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    <subfield code="a">10.1016/j.nrl.2021.03.003</subfield>
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    <subfield code="2">sideral</subfield>
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    <subfield code="a">ART-2021-124265</subfield>
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    <subfield code="a">eng</subfield>
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    <subfield code="a">Caronna, E.</subfield>
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  <datafield tag="245" ind1=" " ind2=" ">
    <subfield code="a">Safety of anti-CGRP monoclonal antibodies in patients with migraine during the COVID-19 pandemic: Present and future implications [Seguridad de los anticuerpos monoclonales anti-CGRP en pacientes con migraña durante la pandemia de COVID-19: implicaciones actuales y futuras]</subfield>
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    <subfield code="c">2021</subfield>
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    <subfield code="a">Access copy available to the general public</subfield>
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    <subfield code="a">Background and objective: CGRP, a neuropeptide involved in migraine pathophysiology, is also known to play a role in the respiratory system and in immunological conditions such as sepsis. We analyzed the impact of the use of CGRP antagonists in patients with migraine during the COVID-19 pandemic, caused by the SARS-CoV-2 coronavirus. Methods: This is a multicentre cross-sectional study. From May to November 2020, through a national survey distributed by the Spanish Society of Neurology, we collected data about the presence of COVID-19 symptoms including headache and their characteristics and severity in patients with migraine treated with anti-CGRP monoclonal antibodies (mAb), and compared them with patients with migraine not receiving this treatment. We also conducted a subanalysis of patients with COVID-19 symptoms. Results: We recruited 300 patients with migraine: 51.7% (155/300) were taking anti-CGRP mAbs; 87.3% were women (262/300). Mean age (standard deviation) was 47.1 years (11.6). Forty-one patients (13.7%) met diagnostic criteria for COVID-19, with no statistically significant difference between patients with and without anti-CGRP mAb treatment (16.1% vs 11.0%, respectively; P = .320). Of the patients with COVID-19, 48.8% (20/41) visited the emergency department and 12.2% (5/41) were hospitalised. Likewise, no clinical differences were found between the groups of patients with and without anti-CGRP mAb treatment. Conclusion: Anti-CGRP mAbs may be safe in clinical practice, presenting no association with increased risk of COVID-19.</subfield>
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    <subfield code="9">info:eu-repo/semantics/openAccess</subfield>
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    <subfield code="u">https://creativecommons.org/licenses/by-nc-nd/4.0/deed.es</subfield>
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    <subfield code="a">Neurology (clinical)</subfield>
    <subfield code="c">2021</subfield>
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    <subfield code="c">2021</subfield>
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    <subfield code="a">José Gallardo, V.</subfield>
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    <subfield code="a">Alpuente, A.</subfield>
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    <subfield code="a">Torres-Ferrus, M.</subfield>
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    <subfield code="a">Sánchez-Mateo, N.M.</subfield>
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    <subfield code="a">Viguera-Romero, J.</subfield>
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    <subfield code="a">López-Veloso, A.C.</subfield>
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    <subfield code="a">López-Bravo, A.</subfield>
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    <subfield code="a">Gago-Veiga, A.B.</subfield>
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    <subfield code="a">Irimia Sieira, P.</subfield>
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    <subfield code="a">Porta-Etessam, J.</subfield>
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    <subfield code="a">Santos-Lasaosa, S.</subfield>
    <subfield code="u">Universidad de Zaragoza</subfield>
    <subfield code="0">(orcid)0000-0001-5139-6031</subfield>
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    <subfield code="a">Pozo-Rosich, P.</subfield>
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    <subfield code="a">Spanish, CGRP-COVID, Study, Group</subfield>
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  <datafield tag="710" ind1="2" ind2=" ">
    <subfield code="1">1007</subfield>
    <subfield code="2">610</subfield>
    <subfield code="a">Universidad de Zaragoza</subfield>
    <subfield code="b">Dpto. Medicina, Psiqu. y Derm.</subfield>
    <subfield code="c">Area Medicina</subfield>
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  <datafield tag="773" ind1=" " ind2=" ">
    <subfield code="g">36 (2021), 611-617</subfield>
    <subfield code="p">Neurología (Barc.)</subfield>
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