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The CINtec PLUS Cytology Kit is an immunocytochemistry assay for the simultaneous qualitative detection of the p16INK4a and Ki-67 proteins in cervical cytology preparations. It is indicated to be used as an aid in the identification of women with high-grade cervical intraepithelial lesions in a screening population, and in the sub-groups of patients with a Pap cytology result of ASC-US (atypical squamous cells of undetermined significance) or LSIL (low-grade squamous intraepithelial lesion), or in patients with positive high-risk HPV test results.Interpretation of the test results may only be made by a certified professional in conjunction with the patient´s clinical history and additional diagnostic tests that have been performed.The product is intended for in vitro diagnostic (IVD) use.
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#0B42CA
Denim
11, 66, 202
223, 90, 42
95, 67, 0, 21
#FFFFFF
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255, 255, 255
0, 0, 100
0, 0, 0, 0
#006674
Mosque
0, 102, 116
187, 100, 23
100, 12, 0, 55
The CINtec PLUS Cytology Kit is an advanced immunocytochemistry assay developed by Roche Diagnostics for the simultaneous detection of the p16INK4a and Ki-67 proteins in cervical cytology specimens. Designed for in vitro diagnostic use, this kit aids in identifying women with high-grade cervical intraepithelial lesions, particularly in those with atypical Pap results or positive high-risk HPV tests. The dual-biomarker technology employed in the CINtec PLUS kit enhances the accuracy of cervical cancer screening by objectively identifying transforming HPV infections.
This approach not only supports laboratory professionals in making informed decisions regarding patient follow-up, but it also seeks to improve clinical outcomes while minimizing unnecessary colposcopies. With a focus on reducing follow-up visits and providing clear, actionable results, the CINtec PLUS Cytology Kit is a crucial tool for effective cervical cancer screening and management, ensuring that women receive timely care based on their individual risk profiles
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