EQA/PT scheme to improve the equivalence of enzymatic results between mutual recognition laboratories in Beijing
Background To utilize the external quality assessment (EQA)/proficiency testing (PT) scheme to evaluate the equivalence of different clinical enzymatic measuring systems in Beijing. Methods The Beijing Center for Clinical Laboratory (BCCL) distributed three investigation samples to mutual recognitio...
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description | Background
To utilize the external quality assessment (EQA)/proficiency testing (PT) scheme to evaluate the equivalence of different clinical enzymatic measuring systems in Beijing.
Methods
The Beijing Center for Clinical Laboratory (BCCL) distributed three investigation samples to mutual recognition clinical laboratories in Beijing including alanine aminotransferase (ALT), aspartate aminotransferase (AST), γ‐glutamyltransferase (GGT), creatine kinase (CK), and lactate dehydrogenase (LDH). These samples were derived from serum pools with values assigned by the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) enzymatic reference measurement procedures (RMPs). Each laboratory performed duplicate tests of the samples. Then, the samples at level 1 were used to recalibrate individual measuring systems for repeating the tests. BCCL collected data for evaluation of their analytical quality.
Results
Before recalibration, the biases of ALT and AST tests were not traceable to the IFCC RMPs, and the bias pass rates of GGT, CK, and LDH tests were only 51.2%, 55.7%, and 48.6% respectively. After recalibration, the pass rates of ALT, AST, GGT, CK, and LDH increased to 95.1%, 82.9%, 95.1%, 97.1%, and 70.0% respectively. The EQA/PT also showed that after recalibration, more than 95% of laboratories met the optimum level specifications of the biological variation for ALT, AST, GGT, and CK tests and the desirable for LDH tests.
Conclusion
The enzymatic tests in Beijing need to be further standardized by category 1 or 2 EQA/PT scheme for mutual recognition between clinical laboratories. The criteria of biological variation are more relevant for determining the equivalence of clinical enzymatic tests.
Using fresh human serum pools which assigned valued by IFCC RMPS performed re‐calibration, the trueness of enzymatic tests results had been improved. It is also necessary to implement Category 1or 2 EQA/PT schemes to monitor the equivalence of results and the success of standardization in Beijing. |
doi_str_mv | 10.1002/jcla.23814 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8183905</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2537673989</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4484-6f33d040a645ebd82b71448ec60683b5343359f81ce8b4fb03fc2bca849d9e343</originalsourceid><addsrcrecordid>eNp9kU1rGzEQhkVpady0l_6AIuilFJxIK-16dCk4JukHhraQnoVWnrVltJIj7Tq4vz5KnYa2h55GzPvwMOIl5DVnZ5yx6nxrvTmrBHD5hEw4UzCtoKqfkgkDmE2BcXFCXuS8ZYyB4s1zciKEkqCgmZDd5ff5-bdrmu0Ge6RDpK7fpbgvzw1SvBnd3ngMFmnsKIafh94MztKEefRDpi0Ot4iB9uMwGl_WNq6DG1wM1Js2JjPE5DBTF-gFuq0L65fkWWd8xlcP85T8uLq8XnyaLr9-_LyYL6dWSpDTphNixSQzjayxXUHVzngJ0DasAdHWQgpRqw64RWhl1zLR2aq1BqRaKSzpKflw9O7GtseVxTAk4_Uuud6kg47G6b-T4DZ6HfcaOAjF6iJ49yBI8WbEPOjeZYvem4BxzLqqq0ooYAIK-vYfdBvHFMr3CiVmzaxwqlDvj5RNMeeE3eMxnOn7IvV9kfpXkQV-8-f5j-jv5grAj8Ct83j4j0p_WSznR-kd7faqcQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2537673989</pqid></control><display><type>article</type><title>EQA/PT scheme to improve the equivalence of enzymatic results between mutual recognition laboratories in Beijing</title><source>DOAJ Directory of Open Access Journals</source><source>Wiley Online Library Journals Frontfile Complete</source><source>Wiley-Blackwell Open Access Titles</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>Tong, Qing ; Zhang, Shunli ; Zuo, Chang</creator><creatorcontrib>Tong, Qing ; Zhang, Shunli ; Zuo, Chang</creatorcontrib><description>Background
To utilize the external quality assessment (EQA)/proficiency testing (PT) scheme to evaluate the equivalence of different clinical enzymatic measuring systems in Beijing.
