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Improved efficiency using sequential automated immunoassays for syphilis screening in blood donors.
Cheng, Anthea; Das, Anindita; Styles, Claire E; Naing, Zin; Rawlinson, William D; Gosbell, Iain B.
Afiliação
  • Cheng A; Pathology and Clinical Governance, Australian Red Cross Lifeblood, West Melbourne, Victoria, Australia.
  • Das A; Pathology and Clinical Governance, Australian Red Cross Lifeblood, West Melbourne, Victoria, Australia.
  • Styles CE; Clinical Microbiology, ACT Pathology, Garran, Australian Capital Territory, Australia.
  • Naing Z; Faculty of Health, University of Canberra, Bruce, Australian Capital Territory, Australia.
  • Rawlinson WD; Pathology and Clinical Governance, Australian Red Cross Lifeblood, West Melbourne, Victoria, Australia.
  • Gosbell IB; Serology and Virology Division (SAViD), NSW Health Pathology, Randwick, New South Wales, Australia.
J Clin Microbiol ; 62(8): e0047624, 2024 Aug 14.
Article em En | MEDLINE | ID: mdl-39007562
ABSTRACT
Using sequential immunoassays for the screening of blood donors is well described for viral serology testing but not for the screening of syphilis. In this study, we report the evaluation results and 2-year sequential testing data using two highly sensitive automated serology assays, the Alinity s Syphilis chemiluminescent immunoassay for screening, with all repeatedly reactive samples then tested on the Elecsys Syphilis electrochemiluminescence immunoassay. We screened 1,767,782 blood donor samples between 7 July 2021 and 6 July 2023 and found the Alinity false-positive rate to be low at 0.08% (1,456/1,767,782). The common false-positive rate between the two assays was also low (3.83%, 58/1,514). Concordantly reactive samples were further tested using a Treponema pallidum particle agglutination test, a rapid plasma reagin test, and a fluorescent treponemal antibody absorption test. There were 262/1,376 concordantly reactive Alinity and Elecsys blood donor samples with reactivity on one or more of the confirmatory tests. A total of 26/1,376 donors had a current syphilis infection, 152/1,376 reported a past history of syphilis and had been treated, and 84/1,376 did not report a past history of syphilis. We suggest that future studies could explore the use of sequential immunoassays to aid in the serodiagnosis for syphilis. IMPORTANCE The serodiagnosis for syphilis usually follows two methodologies-a "traditional" algorithm using a non-treponemal test followed by confirmation using a treponemal test, or a "reverse" algorithm using a treponemal test followed by a non-treponemal test. There are limited reports in the literature of using a modified reverse algorithm (treponemal test followed by a second treponemal test), and to the best of knowledge, there are currently no published articles using two highly sensitive automated immunoassays to aid the serodiagnosis of syphilis. In addition, the Treponema pallidum particle agglutination (TPPA) assay is commonly used as a confirmatory test for the diagnosis of syphilis. With the withdrawal of the TPPA assay from Australia and presumably from the global market also, alternative testing algorithms are now required. This study provides proof of concept for using sequential immunoassays in the diagnosis of syphilis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Treponema pallidum / Doadores de Sangue / Sorodiagnóstico da Sífilis / Sífilis Limite: Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Treponema pallidum / Doadores de Sangue / Sorodiagnóstico da Sífilis / Sífilis Limite: Female / Humans / Male Idioma: En Ano de publicação: 2024 Tipo de documento: Article