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Safety and Adverse Events Among Long-term Care Residents Receiving a Third COVID-19 mRNA Vaccine Booster Dose in Quebec

Quote” Although LTC residents are disproportionately at risk of severe outcomes following COVID-19 infection, our findings suggest that they may also be at greater risk of postvaccination adverse effects “
Introduction

Booster doses of mRNA COVID-19 vaccines are administered worldwide to enhance antibody levels and immunity against Delta, Omicron, and emerging variants. Data on adverse events show a favorable safety profile, with similar reactogenicity for second and third doses. However, safety in older adults in long-term care (LTC) settings has not been well described.1,2 We examined adverse events following mRNA booster vaccination in LTC residents within the context of factors unique to the province of Quebec that may increase reactogenicity: extended interval between doses 1 and 2,3 heterologous vaccination, full dose mRNA-1273 (100 µg) booster,4 and high prevalence of previous COVID-19 infection.5

Methods

This cohort study was approved by the Centre-Sud-de-l’Île-de-Montréal regional health authority (CS-RHA) institutional review board. We followed the STROBE reporting guideline.

We included 280 LTC residents from 6 facilities of the CS-RHA in Quebec. Residents received mRNA booster doses, BNT162b2 (Pfizer [P]), 30 µg, or mRNA-1273 (Moderna [M]), 100 µg, between October 18 and November 1, 2021. In Quebec, a minimal interval of 3 months between doses 1 and 2 was used. The 100-µg mRNA-1273 dosage rollout was planned before the 50-µg booster dose FDA approval. Residents were initially eligible regardless of prior COVID-19 infection status and vaccination combination for the first 2 doses (any combination of BNT162b2 and mRNA-1273), 5 months after the second dose. We excluded residents who received the second dose less than 35 days after the first dose (n = 10) and those who received a third dose for indications related to immunosuppression. We collected age, sex, COVID-19 infection date, vaccination combinations, and dates. The primary outcome was the occurrence of any systemic adverse events (SAEs, ie, fever, malaise, gastrointestinal symptoms, tachycardia, desaturation, respiratory distress, hospital transfer, hypotension, thrombosis, rigors, death), during the first 48 hours. SAEs were collected as part of instructed postvaccination surveillance by health care staff and reported in the medical record. We calculated the proportion of residents reporting SAEs for vaccine combinations with more than 40 participants. To assess factors of reactogenicity, we used logistic regression with vaccine combinations and COVID-19 status as independent variables, adjusted for age (b-splines) and sex. The level of statistical significance was α = .05 (2-sided); analyses were conducted using R version 4.1.2 (R Project for Statistical Computing).

Results

Among 280 participants included, 184 (66%) were female and 96 (34%) were male; the mean (SD) age was 83 (11) years. The Table reports the demographic characteristics by vaccine combinations (MPM, MPP, PPP). The median (IQR) interval between doses 1 and 2 was 111 (1) days and between 2 and 3 was 175 (1) days; the interval between COVID-19 infection and dose 1 was 266 (25) days. Figure A compares SAEs for the MPM combination according to prior COVID-19 infection (+). Figure B, C, and D present results in those without prior infection (−) for MPM, MMP, and PPP. Among residents with MPM+, 46% had a SAE (40% fever) compared with 16% (10% fever) for MPM−, 6% for MMP−, and 2% for PPP−. With the MPM− as reference, the likelihood of SAEs was greater for MPM+ (OR, 4.13; 95% CI, 2.08-8.47) and lower for MPP− (OR, 0.27; 95% CI, 0.06-0.90) and PPP− (OR, 0.12; 95% CI, 0.01-0.63). No resident had a COVID-19 infection within 7 days of vaccination.

