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 inBrain & development (Tokyo. 1979) Vol. 44; no. 10; pp. 743 - 747
Main Authors Tetsuhara, Kenichi, Akamine, Satoshi, Matsubara, Yoshie, Fujii, Shunsuke, Kashimada, Wataru, Marutani, Kentaro, Torio, Michiko, Morooka, Yuya, Hanaoka, Nozomu, Fujimoto, Tsuguto, Nakamura-Miwa, Haruna, Arai, Satoru, Tanaka-Taya, Keiko, Furuno, Kenji, Mizuno, Yumi, Kira, Ryutaro
Format Journal Article
LanguageEnglish
Published 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.
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
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  surname: Morooka
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  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
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  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
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  givenname: Ryutaro
  surname: Kira
  fullname: Kira, Ryutaro
  organization: Department of Pediatric Neurology, Fukuoka Children’s Hospital, Fukuoka, Japan
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Issue 10
Keywords Encephalomalacia
Omicron variant
Severe encephalopathy
Neonate
Coronavirus disease 2019 (COVID-19)
Language English
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Snippet 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...
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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
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0387760422001115
https://dx.doi.org/10.1016/j.braindev.2022.06.010
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