Prognoses of Acute Encephalopathy

  • Kurihara Mana
    Department of Pediatrics, the Kanagawa Rehabilitation Center Department of Pediatrics, Jikei University School of Medicine
  • Kohagizawa Toshitaka
    Department of Pediatrics, the Kanagawa Rehabilitation Center Department of Pediatrics, Jikei University School of Medicine
  • Yoshihashi Manabu
    Department of Pediatrics, the Kanagawa Rehabilitation Center
  • Iino Chieko
    Department of Pediatrics, the Kanagawa Rehabilitation Center
  • Anzai Rie
    Department of Pediatrics, the Kanagawa Rehabilitation Center
  • Ida Hiroyuki
    Department of Pediatrics, Jikei University School of Medicine

Bibliographic Information

Other Title
  • 急性脳症後遺症の検討

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Description

  We investigated the prognoses of 103 children with acute encephalopathy at more than one year from the onset. The patients were divided into five groups according to the clinical courses during the acute stage: group 1: 1 case with metabolic disorder, group, 2: 24 with cytokine storms, group, 3: 68 with prolonged convulsion more than 30 minutes, group, 4: 5 with severe refractory status epilepticus, and group, 5: 5 with the main symptom of impaired consciousness. We checked the past histories, etiologies, severities of consciousness loss, complications and disabilities including higher cortical dysfunction in their medical charts. The average age of onset in all cases was 3 years, with the highest age of 6 years 5 months in group 4. Regarding the past histories, febrile seizures, asthma and theophylline medication were prominent though they were not significantly different. Regarding etiologies, influenza infection, 36 cases, and HHV-6 infection, 7 cases, were prominent though they were not significantly different. Complicating disabilities comprised mental retardation, 89.3%, higher cortical dysfunction, 77.7%, epilepsies, 68.9%, and motor disturbance, 27.2%. The severity of disabilities increased in the order of 1, 2, 3, 4, 5. Attention deficit and visiospacial disturbance were the main symptoms of higher cortical dysfunction.

Journal

  • NO TO HATTATSU

    NO TO HATTATSU 43 (4), 285-290, 2011

    The Japanese Society of Child Neurology

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