Evidence map›Paper›PMID 36661242›Full record

ArticleStatistics in medicine2023

Practical approaches to Bayesian sample size determination in non-inferiority trials with binary outcomes.

Rebecca M Turner, Michelle N Clements, Matteo Quartagno, Victoria Cornelius, Suzie Cro, Deborah Ford, Conor D Tweed, A Sarah Walker, Ian R White

Open access · hybridAbstract read
In one paragraph

Article in Statistics in medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% of its field
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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
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

9 authors at 2 institutions in 1 country.

Rebecca M TurnerMRC Clinical Trials Unit, University College London, London, UK.ORCID 0000-0001-7194-5464
Michelle N ClementsMRC Clinical Trials Unit, University College London, London, UK.
Matteo QuartagnoMRC Clinical Trials Unit, University College London, London, UK.ORCID 0000-0003-4446-0730
Victoria CorneliusImperial Clinical Trials Unit, School of Public Health, Imperial College London, London, UK.
Suzie CroImperial Clinical Trials Unit, School of Public Health, Imperial College London, London, UK.ORCID 0000-0002-6113-1173
Deborah FordMRC Clinical Trials Unit, University College London, London, UK.
Conor D TweedMRC Clinical Trials Unit, University College London, London, UK.
A Sarah WalkerMRC Clinical Trials Unit, University College London, London, UK.
Ian R WhiteMRC Clinical Trials Unit, University College London, London, UK.ORCID 0000-0002-6718-7661
MRC Clinical Trials Unit at UCL · GBImperial College London · GB

Funding

Department of Health NIHR 300593Medical Research Council MC_UU_00004/03Medical Research Council MC_UU_00004/05Medical Research Council MC_UU_00004/09
6 · The paper itself

Abstract

Bayesian analysis of a non-inferiority trial is advantageous in allowing direct probability statements to be made about the relative treatment difference rather than relying on an arbitrary and often poorly justified non-inferiority margin. When the primary analysis will be Bayesian, a Bayesian approach to sample size determination will often be appropriate for consistency with the analysis. We demonstrate three Bayesian approaches to choosing sample size for non-inferiority trials with binary outcomes and review their advantages and disadvantages. First, we present a predictive power approach for determining sample size using the probability that the trial will produce a convincing result in the final analysis. Next, we determine sample size by considering the expected posterior probability of non-inferiority in the trial. Finally, we demonstrate a precision-based approach. We apply these methods to a non-inferiority trial in antiretroviral therapy for treatment of HIV-infected children. A predictive power approach would be most accessible in practical settings, because it is analogous to the standard frequentist approach. Sample sizes are larger than with frequentist calculations unless an informative analysis prior is specified, because appropriate allowance is made for uncertainty in the assumed design parameters, ignored in frequentist calculations. An expected posterior probability approach will lead to a smaller sample size and is appropriate when the focus is on estimating posterior probability rather than on testing. A precision-based approach would be useful when sample size is restricted by limits on recruitment or costs, but it would be difficult to decide on sample size using this approach alone.

Indexed as

Research DesignBayes TheoremChildEquivalence Trials as TopicHumansProbabilitySample SizeUncertaintyBayesian methodsnon-inferiority trialssample sizetrial design

Identifiers

PMID36661242
PMCPMC7615731
OpenAlexW4317538565

What OpenQuestion 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 OpenQuestion graph.