scholarly journals Adverse reactions to Pfizer‐BioNTech vaccination of healthcare workers at Malta’s state hospital

Author(s):  
Sarah Cuschieri ◽  
Michael Borg ◽  
Steve Agius ◽  
Jorgen Souness ◽  
Andre Brincat ◽  
...  
2021 ◽  
Vol 36 (21) ◽  
Author(s):  
Yun Woo Lee ◽  
So Yun Lim ◽  
Ji-Hyang Lee ◽  
Joon Seo Lim ◽  
Miseo Kim ◽  
...  

2011 ◽  
Vol 4 (1) ◽  
Author(s):  
Harald Bias ◽  
David Quarcoo ◽  
Claus Meier-Wronski ◽  
Sabine Wicker ◽  
Joachim Seybold ◽  
...  

2020 ◽  
Author(s):  
Alberto Borobia ◽  
Irene García-García ◽  
Lucía Díaz-García ◽  
Amelia Rodríguez-Mariblanca ◽  
Lucía Martínez de Soto ◽  
...  

BACKGROUND In April 2020, two independent clinical trials (CT) to assess SARS-Cov-2 prophylaxis in healthcare workers were started in our Hospital: MeCOVID (melatonin vs placebo) and EPICOS (tenofovir disoproxil/emtricitabine vs hydroxychloroquine vs the combination of both vs placebo). OBJECTIVE We aim to evaluate the motivations to participate and the reasons to choose one or another. METHODS Both CTs were offered to personnel through the internal news bulletin. After the screening visit, all subjects were asked to answer a web-based survey. RESULTS In the first month, 206 healthcare workers were screened and 160 randomized. Survey participation was quite high, 73.3%. The main motivation to participate was “to contribute to scientific knowledge” 53.0%, followed by “to avoid SARS-Cov-2 infection” and “the interest to be tested for SARS-CoV-2”. We found differences between physicians and nurses in the expected personal benefits (P<0.05). The vast majority of the volunteers selected the MeCOVID study, the main reason was the fear of adverse reactions associated with treatments in EPICOS, 69.4%. CONCLUSIONS Healthcare workers´ motivations to participate in prophylaxis trials in a pandemic context appear to be driven mostly by their desire to contribute to science and getting some health benefits. Safety seems to weight way more than efficacy to choose between CTs.


2021 ◽  
Vol 36 (17) ◽  
Author(s):  
Seongman Bae ◽  
Yun Woo Lee ◽  
So Yun Lim ◽  
Ji-Hyang Lee ◽  
Joon Seo Lim ◽  
...  

Author(s):  
Filippos Filippatos ◽  
Elizabeth-Barbara Tatsi ◽  
Charilaos Dellis ◽  
Nick Dessypris ◽  
Vassiliki Syriopoulou ◽  
...  

Open Medicine ◽  
2016 ◽  
Vol 11 (1) ◽  
pp. 482-488 ◽  
Author(s):  
Taku Ogawa ◽  
Fukumi Uchiyama-Nakamura ◽  
Aiko Sugata-Tsubaki ◽  
Yutaka Yamada ◽  
Kenji Uno ◽  
...  

AbstractThe purpose of this study was to examine the efficacy rendered with a single dose of live attenuated measles, rubella, mumps, and varicella containing vaccine.We inoculated healthcare workers (HCWs) with a single dose of vaccine to a disease lacking in antibody titer for those not meeting the criteria of our hospital (measles: <16.0 (IgG enzyme immunoassay (EIA)), rubella: ≤1:32 (hemagglutination-inhibition), mumps: <4.0 (IgG EIA), and varicella: <4.0 (IgG EIA)). At 28–60 days after vaccination, the antibody titer was tested again.We included 48 HCWs. A total of 32, 15, 31, and 10 individuals were inoculated with a single dose of measles-containing, rubella-containing, mumps, or varicella vaccine, respectively, and showed significant antibody elevation (9.2 ± 12.3 to 27.6 ± 215.6, p<0.001; 8 ± 1.2 to 32 ± 65.5, p<0.001; 3.0 ± 1.0 to 13.1 ± 8.6, p<0.05; and 2.6 ± 1.3 to 11.8 ± 8.1, p<0.001, respectively). Major side effects were not observed.In a limited population, a single dose of live attenuated vaccine showed elevation of antibody titer without any severe adverse reactions. However, whether the post-vaccination response rate criteria of our university was fulfilled could not be determined owing to limited sample size.


2021 ◽  
Author(s):  
Masaaki Takeuchi ◽  
Yukie Higa ◽  
Akina Esaki ◽  
Yosuke Nabeshima ◽  
Akemi Nakazono

Adverse reactions are more common after the second injection of messenger RNA vaccines such as Pfizer/BioNTech's BNT162b2. We hypothesized that the degree and severity of reactogenicity after the second injection reflects the magnitude of antibody production against the SARS CoV-2 virus spike protein (spike IgG). Blood samples were obtained from 67 healthy Japanese healthcare workers three weeks after the first injection and two weeks after the second injection of the BNT162b2 vaccine to measure spike IgG levels. Using questionnaires, we calculated an adverse event (AE) score (0-11) for each participant. The geometric mean of spike IgG titers increased from 1,047 antibody units (AU/mL) (95% CI: 855±1282 AU/mL) after the first injection to 17,378 AU/mL (14,622±20,663 AU/mL) after the second injection. The median AE score increased from 2 to 5. Spike IgG levels after the second injection were negatively correlated with age and positively correlated with spike IgG after the first injection. AE scores after the second injection were not significantly associated with log-transformed spike IgG after the second injection, when adjusted for age, sex, and log-transformed spike IgG after the first injection. Although the sample size was relatively small, reactogenicity after the second injection may not accurately reflect antibody production.


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