Midterm Review Flashcards

(45 cards)

1
Q

What are the 9 Bradford Hill critera?

A

1: Strength of Association
2: Consistency
3: Specificity
4: Temporality
5: Biological Gradient
6: Plausibility
7: Coherence
8: Experiment
9: Analogy

Mnemonic: “Some Assholes Constantly Specify That Bitchy Pigeons Collect Every Ant”

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2
Q

Bradford Hill: Strength

A

Strong associations compelling because weaker
associations could be more easily explained by
confounders etc.

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3
Q

Bradford Hill: Consistency

A

Repeated observation in different populations under different circumstances

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4
Q

Bradford Hill: Specificity

A

A cause leads to a single effect, not multiple effects
An effect has one cause, not multiple causes

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5
Q

Bradford Hill: Temporality

A

Cause precedes effect in time

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6
Q

Bradford Hill: Biologic Gradient

A

Dose-response or exposure-response curve with an expected shape

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7
Q

Bradford Hill: Plausibility

A

Scientific plausibility of an association

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8
Q

Bradford Hill: Coherence

A

Cause-and effect interpretation does not conflict with what is known of natural history and biology of disease
“it makes sense with what we knew before; it is coherent with it”

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9
Q

Bradford Hill: Experimental Evidence

A

Effect of reducing or eliminating putatively
harmful exposure and seeing if there is a resulting decrease in disease

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10
Q

Bradford Hill: Analogy

A

Extension to other similar conditions, exposures.
“when one causal agent is known, the standards of evidence are lowered for a second causal agent that is similar in some way”

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11
Q

Incidence Times

A

Times after a common reference event, when new cases occur among population

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12
Q

Incidence Rate

A

Occurrences of new cases per unit of PERSON-TIME

follow each member of our population to see
specifically how long each person is observed for the outcome of interest…

Note you could also look at this as a time-weighted average of individual rates

IT ISN’t A PROPORTION!

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13
Q

Incidence Proportion

A

Also called Cumulative Incidence
Proportion of people who develop new disease during specified time period

This is a PROPORTION

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14
Q

Prevalence

A

Measures the total number of cases (both new and existing) in a population at a specific point in time (point prevalence) or over a period (period prevalence).

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15
Q

Incidence Time

A

T0 to the point the event occurs

Used in time-to-event (survival) analysis to track when cases occur rather than just counting how many occur.

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16
Q

Censoring

A

Occurs when a study does not observe the exact time of an event (e.g., disease onset, death) for an individual, either because they leave the study early or the study ends before the event occurs.

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17
Q

Post Hoc Fallacy

A

A logical fallacy that assumes “because X happened before Y, X must have caused Y.

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18
Q

Reason to use Kaplan-Meier Curve

A

Cumulative survival will not work when censored observations are in the sample. Kaplan-Meier curves (or other actuarial methods like life tables) account for this

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19
Q

Assumption of Life Tables

A

Uniformity of events and losses within each interval

20
Q

4 Assumptions of Kaplan-Meier Curves

A

1: Independence between censoring and survival
The probability of being censored is not related to the probability of experiencing the event

2: Event Occurs at the Recorded Time
No measurement errors

3: Survival Probabilities are the Same for All Individuals at a Given Time
Every participant who remains at risk has the same probability of survival as others still in the study.

4: No Changes in Risk Over Time (no secular changes)
The conditions affecting survival remain constant throughout the study period.

21
Q

Secular Trends

A

Gradual changes in the occurrence of disease over a long period of time, usually years or decades.They are also known as temporal trends

22
Q

Direction of bias if those censored have HIGHER risk than those not censored

A

Towards null (if outcome is death/illness): study sample is progressively healthy over time (lower risk patients remain in study)

23
Q

Direction of bias if those censored have LOWER risk than those not censored

A

Away from null (if outcome is death/illness): study sample is progressively sicker over time (higher risk patients remain in study)

24
Q

Odds

A

The ratio of the (probability of event) to (probability of non-event)

25
Odds Ratio
A measure of association that compares the odds of an outcome occurring in an exposed group to the odds in an unexposed group. It is commonly used in case-control studies but can also be applied in cohort and cross-sectional studies.
26
Risk
The probability that an individual in a population will develop a disease or experience an event over a specified time period.
27
Risk Ratio
Compares the risk of developing a disease in an exposed group to the risk in an unexposed group.
28
Prevalence Ratio
A measure that compares the prevalence of a disease or condition between two groups—typically an exposed group and an unexposed group. It is similar to Relative Risk (RR) but is used in cross-sectional studies, where disease status is measured at a single point in time rather than over a period.
29
Prevalence Odds Ratio
Similar to the Odds Ratio (OR) but is specifically used in cross-sectional studies. It compares the odds of having a disease (prevalence) between an exposed and unexposed group.
30
Age effect
Change in the rate of a condition according to age, irrespective of birth cohort and calendar time ## Footnote e.g. increased heart disease risk with age
31
Cohort Effect
Change in the rate of a condition according to year of birth, irrespective of birth cohort and calendar time ## Footnote ie: for zika virus, didnt have to do with the cohort of the mom or baby, just the time the baby was born (ie during the outbreak) different from Period Effect bc this only effects birth cohort
32
Period Effect
Change in the rate of a condition affecting an entire population at some point in time, irrespective of age and birth cohort ## Footnote e.g., a pandemic, economic crisis, Introduction of Antibiotics (1940s) → Sharp decline in infectious disease deaths for all age groups. different from Cohort effect bc effects EVERONE in the period
33
3 thing cross sectional studies mask that Birth Cohort Analysis shows
Age effect Period effect Cohort effect
34
Rare Disease Assumption
As a disease becomes more rare the OR more closely approximates the RR
35
Conditions when OR will approximate RR
* Controls are representative of individuals in the base population * Cases are representative of all individuals in the base population with the disease of interest * The disease is** relatively rare (generally < 5%** of the base population)
36
True or false: OR of the event is the reciprocal of the non-event
True! This is because it is a counterfactual; you either did or didn't die NOT SO FOR RR or other risk estimates | Ratio or Risks, NOT complements
37
Incidence density sampling
Also called risk set sampling, is a method used in case-control studies nested within a cohort. It selects controls from individuals who were at risk at the same time cases occurred, preserving the timing of exposure and ensuring comparability between cases and controls.
38
Attributable Risk
A measure of association based on the *absolute difference between two risk estimates*
39
What are the 4 assumptions for Attributable Risk?
1. Causality 2. No Bias 3. No Confounding 4. Reversibility ## Footnote Also Independence, according to sources
40
Population Attributable Risk (Levin's)
Estimates the proportion of the disease risk in the underlying population associated with exposure of interest
41
Ecologic Fallacy, aka Aggregation Bias
Bias that can occur because an association between variables on an aggregate level does not necessarily represent the association that exists on the individual level
42
4 Cohort Study Hightlights
1. Categorized according to exposure 2. All disease free at baseline 3. Exposure occurred first 4. Exposure categorization (exposed vs not exposed) documented prior to outcome ## Footnote Allows for temporality!!!
43
Incidence Denstity Sampling (aka risk set sampling)
A method used in **nested case-control studies** where **controls are selected from individuals who are still at risk at the time each case occurs.** This approach ensures that the control group represents the population at risk at the same time the cases arise, maintaining comparability between cases and controls.
44
Directon of ITT Bias
Intention to Treat will always **underestimate the true impact**
45
Randomization vs Random Allocation
Randomization = Deciding who enters the study (random sampling). Random Allocation = Deciding which group they go into (random assignment).