Evidence map›Paper›PMID 25712447›Full record

ArticleMedical decision making : an international journal of the Society for Medical Decision Making2015

Accounting for Heterogeneity in Relative Treatment Effects for Use in Cost-Effectiveness Models and Value-of-Information Analyses.

Nicky J Welton, Marta O Soares, Stephen Palmer, Anthony E Ades, David Harrison, Manu Shankar-Hari, Kathy M Rowan

Open access · greenAbstract read
In one paragraph

Article in Medical decision making : an international journal of the Society for Medical Decision Making, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
13.7field-weighted citation impact, top 2% of its field
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

10 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  3. Review
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  5. Validating the Assumptions of Population Adjustment: Application of Multilevel Network Meta-regression to a Network of Treatments for Plaque Psoriasis.Medical decision making : an international journal of the Society for Medical Decision Making · 2023
    Article
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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

7 authors at 4 institutions in 1 country.

Nicky J WeltonSchool of Social and Community Medicine, University of Bristol, Bristol, UK (NJW, AEA)
Marta O SoaresCentre for Health Economics, University of York, York, UK (MOS, SP)
Stephen PalmerCentre for Health Economics, University of York, York, UK (MOS, SP)
Anthony E AdesSchool of Social and Community Medicine, University of Bristol, Bristol, UK (NJW, AEA)
David HarrisonIntensive Care National Audit & Research Centre, London, UK (DH, KMR)
Manu Shankar-HariGuy's and St Thomas' Hospital NHS Foundation Trust, London, UK (MS-H)
Kathy M RowanIntensive Care National Audit & Research Centre, London, UK (DH, KMR)
Guy's and St Thomas' NHS Foundation Trust · GBSt Thomas' Hospital · GBUniversity of Bristol · GBUniversity of York · GB

Funding

Department of Health 08/70/01Medical Research Council G0800800Medical Research Council G0802413Medical Research Council MC_U145079307Medical Research Council MRC G0800800Medical Research Council MR/K025643/1
6 · The paper itself

Abstract

Cost-effectiveness analysis (CEA) models are routinely used to inform health care policy. Key model inputs include relative effectiveness of competing treatments, typically informed by meta-analysis. Heterogeneity is ubiquitous in meta-analysis, and random effects models are usually used when there is variability in effects across studies. In the absence of observed treatment effect modifiers, various summaries from the random effects distribution (random effects mean, predictive distribution, random effects distribution, or study-specific estimate [shrunken or independent of other studies]) can be used depending on the relationship between the setting for the decision (population characteristics, treatment definitions, and other contextual factors) and the included studies. If covariates have been measured that could potentially explain the heterogeneity, then these can be included in a meta-regression model. We describe how covariates can be included in a network meta-analysis model and how the output from such an analysis can be used in a CEA model. We outline a model selection procedure to help choose between competing models and stress the importance of clinical input. We illustrate the approach with a health technology assessment of intravenous immunoglobulin for the management of adult patients with severe sepsis in an intensive care setting, which exemplifies how risk of bias information can be incorporated into CEA models. We show that the results of the CEA and value-of-information analyses are sensitive to the model and highlight the importance of sensitivity analyses when conducting CEA in the presence of heterogeneity. The methods presented extend naturally to heterogeneity in other model inputs, such as baseline risk.

Indexed as

Decision Support TechniquesBayes TheoremBiasCost-Benefit AnalysisHumansMeta-Analysis as TopicRegression AnalysisSepsisBayesian meta-analysiscost-effectiveness analysisvalue of information

Identifiers

PMID25712447
PMCPMC4471065
OpenAlexW2099106612

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.