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      SARS-CoV-2 spread and hospitalisations in paediatric patients during the omicron surge

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      The Lancet. Child & Adolescent Health
      Elsevier Ltd

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          Abstract

          The omicron (B.1.1.529) variant of SARS-CoV-2 was first reported to WHO on Nov 24, 2021, and designated a variant of concern 2 days later. 1 Since then, the variant has been detected in many countries and is causing new surges in the COVID-19 pandemic, which has now lasted for over 2 years. In Europe and the Americas, WHO data indicate that spread of the omicron variant has resulted in 5–6 times more confirmed COVID-19 cases during the reporting weeks of Jan 10 and Jan 17, 2022, compared with highest peaks reported in previous waves. The rapid spread of omicron is attributed to multiple mutations on the spike protein that might have conferred increased host-cell receptor binding affinity and the increased ability to escape immunity induced by COVID-19 vaccination and previous infection. 2 Host-cell analysis using pseudotyped SARS-CoV-2 spike proteins indicated that these mutations might have resulted in the omicron variant being more infectious than the delta (B.1.617.2) variant and other variants of concern.2, 3 In The Lancet Child & Adolescent Health, a study by Jeané Cloete and colleagues, 4 published performed in Tshwane District of South Africa, found a rapid increase in paediatric COVID-19-related admissions to hospital (hereafter, hospitalisations) during the 6-week period from Oct 31 to Dec 11, 2021. The rapid increase in hospitalisations was accompanied by widespread community transmission of the omicron variant, as shown by COVID-19 surveillance data from multiple sources and genomic sequencing data. Although the overall number of COVID-19-associated hospitalisations in Tshwane District were lower than in previous waves, admissions among children and adolescents aged 1 years and younger were higher than at any other time during the pandemic. The authors hypothesise that this increase was due to the higher transmission potential of the omicron variant, less frequent facemask wearing among children than adults, and low vaccination rate in the paediatric population, with only children aged 12 years and older being eligible for vaccination at the time of study. Among hospitalised paediatric patients (aged ≤13 years) with a primary COVID-19 diagnosis, seizures were reported in 19 (31%) of 138 patients, with only a small number having comorbid conditions (eg, epilepsy [n=1] and cerebral palsy [n=1]) that explained the seizure manifestations. 4 In a separate multinational study of neurological manifestations by Fink and colleagues, 5 seizures were reported in 108 (8·5%) of 1278 children hospitalised with COVID-19. The study included patients from 30 centres across North and South America. Although Fink and colleagues' study predates the omicron wave of the COVID-19 pandemic, it highlighted that seizures were not previously described as a common manifestation of COVID-19 in children. Whether or not seizures, as reported by Cloete and colleagues, are more common with the omicron variant than with the other variants of concern should be further investigated. Although several studies have shown that the omicron wave is associated with a lower hospitalisation rate per infection than previous COVID-19 waves, primarily because of milder illness, the number of paediatric patients with omicron in many countries is surpassing the number of paediatric COVID-19 cases seen in those previous waves.6, 7, 8 The current study, consistent with previous research, shows the possibility that a large increase in the number of COVID-19 cases, even if milder on average, can increase the absolute number of paediatric patients with severe outcomes. 4 These conditions can overwhelm an already strained health-care system, and be further exacerbated during seasonal increases of expected respiratory illness among children. The emergence and rapid spread of the omicron variant highlights the need to continue to bolster genomic surveillance of SARS-CoV-2, information sharing among global partners, equitable use of COVID-19 vaccination worldwide, and increased vaccine access for paediatric populations. There is a need to investigate clinical manifestations and severity of infection, including risk factors associated with severe paediatric illness, so that both treatment and prevention measures can be improved. Continuing simultaneous application of public health measures during times of high transmission is essential to minimise the burden of illness among children, including vaccine administration for children, prompt testing and isolation of infected individuals, and wider application of preventive measures such as facemask wearing, hand hygiene, cleaning, and ventilation of indoor spaces. We declare no competing interests. The findings and conclusions in this Comment are those of the authors and do not necessarily represent the official position of the US Centres for Disease Control and Prevention.

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          The Omicron variant is highly resistant against antibody-mediated neutralization – implications for control of the COVID-19 pandemic

          The rapid spread of the SARS-CoV-2 Omicron variant suggests that the virus might become globally dominant. Further, the high number of mutations in the viral spike-protein raised concerns that the virus might evade antibodies induced by infection or vaccination. Here, we report that the Omicron spike was resistant against most therapeutic antibodies but remained susceptible to inhibition by Sotrovimab. Similarly, the Omicron spike evaded neutralization by antibodies from convalescent or BNT162b2-vaccinated individuals with 10- to 44-fold higher efficiency than the spike of the Delta variant. Neutralization of the Omicron spike by antibodies induced upon heterologous ChAdOx1/BNT162b2-vaccination or vaccination with three doses of BNT162b2 was more efficient, but the Omicron spike still evaded neutralization more efficiently than the Delta spike. These findings indicate that most therapeutic antibodies will be ineffective against the Omicron variant and that double immunization with BNT162b2 might not adequately protect against severe disease induced by this variant. The SARS-CoV-2 Omicron variant is rapidy spreading worldwide and a public health concern. Experiments show that this variant resistant against several therapeutic antibodies for COVID-19 and efficiently evades antibodies induced upon infection or double BNT162b2 vaccination, however not triple BNT162b2 or ChAdOx1/BNT162b2 vaccination.
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            Omicron variant of SARS‐CoV‐2: Genomics, transmissibility, and responses to current COVID‐19 vaccines

            Abstract Currently, severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has spread worldwide as an Omicron variant. This variant is a heavily mutated virus and designated as a variant of concern by the World Health Organization (WHO). WHO cautioned that the Omicron variant of SARS‐CoV‐2 held a very high risk of infection, reigniting anxieties about the economy's recovery from the 2‐year pandemic. The extensively mutated Omicron variant is likely to spread internationally, posing a high risk of infection surges with serious repercussions in some areas. According to preliminary data, the Omicron variant of SARS‐CoV‐2 has a higher risk of reinfection. On the other hand, whether the current COVID‐19 vaccines could effectively resist the new strain is still under investigation. However, there is very limited information on the current situation of the Omicron variant, such as genomics, transmissibility, efficacy of vaccines, treatment, and management. This review focused on the genomics, transmission, and effectiveness of vaccines against the Omicron variant, which will be helpful for further investigation of a new variant of SARS‐CoV‐2.
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              Is Open Access

              Trends in Disease Severity and Health Care Utilization During the Early Omicron Variant Period Compared with Previous SARS-CoV-2 High Transmission Periods — United States, December 2020–January 2022

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                Author and article information

                Journal
                Lancet Child Adolesc Health
                Lancet Child Adolesc Health
                The Lancet. Child & Adolescent Health
                Elsevier Ltd
                2352-4642
                2352-4650
                18 February 2022
                18 February 2022
                Affiliations
                [a ]COVID-19 Response, Centers for Disease Control and Prevention, Atlanta, GA, 30333, USA
                Article
                S2352-4642(22)00060-8
                10.1016/S2352-4642(22)00060-8
                8856665
                35189084
                537ad72f-453a-4b55-80c0-9a83e67e23f8
                Published by Elsevier Ltd.

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

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