Methods
The Beijing Center for Clinical Laboratory (BCCL) distributed three investigation samples to mutual recognition clinical laboratories in Beijing including alanine aminotransferase (ALT), aspartate aminotransferase (AST), γ‐glutamyltransferase (GGT), creatine kinase (CK), and lactate dehydrogenase (LDH). These samples were derived from serum pools with values assigned by the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) enzymatic reference measurement procedures (RMPs). Each laboratory performed duplicate tests of the samples. Then, the samples at level 1 were used to recalibrate individual measuring systems for repeating the tests. BCCL collected data for evaluation of their analytical quality.
Results
Before recalibration, the biases of ALT and AST tests were not traceable to the IFCC RMPs, and the bias pass rates of GGT, CK, and LDH tests were only 51.2%, 55.7%, and 48.6% respectively. After recalibration, the pass rates of ALT, AST, GGT, CK, and LDH increased to 95.1%, 82.9%, 95.1%, 97.1%, and 70.0% respectively. The EQA/PT also showed that after recalibration, more than 95% of laboratories met the optimum level specifications of the biological variation for ALT, AST, GGT, and CK tests and the desirable for LDH tests.
Conclusion
The enzymatic tests in Beijing need to be further standardized by category 1 or 2 EQA/PT scheme for mutual recognition between clinical laboratories. The criteria of biological variation are more relevant for determining the equivalence of clinical enzymatic tests.
Using fresh human serum pools which assigned valued by IFCC RMPS performed re‐calibration, the trueness of enzymatic tests results had been improved. It is also necessary to implement Category 1or 2 EQA/PT schemes to monitor the equivalence of results and the success of standardization in Beijing.</description><identifier>ISSN: 0887-8013</identifier><identifier>EISSN: 1098-2825</identifier><identifier>DOI: 10.1002/jcla.23814</identifier><identifier>PMID: 33948986</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>Alanine ; Alanine transaminase ; Aspartate aminotransferase ; Bias ; Biological variation ; Creatine ; Creatine kinase ; Dehydrogenases ; enzymatic assay ; Enzymes ; external quality assessment ; L-Lactate dehydrogenase ; Laboratories ; Lactic acid ; Medical laboratories ; proficiency testing ; Quality control ; Reagents ; Reference materials ; Standardization</subject><ispartof>Journal of clinical laboratory analysis, 2021-06, Vol.35 (6), p.e23814-n/a</ispartof><rights>2021 The Authors. published by Wiley Periodicals LLC</rights><rights>2021 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.</rights><rights>2021. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4484-6f33d040a645ebd82b71448ec60683b5343359f81ce8b4fb03fc2bca849d9e343</citedby><cites>FETCH-LOGICAL-c4484-6f33d040a645ebd82b71448ec60683b5343359f81ce8b4fb03fc2bca849d9e343</cites><orcidid>0000-0002-8929-3043</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183905/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8183905/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1417,11562,27924,27925,45574,45575,46052,46476,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33948986$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tong, Qing</creatorcontrib><creatorcontrib>Zhang, Shunli</creatorcontrib><creatorcontrib>Zuo, Chang</creatorcontrib><title>EQA/PT scheme to improve the equivalence of enzymatic results between mutual recognition laboratories in Beijing</title><title>Journal of clinical laboratory analysis</title><addtitle>J Clin Lab Anal</addtitle><description>Background
To utilize the external quality assessment (EQA)/proficiency testing (PT) scheme to evaluate the equivalence of different clinical enzymatic measuring systems in Beijing.
