Evidence map›Paper›PMID 27036963›Full record

ArticleBMC medical research methodology2016

On the use of propensity scores in case of rare exposure.

David Hajage, Florence Tubach, Philippe Gabriel Steg, Deepak L Bhatt, Yann De Rycke

Abstract read
In one paragraph

Article in BMC medical research methodology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 citing papers in PubMed.

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  14. Comparison between treatment effects in a randomised controlled trial and an observational study using propensity scores in primary care.The British journal of general practice : the journal of the Royal College of General Practitioners · 2017
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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.

David HajageAPHP, Hôpital Louis Mourier, Département d'Epidémiologie et Recherche Clinique, 178 Rue des Renouillers, Colombes, 92700, France. david.hajage@aphp.fr.
Florence TubachAPHP, Hôpital Bichat, Département d'Epidémiologie et Recherche Clinique, 46 Rue Henri Huchard, Paris, F-75018, France.
Philippe Gabriel StegFACT, DHU FIRE, Univ Paris-Diderot, Sorbonne Paris-Cité, Paris, F-75018, France.
Deepak L BhattBrigham and Women's Hospital Heart & Vascular Center and Harvard Medical School, Boston, Massachusetts, USA.
Yann De RyckeAPHP, Hôpital Bichat, Département d'Epidémiologie et Recherche Clinique, 46 Rue Henri Huchard, Paris, F-75018, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObservational post-marketing assessment studies often involve evaluating the effect of a rare treatment on a time-to-event outcome, through the estimation of a marginal hazard ratio. Propensity score (PS) methods are the most used methods to estimate marginal effect of an exposure in observational studies. However there is paucity of data concerning their performance in a context of low prevalence of exposure.

methodsWe conducted an extensive series of Monte Carlo simulations to examine the performance of the two preferred PS methods, known as PS-matching and PS-weighting to estimate marginal hazard ratios, through various scenarios.

resultsWe found that both PS-weighting and PS-matching could be biased when estimating the marginal effect of rare exposure. The less biased results were obtained with estimators of average treatment effect in the treated population (ATT), in comparison with estimators of average treatment effect in the overall population (ATE). Among ATT estimators, PS-weighting using ATT weights outperformed PS-matching. These results are illustrated using a real observational study.

conclusionsWhen clinical objectives are focused on the treated population, applied researchers are encouraged to estimate ATT with PS-weighting for studying the relative effect of a rare treatment on time-to-event outcomes.

Indexed as

Monte Carlo MethodPropensity ScoreCardiovascular DiseasesComputer SimulationFemaleHumansMaleModels, StatisticalObservational Studies as TopicProportional Hazards ModelsThiazolidinesThiazolidinesHazard ratioMonte Carlo simulationsObservational studiesPharmacoepidemiologyPropensity scoresRare exposure

Identifiers

PMID27036963
PMCPMC4815252

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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.