[Articles] Global, regional, and national burden of upper respiratory infections and otitis media, 1990–2021: a systematic analysis from the Global Burden of Disease Study 2021

Di |2024-09-10T00:30:06+02:00Settembre 10th, 2024|Categorie: Coronavirus Lancet|

The findings of this study highlight the widespread burden posed by URIs and otitis media across all age groups and both sexes. There is a continued need for surveillance, prevention, and management to better understand and reduce the burden associated...

[Articles] Health outcomes 3 months and 6 months after molnupiravir treatment for COVID-19 for people at higher risk in the community (PANORAMIC): a randomised controlled trial

Di |2024-09-10T00:30:05+02:00Settembre 10th, 2024|Categorie: Coronavirus Lancet|

In a vaccinated population, people treated with molnupiravir for acute COVID-19 felt better, experienced fewer and less severe COVID-19 associated symptoms, accessed health care less often, and took less time off work at 6 months. However, the absolute...

[Articles] Safety and immunogenicity of mRNA-based seasonal influenza vaccines formulated to include multiple A/H3N2 strains with or without the B/Yamagata strain in US adults aged 50–75 years: a phase 1/2, open-label, randomised trial

Di |2024-09-06T00:30:00+02:00Settembre 6th, 2024|Categorie: Coronavirus Lancet|

These data support the continued clinical development of mRNA-based next-generation seasonal influenza vaccines with broadened influenza A/H3N2 strain coverage.

[Articles] The evidence base for the optimal antibiotic treatment duration of upper and lower respiratory tract infections: an umbrella review

Di |2024-09-05T00:30:02+02:00Settembre 5th, 2024|Categorie: Coronavirus Lancet|

The available evidence for non-ICU CAP and AECOPD supports a short-course treatment duration of 5 days in patients who have clinically improved. Efforts of the scientific community should be directed at implementing this evidence in daily practice. Hig...

[Articles] Safety and immunogenicity of a live-attenuated chikungunya virus vaccine in endemic areas of Brazil: interim results of a double-blind, randomised, placebo-controlled phase 3 trial in adolescents

Di |2024-09-05T00:30:01+02:00Settembre 5th, 2024|Categorie: Coronavirus Lancet|

VLA1553 was generally safe and induced seroprotective titres in almost all vaccinated adolescents with favourable safety data in adolescents who were seropositive at baseline. The data support the use of VLA1553 for the prevention of disease caused by ...

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