top of page

Cxbladder Triage 膀胱癌篩查檢測

HK$6,000.00Price

助您排除膀胱癌

Quantity
  • Cxbladder Triage 是一種非侵入性的分子診斷測試,旨在協助臨床醫生排除膀胱癌,為您和您的患者提供更大的安心。

    Cxbladder Triage 的設計目的是利用專有算法結合表型和基因型因素,通過分離指數 ‘G+P INDEX’ 來識別患有尿路上皮癌 (UC) 機率低的患者。使用 G+P INDEX,Cxbladder Triage 專注於準確識別患有血尿且 UC 機率低的患者,這些患者可能不需要進行更廣泛的評估。

    Cxbladder Triage 已在一項包含 587 名出現肉眼血尿患者的臨床研究中得到驗證。該研究顯示,Cxbladder Triage 的敏感性為 95.1%,且具有 98.5% 的高陰性預測值,40% 的患者被準確地分流為 UC 機率低。Cxbladder Triage 尤其適合對出現血尿的低風險患者進行分流[1]。

    Cxbladder Triage is a non-invasive molecular diagnostic test to assist clinicians in ruling out bladder cancer – giving you and your patients greater peace of mind.

    Cxbladder Triage is designed to identify patients with a low probability of having urothelial carcinoma (UC) using a proprietary algorithm combining both phenotypic and genotypic factors into a segregation index – ‘the G+P INDEX’. Using the G+P INDEX, Cxbladder Triage focuses on accurately identifying patients with hematuria who have a low probability of UC, for whom a more extensive evaluation may not be required.

    Cxbladder Triage has been validated in a clinical study with 587 patients presenting with gross hematuria. With a sensitivity of 95.1% and high negative predictive value of 98.5%, the study showed that 40% of patients were accurately triaged out with a low probability of UC. Cxbladder Triage is particularly appropriate for triaging low risk patients presenting with hematuria[1].

    Reference:

    [1] Kavalieris et al: ‘A segregation index combining phenotypic (clinicalcharacteristics) and genotypic (gene expression) biomarkers from a urinesample to triage-out patients presenting with hematuria who have a lowprobability of urothelial carcinoma. BMC urology 2015; 15:23.

No Reviews YetShare your thoughts. Be the first to leave a review.

How To Order?

Related Products

Codex offers hereditary genetic tests for cancer and neuro diseases, and comprehensive genomic profiling for cancer treatments. The services provided by Codex Genetics are for research use only, and they are not suitable for diagnostic and/or treatment use, unless otherwise instructed by licensed medical professionals. 

科德施提供與腦神經退化和癌症基因相關的測試。 除非有醫療專業人員另行指示,此網站的服務只供研究用途,並不供作診斷或治療任何疾病之用。

  • alt.text.label.Facebook
  • alt.text.label.LinkedIn
  • alt.text.label.Instagram

Office Hours:
Monday to Friday 10:00 – 18:00
Closed on Saturdays, Sundays and public holidays.
If you need special arrangements, please contact us during office hours.

Privacy policy
​Terms of Use
Contact us

©2024 by Codex Genetics Limited

bottom of page