Evidence map›Paper›PMID 41893566›Full record

ArticleToxins2026

OnabotulinumToxinA Reduces Pharmacological Burden in Chronic Migraine Patients: A Two-Center Prospective Cohort Study.

Danilo Antonio Montisano, Alessandra Parisi, Alberto Raggi, Claudia Altamura, Luigi D'Onofrio, Marilena Marcosano, Luisa Fofi, Alessia Marcassoli, Fabrizio Vernieri, Licia Grazzi

Abstract readMulticenter Study
In one paragraph

Article in Toxins, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Danilo Antonio MontisanoHeadache Center, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20131 Milano, Italy.ORCID 0000-0003-4834-2045
Alessandra ParisiHeadache Center, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20131 Milano, Italy.ORCID 0000-0002-8570-4175
Alberto RaggiNeurology, Public Health and Disability Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milano, Italy.ORCID 0000-0002-7433-7779
Claudia AltamuraHeadache and Neurosonology Unit, Fondazione Policlinico Campus Bio-Medico, Università Campus Bio-Medico Di Roma, 00128 Rome, Italy.ORCID 0000-0002-5934-5535
Luigi D'OnofrioHeadache and Neurosonology Unit, Fondazione Policlinico Campus Bio-Medico, Università Campus Bio-Medico Di Roma, 00128 Rome, Italy.ORCID 0009-0006-3387-4013
Marilena MarcosanoHeadache and Neurosonology Unit, Fondazione Policlinico Campus Bio-Medico, Università Campus Bio-Medico Di Roma, 00128 Rome, Italy.ORCID 0009-0003-5191-7628
Luisa FofiHeadache and Neurosonology Unit, Fondazione Policlinico Campus Bio-Medico, Università Campus Bio-Medico Di Roma, 00128 Rome, Italy.
Alessia MarcassoliNeurology, Public Health and Disability Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milano, Italy.ORCID 0000-0002-5003-1409
Fabrizio VernieriHeadache and Neurosonology Unit, Fondazione Policlinico Campus Bio-Medico, Università Campus Bio-Medico Di Roma, 00128 Rome, Italy.ORCID 0000-0002-9594-9336
Licia GrazziHeadache Center, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20131 Milano, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic migraine (CM) is a highly disabling and difficult-to-manage condition with a high pharmacological and economic burden. OnabotulinumtoxinA (BTx) was the first treatment specifically approved for CM. The main aim of this study was to assess whether the initiation of BTx is associated with discontinuation of previously prescribed preventive therapies.

methodsThis study was a prospective cohort investigation conducted in two headache centers: Carlo Besta (Milan) and Policlinico Campus Bio-Medico (Rome). We included patients with CM and previous oral preventive treatments initiating BTx. We analyzed persistence with preventive therapies over 12 months of follow-up and evaluated the conversion rate from chronic to episodic migraine (EM), along with change in migraine days, symptomatic intake, and HIT-6.

resultsA total of 95 patients were included in the main analysis, showing a discontinuation of treatment in 28.4% of patients at 12 months. In the exploratory analysis, a CM to EM conversion rate of 58.9% was achieved at 12 months; meanwhile, HIT-6, migraine days, and symptomatic intake showed a sizeable improvement.

conclusionTreatment with BTx was associated with a reduction in drug burden at 12 months and a CM to EM conversion rate of almost 60% at 12 months, also contributing to a reduction in the economic burden of the disease.

Indexed as

Acetylcholine Release InhibitorsBotulinum Toxins, Type AMigraine DisordersAdultChronic DiseaseFemaleHumansMaleMiddle AgedProspective StudiesTreatment OutcomeAcetylcholine Release InhibitorsBotulinum Toxins, Type Aonabotulinum toxin AburdenchronicmigraineOnabotulinumtoxinApharmacologicalpreventive

Identifiers

PMID41893566
PMCPMC13029949

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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 OpenQuestion graph.