Evidence map›Paper›PMID 38323742›Full record

Observational studyEuropean journal of neurology2024

Evaluation of the concomitant use of prophylactic treatments in patients with migraine under anti-calcitonin gene-related peptide therapies: The PREVENAC study.

Ana Beatriz Gago-Veiga, Noelia Lopez-Alcaide, Sonia Quintas, Iris Fernández Lázaro, Javier Casas-Limón, Carlos Calle, Germán Latorre, Nuria González-García, Jesús Porta-Etessam, Jaime Rodriguez-Vico and 11 more

Abstract readObservational StudyMulticenter Study
In one paragraph

Observational study in European journal of neurology, 2024. 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
–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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
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

21 authors.

Ana Beatriz Gago-VeigaHeadache Unit, Hospital Universitario de la Princesa & Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Madrid, Spain.ORCID 0000-0002-0038-3406
Noelia Lopez-AlcaideHeadache Unit, Hospital Universitario de la Princesa & Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Madrid, Spain.
Sonia QuintasHeadache Unit, Hospital Universitario de la Princesa & Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Madrid, Spain.ORCID 0000-0003-0622-8228
Iris Fernández LázaroHeadache Unit, Hospital Universitario de la Princesa & Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Madrid, Spain.
Javier Casas-LimónHeadache Unit, Hospital Universitario Fundación Alcorcón, Alcorcón, Spain.
Carlos CalleHeadache Unit, Hospital de Fuenlabrada, Madrid, Spain.
Germán LatorreHeadache Unit, Hospital de Fuenlabrada, Madrid, Spain.
Nuria González-GarcíaHeadache Unit, Hospital Clínico San Carlos, Madrid, Spain.
Jesús Porta-EtessamHeadache Unit, Hospital Clínico San Carlos, Madrid, Spain.ORCID 0000-0002-7034-682X
Jaime Rodriguez-VicoHeadache Unit, Hospital Fundación Jiménez Díaz, Madrid, Spain.
Alex JaimesHeadache Unit, Hospital Fundación Jiménez Díaz, Madrid, Spain.
Andrea Gómez GarcíaHeadache Unit, Hospital Fundación Jiménez Díaz, Madrid, Spain.
David García-AzorínHeadache Unit, Hospital Clínico Universitario de Valladolid, Valladolid, Spain.ORCID 0000-0002-3132-1064
Ángel Luis Guerrero-PeralHeadache Unit, Hospital Clínico Universitario de Valladolid, Valladolid, Spain.ORCID 0000-0001-7493-6002
Álvaro SierraHeadache Unit, Hospital Clínico Universitario de Valladolid, Valladolid, Spain.ORCID 0000-0002-0022-6064
Alberto Lozano RosHeadache Unit, Hospital Universitario Gregorio Marañón, Madrid, Spain.
Antonio Sánchez-SoblecheroHeadache Unit, Hospital Universitario Gregorio Marañón, Madrid, Spain.ORCID 0000-0002-7098-8494
Javier Díaz-de-TeranHeadache Unit, Hospital Severo Ochoa, Madrid, Spain.
Javier A MembrillaHeadache Unit, Hospital Severo Ochoa, Madrid, Spain.ORCID 0000-0001-6018-6677
Cristina TreviñoHeadache Unit, Hospital Clínico Universitario de la Paz, Madrid, Spain.
Alicia Gonzalez-MartinezHeadache Unit, Hospital Universitario de la Princesa & Instituto de Investigación Sanitaria Princesa (IIS-Princesa), Madrid, Spain.ORCID 0000-0002-1228-1503

Funding

Instituto de Salud Carlos III (ISCIII) and the European Union (ESF+) PMP22/00158Instituto de Salud Carlos III (ISCIII) and the European Union (ESF+) through a Río Hortega and Juan Rodés Fellowship to A.G.M. CM21/00178Instituto de Salud Carlos III (ISCIII) and the European Union (ESF+) through a Río Hortega and Juan Rodés Fellowship to A.G.M. JR23/00005
6 · The paper itself

Abstract

background and purposeAnti-calcitonin gene-related peptide (CGRP) therapies are recent preventive therapies approved for both episodic and chronic migraine. One of the measures of effectiveness is the withdrawal of other preventive treatments. The objective of this study is to quantify the impact of anti-CGRP drugs in concomitant preventive treatment in patients with migraine.

methodsThis was an observational, retrospective, multicenter cohort study with patients from nine national headache units. Patients with migraine undergoing treatment for at least 6 months with anti-CGRP antibodies, who were initially associated with some preventive treatment (oral and/or onabotulinumtoxinA) were included. Demographic and clinical variables were collected, as well as variables related to headache. Differences according to withdrawal or nonwithdrawal were evaluated.

resultsA total of 408 patients were included, 86.52% women, 48.79 (SD = 1.46) years old. Preventive treatment was withdrawn in 43.87% (179/408), 20.83% partially and 23.04% totally. In 27.45% (112/408), it was maintained exclusively due to comorbidity and in 28.6% (117/408) due to partial efficacy. The most frequent time of withdrawal was between 3 and 5 months after the start of treatment. The baseline characteristics associated with nonwithdrawal were comorbidities: insomnia, hypertension and obesity, chronic migraine, and medication overuse. In the multivariate analysis, the absence of high blood pressure, a greater number of preventive treatments at the start, and a lower number of migraine days/month after anti-CGRP treatment were independently associated with withdrawal of the treatment (p < 0.05).

conclusionsAnti-CGRP antibodies allow the withdrawal of associated preventive treatment in a significant percentage of patients, which supports its effectiveness in real-life conditions.

Indexed as

Calcitonin Gene-Related PeptideMigraine DisordersCohort StudiesFemaleHeadacheHumansInfantMaleRetrospective StudiesCalcitonin Gene-Related PeptideCGRPeffectivenessmigraineoral prophylacticsresponse

Identifiers

PMID38323742
PMCPMC11235635

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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 OpenQuestion graph.