Performance of a New HPV Cervi-Collect Collection and Transportation Kit

Author:

Chernesky M.1,Huang S.2,Jang D.1,Erickson B.2,Salituro J.2,Engel H.3,Gilchrist J.1,Neuscheler P.3,Mak W. B.2,Abravaya K.2

Affiliation:

1. St. Joseph's Healthcare Hamilton, McMaster University, Hamilton, ON, Canada L8N 4A6

2. Abbott Molecular Inc., Des Plaines, IL 60018-3315, USA

3. Abbott Diagnostics, 65205 Wiesbaden, Germany

Abstract

Background. Liquid-based Pap (L-Pap) media are used for Pap and human papillomavirus (HPV) testing.Objectives. To compare RealTime High Risk (HR) HPV testing of a new collection kit (Cervi-Collect) and PreservCyt L-Pap specimens. To determine ease of use and safety of Cervi-Collect.Methods. L-Pap samples (n=203) were tested with HC2 and RealTime HR HPV and Cervi-Collect with RealTime HR HPV. Discordant samples were genotyped.Results. L-Pap and Cervi-Collect specimens tested by RealTime HR HPV showed 93.1% agreement (Kappa 0.86). RealTime HR HPV and HC2 on L-Pap had 90.3% agreement (Kappa 0.80). RealTime HR HPV on Cervi-Collect and HC2 on L-Pap showed 88.2% agreement (Kappa 0.76). Sixteen of 21 samples which were HC2 negative and RealTime HR HPV positive on L-Pap or Cervi-Collect contained HR HPV genotypes. Eleven healthcare collectors were in strong agreement on a usability and safety questionnaire.Conclusion. Cervi-Collect samples were easy to collect and showed strong agreement with L-Pap samples tested with RealTime HR HPV or HC2.

Publisher

Hindawi Limited

Subject

Oncology

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