Factors influencing the development of infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion

Infantile traumatic brain injury (TBI) with a biphasic clinical course and late reduced diffusion (TBIRD) has been reported as a type of TBI. However, it remains uncertain which pediatric patients with TBI develop TBIRD. Patients with TBI who were admitted to our hospital and underwent magnetic reso...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of the neurological sciences 2024-02, Vol.457, p.122904-122904, Article 122904
Hauptverfasser: Yasukohchi, Madoka, Omata, Taku, Ochiai, Kenta, Sano, Kentaro, Murofushi, Yuka, Kimura, Sho, Takase, Nanako, Honda, Takafumi, Yasukawa, Kumi, Takanashi, Jun-ichi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 122904
container_issue
container_start_page 122904
container_title Journal of the neurological sciences
container_volume 457
creator Yasukohchi, Madoka
Omata, Taku
Ochiai, Kenta
Sano, Kentaro
Murofushi, Yuka
Kimura, Sho
Takase, Nanako
Honda, Takafumi
Yasukawa, Kumi
Takanashi, Jun-ichi
description Infantile traumatic brain injury (TBI) with a biphasic clinical course and late reduced diffusion (TBIRD) has been reported as a type of TBI. However, it remains uncertain which pediatric patients with TBI develop TBIRD. Patients with TBI who were admitted to our hospital and underwent magnetic resonance imaging (MRI) between December 2006 and October 2022 were included in this study. A diagnosis of TBIRD was made in patients with or suspected TBI, with initial symptoms being convulsions or disturbance of consciousness and late-onset subcortical reduced diffusion, the so-called bright tree appearance. Clinical features, neuroimaging (computed tomography (CT) and MRI) findings, laboratory data, and Tada score were retrospectively compared between TBIRD and non-TBIRD patients. Neurological prognosis was assessed using the Pediatric Cerebral Performance Category scale. Of 21 patients who met the inclusion criteria, a diagnosis of TBIRD was made in 7 patients (median age: 8 months). The factors contributing to TBIRD development were seizures lasting over 30 min as the initial symptom (5/7 in TBIRD vs. 0/14 in non-TBIRD), tracheal intubation during initial treatment (5/7 vs. 0/14), and brain parenchymal lesions on CT (3/7 vs. 0/14), suggesting that severe TBI may progress to TBIRD. The Tada score was more positive in patients with TBIRD (6/7) than in those without (0/14). It is important to monitor infant patients with severe TBI for the development of TBIRD. The Tada score can be a useful tool for TBIRD prediction. •TBIRD usually occurs in clinically and radiologically severe infantile TBI.•TBIRD is characterized by a biphasic clinical course and BTA.•Subdural hematoma (SDH) is observed in almost all patients with TBIRD.•Similar to AESD, the Tada score is useful for predicting TBIRD.•SDH and BTA location are differentiating indicators between AESD and TBIRD.
doi_str_mv 10.1016/j.jns.2024.122904
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2920574830</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022510X2400039X</els_id><sourcerecordid>2920574830</sourcerecordid><originalsourceid>FETCH-LOGICAL-c305t-5df1d66e2d9c2e070c1ad20eb9540ddc6c03b21bf3731848e946cd81bb3c8d8f3</originalsourceid><addsrcrecordid>eNp9kDtvFDEUhS0EIpvAD6BBLmlmubbn4REVihKIFIkGJDrLY1-zHs3Yix9BafnlzGoDJdUtzneOdD9C3jDYM2D9-3k_h7znwNs943yE9hnZMTnIppNSPCc7AM6bjsH3C3KZ8wwAvZTjS3Ih5EaLQe7I71ttSkyZ-uCWisH48IOWA1KLD7jE44qh0OhOsQ7FL0hL0nXVxRs6Je3Dlsw1PdJfvhyoppM_HnTeQrP44I1eqIk1ZaQ6WLrogjShrQYttd65mn0Mr8gLp5eMr5_uFfl2e_P1-nNz_-XT3fXH-8YI6ErTWcds3yO3o-EIAximLQecxq4Fa01vQEycTU4MgslW4tj2xko2TcJIK524Iu_Ou8cUf1bMRa0-G1wWHTDWrPjIoRtaKWBD2Rk1Keac0Klj8qtOj4qBOqlXs9rUq5N6dVa_dd4-zddpRfuv8df1Bnw4A7g9-eAxqWz8ZhytT2iKstH_Z_4PktOXUg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2920574830</pqid></control><display><type>article</type><title>Factors influencing the development of infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion</title><source>Access via ScienceDirect (Elsevier)</source><creator>Yasukohchi, Madoka ; Omata, Taku ; Ochiai, Kenta ; Sano, Kentaro ; Murofushi, Yuka ; Kimura, Sho ; Takase, Nanako ; Honda, Takafumi ; Yasukawa, Kumi ; Takanashi, Jun-ichi</creator><creatorcontrib>Yasukohchi, Madoka ; Omata, Taku ; Ochiai, Kenta ; Sano, Kentaro ; Murofushi, Yuka ; Kimura, Sho ; Takase, Nanako ; Honda, Takafumi ; Yasukawa, Kumi ; Takanashi, Jun-ichi</creatorcontrib><description>Infantile traumatic brain injury (TBI) with a biphasic clinical course and late reduced diffusion (TBIRD) has been reported as a type of TBI. However, it remains uncertain which pediatric patients with TBI develop TBIRD. Patients with TBI who were admitted to our hospital and underwent magnetic resonance imaging (MRI) between December 2006 and October 2022 were included in this study. A diagnosis of TBIRD was made in patients with or suspected TBI, with initial symptoms being convulsions or disturbance of consciousness and late-onset subcortical reduced diffusion, the so-called bright tree appearance. Clinical features, neuroimaging (computed tomography (CT) and MRI) findings, laboratory data, and Tada score were retrospectively compared between TBIRD and non-TBIRD patients. Neurological prognosis was assessed using the Pediatric Cerebral Performance Category scale. Of 21 patients who met the inclusion criteria, a diagnosis of TBIRD was made in 7 patients (median age: 8 months). The factors contributing to TBIRD development were seizures lasting over 30 min as the initial symptom (5/7 in TBIRD vs. 0/14 in non-TBIRD), tracheal intubation during initial treatment (5/7 vs. 0/14), and brain parenchymal lesions on CT (3/7 vs. 0/14), suggesting that severe TBI may progress to TBIRD. The Tada score was more positive in patients with TBIRD (6/7) than in those without (0/14). It is important to monitor infant patients with severe TBI for the development of TBIRD. The Tada score can be a useful tool for TBIRD prediction. •TBIRD usually occurs in clinically and radiologically severe infantile TBI.•TBIRD is characterized by a biphasic clinical course and BTA.•Subdural hematoma (SDH) is observed in almost all patients with TBIRD.•Similar to AESD, the Tada score is useful for predicting TBIRD.•SDH and BTA location are differentiating indicators between AESD and TBIRD.</description><identifier>ISSN: 0022-510X</identifier><identifier>EISSN: 1878-5883</identifier><identifier>DOI: 10.1016/j.jns.2024.122904</identifier><identifier>PMID: 38290378</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) ; Bright tree appearance ; Infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion ; Subdural hematoma ; Tada score ; Traumatic brain injury</subject><ispartof>Journal of the neurological sciences, 2024-02, Vol.457, p.122904-122904, Article 122904</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c305t-5df1d66e2d9c2e070c1ad20eb9540ddc6c03b21bf3731848e946cd81bb3c8d8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jns.2024.122904$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>315,781,785,3551,27926,27927,45997</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38290378$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yasukohchi, Madoka</creatorcontrib><creatorcontrib>Omata, Taku</creatorcontrib><creatorcontrib>Ochiai, Kenta</creatorcontrib><creatorcontrib>Sano, Kentaro</creatorcontrib><creatorcontrib>Murofushi, Yuka</creatorcontrib><creatorcontrib>Kimura, Sho</creatorcontrib><creatorcontrib>Takase, Nanako</creatorcontrib><creatorcontrib>Honda, Takafumi</creatorcontrib><creatorcontrib>Yasukawa, Kumi</creatorcontrib><creatorcontrib>Takanashi, Jun-ichi</creatorcontrib><title>Factors influencing the development of infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion</title><title>Journal of the neurological sciences</title><addtitle>J Neurol Sci</addtitle><description>Infantile traumatic brain injury (TBI) with a biphasic clinical course and late reduced diffusion (TBIRD) has been reported as a type of TBI. However, it remains uncertain which pediatric patients with TBI develop TBIRD. Patients with TBI who were admitted to our hospital and underwent magnetic resonance imaging (MRI) between