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Reactogenicity among health care workers following a BNT162b2 or mRNA-1273 second dose after priming with a ChAdOx1 nCOV-19 vaccine.
Baldolli, Aurelie; Fournier, Anna; Verdon, Renaud; Michon, Jocelyn.
  • Baldolli A; CHU de Caen, Department of Infectious Diseases, Caen, France.
  • Fournier A; CHU de Caen, Department of Infectious Diseases, Caen, France; Groupe de Recherche sur l'Adaptation Microbienne, Université Caen Normandie, Caen, France.
  • Verdon R; CHU de Caen, Department of Infectious Diseases, Caen, France; Groupe de Recherche sur l'Adaptation Microbienne, Université Caen Normandie, Caen, France.
  • Michon J; CHU de Caen, Department of Infectious Diseases, Caen, France. Electronic address: jocelynmichon@gmail.com.
Clin Microbiol Infect ; 28(6): 885.e1-885.e5, 2022 Jun.
Article in English | MEDLINE | ID: covidwho-1763660
ABSTRACT

OBJECTIVES:

In March 2021, French authorities recommended a heterologous second dose of the mRNA vaccine for persons aged <55 years, with administration 9 to 12 weeks after the first dose of ChAdOx1 nCoV-19. This recommendation was despite a lack of data on the reactogenicity and safety of the regimen. Since then, several studies have shown an acceptable short-term safety profile of ChAdOx1 nCoV-19 and BNT162b2 heterologous vaccination, although some transient increased reactogenicity has been described.

METHODS:

We performed a single-centre prospective observational cohort study among health care workers (HCWs) at a tertiary care hospital to assess the reactogenicity of the BNT162b2 and mRNA-1273 vaccines administered as a second dose in participants primed with ChAdOx1 nCoV-19.

RESULTS:

Among 1184 HCWs, 356 (30%) agreed to participate. Of the participants, 32.3% were male, and the mean age was 35 years (standard deviation 10.1 years). Of the participants, 229 received BNT162b2 and 127 received mRNA-1273. A systemic reaction was observed in 130 of 229 (56.8%) and 100 of 127 (78.7%) HCWs, respectively. Injection site reactions were generally limited (grade 1 or 2 in 163 of 229 (97.6%) and 90 of 127 (85.7 %) HCWs, respectively). After adjustment for age, sex, and HCW role, receiving the mRNA-1273 vaccine was associated with higher reactogenicity with more grade 3 side effects (adjusted OR (aOR) 3.34; 95% CI, 1.91-5.85), more systemic symptoms (aOR 2.82; 95% CI, 1.69-4.7), and not being able to work (aOR 8.35; 95% CI, 3.78-18.44) compared with receiving the BNT162b2 vaccine.

DISCUSSION:

Among patients receiving the mRNA1273 vaccine as a second dose, our study confirms good tolerance of the heterologous schedule with a higher risk of short-term side effects in comparison with patients receiving the BNT162b2 vaccine.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Health Personnel / COVID-19 Vaccines / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Adult / Female / Humans / Male Language: English Journal: Clin Microbiol Infect Journal subject: Communicable Diseases / Microbiology Year: 2022 Document Type: Article Affiliation country: J.cmi.2022.02.010

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Health Personnel / COVID-19 Vaccines / COVID-19 Type of study: Cohort study / Observational study / Prognostic study Topics: Vaccines Limits: Adult / Female / Humans / Male Language: English Journal: Clin Microbiol Infect Journal subject: Communicable Diseases / Microbiology Year: 2022 Document Type: Article Affiliation country: J.cmi.2022.02.010