Lecure 8 Flashcards

1
Q

Measures of prevalence relate to

A

Existing cases of disease

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2
Q

Measure of incidence refer to

A

New cases of disease

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3
Q

Prevalence is used up for measuring

A
  • the disease in a community and is often measures in a discription study / survey

E.g: the proportion of students in this class who currently have a cold, the proportion of Otago students in this class who currently have a cold

  • the frequency of risk factor for disease

E.g: the proportion of Otago uni students who use e-cigarettes

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4
Q

Prevalence calculation

A
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5
Q

Prevalence time line

A
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6
Q

Prevalence definition

A

Prevalence is the proportion of people in a population who have the disease at a given point in time

  • the time point may refer to calendar time, or to a fixed point in the course of events (relative to an event rather then an absolute time)
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7
Q

What is incidence and what does is measure

A

Incidence measures the frequency of new cases of a disease
- useful for looking at the cause of disease

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8
Q

What is cumulative incidence

A
  • the proportion of people who become diseased during a specific period of time
  • if follow-up over the time period is complete we can estimate cumulative incidence.
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9
Q

(If follow up over time periods is complete) we can estimate cumulative incidence over the specified time period as:

A
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10
Q

What does cumulative evidence provide?

A
  • an estimate of the probability, or risk, the an individual will develop this disease during the specific period of time
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11
Q
A
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12
Q

For culumulative incidence to be interpretable, what must be specified?

A

Time period

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13
Q

Cumulative incidence with loss to follow up

A

Time to event analyses are able to take account of the censoring of follow-up. We use methods for censored data.
- people are included in the analysis up into the time they are lost to follow up
- bias can still occur if the people who are lost to follow-up are systematically different from those who remain in follow up

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14
Q

What is the difference between these curves

A
  • the curve on the left estimate the proportion who are still disease free at each time point
  • the curve on the right estimates to proportion who have contracted the disease by each time point

If we calculated the cumulative incidence without allowing for loss to follow-up it would be 2/5 = 0.4 by the end of year 5
If we allow for the loss to follow-up using the Kaplan-Meier method, the cumulative incidence at the end of year 5 is greater then 0.4

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15
Q

What also allows for differences in follow-up among participants

A
  • we can compute an incidence rate
  • it is the ratio of the total number of events to the total time on study and at risk over all study participants
    • person-time is the total time each person in the population is part of the study and at risk for the disease
  • it is the same if we follow 16 people for one year or four people for four years, or one person for 16 years
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16
Q

How to calculate the incidence rate

A
  • the denominator for measures of incidence should only include those who are at risk of developing the disease and should exclude those who:
    • already have the disease
    • those who cannot develop the disease
      Failure to do this will lead to an underestimate of the tru incidence since fewer will develop the condition 3
17
Q

Incidence vs prevalence

A
18
Q

Prevalalnce depends on the:

A
  • incidence rate, ASWELL as the duration of the disease