Evidence Based Flashcards

1
Q

Ratio

A

Numerator does not need to be a subset of the denominator
ex. ratio of men to women

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2
Q

Proportion

A

diving one number by another, where the numerator is a subset of the denominator
ex. the proportion of men in a population calculated as the number of men divided by the total population

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3
Q

Rate

A

similar to ratios and proportions, rates are calculated by dividing one number by another, and additionally have a time component of the denominator
ex. the number of people who developed influenza in 2017, the birth rate per year in a population, the mortality rate per year in a population

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4
Q

Observation bias

A

the bias arises from systematic differences in the way information on exposure or disease is obtained from the study groups
occurred only after the participants have entered the study

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5
Q

Methods of controlling for confounding

A

randomization, restriction, matching, standardization, stratification, and conducting a multivariable analysis

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6
Q

Reliability

A

aka repeatability
- repeated measures are close to one another but still misses the bull eye

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7
Q

Validity

A

a screening test is the ability of a test to accurately identify diseases and non-diseases individuals

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8
Q

Lead time bias

A

overestimation of survival duration attributable to earlier detection by screening than by clinical presentation

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9
Q

Length bias

A

screening is more likely to detect cases that are progressing slowly compared with those with rapid progression of disease, who manifest clinically
- slow progressing cases are usually milder and more likely to survive, leading to an overestimation of survival as a result of screening

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10
Q

Descriptive statistics

A

performed on a small subset of a population, known as a sample
- builds on descriptive statistics and allows researchers to draw conclusions on the population based on information collected from the sample

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11
Q

nominal variables

A

data are collected on the category in which the participants falls. The categories have no inherent order (ie. race)

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12
Q

Dichotomous variables

A

variables have only two possible values (i.e. exposure status: exposed or unexposed)

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13
Q

ordinal variables

A

categories have an inherent order (i.e. level of education)

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14
Q

Interval variable

A
  • type of continuous variable
  • have a distinct order
  • lacks a true zero
    (i.e. pH)
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15
Q

Ratio variable

A
  • type of continuous variable
  • true zero
  • values of the variable act as true ratios of one another
    (i.e. temperatures in kelvin)
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16
Q

Z scores table

A

Probabilities for the likelihood that a certain value or a more extreme value would be observed are tabulated through this table
- often uses inferential statistics analyses

17
Q

Poisson distribution

A

count data is the number of occurrences in a group
- distribution is right-skewed because higher counts are less likely to be observed

18
Q

Confidence interval

A

show the strength of association between the exposure and the outcome

19
Q

Pearson correlation of coefficient (r)

A

-1 to +1
reveals both the fit of the data to the regression line and the direction of association between the variables
- negative r = the values of independent variable increase, while dependent variable decrease
- positive r = independent variable increase, while the values of the dependent variable also increase
- 0 reveals the strength of the relationship
- +0.9 or -0.9 = strong positive and negative linear relationship
- +0.1 or -0.1 reveals a weak positive and negative linear relationship

20
Q

Coefficient of determination (r^2)

A

for simple linear regressions, this is the squared value of the pearson product moment correlations coefficient
- standardizes the value to be used as a metric of the fit of the linear regression model for both positively and negatively associated variables
- 0 to 1

21
Q

Case fatality ratio

A

of deaths / # of cases

22
Q

Distribution

A

describes who gets the disease, where people with the disease are located, and how these aspects of the disease change overtime

23
Q

When should sensitivity be increased

A

when the penalty associated with missing a case is high
- when the subsequent diagnostic evaluations are associated with minimal cost and risk

24
Q

When should specificity be increased

A

when the costs associated with further diagnostic techniques are substantial

25
Q

preclinical phase

A

period between the initial biological onset of a disease and the emergence of any noticeable symptoms or clinical signs.

26
Q

clinical phase

A

period during which a disease manifests noticeable symptoms and signs that are detectable through standard diagnostic methods or observable changes in a person’s health