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Delayed encephalopathy after COVID-19: A case series of six patients

Acute encephalopathy is a severe neurological complication of coronavirus disease 2019 (COVID-19). Most cases of acute encephalopathy associated with COVID-19 occur within several weeks of COVID-19 onset. We describe a case series of 6 patients who developed delayed encephalopathy (DE) after COVID-1...

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Autores principales: Akimoto, Takayoshi, Hara, Makoto, Tasaki, Kenta, Kurosawa, Yusuke, Nakamoto, Tadaharu, Hirose, Satoshi, Mizoguchi, Tomotaka, Yokota, Yuki, Ninomiya, Satoko, Nakajima, Hideto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592135/
https://www.ncbi.nlm.nih.gov/pubmed/36281140
http://dx.doi.org/10.1097/MD.0000000000031029
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author Akimoto, Takayoshi
Hara, Makoto
Tasaki, Kenta
Kurosawa, Yusuke
Nakamoto, Tadaharu
Hirose, Satoshi
Mizoguchi, Tomotaka
Yokota, Yuki
Ninomiya, Satoko
Nakajima, Hideto
author_facet Akimoto, Takayoshi
Hara, Makoto
Tasaki, Kenta
Kurosawa, Yusuke
Nakamoto, Tadaharu
Hirose, Satoshi
Mizoguchi, Tomotaka
Yokota, Yuki
Ninomiya, Satoko
Nakajima, Hideto
author_sort Akimoto, Takayoshi
collection PubMed
description Acute encephalopathy is a severe neurological complication of coronavirus disease 2019 (COVID-19). Most cases of acute encephalopathy associated with COVID-19 occur within several weeks of COVID-19 onset. We describe a case series of 6 patients who developed delayed encephalopathy (DE) after COVID-19. PATIENT CONCERNS AND DIAGNOSES: We evaluated patients who recovered from COVID-19 and showed acute disturbance of consciousness or focal neurological deficits without recurrence of pneumonitis. Six patients, 2 females and 4 males, with ages ranging from 65 to 83 years were included. Durations of hospitalization due to COVID-19 were between 25 and 44 days. The severity of COVID-19 was moderate in 5 and severe in 1 patient. Patients were rehospitalized for acute disturbance of consciousness concomitant with postural tremor and, abnormal behavior, hemiplegia, aphasia, or apraxia between 34 and 67 days after the onset of COVID-19. Chest computed tomography showed no exacerbation of pneumonitis. Brain magnetic resonance imaging showed no specific findings except in 1 patient with an acute lacunar infarction. Electroencephalogram demonstrated diffuse slowing in all patients. Repeat electroencephalogram after recovery from encephalopathy demonstrated normal in all patients. One of the 6 patients had cerebrospinal fluid (CSF) pleocytosis. CSF protein levels were elevated in all patients, ranging from 51 to 115 mg/dL. CSF interleukin-6 levels ranged from 2.9 to 10.9 pg/mL. The immunoglobulin index was 0.39 to 0.44. Qlim(alb) < QAlb indicating dysfunction of the blood–brain barrier was observed in all patients. Severe acute respiratory syndrome coronavirus 2 reverse transcription polymerase chain reaction of CSF was negative in all patients. Neuronal autoantibodies were absent in serum and CSF. INTERVENTIONS AND OUTCOMES: Immunotherapy including steroid pulses was administered to 3 patients; however, symptoms of encephalopathy resolved within several days in all patients, regardless of treatment with immunotherapy, and their consciousness levels were recovered fully. Notably, postural tremor remained for 2 weeks to 7 months. LESSONS: In our patients, DE after COVID-19 was characterized by symptoms of acute encephalopathy accompanied with tremor in the absence of worsening pneumonitis after the fourth week of COVID-19 onset. Our findings indicate blood–brain barrier dysfunction may contribute to the pathogenesis of DE after COVID-19.
