Epidemiology case studies etc – Flashcards
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Learning Objectives of Epidemiology and Public Health
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Learning Objectives You should be able to: 1- Define epidemiology & Public Health 2- Compare medicine practised on individuals in a clinical setting to that practised at a population level 3- Understand the strengths & limitations of the population perspective 4- Know what a "rate" is in general terms
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Epidemiology
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the study of the distribution and determinants of diseases in human populations. It seeks to understand the background of a disease and identify its causes, so making possible its prevention
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Public Health Epidemiology
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The study of DISEASE INCIDENCE
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Clinical Epidemiology
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The study of DISEASE PROGNOSIS
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Public Health
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the science and art of prolonging life, preventing disease and promoting health by the organised efforts of society
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Clinical medicine
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is concerned with people who already have the disease, it seeks to understand how the disease progresses what its effects are, and how it can be treated
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Essence of Epidemiology
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lies in comparing incidence or prevalence rates between populations or between groups within a population.
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Epidemiology conclusions
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Because epidemiologists deal in terms of rates, their conclusions relate to GROUPS, rather than individuals. They seek to explain why one population e.g. country or group e.g. poorer families has more illness than another
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Epidemiological "rates"
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"Rate" = Number of cases* / divided by Population at risk eg Number of people in Llandovery with flu / the number of people in Llandovery * Incidence rates (new cases) and mortality rates (fatal cases) also specify a time period Prevalence rates (existing cases only) = number of people with flu NOW # Sometimes called "catchment population"
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Prevalence
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the number of existing cases of the disease / divided by total number of patients in catchment eg number of people with flu NOW in llandovery / number of people in Llandovery ALSO defined as incidence x duration
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Incidence (note: not incidence rate!)
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number of new cases of diseases / number in catchment population
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Cumulative incidence (look at sheet) NOTE NOT INCIDENCE RATE, In some ways, the cumulative word is unecessary
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= d/N where d = the number of cases of disease and N is the catchment population
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Incidence rate (look at sheet)
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= d/Y where d is the cases of disease and Y is the catchment population multiplied by the number of years looked at
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Odds of disease (see sheet)
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= d/(N-d) where d = the number of cases of disease and N is the catchment population so N-d is the number in the population that have not developed the disease
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Cumulative incidence
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number of persons who become diseased during a defined follow up period (d) / divided by number of persons in the population at the start of the follow up period (N)
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Incidence rate
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number of persons who become diseased during a defined period (d) / divided by total person time at risk during the follow up period (Y)
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Cross sectional study
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A study in which a representative cross section of the population is tested or surveyed at one specific time
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CROSS SECTIONAL STUDY
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Do persons with the characteristic HAVE THE DISEASE more frequently than those who do not have the characteristic? i.e= do people who smoke HAVE the disease more frequently than those who DO NOT smoke?
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Advantages of Cross sectional survey
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Suited to study common diseases Relatively quick and easy to carry out Can give estimates of the prevalence of a disease eg so you can tell how many people have the diseases NOW
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Disadvantages of Cross sectional study
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Not suited to study rare conditions as large number of people would need to be sampled to obtain a good estimate of the prevalence Care needs to be taken with the selection of the sample to ensure it is representative of the population No estimates of the incidence of a disease
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Cohort
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A group of people who share a common characteristic (eg smokers) or experience within a defined period (e.g., are born, are exposed to a drug or vaccine or pollutant, or undergo a certain medical procedure). The comparison group may be the general population from which the cohort is drawn, or it may be another cohort of persons thought to have had little or no exposure to the substance under investigation, but otherwise similar. In a cohort study, healthy subjects are defined according to their exposure status and followed over time to determine the incidence of symptoms, disease, or death. The common characteristic for grouping subjects is their exposure level. Usually two groups are compared, an "exposed" and "unexposed" group. The unexposed group is called comparison group
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COHORT STUDY
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Do persons with the characteristic DEVELOP THE DISEASE more frequently than those who do not have the characteristic So we are really looking at two cohorts, i.e. the one exposed to the characteristic and the other cohort that has not been exposed to the characteristic eg = are people who have been exposed to asbestos have lung cancer (mesothelioma) more commonly than those who have never been exposed?
