Cintec plus cytology test
WebMar 16, 2024 · The CINtec Plus cytology test identifies women whose HPV infections are most likely to be associated with cervical precancers. It enables clinicians to determine more confidently which women should be … WebNov 2, 2024 · The CINtec PLUS Cytology test detects the simultaneous presence within a single cell of the two biomarkers—p16 and Ki-67. This abnormality is associated with HPV infections that are transforming and can, if left untreated, progress to pre-cancer or cancer. A positive result of these two biomarkers in a single cell signals that a woman is more ...
Cintec plus cytology test
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WebMar 10, 2024 · What is it? CINtec® PLUS Cytology is a laboratory test doctors can use to detect proteins, called p16 and Ki67, in Pap test specimens obtained from women that … WebThe dual-stain biomarker technology included in the CINtec ® PLUS Cytology test detects the simultaneous presence within a single cell of the two biomarkers -- p16 and Ki-67. This abnormality is associated with …
Web2 days ago · The endpoints were defined as either an HPV-negative cytology test or the worst detected histology diagnoses during follow-up time, as described in BOX 1. ... by use of the CINtec ® PLUS Cytology kit (Roche Diagnostics GmbH, Mannheim, Germany). Smears were processed on a ThinPrep 5000 processor, and immunocytochemistry was … WebAs part of its testing in women’s health, TriCore offers CINtec® PLUS Cytology. CINtec® PLUS Cytology is a P16/Ki67 dual-stain Immunocytochemistry assay test. The presence of co-expression of P16/Ki67 helps identify women with transforming HPV infections and therefore the need for colposcopy.
WebMar 12, 2024 · Roche has obtained the US Food and Drug Administration (FDA) approval of CINtec PLUS Cytology test for women tested positive for the human papillomavirus (HPV) using its cobas 4800 HPV test. The … WebJan 24, 2024 · CINtec ® PLUS is one of the DS techniques specific to p16 and Ki-67, and its accuracy has been clinically and epidemiologically validated. CINtec ® PLUS has also been used as the comparator standard for evaluating various DS tests ( 17, 18 ).
WebApr 10, 2024 · • Screen cytology specimens • Use Thin Prep® Imaging System • Manual Screening of gyn Thin Prep® slides- atypical or other review and non-gynecologic specimens • Direct cytology slides requiring pathologist review to appropriate location • HER2 Dual ISH count interpretation • CINtec PLUS interpretation • Data entry of …
WebResults: The data of this study show that CINtec® PLUS Cytology Kit is a valid test for the diagnosis of persistent HPV lesions (p = 0.0005), with excellent sensitivity and reliable values of specificity. Relevant patient groups to apply the kit are in agreement with the manufacturer recommendations: women with ASC-US/LSIL result and NILM ... mymichigan doctorsWebTo improve performance outcomes, the concept of dual-stain cytology (CINtec ® PLUS Cytology test) has been introduced. In this approach, additional staining with p16/Ki-67 is performed in cases where cytology results are abnormal (LSIL or ASCUS) and/or HPV-positive. Another way to describe this approach might be "diagnostic" cytology. mymichigan employee loginWebCINtec PLUS Cytology is the only FDA approved triage test that uses dual biomarker technology to simultaneously detect p16 and Ki-67 in women with HPV-positive results. … Does your p16 meet the defined criteria for Class II devices like CINtec Histology … mymichigan east endWebSep 16, 2024 · The FDA approved the CINtec PLUS Cytology test to help determine if HPV-positive women need further diagnostic procedures to prevent cervical cancer, thus contributing to the World Health Organization’s (WHO) goal of irradicating the disease by 2030, according to Roche, the manufacturer of the next-generation biomarker test. mymichigan clare michiganWeb开馆时间：周一至周日7:00-22:30 周五 7:00-12:00; 我的图书馆 my michigan cityWebMar 23, 2024 · CINTEC PLUS CYTOLOGY is a qualitative immunocytochemical assay intended for the simultaneous detection of the p16INK4a and Ki-67 proteins in cervical specimens collected by a clinician using an endocervical brush/spatula or broom collection device and placed in the ThinPrep Pap Test PreservCyt Solution. Subsequent to this … my michigan child supportWebTest performance was ascertained with cervical intraepithelial neoplasia grade 2 or worse (CIN2+) and CIN3 or worse (CIN3+) serving as clinical endpoints. Results: In all ages, … mymichigan employee access