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. 2023 Jul 11;8(7):e012311. doi: 10.1136/bmjgh-2023-012311

Table 3.

Participants screened for cervical cancer and the concordance rates

Phase No VIA screened No VIA positive Reviewer diagnosis/case finder Positive concordance (%) Reviewer diagnosis/case finder Negative concordance (%)
Pilot phase (December 2019–June 2020) 182 9 NA NA NA NA
Pre-AVIVA
Phase 1
(July 2020–October 2020)
2892 117 9/35
Sample*
25.71 N/A N/A
Post-VIVA Phase 1 (November 2020–March 2021) 5184 432 65/152
Sample†
42.76 115/144
Sample†
79.86
Phase 2 (April 2021–April 2022) 16 465 907 70/180
Sample†
38.89 671/722
Sample†
92.94
Phase 3
(May 2022– June 2022)
4539 144 5/12
Sample†
41.67 172/180
Sample†
95.56

*Reviewed by gynaecologist on-site.

†Reviewed by gynaecologist using AVIVA.

AVIVA, APIN developed VIA Visual Application; NA, not available; VIA, visual inspection with acetic acid.