An Introduction to Tables

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An Introduction to Tables Confounding and Effect Modification Interpretation and Choices

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An Introduction to Tables. Confounding and Effect Modification Interpretation and Choices. Population characteristics. p = Probability of an event of interest for example: Probability of successful post op probability is thought to be ‘conditional’ on factors of interest - PowerPoint PPT Presentation

Transcript of An Introduction to Tables

Page 1: An Introduction to Tables

An Introduction to Tables

Confounding and Effect Modification

Interpretation and Choices

Page 2: An Introduction to Tables

Population characteristics

• p = Probability of an event of interest• for example: Probability of successful post op• probability is thought to be ‘conditional’ on

factors of interest• for example: pre-op treatments (coded 0 and 1)

• Question: Does the probability of success depend on the choice of pre-op treatment?

Page 3: An Introduction to Tables

But the patients receive a several different operations

• Surgery types are then coded 1 and 2• Question: Does our previous question depend on

the type of surgery?• i.e. Does the comparison between treatments (with

regard to the probability of success) depend on the type of surgery?

• This is addressing whether surgery type is an effect modifier

Page 4: An Introduction to Tables

For example

• . cs suc tr,by(surg)

• surg | RR [95% Conf. Interval] M-H Weight• -----------------+-------------------------------------------------• 1 | 2 .8342841 4.79453 4.545455 • 2 | 1.9 1.759944 2.051202 45.45455 • -----------------+-------------------------------------------------• Crude | .3861386 .3348359 .4453018 • M-H combined | 1.909091 1.71543 2.124615• -------------------------------------------------------------------• Test of homogeneity (M-H) chi2(1) = 0.026 Pr>chi2 = 0.8724

Page 5: An Introduction to Tables

Notice:

• The surgery group specific risk ratios are nearly equal. (2 is ‘close’ to 1.9)

• The test of the null hypothesis of no effect modification (in Stata, it is called the test for homogeneity) has a p-value of 0.8724

• So, on the basis of this test, there is no evidence that surgery type is an effect modifier (0.386 is not ‘close’ to

Page 6: An Introduction to Tables

Since there is no evidence that surgery type is an effect modifier:

• We can assess whether surgery type is a confounder

• We compare the ‘crude’ estimate of the risk ratio with the ‘adjusted’ estimate of the risk ratio ( 0.386 is not ‘close’ to 1.909)

• So, there is ‘evidence’ that surgery type is a confounder.

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Have a look at the surgery type specific tables

• . cs suc tr if surg==1,exact

• | tr |• | Exposed Unexposed | Total• -----------------+------------------------+----------• Cases | 100 5 | 105• Noncases | 900 95 | 995• -----------------+------------------------+----------• Total | 1000 100 | 1100• | |• Risk | .1 .05 | .0954545• | |• | Point estimate | [95% Conf. Interval]• |------------------------+----------------------• Risk difference | .05 | .0034122 .0965878 • Risk ratio | 2 | .8342841 4.79453 • Attr. frac. ex. | .5 | -.1986325 .791429 • Attr. frac. pop | .4761905 |• +-----------------------------------------------• 1-sided Fisher's exact P = 0.0667• 2-sided Fisher's exact P = 0.1503

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…and• . cs suc tr if surg==2,exact

• | tr |• | Exposed Unexposed | Total• -----------------+------------------------+----------• Cases | 95 500 | 595• Noncases | 5 500 | 505• -----------------+------------------------+----------• Total | 100 1000 | 1100• | |• Risk | .95 .5 | .5409091• | |• | Point estimate | [95% Conf. Interval]• |------------------------+----------------------• Risk difference | .45 | .3972264 .5027736 • Risk ratio | 1.9 | 1.759944 2.051202 • Attr. frac. ex. | .4736842 | .4318 .512481 • Attr. frac. pop | .0756303 |• +-----------------------------------------------• 1-sided Fisher's exact P = 0.0000• 2-sided Fisher's exact P = 0.0000

Page 9: An Introduction to Tables

The previous 2 displays highlight the importance of looking at the actual data

• Should the surgery specific risk ratios be offered? • Look at the p-values in each group• Look at the width of the confidence intervals in

each group.• Is a test for homogenity enough here?

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Risk Ratios

• Usually: D - Disease E - Exposure• Risk ratio: RR = Pr(D|E) / Pr(D|not E)• Estimates of RR are usually written:

• Crude: Adjusted:

• Stratum specific:

• we can say that the risk of disease with exposure is estimated to be X times the risk of disease without exposure (with a p-value and/or a CI)

RR

cr

RR adj

RR

2RR

1RR

X,RR isIf

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Risk Difference

• RD = Pr(D|E) - Pr(D|not E)

• Estimate is:

• Crude, Adjusted, Stratum-specific….

• then the risk of disease with exposure is estimated to be X higher than the risk of disease without exposure

RD

,XRD isIf

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Odds

• Odds(E|D) = Pr(E|D)/Pr(not E|D)

• for example, if Pr(E|D) = 2/3, then odds(E|D) = 2

• notice: odds risk

• odds can be any positive number

• risk (is a probability) and must be between 0 and 1

Page 13: An Introduction to Tables

Odds Ratios

• OR = odds(E|D)/odds(E|not D)• most useful in case-control studies• OR can be any positive number• log(OR) = logit can be any number (positive or

negative)• logits provide a ‘natural’ outcome for modelling• estimates written:• crude, adjusted, stratum-specific...

OR

Page 14: An Introduction to Tables

Interpretation of Odds Ratios

• we can say that the odds of exposure with disease is estimated to be X times the odds of exposure without disease (with a p-value and/or a CI)

• But we can also say that the odds of disease with exposure is estimated to be X times the odds of disease without exposure (with a p-value and/or a CI)

• Odds ratio’s magic property!

X,OR isIf