EPI Final Exam Flashcards

1
Q

How to Calculate Prevalence Period

A

existing cases at start + new cases over a period of time/ size of population at start of time period = %

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2
Q

How to calculate prevalence point

A

existing cases at “point” in time/ size of population at “point” in time = %

a single point in time

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3
Q

how to calculate incidence proportion (cumulative incidence= CI)

A

number of people developing the outcome/ number of people at risk

CI=IR x time

estimation for risk in a population “at risk” (candidate population)- fixed population

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4
Q

how to calculate incidence rate (IR)

A

number of people developing the outcome/ total time at risk

estimates change in risk over time in a population at risk- fixed or dynamic population (instantaneous risk)

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5
Q

how to calculate incidence density

A

number of new cases / sum of the person-time of the at-risk population

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6
Q

how to calculate person time incidence

A

the number of new cases/ person time at risk through observation

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7
Q

how to calculate crude death rate

A

number of death in a given period/ the population exposed to risk of death in that period

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8
Q

how to calculate proportionate mortality

A

number of deaths from a given cause in a specific period of time/ total number of deaths in the same period

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9
Q

how to calculate case fatality rate

A

proportion of individuals with a disease who die from the disease

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10
Q

what is age adjustment

A

standardization

  • provides a valid comparison using a single number for each population
  • transform a measure based on a specific factor composition of a reference population
  • referred to as the direct method of standardization
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11
Q

why is age adjustment used

A

almost all diseases occur at different rates in different age groups, so for accurate analysis- its going to be important to take this into account

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12
Q

what are age specific rates

A

total number of health events for the specific age group of interest/ total population in that age group

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13
Q

how are age specific rates used

A

multiplying the age-specific rates of disease by age- specific weights

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14
Q

what is the formula for risk difference/excess risk

A

Re-Ru/Ru = RR -1 (expressed as percent

the null value is 0%
not a proportion just a ratio

“relative risk”- often described as the percent change relative to the reference risk

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15
Q

what is the formula for risk ratio

A

RR = Re/ Ru
Risk ratio & rate Ratio
Rate Ratio : Rr = IRe/ IRu

Prevalence ration = Pe/Pu

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16
Q

what is the formula for odds ratio

A

(a/b)/ (c/d) or ad/bc

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17
Q

what is the formula for relative risk

A

deaths or disease risk in a specific population/ risk of people from all other groups

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18
Q

how do you calculate and interpret risk difference/excess risk

A

RE-Ru/Ru = RR -1 (expressed as a percent)

  • increase linearly above one and exponentially below one

RR= Rm/Rf and RR = Rf/Rm

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19
Q

how do you calculate and interpret risk ratio

A
no effect (null value) is 1.0 
RR >1 indicates GREATER risk for exposed population relative to reference population 

RR < 1 indicates lesser risk for exposed population relative to reference population

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20
Q

how do you calculate and interpret odds ratio

A

odds of the first group/ odds in the seconds grouphow

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21
Q

how do you calculate and interpret relative risk

A

death or disease risk in a specific population/ risk of people from all other groups

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22
Q

definition of attributable risk

A

amount of proportion of incidence of disease or death in individuals exposed to a specific risk factor

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23
Q

definition of population attributable risk

A

risk in the total population that would not have occurred if exposure had not occurred )may also be expressed as number of cases)

PRD = R total - Ru

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24
Q

what type of epi study uses case control sutdies

A

main features:

