Journal article
Performance of clinical screening algorithms comprising point-of-care HPV-DNA testing using self-collected vaginal specimens, and visual inspection of the cervix with acetic acid, for the detection of underlying high-grade squamous intraepithelial lesions in Papua New Guinea
PJ Toliman, JM Kaldor, SG Badman, J Gabuzzi, S Silim, A Kumbia, B Kombuk, Z Kombati, G Munnull, R Guy, LM Vallely, A Kelly-Hanku, H Wand, C Ryan, G Tan, J Brotherton, M Saville, GDL Mola, SM Garland, SN Tabrizi Show all
Papillomavirus Research | ELSEVIER | Published : 2018
Abstract
The performance of different clinical screening algorithms comprising point-of-care HPV-DNA testing using self-collected vaginal (‘V’) specimens, and visual inspection of the cervix with acetic acid (VIA) was evaluated in Papua New Guinea. Women aged 30–59 years provided V specimens that were tested at point-of-care using the Xpert HPV Test (Cepheid, Sunnyvale, CA). A clinician-collected cervical (‘C’) specimen was then collected for point-of-care Xpert testing, and liquid-based cytology (LBC). Following this, VIA examination was conducted, blind to HPV test results, and ablative cervical cryotherapy provided if indicated. Detection of high-grade squamous intraepithelial lesion (HSIL) by LBC..
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Awarded by National Health and Medical Research Council
Funding Acknowledgements
This work was funded through the National Health and Medical Research Council of Australia (NHMRC) (1071269) and the Papua New Guinea Institute of Medical Research (PNGIMR) Internal Competitive Research Award Scheme (297/1). The funders had no role in study design, data collection, data analysis, data interpretation, or writing of the report. The corresponding author had full access to all data in the study and had final responsibility for the decision to submit for publication.