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Waning of vaccine effectiveness against moderate and severe covid-19 among adults in the US from the VISION network: test negative, case-control study.
Ferdinands, Jill M; Rao, Suchitra; Dixon, Brian E; Mitchell, Patrick K; DeSilva, Malini B; Irving, Stephanie A; Lewis, Ned; Natarajan, Karthik; Stenehjem, Edward; Grannis, Shaun J; Han, Jungmi; McEvoy, Charlene; Ong, Toan C; Naleway, Allison L; Reese, Sarah E; Embi, Peter J; Dascomb, Kristin; Klein, Nicola P; Griggs, Eric P; Liao, I-Chia; Yang, Duck-Hye; Fadel, William F; Grisel, Nancy; Goddard, Kristin; Patel, Palak; Murthy, Kempapura; Birch, Rebecca; Valvi, Nimish R; Arndorfer, Julie; Zerbo, Ousseny; Dickerson, Monica; Raiyani, Chandni; Williams, Jeremiah; Bozio, Catherine H; Blanton, Lenee; Link-Gelles, Ruth; Barron, Michelle A; Gaglani, Manjusha; Thompson, Mark G; Fireman, Bruce.
  • Ferdinands JM; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA zdn5@cdc.gov.
  • Rao S; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Dixon BE; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, IN, USA.
  • Mitchell PK; Fairbanks School of Public Health, Indiana University, Indianapolis, IN, USA.
  • DeSilva MB; Westat, Rockville, MD, USA.
  • Irving SA; HealthPartners Institute, Minneapolis, MN, USA.
  • Lewis N; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Natarajan K; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, CA, USA.
  • Stenehjem E; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
  • Grannis SJ; New York Presbyterian Hospital, New York, NY, USA.
  • Han J; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, UT, USA.
  • McEvoy C; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, IN, USA.
  • Ong TC; Indiana University School of Medicine, Indianapolis, IN, USA.
  • Naleway AL; Department of Biomedical Informatics, Columbia University Irving Medical Center, New York, NY, USA.
  • Reese SE; HealthPartners Institute, Minneapolis, MN, USA.
  • Embi PJ; Department of Pediatrics, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
  • Dascomb K; Center for Health Research, Kaiser Permanente Northwest, Portland, OR, USA.
  • Klein NP; Westat, Rockville, MD, USA.
  • Liao IC; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, UT, USA.
  • Yang DH; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, CA, USA.
  • Fadel WF; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
  • Grisel N; Baylor Scott &White Health, Temple, TX, USA.
  • Goddard K; Westat, Rockville, MD, USA.
  • Patel P; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, IN, USA.
  • Murthy K; Fairbanks School of Public Health, Indiana University, Indianapolis, IN, USA.
  • Birch R; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, UT, USA.
  • Valvi NR; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, CA, USA.
  • Arndorfer J; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
  • Zerbo O; Baylor Scott &White Health, Temple, TX, USA.
  • Dickerson M; Westat, Rockville, MD, USA.
  • Raiyani C; Center for Biomedical Informatics, Regenstrief Institute, Indianapolis, IN, USA.
  • Williams J; Division of Infectious Diseases and Clinical Epidemiology, Intermountain Healthcare, Salt Lake City, UT, USA.
  • Bozio CH; Kaiser Permanente Vaccine Study Center, Kaiser Permanente Northern California Division of Research, Oakland, CA, USA.
  • Blanton L; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
  • Link-Gelles R; Baylor Scott &White Health, Temple, TX, USA.
  • Barron MA; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
  • Gaglani M; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
  • Thompson MG; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
  • Fireman B; Centers for Disease Control and Prevention COVID-19 Response Team, Atlanta, GA, USA.
BMJ ; 379: e072141, 2022 10 03.
Article in English | MEDLINE | ID: covidwho-2053175
ABSTRACT

OBJECTIVE:

To estimate the effectiveness of mRNA vaccines against moderate and severe covid-19 in adults by time since second, third, or fourth doses, and by age and immunocompromised status.

DESIGN:

Test negative case-control study.

SETTING:

Hospitals, emergency departments, and urgent care clinics in 10 US states, 17 January 2021 to 12 July 2022.

PARTICIPANTS:

893 461 adults (≥18 years) admitted to one of 261 hospitals or to one of 272 emergency department or 119 urgent care centers for covid-like illness tested for SARS-CoV-2. MAIN OUTCOME

MEASURES:

The main outcome was waning of vaccine effectiveness with BNT162b2 (Pfizer-BioNTech) or mRNA-1273 (Moderna) vaccine during the omicron and delta periods, and the period before delta was dominant using logistic regression conditioned on calendar week and geographic area while adjusting for age, race, ethnicity, local virus circulation, immunocompromised status, and likelihood of being vaccinated.

RESULTS:

45 903 people admitted to hospital with covid-19 (cases) were compared with 213 103 people with covid-like illness who tested negative for SARS-CoV-2 (controls), and 103 287 people admitted to emergency department or urgent care with covid-19 (cases) were compared with 531 168 people with covid-like illness who tested negative for SARS-CoV-2. In the omicron period, vaccine effectiveness against covid-19 requiring admission to hospital was 89% (95% confidence interval 88% to 90%) within two months after dose 3 but waned to 66% (63% to 68%) by four to five months. Vaccine effectiveness of three doses against emergency department or urgent care visits was 83% (82% to 84%) initially but waned to 46% (44% to 49%) by four to five months. Waning was evident in all subgroups, including young adults and individuals who were not immunocompromised; although waning was morein people who were immunocompromised. Vaccine effectiveness increased among most groups after a fourth dose in whom this booster was recommended.

CONCLUSIONS:

Effectiveness of mRNA vaccines against moderate and severe covid-19 waned with time after vaccination. The findings support recommendations for a booster dose after a primary series and consideration of additional booster doses.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Limits: Adult / Humans / Young adult Language: English Journal: BMJ Journal subject: Medicine Year: 2022 Document Type: Article Affiliation country: Bmj-2022-072141

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 Type of study: Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines / Variants Limits: Adult / Humans / Young adult Language: English Journal: BMJ Journal subject: Medicine Year: 2022 Document Type: Article Affiliation country: Bmj-2022-072141