Methods
The Beijing Center for Clinical Laboratory (BCCL) distributed three investigation samples to mutual recognition clinical laboratories in Beijing including alanine aminotransferase (ALT), aspartate aminotransferase (AST), γ‐glutamyltransferase (GGT), creatine kinase (CK), and lactate dehydrogenase (LDH). These samples were derived from serum pools with values assigned by the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) enzymatic reference measurement procedures (RMPs). Each laboratory performed duplicate tests of the samples. Then, the samples at level 1 were used to recalibrate individual measuring systems for repeating the tests. BCCL collected data for evaluation of their analytical quality.
Results
Before recalibration, the biases of ALT and AST tests were not traceable to the IFCC RMPs, and the bias pass rates of GGT, CK, and LDH tests were only 51.2%, 55.7%, and 48.6% respectively. After recalibration, the pass rates of ALT, AST, GGT, CK, and LDH increased to 95.1%, 82.9%, 95.1%, 97.1%, and 70.0% respectively. The EQA/PT also showed that after recalibration, more than 95% of laboratories met the optimum level specifications of the biological variation for ALT, AST, GGT, and CK tests and the desirable for LDH tests.
Conclusion
The enzymatic tests in Beijing need to be further standardized by category 1 or 2 EQA/PT scheme for mutual recognition between clinical laboratories. The criteria of biological variation are more relevant for determining the equivalence of clinical enzymatic tests.
Using fresh human serum pools which assigned valued by IFCC RMPS performed re‐calibration, the trueness of enzymatic tests results had been improved. It is also necessary to implement Category 1or 2 EQA/PT schemes to monitor the equivalence of results and the success of standardization in Beijing.</description><subject>Alanine</subject><subject>Alanine transaminase</subject><subject>Aspartate aminotransferase</subject><subject>Bias</subject><subject>Biological variation</subject><subject>Creatine</subject><subject>Creatine kinase</subject><subject>Dehydrogenases</subject><subject>enzymatic assay</subject><subject>Enzymes</subject><subject>external quality assessment</subject><subject>L-Lactate dehydrogenase</subject><subject>Laboratories</subject><subject>Lactic acid</subject><subject>Medical laboratories</subject><subject>proficiency testing</subject><subject>Quality control</subject><subject>Reagents</subject><subject>Reference materials</subject><subject>Standardization</subject><issn>0887-8013</issn><issn>1098-2825</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU1rGzEQhkVpady0l_6AIuilFJxIK-16dCk4JukHhraQnoVWnrVltJIj7Tq4vz5KnYa2h55GzPvwMOIl5DVnZ5yx6nxrvTmrBHD5hEw4UzCtoKqfkgkDmE2BcXFCXuS8ZYyB4s1zciKEkqCgmZDd5ff5-bdrmu0Ge6RDpK7fpbgvzw1SvBnd3ngMFmnsKIafh94MztKEefRDpi0Ot4iB9uMwGl_WNq6DG1wM1Js2JjPE5DBTF-gFuq0L65fkWWd8xlcP85T8uLq8XnyaLr9-_LyYL6dWSpDTphNixSQzjayxXUHVzngJ0DasAdHWQgpRqw64RWhl1zLR2aq1BqRaKSzpKflw9O7GtseVxTAk4_Uuud6kg47G6b-T4DZ6HfcaOAjF6iJ49yBI8WbEPOjeZYvem4BxzLqqq0ooYAIK-vYfdBvHFMr3CiVmzaxwqlDvj5RNMeeE3eMxnOn7IvV9kfpXkQV-8-f5j-jv5grAj8Ct83j4j0p_WSznR-kd7faqcQ</recordid><startdate>202106</startdate><enddate>202106</enddate><creator>Tong, Qing</creator><creator>Zhang, Shunli</creator><creator>Zuo, Chang</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8929-3043</orcidid></search><sort><creationdate>202106</creationdate><title>EQA/PT scheme to improve the equivalence of enzymatic results between mutual recognition laboratories in Beijing</title><author>Tong, Qing ; Zhang, Shunli ; Zuo, Chang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4484-6f33d040a645ebd82b71448ec60683b5343359f81ce8b4fb03fc2bca849d9e343</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Alanine</topic><topic>Alanine transaminase</topic><topic>Aspartate aminotransferase</topic><topic>Bias</topic><topic>Biological variation</topic><topic>Creatine</topic><topic>Creatine kinase</topic><topic>Dehydrogenases</topic><topic>enzymatic