What does CNCR mean in CANCER
The Czech National Cancer Registry, often abbreviated to CNCR, is an invaluable resource for tracking and understanding cancer cases in the Czech Republic. It has been collating data on cancer diagnoses since its establishment in 1999, making it one of the longest-standing cancer registries in Europe. In addition to collecting information on individual cases, the CNCR also actively works to inform public health initiatives related to cancer prevention and control.
CNCR meaning in Cancer in Medical
CNCR mostly used in an acronym Cancer in Category Medical that means Czech National Cancer Registry
Shorthand: CNCR,
Full Form: Czech National Cancer Registry
For more information of "Czech National Cancer Registry", see the section below.
What Does The Czech National Cancer Registry Do?
The main function of the CNCR is to collect accurate records of all cases of cancer diagnosed within the Czech Republic. This includes gathering detailed patient information such as age, gender, type and stage of disease and any treatments that have been administered. The registry also collects data from death certificates when applicable. All this information helps support accurate estimates of incidence, mortality and survival rates for different types of cancers in different areas of the country. This allows healthcare professionals and public health organizations to create more effective strategies for reducing the burden of cancer across populations. In addition to simply collecting data, the CNCR also carries out analyses aimed at understanding trends and patterns in cancer incidence that can help guide public health interventions. The registry also provides training opportunities for researchers interested in conducting their own investigations into cancer.
Essential Questions and Answers on Czech National Cancer Registry in "MEDICAL»CANCER"
What is the Czech National Cancer Registry?
The Czech National Cancer Registry (CNCR) is a national database that collects data on cancer patients in the Czech Republic. The registry includes information on diagnosis, treatment, and outcomes of cancer patients, allowing health authorities to plan systematic cancer control activities.
How long has the Czech National Cancer Registry been around?
The CNCR has been collecting data since 1993.
Who can access the Czech National Cancer Registry?
Access to the CNCR is restricted to authorized personnel only, such as physicians and researchers who are researching specific cancers or treatments.
What types of information does the Dutch National Cancer Society collect?
The CNCR collects patient-specific data such as age, sex, date of diagnosis, tumor characteristics (size and location), treatment information (surgery types, drugs administered), and outcome measures (survival time and status).
Where does the CNCR get its data from?
The CNCR collects its data from hospitals, laboratories and other healthcare providers across the country. Each participating facility is required to provide detailed records for each case of cancer diagnosed there.
How often is the data updated?
Data within the CNCR is regularly updated every three months so that health officials are able to monitor cancer trends over time.
Is there a fee associated with accessingdata from the CNCR?
No, there are no fees associated with accessing or using data from the CNCR. Health professionals may use the system free of charge for research purposes or clinical decision support applications.
Does the CNCR have a public website where anyone can access information about cancer in Europe?
Yes! The registry's website provides users with an overview of current statistics on incidence rates gathered from various European countries including Switzerland and Austria as well as relevant publications related to published research conducted by experts in relation to cancer care in Europe.
Final Words:
Overall, the Czech National Cancer Registry (CNCR) plays an important role in helping us better understand and respond effectively to cancer cases within the Czech Republic. This valuable resource helps us implement preventative measures, develop effective treatment plans, identify high risk groups and provide personalized care for those affected by a diagnosis of cancer.
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