Evidence map›Paper›PMID 35044274›Full record

ArticleStatistical methods in medical research2022

A comparison of various aggregation functions in multi-criteria decision analysis for drug benefit-risk assessment.

Tom Menzies, Gaelle Saint-Hilary, Pavel Mozgunov

Abstract read
In one paragraph

Article in Statistical methods in medical research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

3 authors.

Tom MenziesClinical Trials Research Unit, Leeds Institute of Clinical Trials Research, 4468University of Leeds, UK.ORCID 0000-0003-3896-7228
Gaelle Saint-HilaryDepartment of Biostatistics, 154729Institut de Recherches Internationales Servier (IRIS), France.ORCID 0000-0003-1643-3348
Pavel MozgunovMRC Biostatistics Unit, 2152University of Cambridge, UK.ORCID 0000-0001-6810-0284

Funding

Department of Health NIHR300576Medical Research Council MC UU 00002/14Medical Research Council MC_UU_00002/14
6 · The paper itself

Abstract

Multi-criteria decision analysis is a quantitative approach to the drug benefit-risk assessment which allows for consistent comparisons by summarising all benefits and risks in a single score. The multi-criteria decision analysis consists of several components, one of which is the utility (or loss) score function that defines how benefits and risks are aggregated into a single quantity. While a linear utility score is one of the most widely used approach in benefit-risk assessment, it is recognised that it can result in counter-intuitive decisions, for example, recommending a treatment with extremely low benefits or high risks. To overcome this problem, alternative approaches to the scores construction, namely, product, multi-linear and Scale Loss Score models, were suggested. However, to date, the majority of arguments concerning the differences implied by these models are heuristic. In this work, we consider four models to calculate the aggregated utility/loss scores and compared their performance in an extensive simulation study over many different scenarios, and in a case study. It is found that the product and Scale Loss Score models provide more intuitive treatment recommendation decisions in the majority of scenarios compared to the linear and multi-linear models, and are more robust to the correlation in the criteria.

Indexed as

Decision Support TechniquesComputer SimulationRisk AssessmentAggregation functionbenefit–riskdecision-makingloss scoremulti-criteria decision analysis

Identifiers

PMID35044274
PMCPMC7612697

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.