Case report: Consecutive hyperbaric oxygen therapy for delayed post-hypoxic leukoencephalopathy resulting from CHANTER syndrome caused by opioid intoxication

Delayed post-hypoxic leukoencephalopathy (DPHL) is a poorly recognized syndrome characterized by neuropsychiatric symptoms following recovery from an acute hypoxic episode. Although most cases are related to carbon monoxide poisoning, some have been linked to excessive opioid use. Opioid intoxicatio...

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Main Authors: Naoto Jingami, Kosai Cho, Takayuki Nitta, Miwa Takatani, Katsuya Kobayashi, Ryo Takenaka, Naoko Sugita, Shigeru Ohtsuru
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-04-01
Series:Frontiers in Medicine
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fmed.2024.1364038/full
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author Naoto Jingami
Naoto Jingami
Naoto Jingami
Kosai Cho
Takayuki Nitta
Miwa Takatani
Katsuya Kobayashi
Ryo Takenaka
Naoko Sugita
Shigeru Ohtsuru
Shigeru Ohtsuru
author_facet Naoto Jingami
Naoto Jingami
Naoto Jingami
Kosai Cho
Takayuki Nitta
Miwa Takatani
Katsuya Kobayashi
Ryo Takenaka
Naoko Sugita
Shigeru Ohtsuru
Shigeru Ohtsuru
author_sort Naoto Jingami
collection DOAJ
description Delayed post-hypoxic leukoencephalopathy (DPHL) is a poorly recognized syndrome characterized by neuropsychiatric symptoms following recovery from an acute hypoxic episode. Although most cases are related to carbon monoxide poisoning, some have been linked to excessive opioid use. Opioid intoxication has recently become known for manifesting the characteristic imaging findings involving cerebellar, hippocampal, and basal nuclei transient edema with restricted diffusion (CHANTER) syndrome. Herein, we present a patient with severe disturbances in consciousness who was initially diagnosed with CO poisoning but was later found to have taken excessive tramadol. Magnetic resonance imaging (MRI) in the acute phase revealed abnormal intensities in the bilateral globus pallidus and the cerebellum, indicative of CHANTER syndrome. After intensive care, his level of consciousness was restored. However, around the 3rd week after hospitalization, his consciousness gradually deteriorated and he developed severe neurological symptoms. Another MRI on day 25 revealed a new diffuse white matter abnormality; DPHL was suspected. Cerebrospinal fluid collected on day 28 revealed significantly elevated myelin basic protein levels. Although it was challenging to decide on a treatment plan, hyperbaric oxygen (HBO) therapy trials were initiated on day 58; the patient's condition improved after a series of HBO sessions. MRI revealed gradual shrinkage of the white matter abnormality. A total of 63 consecutive HBO sessions were performed, leading to the successful resolution of the serious neurological symptoms. While the effectiveness of HBO therapy for DPHL remains inconclusive, especially in opioid-related cases, this patient made a remarkable recovery, likely due to the therapeutic effect of improved cerebral blood flow and oxygenation.
