Registry Data & Mortality Statistics

Registry data & Mortality statistics

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PART A: Registry data

For a couple of years, many clinicians in the state health departments have taken into use and benefited from many data sources including clinical and population data linked resources to produce new health insights and stimulate advanced health research programs. Registry data will therefore act as a core research propellant in state healthcare. Combining the possible multiple data sources like administrative database systems and patient report records has for example helped the improve healthcare service provision in the United States. Clinicians in the U.S have made good use of such records to make an in-depth understanding of disease prevalence and incidences over the past decade.

Invasive cancers survey done in the United States in 2011, data for the project were obtained from a population-based registry for cancer records and affiliated by the SEER programs. This was conducted in the District of Columbia and Puerto. This was assumed to cover approximately 99% of the total population of the United States. In the year 2011, a total population of 1,532,066 incidents of cancer were reported to the national health registry (Gliklich, Dreyer & Leavy, 2014). Proportions of survivors for more than 5 years were recorded and taken more serious in the database. These cancer registry reports are what the US use in development of effective and comprehensive cancer control strategies and supporting needs services for cancer survivors.

Similarly, ATSDR in collaboration with the US healthcare providers after case investigations and clinical trials. The proposed biorepository helps researchers in better understanding diseases after pairing prevalence and the existing risk-factor. In addition, the National ALS registry reports with the secure Web portal programs are a better research data sources that were useful in investigating the incidences of Amyotrophic lateral sclerosis...