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Effect of vaccination on the case fatality rate for COVID-19 infections 2020-2021: multivariate modelling of data from the US Department of Veterans Affairs.
Murata, Glen H; Murata, Allison E; Perkins, Douglas J; Campbell, Heather M; Mao, Jenny T; Wagner, Brent; McMahon, Benjamin H; Hagedorn, Curt H.
  • Murata GH; Research Service, New Mexico VA Health Care System, Albuquerque, New Mexico, USA.
  • Murata AE; Clinical Research Pharmacy Coordinating Center, VHA Cooperative Studies Program, Albuquerque, New Mexico, USA.
  • Perkins DJ; Center for Global Health, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA.
  • Campbell HM; Clinical Research Pharmacy Coordinating Center, VHA Cooperative Studies Program, Albuquerque, New Mexico, USA.
  • Mao JT; Medicine Service, New Mexico VA Health Care System, Albuquerque, New Mexico, USA.
  • Wagner B; Research Service, New Mexico VA Health Care System, Albuquerque, New Mexico, USA brent.wagner@va.gov.
  • McMahon BH; Medicine Service, New Mexico VA Health Care System, Albuquerque, New Mexico, USA.
  • Hagedorn CH; Kidney Institute of New Mexico, University of New Mexico Health Sciences Center, Albuquerque, New Mexico, USA.
BMJ Open ; 12(12): e064135, 2022 12 23.
Article in English | MEDLINE | ID: covidwho-2193776
ABSTRACT

OBJECTIVES:

To evaluate the benefits of vaccination on the case fatality rate (CFR) for COVID-19 infections. DESIGN, SETTING AND

PARTICIPANTS:

The US Department of Veterans Affairs has 130 medical centres. We created multivariate models from these data-339 772 patients with COVID-19-as of 30 September 2021. OUTCOME

MEASURES:

The primary outcome for all models was death within 60 days of the diagnosis. Logistic regression was used to derive adjusted ORs for vaccination and infection with Delta versus earlier variants. Models were adjusted for confounding factors, including demographics, comorbidity indices and novel parameters representing prior diagnoses, vital signs/baseline laboratory tests and outpatient treatments. Patients with a Delta infection were divided into eight cohorts based on the time from vaccination to diagnosis. A common model was used to estimate the odds of death associated with vaccination for each cohort relative to that of unvaccinated patients.

RESULTS:

9.1% of subjects were vaccinated. 21.5% had the Delta variant. 18 120 patients (5.33%) died within 60 days of their diagnoses. The adjusted OR for a Delta infection was 1.87±0.05, which corresponds to a relative risk (RR) of 1.78. The overall adjusted OR for prior vaccination was 0.280±0.011 corresponding to an RR of 0.291. Raw CFR rose steadily after 10-14 weeks. The OR for vaccination remained stable for 10-34 weeks.

CONCLUSIONS:

Our CFR model controls for the severity of confounding factors and priority of vaccination, rather than solely using the presence of comorbidities. Our results confirm that Delta was more lethal than earlier variants and that vaccination is an effective means of preventing death. After adjusting for major selection biases, we found no evidence that the benefits of vaccination on CFR declined over 34 weeks. We suggest that this model can be used to evaluate vaccines designed for emerging variants.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Veterans / Hepatitis D / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: BMJ Open Year: 2022 Document Type: Article Affiliation country: Bmjopen-2022-064135

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Veterans / Hepatitis D / COVID-19 Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Topics: Vaccines / Variants Limits: Humans Language: English Journal: BMJ Open Year: 2022 Document Type: Article Affiliation country: Bmjopen-2022-064135