assay</topic><topic>Enzymes</topic><topic>external quality assessment</topic><topic>L-Lactate dehydrogenase</topic><topic>Laboratories</topic><topic>Lactic acid</topic><topic>Medical laboratories</topic><topic>proficiency testing</topic><topic>Quality control</topic><topic>Reagents</topic><topic>Reference materials</topic><topic>Standardization</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tong, Qing</creatorcontrib><creatorcontrib>Zhang, Shunli</creatorcontrib><creatorcontrib>Zuo, Chang</creatorcontrib><collection>Wiley-Blackwell Open Access Titles</collection><collection>Wiley Free Content</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of clinical laboratory analysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tong, Qing</au><au>Zhang, Shunli</au><au>Zuo, Chang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EQA/PT scheme to improve the equivalence of enzymatic results between mutual recognition laboratories in Beijing</atitle><jtitle>Journal of clinical laboratory analysis</jtitle><addtitle>J Clin Lab Anal</addtitle><date>2021-06</date><risdate>2021</risdate><volume>35</volume><issue>6</issue><spage>e23814</spage><epage>n/a</epage><pages>e23814-n/a</pages><issn>0887-8013</issn><eissn>1098-2825</eissn><abstract>Background
To utilize the external quality assessment (EQA)/proficiency testing (PT) scheme to evaluate the equivalence of different clinical enzymatic measuring systems in Beijing.
Methods
The Beijing Center for Clinical Laboratory (BCCL) distributed three investigation samples to mutual recognition clinical laboratories in Beijing including alanine aminotransferase (ALT), aspartate aminotransferase (AST), γ‐glutamyltransferase (GGT), creatine kinase (CK), and lactate dehydrogenase (LDH). These samples were derived from serum pools with values assigned by the International Federation of Clinical Chemistry and Laboratory Medicine (IFCC) enzymatic reference measurement procedures (RMPs). Each laboratory performed duplicate tests of the samples. Then, the samples at level 1 were used to recalibrate individual measuring systems for repeating the tests. BCCL collected data for evaluation of their analytical quality.
Results
Before recalibration, the biases of ALT and AST tests were not traceable to the IFCC RMPs, and the bias pass rates of GGT, CK, and LDH tests were only 51.2%, 55.7%, and 48.6% respectively. After recalibration, the pass rates of ALT, AST, GGT, CK, and LDH increased to 95.1%, 82.9%, 95.1%, 97.1%, and 70.0% respectively. The EQA/PT also showed that after recalibration, more than 95% of laboratories met the optimum level specifications of the biological variation for ALT, AST, GGT, and CK tests and the desirable for LDH tests.
Conclusion
The enzymatic tests in Beijing need to be further standardized by category 1 or 2 EQA/PT scheme for mutual recognition between clinical laboratories. The criteria of biological variation are more relevant for determining the equivalence of clinical enzymatic tests.
Using fresh human serum pools which assigned valued by IFCC RMPS performed re‐calibration, the trueness of enzymatic tests results had been improved. It is also necessary to implement Category 1or 2 EQA/PT schemes to monitor the equivalence of results and the success of standardization in Beijing.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>33948986</pmid><doi>10.1002/jcla.23814</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-8929-3043</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Alanine Alanine transaminase Aspartate aminotransferase Bias Biological variation Creatine Creatine kinase Dehydrogenases enzymatic assay Enzymes external quality assessment L-Lactate dehydrogenase Laboratories Lactic acid Medical laboratories proficiency testing Quality control Reagents Reference materials Standardization |
title | EQA/PT scheme to improve the equivalence of enzymatic results between mutual recognition laboratories in Beijing |
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