Subscribe to RSS
DOI: 10.1055/s-0044-1788586
Brazilian consensus recommendations on the diagnosis and treatment of autoimmune encephalitis in the adult and pediatric populations
Consenso brasileiro sobre o diagnóstico e o tratamento de encefalites autoimunes nas populações adulta e pediátricaAbstract
Background Autoimmune encephalitis (AIE) is a group of inflammatory diseases characterized by the presence of antibodies against neuronal and glial antigens, leading to subacute psychiatric symptoms, memory complaints, and movement disorders. The patients are predominantly young, and delays in treatment are associated with worse prognosis.
Objective With the support of the Brazilian Academy of Neurology (Academia Brasileira de Neurologia, ABN) and the Brazilian Society of Child Neurology (Sociedade Brasileira de Neurologia Infantil, SBNI), a consensus on the diagnosis and treatment of AIE in Brazil was developed using the Delphi method.
Methods A total of 25 panelists, including adult and child neurologists, participated in the study.
Results The panelists agreed that patients fulfilling criteria for possible AIE should be screened for antineuronal antibodies in the serum and cerebrospinal fluid (CSF) using the tissue-based assay (TBA) and cell-based assay (CBA) techniques. Children should also be screened for anti-myelin oligodendrocyte glucoprotein antibodies (anti-MOG). Treatment should be started within the first 4 weeks of symptoms. The first-line option is methylprednisolone plus intravenous immunoglobulin (IVIG) or plasmapheresis, the second-line includes rituximab and/or cyclophosphamide, while third-line treatment options are bortezomib and tocilizumab. Most seizures in AIE are symptomatic, and antiseizure medications may be weaned after the acute stage. In anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis, the panelists have agreed that oral immunosuppressant agents should not be used. Patients should be evaluated at the acute and postacute stages using functional and cognitive scales, such as the Mini-Mental State Examination (MMSE), the Montreal Cognitive Assessment (MoCA), the Modified Rankin Scale (mRS), and the Clinical Assessment Scale in Autoimmune Encephalitis (CASE).
Conclusion The present study provides tangible evidence for the effective management of AIE patients within the Brazilian healthcare system.
Resumo
Antecedentes Encefalites autoimunes (EAIs) são um grupo de doenças inflamatórias caracterizadas pela presença de anticorpos contra antígenos neuronais e gliais, que ocasionam sintomas psiquiátricos subagudos, queixas de memória e distúrbios anormais do movimento. A maioria dos pacientes é jovem, e o atraso no tratamento está associado a pior prognóstico.
Objetivo Com o apoio da Academia Brasileira de Neurologia (ABN) e da Sociedade Brasileira de Neurologia Infantil (SBNI), desenvolvemos um consenso sobre o diagnóstico e o tratamento da EAIs no Brasil utilizando a metodologia Delphi.
Métodos Um total de 25 especialistas, incluindo neurologistas e neurologistas infantis, foram convidados a participar.
Resultados Os especialistas concordaram que os pacientes com critérios de possíveis EAIs devem ser submetidos ao rastreio de anticorpos antineuronais no soro e no líquido cefalorraquidiano (LCR) por meio das técnicas de ensaio baseado em tecidos (tissue-based assay, TBA, em inglês) e ensaio baseado em células (cell-based assay, CBA, em inglês). As crianças também devem ser submetidas ao rastreio de de anticorpo contra a glicoproteína da mielina de oligodendrócitos (anti-myelin oligodendrocyte glycoprotein, anti-MOG, em inglês). O tratamento deve ser iniciado dentro das primeiras 4 semanas dos sintomas, sendo as opções de primeira linha metilprednisolona combinada com imunoglobulina intravenosa (IGIV) ou plasmaférese. O tratamento de segunda linha inclui rituximabe e ciclofosfamida. Bortezomib e tocilizumab são opções de tratamento de terceira linha. A maioria das crises epilépticas nas EAIs são sintomáticas, e os fármacos anticrise podem ser desmamadas após a fase aguda. Em relação à encefalite antirreceptor de N-metil-D-aspartato (anti-N-methyl-D-aspartate receptor, anti-NMDAR, em inglês), os especialistas concordaram que agentes imunossupressores orais não devem ser usados. Os pacientes devem ser avaliados na fase aguda e pós-aguda mediante escalas funcionais e cognitivas, como Mini-Mental State Examination (MMSE), Montreal Cognitive Assessment (MoCA), Modified Rankin Scale (mRS), e Clinical Assessment Scale in Autoimmune Encephalitis (CASE).
Conclusão Esta pesquisa oferece evidências tangíveis do manejo efetivo de pacientes com EAIs no sistema de saúde Brasileiro.
