Introduction to Non Influenza Respiratory
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In addition, we studied the potential interference between SIV and ILI caused by non-influenza respiratory viruses (NIRV) based on data collated from 2017/18 to 2019/20 seasons.
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Increasing evidence indicates that non-influenza respiratory viruses (NIRV) also contribute to the burden of SARI.
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Increasing evidence indicates that non-influenza respiratory viruses (NIRVs) also contribute to the burden of SARI.
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Conclusions Patients infected with SARS-CoV-2 along with a non-influenza respiratory virus had less severe disease on presentation and were more likely to be admitted—but did not have more severe outcomes—than those infected with SARS-CoV-2 alone.
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The authors come to the curious conclusion that patients infected with SARS-CoV-2 along with a non-influenza respiratory virus had less-severe disease on presentation and did not have more severe outcomes than those infected with SARS-CoV-2 alone.
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CONCLUSIONS
Influenza vaccination coverage over eight seasons among outpatients with non-influenza respiratory illness was slightly higher than coverage in the general population but 15% lower than national targets.
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Background
Although influenza vaccines provide protection against influenza viruses, concern has been raised that they may increase susceptibility to non-influenza respiratory viruses.
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OBJECTIVE
We evaluated the incidence of influenza and non-influenza respiratory viruses (NIRVs) pre-/post-implementation of public health (PH) measures aimed to decrease COVID-19 transmission using population-based surveillance data.
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Although broad knowledge of influenza viral pneumonia has been established, the significance of non-influenza respiratory viruses in community-acquired pneumonia (CAP) and their impact on clinical outcomes remains unclear, especially in the non-immunocompromised adult population.
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Transmission of non-influenza respiratory viruses in households can inform preventative interventions and has not been well-characterised in South Asia.
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All samples were tested for RSV A and B using real-time polymerase chain reaction for non-influenza respiratory viruses.
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Conclusions
Non-influenza respiratory microorganisms frequently co-circulated during the epidemic peaks of influenza, which easily being ignored in CAP therapy.
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Respondents were asked to (1) rate daily workload increase as 60 minutes in response to five exposure (lice/scabies, mumps/measles, pertussis, tuberculosis, influenza) and outbreak scenarios (methicillin-resistant Staphylococcus aureus, other multidrug-resistant organisms, non-influenza respiratory viruses, Clostridium difficile, gastrointestinal viruses), and (2) rank most time consuming activities during exposure/outbreak responses.
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CONCLUSIONS
This study revealed that non-influenza respiratory viruses were a major contributor to ILI.
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Patients with a non-influenza respiratory virus were less likely to experience severe clinical outcomes than patients with A/H1, however, had similar likelihood when compared to patients with A/H3.
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Background The population-based incidence and burden of community-onset non-influenza respiratory viruses associated with hospitalization in adults has not been systematically assessed.
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