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. 2022 Feb 7;31(2):486–492. doi: 10.1158/1055-9965.EPI-21-0865

Table 3.

History of screening and treatment by baseline cotest result among individuals in IRIS cohort.

Baseline cotest result
High-grade+ LSIL ASC-US NILM
Participant clinical historya IRIS cohort % of IRIS cohort % of KPNC populationa,b HPV+ HPV HPV+ HPV HPV+ HPV HPV+ HPV
Total 77,920 100% 100% 3,449 1,031 11,678 1,272 15,984 7,912 23,846 12,748
Routine screening 30,520 39.2% 58.4% 722 427 3,418 506 4,824 3,894 8,964 7,765
(previous screen negative) 20.9% 41.4% 29.3% 39.8% 30.2% 49.2% 37.6% 60.9%
 Early (≤30 months) 4,473 5.7% 14.6% 87 54 600 66 782 568 1,371 945
2.5% 5.2% 5.1% 5.2% 4.9% 7.2% 5.7% 7.4%
 Timely (≤42 months) 17,630 22.6% 37.7% 349 267 1,801 316 2,646 2,316 4,941 4,994
10.1% 25.9% 15.4% 24.8% 16.6% 29.3% 20.7% 39.2%
 Late (>42 months) 8,417 10.8% 7.1% 286 106 1,017 124 1,396 1,010 2,652 1,826
8.3% 10.3% 8.7% 9.7% 8.7% 12.8% 11.1% 14.3%
Previous screen abnormal 4,854 6.2% 3.3% 258 16 812 56 1,227 229 2,052 204
7.5% 1.6% 7.0% 4.4% 7.7% 2.9% 8.6% 1.6%
Postcolposcopy 17,130 22.0% 10.3% 892 245 3,302 305 4,465 1,551 4,985 1,385
25.9% 23.8% 28.3% 24.0% 27.9% 19.6% 20.9% 10.9%
 Recent (<42 months) 11,225 14.4% 3.2% 659 151 2,545 182 3,191 748 3,255 494
19.1% 14.6% 21.8% 14.3% 20.0% 9.5% 13.7% 3.9%
 Distant (42+ months) 5,905 7.6% 7.1% 233 94 757 123 1,274 803 1,730 891
6.8% 9.1% 6.5% 9.7% 8.0% 10.1% 7.3% 7.0%
Posttreatment 4,095 5.3% 2.5% 392 130 631 83 807 453 1,133 466
11.4% 12.6% 5.4% 6.5% 5.0% 5.7% 4.8% 3.7%
Unknown clinical history 21,321 27.4% 25.5% 1,185 213 3,515 322 4,661 1,785 6,712 2,928
34.4% 20.7% 30.1% 25.3% 29.2% 22.6% 28.1% 23.0%

Note: High-grade+ includes atypical glandular cells of undetermined significance (AGUS), atypical squamous cells, cannot rule out high-grade squamous intraepithelial lesion (ASC-H), HSILs, and carcinoma.

Abbreviation: NILM, negative for intraepithelial lesion or malignancy.

aClinical history at first cotest during period between January 2016 and August 2018.

bDistribution at KPNC for individuals with one or more cotest results between January 2016 and August 2018.