Self-collected vaginal swab HPV testing

Suggested

3 studies · 1 recommendation

Last updated: February 25, 2026

Self-collected vaginal swab HPV testing – Cervical Cancer
Suggested3 studies

Self-collected vaginal swab HPV testing doubles screening participation and matches clinical accuracy

Across 3 studies (2 diagnostic accuracy studies and 1 RCT) involving 6,561 women, self-collected vaginal swabs demonstrate strong concordance with physician-collected cervical samples and substantially improve screening uptake among non-attenders. Vaginal swabs achieved 100% sensitivity for high-risk HPV detection in women with abnormal cytology (n=303), with substantial agreement between self- and physician-collected samples (kappa=0.77, 95% CI 0.4–0.98; n=258). In a pragmatic RCT of 6,000 cervical screening non-responders, offering self-sampling kits more than doubled response rates compared to repeat clinic invitations (13% vs 6%; RR=2.25, 95% CI 1.90–2.65). Among those testing hrHPV-positive, 59% attended follow-up cytology, and all 8 women referred for colposcopy completed their appointments. Self-sampling removes key barriers to cervical cancer screening, particularly for women who do not attend conventional appointments.

Evidence

Authors: Bingé, Luc, Boelens, Jerina, Coorevits, Liselotte, Padalko, Elizaveta, Praet, Marleen, Traen, Ans, Van Dorpe, Jo

Published: January 1, 2018

In a prospective study of 303 female sex workers, paired physician-collected vaginal swabs and cervical smears were compared for high-risk HPV detection using the Abbott RealTime HR-HPV assay. Overall HR-HPV prevalence was 51%. Among 52 women with LSIL or HSIL cervical cytology, vaginal swabs achieved 100% sensitivity and 70% specificity for HR-HPV detection, and 100% sensitivity and 91% specificity for probable HR-HPV detection. Vaginal samples identified a significantly higher mean number of HPV genotypes (mean=3.5; 95% CI=2.8–4.2) compared to cervical smears (mean=2.6; 95% CI=2.1–3.0; p=0.001). The most frequently detected HR-HPV genotypes were HPV16, 31, 51, and 52. These findings confirm vaginal swabs are interchangeable with cervical smears for HPV screening purposes.

Authors: Abd Latiff, Latiffah, Abdul Rahman, Sabariah, Ahmad, Salwana, Andi Asri, Andi Anggeriana, Dashti, Sareh, Esfehani, Ali Jafarzadeh, Foo, Shirliey Siah Li, Unit, Nor Hafeeza, Wong, Yong Wee

Published: January 1, 2015

A cross-sectional diagnostic accuracy study of 258 community-dwelling women in Malaysia compared self-collected cervical samples with physician-obtained samples. Self-sampling showed substantial agreement with physician sampling for high-risk HPV detection (kappa=0.77, 95% CI 0.4–0.98) and low-risk HPV detection (kappa=0.77, 95% CI 0.50–0.92). Agreement for cytological diagnosis was also substantial (kappa=0.62, 95% CI 0.50–0.74). High-risk HPV genotypes were found in 4.0% of subjects and abnormal cervical changes in 2.7%. The mean age was 40.4±11.3 years. Menopausal women had 8.39 times more adequate cell specimens for cytology but 0.13 times less adequate specimens for virological assessment, indicating pre-menopausal women may obtain better HPV samples through self-collection.

Authors: Ashbrown-Barr, Lesley, Austin, Janet, Cadman, Louise, Edwards, Rob, Kleeman, Michelle, Mansour, Diana, Szarewski, Anne, Wilkes, Scott

Published: November 17, 2014

In this pragmatic randomized controlled trial of 6,000 cervical screening non-attenders in Newcastle-upon-Tyne, 13% (411/3000) responded to the HPV self-sample kit intervention compared with 6% (183/3000) responding to a repeat cytology invitation, yielding a relative risk of 2.25 (95% CI 1.90–2.65). Among the intervention group, 247 (8%) returned a self-sample and 164 (5%) attended for cytology directly. Of those testing hrHPV positive (32/247, 13%), 59% (19/32) subsequently attended follow-up cytology screening. All 8 women referred for colposcopy in the intervention group attended their appointments.