Presenting clinical trials data Flashcards

1
Q

Confidence interval

A

A confidence interval gives an estimated range of values which is likely to include an unknown population parameter, the estimated range being calculated from a given set of sample data.

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2
Q

why are confidence intervals more informative than the simple results of hypothesis tests

A

since they provide a range of plausible values for the unknown parameter.

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3
Q

what is the point estimate

A

(usually the mean) indicates the magnitude of the effect of the experimental intervention compared to the control intervention (Risk ratio is 0.7 of that in the control group).

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4
Q

what does the confidence interval describe

A

the uncertainty of the point estimate

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5
Q

what does the confidence interval describe

A

range of values within which we can be reasonably sure that the true effect actually lies.

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6
Q

narrow confidence intervals

A

there is a HIGHER level of confidence int he results

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7
Q

wide confidence intervals

A

means there is LOWER confidence in the results

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8
Q

why are confidence intervals better than p values

A
  1. Give a range of possible effect sizes
  2. Embrace the value of no difference between treatments (not significantly different from the control)
  3. Help interpret clinical trial data by placing upper and lower bounds on the true effect size
  4. Statistically significant does not mean clinically important –the size of the effect determines importance!
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9
Q

Measuring the effectiveness of interventions

A
  1. Number needed to treat
  2. Relative risk
  3. Odds ratio
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10
Q

what is NNT (number needed to treat) a measure of the effectiveness of interventions

A

the difference between treatment and control in achieving a particular clinical outcome and is TREATMENT specific

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11
Q

relative risk =

A

probability of getting disease if exposed / probability of getting disease if not exposed

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12
Q

relative risk of a drug =

A

probability of outcome if on drug / probability of outcome if on placebo

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13
Q

odds ratio =

A

odds that the disease was exposed / odds the control were exposed

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14
Q

when would you use relative risk

A

cohort studies and clinical trials

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15
Q

when would you use odds ratio

A

case-control studies

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16
Q

Heterogeneity

A

this is the extent to which outcomes vary
• Clinical baseline
• Design related
• Statistical heterogeneity

17
Q

what is I squared in heterogeneity

A

the amount of variation not caused by sampling error