1 / 44

is for Epi

is for Epi. Epidemiology basics for non-epidemiologists. Session III Part II. Descriptive and Analytic Epidemiology. Analytic Epidemiology. Hypotheses and Study Designs. Descriptive vs. Analytic Epidemiology. Descriptive epidemiology deals with the questions: Who, What, When, and Where

azure
Download Presentation

is for Epi

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. is for Epi Epidemiology basics for non-epidemiologists

  2. Session IIIPart II Descriptive and Analytic Epidemiology

  3. Analytic Epidemiology Hypotheses and Study Designs

  4. Descriptive vs. Analytic Epidemiology • Descriptive epidemiology deals with the questions: Who, What, When, and Where • Analytic epidemiology deals with the remaining questions: Why and How

  5. Analytic Epidemiology • Used to help identify the cause of disease • Typically involves designing a study to test hypotheses developed using descriptive epidemiology

  6. Borgman, J (1997). The Cincinnati Enquirer. King Features Syndicate.

  7. Exposure and Outcome A study considers two main factors: exposure and outcome • Exposure refers to factors that might influence one’s risk of disease • Outcome refers to case definitions

  8. Case Definition • A set of standard diagnostic criteria that must be fulfilled in order to identify a person as a case of a particular disease • Ensures that all persons who are counted as cases actually have the same disease • Typically includes clinical criteria (lab results, symptoms, signs) and sometimes restrictions on person, place, and time

  9. Developing Hypotheses • A hypothesis is an educated guess about an association that is testable in a scientific investigation • Descriptive data provide information to develop hypotheses • Hypotheses tend to be broad initially and are then refined to have a narrower focus

  10. Example • Hypothesis: People who ate at the church picnic were more likely to become ill • Exposure is eating at the church picnic • Outcome is illness – this would need to be defined, for example, ill persons are those who have diarrhea and fever • Hypothesis: People who ate the egg salad at the church picnic were more likely to have laboratory-confirmed Salmonella • Exposure is eating egg salad at the church picnic • Outcome is laboratory confirmation of Salmonella

  11. Types of Studies Two main categories: • Experimental • Observational • Experimental studies – exposure status is assigned • Observational studies – exposure status is not assigned

  12. Experimental Studies • Can involve individuals or communities • Assignment of exposure status can be random or non-random • The non-exposed group can be untreated (placebo) or given a standard treatment • Most common is a randomized clinical trial

  13. Experimental Study Examples • Randomized clinical trial to determine if giving magnesium sulfate to pregnant women in preterm labor decreases the risk of their babies developing cerebral palsy • Randomized community trial to determine if fluoridation of the public water supply decreases dental cavities

  14. Observational Studies Three main study designs: • Cross-sectional study • Cohort study • Case-control study

  15. Cross-Sectional Studies • Exposure and outcome status are determined at the same time • Examples include: • Behavioral Risk Factor Surveillance System (BRFSS) - http://www.cdc.gov/brfss/ • National Health and Nutrition Surveys (NHANES) - http://www.cdc.gov/nchs/nhanes.htm • Also include most opinion and political polls

  16. Cohort Studies • Study population is grouped by exposure status • Groups are then followed to determine if they develop the outcome

  17. Cohort Studies Study Population Exposure is self selected Non-exposed Exposed Follow through time Disease No Disease Disease No Disease

  18. Cohort Study Examples • Study to determine if smokers have a higher risk of lung cancer • Study to determine if children who receive influenza vaccination miss fewer days of school • Study to determine if the coleslaw was the cause of a foodborne illness outbreak

  19. Case-Control Studies • Study population is grouped by outcome • Cases are persons who have the outcome • Controls are persons who do not have the outcome • Past exposure status is then determined

  20. Case-Control Studies Study Population Controls Cases Had Exposure No Exposure Had Exposure No Exposure

  21. Case-Control Study Examples • Study to determine an association between autism and vaccination • Study to determine an association between lung cancer and radon exposure • Study to determine an association between salmonella infection and eating at a fast food restaurant

  22. Cohort versus Case-Control Study

  23. Classification of Study Designs Source: Grimes DA, Schulz KF. Lancet 2002; 359: 58

  24. Analytic Epidemiology Measures of Association and Statistical Tests

  25. Measures of Association • Assess the strength of an association between an exposure and the outcome of interest • Indicate how more or less likely a group is to develop disease as compared to another group • Two widely used measures: • Relative risk (a.k.a. risk ratio, RR) • Odds ratio (a.k.a. OR)

  26. 2 x 2 Tables Used to summarize counts of disease and exposure in order to do calculations of association

  27. 2 x 2 Tables a = number who are exposed and have the outcome b = number who are exposed and do not have the outcome c = number who are not exposed and have the outcome d = number who are not exposed and do not have the outcome ****************************************************************** a + b = total number who are exposed c + d = total number who are not exposed a + c = total number who have the outcome b + d = total number who do not have the outcome a + b + c + d = total study population Outcome Yes No Yes Exposure No

