Performance and reproducibility of gynecologic cytology interpretation using the focalpoint system: Results of the RODEO study team

Maíra Degiovani Stein, José Humberto T.G. Fregnani, Cristovam Scapulatempo, Allini Mafra, Natália Campacci, Adhemar Longatto-Filho*, Teóclito Saccheto De Carvalho, Fábio De Paula Mateus, Eduardo Tadeu Da Silva, Michele M.Castro Alves, Fábio Cardoso De Lima, Erlaine Martins Suriano, Eduardo C.A. Da Silva, Sandra M. Da Silva, Ligia Maria Kerr, Lucas F.A. Machado, Edmundo C. Mauad

*Corresponding author for this work

Research output: Contribution to journalArticleResearchpeer-review

13 Citations (Scopus)

Abstract

Objectives: To assess whether automated screening in the cytologic examination of Papanicolaou smear slides results in smaller margins of error than manual screening. Methods: We compared cytotechnologists' performance and reproducibility of manual and automated screening of 10,165 consecutive cervical cytology slides examined at Barretos Cancer Hospital using the FocalPoint system. Results: In total, 83% of atypical squamous cells of undetermined significance and greater were classified as quintiles 1 and 2; no high-grade squamous intraepithelial lesions and greater were observed in quintile 5. No statistically significant differences were found between manual and automated screening, using cervical biopsy specimens as the gold standard. Conclusions: FocalPoint safely screened high-grade lesions, which can be valuable for high-workload routines.

Original languageEnglish
Pages (from-to)567-571
Number of pages5
JournalAmerican Journal of Clinical Pathology
Volume140
Issue number4
DOIs
Publication statusPublished - Oct 2013
Externally publishedYes

Keywords

  • Automation
  • FocalPoint
  • Pap test
  • Quality control
  • SurePath

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