Citation
Link-Gelles, Ruth, et al. "Effectiveness of 2, 3, and 4 COVID-19 mRNA Vaccine Doses Among Immunocompetent Adults During Periods when SARS-CoV-2 Omicron BA.1 and BA.2/BA.2.12.1 Sublineages Predominated - VISION Network, 10 States, December 2021-June 2022." MMWR. Morbidity and Mortality Weekly Report, vol. 71, no. 29, 2022, pp. 931-939.
Link-Gelles R, Levy ME, Gaglani M, et al. Effectiveness of 2, 3, and 4 COVID-19 mRNA Vaccine Doses Among Immunocompetent Adults During Periods when SARS-CoV-2 Omicron BA.1 and BA.2/BA.2.12.1 Sublineages Predominated - VISION Network, 10 States, December 2021-June 2022. MMWR Morb Mortal Wkly Rep. 2022;71(29):931-939.
Link-Gelles, R., Levy, M. E., Gaglani, M., Irving, S. A., Stockwell, M., Dascomb, K., DeSilva, M. B., Reese, S. E., Liao, I. C., Ong, T. C., Grannis, S. J., McEvoy, C., Patel, P., Klein, N. P., Hartmann, E., Stenehjem, E., Natarajan, K., Naleway, A. L., Murthy, K., ... Tenforde, M. W. (2022). Effectiveness of 2, 3, and 4 COVID-19 mRNA Vaccine Doses Among Immunocompetent Adults During Periods when SARS-CoV-2 Omicron BA.1 and BA.2/BA.2.12.1 Sublineages Predominated - VISION Network, 10 States, December 2021-June 2022. MMWR. Morbidity and Mortality Weekly Report, 71(29), 931-939. https://doi.org/10.15585/mmwr.mm7129e1
Link-Gelles R, et al. Effectiveness of 2, 3, and 4 COVID-19 mRNA Vaccine Doses Among Immunocompetent Adults During Periods when SARS-CoV-2 Omicron BA.1 and BA.2/BA.2.12.1 Sublineages Predominated - VISION Network, 10 States, December 2021-June 2022. MMWR Morb Mortal Wkly Rep. 2022 Jul 22;71(29):931-939. PubMed PMID: 35862287.
TY - JOUR
T1 - Effectiveness of 2, 3, and 4 COVID-19 mRNA Vaccine Doses Among Immunocompetent Adults During Periods when SARS-CoV-2 Omicron BA.1 and BA.2/BA.2.12.1 Sublineages Predominated - VISION Network, 10 States, December 2021-June 2022.
AU - Link-Gelles,Ruth,
AU - Levy,Matthew E,
AU - Gaglani,Manjusha,
AU - Irving,Stephanie A,
AU - Stockwell,Melissa,
AU - Dascomb,Kristin,
AU - DeSilva,Malini B,
AU - Reese,Sarah E,
AU - Liao,I-Chia,
AU - Ong,Toan C,
AU - Grannis,Shaun J,
AU - McEvoy,Charlene,
AU - Patel,Palak,
AU - Klein,Nicola P,
AU - Hartmann,Emily,
AU - Stenehjem,Edward,
AU - Natarajan,Karthik,
AU - Naleway,Allison L,
AU - Murthy,Kempapura,
AU - Rao,Suchitra,
AU - Dixon,Brian E,
AU - Kharbanda,Anupam B,
AU - Akinseye,Akintunde,
AU - Dickerson,Monica,
AU - Lewis,Ned,
AU - Grisel,Nancy,
AU - Han,Jungmi,
AU - Barron,Michelle A,
AU - Fadel,William F,
AU - Dunne,Margaret M,
AU - Goddard,Kristin,
AU - Arndorfer,Julie,
AU - Konatham,Deepika,
AU - Valvi,Nimish R,
AU - Currey,J C,
AU - Fireman,Bruce,
AU - Raiyani,Chandni,
AU - Zerbo,Ousseny,
AU - Sloan-Aagard,Chantel,
AU - Ball,Sarah W,
AU - Thompson,Mark G,
AU - Tenforde,Mark W,
Y1 - 2022/07/22/
PY - 2022/7/21/entrez
PY - 2022/7/22/pubmed
PY - 2022/7/26/medline
SP - 931
EP - 939
JF - MMWR. Morbidity and mortality weekly report
JO - MMWR Morb Mortal Wkly Rep
VL - 71
IS - 29
N2 - The Omicron variant (B.1.1.529) of SARS-CoV-2, the virus that causes COVID-19, was first identified in the United States in November 2021, with the BA.1 sublineage (including BA.1.1) causing the largest surge in COVID-19 cases to date. Omicron sublineages BA.2 and BA.2.12.1 emerged later and by late April 2022, accounted for most cases.* Estimates of COVID-19 vaccine effectiveness (VE) can be reduced by newly emerging variants or sublineages that evade vaccine-induced immunity (1), protection from previous SARS-CoV-2 infection in unvaccinated persons (2), or increasing time since vaccination (3). Real-world data comparing VE during the periods when the BA.1 and BA.2/BA.2.12.1 predominated (BA.1 period and BA.2/BA.2.12.1 period, respectively) are limited. The VISION network† examined 214,487 emergency department/urgent care (ED/UC) visits and 58,782 hospitalizations with a COVID-19-like illness§ diagnosis among 10 states during December 18, 2021-June 10, 2022, to evaluate VE of 2, 3, and 4 doses of mRNA COVID-19 vaccines (BNT162b2 [Pfizer-BioNTech] or mRNA-1273 [Moderna]) compared with no vaccination among adults without immunocompromising conditions. VE against COVID-19-associated hospitalization 7-119 days and ≥120 days after receipt of dose 3 was 92% (95% CI = 91%-93%) and 85% (95% CI = 81%-89%), respectively, during the BA.1 period, compared with 69% (95% CI = 58%-76%) and 52% (95% CI = 44%-59%), respectively, during the BA.2/BA.2.12.1 period. Patterns were similar for ED/UC encounters. Among adults aged ≥50 years, VE against COVID-19-associated hospitalization ≥120 days after receipt of dose 3 was 55% (95% CI = 46%-62%) and ≥7 days (median = 27 days) after a fourth dose was 80% (95% CI = 71%-85%) during BA.2/BA.2.12.1 predominance. Immunocompetent persons should receive recommended COVID-19 booster doses to prevent moderate to severe COVID-19, including a first booster dose for all eligible persons and second booster dose for adults aged ≥50 years at least 4 months after an initial booster dose. Booster doses should be obtained immediately when persons become eligible.¶.
SN - 1545-861X
UR - https://www.unboundmedicine.com/medline/citation/35862287/Effectiveness_of_2_3_and_4_COVID_19_mRNA_Vaccine_Doses_Among_Immunocompetent_Adults_During_Periods_when_SARS_CoV_2_Omicron_BA_1_and_BA_2/BA_2_12_1_Sublineages_Predominated___VISION_Network_10_States_December_2021_June_2022_
DB - PRIME
DP - Unbound Medicine
ER -