Re-testing as a method of implementing external quality assessment program for COVID-19 real time PCR testing in Uganda
Significant milestones have been made in the development of COVID19 diagnostics Technologies. Government of the republic of Uganda and the line Ministry of Health mandated Uganda Virus Research Institute to ensure quality of COVID19 diagnostics. Re-testing was one of the methods initiated by the UVR...
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creator | Okek, Erick Jacob Masembe, Fredrick Joshua Kiconco, Jocelyn Kayiwa, John Amwine, Esther Obote, Daniel Alele, Stephen Nahabwe, Charles Were, Jackson Bagaya, Bernard Balinandi, Stephen Lutwama, Julius Kaleebu, Pontiano |
description | Significant milestones have been made in the development of COVID19 diagnostics Technologies. Government of the republic of Uganda and the line Ministry of Health mandated Uganda Virus Research Institute to ensure quality of COVID19 diagnostics. Re-testing was one of the methods initiated by the UVRI to implement External Quality assessment of COVID19 molecular diagnostics.
participating laboratories were required by UVRI to submit their already tested and archived nasopharyngeal samples and corresponding meta data. These were then re-tested at UVRI using the WHO Berlin protocol, the UVRI results were compared to those of the primary testing laboratories in order to ascertain performance agreement for the qualitative & quantitative results obtained. Ms Excel window 12 and GraphPad prism ver 15 was used in the analysis. Bar graphs, pie charts and line graphs were used to compare performance agreement between the reference Laboratory and primary testing Laboratories.
Eleven (11) Ministry of Health/Uganda Virus Research Institute COVID19 accredited laboratories participated in the re-testing of quality control samples. 5/11 (45%) of the primary testing laboratories had 100% performance agreement with that of the National Reference Laboratory for the final test result. Even where there was concordance in the final test outcome (negative or positive) between UVRI and primary testing laboratories, there were still differences in CT values. The differences in the Cycle Threshold (CT) values were insignificant except for Tenna & Pharma Laboratory and the UVRI(p = 0.0296). The difference in the CT values were not skewed to either the National reference Laboratory(UVRI) or the primary testing laboratory but varied from one laboratory to another. In the remaining 6/11 (55%) laboratories where there were discrepancies in the aggregate test results, only samples initially tested and reported as positive by the primary laboratories were tested and found to be false positives by the UVRI COVID19 National Reference Laboratory.
False positives were detected from public, private not for profit and private testing laboratories in almost equal proportion. There is need for standardization of molecular testing platforms in Uganda. There is also urgent need to improve on the Laboratory quality management systems of the molecular testing laboratories in order to minimize such discrepancies. |
doi_str_mv | 10.1371/journal.pone.0287272 |
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participating laboratories were required by UVRI to submit their already tested and archived nasopharyngeal samples and corresponding meta data. These were then re-tested at UVRI using the WHO Berlin protocol, the UVRI results were compared to those of the primary testing laboratories in order to ascertain performance agreement for the qualitative & quantitative results obtained. Ms Excel window 12 and GraphPad prism ver 15 was used in the analysis. Bar graphs, pie charts and line graphs were used to compare performance agreement between the reference Laboratory and primary testing Laboratories.
Eleven (11) Ministry of Health/Uganda Virus Research Institute COVID19 accredited laboratories participated in the re-testing of quality control samples. 5/11 (45%) of the primary testing laboratories had 100% performance agreement with that of the National Reference Laboratory for the final test result. Even where there was concordance in the final test outcome (negative or positive) between UVRI and primary testing laboratories, there were still differences in CT values. The differences in the Cycle Threshold (CT) values were insignificant except for Tenna & Pharma Laboratory and the UVRI(p = 0.0296). The difference in the CT values were not skewed to either the National reference Laboratory(UVRI) or the primary testing laboratory but varied from one laboratory to another. In the remaining 6/11 (55%) laboratories where there were discrepancies in the aggregate test results, only samples initially tested and reported as positive by the primary laboratories were tested and found to be false positives by the UVRI COVID19 National Reference Laboratory.
