Comparison of commercial hybridization and automated transcription-mediated amplification modalities for detection of high-risk human papillomavirus nucleic acid

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Abstract

Assessment of 4,056 cytology collections by Cervista HPV HR and APTIMA HPV yielded 88.7% concordance, with increased detection by Cervista in patients with atypical squamous cells of undetermined significance (ASC-US) and patients negative for intraepithelial lesions and malignancy (NILM) (P<0.02). Both assays detected>91.7% of cervical intraepithelial neoplasia grade 2(CIN2) lesions. A total of 262 specimens demonstrated luminescence within all three Cervista oligonucleotide mixtures (triple positive). APTIMA HPV and PCR-based microarray confirmed triple-positive results at rates of 7.3% and 5.9%, respectively. Copyright © 2014, American Society for Microbiology.

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Munson, E., Kroeger, L., Balzer, S., Amrhein, R., Munson, K. L., Napierala, M., … Dillon, P. J. (2014). Comparison of commercial hybridization and automated transcription-mediated amplification modalities for detection of high-risk human papillomavirus nucleic acid. Journal of Clinical Microbiology, 52(1), 331–334. https://doi.org/10.1128/JCM.03066-13

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