1 / 52

Definitions, History and Infections

Definitions, History and Infections. September 30 2004 Epidemiology 511 Autumn 2004 W.A. Kukull. Forecasting the future.

cmishler
Download Presentation

Definitions, History and Infections

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. Definitions, History and Infections September 30 2004 Epidemiology 511 Autumn 2004 W.A. Kukull

  2. Forecasting the future • “On the basis of what has happened in the last 30 years…the most likely forecast about the future of infectious disease is that it will be very dull…outbreaks of infections from exotic animals…will doubtless occur in the future but they will presumably be safely contained”.Nobel Laureate, Sir McFarland Burnet, 1972

  3. Definitions of Epidemiology • The study of the distribution and determinants of health and diseases, morbidity, injuries, disability, and mortality in populations. • The study of the distribution and determinants of health-related states or events in specified populations and the application of this study to control of health problems [Gordis]

  4. Assumptions • “Disease” does not occur at random • “Disease” has causal and preventive factors that can be identified through systematic study of populations (persons, places, times) • Factors may be genetic or environmental

  5. Prevention of disease • Primary Prevention: prevent the disease from occurring in a well person • Secondary Prevention: early detection of disease to change the natural history • Tertiary Prevention: reducing disease disability after clinical treatment

  6. Determinants? • Infectious agents • Carcinogens, chemicals • Behaviors/Habits/Lifestyle • Occupational exposures • Aging • Genetic constitution • Socio-political factors

  7. Distribution • Who is affected? • what are their characteristics? • Where are the affected persons? • When are persons affected ? • How many persons are affected? • Is the distribution changing; how?

  8. Population ? • Geographic • Organization Membership • Employment • School • High risk subgroups vs entire Population • Can we enumerate (count) all members?

  9. West Nile Virus numbersScience,297:1988,(2002) and CDC

  10. U.S. counties reportinghumanWNV disease cases, 1999(N = 6 counties)

  11. U.S. counties reportinghumanWNV disease cases, 2000(N = 10 counties)

  12. Incidence of WNME in Humans, by County, United States, 2002* *Reported as of 01/21/2003

  13. U.S. Counties Reporting Human WNV Disease Cases, 2002* 3,862 cases 708 counties 39 states & D.C.

  14. WNV Human Disease Cases, Demographics & Mortality, United States, 1999-2002* * Reported as of 01/21/2003 ** 9% of WN ME cases

  15. Human WNV Disease Incidence, by Age Group and Clinical Category, United States, 2002* * Reported as of 01/21/2003 * *Entire US population

  16. John Snow and Cholera (1) • Snow: vital statistics for 1832 epidemic • higher cholera death rates in areas served by Southwark (11 per 1000 vs. 2 per 1000) • Epidemic of 1848-49: observed similar death rates in areas served by Southwark, and Lambeth water companies • all draw water from same place on Thames

  17. Cholera (2) • William Farr, 1848-49 epidemic: low altitude associated with higher death rate: Miasma or cloud transmitted disease • Snow, 1853: Lambeth water source now moved upstream => Cleaner water • lower death rates in Lambeth service areas: ECOLOGIC design

  18. Materies Morbi: Snow’s hypothesis • Living transmissible agents • small amounts can enter host and multiply • transmitted by contact with patient or fomites • agent can remain dormant, like a seed • can be transmitted great distances while dormant, e.g. by water supply • body portal of entry and exit

  19. Cholera (3) • Snow, 1854 Epidemic, Field epidemiology • 3 water companies served households in the area in a “random” distribution • Determined # of deaths in households served by each water company. • S&V= 71 per 10,000; Lambeth 5 per 10,000 • RETROSPECTIVE COHORT Design

  20. Cholera (4) • 1854 The Broad Street Pump • remove the handle: public policy change • Did cholera cases use Pump? • Did Non-Cases use pump? • Brewery workers • Workhouse inmates • Other pumps • CASE-CONTROL design

  21. Important generalizations: Snow and Cholera • Careful observation of vital statistics • numerators: numbers of events (deaths) • denominators: total persons at risk • calculation of rates • Etiology: causal hypothesis • Exposure ascertainment: field epidemiology • Public policy change

  22. Koch’s postulates • The agent must be recovered from all individuals with disease • Recovered agent must grow in culture • Cultured organism must cause disease in susceptible animal • Agent must be recovered from diseased experimental animal

  23. Revised causal criteria • Temporal relationship • Strength of Association (RR) • Biologic plausibility • Risk factor changes occurrence or severity of disease • Consistency : association is replicated by other investigators • Dose-response

  24. Endemic or Epidemic Cases per 1000 population/time Expected Level Time

  25. The Epidemiologic Triad of a Disease Host Vector Agent Environment

  26. Influenza A epidemic excess mortality in U.S. • A/Japan/57 (H2N2) 1957-58 69,800 • A/Japan/62 (H2N2) 1963 43,200 • A/HK/68 (H3N2) 1968-69 33,800 • A/Eng/72 (H3N2) 1972-73 24,800

  27. Influenza • Surface Antigens: Hemagglutinin; Neuraminidase • Antigenic Shift: MAJOR changes in H, N • May cause pandemics • Antigenic Drift: MINOR changes in H, N • RNA mutation • Change in antigenicity but not serotype

  28. Antigenic Shift serotypes

  29. Antigenic Drift • A/Sidney/5/97 H3N2 • Many variants of H3N2 since 1968 • A/New Caledonia/20/99 H1N1 • Over 66% of H1N1 strains isolated in 1999-2000 were antigenically different from previous • Included in 2000-01 vaccine

  30. Natural Hx of infection Observable illness Outcome Treatment Infection Exposure Incubation period Pre Clinical period Clinical Period

  31. Outbreak Investigation (1)Define the epidemic • Define the numerator (cases) • Clinical features • Culture, serology • other causes • Define denominator • population at risk; susceptibles • Calculate Attack Rates

  32. Outbreak investigation (2)Distribution of cases • Time-Place interactions • Characteristics of persons; risk subgroups • Combinations of relevant variables • cross-tabulation of attack rates • Develop hypotheses • existing knowledge of disease (if any) • analogy to known diseases

  33. Outbreak investigation (3) • Test Hypotheses • Calculate ratios of Attack rates • Further analyze existing data • Collect additional data • Recommend Control Measures • Control present outbreak • Prevent future outbreaks

  34. Critical Questions • When did exposure take place? • When did disease begin? • What was disease incubation period? • If we know any two answers, we can calculate the answer to the other.

  35. Herd Immunity • Number of susceptibles • Does infection induce persistent immunity? • Is agent restricted to single host--humans? • Is transmission relatively direct? • High proportion immune protects others • Vaccine programs • lack of susceptibles limits spread

  36. Attack Rates Attack Rate = Number of people at risk who develop illness Total number of people at risk Secondary Attack Rate = Number of contacts developing disease within one incubation period Total number of susceptible contacts Measure of the disease’s tendency to spread in a population

  37. Distribution of SARS cases by days since exposure Average days estimates incubation period

  38. Estimated Incubation Period

  39. Age-specific case fatality rate

  40. Time before hospital admission after symptoms had occurred

  41. Secondary Attack Cases (SSE= super spreading event)

  42. Attack Rates(% who became ill) Which one is the cause of illness?

  43. Attack Rates (2)

  44. Emerging Infections:newly appeared or has existed but is rapidly increasing in incidence or geographical range • Promoters of pre-existing pathogens • Ecologic changes; shifts in human populations • International travel/commerce • changing industry and technology • microbial adaptation; lapses in public health system

More Related