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Correlation between the severity of COVID-19 vaccine-related adverse events and the blood group of the vaccinees in Saudi Arabia: A web-based survey.
Almalki, Ohoud S; Khalifa, Amany S; Alhemeidi, Ozouf F; Ewis, Ashraf A; Shady, Abeer M; Abdelwahab, Sayed F.
Afiliação
  • Almalki OS; Department of Clinical Pharmacy, College of Pharmacy, Taif University, Taif, Saudi Arabia.
  • Khalifa AS; Department of Pharmaceutics and Industrial pharmacy, College of Pharmacy, Taif University, Taif, Saudi Arabia.
  • Alhemeidi OF; Department of Clinical Pharmacy, College of Pharmacy, Taif University, Taif, Saudi Arabia.
  • Ewis AA; Department of Public Health, Faculty of Health Sciences-AlQunfudah, Umm Al-Qura University, Makkah, Saudi Arabia.
  • Shady AM; Department of Public Health and Occupational Medicine, Faculty of Medicine, Minia University, El-Minia, Egypt.
  • Abdelwahab SF; Department of Pharmaceutics and Industrial pharmacy, College of Pharmacy, Taif University, Taif, Saudi Arabia.
Front Pharmacol ; 13: 1006333, 2022.
Article em En | MEDLINE | ID: mdl-36561341
ABSTRACT

Background:

Recent epidemiological studies have reported an association between the ABO blood group and the acquisition, symptom severity, and mortality rate of coronavirus disease 2019 (COVID-19). However, the association between the ABO blood group antigens and the type and severity of COVID-19 vaccine-related adverse reactions has not been elucidated. Patients and

Methods:

We conducted a cross-sectional, questionnaire-based study in Saudi Arabia from February to April 2022. The study cohort included adults who had received or were willing to receive at least two doses of a COVID-19 vaccine of any type. We used Chi-square test to assess the association between the ABO blood groups and vaccine-related adverse reactions. p values of <0.05 were considered significant.

Results:

Of the 1180 participants, approximately half were aged 18-30 years old, 69.2% were female, and 41.6% reported their blood group as O. The most frequent COVID-19 vaccine-related adverse reactions were fatigue (65%), pain at the injection site (56%), and headache (45.9%). These adverse reactions demonstrated significant correlations with the education level (p = 0.003) and nationality (p = 0.018) of the participants following the first dose, with gender (p < 0.001) following the second dose, and with the general health status (p < 0.001) after all the doses. Remarkably, no correlation was observed between the severity of the vaccine-related adverse reactions and ABO blood groups.

Conclusion:

Our findings do not support a correlation between the severity of COVID-19 vaccine-related adverse reactions and the ABO blood groups of the vaccinees. The creation of a national database is necessary to account for population differences.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article