midterm Flashcards

(36 cards)

1
Q

Descriptive epidemiology

A

Classify according to person, place and time variables

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2
Q

analytical epidemiology

A

explores causal hypotheses between exposures and health conditions

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3
Q

Simple random sampling (SRS)

A

sample is selected using random processes

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4
Q

stratified random sampling

A

to ensure adequate representation of minority groups that might be underrepresented in SRS

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5
Q

convenience sampling

A

selecting individuals from easily accessible and available groups such as those who visit a specific clinic

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6
Q

Systematic sampling

A

choosing via a systematic, predetermined approach from the sampling frame

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7
Q

Cluster sampling

A

selecting groups of individuals

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8
Q

Central tendency

A

in normal distribution, mean, median and mode are equal and situated at center of distribution with values symmetrically distributed around central point

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9
Q

skewed distribution

A

mean, median and mode are often different- median is most accurate because it is resistant to outliers

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10
Q

symmetric distribution

A

mean and median are equivalent- mean is preferred bc it is more stable/precise across different sample sizes

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11
Q

Multimodal distribution

A

several peaks in frequency of data marking distinct groups/clusters within dataset (ex. Age-related changes)

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12
Q

Epidemic curve

A

represents distribution of cases over specified time frame to identity patterns in disease outbreaks

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13
Q

Dose-response curve

A

correlation between exposure and effect

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14
Q

Incidence

A

number of new cases occurring in specific population in specific time period

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15
Q

Prevalence

A

total number of existing cases in population at specific time, expressed as proportion, New cases and treatment advances that extend survival can boost prevalence

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16
Q

person variables

A

Age, sex, race, socioeconomic status, marital status

17
Q

place variables

A

Morbidity and mortality influenced by geographic factors (ie life expectancy), urban vs rural, localized patterns of disease

18
Q

time variables

A

Secular trends (long-term changes in frequency of diseases), cyclic (seasonal) trends, point epidemics, clustering

19
Q

Criteria for causal relationship

A

Strength of association
Consistency
Specificity
Temporality- establishing that exposure occurs before health outcome
Biological gradient- depicting how increased exposure correlates with increased disease incidence
Plausibility
Coherence
Experimental evidence
Analogy in causality- comparison against established causal relationships

20
Q

Risk factor

A

Factors correlated with an increased likelihood of disease but are not sufficient on their own to cause it

21
Q

observational studies

A

ecological, case-control, cohort, cross-sectional

22
Q

experimental studies

A

clinical trials, field trials, community trials
Advantages: less prone to biases, control for confounding variables, causal relationships
Disadvantages: complex and costly, large sample size, ethical considerations, patient non-compliance

23
Q

bias

A

Systematic error that leads to deviation from truth

24
Q

Hawthorne effect

A

altered behavior bc know they’re being studied

25
Recall bias
remembering exposure history
26
Selection bias
selecting participants leads to misrepresentation of association between exposure and outcome
27
ecological studies
estimate exposure levels for groups based on data from environment, applying same exposure level to all group members despite variations within group Advantages: broader context, conducted quickly with less resources because data is more readily available, useful when cant get individual level data Disadvantages: ecologic fallacy- correlations at group do not necessarily apply to individuals, overlook individual/personal behaviors and genetic predispositions
28
case-control studies
cases have outcome/disease, retrospective approach Advantages: useful for studying low-prevalence conditions or rare diseases, fewer resources and quicker than traditional follow up studies Disadvantages: innacurate exposure measurements, representativeness of cases and controls may be uncertain, indirect estimates of risk, temporal relationships may not be clear
29
cohort studies
tracks incidence overtime following cohort that shares common characteristic Fixed- individuals classified as exposed or unexposed at specific baseline time and followed Dynamic- continuous recruitment of new eligible candidates over time- inds may shift from unexposed to exposed group Advantages- evaluating incidence rates, direct observation of risk, relationship between exposure and outcomes over time, uncommon exposures or diseases with clear temporal relationships between exposures and outcomes Disadvantages- costly and time consuming, not useful in rare conditions, planning and tracking large groups, non-participation may affect demographics
30
cross-sectional studies
examines defined population or random sample at specific point in time- assessing both presence of disease and potential determinants, mainly descriptive (not causal relationships) Advantages: snapshot, inexpensive and easy bc do not follow over time Disadvantages: establishing causal, controlling for confounding variables, accurate reporting of exposure by patients, selection bias, length bias
31
clinical trials- randomized controlled trials (RCTs)
phase 1 tests safety, phase 2 immune responses and phase 3 randomization randomly allocated into test and control groups
32
field trials and community trials
involve healthy individuals at risk, data collection in natural settings, evaluate intervention designed to prevent diseases involve groups, can be harder
33
environmental epidemiology
etiology (causes/origins), natural history, health status of pop, effectiveness of interventions, geographic focus
34
Natural history of disease
Pathological onset, presymptomatic stage, clinical stage Prognosis- predicting likely course of disease Efficacy- benefits of treatment under ideal conditions Effectiveness- benefits in real-world clinical settings (RCTs)
35
dose-effect/dose-response relationship
Does-effect identify which adverse effects should be prioritized for prevention Dose-response to determine what constitutes acceptable level for exposure
36
directed acyclic graphs (DAGs)
relationships/causal links (arrows) between variables (nodes), no sequence of arrows forms a closed loop, if 2 or more variables share same cause ("parent" cause should be included), unmeasured confounding/cause (arrow pointing both directions between 2 nodes)