a 0-450 scale) in RV analyses at one point in time. The ability of the calibrated scale scores to discriminate between groups was at least as good as the ability of the observed sum scales and often remarkably better. CONCLUSION: The theoretical advantage of IRT models in scale calibration is supported by our results. This approach to achieving comparability of new and widely-used scales and accelerating the accumulation of interpretation guidelines based on previous work warrant testing for measures of other generic and disease-specific concepts.

Adolescent↗

Goldmann applanation tonometer calibration error checks: current practice in the UK.

AIM: Assess current practice and views regarding checking Goldmann applanation tonometers for calibration errors in the United Kingdom. DESIGN: Questionnaire survey. METHODS: A total of 100 ophthalmology residents from England, Wales, and Scotland attending the 2004 Congress of the Royal College of Ophthalmologists, UK, responded to a structured questionnaire. They were asked the following: how often they used different tonometers between clinical sessions; how often they checked their tonometers for errors; and who they felt was responsible for checking tonometers for calibration errors. RESULTS: All respondents were using a different Goldmann tonometer for each clinic: 85% never check tonometers for errors; only 7% perform checks at the start of each clinical session; and 8% would only check the tonometer for calibration errors if they had suspicious or unexpected measurements. A total of 70% of respondents felt that calibration checks are not part of their responsibility. They believe that either nursing staff or other hospital staff should carry out calibration checks and ensure that tonometers are accurate. The remaining 30% felt that calibration checks should be carried out by the doctor using the tonometer. CONCLUSION: Despite evidence that Goldmann tonometers lose accuracy during routine use in clinical practice, only a minority are checking the tonometers for calibration errors. There is no consensus as to who should be responsible for ensuring that tonometer calibration is maintained. We recommend that tonometers should be checked for calibration errors at least on a monthly basis by individuals identified by departmental protocols.

Calibration↗

The extent and implications of sphygmomanometer calibration error in primary care.

AIM: The sphygmomanometer is an essential piece of diagnostic equipment, used in many routine consultations in primary care. Its accuracy depends on correct maintenance and calibration. This study was designed to: (1) assess the maintenance and calibration of sphygmomanometers in use in primary care; (2) assess the clinical, ethical, legal and public health implications of our findings. METHOD: A researcher assessed the accuracy of mercury and aneroid sphygmomanometers in use in 231 English general practices. He also made enquiries about arrangements for the maintenance and calibration of sphygmomanometers. We conducted a small telephone survey in general practices across the country to determine maintenance and calibration arrangements across the country. We carried out a modelling exercise to explore the clinical, ethical and public health implications of our findings. RESULTS: Of 1462 sphygmomanometers, 9.2% gave readings were more than 5 mm Hg inaccurate. No practice had arrangements for maintenance and calibration of sphygmomanometers. Nationally, one of 54 practices had an arrangement for maintenance and calibration. True hypertension is very uncommon in women under 35, a blood pressure which is measured as high is much more likely to be caused by calibration error than by hypertension. CONCLUSION: It is rare for sphygmomanometers used in primary care to be maintained and calibrated. Because of this women under 35 are at risk of misclassification and inappropriate treatment. This has ethical and public health implications. Clinicians using equipment which has not been maintained and calibrated may be medically negligent.

Adolescent↗

Effect of non-invasive calibration of radial waveforms on error in transfer-function-derived central aortic waveform characteristics.

Transfer function techniques are increasingly used for non-invasive estimation of central aortic waveform characteristics. Non-invasive radial waveforms must be calibrated for this purpose. Most validation studies have used invasive pressures for calibration, with little data on the impact of non-invasive calibration on transfer-function-derived aortic waveform characteristics. In the present study, simultaneous invasive central aortic (Millar Mikro-tip catheter transducer) and non-invasive radial (Millar Mikro-tip tonometer) pressure waveforms and non-invasive brachial pressures (Dinamap) were measured in 42 subjects. In this cohort, radial waveforms were calibrated to both invasive and non-invasive mean and diastolic pressures. From each of these, central waveforms were reconstructed using a generalized transfer function obtained by us from a previous cohort [Hope, Tay, Meredith and Cameron (2002) Am. J. Physiol. Heart Circ. Physiol. 283, H1150-H1156]. Waveforms were analysed for parameters of potential clinical interest. For calibrated radial and reconstructed central waveforms, different methods of calibration were associated with differences in pressure (P<0.001), but not time parameters or augmentation index. Whereas invasive calibration resulted in little error in transfer function estimation of central systolic pressure (difference -1+/-8 mmHg; P=not significant), non-invasive calibration resulted in significant underestimation (7+/-12 mmHg; P<0.001). Errors in estimated aortic parameters differed with non-invasively calibrated untransformed radial and transfer-function-derived aortic waveforms (all P<0.01), with smaller absolute errors with untransformed radial waveforms for most pressure parameters [systolic pressure, 5+/-16 and 7+/-12 mmHg; pulse pressure, 0+/-16 and 4+/-12 mmHg (radial and derived aortic respectively)]. When only non-invasive pressures are accessible, analysis of untransformed radial waveforms apparently produces smaller errors in the estimation of central aortic systolic pressure, and other waveform parameters, than using a generalized transfer function.

