DR. GEORGE Flashcards
Comparison of populations in different places at the same time or in a time series.
Ecological study
i. These studies are also called follow-up or incidence studies
ii. Begins with a group of people who are free of disease or outcome of interest and who are classified into subgroups according to exposure to a potential cause of disease or outcome
Cohort study
i. Investigates the causes of diseases
ii. Incudes people with a disease of interest and a suitable control (comparison or reference) group of people unaffected by the disease or outcome variable
iii. Compares the occurrence of the possible cause in cases and in controls
iv. Data is collected on disease occurrence at one point in time and exposures at a previous point in time
v. They are longitudinal studies/retrospective/prospective studies
Case control study
i. Measure the prevalence of disease
ii. The measurements of exposure and effect are made at the same time1. E.g. Risk factor survey for non-communicable diseases
Cross-sectional study
i. An experiment designed to study the effects of a particular intervention (clinical trial)
ii. Subjects are randomly allocated to intervention and control groups and the results are assessed by comparing outcomes
Randomized control study
i. Involve people who are healthy but presumed to be at risk
ii. Data takes place in the field among non-institutionalized people in the general population
iii. Useful to evaluate interventions aimed at reducing exposure without necessarily measuring the occurrence of health effects
1. E.g. Testing of the Salk vaccine for the prevention of poliomyelitis
Field trial
i. The treatment groups are communities rather than individuals
ii. Appropriate for diseases that are influenced by social conditions and for which prevention efforts target group behavior
Community trial
a. When a value of the sample measurement diverges – due to chance alone – from that of the true population value
b. Causes inaccurate measures of association
a. Random error
c. There are three (3) major sources of random error
i. Individual biological variation
ii. Sampling error (small sample is not representative of the population)
iii. Measurement error (reduce through protocols and quality control procedures)
a. Must be large enough for the study to have sufficient statistical power to detect the differences
Sample size
b. Parameters required for calculation of sample size:
i. Required level of statistical significance of the ability to detect a difference
ii. Acceptable error
iii. Magnitude of the effect under investigation
iv. Amount of disease in the population
v. Relative sizes of the groups being compared
a. When results differ in a systematic manner from the true values
Systematic error
b. A study with a small systematic error is said to have a
high accuracy
d. The principle biases are
i. Selection bias
ii. Measurement or classification bias
a. When patients included in the study are not representative of the population to which the results will be applied
b. When there is systematic difference between the characteristics of the people selected for a study and the characteristics of those who are not
c. E.G
i. When participants select themselves for a study
ii. When the disease or factor under investigation itself makes people unavailable for study
Selection bias
a. When the individual measurements or classifications of disease or exposure are inaccurate – they do not measure correctly what they are supposed to measure
b. E.G. Biochemical or physiological measurements are never completely accurate and different laboratories produce different results on the same specimen
Measurement bias
Relative Risk
Relative Risk = Risk in exposed/Risk in non-exposed
Determines the ratio of the risk of disease in exposed individuals to the risk of disease in non-exposed individuals