  • individuals with the outcome are identified (cases)
  • individuals without the outcome are identified (controls or referents)
  • exposure is determined for cases and controls at an appropriate time IN THE PAST (there is no follow-up)
  • the association between exposure and health outcome is quantified using the odds ratio
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25
what type of epi study uses cohort studies
population with one or more common characteristics or experiences experimental (intervention) studies Observational Cohort Studies - prospective cohort - retrospective cohort
26
what type of epi study uses ecological studies
data representing entire populations are used to evaluate an association exposure status and outcome status are single values applied to the entire population correlations can be positive, negative, or zero may not represent the association that exists on the individual level (ecological fallacy) more complicated relationships can be masked
27
what type of epi study uses cross sectional studies
Assess prevalence of population in characteristics at a "point in time" this means information on current status is collected from a participant only once (no follow up) information on individuals associations but lacks temporal relationship between :exposure" and outcome measure of association is the odds ratio (not an estimate of RR for cross-sectional studies) classified by whether the data is provided by participants for come from an evaluation - interview or examination
28
conditions to use a case control study
exposure data are difficult or expensive to obtain small number of participants disease is rare disease has long induction and latent period little is known about the disease
29
conditions to use a cohort study
good evidence is needed for risk factor exposure is rare desire accurate measurement of exposure little is known about the exposure limitations: expensive, long time commitment
30
conditions to use an ecological study
One of the least valid data representing entire populations are used to evaluate an association exposure status and outcome status are single values applied to the entire population correlations can be positive, negative, or zero may not represent the association that exists on the individual level (ecological fallacy) more complicated relationships can be masked
31
conditions to use a cross sectional study
Almost the least valid strengths: inexpensive and quick , generalizability , useful for public health planning limitations: prevalence is the measure of disease frequency, not time separation between exposure and outcome, data are prone to bias and often self reported
32
death rate
number of people dying from a condition in a specified population/ number of people in the specified population = deaths per 100,00
33
What is external validity
the relevance of internally valid study results to populations with characteristics different from the source population, also called generalizability
34
What is internal validity
the extent to which studies result represent the true association between a factor of interest and the health-related outcome for the source population
35
What is the major differences between internal and external validity
When the goal of the study is to evaluate a potential association between a factor and health related outcome, there are two types of validity when the goal of the study is to estimate a characteristic of a source population, then there is onyl one validity
36
What is systematic error
always results in bias
37
what is random error
may result from bias for an individual measurement but not necessarily an average measurement
38
what is included under systematic error
misclassification, information, selection
39
what is confouding
mixing of effects between a factor of interest, a health outcome, and a third factor that is a risk factor for the health outcome of interest, but is not of interest in the study. This third factor is often referred to as a confounder
40
what are the 3 criteria for confounding
1. variable must be a risk factor for the outcome in BOTH the exposed and unexposed populations 2. the potential confounder must be associated with the exposure in the population that produced the cases 3. the confounder can not be an intermediate step in the causal pathway between the factor of interest and the health outcome
41
what is selection bias
bias that occurs at the selection of participants
42
what is information bias
incorrect portrayal or records of information or calculation
43
what is misclassification bias
individual is assigned to a different category than they should be
44
What are the strategies to control confounding
``` randomization restriction matching stratification adjustment multivariate analysis ```
45
What is used to reduce bias
placebo- pharmacologically inactive substance given as a substitute for an active substance sham procedure-bogus procedure designed to resemble a legitimate procedure blinding- withholding idtentiy of group assignment
46
what is confounding ( direction away, towards the null)
occurs when risk factors for the outcome, other than that being studied distorts the measures association between the factor being studied and the outcome
47
What is matching
selection of unexposed subjects that have characteristics identical to cases
48
What sets the data towards the null (ex)
ex. CRUDE RR = 1.5 Adjusted RR = 2.5 CRUDE less than negative confounding-bias towards the null
49
What sets the data away from the null (ex)
ex. CRUDE RR= 3 Adjusted RR = 2 CRUDE larger positive confounding- bias away from the null
50
Define sensitivity
proportion of people with the disease who have also a positive result for the test, sign, or symptom. this is a measure of the ability of a screening test to correctly identify people WITH the outcome of interest
51
Define specificity
the proportion of people among those who do not have the disease who also have a negative result for the test, sign, or symptom. This is a measure of the ability of a screening test to correctly identify people WITHOUT the outcome of interest
52
Define negative predictive value
proportion of people with a negative test results who actually do not have the outcome of interest- measures accuracy of negative test results
53
define positive predictive value
