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Temporal rank of clinical characteristics and prognosis of anti‐N‐methyl‐d‐aspartate receptor encephalitis

OBJECTIVES: Early recognition and intervention of patients with the anti‐N‐methyl‐d‐aspartate receptor (NMDAR) encephalitis are important to achieve a better prognosis. The study aims to summarize the real‐world perspectives of anti‐NMDAR encephalitis patients in China via electronic medical records...

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Autores principales: Yang, Runnan, Ge, Fenfen, Jiang, Jingwen, Wang, Yue, Wan, Mengtong, Zhang, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413795/
https://www.ncbi.nlm.nih.gov/pubmed/34232562
http://dx.doi.org/10.1002/brb3.2277
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author Yang, Runnan
Ge, Fenfen
Jiang, Jingwen
Wang, Yue
Wan, Mengtong
Zhang, Wei
author_facet Yang, Runnan
Ge, Fenfen
Jiang, Jingwen
Wang, Yue
Wan, Mengtong
Zhang, Wei
author_sort Yang, Runnan
collection PubMed
description OBJECTIVES: Early recognition and intervention of patients with the anti‐N‐methyl‐d‐aspartate receptor (NMDAR) encephalitis are important to achieve a better prognosis. The study aims to summarize the real‐world perspectives of anti‐NMDAR encephalitis patients in China via electronic medical records (EMRs). METHODS: Using EMRs of patients from 2013 to 2019 from West China Hospital in China, a retrospective research was conducted to demonstrate the temporary rank of clinical characteristics and disease prognosis of anti‐NMDAR encephalitis. The modified Rankin Scale (mRS) scores were used to divide the anti‐NMDAR‐encephalitis into two groups (poor prognosis vs. good prognosis). Chi‐square test and logistic regression were used to analyze factors associated with prognosis. RESULTS: Here, 78 patients were included. The most common clinical characteristics are cognitive dysfunction (86.0%) and thought disorder (86.0%). Cognitive dysfunction, thought disorder, and seizures tended to appear soon after prodrome symptoms. Logistics analysis results showed that cognitive dysfunction (OR = 4.48, 95% CI = 1.09–18.47), the score of (GCS ≤ 8) (OR = 4.52, 95% CI = 1.18–17.32), positive antibodies in serum (OR = 4.89, 95% CI = 1.19–20.13) and delay immunotherapy (OR = 4.76, 95% CI = 1.79–12.60) were risk factors of poor clinical outcomes. CONCLUSIONS: There are two peaks in the development of autoimmune encephalitis (AE). The first peak is cognitive dysfunction, and the second peak is autonomic dysfunction. Cognitive dysfunction and GCS score ≤8 at admission, antibodies positive in serum, and delay immunotherapy were risk factors for a poor prognosis at discharge.
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spelling pubmed-84137952021-09-07 Temporal rank of clinical characteristics and prognosis of anti‐N‐methyl‐d‐aspartate receptor encephalitis Yang, Runnan Ge, Fenfen Jiang, Jingwen Wang, Yue Wan, Mengtong Zhang, Wei Brain Behav Original Research OBJECTIVES: Early recognition and intervention of patients with the anti‐N‐methyl‐d‐aspartate receptor (NMDAR) encephalitis are important to achieve a better prognosis. The study aims to summarize the real‐world perspectives of anti‐NMDAR encephalitis patients in China via electronic medical records (EMRs). METHODS: Using EMRs of patients from 2013 to 2019 from West China Hospital in China, a retrospective research was conducted to demonstrate the temporary rank of clinical characteristics and disease prognosis of anti‐NMDAR encephalitis. The modified Rankin Scale (mRS) scores were used to divide the anti‐NMDAR‐encephalitis into two groups (poor prognosis vs. good prognosis). Chi‐square test and logistic regression were used to analyze factors associated with prognosis. RESULTS: Here, 78 patients were included. The most common clinical characteristics are cognitive dysfunction (86.0%) and thought disorder (86.0%). Cognitive dysfunction, thought disorder, and seizures tended to appear soon after prodrome symptoms. Logistics analysis results showed that cognitive dysfunction (OR = 4.48, 95% CI = 1.09–18.47), the score of (GCS ≤ 8) (OR = 4.52, 95% CI = 1.18–17.32), positive antibodies in serum (OR = 4.89, 95% CI = 1.19–20.13) and delay immunotherapy (OR = 4.76, 95% CI = 1.79–12.60) were risk factors of poor clinical outcomes. CONCLUSIONS: There are two peaks in the development of autoimmune encephalitis (AE). The first peak is cognitive dysfunction, and the second peak is autonomic dysfunction. Cognitive dysfunction and GCS score ≤8 at admission, antibodies positive in serum, and delay immunotherapy were risk factors for a poor prognosis at discharge. John Wiley and Sons Inc. 2021-07-07 /pmc/articles/PMC8413795/ /pubmed/34232562 http://dx.doi.org/10.1002/brb3.2277 Text en © 2021 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Yang, Runnan
Ge, Fenfen
Jiang, Jingwen
Wang, Yue
Wan, Mengtong
Zhang, Wei
Temporal rank of clinical characteristics and prognosis of anti‐N‐methyl‐d‐aspartate receptor encephalitis
title Temporal rank of clinical characteristics and prognosis of anti‐N‐methyl‐d‐aspartate receptor encephalitis
title_full Temporal rank of clinical characteristics and prognosis of anti‐N‐methyl‐d‐aspartate receptor encephalitis
title_fullStr Temporal rank of clinical characteristics and prognosis of anti‐N‐methyl‐d‐aspartate receptor encephalitis
title_full_unstemmed Temporal rank of clinical characteristics and prognosis of anti‐N‐methyl‐d‐aspartate receptor encephalitis
title_short Temporal rank of clinical characteristics and prognosis of anti‐N‐methyl‐d‐aspartate receptor encephalitis
title_sort temporal rank of clinical characteristics and prognosis of anti‐n‐methyl‐d‐aspartate receptor encephalitis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8413795/
https://www.ncbi.nlm.nih.gov/pubmed/34232562
http://dx.doi.org/10.1002/brb3.2277
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