Keywords
Autoimmune Encephalitis - Anti-N-Methyl-D-Aspartate Receptor Encephalitis - Delphi Technique - Rituximab - TocilizumabPalavras-chave
Doenças Autoimunes do Sistema Nervoso - Encefalite Antirreceptor de N-Metil-D-Aspartato - Técnica Delphi - Rituximab - TocilizumabAuthors' Contributions
LAD, PVCS: conceptualization, data curation, formal analysis, investigation, methodology, project administration, supervision, validation, writing of the original draft, and writing – review and editing. JHFF, ACM, FFT, CCFV, DGB, SLAP, TA, LJAR, LPBS, NACS, FVG: conceptualization, methodology, supervision, and writing – review and editing. ADP, BKDC, CCDD, CP, DADV, DSD, FFA, FRS, FTM, GJM, GDS, KL, LFP, MLSFS, MVMG, MBK, MEJH, OGPD, OJMN, PRN, PMP, RMPC, VD: writing – review and editing. All authors approved the final version of the manuscript and agree to be responsible for all aspects of the work.
Publication History
Received: 07 January 2024
Accepted: 27 April 2024
Article published online:
01 August 2024
© 2024. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)
Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
Lívia Almeida Dutra, Pedro Victor de Castro Silva, João Henrique Fregadolli Ferreira, Alexandre Coelho Marques, Fabio Fieni Toso, Claudia Cristina Ferreira Vasconcelos, Doralina Guimarães Brum, Samira Luisa dos Apóstolos Pereira, Tarso Adoni, Leticia Januzi de Almeida Rocha, Leticia Pereira de Brito Sampaio, Nise Alessandra de Carvalho Sousa, Renata Barbosa Paolilo, Angélica Dal Pizzol, Bruna Klein da Costa, Caio César Diniz Disserol, Camila Pupe, Daniel Almeida do Valle, Denise Sisterolli Diniz, Fabiano Ferreira de Abrantes, Felipe da Rocha Schmidt, Fernando Cendes, Francisco Tomaz Meneses de Oliveira, Gabriela Joca Martins, Guilherme Diogo Silva, Katia Lin, Lécio Figueira Pinto, Mara Lúcia Schimtz Ferreira Santos, Marcus Vinícius Magno Gonçalves, Mariana Braatz Krueger, Michel Elyas Jung Haziot, Orlando Graziani Povoas Barsottini, Osvaldo José Moreira do Nascimento, Paulo Ribeiro Nóbrega, Priscilla Mara Proveti, Raphael Machado do Castilhos, Vanessa Daccach, Felipe von Glehn. Brazilian consensus recommendations on the diagnosis and treatment of autoimmune encephalitis in the adult and pediatric populations. Arq Neuropsiquiatr 2024; 82: s00441788586.
DOI: 10.1055/s-0044-1788586
-
References
- 1 Vitaliani R, Mason W, Ances B, Zwerdling T, Jiang Z, Dalmau J. Paraneoplastic encephalitis, psychiatric symptoms, and hypoventilation in ovarian teratoma. Ann Neurol 2005; 58 (04) 594-604
- 2 Dalmau J, Gleichman AJ, Hughes EG. et al. Anti-NMDA-receptor encephalitis: case series and analysis of the effects of antibodies. Lancet Neurol 2008; 7 (12) 1091-1098
- 3 Dalmau J, Graus F. Antibody-Mediated Encephalitis. N Engl J Med 2018; 378 (09) 840-851
- 4 Dubey D, Pittock SJ, Kelly CR. et al. Autoimmune encephalitis epidemiology and a comparison to infectious encephalitis. Ann Neurol 2018; 83 (01) 166-177
- 5 Hor JY, Asgari N, Nakashima I. et al. Epidemiology of Neuromyelitis Optica Spectrum Disorder and Its Prevalence and Incidence Worldwide. Front Neurol 2020; 11: 501
- 6 Dutra LA, Abrantes F, Toso FF, Pedroso JL, Barsottini OGP, Hoftberger R. Autoimmune encephalitis: a review of diagnosis and treatment. . Arq Neuropsiquiatr 2018; 76 (01) 41-49
- 7 Titulaer MJ, McCracken L, Gabilondo I. et al. Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study. Lancet Neurol 2013; 12 (02) 157-165
- 8 van Sonderen A, Thijs RD, Coenders EC. et al. Anti-LGI1 encephalitis: Clinical syndrome and long-term follow-up. Neurology 2016; 87 (14) 1449-1456
