Knowledge managemnet Flashcards

1
Q

primary research

A

the original study

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2
Q

SECONDARY RESEARCH

A

the combo of studies that has been synthesized, summarized n analysed. the results are systematic reviews, practice guidelines, economic health analyses etc

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3
Q

critical apppraisal tool

A

guides

checklists, which are based around these 5 type of qs:
therapy
diagnosis
prognosis
prevention
atielogy
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4
Q

3 things to consider when critically appraising any study

A

VALIDITY, RELIABILITY, APPLICABILITY

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5
Q

validity definition

A

The validity of a study is the extent to which its design and conduct are likely to prevent systematic errors, or bias.
 More methodologically rigorous studies may be more likely to yield results that are closer to the “truth”

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6
Q

Qs about validity

A

• Are the results of the study valid?
• Did the trial address a clearly focused issue
• Was the assignment of the participants randomized AND concealed?
• Were all of the participants who entered the trial properly accounted for at its conclusion?
• Was the study conducted with an intention to treat?
• Were participants, professionals and study personnel ‘blind’ to the intervention(s)?
• Were the groups similar at the start of the trial?
• Aside from the experimental intervention, were the groups treated equally?
• the qs are really about randomisation with concealment, the follow up of both groups to completion, intention to treat analysis, and making sure that there were no co-interventions

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7
Q

confidence intervals

A

Precision is another measure of the likelihood of random errors. It is reflected in the confidence interval around the estimate of effect.
 Confidence intervals do more than indicate whether the results might be a chance effect. They illustrate, allowing for the role of chance, how small or how large the true effect size might be.
The narrower the confidence interval the more certain one can be about the size of the true effect.
 If an unbiased study reports a 95% confidence interval this means that there is a 95% chance that the true effect lies within the confidence interval.

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8
Q

Statistical significance

A
  • Doesn’t tell u anything about bias
  • Could still be high even if methods were poor
  • Ie the idea that this result occurred due to a particular cause, rather than just chance
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9
Q

p value

A

type 1 statistical error

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10
Q

event rate in placebo group

A

X

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11
Q

event rate in the treatment group

A

Y

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12
Q

Absolute risk reduction (ARR)

A

ARR = X-Y.

difference in the proportion of subjects with the outcome of interest in each group

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13
Q

relative risk (RR)

A

RR = Y/X

the probability of an event in the active treatment group divided by the probability of an event in the control group.

A relative risk of 1 is the null value or no difference.

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14
Q

Relative risk reduction (RRR)

A

100*(X-Y)/X

standardised measure of the absolute risk reduction. It can be expressed as the absolute risk reduction divided by the probability of an event in the control group.

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15
Q

Number needed to treat (NNT)

A

NNT= 1/ARR).

how many ppl u have to treat to prevent one more death / get a desired outcome

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