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Rescreening Practices of Negative Papanicolaou Tests With Positive Human Papillomavirus Test Result.
Goyal, Abha; Davey, Diane D; Souers, Rhona J; Tabbara, Sana O; Goodrich, Kelly; Booth, Christine N.
Affiliation
  • Goyal A; From the Department of Pathology and Laboratory Medicine, Weill Cornell Medicine-New York Presbyterian Hospital, New York, New York (Goyal).
  • Davey DD; The Department of Clinical Sciences, University of Central Florida College of Medicine, Orlando (Davey).
  • Souers RJ; Statistics/Biostatistics (Souers).
  • Tabbara SO; The Department of Pathology, the George Washington University, Washington, District of Columbia (Tabbara).
  • Goodrich K; Surveys Department (Goodrich), College of American Pathologists, Northfield, Illinois.
  • Booth CN; The Department of Pathology, Cleveland Clinic, Cleveland, Ohio (Booth).
Arch Pathol Lab Med ; 146(1): 78-83, 2022 01 01.
Article in En | MEDLINE | ID: mdl-33929528
ABSTRACT
CONTEXT.­ The yield of the prospective rescreening process for "negative for intraepithelial lesion or malignancy" (NILM) Papanicolaou (Pap) tests is higher with the inclusion of a greater proportion of high-risk cases. One of the suggested criteria for classifying a Pap test finding as high risk is recent or concurrent high-risk human papillomavirus (HPV) positivity. OBJECTIVE.­ To evaluate how the results of HPV testing have been incorporated in the prospective rescreening of NILM Pap tests across a wide range of laboratories. DESIGN.­ A questionnaire survey was sent to laboratories participating in the 2019 College of American Pathologists (CAP) Gynecologic Cytology (PAP Education) Program. RESULTS.­ Of the 1507 participating laboratories, 667 (44%) responded to the survey. Most laboratories (59.4%; 396 of 667) had not incorporated HPV test/genotyping results to select NILM Pap tests for rescreening. Amongst the remaining laboratories, for NILM HPV-positive Pap test results, 112 (16.8%) had a policy to rescreen by a cytotechnologist only, 51 (7.6%) by a pathologist only, and 86 (12.9%) by both. Of 264 laboratories, 181 (68.6%) reported the cytology upon availability of the HPV test result and completion of the secondary review. Of 661 laboratories, 145 (21.9%) included consensus-type recommendations in the cytology report for such Pap tests. CONCLUSIONS.­ This CAP survey provides significant information regarding the current trends in the use of HPV test results in prospective rescreening of NILM Pap tests. Future studies on quality improvement can further assist in the standardization of this process across different laboratories.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Uterine Cervical Dysplasia / Uterine Cervical Neoplasms / Papillomavirus Infections / Alphapapillomavirus Type of study: Diagnostic_studies / Observational_studies Limits: Female / Humans Language: En Journal: Arch Pathol Lab Med Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Uterine Cervical Dysplasia / Uterine Cervical Neoplasms / Papillomavirus Infections / Alphapapillomavirus Type of study: Diagnostic_studies / Observational_studies Limits: Female / Humans Language: En Journal: Arch Pathol Lab Med Year: 2022 Document type: Article