Effectiveness of Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccines for Preventing Coronavirus Disease 2019 Hospitalizations in the United States. (6th August 2021)
- Record Type:
- Journal Article
- Title:
- Effectiveness of Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccines for Preventing Coronavirus Disease 2019 Hospitalizations in the United States. (6th August 2021)
- Main Title:
- Effectiveness of Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccines for Preventing Coronavirus Disease 2019 Hospitalizations in the United States
- Authors:
- Tenforde, Mark W
Patel, Manish M
Ginde, Adit A
Douin, David J
Talbot, H Keipp
Casey, Jonathan D
Mohr, Nicholas M
Zepeski, Anne
Gaglani, Manjusha
McNeal, Tresa
Ghamande, Shekhar
Shapiro, Nathan I
Gibbs, Kevin W
Files, D Clark
Hager, David N
Shehu, Arber
Prekker, Matthew E
Erickson, Heidi L
Exline, Matthew C
Gong, Michelle N
Mohamed, Amira
Henning, Daniel J
Steingrub, Jay S
Peltan, Ithan D
Brown, Samuel M
Martin, Emily T
Monto, Arnold S
Khan, Akram
Hough, Catherine L
Busse, Laurence W
ten Lohuis, Caitlin C
Duggal, Abhijit
Wilson, Jennifer G
Gordon, Alexandra June
Qadir, Nida
Chang, Steven Y
Mallow, Christopher
Gershengorn, Hayley B
Babcock, Hilary M
Kwon, Jennie H
Halasa, Natasha
Chappell, James D
Lauring, Adam S
Grijalva, Carlos G
Rice, Todd W
Jones, Ian D
Stubblefield, William B
Baughman, Adrienne
Womack, Kelsey N
Lindsell, Christopher J
Hart, Kimberly W
Zhu, Yuwei
Olson, Samantha M
Stephenson, Meagan
Schrag, Stephanie J
Kobayashi, Miwako
Verani, Jennifer R
Self, Wesley H
… (more) - Abstract:
- Abstract: Background: As severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination coverage increases in the United States, there is a need to understand the real-world effectiveness against severe coronavirus disease 2019 (COVID-19) and among people at increased risk for poor outcomes. Methods: In a multicenter case-control analysis of US adults hospitalized March 11–May 5, 2021, we evaluated vaccine effectiveness to prevent COVID-19 hospitalizations by comparing odds of prior vaccination with a messenger RNA (mRNA) vaccine (Pfizer-BioNTech or Moderna) between cases hospitalized with COVID-19 and hospital-based controls who tested negative for SARS-CoV-2. Results: Among 1212 participants, including 593 cases and 619 controls, median age was 58 years, 22.8% were Black, 13.9% were Hispanic, and 21.0% had immunosuppression. SARS-CoV-2 lineage B0.1.1.7 (Alpha) was the most common variant (67.9% of viruses with lineage determined). Full vaccination (receipt of 2 vaccine doses ≥14 days before illness onset) had been received by 8.2% of cases and 36.4% of controls. Overall vaccine effectiveness was 87.1% (95% confidence interval [CI], 80.7–91.3). Vaccine effectiveness was similar for Pfizer-BioNTech and Moderna vaccines, and highest in adults aged 18–49 years (97.4%; 95% CI, 79.3–9.7). Among 45 patients with vaccine-breakthrough COVID hospitalizations, 44 (97.8%) were ≥50 years old and 20 (44.4%) had immunosuppression. Vaccine effectiveness was lower among patientsAbstract: Background: As severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination coverage increases in the United States, there is a need to understand the real-world effectiveness against severe coronavirus disease 2019 (COVID-19) and among people at increased risk for poor outcomes. Methods: In a multicenter case-control analysis of US adults hospitalized March 11–May 5, 2021, we evaluated vaccine effectiveness to prevent COVID-19 hospitalizations by comparing odds of prior vaccination with a messenger RNA (mRNA) vaccine (Pfizer-BioNTech or Moderna) between cases hospitalized with COVID-19 and hospital-based controls who tested negative for SARS-CoV-2. Results: Among 1212 participants, including 593 cases and 619 controls, median age was 58 years, 22.8% were Black, 13.9% were Hispanic, and 21.0% had immunosuppression. SARS-CoV-2 lineage B0.1.1.7 (Alpha) was the most common variant (67.9% of viruses with lineage determined). Full vaccination (receipt of 2 vaccine doses ≥14 days before illness onset) had been received by 8.2% of cases and 36.4% of controls. Overall vaccine effectiveness was 87.1% (95% confidence interval [CI], 80.7–91.3). Vaccine effectiveness was similar for Pfizer-BioNTech and Moderna vaccines, and highest in adults aged 18–49 years (97.4%; 95% CI, 79.3–9.7). Among 45 patients with vaccine-breakthrough COVID hospitalizations, 44 (97.8%) were ≥50 years old and 20 (44.4%) had immunosuppression. Vaccine effectiveness was lower among patients with immunosuppression (62.9%; 95% CI, 20.8–82.6) than without immunosuppression (91.3%; 95% CI, 85.6–94.8). Conclusion: During March–May 2021, SARS-CoV-2 mRNA vaccines were highly effective for preventing COVID-19 hospitalizations among US adults. SARS-CoV-2 vaccination was beneficial for patients with immunosuppression, but effectiveness was lower in the immunosuppressed population. Abstract : From March to May 2021, full vaccination using authorized mRNA products was associated with 87.1% (95% CI, 80.7–91.3) protection against COVID-19 hospitalization among US adults. Vaccine effectiveness was lower in adults with versus without immunosuppression (62.9% versus 91.3%). … (more)
- Is Part Of:
- Clinical infectious diseases. Volume 74:Number 9(2022)
- Journal:
- Clinical infectious diseases
- Issue:
- Volume 74:Number 9(2022)
- Issue Display:
- Volume 74, Issue 9 (2022)
- Year:
- 2022
- Volume:
- 74
- Issue:
- 9
- Issue Sort Value:
- 2022-0074-0009-0000
- Page Start:
- 1515
- Page End:
- 1524
- Publication Date:
- 2021-08-06
- Subjects:
- COVID-19 -- vaccine effectiveness -- mRNA vaccines -- hospitalized -- immunocompromised
Communicable diseases -- Periodicals
616.905 - Journal URLs:
- http://cid.oxfordjournals.org ↗
http://ukcatalogue.oup.com/ ↗
http://www.journals.uchicago.edu/CID/journal ↗
http://www.jstor.org/journals/10584838.html ↗ - DOI:
- 10.1093/cid/ciab687 ↗
- Languages:
- English
- ISSNs:
- 1058-4838
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.293860
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