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	<title>Analytical Performance &#8211; mikrobik.net</title>
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		<title>Use of Capability Index to Improve Laboratory Analytical Performance</title>
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		<pubDate>Fri, 20 Nov 2009 14:29:00 +0000</pubDate>
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		<category><![CDATA[Analytical Performance]]></category>
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					<description><![CDATA[Use of Capability Index to Improve Laboratory Analytical Performance Renze Bais Clin Biochem Rev Vol 29 Suppl (i) August 2008 Summary • For detection of errors where the standard deviation is wide compared...]]></description>
										<content:encoded><![CDATA[<p><strong><span style="color:#5C3566;">Use of Capability Index to Improve Laboratory Analytical Performance</span></strong><br />
Renze Bais</p>
<p><a href="http://old.aacb.asn.au/pubs/2008%20cbr%20articles/august%20cbr%202008%20bais.pdf" target="_blank" rel="noopener">Clin Biochem Rev Vol 29 Suppl (i) August 2008</a></p>
<p>Summary<br />
• For detection of errors where the standard deviation is wide compared to clinical requirements, consider use of the Capability Index (Cps).<br />
• Cps is defined as ‘Allowable Limit of Error divided by the standard deviation of between-batch QC measurement’.<br />
• ‘Capable’ assays have Cps >4 compared with ‘incapable’ ones with Cps <4.
• Capability of an analyte can be used to optimise the amount of quality control (QC) required and still maintain appropriate error detection.
• For EQA material, Cps can be used for continuously monitoring individual analytes, comparing laboratory performance with peers and comparison with industry-wide performance.
• The capability approach can result in reducing the number of QCs run per day, reducing costs as well as significantly improving the performance of a number of assays.
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