Aorta↗

Direct calibration of a reference standard against the air kerma strength primary standard, at 192Ir HDR energy.

The primary standard of low air kerma rate sources or beams, maintained at the Radiological Standards Laboratory (RSL) of the Bhabha Atomic Research Centre (BARC), is a 60 cm3 spherical graphite ionization chamber. A 192Ir HDR source was standardized at the hospital site in units of air kerma strength (AKS) using this primary standard. A 400 cm3 bakelite chamber, functioning as a reference standard at the RSL for a long period, at low air kerma rates (compared to external beam dose rates), was calibrated against the primary standard. It was seen that the primary standard and the reference standard, both being of low Z, showed roughly the same scatter response and yielded the same calibration factor for the 400 cm3 reference chamber, with or without room scatter. However, any likelihood of change in the reference chamber calibration factor would necessitate the re-transport of the primary standard to the hospital site for re-calibration. Frequent transport of the primary standard can affect the long-term stability of the primary standard, due to its movement or other extraneous causes. The calibration of the reference standard against the primary standard at the RSL, for an industrial type 192Ir source maintained at the laboratory, showed excellent agreement with the hospital calibration, making it possible to check the reference chamber calibration at RSL itself. Further calibration procedures have been developed to offer traceable calibration of the hospital well ionization chambers.

Air↗

Calculation vs calibration curve for INR determination. Results of an interlaboratory proficiency scheme.

We surveyed 271 laboratories participating in a quality assessment program to ascertain whether the use of a calibration curve for determining the international normalized ratio (INR) would improve interlaboratory accuracy and precision. Lyophilized warfarinized samples with INR values assigned through manual calibration against internationally assigned rabbit reference thromboplasts were assayed for prothrombin time. Calibration analysis on the results was performed by linear regression. In all but 1 sample, the mean INR value computed by the calibration method was closer to the "true" value than the mean for the conventional calculation method using the International Sensitivity Index (ISI); the ISI calculation consistently overestimated the true value. Interlaboratory variation decreased using the calibration method. Variation from reagent to reagent was greater than from instrument to instrument, but was reduced by the calibration method. The specificity of the ISI for instrument type did not seem to alter the findings. Use of in-house calibrators to verify the ISI improved precision but not necessarily accuracy. The formation of a stable calibration line is consistent over time, but further studies are required to confirm whether such calibration improves the accuracy and precision of INR determination in practice.

Animals↗

Regression calibration in studies with correlated variables measured with error.

Regression calibration is a technique that corrects biases in regression results in situations where exposure variables are measured with error. The existence of a calibration substudy, where accurate and crude measurement methods are related by a second regression analysis, is assumed. The cost of measurement error in multivariate analyses is loss of statistical power. In this paper, calibration data from California Seventh-day Adventists are used to simulate study populations and new calibration studies. Applying regression calibration logistic analyses, the authors estimate power for pairs of nutritional variables. The results demonstrate substantial loss of power if variables measured with error are strongly correlated. Biases in estimated effects in cases where regression calibration is not performed can be large and are corrected by regression calibration. When the true coefficient has zero value, the corresponding coefficient in a crude analysis will usually have a nonzero expected value. Then type I error probabilities are not nominal, and the erroneous appearance of statistical significance can readily occur, particularly in large studies. Major determinants of power with use of regression calibration are collinearity between the variables measured with error and the size of correlations between crude and corresponding true variables. Where there is important collinearity, useful gains in power accrue with calibration study size up to 1,000 subjects.

Bias↗

Calibration of avian molecular clocks.