  28. Relative Risk • The relative risk is the risk of disease in the exposed group divided by the risk of disease in the non-exposed group • RR is the measure used with cohort studies a a + b RR = c c + d Outcome Yes No Total Risk among the exposed Yes Exposure No a + b c + d Risk among the unexposed

  29. Relative Risk Example a / (a + b) 23 / 33 RR = = = 6.67 c / (c + d) 7 / 67

  30. Odds Ratio • In a case-control study, the risk of disease cannot be directly calculated because the population at risk is not known • OR is the measure used with case-control studies a x d OR = b x c

  31. Odds Ratio Example a x d 130 x 135 OR = = = 1.27 b x c 115 x 120

  32. Interpretation Both the RR and OR are interpreted as follows: = 1 - indicates no association > 1 - indicates a positive association < 1 - indicates a negative association

  33. Interpretation • If the RR = 5 • People who were exposed are 5 times more likely to have the outcome when compared with persons who were not exposed • If the RR = 0.5 • People who were exposed are half as likely to have the outcome when compared with persons who were not exposed • If the RR = 1 • People who were exposed are no more or less likely to have the outcome when compared to persons who were not exposed

  34. Tests of Significance • Indication of reliability of the association that was observed • Answers the question “How likely is it that the observed association may be due to chance?” • Two main tests: • 95% Confidence Intervals (CI) • p-values

  35. 95% Confidence Interval (CI) • The 95% CI is the range of values of the measure of association (RR or OR) that has a 95% chance of containing the true RR or OR • One is 95% “confident” that the true measure of association falls within this interval

  36. 95% CI Example Grodstein F, Goldman MB, Cramer DW. Relation of tubal infertility to history of sexually transmitted diseases. Am J Epidemiol. 1993 Mar 1;137(5):577-84

  37. Interpreting 95% Confidence Intervals • To have a significant association between exposure and outcome, the 95% CI should not include 1.0 • A 95% CI range below 1 suggests less risk of the outcome in the exposed population • A 95% CI range above 1 suggests a higher risk of the outcome in the exposed population

  38. p-values • The p-value is a measure of how likely the observed association would be to occur by chance alone, in the absence of a true association • A very small p-value means that you are very unlikely to observe such a RR or OR if there was no true association • A p-value of 0.05 indicates only a 5% chance that the RR or OR was observed by chance alone

  39. p-value Example Grodstein F, Goldman MB, Cramer DW. Relation of tubal infertility to history of sexually transmitted diseases. Am J Epidemiol. 1993 Mar 1;137(5):577-84

  40. Summary • Descriptive Epidemiology • Answers: Who, what, where, when • Key Terms: Prevalence, person, place, time • Hypothesis-generating • Analytic Epidemiology • Answers: Why, how • Key Terms: Measure of association • Hypothesis-testing

  41. References and Resources • Centers for Disease Control and Prevention (1992). Principles of Epidemiology: 2nd Edition. Public Health Practice Program Office: Atlanta, GA. • Gordis, L. (2000). Epidemiology: 2nd Edition. W.B. Saunders Company: Philadelphia, PA. • Gregg, M.B. (2002). Field Epidemiology: 2nd Edition. Oxford University Press: New York. • Hennekens, C.H. and Buring, J.E. (1987). Epidemiology in Medicine. Little, Brown and Company: Boston/Toronto.

  42. References and Resources • Last, J.M. (2001). A Dictionary of Epidemiology: 4th Edition. Oxford University Press: New York. • McNeill, A. (January 2002). Measuring the Occurrence of Disease: Prevalence and Incidence. Epid 160 lecture series, UNC Chapel Hill School of Public Health, Department of Epidemiology. • Morton, R.F, Hebel, J.R., McCarter, R.J. (2001). A Study Guide to Epidemiology and Biostatistics: 5th Edition. Aspen Publishers, Inc.: Gaithersburg, MD. • University of North Carolina at Chapel Hill School of Public Health, Department of Epidemiology, and the Epidemiologic Research & Information Center (June 1999). ERIC Notebook. Issue 2. http://www.sph.unc.edu/courses/eric/eric_notebooks.htm

  43. References and Resources • University of North Carolina at Chapel Hill School of Public Health, Department of Epidemiology, and the Epidemiologic Research & Information Center (July 1999). ERIC Notebook. Issue 3. http://www.sph.unc.edu/courses/eric/eric_notebooks.htm • University of North Carolina at Chapel Hill School of Public Health, Department of Epidemiology, and the Epidemiologic Research & Information Center (September 1999). ERIC Notebook. Issue 5. http://www.sph.unc.edu/courses/eric/eric_notebooks.htm • University of North Carolina at Chapel Hill School of Public Health, Department of Epidemiology (August 2000). Laboratory Instructor’s Guide: Analytic Study Designs. Epid 168 lecture series. http://www.epidemiolog.net/epid168/labs/AnalyticStudExerInstGuid2000.pdf

More Related