Evidence map›Paper›PMID 38291203›Full record

ArticleInternational journal of obesity (2005)2024

Cost-effectiveness of weight-management pharmacotherapies in Canada: a societal perspective.

Anamaria-Vera Olivieri, Sergey Muratov, Sara Larsen, Maria Luckevich, Katalina Chan, Mark Lamotte, David C W Lau

Abstract read
In one paragraph

Article in International journal of obesity (2005), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. 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

7 authors.

Anamaria-Vera OlivieriQVIA, Basel, Switzerland.ORCID 0000-0002-0947-3002
Sergey MuratovQVIA Mississauga, Mississauga, ON, Canada.
Sara LarsenNovo Nordisk A/S, Søborg, Bagsværd, Denmark.
Maria LuckevichNovo Nordisk Canada Inc, Mississauga, ON, Canada. MLVH@novonordisk.com.ORCID 0000-0002-4308-2574
Katalina ChanNovo Nordisk Canada Inc, Mississauga, ON, Canada.
Mark LamotteQVIA, Zaventem, Zaventem, Belgium.
David C W LauDepartment of Medicine, University of Calgary Cumming School of Medicine, Calgary, AB, Canada.ORCID 0000-0002-1780-9039

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis study aimed to assess the cost-effectiveness of weight-management pharmacotherapies approved by Canada Health, i.e., orlistat, naltrexone 32 mg/bupropion 360 mg (NB-32), liraglutide 3.0 mg and semaglutide 2.4 mg as compared to the current standard of care (SoC).

methodsAnalyses were conducted using a cohort with a mean starting age 50 years, body mass index (BMI) 37.5 kg/m

resultsFrom a societal perspective, at a willingness-to-pay (WTP) threshold of CAD 50 000 per QALY, semaglutide 2.4 mg was the most cost-effective treatment, at an incremental cost-utility ratio (ICUR) of CAD 31 243 and CAD 29 014 per QALY gained versus the next best alternative, i.e., orlistat, and SoC, respectively. Semaglutide 2.4 mg extendedly dominated other pharmacotherapies such as NB-32 or liraglutide 3.0 mg and remained cost-effective both under a public and private payer perspective. Results were robust to sensitivity analyses varying post-treatment catch-up rates, longer treatment durations and using real-world cohort characteristics. Semaglutide 2.4 mg was the preferred intervention, with a likelihood of 70% at a WTP threshold of CAD 50 000 per QALY gained. However, when the modeled benefits of weight-loss on cancer, mortality, cardiovascular disease (CVD) or osteoarthritis surgeries were removed simultaneously, orlistat emerged as the best value for money compared with SoC, with an ICUR of CAD 35 723 per QALY gained.

conclusionSemaglutide 2.4 mg was the most cost-effective treatment alternative compared with D&E or orlistat alone, and extendedly dominated other pharmacotherapies such as NB-32 or liraglutide 3.0 mg. Results were sensitive to the inclusion of the combined benefits of mortality, cancer, CVD, and knee osteoarthritis.

Indexed as

Anti-Obesity AgentsCost-Benefit AnalysisObesityOrlistatBupropionCanadaDiabetes Mellitus, Type 2FemaleGlucagon-Like PeptidesHumansLiraglutideMaleMiddle AgedNaltrexoneQuality-Adjusted Life YearsSemaglutideAnti-Obesity AgentsBupropionGlucagon-Like PeptidesLiraglutideNaltrexoneOrlistatSemaglutide

Identifiers

PMID38291203
PMCPMC11058048

What OpenQuestion holds

Texttitle and abstract
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.