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Cohort study
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A form of longitudinal study (a type of observational study) used in medicine. It is an analysis of risk factors and follows a group of people who do not have the disease, and uses correlations to determine the absolute risk of people catching the disease
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Definition of a case control study
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A case - control study starts with the identification of a group of CASES (individuals with a particular illness or condition) and a group of CONTROLS (individuals without a particular illness or condition). The prevalence of a particular EXPOSURE is then measured in the two groups and compared. If the exposure is more common among the cases than controls, it may be a RISK FACTOR for the disease. If it is less common, it may be a PROTECTIVE FACTOR CASE CONTROLS ARE QUICK TO CARRY OUT
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CASE CONTROL STUDY
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Do persons with the disease HAVE A CHARACTERISTIC more frequently than those without the disease Those who have the disease are termed cases, and those who do not have the disease are termed controls. The exposure histories of cases and controls are then obtained and compared.
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Endemic
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when a disease persist for a long period within a community
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Epidemic
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when the occurrence of disease episodes increase substantially for a limited period of time
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Definition of disease outbreak can be defined in two ways
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1 An incident affecting two or more people within a given period of time /place with a common exposure to a potential source and experiencing a similar or proven illness OR a rate of infection greater than the expected rate for that place and time, where spread is occurring through cross infection, or person to person
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A Point Source Outbreak suggests
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an introduction of an infection to a group of people at ONE POINT in time
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A SECONDARY (person to person) spread suggests
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infection spread from one person to another person, rather than the initial point source outbreak
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Risk ratio = (must look at image on questions 12,13,and 14 above)
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Cumulative incidence in exposed group / cumulative incidence in non-exposed group d/N (of exposed group) divided by d*/N* (of non exposed group)
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rate ratio = (must look at image on questions 12,13,and 14 above)
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incidence rate in exposed group / incidence rate in non-exposed group d/Y (of exposed group) divided by d*/Y* (of non exposed group)
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Odds ratio = (must look at image on questions 12,13,and 14 above)
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Odds of disease in exposed group / Odds of disease in unexposed group d/(N-d) (of exposed group) divided by d*/N-d*)* (of non exposed group)
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Rate ratios, risk ratios and Odds ratios are examples of
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Relative Risk
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Relative Risk = ( see example on separate sheet word document Relative and Absolute excess GOOD EXAMPLES)
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A measure of the STRENGTH of an association. It has NO units e.g.
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A relative risk of 1.0
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This implies NO EFFECT to an exposure of a disease occurring
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The most helpful measure to establish causation is
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Relative Risk
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Null hypothesis
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A general or default position is that there is no relationship between two measured phenomena, (e.g. that a potential medical treatment has no effect
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If the NULL HYPOTHESIS IS TRUE, the odds ratio (i.e. relative risk) will be
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1 (ONE)
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p-value
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the probability of obtaining a test statistic at least as extreme as the one that was actually observed, assuming that the null hypothesis is true
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Confidence Interval
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CI around a result obtained from a study sample indicates the range of values within which there is a specific level of certainty (usually 95%) that the true population value for that result lies A confidence interval gives an estimated range of values which is likely to include an unknown population parameter, the estimated range being calculated from a given set of sample data.
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"Attributable risk" and "Population Attributable risk" are examples of ( see example on separate sheet word document Relative and Absolute excess GOOD EXAMPLES)
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Absolute risk
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The most helpful measure for Policy Making is
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Absolute Risk
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Explaining Confounding
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In an ideal laboratory experiment the investigator alters only one variable at a time, so that any effect he observes can only be due to that variable. Most epidemiological studies are observational, not experimental, and compare people who differ in all kinds of ways, known and unknown. If such differences determine risk of disease independently of the exposure under investigation, they are said to confoundits association with the disease. ("Confoundits complicate the results, and this can be either negatively or positively") For example, several studies have indicated high rates of lung cancer in cooks. Though this could be a consequence of their work (perhaps caused by carcinogens in fumes from frying), it may be simply because professional cooks smoke more than the average. In other words, smoking might confound the association with cooking. Confounding determines the extent to which observed associations are causal. It may give rise to spurious associations when in fact there is no causal relation, or at the other extreme, it may obscure the effects of a true cause. Two common confounding factors are age and sex. Crude mortality from all causes in males over a five year period was higher in Bournemouth than in Southampton. However, this difference disappeared when death rates were compared for specific age groups. It occurred not because Bournemouth is a less healthy place than Southampton but because, being a town to which people retire, it has a more elderly population.
