Cohort Studies Flashcards

1
Q

Cohort study definition

A

Cohort studies define and measure the risk factor and then evaluate the outcome in a suitable demographic group over time (you get to pick the people), outcome can be the presence or absence of disease associated with a single RF (not multiple)

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2
Q

What is a major difference between Cohort and CCS?

A

Cohort studies have a well defined population in demographics and numbers. Bias and confounding controlled better

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3
Q

What are the two types of cohort studies?

A

prospective and retrospective

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4
Q

What is usually done before a cohort study?

A

a case control study

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5
Q

What is ideal for the control group?

A

It is ideal for the control group to have no exposure to the RF. Best if personal interviews are performed. Can be complicated if using published data or environmental RF.

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6
Q

What is the key point for Cohort studies?

A

Presence or absence of risk factor is determined before outcome occurs

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7
Q

How do you calculate risk?

A

a/(a+b)

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8
Q

How do you calculate relative risk?

A

a/(a+b) / c(c+d) =

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9
Q

How do you form a 2x2?

A

Risk factor on side and Disease on top

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10
Q

What does a RR of 6 tell you?

A

6x more likely to get disease if exposed

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11
Q

Odds Ratio calculation

A

(a/c) / (b/d), include an error factor

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12
Q

Person Years

A

This adjusts for the amount of time that any individual member of the cohort’s data is available; some in study longer, evaluate number of person years instead of number of people

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13
Q

Confounding in Cohort studies

A

Associations between risk factors and cardiovascular disease outcomes are confounded by pre-existing cardiac, renal and other diseases

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14
Q

Bias

A

Anything that might negatively affect the representativity of the cohorts studied

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15
Q

Information bias

A

Is information about outcome obtained in the same way for those exposed and those not?

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16
Q

Features to look for in cohort studies

A
  1. What steps were taken to minimize information bias?
  2. How complete was the follow up in both groups?
  3. Were potential confounding factors sought and controlled for in the analysis?
17
Q

Cohort vs Case study

A

Long term and require a lot of planning, less useful in study of diseases of low prevalence or exposure, deals better with confounding and bias, strength of association of RR stronger than OR

18
Q

Why can you extrapolate the results in a case control study?

A

the demographic latitudes inherent in control group formation and the additional variation built into the confidence interval by including factorials for control groups

19
Q

Clinical trials

A

A cohort study in which the exposure to the effector is controlled. (Placebo controlled, single/double/triple blind)

20
Q

Triple blind experiment

A

Patient, clinician, and lab analyzing does not know groups

21
Q

Diagnosis can be made through?

A

quantitative or qualitative, subjective or objective methods: serology assays, PCR, X-Ray, CAT scans, experience

22
Q

2x2 Table for test sensitivity and specificity

A

side has test positive and negative; top has disease positive and negative

23
Q

How to calculate sensitivity from 2x2?

A

a / total disease positives

24
Q

How to calculate specificity from 2x2?

A

d / total disease negatives

25
Q

Sensitivity tests…

A

true postives

26
Q

Specificity tests….

A

true negatives

27
Q

How is true disease status determined?

A

By a gold standard method

28
Q

How do specificity and sensitivity relate?

A

Inverse; as sensitivity increases specificity decreases

29
Q

Sensitivity definition

A

the capacity of the test to correctly identify diseased individuals in a population; true positives. Greater sensitivity means smaller number of false negatives.

30
Q

Specificity definition

A

the capacity of the test to correctly exclude individuals who are free of the disease, true negatives; the greater specificity means the fewer false positives

31
Q

Positive predictive value

A

the probability of the disease being present, among those with positive diagnostic test results

32
Q

Negative predictive value

A

the probability that the disease was absent among those whose diagnostic test results were negative

33
Q

positivity rate =

A

total positives/total tested x 100

34
Q

negativity rate =

A

total negatives/total tested x 100

35
Q

Reliable and reproducible results?

A

How often using the same tests and samples will you get the same results; different test lots, different personnel, equipment variation

36
Q

Misclassification

A

the placement of subjects into inappropriate group or classification; occurs when the means by which we measure risk are not perfect; may reduce the true value of OR or RR, highlights the need to know the limits and parameters of assessment

37
Q

Non-random misclassification

A

when exposure or disease status influences group assignment; typically insert unwarranted bias