Comparison of the Roche Cobas® 4800 HPV assay to Roche Amplicor for detection of high-risk human papillomavirus

被引:0
作者
S. Phillips
A. M. Cornall
D. A. Machalek
S. M. Garland
D. Bateson
M. Garefalakis
S. N. Tabrizi
机构
[1] The Royal Women’s Hospital,Regional HPV Lab Net Reference Laboratory, Department of Microbiology and Infectious Diseases
[2] The Royal Women’s Hospital,Department of Microbiology and Infectious Diseases
[3] Murdoch Childrens Research Institute,Department of Obstetrics and Gynaecology
[4] University of Melbourne,undefined
[5] Family Planning New South Wales,undefined
[6] Family Planning Western Australia,undefined
来源
European Journal of Clinical Microbiology & Infectious Diseases | 2016年 / 35卷
关键词
Family Planning Clinic; Discrepant Sample; Roche Linear Array; Cobas Testing; Attend Family Planning Clinic;
D O I
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学科分类号
摘要
Roche Amplicor HPV (AMP) had previously been used for detection of high-risk human papillomavirus (HR-HPV) in epidemiological and clinical studies. As this assay is no longer available, we compared its performance using PreservCyt samples from women aged of 18–24 years attending for routine cervical cytology screening to Roche Cobas® 4800 (Cobas) to determine if subsequent studies could continue using the Cobas assay. Overall 507 samples were tested on Cobas and compared to previous AMP results, with discrepant samples tested on Roche Linear Array. Results: Overall, agreement between the Cobas and AMP for the presence of HR HPV types was very high (κ = 0.81) (95 % CI: 0.76 - 0.87) with percentage agreement of 91.57 %. Cobas is comparable to AMP for the detection of HR-HPV types in a community recruited cohort of healthy women.
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页码:1305 / 1307
页数:2
相关论文
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