Evidence map›Paper›PMID 31691322›Full record

ArticleStatistics in medicine2019

A new Bayesian joint model for longitudinal count data with many zeros, intermittent missingness, and dropout with applications to HIV prevention trials.

Jing Wu, Ming-Hui Chen, Elizabeth D Schifano, Joseph G Ibrahim, Jeffrey D Fisher

Abstract read
In one paragraph

Article in Statistics in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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.

Jing WuDepartment of Computer Science and Statistics, University of Rhode Island, Kingston, Rhode Island.ORCID 0000-0001-7808-6981
Ming-Hui ChenDepartment of Statistics, University of Connecticut, Storrs, Connecticut.ORCID 0000-0003-1935-2447
Elizabeth D SchifanoDepartment of Statistics, University of Connecticut, Storrs, Connecticut.ORCID 0000-0002-9793-332X
Joseph G IbrahimDepartment of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.ORCID 0000-0003-2428-6552
Jeffrey D FisherDepartment of Psychology and Institute for Collaboration on Health, Intervention, and Policy (InCHIP), University of Connecticut, Storrs, Connecticut.

Funding

Statistical Methods for Cancer Clinical TrialsP01CA142538 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KOSOROK, MICHAEL R · 2010 to 2019
$21.3M
Integrating HIV Prevention into Clinical Care for PLWHA in South AfricaR01MH077524 · NIMH · UNIVERSITY OF CONNECTICUT STORRS · PI FISHER, JEFFREY D · 2007 to 2011
$6.9M
Bayesian Approaches to Model Selection for Survival DataR01GM070335 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI IBRAHIM, JOSEPH G · 2003 to 2019
$4.0M
NCI NIH HHS P01 CA142538NIGMS NIH HHS R01 GM070335NIMH NIH HHS R01 MH077524
6 · The paper itself

Abstract

In longitudinal clinical trials, it is common that subjects may permanently withdraw from the study (dropout), or return to the study after missing one or more visits (intermittent missingness). It is also routinely encountered in HIV prevention clinical trials that there is a large proportion of zeros in count response data. In this paper, a sequential multinomial model is adopted for dropout and subsequently a conditional model is constructed for intermittent missingness. The new model captures the complex structure of missingness and incorporates dropout and intermittent missingness simultaneously. The model also allows us to easily compute the predictive probabilities of different missing data patterns. A zero-inflated Poisson mixed-effects regression model is assumed for the longitudinal count response data. We also propose an approach to assess the overall treatment effects under the zero-inflated Poisson model. We further show that the joint posterior distribution is improper if uniform priors are specified for the regression coefficients under the proposed model. Variations of the g-prior, Jeffreys prior, and maximally dispersed normal prior are thus established as remedies for the improper posterior distribution. An efficient Gibbs sampling algorithm is developed using a hierarchical centering technique. A modified logarithm of the pseudomarginal likelihood and a concordance based area under the curve criterion are used to compare the models under different missing data mechanisms. We then conduct an extensive simulation study to investigate the empirical performance of the proposed methods and further illustrate the methods using real data from an HIV prevention clinical trial.

Indexed as

Models, StatisticalBayes TheoremBiostatisticsComputer SimulationData Interpretation, StatisticalFemaleHIV InfectionsHumansLikelihood FunctionsLongitudinal StudiesMalePatient DropoutsPoisson DistributionRandomized Controlled Trials as TopicRegression AnalysisSexual BehaviorAUCG-priorJeffreys priorLPMLmaximally dispersed normal priorzero-inflated Poisson

Identifiers

PMID31691322
PMCPMC6891130

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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.