CM: Epidemiology and biostatistics Flashcards

1
Q

Definition of epidemiology

A

study the occurence and distribution of disease-related events, states, and processes in specified population, including the study of determinants, and apply the knowledge to control relevant health problems

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2
Q

Roles of epidemiology (2)

A
  1. describe disease pattern (descriptive)
  2. identify disease determinants (analytical)
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3
Q

Definition of prevalence

A

number of existing cases / population of interest at a designated point of time

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4
Q

Advantages of using prevalence (3)

A
  • time- and resource-saving
  • quickly assessing current health needs, and useful to anticipate future needs
  • generate ideas for future studies / formulate research hypothesis
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5
Q

Limitations of using prevalence (3)

A
  • good for chronic diseases but not for disease in a short duration
  • cannot tell the number of new cases
  • some cases are not present / detected at the time of study (e.g. early death, cured, sub-clinical)
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6
Q

Reasons for false changes in disease frequency (4)

A
  • better diagnostic method
  • change in diagnostic criteria
  • increase in screening coverage
  • change in law (compulsory reporting)
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7
Q

Descriptive studies vs Analytical studies

A

D: describe disease pattern and distribution, for formulating research hypothesis and better allocating public health resources
- e.g. Case study, Correlational study, Cross-sectional study

A: identify disease determinants, for evaluating the casual relationship between exposure and outcomes
- e.g. Cohort study, Case-control study, RCT

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8
Q

Advantages of case report (3)

A
  • alert public health workers for new disease / new therapy
  • risk communication
  • formulate research hypothesis
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9
Q

Definition of case report

A

detailed clinical report by doctors of a single patient with unusual clinical features

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10
Q

Limitations of case report (3)

A
  • no control
  • small sample size
  • limited generalizability and interpretability
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11
Q

Steps of conducting a cross-sectional study

A
  1. select a study sample, as a representative of the population of interest
  2. simultaneously determine both the exposure and disease status, with no follow up
  3. construct a contingency table to calculate the prevalence in exposure & non-exposure groups, and thus the relative risk
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12
Q

Pros of cross-sectional studies (3)

A

(same as the advantages of using prevalence)

  • time- and resource-saving
  • quickly assessing current health needs, and useful to anticipate future needs
  • generate ideas for future studies / formulate research hypothesis
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13
Q

Cons of cross-sectional studies (3)

A
  • use of prevalence: detectable cases may not be representative of all cases; not cost-effective for diseases with short duration
  • lack of follow up: may misclassify exposure or outcome groups
  • no temporal sequence –> cannot establish casuality between exposure & outcome
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14
Q

What is cohort?

A

designated group of individuals who are followed up over a period of time

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15
Q

What is birth cohort?

A

a group of people who born in the same year, being followed up over a period of time

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16
Q

What is cohort study?

A

a longitudinal study, in which people who are (a) initially disease-free but (b) at risk of the disease are followed up over time, to (1) measure the incidence of the population and (2) test the casual relationship between exposures and outcomes

17
Q

Cumulative incidence v.s. Incidence rate (in cohort study)

A

CI = # of new cases / # of individuals at risk (used in closed cohort)

IR = # of new cases / sum of person-years of individuals at risk (used in open cohort)

18
Q

4 steps of conducting cohort study

A
  1. Select study samples (initially disease-free, and at risk)
  2. Determine exposure status
  3. Follow up and measure incidence of the disease
  4. Measure association
19
Q

Advantages of prospective vs retrospective cohort studies

A

P: (1) Better control of quantity and quality of the data; (2) less potential for bias

R: (1) Less expensive; (2) Less time-consuming

20
Q

How to obtain high FU rate in cohort studies?

A
  1. Remove barriers to FU
  2. Give incentives
  3. Tracking software
21
Q

Pros of cohort studies (5)

A
  • Able to measure the incidence
  • Able to study multiple exposures
  • Able to test on harmful exposures
  • Clear temporal sequence
  • Less potential to recall bias
22
Q

Cons of cohort studies (5)

A
  • Large sample size
  • Expensive
  • Long FU time
  • Loss to FU
  • Inefficient for rare outcomes
23
Q

When to use case-control studies? (3)

A
  • rare disease
  • long latent period
  • little knowledge about the causes so multiple risk factors are of interest
24
Q

4 Steps of conducting a case-control study

A
  1. Case selection
  2. Control selection
  3. Measure exposures
  4. Measure association
25
Q

3 Criteria of confounders

A
  1. Independent risk or protective factor of the disease
  2. Associated with the main exposure
  3. Not on the casual pathway between exposure & outcome
26
Q

Controls of confounders (3+2)

A
  • restriction, randomization, matching
  • stratification, multi-variable statistical analysis
27
Q

Pros of case-control study (5)

A
  • Cases easily available
  • Efficient for rare diseases
  • Quick, relatively inexpensive
  • Able to measure multiple exposures
  • Small sample size
28
Q

Cons of case-control study (5)

A
  • Time sequence may not be clear
  • Cases may be selective survivors
  • Able to measure one outcome only
  • Recall bias
  • Difficult to select appropriate controls
29
Q

What is external validity?

A

Generalizability of a study result to be applied to the population

30
Q
A