- 9 Gadoth A, Nisnboym M, Alcalay Y, Weinstein T. LGI1 encephalitis associated hyponatremia, is it all in the brain? (2256). Neurology 2021; 96 (15) , Supplement) 2256
- 10 Graus F, Titulaer MJ, Balu R. et al. A clinical approach to diagnosis of autoimmune encephalitis. Lancet Neurol 2016; 15 (04) 391-404
- 11 Cellucci T, Van Mater H, Graus F. et al. Clinical approach to the diagnosis of autoimmune encephalitis in the pediatric patient. Neurol Neuroimmunol Neuroinflamm 2020; 7 (02) e663
- 12 Ricken G, Schwaiger C, De Simoni D. et al. Detection Methods for Autoantibodies in Suspected Autoimmune Encephalitis. Front Neurol 2018; 9: 841
- 13 Ruiz-García R, Muñoz-Sánchez G, Naranjo L. et al. Limitations of a Commercial Assay as Diagnostic Test of Autoimmune Encephalitis. Front Immunol 2021; 12: 691536
- 14 Fredrich SE, Vernino S, Blackburn KM. Antibody Testing for Neurological Autoimmune Disorders: Evaluation of Best Practices at a Tertiary Referral Center. Front Neurol 2021; 12: 690415
- 15 Bien CG, Bien CI, Dogan Onugoren M. et al. Routine diagnostics for neural antibodies, clinical correlates, treatment and functional outcome. J Neurol 2020; 267 (07) 2101-2114
- 16 McCracken L, Zhang J, Greene M. et al. Improving the antibody-based evaluation of autoimmune encephalitis. Neurol Neuroimmunol Neuroinflamm 2017; 4 (06) e404
- 17 Dalmau J, Geis C, Graus F. Autoantibodies to Synaptic Receptors and Neuronal Cell Surface Proteins in Autoimmune Diseases of the Central Nervous System. Physiol Rev 2017; 97 (02) 839-887
- 18 Flanagan EP, Geschwind MD, Lopez-Chiriboga AS. et al. Autoimmune Encephalitis Misdiagnosis in Adults. JAMA Neurol 2023; 80 (01) 30-39
- 19 Dinoto A, Zara P, Mariotto S. et al. Autoimmune encephalitis misdiagnosis and mimics. J Neuroimmunol 2023; 378: 578071
- 20 Van Steenhoven RW, de Vries JM, Bruijstens AL. et al. Mimics of Autoimmune Encephalitis: Validation of the 2016 Clinical Autoimmune Encephalitis Criteria. Neurol Neuroimmunol Neuroinflamm 2023; 10 (06) e200148
- 21 Dalmau J, Graus F. Autoimmune Encephalitis-Misdiagnosis, Misconceptions, and How to Avoid Them. JAMA Neurol 2023; 80 (01) 12-14
- 22 Cohen J, Sotoca J, Gandhi S. et al. Autoimmune encephalitis: A costly condition. Neurology 2019; 92 (09) e964-e972
- 23 Uy CE, Binks S, Irani SR. Autoimmune encephalitis: clinical spectrum and management. Pract Neurol 2021; 21 (05) 412-423
- 24 Abboud H, Probasco JC, Irani S. et al; Autoimmune Encephalitis Alliance Clinicians Network. Autoimmune encephalitis: proposed best practice recommendations for diagnosis and acute management. J Neurol Neurosurg Psychiatry 2021; 92 (07) 757-768
- 25 Ganesh A, Wesley SF. Practice Current: When do you suspect autoimmune encephalitis and what is the role of antibody testing?. Neurol Clin Pract 2018; 8 (01) 67-73
- 26 Nissen MS, Ryding M, Meyer M, Blaabjerg M. Autoimmune Encephalitis: Current Knowledge on Subtypes, Disease Mechanisms and Treatment. CNS Neurol Disord Drug Targets 2020; 19 (08) 584-598
- 27 Nosadini M, Thomas T, Eyre M. et al. International Consensus Recommendations for the Treatment of Pediatric NMDAR Antibody Encephalitis. Neurol Neuroimmunol Neuroinflamm 2021; 8 (05) e1052
- 28 Ellul M, Solomon T. Acute encephalitis - diagnosis and management. Clin Med (Lond) 2018; 18 (02) 155-159
- 29 Nosadini M, Eyre M, Molteni E. et al; International NMDAR Antibody Encephalitis Consensus Group. Use and Safety of Immunotherapeutic Management of N-Methyl-d-Aspartate Receptor Antibody Encephalitis: A Meta-analysis. JAMA Neurol 2021; 78 (11) 1333-1344
- 30 Beiderbeck D, Frevel N, von der Gracht HA, Schmidt SL, Schweitzer VM. Preparing, conducting, and analyzing Delphi surveys: Cross-disciplinary practices, new directions, and advancements. MethodsX 2021; 8: 101401