False positives were detected from public, private not for profit and private testing laboratories in almost equal proportion. There is need for standardization of molecular testing platforms in Uganda. There is also urgent need to improve on the Laboratory quality management systems of the molecular testing laboratories in order to minimize such discrepancies.</description><identifier>ISSN: 1932-6203</identifier><identifier>EISSN: 1932-6203</identifier><identifier>DOI: 10.1371/journal.pone.0287272</identifier><identifier>PMID: 38265993</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Academies and Institutes ; Archives & records ; Biobanks ; Biology and Life Sciences ; COVID-19 ; COVID-19 - diagnosis ; COVID-19 Testing ; Engineering and Technology ; Graphs ; Hospitals ; Humans ; Laboratories ; Management systems ; Medical care ; Medicine and Health Sciences ; Metadata ; People and Places ; Pharmaceuticals ; Polymerase chain reaction ; Qualitative analysis ; Quality assessment ; Quality control ; Quality management ; Real time ; Real-Time Polymerase Chain Reaction ; Research and Analysis Methods ; Research centers ; Standardization ; Supervision ; Testing ; Testing laboratories ; Uganda</subject><ispartof>PloS one, 2024-01, Vol.19 (1), p.e0287272-e0287272</ispartof><rights>Copyright: © 2024 Okek et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</rights><rights>COPYRIGHT 2024 Public Library of Science</rights><rights>2024 Okek et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 Okek et al 2024 Okek et al</rights><rights>2024 Okek et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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><cites>FETCH-LOGICAL-c642t-80ba52f4bcc666e6f93929858be7258c13928d6a406481177c2e904214990b03</cites><orcidid>0000-0002-1840-1801 ; 0000-0002-2836-7141</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/PMC10807774/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10807774/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,2095,2914,23846,27903,27904,53769,53771,79346,79347</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38265993$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Onwuamah, Chika Kingsley</contributor><creatorcontrib>Okek, Erick Jacob</creatorcontrib><creatorcontrib>Masembe, Fredrick Joshua</creatorcontrib><creatorcontrib>Kiconco, Jocelyn</creatorcontrib><creatorcontrib>Kayiwa, John</creatorcontrib><creatorcontrib>Amwine, Esther</creatorcontrib><creatorcontrib>Obote, Daniel</creatorcontrib><creatorcontrib>Alele, Stephen</creatorcontrib><creatorcontrib>Nahabwe, Charles</creatorcontrib><creatorcontrib>Were, Jackson</creatorcontrib><creatorcontrib>Bagaya, Bernard</creatorcontrib><creatorcontrib>Balinandi, Stephen</creatorcontrib><creatorcontrib>Lutwama, Julius</creatorcontrib><creatorcontrib>Kaleebu, Pontiano</creatorcontrib><title>Re-testing as a method of implementing external quality assessment program for COVID-19 real time PCR testing in Uganda</title><title>PloS one</title><addtitle>PLoS One</addtitle><description>Significant milestones have been made in the development of COVID19 diagnostics Technologies. Government of the republic of Uganda and the line Ministry of Health mandated Uganda Virus Research Institute to ensure quality of COVID19 diagnostics. Re-testing was one of the methods initiated by the UVRI to implement External Quality assessment of COVID19 molecular diagnostics.
participating laboratories were required by UVRI to submit their already tested and archived nasopharyngeal samples and corresponding meta data. These were then re-tested at UVRI using the WHO Berlin protocol, the UVRI results were compared to those of the primary testing laboratories in order to ascertain performance agreement for the qualitative & quantitative results obtained. Ms Excel window 12 and GraphPad prism ver 15 was used in the analysis. Bar graphs, pie charts and line graphs were used to compare performance agreement between the reference Laboratory and primary testing Laboratories.