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spelling doaj.art-4acfee989dae424fb7c79f8220f915312024-04-17T04:43:51ZengFrontiers Media S.A.Frontiers in Medicine2296-858X2024-04-011110.3389/fmed.2024.13640381364038Case report: Consecutive hyperbaric oxygen therapy for delayed post-hypoxic leukoencephalopathy resulting from CHANTER syndrome caused by opioid intoxicationNaoto Jingami0Naoto Jingami1Naoto Jingami2Kosai Cho3Takayuki Nitta4Miwa Takatani5Katsuya Kobayashi6Ryo Takenaka7Naoko Sugita8Shigeru Ohtsuru9Shigeru Ohtsuru10Department of Primary Care and Emergency Medicine, Kyoto University Graduate School of Medicine, Kyoto, JapanHyperbaric Oxygen Therapy Center, Kyoto University Hospital, Kyoto, JapanDepartment of Neurology, Kyoto University Graduate School of Medicine, Kyoto, JapanDepartment of Primary Care and Emergency Medicine, Kyoto University Graduate School of Medicine, Kyoto, JapanHyperbaric Oxygen Therapy Center, Kyoto University Hospital, Kyoto, JapanDepartment of Neurology, Kyoto University Graduate School of Medicine, Kyoto, JapanDepartment of Neurology, Kyoto University Graduate School of Medicine, Kyoto, JapanDepartment of Psychiatry, Kyoto University Graduate School of Medicine, Kyoto, JapanDepartment of Psychiatry, Kyoto University Graduate School of Medicine, Kyoto, JapanDepartment of Primary Care and Emergency Medicine, Kyoto University Graduate School of Medicine, Kyoto, JapanHyperbaric Oxygen Therapy Center, Kyoto University Hospital, Kyoto, JapanDelayed post-hypoxic leukoencephalopathy (DPHL) is a poorly recognized syndrome characterized by neuropsychiatric symptoms following recovery from an acute hypoxic episode. Although most cases are related to carbon monoxide poisoning, some have been linked to excessive opioid use. Opioid intoxication has recently become known for manifesting the characteristic imaging findings involving cerebellar, hippocampal, and basal nuclei transient edema with restricted diffusion (CHANTER) syndrome. Herein, we present a patient with severe disturbances in consciousness who was initially diagnosed with CO poisoning but was later found to have taken excessive tramadol. Magnetic resonance imaging (MRI) in the acute phase revealed abnormal intensities in the bilateral globus pallidus and the cerebellum, indicative of CHANTER syndrome. After intensive care, his level of consciousness was restored. However, around the 3rd week after hospitalization, his consciousness gradually deteriorated and he developed severe neurological symptoms. Another MRI on day 25 revealed a new diffuse white matter abnormality; DPHL was suspected. Cerebrospinal fluid collected on day 28 revealed significantly elevated myelin basic protein levels. Although it was challenging to decide on a treatment plan, hyperbaric oxygen (HBO) therapy trials were initiated on day 58; the patient's condition improved after a series of HBO sessions. MRI revealed gradual shrinkage of the white matter abnormality. A total of 63 consecutive HBO sessions were performed, leading to the successful resolution of the serious neurological symptoms. While the effectiveness of HBO therapy for DPHL remains inconclusive, especially in opioid-related cases, this patient made a remarkable recovery, likely due to the therapeutic effect of improved cerebral blood flow and oxygenation.https://www.frontiersin.org/articles/10.3389/fmed.2024.1364038/fullhyperbaric oxygen therapydelayed post-hypoxic leukoencephalopathydelayed neurological sequelaeopioid intoxicationcarbon monoxide
spellingShingle Naoto Jingami
Naoto Jingami
Naoto Jingami
Kosai Cho
Takayuki Nitta
Miwa Takatani
Katsuya Kobayashi
Ryo Takenaka
Naoko Sugita
Shigeru Ohtsuru
Shigeru Ohtsuru
Case report: Consecutive hyperbaric oxygen therapy for delayed post-hypoxic leukoencephalopathy resulting from CHANTER syndrome caused by opioid intoxication
Frontiers in Medicine
hyperbaric oxygen therapy
delayed post-hypoxic leukoencephalopathy
delayed neurological sequelae
opioid intoxication
carbon monoxide
title Case report: Consecutive hyperbaric oxygen therapy for delayed post-hypoxic leukoencephalopathy resulting from CHANTER syndrome caused by opioid intoxication
title_full Case report: Consecutive hyperbaric oxygen therapy for delayed post-hypoxic leukoencephalopathy resulting from CHANTER syndrome caused by opioid intoxication
title_fullStr Case report: Consecutive hyperbaric oxygen therapy for delayed post-hypoxic leukoencephalopathy resulting from CHANTER syndrome caused by opioid intoxication
title_full_unstemmed Case report: Consecutive hyperbaric oxygen therapy for delayed post-hypoxic leukoencephalopathy resulting from CHANTER syndrome caused by opioid intoxication
title_short Case report: Consecutive hyperbaric oxygen therapy for delayed post-hypoxic leukoencephalopathy resulting from CHANTER syndrome caused by opioid intoxication
title_sort case report consecutive hyperbaric oxygen therapy for delayed post hypoxic leukoencephalopathy resulting from chanter syndrome caused by opioid intoxication
topic hyperbaric oxygen therapy
delayed post-hypoxic leukoencephalopathy
delayed neurological sequelae
opioid intoxication
carbon monoxide
url https://www.frontiersin.org/articles/10.3389/fmed.2024.1364038/full
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