Safety Assessment of Concurrent Vaccination with the HPV Vaccine and the COVID-19 Vaccine in Fujian Province, China: A Retrospective Study

Author:

Zhang Yan123,Zhang Yuhang123,Dong Binhua234,Lin Wenyu234ORCID,Huang Yuxuan234,Osafo Kelvin Stefan234ORCID,Lin Xite234,Jiang Tingting234,Zhang Yu56,Zou Huachun78ORCID,Sun Pengming2349ORCID

Affiliation:

1. The State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics, National Institute of Diagnostics and Vaccine Development in Infectious Diseases, School of Public Health, Xiamen University, Xiamen 361102, China

2. Laboratory of Gynecologic Oncology, Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou 350001, China

3. Fujian Clinical Research Center for Gynecologic Oncology, Fujian Maternity and Child Health Hospital, Fuzhou 350001, China

4. Fujian Key Laboratory of Women and Children’s Critical Diseases Research, Fujian Maternity and Child Health Hospital, Fuzhou 350001, China

5. Department of Gynecology, Xiangya Hospital, Central South University, Changsha 410008, China

6. Gynecological Oncology Research and Engineering Center of Hunan Province, Changsha 410008, China

7. School of Public Health, Fudan University, Shanghai 200433, China

8. Fujian Maternity and Child Health Hospital, College of Clinical Medicine for Obstetrics and Gynecology and Pediatrics, Fujian Medical University, Fuzhou 350001, China

9. School of Public Health, Xiamen University, Xiamen 361102, China

Abstract

During acute respiratory infections, women may concurrently receive human papillomavirus (HPV) and respiratory vaccines, as observed during the coronavirus disease 2019 (COVID-19) pandemic in China. However, few studies have assessed the safety of such concurrent administration, which could impact HPV vaccination schedules. This study analyzes the safety and optimal sequence of concurrent HPV and COVID-19 vaccinations. For this purpose, we surveyed women with both vaccines from January to October 2023 in Fujian Province, China. During this process, we collected vaccination history and adverse event (AE) data via telephone or interviews. Participants were grouped as Before, Concurrent, or After based on their vaccination sequence. A Chi-squared test, exact Fisher tests, and logistic regression were used to analyze the incidence of AEs and factors influencing vaccine safety. Overall, 1416 eligible participants were included. Although overall AE risk with the HPV vaccine was unaffected by vaccination sequence, individual AEs varied statistically between groups, including pain at the vaccination site (p < 0.001) and prolonged menstruation duration (p = 0.003). Based on the results, the optimal sequence would be to receive the HPV vaccine after the COVID-19 vaccine (After group). This insight may guide future emergency vaccination sequences for HPV and other respiratory infectious diseases.

Funder

National Key R&D Program of China

National Natural Science Foundation of China

Major Scientific Research Program for Young and Middle-aged Health Professionals of Fujian Province, China

Fujian Province Central Government-Guided Local Science and Technology Development Project

Fujian Clinical Medical Research Center for Gynecologic Oncology

Fujian Province’s Third Batch of Flexible Introduction of High-Level Medical Talent Teams

Fujian Provincial Natural Science Foundation of China

Fujian Provincial Science and Technology Innovation Joint Fund

Publisher

MDPI AG

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