Adverse events following third dose of mRNA COVID‐19 vaccination among nursing home residents who received the primary series. Issue 6 (27th April 2022)

• Record Type: Journal Article
• Authors: Bardenheier, Barbara H.; White, Elizabeth M.; Blackman, Carolyn; Gravenstein, Stefan; Gutman, Roee; Sarkar, Indra Neil; Feifer, Richard A.; McConeghy, Kevin; Nanda, Aman; Duprey, Matthew; Mor, Vincent
• Is Part Of: Journal of the American Geriatrics Society. Volume 70:Issue 6(2022)
• Page Start: 1642
• Page End: 1647
• Publication Date: 2022-04-27
• Subjects: adverse events after vaccination -- booster COVID‐19 vaccination -- nursing home; Geriatrics -- Periodicals; 618.97
• DOI: 10.1111/jgs.17812
• Languages: English
• ISSNs: 0002-8614

Abstract

Abstract: Background: We sought to compare rates of adverse events among nursing home residents who received an mRNA COVID‐19 vaccine booster dose with those who had not yet received their booster. Methods: We assessed a prospective cohort of 11, 200 nursing home residents who received a primary COVID‐19 mRNA vaccine series at least 6 months prior to September 22, 2021 and received a third "booster dose" between September 22, 2021 and February 2, 2022. Residents lived in 239 nursing homes operated by Genesis HealthCare, spanning 21 U.S. states. We screened electronic health records for 20 serious vaccine‐related adverse events that are monitored following receipt of COVID‐19 vaccination by the CDC's Vaccine Safety Datalink. We matched boosted and yet‐to‐be boosted residents during the same time period, comparing rates of events occurring 14 days after booster administration with those occurring 14 days prior to booster administration. To supplement previously reported background rates of adverse events, we report background rates of medical conditions among nursing home residents during 2020, before COVID‐19 vaccines were administered in nursing homes. Events occurring in 2021–2022 were confirmed by physician chart review. We report unadjusted rates of adverse events and used a false discovery rate procedure to adjust for multiplicity of events tested. Results: No adverse events were reported during the 14 days post‐booster. A few adverse events occurred prior to booster (ischemic stroke: 49.4 per 100, 000 residents, 95% CI: 21.2, 115.7; venous thromboembolism: 9.9 per 100, 000 residents, 95% CI: 1.7, 56.0), though differences in event rates pre‐ versus post‐booster were not statistically significant ( p < 0.05) after adjusting for multiple comparisons. No significant differences were detected between post‐booster vaccination rates and prior year 14‐day background rates of medical conditions. Conclusions: No safety signals were detected following a COVID‐19 mRNA vaccine booster dose in this large multi‐state sample of nursing home residents.