Evidence map›Paper›PMID 38487976›Full record

ArticleStatistics in medicine2024

Categorisation of continuous covariates for stratified randomisation: How should we adjust?

Thomas R Sullivan, Tim P Morris, Brennan C Kahan, Alana R Cuthbert, Lisa N Yelland

Abstract read
In one paragraph

Article in Statistics in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Thomas R SullivanWomen and Kids Theme, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.ORCID 0000-0002-6930-5406
Tim P MorrisMRC Clinical Trials Unit, UCL, London, UK.ORCID 0000-0001-5850-3610
Brennan C KahanMRC Clinical Trials Unit, UCL, London, UK.ORCID 0000-0001-9957-0844
Alana R CuthbertWomen and Kids Theme, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.ORCID 0000-0002-3142-256X
Lisa N YellandWomen and Kids Theme, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.ORCID 0000-0003-3803-8728

Funding

Medical Research Council MC_UU_00004/09National Health and Medical Research Council 1173576
6 · The paper itself

Abstract

To obtain valid inference following stratified randomisation, treatment effects should be estimated with adjustment for stratification variables. Stratification sometimes requires categorisation of a continuous prognostic variable (eg, age), which raises the question: should adjustment be based on randomisation categories or underlying continuous values? In practice, adjustment for randomisation categories is more common. We reviewed trials published in general medical journals and found none of the 32 trials that stratified randomisation based on a continuous variable adjusted for continuous values in the primary analysis. Using data simulation, this article evaluates the performance of different adjustment strategies for continuous and binary outcomes where the covariate-outcome relationship (via the link function) was either linear or non-linear. Given the utility of covariate adjustment for addressing missing data, we also considered settings with complete or missing outcome data. Analysis methods included linear or logistic regression with no adjustment for the stratification variable, adjustment for randomisation categories, or adjustment for continuous values assuming a linear covariate-outcome relationship or allowing for non-linearity using fractional polynomials or restricted cubic splines. Unadjusted analysis performed poorly throughout. Adjustment approaches that misspecified the underlying covariate-outcome relationship were less powerful and, alarmingly, biased in settings where the stratification variable predicted missing outcome data. Adjustment for randomisation categories tends to involve the highest degree of misspecification, and so should be avoided in practice. To guard against misspecification, we recommend use of flexible approaches such as fractional polynomials and restricted cubic splines when adjusting for continuous stratification variables in randomised trials.

Indexed as

Randomized Controlled Trials as TopicComputer SimulationData Interpretation, StatisticalHumansLinear ModelsLogistic ModelsRandom Allocationcategorisecovariate adjustmentdichotomiserandomised trialstratification variable

Identifiers

PMID38487976
PMCPMC7616414

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.