Evidence map›Paper›PMID 27470429›Full record

ArticleClinical drug investigation2016

A Comparison of Markov and Discrete-Time Microsimulation Approaches: Simulating the Avoidance of Alcohol-Attributable Harmful Events from Reduction of Alcohol Consumption Through Treatment of Alcohol Dependence.

Philippe Laramée, Aurélie Millier, Thor-Henrik Brodtkorb, Nora Rahhali, Olivier Cristeau, Samuel Aballéa, Stephen Montgomery, Sara Steeves, Mondher Toumi, Jürgen Rehm

Abstract readComparative Study
PubMed Publisher
In one paragraph

Article in Clinical drug investigation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Review
  2. Article
  3. 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

10 authors at 6 institutions in 5 countries.

Philippe LaraméeSocial and Epidemiological Research Department, Centre for Addiction and Mental Health, Toronto, ON, M5S 2S1, Canada. plaramee@outlook.com.
Aurélie MillierHealth Economics and Outcomes Research, Creativ-Ceutical, 75008, Paris, France.
Thor-Henrik BrodtkorbHealth Economics, RTI Health Solutions, 45930, Ljungskile, Sweden.
Nora RahhaliGlobal Analytics, Lundbeck SAS, 92445, Issy-les-Moulineaux CEDEX, France.
Olivier CristeauHealth Economics and Outcomes Research, Creativ-Ceutical, 75008, Paris, France.
Samuel AballéaHealth Economics and Outcomes Research, Creativ-Ceutical, 75008, Paris, France.
Stephen MontgomeryCostello Medical Consulting Ltd, Cambridge, CB2 1RE, UK.
Sara SteevesCostello Medical Consulting Ltd, Cambridge, CB2 1RE, UK.
Mondher ToumiLaboratoire de Santé Publique, Faculté de Médecine, Université de la Méditerranée, 13385, Marseille, France.
Jürgen RehmSocial and Epidemiological Research Department, Centre for Addiction and Mental Health, Toronto, ON, M5S 2S1, Canada.
Creativ-Ceutical (France) · FRCostello Medical Consulting (United Kingdom) · GBCentre for Addiction and Mental Health · CAHealth Solutions (Sweden) · SEInstitut de Neurobiologie de la Méditerranée · FRUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveWhen modelling the pathophysiology of a disease, it is important to select a modelling approach that can adequately replicate its course. The objective of this paper was to compare the outcomes obtained by the Markov and discrete-time microsimulation modelling approaches using nalmefene clinical trial data.

methodsMarkov and microsimulation modelling approaches assessing alcohol dependence treatment with psychosocial support with or without nalmefene were compared in terms of the modelled evolution of patients' alcohol consumption and the resulting occurrence of alcohol-attributable harmful events over 1 year.

resultsComparison of the proportion of the modelled population at different levels of alcohol consumption over time revealed systematic differences arising from the different modelling techniques: a lower number of patients reaching abstinence, a higher number of patients at higher drinking levels, and, overall, a smoother evolution of alcohol consumption in the microsimulation. Reasons are discussed in the paper. While the models produced similar occurrences of alcohol-attributable harmful events as a whole, distinct results for the individual events were observed, explained by the specific pathophysiology of occurrence of these events and how their implementation was adapted to fit the limitations of the compared modelling approaches; however, these differences were only statistically significant for one of the eight events.

conclusionsFor a general public health or health economic assessment of alcohol use disorders, it is possible to achieve similar results with the compared approaches. To assess a patients' disease course, taking into consideration alcohol-attributable harmful events, the microsimulation approach may provide more precise results. However, further external validation of the models is needed and this additional precision may be outweighed by the greater computational burden of a microsimulation approach.

Indexed as

AdultAlcohol DrinkingAlcoholismAlcohol-Related DisordersFemaleHumansNaltrexonenalmefeneNaltrexone

Identifiers

PMID27470429
OpenAlexW2494421376

What OpenQuestion holds

Textmetadata
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.