proportion of people with a positive test result who actually have the outcome of interest- measure of the accuracy of a positive test result
54
what is a p-value
the probability the point estimate based on data would be as far from the null hypothesis or farther than that actually obtained - probability of a false positive conclusion
55
how do you interpret a p-value
p value LESS than a predetermined cutoof is taken to indicated as "statistically significant" result most typical cutoff is p = .05 Null hypothesis is true, do not reject - correct Null is true, rejct - type 1 error (fals pos) Null false, do not reject - type 2 error (false neg) Null false, reject- correct
56
what is an epidemic
increase in disease frequency of a disease above what is normally expected in a given population and area
57
what is an endemic
constant presence and/or usual prevalence of a disease or infectious agent in a population within a geographic area. Hyperendemic refers to persistent high levels of disease occurrence
58
what is a pandemic
an international epidemic
59
what is the difference in epidemic, endemic, and pandemic
epi is in a given area pan is worldwid end is a geographic area
60
Who is included in "externally valid"
entire Us population, reference target popualtion, source population
61
Null hypothesis: Ho
assumed value or preconceived notion for a population parameter (usually the null value for the RR or OR is =1)
62
what is infectivity
capacity of an agent to enter and multiply in a susceptible host
63
what is virulence
capacity of an agent to produce a sever outcome course the most severe outcome would be death
64
what is antigenicity
capacity of an agent to induce antibody production in a host
65
what is pathogenicity
capacity of an agent to cause disease in the infected host
66
what are the types of transmission
direct or indirect
67
what is reproductive number
r= 1 correspond to constant disease r> 1 corresponds to increased disease r<1 corresponds to reduced disease empirical measure that allows comparison of epidemic potential for different infectious disease under different conditions
68
what is vector born transmission
indirect infectious agent is conveyed to a susceptible host by some form of living organism called a vector
69
Alternative Hypothesis Ha
the opposite or complement of the null hypothesis- usually not one but could be greater or less than
70
Direct transmission
immediate transfer of an infectious agent from an infected host or reservoir to a susceptible host airborne, direct contact, bites
71
indirect transmission
vehicle borne, vector born
72
indirect transmission
vehicle borne, vector born
73
Type of carriers
inapparent incubating convalescent chronic
74
inapparent carrier
individual that is infectious in the absence of symptoms throughout the course of their infection
75
incubating carrier
an individual that is infectious during the incubation period
76
convalescent carrier
an individual that has recovered from disease but remains infectious
77
chronic carrier
an individual continues to harbor the viable organism indefinitely and remains infectious to others
78
chronic carrier
an individual continues to harbor the viable organism indefinitely and remains infectious to others
79
Active Immunity
attained naturally by infection or immunization
80
passive immunity
attained naturally but WITHOUT infection
81
validity =
accuracy
82
reliability=
precision
83
reliability=
precision
84
true or false: the purpose of screening is to identify symptomatic cases of disease
false
85
true or false: screening is conducted in order to reduce morbidity and improve survival
true
86
true or false: the positive predictive value is more influence by the specificity than the sensitivity of the screening test
true
87
true or false: the positive predictive value is more influence by the specificity than the sensitivity of the screening test
true
88
In the definition of epidemiology, the phrase "determinants of disease frequency in human population" refers to which of the following
WHY it is occuring
89
A study of retirees from a large manufacturing facility found that the average age death among the retirees was greater than the average age death for the general population. What is the best interpretation of this finding
the comparison is not valid because the general population contains many individuals that die young
90
Who created the life table
John Graunt
91
John Snow's investigation of cholera epidemic in the mid 19th century was an example of which advance in the history of epi?
disease etiology can be investigated in natural experiments
92
Who observed that during the 1918 influenza pandemic, young adults were at greater risk of dying from influenza if they became infected than were middle age adults
wade hampton frost
93
What is one reason why randomized clinical trails were developed in the mid 20th century
to improve the assessment of efficacy and safety of drug vaccines
94
What is one reason why randomized clinical trails were developed in the mid 20th century
to improve the assessment of efficacy and safety of drug vaccines
95
When a single agent can cause multiple different adverse health outcomes and a particular adverse health outcome can be the result of several distinctly different factors, this is referred to as lack of ____
specificity
96
Why is it difficult to accurately estimate the average induction and average latent period
the start of disease can't be determined
97
in the causal model for the natural history of disease during the___ period the disease process has already started
latent
98
in the causal model for the natural history of disease, the time from the first action of component cause to development of disease is call the ____ period
induction
99
a _____ cause is all that is needed for disease to occur
sufficient
100
a _____ cause must always be present, but may require additional factors to cause the outcome
necessary
101
Which of hill guidelines for causality comes closest to being a requirement for causality
temporality
102
several different epi studies on diabetes as a risk factor for dementia found similar results. This support which causality guidline
consistency
103
Hill guidelines for causality _____ would be satisfied is the effect of exposure increased as the exposure level increased
biological gradient
104
the relationship between the flu virus and the flu could be used as an example of which of the guidelines for causality
specificity