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spelling pubmed-95921352022-10-25 Delayed encephalopathy after COVID-19: A case series of six patients Akimoto, Takayoshi Hara, Makoto Tasaki, Kenta Kurosawa, Yusuke Nakamoto, Tadaharu Hirose, Satoshi Mizoguchi, Tomotaka Yokota, Yuki Ninomiya, Satoko Nakajima, Hideto Medicine (Baltimore) 5300 Acute encephalopathy is a severe neurological complication of coronavirus disease 2019 (COVID-19). Most cases of acute encephalopathy associated with COVID-19 occur within several weeks of COVID-19 onset. We describe a case series of 6 patients who developed delayed encephalopathy (DE) after COVID-19. PATIENT CONCERNS AND DIAGNOSES: We evaluated patients who recovered from COVID-19 and showed acute disturbance of consciousness or focal neurological deficits without recurrence of pneumonitis. Six patients, 2 females and 4 males, with ages ranging from 65 to 83 years were included. Durations of hospitalization due to COVID-19 were between 25 and 44 days. The severity of COVID-19 was moderate in 5 and severe in 1 patient. Patients were rehospitalized for acute disturbance of consciousness concomitant with postural tremor and, abnormal behavior, hemiplegia, aphasia, or apraxia between 34 and 67 days after the onset of COVID-19. Chest computed tomography showed no exacerbation of pneumonitis. Brain magnetic resonance imaging showed no specific findings except in 1 patient with an acute lacunar infarction. Electroencephalogram demonstrated diffuse slowing in all patients. Repeat electroencephalogram after recovery from encephalopathy demonstrated normal in all patients. One of the 6 patients had cerebrospinal fluid (CSF) pleocytosis. CSF protein levels were elevated in all patients, ranging from 51 to 115 mg/dL. CSF interleukin-6 levels ranged from 2.9 to 10.9 pg/mL. The immunoglobulin index was 0.39 to 0.44. Qlim(alb) < QAlb indicating dysfunction of the blood–brain barrier was observed in all patients. Severe acute respiratory syndrome coronavirus 2 reverse transcription polymerase chain reaction of CSF was negative in all patients. Neuronal autoantibodies were absent in serum and CSF. INTERVENTIONS AND OUTCOMES: Immunotherapy including steroid pulses was administered to 3 patients; however, symptoms of encephalopathy resolved within several days in all patients, regardless of treatment with immunotherapy, and their consciousness levels were recovered fully. Notably, postural tremor remained for 2 weeks to 7 months. LESSONS: In our patients, DE after COVID-19 was characterized by symptoms of acute encephalopathy accompanied with tremor in the absence of worsening pneumonitis after the fourth week of COVID-19 onset. Our findings indicate blood–brain barrier dysfunction may contribute to the pathogenesis of DE after COVID-19. Lippincott Williams & Wilkins 2022-10-21 /pmc/articles/PMC9592135/ /pubmed/36281140 http://dx.doi.org/10.1097/MD.0000000000031029 Text en Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle 5300
Akimoto, Takayoshi
Hara, Makoto
Tasaki, Kenta
Kurosawa, Yusuke
Nakamoto, Tadaharu
Hirose, Satoshi
Mizoguchi, Tomotaka
Yokota, Yuki
Ninomiya, Satoko
Nakajima, Hideto
Delayed encephalopathy after COVID-19: A case series of six patients
title Delayed encephalopathy after COVID-19: A case series of six patients
title_full Delayed encephalopathy after COVID-19: A case series of six patients
title_fullStr Delayed encephalopathy after COVID-19: A case series of six patients
title_full_unstemmed Delayed encephalopathy after COVID-19: A case series of six patients
title_short Delayed encephalopathy after COVID-19: A case series of six patients
title_sort delayed encephalopathy after covid-19: a case series of six patients
topic 5300
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9592135/
https://www.ncbi.nlm.nih.gov/pubmed/36281140
http://dx.doi.org/10.1097/MD.0000000000031029
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