December 2006 and October 2022 were included in this study. A diagnosis of TBIRD was made in patients with or suspected TBI, with initial symptoms being convulsions or disturbance of consciousness and late-onset subcortical reduced diffusion, the so-called bright tree appearance. Clinical features, neuroimaging (computed tomography (CT) and MRI) findings, laboratory data, and Tada score were retrospectively compared between TBIRD and non-TBIRD patients. Neurological prognosis was assessed using the Pediatric Cerebral Performance Category scale. Of 21 patients who met the inclusion criteria, a diagnosis of TBIRD was made in 7 patients (median age: 8 months). The factors contributing to TBIRD development were seizures lasting over 30 min as the initial symptom (5/7 in TBIRD vs. 0/14 in non-TBIRD), tracheal intubation during initial treatment (5/7 vs. 0/14), and brain parenchymal lesions on CT (3/7 vs. 0/14), suggesting that severe TBI may progress to TBIRD. The Tada score was more positive in patients with TBIRD (6/7) than in those without (0/14). It is important to monitor infant patients with severe TBI for the development of TBIRD. The Tada score can be a useful tool for TBIRD prediction. •TBIRD usually occurs in clinically and radiologically severe infantile TBI.•TBIRD is characterized by a biphasic clinical course and BTA.•Subdural hematoma (SDH) is observed in almost all patients with TBIRD.•Similar to AESD, the Tada score is useful for predicting TBIRD.•SDH and BTA location are differentiating indicators between AESD and TBIRD.</description><subject>Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD)</subject><subject>Bright tree appearance</subject><subject>Infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion</subject><subject>Subdural hematoma</subject><subject>Tada score</subject><subject>Traumatic brain injury</subject><issn>0022-510X</issn><issn>1878-5883</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9kDtvFDEUhS0EIpvAD6BBLmlmubbn4REVihKIFIkGJDrLY1-zHs3Yix9BafnlzGoDJdUtzneOdD9C3jDYM2D9-3k_h7znwNs943yE9hnZMTnIppNSPCc7AM6bjsH3C3KZ8wwAvZTjS3Ih5EaLQe7I71ttSkyZ-uCWisH48IOWA1KLD7jE44qh0OhOsQ7FL0hL0nXVxRs6Je3Dlsw1PdJfvhyoppM_HnTeQrP44I1eqIk1ZaQ6WLrogjShrQYttd65mn0Mr8gLp5eMr5_uFfl2e_P1-nNz_-XT3fXH-8YI6ErTWcds3yO3o-EIAximLQecxq4Fa01vQEycTU4MgslW4tj2xko2TcJIK524Iu_Ou8cUf1bMRa0-G1wWHTDWrPjIoRtaKWBD2Rk1Keac0Klj8qtOj4qBOqlXs9rUq5N6dVa_dd4-zddpRfuv8df1Bnw4A7g9-eAxqWz8ZhytT2iKstH_Z_4PktOXUg</recordid><startdate>20240215</startdate><enddate>20240215</enddate><creator>Yasukohchi, Madoka</creator><creator>Omata, Taku</creator><creator>Ochiai, Kenta</creator><creator>Sano, Kentaro</creator><creator>Murofushi, Yuka</creator><creator>Kimura, Sho</creator><creator>Takase, Nanako</creator><creator>Honda, Takafumi</creator><creator>Yasukawa, Kumi</creator><creator>Takanashi, Jun-ichi</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20240215</creationdate><title>Factors influencing the development of infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion</title><author>Yasukohchi, Madoka ; Omata, Taku ; Ochiai, Kenta ; Sano, Kentaro ; Murofushi, Yuka ; Kimura, Sho ; Takase, Nanako ; Honda, Takafumi ; Yasukawa, Kumi ; Takanashi, Jun-ichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c305t-5df1d66e2d9c2e070c1ad20eb9540ddc6c03b21bf3731848e946cd81bb3c8d8f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD)</topic><topic>Bright tree appearance</topic><topic>Infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion</topic><topic>Subdural hematoma</topic><topic>Tada score</topic><topic>Traumatic brain injury</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yasukohchi, Madoka</creatorcontrib><creatorcontrib>Omata, Taku</creatorcontrib><creatorcontrib>Ochiai, Kenta</creatorcontrib><creatorcontrib>Sano, Kentaro</creatorcontrib><creatorcontrib>Murofushi, Yuka</creatorcontrib><creatorcontrib>Kimura, Sho</creatorcontrib><creatorcontrib>Takase, Nanako</creatorcontrib><creatorcontrib>Honda, Takafumi</creatorcontrib><creatorcontrib>Yasukawa, Kumi</creatorcontrib><creatorcontrib>Takanashi, Jun-ichi</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the