Intention to Treat Flashcards

1
Q

What is the intention to treat principle?

A

Participants must be counted in the groups to which they were initially assigned, regardless of whether they were compliant with the intervention.
Includes those who withdraw.

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2
Q

Rationale behind intention to treat principle?

A

In an RCT one sets out to estimate broader effects of allocating intervention to a group and not the narrow effects of those who comply.
In reality, few people adhere to treatments strictly.

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3
Q

What does intention to treat principle give us?

A

Conservative estimate of treatment effect compared with what would be expected in ideal world of full compliance

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4
Q

Advantages of intention to treat principle

A

Makes results from RCT more generalisable and pragmatic

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5
Q

When might intention to treat principle not be suitable?

A

RCTs where investigation is of biological effects of drugs

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6
Q

Impact of ITT analysis in non inferiority trials?

A

Will favour equality due to dilution

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7
Q

When is ITT difficult to interpret?

A

If number of crossovers are high

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8
Q

Ways of dealing with missing data

A

Test the difference
Use available data
Imputation of data
Statistical methods

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9
Q

What is test the difference?

A

Test for difference between drop out group and available subject group.
Baseline characteristics if comparable can substantiate loss without further adjustment

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10
Q

Ways of using available data to deal with missing data

A

LOCF

Worst case scenario analysis

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11
Q

What does LOCF stand for?

A

Last observation carried forward

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12
Q

When is LOCF useful?

A

Only for longitudinal observations where continuous scales are used

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13
Q

Disadvantages of LOCF

A

Many psychiatric diseases have natural course of remission - LOCF does not allow for this’
‘Too good’ for controls and ‘too stringent’ for patient group

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14
Q

What is worst case scenario analysis?

A

Assumes that those lost to follow-up did not improve on trial intervention. Hence, data of treatment failure subjects used as proxy.

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15
Q

When is worst case scenario analysis used?

A

As part of sensitivity analysis

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16
Q

Types of imputations of data

A

Replacing missing values with mean of group

Hot deck imputation

17
Q

What are some statistical methods to make up for missing data?

A

Multiple regression
Growth curve analysis
Random effects modelling
Multiple imputation

18
Q

What is hot desk imputation?

A

Involves finding similar person among subjects and using that persons score

19
Q

What is multiple regression?

A

Used to predict missing values based on several other variables in data set

20
Q

What is growth curve analysis?

A

Line is fitted through existing data points for each subject. From 2 data points, we can derive parameters for straight line. For 3; quadratic curve. For 4; cubic curve.

21
Q

What is needed for growth curve analysis

A

At least 2 follow-up visits

22
Q

What is the definition of random effects modelling?

A

Derives from the fact that, when we usually fit a regression line to data, we assume that the parameters are fixed i.e. the same for all subjects
In random effects model, we allow them to differ for each person

23
Q

Who defined random effects modelling?

A

Streiner

24
Q

Implications of random effects modelling?

A

We do not expect curves for people who drop out to be same as for people who complete study

25
Q

What is multiple imputation?

A

Sophisticated and accurate methods which use maximum likelihood and Monte Carlo procedures.

26
Q

Recommendations if missing data are imputed?

A

Some sensitivity analysis is performed to ensure study conclusions are not misleading

27
Q

Alternatives to ITT

A

Per-protocol analysis

Treatment-received analysis

28
Q

What is per-protocol analysis?

A

Only patient who sufficiently complied with trials protocol are considered in final analysis.

29
Q

Another name for per-protocol analysis?

A

On treatment analysis

30
Q

Which types of RCTs use per-protocol analysis?

A

Biological explanatory RCTs

Secondary analysis in effectiveness trials

31
Q

What is treatment-received analysis?

A

Analyse subjects according to actual treatment received - not allocation made.

32
Q

Disadvantage of treatment-received analysis?

A

Effect of randomisation is compromised due to contamination of trial by one group of subjects moving to other group

33
Q

ITT is the norm except when?

A

Overwhelming justification of different analysis policy

34
Q

Advantages of ITT

A

Retains balance of prognostic factors arising from original random treatment allocation
Gives unbiased estimate of treatment effect
Admits non-compliance and protocol deviations, reflecting clinical life

35
Q

Limitations of ITT

A

Estimate of treatment effect is conservative
In equivalence trials, ITT will favour equality of treatment
Interpretation is difficult if large proportion of participants cross over to opposite treatment arms

36
Q

Why is estimate of treatment effect conservative in ITT?

A

Dilution effect of non-compliance

37
Q

Requirements for ideal ITT

A

Full compliance with randomised treatment
No missing responses
Follow-up of all participants