Author
Listed:
- Francisco Tsz Tsun Lai
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong
Laboratory of Data Discovery for Health (D24H), Hong Kong Science Park, Hong Kong Science and Technology Park)
- Lei Huang
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong)
- Celine Sze Ling Chui
(Laboratory of Data Discovery for Health (D24H), Hong Kong Science Park, Hong Kong Science and Technology Park
School of Nursing, Li Ka Shing Faculty of Medicine, The University of Hong Kong
School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong)
- Eric Yuk Fai Wan
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong
Laboratory of Data Discovery for Health (D24H), Hong Kong Science Park, Hong Kong Science and Technology Park
Li Ka Shing Faculty of Medicine, The University of Hong Kong)
- Xue Li
(Laboratory of Data Discovery for Health (D24H), Hong Kong Science Park, Hong Kong Science and Technology Park
Li Ka Shing Faculty of Medicine, The University of Hong Kong)
- Carlos King Ho Wong
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong
Laboratory of Data Discovery for Health (D24H), Hong Kong Science Park, Hong Kong Science and Technology Park
Li Ka Shing Faculty of Medicine, The University of Hong Kong)
- Edward Wai Wa Chan
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong)
- Tiantian Ma
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong
Laboratory of Data Discovery for Health (D24H), Hong Kong Science Park, Hong Kong Science and Technology Park)
- Dawn Hei Lum
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong)
- Janice Ching Nam Leung
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong
Laboratory of Data Discovery for Health (D24H), Hong Kong Science Park, Hong Kong Science and Technology Park)
- Hao Luo
(The University of Hong Kong
The University of Hong Kong)
- Esther Wai Yin Chan
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong
Laboratory of Data Discovery for Health (D24H), Hong Kong Science Park, Hong Kong Science and Technology Park)
- Ian Chi Kei Wong
(Centre for Safe Medication Practice and Research, Department of Pharmacology and Pharmacy, Li Ka Shing Faculty of Medicine, The University of Hong Kong
Laboratory of Data Discovery for Health (D24H), Hong Kong Science Park, Hong Kong Science and Technology Park
University College London)
Abstract
Prior research using electronic health records for Covid-19 vaccine safety monitoring typically focuses on specific disease groups and excludes individuals with multimorbidity, defined as ≥2 chronic conditions. We examine the potential additional risk of adverse events 28 days after the first dose of CoronaVac or Comirnaty imposed by multimorbidity. Using a territory-wide public healthcare database with population-based vaccination records in Hong Kong, we analyze a retrospective cohort of patients with chronic conditions. Thirty adverse events of special interest according to the World Health Organization are examined. In total, 883,416 patients are included and 2,807 (0.3%) develop adverse events. Results suggest vaccinated patients have lower risks of adverse events than unvaccinated individuals, multimorbidity is associated with increased risks regardless of vaccination, and the association of vaccination with adverse events is not modified by multimorbidity. To conclude, we find no evidence that multimorbidity imposes extra risks of adverse events following Covid-19 vaccination.
Suggested Citation
Francisco Tsz Tsun Lai & Lei Huang & Celine Sze Ling Chui & Eric Yuk Fai Wan & Xue Li & Carlos King Ho Wong & Edward Wai Wa Chan & Tiantian Ma & Dawn Hei Lum & Janice Ching Nam Leung & Hao Luo & Esthe, 2022.
"Multimorbidity and adverse events of special interest associated with Covid-19 vaccines in Hong Kong,"
Nature Communications, Nature, vol. 13(1), pages 1-8, December.
Handle:
RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-28068-3
DOI: 10.1038/s41467-022-28068-3
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