Questions Flashcards

1
Q

What is the relationship between prevalence, incidence and duration?

A
Prevalence = Incidence x Average Duration
Incidence = Prevalence / Duration 
Duration = Prevalence / Incidence
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2
Q

What is the difference btwn odds and probability?

A

Odds is a ratio (A/B), probability is a proportion (A/A+B)

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3
Q

How do you control confounding?

A

At the design stage: randomization, restriction, matching

At the analysis stage: stratification, multivariable adjustment (logistic regressions)

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4
Q

How do you control bias?

A
  • must control selection and measurement (information?) bias at design stage (representative sampling from same pop, and blinding)
  • once study is done, it’s too late; must just assess likelihood of bias
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5
Q

Which study design is best for measuring prevalence?

A

Cross-sectional

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6
Q

Which study design is best for risk of harm?

A

cohort, case control

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7
Q

Which study design is best for treatment or prevention?

A

RCT, cohort, case control

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8
Q

Which study design is best for prognosis?

A

cohort

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9
Q

Which study design is best for screening?

A

RCT, cohort, case control

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10
Q

What are the strengths and weaknesses of cohort studies?

A

Strengths (4): good for relatively rare exposures, can minimize selection and measurement bias, can directly determine incidence rate and risk, can look at multiple outcomes from a single exposure

Weaknesses (6): ineffective for rare outcomes, often requires large sample size, takes a long time, expensive, potential ethical issues

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11
Q

Who was Karl Popper?

A
  • associated with deductive approach to epidemiology: science advances only through disproofs, not proofs (rejecting null hypotheses)
  • hypothesis must be testable/falsifiable; must frame a question that can be tested and rejected or not rejected by your data
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12
Q

What type of errors can False Positives and False Negatives create, respectively?

A

FP –> Type I

FN –> Type II

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13
Q

What determines Power?

A
our choice of alpha
our choice of beta
underlying prevalence of the condition
magnitude of effect we hope to find
sample size we can gather (usually more subjects --> more power; the smaller effect size you want to detect, the larger the sample size needed - must predict an effect size in order to calculate power)
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14
Q

What reduces the power of a study?

A
  • inadequate sample size (hard to recruit, loss to follow up, misclassification; random misclassification biases toward the null)
  • making alpha too stringent
  • making beta too lax
  • finding a study pop with low prevalence
  • adjusting for multiple comparisons unnecessarily (Bonferroni adjustment)
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15
Q

How do you solve selection bias?

A

randomization

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16
Q

What is the difference btwn a t test and a Mann Whitney test?

A

T: parametric

  • relies on mean and standard deviation (which are distribution parameters)
  • assumes equal variances

MW: non-parametric

  • ignores mean and median
  • distribution free
  • operates on the ranks
17
Q

What are the three levels of prevention?

A

Primary: before exposure (sanitation, education, nutrition, immunization)
Secondary: after exposure (early detection/screening, early intervention)
Tertiary: after disease process (reverse course of treatment, rehab, treatment)

18
Q

What are the main environments patients experience?

A

Physical (home, work, school, community, intrauterine, etc)
Social (family, community, co-workers, etc)
Personal (lifestyle, behaviors, substance use, nutrition, attitudes, etc)
Chemical (workplace exposures, toxins, etc)
Biological (infectious agents, allergens)
Psychosocial (stress, depression, type A personality)
Mechanical (repetitive motion jobs, heavy lifting)

19
Q

Who was John Snow?

A
  • father of modern epi
  • mapped the cholera cases in London epidemic (1854) –> determined it was a water-borne disease coming from Broad Street pump –> removed the lever so couldn’t be used, epidemic ended
  • based his inference on analysis of spatial patterns of cases (maps)
  • encountered a lot of resistance bc of common theory of ‘miasmas’
20
Q

What are the three types of Data?

A

Nominal (Categorical): no high/low or rank (ex: male/female, yes/no)
Ordinal: there is a rank (ex: high/low, 1+ t 4+)
Interval: there is a rank and the intervals are equal (1, 2, 3, 4)
- continuous: can take any value
- discrete: expressed as counts

21
Q

Types of Variability

A

Measurement
Biological
Inter-Observer
Intra-Individual