Discussion

In comparison with previous reports of third doses’ reactogenicity,2,4 our findings indicate a high proportion of systemic adverse events, specifically among LTC residents with prior infection. SAEs were also more likely with MPM compared with MPP and PPP, suggesting that the mRNA-1273 100-µg booster dose and heterologous vaccination may increase reactogenicity.6 The extended interval between doses 1 and 2 may have increased immunogenicity.3 Although LTC residents are disproportionately at risk of severe outcomes following COVID-19 infection, our findings suggest that they may also be at greater risk of postvaccination adverse effects. As additional booster doses are considered due to waning immunity and variants, examination of past vaccines and intervals, immunity status, and booster dosage may be required to weigh their potential benefits against the risk of adverse effects.

Limitations of our study include absence of antibody testing for prior infections, infections prior to the Omicron variant, and no direct comparison of SAEs between the third and previous doses. Our results may not be generalizable to other older adult populations.

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Article Information

Accepted for Publication: June 6, 2022.

Published: July 21, 2022. doi:10.1001/jamanetworkopen.2022.23401

Open Access: This is an open access article distributed under the terms of the CC-BY License. © 2022 Zhang XS et al. JAMA Network Open.

Corresponding Author: Quoc Dinh Nguyen, MD, MPH, PhD, Division of Geriatrics, Department of Medicine, Centre hospitalier de l’Université de Montréal, 1000 rue Saint-Denis, Montreal, QC H2X 0C1, Canada (quoc.dinh.nguyen@umontreal.ca).

Author Contributions: Dr Nguyen had full access to all of the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Concept and design: Zhang, Moreau, Nguyen.

Acquisition, analysis, or interpretation of data: All authors.

Drafting of the manuscript: Nguyen.

Critical revision of the manuscript for important intellectual content: All authors.

Statistical analysis: Nguyen.

Administrative, technical, or material support: Zhang, Moreau, Cruz-Santiago, Nguyen.

Supervision: Zhang, Moreau, Nguyen.

Conflict of Interest Disclosures: None reported.

References
1.
Barda  N, Dagan  N, Cohen  C,  et al.  Effectiveness of a third dose of the BNT162b2 mRNA COVID-19 vaccine for preventing severe outcomes in Israel: an observational study.   Lancet. 2021;398(10316):2093-2100. doi:10.1016/S0140-6736(21)02249-2PubMedGoogle ScholarCrossref
2.
Hause  AM, Baggs  J, Marquez  P,  et al.  Safety monitoring of COVID-19 vaccine booster doses among adults — United States, September 22, 2021–February 6, 2022.   MMWR Morb Mortal Wkly Rep. 2022;71(7):249-254. doi:10.15585/mmwr.mm7107e1PubMedGoogle ScholarCrossref
3.
Grunau  B, Goldfarb  DM, Asamoah-Boaheng  M,  et al.  Immunogenicity of extended mRNA SARS-CoV-2 vaccine dosing intervals.   JAMA. 2022;327(3):279-281. doi:10.1001/jama.2021.21921
ArticlePubMedGoogle ScholarCrossref
4.
Atmar  RL, Lyke  KE, Deming  ME,  et al; DMID 21-0012 Study Group.  Homologous and heterologous Covid-19 booster vaccinations.   N Engl J Med. 2022;386(11):1046-1057. Published online January 26, 2022. doi:10.1056/NEJMoa2116414PubMedGoogle ScholarCrossref
5.
Wang  Z, Muecksch  F, Schaefer-Babajew  D,  et al.  Naturally enhanced neutralizing breadth against SARS-CoV-2 one year after infection.   Nature. 2021;595(7867):426-431. doi:10.1038/s41586-021-03696-9PubMedGoogle ScholarCrossref
6.
Munro  APS, Janani  L, Cornelius  V,  et al; COV-BOOST study group.  Safety and immunogenicity of seven COVID-19 vaccines as a third dose (booster) following two doses of ChAdOx1 nCov-19 or BNT162b2 in the UK (COV-BOOST): a blinded, multicentre, randomised, controlled, phase 2 trial.   Lancet. 2021;398(10318):2258-2276. doi:10.1016/S0140-6736(21)02717-3PubMedGoogle ScholarCrossref

Source: Safety of third dose of mRNA COVID-19 vaccine in long-term care residents

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