Podcast
Questions and Answers
What is the main advantage of patient-based real-time quality control (PBRTQC) techniques over traditional quality control?
What is the main advantage of patient-based real-time quality control (PBRTQC) techniques over traditional quality control?
In the study, what technique was used to compare different PBRTQC techniques?
In the study, what technique was used to compare different PBRTQC techniques?
For analytes with skewed distributions, what was investigated in addition to moving averages and moving medians?
For analytes with skewed distributions, what was investigated in addition to moving averages and moving medians?
What was shown to be similar for analytes with symmetrical distributions?
What was shown to be similar for analytes with symmetrical distributions?
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What was the main focus of the study in terms of detecting analytical bias and shifts?
What was the main focus of the study in terms of detecting analytical bias and shifts?
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Which statistical transformation is proposed to normalize skewed distributions for some analytes in PBRTQC techniques?
Which statistical transformation is proposed to normalize skewed distributions for some analytes in PBRTQC techniques?
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What is the main advantage of Box–Cox transformation in PBRTQC programs?
What is the main advantage of Box–Cox transformation in PBRTQC programs?
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What is the purpose of moving medians in PBRTQC techniques for skewed distributions?
What is the purpose of moving medians in PBRTQC techniques for skewed distributions?
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What is the challenge associated with using moving averages for right skewed distributions in PBRTQC?
What is the challenge associated with using moving averages for right skewed distributions in PBRTQC?
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What is the key consideration for the optimal approach in PBRTQC programs?
What is the key consideration for the optimal approach in PBRTQC programs?
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What block size was used for mean calculation in the study?
What block size was used for mean calculation in the study?
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What was the false rejection rate allowed for control limits?
What was the false rejection rate allowed for control limits?
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Which package in R was used for calculating moving averages and medians?
Which package in R was used for calculating moving averages and medians?
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What was the method used to assess the performance of each PBRTQC protocol?
What was the method used to assess the performance of each PBRTQC protocol?
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How was bias introduced for simulation and detection in the study?
How was bias introduced for simulation and detection in the study?
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What is the main challenge associated with patient-based real-time quality control (PBRTQC) techniques?
What is the main challenge associated with patient-based real-time quality control (PBRTQC) techniques?
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What was the primary focus of the study in terms of patient-based real-time quality control (PBRTQC) techniques?
What was the primary focus of the study in terms of patient-based real-time quality control (PBRTQC) techniques?
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What was the impact of Box–Cox transformation on the performance of moving averages for analytes with skewed distributions?
What was the impact of Box–Cox transformation on the performance of moving averages for analytes with skewed distributions?
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What was the key finding regarding the performance of moving averages for right skewed distributions such as alanine aminotransferase and creatinine?
What was the key finding regarding the performance of moving averages for right skewed distributions such as alanine aminotransferase and creatinine?
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What did the study emphasize regarding the optimal approaches for PBRTQC techniques?
What did the study emphasize regarding the optimal approaches for PBRTQC techniques?
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What technique was used to assess the distribution of patient results?
What technique was used to assess the distribution of patient results?
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What was found to have little benefit over a simple moving average with no truncation, except for magnesium?
What was found to have little benefit over a simple moving average with no truncation, except for magnesium?
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What markedly improved the performance of simple moving averages for several analytes?
What markedly improved the performance of simple moving averages for several analytes?
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What did the study assess the retrospective detection of, affecting creatinine and urea?
What did the study assess the retrospective detection of, affecting creatinine and urea?
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What varied depending on the analyte, PBRTQC protocol used, and whether the bias was positive or negative?
What varied depending on the analyte, PBRTQC protocol used, and whether the bias was positive or negative?
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What is the average number of patient samples until error is detected (ANPed) for negative shifts in bicarbonate?
What is the average number of patient samples until error is detected (ANPed) for negative shifts in bicarbonate?
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What did the study find regarding the performance of moving averages for right skewed distributions, such as alanine aminotransferase and creatinine?
What did the study find regarding the performance of moving averages for right skewed distributions, such as alanine aminotransferase and creatinine?
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What is the primary purpose of Box-Cox transformation in the context of the study?
What is the primary purpose of Box-Cox transformation in the context of the study?
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What was shown to have little benefit over a simple moving average with no truncation, except for magnesium?
What was shown to have little benefit over a simple moving average with no truncation, except for magnesium?
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What was the impact of excluding abnormal results with narrow truncation limits for symmetrical distributions?
What was the impact of excluding abnormal results with narrow truncation limits for symmetrical distributions?
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Study Notes
Analytical Performance of Moving Averages and Moving Medians for Skewed Distributions
- Moving averages and moving medians were used for skewed distributions, as well as for symmetrical distributions.
- Normal QQ plots were used to assess the distribution of patient results.
- Truncation limits were set based on deviation from the linear portion of the Q-Q plot to minimize the influence of diseased population on the moving average.
- Bias detection curves for symmetrical distributions and skewed distributions were examined for different PBRTQC approaches.
- Error detection varied depending on the analyte, PBRTQC protocol used, and whether the bias was positive or negative.
- Detection of bias was difficult for certain analytes, requiring a large number of samples to detect shifts.
- The addition of wide truncation limits had little benefit over a simple moving average with no truncation, except for magnesium.
- Error detection for right skewed analytes was generally poorer compared to symmetrically distributed analytes.
- Box-Cox transformation of the data markedly improved the performance of simple moving averages for several analytes.
- The performance of the moving median was also improved by the Box-Cox transformation of the data.
- The study assessed the retrospective detection of a real instrument failure affecting creatinine and urea.
- Different algorithms were applied to patient results retrospectively, and error detection time of the algorithms was summarized in Table 2.
Analytical Performance of Patient-Based Retrospective TQC Protocols
- The study compares different patient-based retrospective TQC protocols for skewed and symmetrical patient data distributions.
- The protocols aim to minimize the influence of diseased patients on the moving average (MA) and detect bias in patient results.
- For skewed distributions, truncation limits are used to censor patient data at the inflection point of the frequency distribution curve.
- The detection of bias varies based on the analyte, protocol used, and the nature of the bias (positive or negative).
- Negative bias in albumin and positive bias in bicarbonate are difficult to detect, requiring more than 300 samples for each protocol.
- Error detection is better for negative shifts in bicarbonate, with an average number of patient samples until error detected (ANPed) of less than 50 samples.
- For symmetrical distributions, adding wide truncation limits offers little benefit over a simple MA with no truncation, except for magnesium.
- Excluding abnormal results with narrow truncation limits paradoxically increases ANPed for larger shifts.
- For right skewed distributions, error detection is generally poorer than for symmetrically distributed analytes, and differences between protocols are more marked.
- Box-Cox transformation of the data improves the performance of the MA and moving median for detecting negative shifts in certain analytes.
- The study retrospectively assessed the detection of a real instrument failure affecting creatinine and urea, with the MA and moving median showing improved detection.
- Table 2 summarizes the error detection time of the different algorithms for the real instrument failure affecting creatinine and urea.
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Description
Test your knowledge of patient-based real-time quality control techniques in clinical laboratories with this quiz. Explore statistical methods for reducing the impact of population variation, such as moving averages, moving medians, and Box-Cox transformation for skewed analyte distributions.