Severe encephalopathy associated with SARS-CoV-2 Omicron BA.1 variant infection in a neonate
The coronavirus disease 2019 (COVID-19), including the Omicron variant, is less severe in children than in adults. To date, there has been no detailed description of COVID-19-associated severe encephalopathy due to the Omicron variant during the neonatal and early infantile periods. During the outbr...
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Published in | Brain & development (Tokyo. 1979) Vol. 44; no. 10; pp. 743 - 747 |
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Elsevier B.V
01.11.2022
Published by Elsevier B.V. on behalf of The Japanese Society of Child Neurology |
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Abstract | The coronavirus disease 2019 (COVID-19), including the Omicron variant, is less severe in children than in adults. To date, there has been no detailed description of COVID-19-associated severe encephalopathy due to the Omicron variant during the neonatal and early infantile periods.
During the outbreak of the Omicron variant, a 29-day-old male presented with a pale and ill appearance. The patient was intubated for mechanical ventilation owing to recurrent apnea, which subsequently turned out to be a breath-holding that may have been caused by seizure. In addition, nonconvulsive status epilepticus was observed. Total duration of repetitive seizure activities was approximately 30 min per hour when seizures were most severe. Brain magnetic resonance imaging (MRI) on day 14 revealed extensive hyperintensity in the T2 sequence, hypointensity in the fluid-attenuated inversion recovery (FLAIR) sequence in the deep and subcortical white matter, and diffusion restriction in the corpus callosum. The Omicron BA.1 variant of the severe acute respiratory syndrome coronavirus 2 was detected in his respiratory sample. Follow-up MRI on day 45 revealed multiple cystic cavitations.
Although COVID-19 is not severe in most children, life-threatening conditions such as COVID-19-associated severe encephalopathy can occur during the neonatal and early infantile periods. |
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AbstractList | The coronavirus disease 2019 (COVID-19), including the Omicron variant, is less severe in children than in adults. To date, there has been no detailed description of COVID-19-associated severe encephalopathy due to the Omicron variant during the neonatal and early infantile periods.
During the outbreak of the Omicron variant, a 29-day-old male presented with a pale and ill appearance. The patient was intubated for mechanical ventilation owing to recurrent apnea, which subsequently turned out to be a breath-holding that may have been caused by seizure. In addition, nonconvulsive status epilepticus was observed. Total duration of repetitive seizure activities was approximately 30 min per hour when seizures were most severe. Brain magnetic resonance imaging (MRI) on day 14 revealed extensive hyperintensity in the T2 sequence, hypointensity in the fluid-attenuated inversion recovery (FLAIR) sequence in the deep and subcortical white matter, and diffusion restriction in the corpus callosum. The Omicron BA.1 variant of the severe acute respiratory syndrome coronavirus 2 was detected in his respiratory sample. Follow-up MRI on day 45 revealed multiple cystic cavitations.
Although COVID-19 is not severe in most children, life-threatening conditions such as COVID-19-associated severe encephalopathy can occur during the neonatal and early infantile periods. The coronavirus disease 2019 (COVID-19), including the Omicron variant, is less severe in children than in adults. To date, there has been no detailed description of COVID-19-associated severe encephalopathy due to the Omicron variant during the neonatal and early infantile periods.INTRODUCTIONThe coronavirus disease 2019 (COVID-19), including the Omicron variant, is less severe in children than in adults. To date, there has been no detailed description of COVID-19-associated severe encephalopathy due to the Omicron variant during the neonatal and early infantile periods.During the outbreak of the Omicron variant, a 29-day-old male presented with a pale and ill appearance. The patient was intubated for mechanical ventilation owing to recurrent apnea, which subsequently turned out to be a breath-holding that may have been caused by seizure. In addition, nonconvulsive status epilepticus was observed. Total duration of repetitive seizure activities was approximately 30 min per hour when seizures were most severe. Brain magnetic resonance imaging (MRI) on day 14 revealed extensive hyperintensity in the T2 sequence, hypointensity in the fluid-attenuated inversion recovery (FLAIR) sequence in the deep and subcortical white matter, and diffusion restriction in the corpus callosum. The Omicron BA.1 variant of the severe acute respiratory syndrome coronavirus 2 was detected in his respiratory sample. Follow-up MRI on day 45 