Eleven (11) Ministry of Health/Uganda Virus Research Institute COVID19 accredited laboratories participated in the re-testing of quality control samples. 5/11 (45%) of the primary testing laboratories had 100% performance agreement with that of the National Reference Laboratory for the final test result. Even where there was concordance in the final test outcome (negative or positive) between UVRI and primary testing laboratories, there were still differences in CT values. The differences in the Cycle Threshold (CT) values were insignificant except for Tenna & Pharma Laboratory and the UVRI(p = 0.0296). The difference in the CT values were not skewed to either the National reference Laboratory(UVRI) or the primary testing laboratory but varied from one laboratory to another. In the remaining 6/11 (55%) laboratories where there were discrepancies in the aggregate test results, only samples initially tested and reported as positive by the primary laboratories were tested and found to be false positives by the UVRI COVID19 National Reference Laboratory.
False positives were detected from public, private not for profit and private testing laboratories in almost equal proportion. There is need for standardization of molecular testing platforms in Uganda. 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One</addtitle><date>2024-01-24</date><risdate>2024</risdate><volume>19</volume><issue>1</issue><spage>e0287272</spage><epage>e0287272</epage><pages>e0287272-e0287272</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Significant milestones have been made in the development of COVID19 diagnostics Technologies. Government of the republic of Uganda and the line Ministry of Health mandated Uganda Virus Research Institute to ensure quality of COVID19 diagnostics. Re-testing was one of the methods initiated by the UVRI to implement External Quality assessment of COVID19 molecular diagnostics.
participating laboratories were required by UVRI to submit their already tested and archived nasopharyngeal samples and corresponding meta data. These were then re-tested at UVRI using the WHO Berlin protocol, the UVRI results were compared to those of the primary testing laboratories in order to ascertain performance agreement for the qualitative & quantitative results obtained. Ms Excel window 12 and GraphPad prism ver 15 was used in the analysis. Bar graphs, pie charts and line graphs were used to compare performance agreement between the reference Laboratory and primary testing Laboratories.
Eleven (11) Ministry of Health/Uganda Virus Research Institute COVID19 accredited laboratories participated in the re-testing of quality control samples. 5/11 (45%) of the primary testing laboratories had 100% performance agreement with that of the National Reference Laboratory for the final test result. Even where there was concordance in the final test outcome (negative or positive) between UVRI and primary testing laboratories, there were still differences in CT values. The differences in the Cycle Threshold (CT) values were insignificant except for Tenna & Pharma Laboratory and the UVRI(p = 0.0296). The difference in the CT values were not skewed to either the National reference Laboratory(UVRI) or the primary testing laboratory but varied from one laboratory to another. In the remaining 6/11 (55%) laboratories where there were discrepancies in the aggregate test results, only samples initially tested and reported as positive by the primary laboratories were tested and found to be false positives by the UVRI COVID19 National Reference Laboratory.
False positives were detected from public, private not for profit and private testing laboratories in almost equal proportion. There is need for standardization of molecular testing platforms in Uganda. There is also urgent need to improve on the Laboratory quality management systems of the molecular testing laboratories in order to minimize such discrepancies.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>38265993</pmid><doi>10.1371/journal.pone.0287272</doi><tpages>e0287272</tpages><orcidid>https://orcid.org/0000-0002-1840-1801</orcidid><orcidid>https://orcid.org/0000-0002-2836-7141</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1932-6203 |
ispartof | PloS one, 2024-01, Vol.19 (1), p.e0287272-e0287272 |
issn | 1932-6203 1932-6203 |
language | eng |
recordid | cdi_plos_journals_3069270234 |
source | MEDLINE; DOAJ Directory of Open Access Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Public Library of Science (PLoS); PubMed Central; Free Full-Text Journals in Chemistry |
subjects | Academies and Institutes Archives & records Biobanks Biology and Life Sciences COVID-19 COVID-19 - diagnosis COVID-19 Testing Engineering and Technology Graphs Hospitals Humans Laboratories Management systems Medical care Medicine and Health Sciences Metadata People and Places Pharmaceuticals Polymerase chain reaction Qualitative analysis Quality assessment Quality control Quality management Real time Real-Time Polymerase Chain Reaction Research and Analysis Methods Research centers Standardization Supervision Testing Testing laboratories Uganda |
title | Re-testing as a method of implementing external quality assessment program for COVID-19 real time PCR testing in Uganda |
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