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Relative Vaccine Effectiveness of a Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccine Booster Dose Against the Omicron Variant.
Clin Infect Dis. 2022 12 19; 75(12):2161-2168.CI

Abstract

BACKGROUND

The current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines may be less effective against the Omicron variant than against earlier variants. With recent resurgence of SARS-CoV-2 cases, the role of booster doses of the vaccine needs to be highlighted.

METHODS

Using a retrospective cohort study design emulating a target trial, we determined the relative vaccine effectiveness (RVE) of a homologous booster dose of a SARS-CoV-2 messenger RNA (mRNA) vaccine compared with the primary vaccine series alone in preventing infection, hospitalization, and intensive care unit admission, and death in the Department of Veterans Affairs healthcare system in the United States. Among infection-free survivors who received 2 doses of a mRNA vaccine before 30 April 2021, we identified those who received a booster between 22 September and 25 December 2021 and matched them 1:1 with individuals who did not receive a booster.

RESULTS

Among 2 384 272 previously uninfected persons with 2 doses of an mRNA vaccine by 30 April 2021, we identified 462 950 booster recipients between 22 September and 25 December 2021, who were matched 1:1 with non-booster recipients. The RVE (95% confidence interval) was 19% (17%-22%) for confirmed infection, 52% (46%-57%) for hospitalization, and 83% (65%-92%) for intensive care unit admission or death. Recipients of the mRNA-1273 vaccine had a lower cumulative incidence of infections and hospitalizations than recipients of the BNT162b2 vaccine (log-rank P <.001 for both comparisons).

CONCLUSIONS

While the RVE of SARS-CoV-2 mRNA booster vaccine dose in preventing infection against the Omicron variant is low, it is substantial in preventing hospitalization and high in preventing the most severe/critical disease.

Authors+Show Affiliations

VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, USA. Departments of Medicine and Population Health Sciences, Weill Cornell Medicine, New York, New York, USA. Departments of Medicine and Population Health Sciences, Weill Cornell Medicine, Doha, Qatar.VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, USA. CRISMA Center, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, USA. Division of Gastroenterology, Hepatology and Nutrition, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA.Yale Institute for Global Health, Yale University, New Haven, Connecticut, USA.VA Pittsburgh Healthcare System, Pittsburgh, Pennsylvania, USA. CRISMA Center, Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

35511586

Citation

Butt, Adeel A., et al. "Relative Vaccine Effectiveness of a Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccine Booster Dose Against the Omicron Variant." Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America, vol. 75, no. 12, 2022, pp. 2161-2168.
Butt AA, Talisa VB, Shaikh OS, et al. Relative Vaccine Effectiveness of a Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccine Booster Dose Against the Omicron Variant. Clin Infect Dis. 2022;75(12):2161-2168.
Butt, A. A., Talisa, V. B., Shaikh, O. S., Omer, S. B., & Mayr, F. B. (2022). Relative Vaccine Effectiveness of a Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccine Booster Dose Against the Omicron Variant. Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America, 75(12), 2161-2168. https://doi.org/10.1093/cid/ciac328
Butt AA, et al. Relative Vaccine Effectiveness of a Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccine Booster Dose Against the Omicron Variant. Clin Infect Dis. 2022 12 19;75(12):2161-2168. PubMed PMID: 35511586.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Relative Vaccine Effectiveness of a Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccine Booster Dose Against the Omicron Variant. AU - Butt,Adeel A, AU - Talisa,Victor B, AU - Shaikh,Obaid S, AU - Omer,Saad B, AU - Mayr,Florian B, PY - 2022/03/30/received PY - 2022/5/6/pubmed PY - 2022/12/22/medline PY - 2022/5/5/entrez KW - Delta variant KW - Omicron variant KW - SARS-CoV-2 KW - booster KW - vaccine effectiveness SP - 2161 EP - 2168 JF - Clinical infectious diseases : an official publication of the Infectious Diseases Society of America JO - Clin Infect Dis VL - 75 IS - 12 N2 - BACKGROUND: The current severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccines may be less effective against the Omicron variant than against earlier variants. With recent resurgence of SARS-CoV-2 cases, the role of booster doses of the vaccine needs to be highlighted. METHODS: Using a retrospective cohort study design emulating a target trial, we determined the relative vaccine effectiveness (RVE) of a homologous booster dose of a SARS-CoV-2 messenger RNA (mRNA) vaccine compared with the primary vaccine series alone in preventing infection, hospitalization, and intensive care unit admission, and death in the Department of Veterans Affairs healthcare system in the United States. Among infection-free survivors who received 2 doses of a mRNA vaccine before 30 April 2021, we identified those who received a booster between 22 September and 25 December 2021 and matched them 1:1 with individuals who did not receive a booster. RESULTS: Among 2 384 272 previously uninfected persons with 2 doses of an mRNA vaccine by 30 April 2021, we identified 462 950 booster recipients between 22 September and 25 December 2021, who were matched 1:1 with non-booster recipients. The RVE (95% confidence interval) was 19% (17%-22%) for confirmed infection, 52% (46%-57%) for hospitalization, and 83% (65%-92%) for intensive care unit admission or death. Recipients of the mRNA-1273 vaccine had a lower cumulative incidence of infections and hospitalizations than recipients of the BNT162b2 vaccine (log-rank P <.001 for both comparisons). CONCLUSIONS: While the RVE of SARS-CoV-2 mRNA booster vaccine dose in preventing infection against the Omicron variant is low, it is substantial in preventing hospitalization and high in preventing the most severe/critical disease. SN - 1537-6591 UR - https://www.unboundmedicine.com/medline/citation/35511586/Relative_Vaccine_Effectiveness_of_a_Severe_Acute_Respiratory_Syndrome_Coronavirus_2_Messenger_RNA_Vaccine_Booster_Dose_Against_the_Omicron_Variant_ DB - PRIME DP - Unbound Medicine ER -