Evidence map›Paper›PMID 40165130›Full record

ArticleBMC neurology2025

Quickest way to less headache days: an operational research model and its implementation for chronic migraine.

Irene Lo, Pengfei Zhang

Abstract read
In one paragraph

Article in BMC neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Irene LoDepartment of Management Science & Engineering, Stanford University, Stanford, CA, USA.
Pengfei ZhangDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, MA, USA. pzhang7@bidmc.harvard.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveChoosing migraine prevention medications often involves trial and error. Operations research methodologies, however, allow us to derive a mathematically optimum way to conduct such trial and error processes.

backgroundGiven probability of success (defined as 50% reduction in headache days) and adverse events as a function of time, we seek to develop and solve an operations research model, applicable to any arbitrary patient, minimizing time until discovery of an effective migraine prevention medication. We then seek to apply our model to real life data for chronic migraine prevention.

methodsAn operations research model is developed and then solved for the optimum solution, taking into account the likelihood of reaching 50% headache day reduction as a function of time. We then estimate key variables using FORWARD study by Rothrock et al. as well as erenumab data published by Barbanti et al. at International Headache Congress 2019.

resultsThe solution for our model is to order the medications in decreasing order by probability of efficacy per unit time. This result can be generalized through calculation of Gittins index. In the case of chronic migraine the optimum sequence of chronic migraine prevention medication is a trial of erenumab for 12 weeks, followed by a trial of onabotulinumtoxinA for 32 weeks, followed by a trial of topiramate for 32 weeks.

conclusionsWe propose an optimal sequence for preventive medication trial for patients with chronic migraine. Since our model makes limited assumptions on the characteristics of disease, it can be readily applied also to episodic migraine, given the appropriate data as input. Indeed, our model can be applied to other scenarios so long as probability of success/adverse event as a function of time can be estimated. As such, we believe our model may have implications beyond our sub-specialty.

Indexed as

Migraine DisordersModels, TheoreticalAntibodies, Monoclonal, HumanizedBotulinum Toxins, Type ACalcitonin Gene-Related Peptide Receptor AntagonistsChronic DiseaseHumansAntibodies, Monoclonal, HumanizedBotulinum Toxins, Type ACalcitonin Gene-Related Peptide Receptor AntagonistserenumabHeadachesMedication selectionMigraineMigraine preventionOperations research

Identifiers

PMID40165130
PMCPMC11956327

What Socratic holds

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Registered trials

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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 Socratic graph.