Jul 21, 2017

Epidemiology (BHS210-Mod5 Case)

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Epidemiology (BHS210-Mod5 Case)


Module 5 - Case ANALYTIC EPIDEMIOLOGY You are a Health Officer for a rural county health department and have been assigned to study the frequency of an infectious disease such as tuberculosis or HIV/AIDS. Write a 2- to 3-page essay in which you do the following: Describe observational and experimental epidemiology as the two (2) study designs apply to either of the diseases you have chosen. Be sure to identify differences between these two types of analytic epidemiology. Under what conditions will you conduct a case-control study as opposed to a cohort study? Be sure to support your opinion with evidence from the literature. ANALYTIC EPIDEMIOLOGY Required Reading Analytic Study Design (n.d.). Retrieved on 10/1/13 from http://www.epidemiolog.net/evolving/AnalyticStudyDesigns.pdf Optional Reading Aschengrau A, Seage GR (2003). Chapter 6: Overview of Epidemiologic Study Designs. Essentials of Epidemiology in Public Health, Boston: Jones & Bartlett Publishers. Retrieved on 10/1/13 from http://publichealth.jbpub.com/aschengrau/Aschengrau06.pdf Cosio G (2005). Epidemiological Overview of Tuberculosis [Presentation]. Retrieved on 10/1/13 from www.paho.org/cdmedia/dpccd01/Presentations/Day1/EPIDEMIOLOGICAL%20OVERVIEW%20OF%20TUBERCULOSIS%202.ppt

EPIDEMIOLOGYName:Institution: Epidemiology Working in a remote village, where there is a high prevalence in the number of patients with HIV there are a number of researches that can be conducted to reduce the infection rates to the minimum (Song & Chung, 2010). Depending on the research question, the research can take the observational form or the experimental form.Observational and Experimental Designs With reference to observational studies that can be carried out in the village on HIV, patients experience side effects with respect to using a certain drug. Most of the drugs tend to have some form of side effects that may come within a short while or may take quite some time. In this study, 300 participants will be selected from different age groups, ranging from 20 to 50 years. There will be three subsets, where the age groups will be distributed within 10 years of each other. This distribution will ensure that the patients are observed across the age divide to establish if there is a chance that there may be differences in side effects with respect to age. Observed over a period of two years, the patients will be monitored for any changes in the health alongside the drug that the...

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