Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory Data

Background: Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) often causes various neurological sequelae, necessitating early and objective differentiation of AESD from a febrile seizure (FS). Therefore, we developed a scoring system that predicts AESD onset using only ea...

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Main Authors: Masanori Maeda, Tohru Okanishi, Yosuke Miyamoto, Takuya Hayashida, Tatsuya Kawaguchi, Sotaro Kanai, Yoshiaki Saito, Yoshihiro Maegaki
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-11-01
Series:Frontiers in Neurology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fneur.2021.730535/full
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author Masanori Maeda
Masanori Maeda
Tohru Okanishi
Yosuke Miyamoto
Yosuke Miyamoto
Takuya Hayashida
Takuya Hayashida
Tatsuya Kawaguchi
Sotaro Kanai
Yoshiaki Saito
Yoshiaki Saito
Yoshihiro Maegaki
author_facet Masanori Maeda
Masanori Maeda
Tohru Okanishi
Yosuke Miyamoto
Yosuke Miyamoto
Takuya Hayashida
Takuya Hayashida
Tatsuya Kawaguchi
Sotaro Kanai
Yoshiaki Saito
Yoshiaki Saito
Yoshihiro Maegaki
author_sort Masanori Maeda
collection DOAJ
description Background: Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) often causes various neurological sequelae, necessitating early and objective differentiation of AESD from a febrile seizure (FS). Therefore, we developed a scoring system that predicts AESD onset using only early laboratory data.Methods: We selected patients with AESD or FS admitted to the Tottori University Hospital between November 2005 and September 2020 and collected laboratory data from onset to discharge in patients with FS and from onset to the second neurological events in patients with AESD.Results: We identified 18 patients with AESD and 181 patients with FS. In comparison with patients with FS, patients with AESD showed statistically significant increases in ammonia (NH3), blood sugar (BS), and serum creatinine (Cr) levels, and the white blood cell (WBC) count, and a significant decrease in pH at <3 h from onset. We set the cut-off values and adjusted the weight of each of these parameters based on data obtained <3 h from onset and proposed a scoring system for predicting AESD. This system showed 91% sensitivity and 94% specificity for distinguishing AESD from FS. These accuracies were only slightly improved by the addition of information related to consciousness and seizure duration (sensitivity, 91%; specificity, 96%).Conclusion: NH3, BS, and Cr levels, WBC count, and pH were significantly different between patients with AESD and patients with FS at <3 h from seizure onset. This scoring system using these data may enable the prediction of AESD onset for patients under sedation or without precise clinical information.
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spelling doaj.art-30c8d6659220406c8283b69a88a70a252022-12-21T23:09:12ZengFrontiers Media S.A.Frontiers in Neurology1664-22952021-11-011210.3389/fneur.2021.730535730535Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory DataMasanori Maeda0Masanori Maeda1Tohru Okanishi2Yosuke Miyamoto3Yosuke Miyamoto4Takuya Hayashida5Takuya Hayashida6Tatsuya Kawaguchi7Sotaro Kanai8Yoshiaki Saito9Yoshiaki Saito10Yoshihiro Maegaki11Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, JapanDepartment of Pediatrics, Wakayama Medical University, Wakayama, JapanDivision of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, JapanDivision of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, JapanDepartment of Pediatrics, Kyoto Prefectural University of Medicine, Kyoto, JapanDivision of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, JapanDepartment of Pediatrics, Nagasaki University, Nagasaki, JapanDivision of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, JapanDivision of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, JapanDivision of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, JapanDivision of Child Neurology, Saiseikai Yokohama City Tobu Hospital, Yokohama, JapanDivision of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, JapanBackground: Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) often causes various neurological sequelae, necessitating early and objective differentiation of AESD from a febrile seizure (FS). Therefore, we developed a scoring system that predicts AESD onset using only early laboratory data.Methods: We selected patients with AESD or FS admitted to the Tottori University Hospital between November 2005 and September 2020 and collected laboratory data from onset to discharge in patients with FS and from onset to the second neurological events in patients with AESD.Results: We identified 18 patients with AESD and 181 patients with FS. In comparison with patients with FS, patients with AESD showed statistically significant increases in ammonia (NH3), blood sugar (BS), and serum creatinine (Cr) levels, and the white blood cell (WBC) count, and a significant decrease in pH at <3 h from onset. We set the cut-off values and adjusted the weight of each of these parameters based on data obtained <3 h from onset and proposed a scoring system for predicting AESD. This system showed 91% sensitivity and 94% specificity for distinguishing AESD from FS. These accuracies were only slightly improved by the addition of information related to consciousness and seizure duration (sensitivity, 91%; specificity, 96%).Conclusion: NH3, BS, and Cr levels, WBC count, and pH were significantly different between patients with AESD and patients with FS at <3 h from seizure onset. This scoring system using these data may enable the prediction of AESD onset for patients under sedation or without precise clinical information.https://www.frontiersin.org/articles/10.3389/fneur.2021.730535/fullacute encephalopathybiphasic seizuresdiffusionchildrenearly diagnosislaboratory data
spellingShingle Masanori Maeda
Masanori Maeda
Tohru Okanishi
Yosuke Miyamoto
Yosuke Miyamoto
Takuya Hayashida
Takuya Hayashida
Tatsuya Kawaguchi
Sotaro Kanai
Yoshiaki Saito
Yoshiaki Saito
Yoshihiro Maegaki
Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory Data
Frontiers in Neurology
acute encephalopathy
biphasic seizures
diffusion
children
early diagnosis
laboratory data
title Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory Data
title_full Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory Data
title_fullStr Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory Data
title_full_unstemmed Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory Data
title_short Predicting the Onset of Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion by Using Early Laboratory Data
title_sort predicting the onset of acute encephalopathy with biphasic seizures and late reduced diffusion by using early laboratory data
topic acute encephalopathy
biphasic seizures
diffusion
children
early diagnosis
laboratory data
url https://www.frontiersin.org/articles/10.3389/fneur.2021.730535/full
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