neurological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yasukohchi, Madoka</au><au>Omata, Taku</au><au>Ochiai, Kenta</au><au>Sano, Kentaro</au><au>Murofushi, Yuka</au><au>Kimura, Sho</au><au>Takase, Nanako</au><au>Honda, Takafumi</au><au>Yasukawa, Kumi</au><au>Takanashi, Jun-ichi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Factors influencing the development of infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion</atitle><jtitle>Journal of the neurological sciences</jtitle><addtitle>J Neurol Sci</addtitle><date>2024-02-15</date><risdate>2024</risdate><volume>457</volume><spage>122904</spage><epage>122904</epage><pages>122904-122904</pages><artnum>122904</artnum><issn>0022-510X</issn><eissn>1878-5883</eissn><abstract>Infantile traumatic brain injury (TBI) with a biphasic clinical course and late reduced diffusion (TBIRD) has been reported as a type of TBI. However, it remains uncertain which pediatric patients with TBI develop TBIRD. Patients with TBI who were admitted to our hospital and underwent magnetic resonance imaging (MRI) between December 2006 and October 2022 were included in this study. A diagnosis of TBIRD was made in patients with or suspected TBI, with initial symptoms being convulsions or disturbance of consciousness and late-onset subcortical reduced diffusion, the so-called bright tree appearance. Clinical features, neuroimaging (computed tomography (CT) and MRI) findings, laboratory data, and Tada score were retrospectively compared between TBIRD and non-TBIRD patients. Neurological prognosis was assessed using the Pediatric Cerebral Performance Category scale. Of 21 patients who met the inclusion criteria, a diagnosis of TBIRD was made in 7 patients (median age: 8 months). The factors contributing to TBIRD development were seizures lasting over 30 min as the initial symptom (5/7 in TBIRD vs. 0/14 in non-TBIRD), tracheal intubation during initial treatment (5/7 vs. 0/14), and brain parenchymal lesions on CT (3/7 vs. 0/14), suggesting that severe TBI may progress to TBIRD. The Tada score was more positive in patients with TBIRD (6/7) than in those without (0/14). It is important to monitor infant patients with severe TBI for the development of TBIRD. The Tada score can be a useful tool for TBIRD prediction. •TBIRD usually occurs in clinically and radiologically severe infantile TBI.•TBIRD is characterized by a biphasic clinical course and BTA.•Subdural hematoma (SDH) is observed in almost all patients with TBIRD.•Similar to AESD, the Tada score is useful for predicting TBIRD.•SDH and BTA location are differentiating indicators between AESD and TBIRD.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>38290378</pmid><doi>10.1016/j.jns.2024.122904</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-510X
ispartof Journal of the neurological sciences, 2024-02, Vol.457, p.122904-122904, Article 122904
issn 0022-510X
1878-5883
language eng
recordid cdi_proquest_miscellaneous_2920574830
source Access via ScienceDirect (Elsevier)
subjects Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD)
Bright tree appearance
Infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion
Subdural hematoma
Tada score
Traumatic brain injury
title Factors influencing the development of infantile traumatic brain injury with a biphasic clinical course and late reduced diffusion
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T11%3A44%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Factors%20influencing%20the%20development%20of%20infantile%20traumatic%20brain%20injury%20with%20a%20biphasic%20clinical%20course%20and%20late%20reduced%20diffusion&rft.jtitle=Journal%20of%20the%20neurological%20sciences&rft.au=Yasukohchi,%20Madoka&rft.date=2024-02-15&rft.volume=457&rft.spage=122904&rft.epage=122904&rft.pages=122904-122904&rft.artnum=122904&rft.issn=0022-510X&rft.eissn=1878-5883&rft_id=info:doi/10.1016/j.jns.2024.122904&rft_dat=%3Cproquest_cross%3E2920574830%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2920574830&rft_id=info:pmid/38290378&rft_els_id=S0022510X2400039X&rfr_iscdi=true