[1087] Does the LSIL-H Designation in Pap Tests Impact Patient Management?
SK Galfione, DA Smith, MJ Thrall. The Methodist Hospital, Houston, TX
Background: There has been some controversy regarding the use of the interpretive category Low Grade Squamous Intraepithelial Lesion (LSIL) cannot exclude High Grade Squamous Intraepithelial Lesion (LSIL-H) in Papanicolaou (Pap) tests. Since ASCCP guidelines recommend biopsy for all LSIL (except in adolescents and menopausal women), the clinical significance of this category is unclear. LSIL-H is not currently endorsed by the Bethesda System and is only currently used in some laboratories. This study aims to determine whether the designation of LSIL-H changes the gynecologic management of patients.
Design: We identified all LSIL and LSIL-H Pap tests in women with no prior abnormal Pap tests or cervical biopsies from 5/1/2007 to 10/31/2008. The total Pap test volume for this period was 67,223 (80% ThinPrep and 20% SurePath), of which 4.3% were LSIL. Biopsy and Pap test follow-up was compiled from 5/1/2007 to 9/30/09.
Results:
| total | biopsy as first follow-up | pap as first follow-up | CIN 2-3 | |
| LSIL-H | 66 | 44 (66.7%) | 7 (10.6%) | 15 |
| LSIL | 1249 | 618 (49.5%) | 208 (16.7%) | 47 |
| total | biopsy as first follow-up | Pap as first follow-up | CIN 2-3 | |
| LSIL-H | 51 | 34 (66.7%) | 5 (9.8%) | 11 |
| LSIL | 854 | 470 (55.0%) | 133 (15.6%) | 36 |