Prolonged headache with vaccine- and dose-specific headache pattern associated with vaccine against SARS-CoV-2 in patients with migraine

Author:

Kuan Ai Seon123ORCID,Chen Shih-Pin3456ORCID,Wang Yen-Feng35,Wang Shuu-Jiun357ORCID

Affiliation:

1. Department of Neurosurgery, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan

2. Institute of Public Health, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan

3. School of Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan

4. Institute of Clinical Medicine, College of Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan

5. Department of Neurology, Neurological Institute, Taipei Veterans General Hospital, Taipei, Taiwan

6. Division of Translational Research, Department of Medical Research, Taipei Veterans General Hospital, Taipei, Taiwan

7. Brain Research Center, National Yang Ming Chiao Tung University, Taipei, Taiwan

Abstract

Objective To examine SARS-CoV-2 vaccine-related headache characteristics and risk factors in migraine patients. Methods This retrospective cohort study included 732 migraine patients who had AstraZeneca Vaxzevria, Pfizer-BioNTech Comirnaty, or Moderna Spikevax vaccines. Participants provided information through questionnaires and headache diaries. Headache frequency before and after vaccination and factors associated with headache risk were examined. Results Approximately a third of patients reported increased headache the day after having primary and booster doses, with mean increase ± SD of 1.9 ± 1.2 and 1.8 ± 1.1 days/week, respectively. Proportions of migraine patients with headache (after vaccination vs. before vaccination) increased after having primary-dose Vaxzevria (35.3% vs. 22.8%, p < 0.001) but not Spikevax (23.8% vs. 26.7%, p = 0.700) or Comirnaty (33.2% vs. 25.8%, p = 0.058). Headache proportion increased after having all three boosters (Vaxzevria 27.1% vs. 17.9% p = 0.003; Comirnaty 34.1% vs. 24.5% p = 0.009; Spikevax 35.2% vs. 24.8% p = 0.031). For primary dose with Vaxzevria and Comirnaty, headache risk increased on the vaccination day, peaked on the day after vaccination, and subsided within a week, while for Spikevax headache risk rose gradually after vaccination, peaked on the seventh post-vaccination day and subsided subsequently. For booster dose, headache risk generally increased on the vaccination day, peaked on the day after vaccination, and subsided gradually with fluctuating pattern within a month. Our study also showed that headache increased on the day before primary dose but not booster dose vaccination and it may be attributable to stress associated with having to undertake new vaccines. Multivariable analyses showed that depression was associated with headache. Conclusion Prolonged headache with vaccine- and dose-specific headache pattern was found. Patients with higher risks of vaccine-related headache must be informed of the potential worsening headache.

Funder

Ministry of Science and Technology, Taiwan

National Yang Ming Chiao Tung University

Taipei Veterans General Hospital

Publisher

SAGE Publications

Subject

Neurology (clinical),General Medicine

Reference26 articles.

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