revealed multiple cystic cavitations.CASE PRESENTATIONDuring the outbreak of the Omicron variant, a 29-day-old male presented with a pale and ill appearance. The patient was intubated for mechanical ventilation owing to recurrent apnea, which subsequently turned out to be a breath-holding that may have been caused by seizure. In addition, nonconvulsive status epilepticus was observed. Total duration of repetitive seizure activities was approximately 30 min per hour when seizures were most severe. Brain magnetic resonance imaging (MRI) on day 14 revealed extensive hyperintensity in the T2 sequence, hypointensity in the fluid-attenuated inversion recovery (FLAIR) sequence in the deep and subcortical white matter, and diffusion restriction in the corpus callosum. The Omicron BA.1 variant of the severe acute respiratory syndrome coronavirus 2 was detected in his respiratory sample. Follow-up MRI on day 45 revealed multiple cystic cavitations.Although COVID-19 is not severe in most children, life-threatening conditions such as COVID-19-associated severe encephalopathy can occur during the neonatal and early infantile periods.CONCLUSIONAlthough COVID-19 is not severe in most children, life-threatening conditions such as COVID-19-associated severe encephalopathy can occur during the neonatal and early infantile periods. |
Author | Kira, Ryutaro Kashimada, Wataru Torio, Michiko Fujimoto, Tsuguto Matsubara, Yoshie Fujii, Shunsuke Marutani, Kentaro Morooka, Yuya Tanaka-Taya, Keiko Nakamura-Miwa, Haruna Furuno, Kenji Akamine, Satoshi Hanaoka, Nozomu Arai, Satoru Tetsuhara, Kenichi Mizuno, Yumi |
Author_xml | – sequence: 1 givenname: Kenichi surname: Tetsuhara fullname: Tetsuhara, Kenichi email: ken-tetsuhara@mti.biglobe.ne.jp organization: Department of Critical Care Medicine, Fukuoka Children’s Hospital, Fukuoka, Japan – sequence: 2 givenname: Satoshi surname: Akamine fullname: Akamine, Satoshi organization: Department of Pediatric Neurology, Fukuoka Children’s Hospital, Fukuoka, Japan – sequence: 3 givenname: Yoshie surname: Matsubara fullname: Matsubara, Yoshie organization: Department of Pediatric Neurology, Fukuoka Children’s Hospital, Fukuoka, Japan – sequence: 4 givenname: Shunsuke surname: Fujii fullname: Fujii, Shunsuke organization: Department of Critical Care Medicine, Fukuoka Children’s Hospital, Fukuoka, Japan – sequence: 5 givenname: Wataru surname: Kashimada fullname: Kashimada, Wataru organization: Department of Cardiology, Fukuoka Children’s Hospital, Fukuoka, Japan – sequence: 6 givenname: Kentaro surname: Marutani fullname: Marutani, Kentaro organization: Department of Critical Care Medicine, Fukuoka Children’s Hospital, Fukuoka, Japan – sequence: 7 givenname: Michiko surname: Torio fullname: Torio, Michiko organization: Department of Pediatric Neurology, Fukuoka Children’s Hospital, Fukuoka, Japan – sequence: 8 givenname: Yuya surname: Morooka fullname: Morooka, Yuya organization: Department of General Pediatrics and Interdisciplinary Medicine, Fukuoka Children’s Hospital, Fukuoka, Japan – sequence: 9 givenname: Nozomu surname: Hanaoka fullname: Hanaoka, Nozomu organization: Center for Emergency Preparedness and Response, National Institute of Infectious Diseases, Tokyo, Japan – sequence: 10 givenname: Tsuguto surname: Fujimoto fullname: Fujimoto, Tsuguto organization: Center for Emergency Preparedness and Response, National Institute of Infectious Diseases, Tokyo, Japan – sequence: 11 givenname: Haruna surname: Nakamura-Miwa fullname: Nakamura-Miwa, Haruna organization: Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan – sequence: 12 givenname: Satoru surname: Arai fullname: Arai, Satoru organization: Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan – sequence: 13 givenname: Keiko surname: Tanaka-Taya fullname: Tanaka-Taya, Keiko organization: Center for Surveillance, Immunization, and Epidemiologic Research, National Institute of Infectious Diseases, Tokyo, Japan – sequence: 14 givenname: Kenji surname: Furuno fullname: Furuno, Kenji organization: Department of General Pediatrics and Interdisciplinary Medicine, Fukuoka Children’s Hospital, Fukuoka, Japan – sequence: 15 givenname: Yumi surname: Mizuno fullname: Mizuno, Yumi organization: Department of Pediatric Infectious Disease and Immunology, Fukuoka Children's Hospital, Fukuoka, Japan – sequence: 16 givenname: Ryutaro surname: Kira fullname: Kira, Ryutaro organization: Department of Pediatric Neurology, Fukuoka Children’s Hospital, Fukuoka, Japan |
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Keywords | Encephalomalacia Omicron variant Severe encephalopathy Neonate Coronavirus disease 2019 (COVID-19) |
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SubjectTerms | Case Report Coronavirus disease 2019 (COVID-19) Encephalomalacia Neonate Omicron variant Severe encephalopathy |
Title | Severe encephalopathy associated with SARS-CoV-2 Omicron BA.1 variant infection in a neonate |
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