Epidemiology and Biostats Pt. 3 Flashcards

1
Q

Epi triad

A

agent
host
environment

sometimes vector is shown in the center of the triangle with lines radiating out to each of the three parts of the triad

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2
Q

factors that affect the agent

A

type, presence or absence, pathogenicity, dose, chemical and physical causes of injury and disease

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3
Q

factors that affect the host

A

exposure, susceptibility, age, sex, genetic composition, nutritional and immunologic status, anatomic structure, presence of disease or medications, psychological makeup, behaviors

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4
Q

factors that affect the environment

A

geology and climate, biologic factors that transmit agent (vectors or fomites), socioeconomic factors (crowding, sanitation, etc)

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5
Q

2 types of herd immunity

A

innate and acquired

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6
Q

2 main mechanisms of disease transmission

A

1) direct (direct contact, droplet spread)
2) indirect (airborne - from droplets suspended in the air or dust and blown around, vehicle-born (food, water, blood, fomites), vector-borne(mosquitoes, fleas, ticks))

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7
Q

examples of diseases spread by droplet spread

A

pertussis, meningococcal infection

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8
Q

modifiable risk factors

A

tobacco use
alcohol abuse
unhealthy diet
physical inactivity

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9
Q

non-modifiable risk factors

A

age
sex
heredity

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10
Q

intermediate risk factors

A

increased BP, BG, overweight/obesity, etc.

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11
Q

aims of levels of prevention

A

primordial: establish and maintain conditions that minimize hazards to health
Primary: reduce incidence of disease
Secondary: reduce prevalence of dz/shorten its duration
Tertiary: reduce number/impact of complications

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12
Q

Koch’s postulates

A

1) organism must be in every case of dz
2) organism must be isolated from diseased organism and grown in pure culture
3) cultured organism should cause dz when introduced into a healthy organism
4) organisms must be reisolated from the inoculated, diseased experimental host and identified as being identical to the original specific causative agent

nowadays, not all diseases fit perfectly into this model (ie. prion dz)

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13
Q

Hill’s causal criteria

A

There should be:
-strength (there is a strong association between cause and effect)
-consistency (repeatable results)
-specificity (cause leads to specific effect and not multiple ones)
-temporality (cause should precede effect)
-biological gradient (presence of unidirectional dose-response curve)
-plausibility
-coherence (studies must not contradict each other)
-experiment (experimental evidence is provided)
-analogy (same effect shown in animal studies prior to human studies)

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14
Q

necessary vs. sufficient causes

A

necessary - a factor must happen for disease to occur (a critical ingredient)

sufficient - that factor alone is sufficient in causing disease (other factors are not needed), but it doesn’t necessarily have to come from that factor

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15
Q

What are directed acyclic graphs

A

causal path diagrams that consist of nodes (variables) and arrows that indicate causal effect

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16
Q

Effect Modification

A

association between exposure and disease is different for different levels of a third variable
-the effect of the exposure on the disease is modified by a third variable

17
Q

to be a confounder, a variable must be:

A

-associated with the outcome (ie. is a risk factor for the disease)
-associated with the exposure, but is not a result of the exposure (ie. is not on the casual pathway from exposure to outcome)

18
Q

variables can be classified into 1 of 4 types depending on the type of scale used to characterize their values

A

1) Nominal: values are categories (ie. country of residence)

2) Ordinal: values can be ranked but not necessarily evenly spaced (ie. stages of cancer)

3) Interval: variable is measured on a scale with equally spaced units, but without a true zero (ie. date of birth), a continuous variable

4) Ratio: interval variable with a true zero point (ie. height in cm), a continuous variable

19
Q

A frequency distribution displays:

A

values a variable can take and the number of persons or records with each value

20
Q

categorical variables can be summarized as ratios, proportions, and rates

A

T

21
Q

Central location aka central tendency

A

the clustering of a distrubution at a particular value (ie. the top of the bell curve)

22
Q

Range

A

the difference between its largest (maximum) value and smallest (minimum) value

23
Q

Spread

A

the distribution out from a central value; how wide the bell curve is

24
Q

how to calculate standard deviation

A

1) calculate the mean
2) subtract the mean from each observation, then square the difference
3) sum the squared differences
4) divide the sum of squared differences by (n-1) where n = the total number of values. This is the variance.
5) take the square root of the variance. This is the standard deviation.

25
Q

Steps for general hypothesis testing

A

1) specify the null and alternative hypotheses
2) specify the type 1 error level
3) calculate a test statistic under the assumption that the null hypothesis is true. (The test statistic is a random variable number reflecting how well the data conforms to the null hypothesis)
4) compare the test statistic to what is expected if the null hypothesis were true (compute the p-value)

26
Q

How to decide what statistical test to use

A

1) decide what scale of measurement your data is (nominal, ordinal, interval, etc.)
2) consider the type of analysis required (comparison of independent or paired groups?)

27
Q

parametric vs. non-parametric tests

A

Parametric tests assume a normal distribution in the underlying population

non-parametric tests rely on no or few assumptions about the population distribution.
-Has less statistical power with the same sample size compared to parametric tests

28
Q

correlation coefficient

A

represents the strength of a linear relationship between two continuous variables. Ranges from -1 to 1. Does NOT prove causation.

0 = variables are uncorrelated
positive = variables positively correlated
negative = variables negatively correlated

29
Q

Modeling

A

the representation of physical processes, designed to increase appreciation and understanding of them

Types:
density model
prevalence model
stochastic model
empirical simulation modeling
Monte Carlo simulation modeling

30
Q

Density model

A

considers the absolute number of infectious agents in each host

31
Q

Prevalence model

A

considers the presence/absence of infection in various host cohorts

32
Q

Deterministic model

A

Fixed input parameters do not allow for random variation

33
Q

stochastic model

A

model that allows for random variation

34
Q

empirical simulation modeling

A

simulation of performance of dz in relation to changing parameters

35
Q

Monte Carlo simulation modeling

A

repeated simulations using random numbers to decide whether or not an event takes place