Molecular clocks can be calibrated using fossils within the group under study (internal calibration) or outside of the group (external calibration). Both types of calibration have their advantages and disadvantages. An internal calibration may reduce extrapolation error but may not be from the best fossil record, raising the issue of nonindependence. An external calibration may be more independent but also may have a greater extrapolation error. Here, we used the advantages of both methods by applying a sequential calibration to avian molecular clocks. We estimated a basal divergence within birds, the split between fowl (Galliformes) and ducks (Anseriformes), to be 89.8 +/- 6.97 MYA using an external calibration and 12 rate-constant nuclear genes. In turn, this time estimate was used as an internal calibration for three species-rich avian molecular data sets: mtDNA, DNA-DNA hybridization, and transferrin immunological distances. The resulting time estimates indicate that many major clades of modern birds had their origins within the Cretaceous. This supports earlier studies that identified large gaps in the avian fossil record and suggests that modern birds may have coexisted with other avian lineages for an extended period during the Cretaceous. The new time estimates are concordant with a continental breakup model for the origin of ratites.

Animals↗

Automated VO2max calibrator for open-circuit indirect calorimetry systems.

The complete calibration of indirect calorimetry systems involves simultaneous checks of gas analyzers, volume device, and software, and this requires a machine that can mimic accurately and precisely the ventilation and expired gases of an athlete. While previous calibrators have been built successfully, none have matched the ventilatory flows produced by athletes during high intensity exercise. A calibrator able to simulate high aerobic power (VO2max calibrator) was fabricated and tested against conventional indirect calorimetry systems that use chain-compensated gasometers to measure expired volume (VE systems) and calibrated electronic gas analyzers. The calibrator was also checked against a system that measures inspired volume (VI system) with a turbine ventilometer. The pooled data from both VE and VI systems for predicted VO2 ranging from 2.9 to 7.9 L.min-1 and ventilation ranging from 89 to 246 L.min-1 how that the absolute accuracy (bias) of values measured by conventional indirect calorimetry systems compared with those predicted by the calibrator was excellent. The bias was < 35 mL.min-1 for VO2 and carbon dioxide production, < 0.50 L.min-1 for ventilator (VE BTPS), -0.02% absolute for the percentage of expired O2 and +0.02% absolute for the percentage of expired CO2. Overall, the precision of the measured VO2, VCO2, and VE BTPS was approximately 1%. This VO2max calibrator is a versatile device that can be used for routine calibration of most indirect calorimetry systems that assess the ventilation and aerobic power of athletes.

Blood Gas Analysis↗

Calibration of an amorphous-silicon flat panel portal imager for exit-beam dosimetry.

Amorphous-silicon flat panel detectors are currently used to acquire digital portal images with excellent image quality for patient alignment before external beam radiation therapy. As a first step towards interpreting portal images acquired during treatment in terms of the actual dose delivered to the patient, a calibration method is developed to convert flat panel portal images to the equivalent water dose deposited in the detector plane and at a depth of 1.5 cm. The method is based on empirical convolution models of dose deposition in the flat panel detector and in water. A series of calibration experiments comparing the response of the flat panel imager and ion chamber measurements of dose in water determines the model parameters. Kernels derived from field size measurements account for the differences in the production and detection of scattered radiation in the two systems. The dissimilar response as a function of beam energy spectrum is characterized from measurements performed at various off-axis positions and for increasing attenuator thickness in the beam. The flat panel pixel inhomogeneity is corrected by comparing a large open field image with profiles measured in water. To verify the accuracy of the calibration method, calibrated flat panel profiles were compared with measured dose profiles for fields delivered through solid water slabs, a solid water phantom containing an air cavity, and an anthropomorphic head phantom. Open rectangular fields of various sizes and locations as well as a multileaf collimator-shaped field were delivered. For all but the smallest field centered about the central axis, the calibrated flat panel profiles matched the measured dose profiles with little or no systematic deviation and approximately 3% (two standard deviations) accuracy for the in-field region. The calibrated flat panel profiles for fields located off the central axis showed a small -1.7% systematic deviation from the measured profiles for the in-field region. Out of the field, the differences between the calibrated flat panel and measured profiles continued to be small, approximately 0%-2% of the mean in-field dose. Further refinement of the calibration model should increase the accuracy of the procedure. This calibration method for flat panel portal imagers may be used as part of a validation scheme to verify the dose delivered to the patient during treatment.

Calibration↗