Quality Requirements - Westgard QC - Blog - Page 2 - Results from #20

Tools, Technologies and Training for Healthcare Laboratories

Q & A: Why not just change our SD?

Posted by Sten Westgard, MS

Here's a question that came in about setting the control limits (or range) for a test:

"for some assays we're using this formula: actual SD * 3 and then divided by 2 plus or minus the mean is this acceptable or not because when we use that give us abit wider range than using the mean plus minus 2SD."

When we asked for an example, we got this data:

Manufacturer Data: SD = 22.5, Mean = 224
Actual Data: SD = 8.79, Mean = 223

"We're multiplying ourSD (8.79) by 3 and then we divide it by 2 to give us the new SD which is 13 (8.79*3/2 = 13).
Then we multiply this new SD 13 by 2 to give us the real 2 SD range which is 26.
So our range is now 197 - 249.
Are we following the right way or not?"

The answer, after the jump...

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New Diagnosis: HbA1c for Diabetes

Posted by Sten Westgard, MS

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What's the Q of D? 2012 update

Posted by Sten Westgard, MS

In the recent issue of Clinical Chemistry, an editorial reviews the current state of Vitamin D testing: "There is common agreement that 25-OHD is a 'difficult' analyte."

25-Hydroxyvitamin D: A Difficult Analyte, Graham D. Carter, Clin Chem 58:3; 486-488 (2012).

At the same time, the editorial notes that marked process is being made:

"Nevertheless, results submitted to the international Vitamin D External Quality Assessment (DEQAS) have shown a gradual reduction in interlaboratory imprecision (CV) in recent years - from >30% in 1995 to 15% in 2011."

The question is, is that reduction in imprecision good enough? Or is the quality required by Vitamin D still too "difficult"?

More after the jump...

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New Paper on MU, TE, and the unnecessary struggle

Posted by Sten Westgard, MS

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Wanted: Data that's live

Posted by Sten Westgard, MS

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New Paper: Risk-Based QC Strategies with Six Sigma Nomograms

Posted by Sten Westgard, MS

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Are there new (Erna Lenters-)"Westra Rules" for HbA1c?

Posted by Sten Westgard, MS

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Sigma-metrics in Korea PT

Posted by Sten Westgard, MS

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Q&A: 10 Questions on QC from the first webinar

Posted by Sten Westgard, MS

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Budgets aren't the only things getting squeezed in the lab...

Posted by Sten Westgard, MS

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Setting specifications for setting specifications for...

Posted by Sten Westgard, MS

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Coming to Croatia: Zagreb's EFLM course

Posted by Sten Westgard, MS

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New Publication: Useful measures and models for quality

Posted by Sten Westgard, MS

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Losing ground on HbA1c

Posted by Sten Westgard, MS

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Are performance specifications based on biological variation for hemostatis unfit-for-purpose?

Posted by Sten Westgard, MS

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AACC comments on Proposed New CLIA goals

Posted by Sten Westgard, MS

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NY Times Editorial Focuses on Failures in Medical Device Regulation

A recent New York Times Sunday editorial focused on the deplorable state of medical device regulation. We simply can no longer trust FDA clearances, particularly 510ks:

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Six Sigma Metrics ... Surging in China

Posted by Sten Westgard, MS

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EFLM database: 78 steps forward, 272 steps back

Posted by Sten Westgard, MS

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Q and A: Is the 10:x rule still compulsory?

A recent question came to me via social media: "Hello Sir, Good morning, How are you? I wanted to know is still 10x rule is coumpulsary?[stet.]  Even [when] we are using lab mean and lab SD. Please share the details.Thanks and Regards, [anonymous]"10:x is not compulsory by any regulation that I am aware of. Many regulations require you to...

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