Reviews and Sensitization About Cancer in Algeria
Journal Title: UNKNOWN - Year 2017, Vol 1, Issue 1
Abstract
Having cancer data is a necessity for several reasons. Researchers need accurate data and updates on cancer for the study of possible causes, managers for decisions concerning the acquisition of equipment and/or development activities or programs for treatment, screening and prevention, and the health authorities to investigate cancer groups, their trends and their causes. Where does the data come, and how is it collected? In fact, all these cancer statistics are collected and provided by the Cancer Registry, from clinical records, and from biological and care institutions. By definition, a cancer registry is an information system and an epidemiological surveillance tool for the collection, storage, management, data analysis, and dissemination on incident cases of cancer, covering a geographically defined population. The cancer registry is an essential tool of any program against cancer. Its primary objective is, indeed, the description of the epidemiological situation, the study of trends and geographic distribution of cases, but it is essential to other areas in particular:
Authors and Affiliations
Kaouel Meguenni
Keywords
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- EP ID EP201694
- DOI 10.26415/2572-004X-vol1iss1p7-7
- Views 37
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