Evidence map›Paper›PMID 30279658›Full record

ArticleFrontiers in pharmacology2018

Propensity Score-Based Approaches in High Dimension for Pharmacovigilance Signal Detection: an Empirical Comparison on the French Spontaneous Reporting Database.

Émeline Courtois, Antoine Pariente, Francesco Salvo, Étienne Volatier, Pascale Tubert-Bitter, Ismaïl Ahmed

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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, 1 synthesis or guideline pooled it.

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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

6 authors.

Émeline CourtoisBiostatistics, Biomathematics, Pharmacoepidemiology and Infectious Diseases, INSERM, UVSQ (Université Paris-Saclay), Institut Pasteur, Villejuif, France.
Antoine ParienteBordeaux Population Health Research Center, Pharmacoepidemiology Team (UMR 1219), INSERM, University of Bordeaux, Bordeaux, France.
Francesco SalvoBordeaux Population Health Research Center, Pharmacoepidemiology Team (UMR 1219), INSERM, University of Bordeaux, Bordeaux, France.
Étienne VolatierBiostatistics, Biomathematics, Pharmacoepidemiology and Infectious Diseases, INSERM, UVSQ (Université Paris-Saclay), Institut Pasteur, Villejuif, France.
Pascale Tubert-BitterBiostatistics, Biomathematics, Pharmacoepidemiology and Infectious Diseases, INSERM, UVSQ (Université Paris-Saclay), Institut Pasteur, Villejuif, France.
Ismaïl AhmedBiostatistics, Biomathematics, Pharmacoepidemiology and Infectious Diseases, INSERM, UVSQ (Université Paris-Saclay), Institut Pasteur, Villejuif, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classical methods used for signal detection in pharmacovigilance rely on disproportionality analysis of counts aggregating spontaneous reports of a given adverse drug reaction. In recent years, alternative methods have been proposed to analyze individual spontaneous reports such as penalized multiple logistic regression approaches. These approaches address some well-known biases resulting from disproportionality methods. However, while penalization accounts for computational constraints due to high-dimensional data, it raises the issue of determining the regularization parameter and eventually that of an error-controlling decision rule. We present a new automated signal detection strategy for pharmacovigilance systems, based on propensity scores (PS) in high dimension. PSs are increasingly used to assess a given association with high-dimensional observational healthcare databases in accounting for confusion bias. Our main aim was to develop a method having the same advantages as multiple regression approaches in dealing with bias, while relying on the statistical multiple comparison framework as regards decision thresholds, by considering false discovery rate (FDR)-based decision rules. We investigate four PS estimation methods in high dimension: a gradient tree boosting (GTB) algorithm from machine-learning and three variable selection algorithms. For each (drug, adverse event) pair, the PS is then applied as adjustment covariate or by using two kinds of weighting: inverse proportional treatment weighting and matching weights. The different versions of the new approach were compared to a univariate approach, which is a disproportionality method, and to two penalized multiple logistic regression approaches, directly applied on spontaneous reporting data. Performance was assessed through an empirical comparative study conducted on a reference signal set in the French national pharmacovigilance database (2000-2016) that was recently proposed for drug-induced liver injury. Multiple regression approaches performed better in detecting true positives and false positives. Nonetheless, the performances of the PS-based methods using matching weights was very similar to that of multiple regression and better than with the univariate approach. In addition to being able to control FDR statistical errors, the proposed PS-based strategy is an interesting alternative to multiple regression approaches.

Indexed as

FDRpenalized multiple regressionpharmacovigilancepropensity score in high dimensionsignal detectionspontaneous reports

Identifiers

PMID30279658
PMCPMC6153352

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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.