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variance
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is a measure of the spread of observations around a mean. It is the square of the standard deviation.
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memory bias / recall bias
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A cognitive bias that either enhances or impairs the recall of a memory , or that alters the content of a reported memory.
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Chi-square
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Is a statistical test commonly used to compare observed data with data we would expect to obtain according to a specific hypothesis. For example, if, according to Mendel's laws, you expected 10 of 20 offspring from a cross to be male and the actual observed number was 8 males, then you might want to know about the "goodness to fit" between the observed and expected. Were the deviations (differences between observed and expected) the result of chance, or were they due to other factors. How much deviation can occur before you, the investigator, must conclude that something other than chance is at work, causing the observed to differ from the expected. The chi-square test is always testing what scientists call the null hypothesis, which states that there is no significant difference between the expected and observed result.
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bias
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a partiality that prevents objective consideration of an issue or situation i.e. a lack of pure objectivity e.g. selection bias or recall/memory bias
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Risk Factor
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A risk factor is anything which DISTINGUISHES groups at highet or lower risk of disease. It need not be CAUSAL
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Examples of FIXED RISK FACTORS include
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age, sex, family history and genes
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Examples of potentially MODIFIABLE RISK FACTORS (e.g. in heart disease) include
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Obesity, smoking, blood pressure, plasma cholesterol.
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A plasma cholesterol of 6.5 is regarded a upper limit of normal. What criteria might have been used to define "upper level of normal"
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NORMALITY and ABNORMALITY may be defined as i STATISTICALLY (e.g. a certain % of the population exceed the cut off (above 2 Standard Deviations) ii with reference to SYMPTOMS (not relevant to cholesterol) iii with reference to future COMPLICATIONS iv with reference to the BENEFITS OF TREATMENT In case of cholesterol i and iv are used
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CLASSIFICATION OF PREVENTION
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Primary, secondary, tertiary prevention
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How do we define these and distinguish between classifications of prevention?
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On the basis of the stage of disease
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No disease developed =
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Primary Prevention e.g. immunization, or stopping smoking before Lung cancer develops
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Early disease =
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Secondary Prevention e.g. treating patients with early atheroma for high BP or high cholesterol to stop heart attacks or strokes occurring
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Late disease =
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Tertiary prevention - putting a stent into a patient who has had a heart attack to try and prevent another MI occurring
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STRENGTHS OF HIGH RISK STRATEGY
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Can offer intervention appropriate to individual because subject at high risk, intervention could be:- Effective Cost effective Motivation of subject and doctor usually high Approach fits within medical model Avoids interference with low risk population
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WEAKNESSES OF HIGH RISK STRATEGY
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Process involves risk factor SCREENING which provides imperfect prediction of those at risk has costs has risks offers imperfect prediction of those at high risk - * Some high risk subjects will have developed disease (secondary not primary prevention) No attempt to interfere with the incidence of disease - this is a palliative strategy for prevention, not a radical one Represents medicalization of health and prevention Often socially or behaviourally inappropriate - singling out a small subset of the population who have to behave differently
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STRENGTHS OF POPULATION STRATEGY
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Radical, aiming to reduce disease incidence Large potential benefits especially where risk is widespread in population Often behaviourally appropriate - no need for some individuals to behave differently Does not require screening/identification of high risk group Does not depend on medical care services, which tend to be expensive
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WEAKNESSES OF POPULATION STRATEGY
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Usually depends on a sense of public purpose and/or political will - individuals and health professionals are poorly motivated Measures needed may be complex (see next) Though benefit for the population can be large, benefit for individuals (even high risk individuals) is small - `prevention paradox' If the population strategy involves adding a new factor with potential adverse effects (e.g. fluoride into drinking water) balance of benefit and harm may be narrow
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95% central reference range
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The SD is a measure of the spread of values in individual people about a mean. The 95% reference range is where 95% of the values fall as is given bu the mnean +/-2 x SD.
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Blinding
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