Evidence map›Paper›PMID 39538117›Full record

ArticleBMC medical research methodology2024

Accounting for bias due to outcome data missing not at random: comparison and illustration of two approaches to probabilistic bias analysis: a simulation study.

Emily Kawabata, Daniel Major-Smith, Gemma L Clayton, Chin Yang Shapland, Tim P Morris, Alice R Carter, Alba Fernández-Sanlés, Maria Carolina Borges, Kate Tilling, Gareth J Griffith and 4 more

Abstract readComparative Study
In one paragraph

Article in BMC medical research methodology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

14 authors.

Emily Kawabata *MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Daniel Major-Smith *MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Gemma L Clayton *MRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Chin Yang ShaplandMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Tim P MorrisMRC Clinical Trials Unit at UCL, London, UK.
Alice R CarterMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Alba Fernández-SanlésMRC Unit for Lifelong Health and Ageing at University College London, London, UK.
Maria Carolina BorgesMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Kate TillingMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Gareth J GriffithMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Louise A C MillardMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
George Davey SmithMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Deborah A LawlorMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK.
Rachael A HughesMRC Integrative Epidemiology Unit, University of Bristol, Bristol, UK. rachael.hughes@bristol.ac.uk.

Funding

Wellcome Trust and Royal Society 215408/Z/19/Z
6 · The paper itself

Abstract

backgroundBias from data missing not at random (MNAR) is a persistent concern in health-related research. A bias analysis quantitatively assesses how conclusions change under different assumptions about missingness using bias parameters that govern the magnitude and direction of the bias. Probabilistic bias analysis specifies a prior distribution for these parameters, explicitly incorporating available information and uncertainty about their true values. A Bayesian bias analysis combines the prior distribution with the data's likelihood function whilst a Monte Carlo bias analysis samples the bias parameters directly from the prior distribution. No study has compared a Monte Carlo bias analysis to a Bayesian bias analysis in the context of MNAR missingness.

methodsWe illustrate an accessible probabilistic bias analysis using the Monte Carlo bias analysis approach and a well-known imputation method. We designed a simulation study based on a motivating example from the UK Biobank study, where a large proportion of the outcome was missing and missingness was suspected to be MNAR. We compared the performance of our Monte Carlo bias analysis to a principled Bayesian bias analysis, complete case analysis (CCA) and multiple imputation (MI) assuming missing at random.

resultsAs expected, given the simulation study design, CCA and MI estimates were substantially biased, with 95% confidence interval coverages of 7-48%. Including auxiliary variables (i.e., variables not included in the substantive analysis that are predictive of missingness and the missing data) in MI's imputation model amplified the bias due to assuming missing at random. With reasonably accurate and precise information about the bias parameter, the Monte Carlo bias analysis performed as well as the Bayesian bias analysis. However, when very limited information was provided about the bias parameter, only the Bayesian bias analysis was able to eliminate most of the bias due to MNAR whilst the Monte Carlo bias analysis performed no better than the CCA and MI.

conclusionThe Monte Carlo bias analysis we describe is easy to implement in standard software and, in the setting we explored, is a viable alternative to a Bayesian bias analysis. We caution careful consideration of choice of auxiliary variables when applying imputation where data may be MNAR.

Indexed as

Bayes TheoremBiasComputer SimulationMonte Carlo MethodAlgorithmsData Interpretation, StatisticalHumansModels, StatisticalProbabilityResearch DesignBayesian bias analysisInverse probability weightingMissing not at randomMonte Carlo bias analysisMultiple imputationProbabilistic bias analysisSensitivity analysisUK Biobank

Identifiers

PMID39538117
PMCPMC11558901

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LicenceCC BY
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Registered trials

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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.