Evidence map›Paper›PMID 41716073›Full record

ArticleResearch synthesis methods2026

Producing treatment hierarchies in network meta-analysis using probabilistic models and treatment-choice criteria.

Theodoros Evrenoglou, Adriani Nikolakopoulou, Guido Schwarzer, Gerta Rücker, Anna Chaimani

Abstract read
In one paragraph

Article in Research synthesis methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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.

Theodoros EvrenoglouInstitute of Medical Biometry and Statistics, https://ror.org/03vzbgh69Faculty of Medicine and Medical Center-University of Freiburg, Freiburg im Breisgau, Germany.ORCID https://orcid.org/0000-0003-3336-8058
Adriani NikolakopoulouInstitute of Medical Biometry and Statistics, https://ror.org/03vzbgh69Faculty of Medicine and Medical Center-University of Freiburg, Freiburg im Breisgau, Germany.ORCID https://orcid.org/0000-0001-5884-4319
Guido SchwarzerInstitute of Medical Biometry and Statistics, https://ror.org/03vzbgh69Faculty of Medicine and Medical Center-University of Freiburg, Freiburg im Breisgau, Germany.ORCID https://orcid.org/0000-0001-6214-9087
Gerta RückerInstitute of Medical Biometry and Statistics, https://ror.org/03vzbgh69Faculty of Medicine and Medical Center-University of Freiburg, Freiburg im Breisgau, Germany.ORCID https://orcid.org/0000-0002-2192-2560
Anna ChaimaniCenter of Research in Epidemiology and Statistics (CRESS-U1153), https://ror.org/05f82e368Université Paris Cité, INSERM, Paris, France.ORCID https://orcid.org/0000-0003-2828-6832

Funding

Agence Nationale de la Recherche ANR-22-CE36-0013-01Deutsche Forschungsgemeinschaft 499552394 - SFB 1597,554095932,NI 2226/1-1
6 · The paper itself

Abstract

A key output of network meta-analysis (NMA) is the relative ranking of treatments; nevertheless, it has attracted substantial criticism. Existing ranking methods often lack clear interpretability and fail to adequately account for uncertainty, overemphasizing small differences in treatment effects. We propose a novel framework to estimate treatment hierarchies in NMA using a probabilistic model, focusing on a clinically relevant treatment-choice criterion (TCC). Initially, we define a TCC based on smallest worthwhile differences (SWD), converting NMA relative treatment effects into treatment preference format. These data are then synthesized using a probabilistic ranking model, assigning each treatment a latent "ability" parameter, representing its propensity to yield clinically important and beneficial true treatment effects relative to the rest of the treatments in the network. Parameter estimation relies on the maximum likelihood theory, with standard errors derived asymptotically from the Hessian matrix. To facilitate the use of our methods, we launched the R package mtrank. We applied our method to two clinical datasets: one comparing 18 antidepressants for major depression and another comparing 6 antihypertensives for the incidence of diabetes. Our approach provided robust, interpretable treatment hierarchies that account for a concrete TCC. We further examined the agreement between the proposed method and existing ranking metrics in 153 published networks, concluding that the degree of agreement depends on the precision of the NMA estimates. Our framework offers a valuable alternative for NMA treatment ranking, mitigating overinterpretation of minor differences. This enables more reliable and clinically meaningful treatment hierarchies.

Indexed as

clinically important differencenetwork of interventionsprobabilistic regression modelsmallest worthwhile differencetreatment hierarchy

Identifiers

PMID41716073
PMCPMC13311357

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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.