Evidence map›Paper›PMID 31311500›Full record

ArticleBMC medical research methodology2019

Adaptive propensity score procedure improves matching in prospective observational trials.

Dorothea Weber, Lorenz Uhlmann, Silvia Schönenberger, Meinhard Kieser

Abstract read
In one paragraph

Article in BMC medical research methodology, 2019. 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

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

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

4 authors.

Dorothea WeberInstitute of Medical Biometry and Informatics, University of Heidelberg, Marsilius Arkaden, Im Neuenheimer Feld 130.3, Heidelberg, 69120, Germany. weber@imbi.uni-heidelberg.de.ORCID 0000-0003-4850-9116
Lorenz UhlmannInstitute of Medical Biometry and Informatics, University of Heidelberg, Marsilius Arkaden, Im Neuenheimer Feld 130.3, Heidelberg, 69120, Germany.
Silvia SchönenbergerDepartment of Neurology, Heidelberg University Hospital, Im Neuenheimer Feld 400, Heidelberg, 69120, Germany.
Meinhard KieserInstitute of Medical Biometry and Informatics, University of Heidelberg, Marsilius Arkaden, Im Neuenheimer Feld 130.3, Heidelberg, 69120, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRandomized controlled trials are the gold-standard for clinical trials. However, randomization is not always feasible. In this article we propose a prospective and adaptive matched case-control trial design assuming that a control group already exists.

methodsWe propose and discuss an interim analysis step to estimate the matching rate using a resampling step followed by a sample size recalculation. The sample size recalculation is based on the observed mean resampling matching rate. We applied our approach in a simulation study and to a real data set to evaluate the characteristics of the proposed design and to compare the results to a naive approach.

resultsThe proposed design achieves at least 10% higher matching rate than the naive approach at final analysis, thus providing a better estimation of the true matching rate. A good choice for the interim analysis seems to be a fraction of around [Formula: see text] to [Formula: see text] of the control patients.

conclusionThe proposed resampling step in a prospective matched case-control trial design leads to an improved estimate of the final matching rate and, thus, to a gain in power of the approach due to sensible sample size recalculation.

Indexed as

Models, StatisticalPropensity ScoreResearch DesignBrain IschemiaCase-Control StudiesHumansObservational Studies as TopicProcedural SedationProspective StudiesSample SizeStrokeAdaptive designClinical TrialsMatched cohortProspective matchingSample size recalculation

Identifiers

PMID31311500
PMCPMC6636117

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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.