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SOP: antibody-associated autoimmune encephalitis

BACKGROUND: Antibody-mediated and paraneoplastic autoimmune encephalitides (AE) present with a broad spectrum of clinical symptoms. They often lead to progressing inflammatory changes of the central nervous system with subacute onset and can cause persistent brain damage. Thus, to promptly start the...

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Autores principales: Rössling, Rosa, Prüss, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650054/
https://www.ncbi.nlm.nih.gov/pubmed/33324907
http://dx.doi.org/10.1186/s42466-019-0048-7
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author Rössling, Rosa
Prüss, Harald
author_facet Rössling, Rosa
Prüss, Harald
author_sort Rössling, Rosa
collection PubMed
description BACKGROUND: Antibody-mediated and paraneoplastic autoimmune encephalitides (AE) present with a broad spectrum of clinical symptoms. They often lead to progressing inflammatory changes of the central nervous system with subacute onset and can cause persistent brain damage. Thus, to promptly start the appropriate and AE-specific therapy, recognition of symptoms, initiation of relevant antibody diagnostics and confirmation of the clinical diagnosis are crucial, in particular as the diseases are relatively rare. AIM: This standard operating procedure (SOP) should draw attention to the clinical presentation of AE, support the diagnostic approach to patients with suspected AE and guide through the necessary steps including therapeutic decisions, tumour screening and exclusion of differential diagnoses. METHOD: Based on existing diagnostic algorithms, treatment recommendations and personal experiences, this SOP gives an overview of clinical presentation, diagnostic procedures and therapy in AE. Additional information is provided within an accompanying text and a table describing the most important autoantibodies and their characteristics. RESULTS: The initial steps of the AE flow chart are based on clinical symptoms and the patient’s history. Assignment to paraneoplastic or antibody-mediated AE is sometimes clinically possible. Diagnostics should include MRI, EEG and CSF analysis with antibody panel diagnostic. Definite AE can be diagnosed if the underlying antibody is compatible with the clinical presentation. Classification of probable AE may be possible even with negative anti-neuronal autoantibodies if the clinical presentation and laboratory abnormalities are highly suggestive of AE. The confirmed AE diagnosis requires immediate initiation of immunotherapy. CONCLUSION: The SOP facilitates the recognition of patients with AE and presents the necessary diagnostic and therapeutic steps.
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spelling pubmed-76500542020-12-14 SOP: antibody-associated autoimmune encephalitis Rössling, Rosa Prüss, Harald Neurol Res Pract Standard Operating Procedure BACKGROUND: Antibody-mediated and paraneoplastic autoimmune encephalitides (AE) present with a broad spectrum of clinical symptoms. They often lead to progressing inflammatory changes of the central nervous system with subacute onset and can cause persistent brain damage. Thus, to promptly start the appropriate and AE-specific therapy, recognition of symptoms, initiation of relevant antibody diagnostics and confirmation of the clinical diagnosis are crucial, in particular as the diseases are relatively rare. AIM: This standard operating procedure (SOP) should draw attention to the clinical presentation of AE, support the diagnostic approach to patients with suspected AE and guide through the necessary steps including therapeutic decisions, tumour screening and exclusion of differential diagnoses. METHOD: Based on existing diagnostic algorithms, treatment recommendations and personal experiences, this SOP gives an overview of clinical presentation, diagnostic procedures and therapy in AE. Additional information is provided within an accompanying text and a table describing the most important autoantibodies and their characteristics. RESULTS: The initial steps of the AE flow chart are based on clinical symptoms and the patient’s history. Assignment to paraneoplastic or antibody-mediated AE is sometimes clinically possible. Diagnostics should include MRI, EEG and CSF analysis with antibody panel diagnostic. Definite AE can be diagnosed if the underlying antibody is compatible with the clinical presentation. Classification of probable AE may be possible even with negative anti-neuronal autoantibodies if the clinical presentation and laboratory abnormalities are highly suggestive of AE. The confirmed AE diagnosis requires immediate initiation of immunotherapy. CONCLUSION: The SOP facilitates the recognition of patients with AE and presents the necessary diagnostic and therapeutic steps. BioMed Central 2020-01-15 /pmc/articles/PMC7650054/ /pubmed/33324907 http://dx.doi.org/10.1186/s42466-019-0048-7 Text en © The Author(s) 2020 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Standard Operating Procedure
Rössling, Rosa
Prüss, Harald
SOP: antibody-associated autoimmune encephalitis
title SOP: antibody-associated autoimmune encephalitis
title_full SOP: antibody-associated autoimmune encephalitis
title_fullStr SOP: antibody-associated autoimmune encephalitis
title_full_unstemmed SOP: antibody-associated autoimmune encephalitis
title_short SOP: antibody-associated autoimmune encephalitis
title_sort sop: antibody-associated autoimmune encephalitis
topic Standard Operating Procedure
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7650054/
https://www.ncbi.nlm.nih.gov/pubmed/33324907
http://dx.doi.org/10.1186/s42466-019-0048-7
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