Evidence map›Paper›PMID 37303120›Full record

ArticleStatistical methods in medical research2023

Methods for comparative effectiveness based on time to confirmed disability progression with irregular observations in multiple sclerosis.

Thomas Pa Debray, Gabrielle Simoneau, Massimiliano Copetti, Robert W Platt, Changyu Shen, Fabio Pellegrini, Carl de Moor

Abstract read
In one paragraph

Article in Statistical methods in medical research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Thomas Pa DebrayJulius Centrum voor Gezondheidswetenschappen en Eerstelijns Geneeskunde, Utrecht, Netherlands.ORCID 0000-0002-1790-2719
Gabrielle SimoneauBiogen, Toronto, Canada.ORCID 0000-0001-9310-6274
Massimiliano CopettiFondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy.ORCID 0000-0002-7960-5947
Robert W PlattDepartment of Epidemiology, Bioastatistics and Occupational Health, McGill University, Quebec, Canada.ORCID 0000-0002-5981-8443
Changyu ShenBiogen Inc, Cambridge, USA.
Fabio PellegriniBiogen Spain SL, Madrid, Spain.
Carl de MoorBiogen Inc, Cambridge, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Real-world data sources offer opportunities to compare the effectiveness of treatments in practical clinical settings. However, relevant outcomes are often recorded selectively and collected at irregular measurement times. It is therefore common to convert the available visits to a standardized schedule with equally spaced visits. Although more advanced imputation methods exist, they are not designed to recover longitudinal outcome trajectories and typically assume that missingness is non-informative. We, therefore, propose an extension of multilevel multiple imputation methods to facilitate the analysis of real-world outcome data that is collected at irregular observation times. We illustrate multilevel multiple imputation in a case study evaluating two disease-modifying therapies for multiple sclerosis in terms of time to confirmed disability progression. This survival outcome is derived from repeated measurements of the Expanded Disability Status Scale, which is collected when patients come to the healthcare center for a clinical visit and for which longitudinal trajectories can be estimated. Subsequently, we perform a simulation study to compare the performance of multilevel multiple imputation to commonly used single imputation methods. Results indicate that multilevel multiple imputation leads to less biased treatment effect estimates and improves the coverage of confidence intervals, even when outcomes are missing not at random.

Indexed as

Multiple SclerosisComputer SimulationData Interpretation, StatisticalHumansResearch DesignClustered datacomparative effectivenessconfirmed disability progressionlongitudinal datamultiple imputationmultiple sclerosisreal-world data

Identifiers

PMID37303120
PMCPMC10500950

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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.