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Evaluation of the Abbott Alinity m STI assay for diagnosis of the primary causes of sexually transmitted infections in the United States

OBJECTIVES: The sexually transmitted infections, Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Trichomonas vaginalis (TV), and Mycoplasma genitalium (MG), have similar risk factors and symptoms, supporting use of a quadruplex test as an efficient diagnostic modality. We assessed the clinic...

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Autores principales: Matysiak, Colette, Cheng, Annie, Kirby, James E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495529/
https://www.ncbi.nlm.nih.gov/pubmed/37705589
http://dx.doi.org/10.1016/j.plabm.2023.e00332
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author Matysiak, Colette
Cheng, Annie
Kirby, James E.
author_facet Matysiak, Colette
Cheng, Annie
Kirby, James E.
author_sort Matysiak, Colette
collection PubMed
description OBJECTIVES: The sexually transmitted infections, Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Trichomonas vaginalis (TV), and Mycoplasma genitalium (MG), have similar risk factors and symptoms, supporting use of a quadruplex test as an efficient diagnostic modality. We assessed the clinical and analytical performance of the Abbott Alinity m STI assay to detect these pathogens. DESIGN AND METHODS: Urine and genital swabs from 142 patient samples were tested from an adult outpatient population in the Northeast United States. The positive and negative percent agreement for CT, NG, and TV were determined by comparison with the Hologic Panther Aptima assay. The analytical sensitivity was determined through serial dilution of standards for CT, NG, TV, and MG in negative urine and swab matrix. RESULTS: The positive and negative percent agreement of the Alinity m assay in comparison with the Hologic Panther Aptima assay were, respectively: CT [100.0% (90.6–100.0%) and 99.1% (94.8–100.0%)], NG [100.0% (89.6–100.0%) and 99.1% (94.9–100.0%)]; and TV [96.3% (81.7–99.8%) and 99.1% (95.2–100.0%)]. The limits of detection in urine and swab matrix were, respectively: CT ≤ 5, ≤1; NG ≤ 5, ≤5; TV ≤ 0.5, ≤0.5; and MG ≤ 500, ≤250 genome copies/mL. CONCLUSIONS: The Alinity m assay demonstrated excellent performance characteristics and identifies CT, NG, and TV accurately compared with a well-established comparator.
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spelling pubmed-104955292023-09-13 Evaluation of the Abbott Alinity m STI assay for diagnosis of the primary causes of sexually transmitted infections in the United States Matysiak, Colette Cheng, Annie Kirby, James E. Pract Lab Med Original Research Article OBJECTIVES: The sexually transmitted infections, Chlamydia trachomatis (CT), Neisseria gonorrhoeae (NG), Trichomonas vaginalis (TV), and Mycoplasma genitalium (MG), have similar risk factors and symptoms, supporting use of a quadruplex test as an efficient diagnostic modality. We assessed the clinical and analytical performance of the Abbott Alinity m STI assay to detect these pathogens. DESIGN AND METHODS: Urine and genital swabs from 142 patient samples were tested from an adult outpatient population in the Northeast United States. The positive and negative percent agreement for CT, NG, and TV were determined by comparison with the Hologic Panther Aptima assay. The analytical sensitivity was determined through serial dilution of standards for CT, NG, TV, and MG in negative urine and swab matrix. RESULTS: The positive and negative percent agreement of the Alinity m assay in comparison with the Hologic Panther Aptima assay were, respectively: CT [100.0% (90.6–100.0%) and 99.1% (94.8–100.0%)], NG [100.0% (89.6–100.0%) and 99.1% (94.9–100.0%)]; and TV [96.3% (81.7–99.8%) and 99.1% (95.2–100.0%)]. The limits of detection in urine and swab matrix were, respectively: CT ≤ 5, ≤1; NG ≤ 5, ≤5; TV ≤ 0.5, ≤0.5; and MG ≤ 500, ≤250 genome copies/mL. CONCLUSIONS: The Alinity m assay demonstrated excellent performance characteristics and identifies CT, NG, and TV accurately compared with a well-established comparator. Elsevier 2023-08-22 /pmc/articles/PMC10495529/ /pubmed/37705589 http://dx.doi.org/10.1016/j.plabm.2023.e00332 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research Article
Matysiak, Colette
Cheng, Annie
Kirby, James E.
Evaluation of the Abbott Alinity m STI assay for diagnosis of the primary causes of sexually transmitted infections in the United States
title Evaluation of the Abbott Alinity m STI assay for diagnosis of the primary causes of sexually transmitted infections in the United States
title_full Evaluation of the Abbott Alinity m STI assay for diagnosis of the primary causes of sexually transmitted infections in the United States
title_fullStr Evaluation of the Abbott Alinity m STI assay for diagnosis of the primary causes of sexually transmitted infections in the United States
title_full_unstemmed Evaluation of the Abbott Alinity m STI assay for diagnosis of the primary causes of sexually transmitted infections in the United States
title_short Evaluation of the Abbott Alinity m STI assay for diagnosis of the primary causes of sexually transmitted infections in the United States
title_sort evaluation of the abbott alinity m sti assay for diagnosis of the primary causes of sexually transmitted infections in the united states
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10495529/
https://www.ncbi.nlm.nih.gov/pubmed/37705589
http://dx.doi.org/10.1016/j.plabm.2023.e00332
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