Search results - 5 results
Equivalent Clinical Accuracy of Human Papillomavirus DNA Testing Using Cobas 4800 and 6800 Human Papillomavirus Systems in Paired Urine and Cervical Samples.
first-void urine. In the total study population, HPV testing on first-void urine was similarly sensitive [ratio, 0.98; 95% CI, 0.93-1.02] and specific for cobas 4800 HPV (ratio, 1.00; 95% CI, 0.91-1.10) and ...
Accuracy of Liferiver HarmoniaHPV and VenusHPV Assays on Urine and Vaginal Self-Samples.
self-sample types, whereas the specificity was similar to cervical samples. Post-hoc adjustment of the VenusHPV C-values improved sensitivity (ratio FVU /cervical = 0.94 [95% CI 0.88-1.00]; ratio ...
Meta-analysis of the accuracy of p16 or p16/Ki-67 immunocytochemistry versus HPV testing for the detection of CIN2+/CIN3+ in triage of women with minor abnormal cytology.
RESULTS: Thirty-eight studies were eligible. The sensitivity of p16 staining for CIN3 + was significantly lower than that of hrHPV DNA testing (ratio for ASC- US, 0.87; 95% confidence interval [CI], ...
Impact of the human papillomavirus status on the development of high-grade cervical intraepithelial neoplasia in women negative for intraepithelial lesions or malignancy at the baseline: A 9-year Swedish nested case-control follow-up study.
Baseline liquid-based cytology samples were tested for HPV. Conditional logistic regression analysis was used to calculate odds ratios (OR s) with confidence intervals (CI s). RESULTS The risk of future ...
Detecting cervical precancer and reaching underscreened women by using HPV testing on self samples: updated meta-analyses.
participation trials were included. hrHPV assays based on polymerase chain reaction were as sensitive on self samples as on clinician samples to detect CIN2 + or CIN3 + (pooled ratio 0.99, 95% confidence interval ...