- 31 Schmalz U, Spinler S, Ringbeck J. Lessons Learned from a Two-Round Delphi-based Scenario Study. MethodsX 2020; 8: 101179
- 32 Vasconcelos GA, Barreira RM, Antoniollo KENT. et al. Autoimmune Encephalitis in Latin America: A Critical Review. Front Neurol 2021; 11: 606350
- 33 de Freitas Dias B, Fieni Toso F, Slhessarenko Fraife Barreto ME. et al. Brazilian autoimmune encephalitis network (BrAIN): antibody profile and clinical characteristics from a multicenter study. Front Immunol 2023; 14: 1256480
- 34 Dalmau J, Graus F. Antibody-mediated neuropsychiatric disorders. J Allergy Clin Immunol 2022; 149 (01) 37-40
- 35 Lim J-A, Lee S-T, Moon J. et al. Development of the clinical assessment scale in autoimmune encephalitis. Ann Neurol 2019; 85 (03) 352-358
- 36 Thaler FS, Zimmermann L, Kammermeier S. et al; German Network for Research on Autoimmune Encephalitis (GENERATE). Rituximab Treatment and Long-term Outcome of Patients With Autoimmune Encephalitis: Real-world Evidence From the GENERATE Registry. Neurol Neuroimmunol Neuroinflamm 2021; 8 (06) e1088
- 37 Wendel EM, Thonke HS, Bertolini A. et al; BIOMARKER Study Group. Temporal Dynamics of MOG Antibodies in Children With Acquired Demyelinating Syndrome. Neurol Neuroimmunol Neuroinflamm 2022; 9 (06) e200035
- 38 Dalmau J, Graus F. Diagnostic criteria for autoimmune encephalitis: utility and pitfalls for antibody-negative disease. Lancet Neurol 2023; 22 (06) 529-540
- 39 Bastiaansen AEM, van Steenhoven RW, Te Vaarwerk ES. et al. Antibodies Associated With Autoimmune Encephalitis in Patients With Presumed Neurodegenerative Dementia. Neurol Neuroimmunol Neuroinflamm 2023; 10 (05) e200137
- 40 Venkatesan A, Probasco JC. Autoimmune encephalitis: chasing a moving target. Lancet Neurol 2023; 22 (06) 460-462
- 41 Armangué T, Olivé-Cirera G, Martínez-Hernandez E. et al. Neurologic complications in herpes simplex encephalitis: clinical, immunological and genetic studies. Brain 2023; 146 (10) 4306-4319
- 42 Danieli D, Moraes ACM, Alves MP. et al. Anti-N-methyl-D-aspartate receptor encephalitis and Epstein-Barr virus: another tale on autoimmunity?. Eur J Neurol 2017; 24 (08) e46-e47
- 43 Armangue T, Spatola M, Vlagea A. et al; Spanish Herpes Simplex Encephalitis Study Group. Frequency, symptoms, risk factors, and outcomes of autoimmune encephalitis after herpes simplex encephalitis: a prospective observational study and retrospective analysis. Lancet Neurol 2018; 17 (09) 760-772
- 44 Budhram A, Dubey D, Sechi E. et al. Neural Antibody Testing in Patients with Suspected Autoimmune Encephalitis. Clin Chem 2020; 66 (12) 1496-1509
- 45 Budhram A, Mirian A, McFadden S, Edmond P, Bhayana V, Yang L. Neural Antibody Testing for Autoimmune Encephalitis: A Canadian Single-Centre Experience. Can J Neurol Sci 2021; 48 (06) 859-863
- 46 Budhram A, Yang L, Bhayana V, Mills JR, Dubey D. Clinical Sensitivity, Specificity, and Predictive Value of Neural Antibody Testing for Autoimmune Encephalitis. J Appl Lab Med 2022; 7 (01) 350-356
- 47 Bastiaansen AEM, van Sonderen A, Titulaer MJ. Autoimmune encephalitis with anti-leucine-rich glioma-inactivated 1 or anti-contactin-associated protein-like 2 antibodies (formerly called voltage-gated potassium channel-complex antibodies). Curr Opin Neurol 2017; 30 (03) 302-309
- 48 Michael S, Waters P, Irani SR. Stop testing for autoantibodies to the VGKC-complex: only request LGI1 and CASPR2. Pract Neurol 2020; 20 (05) 377-384
- 49 Buckley C, Oger J, Clover L. et al. Potassium channel antibodies in two patients with reversible limbic encephalitis. Ann Neurol 2001; 50 (01) 73-78
- 50 Shillito P, Molenaar PC, Vincent A. et al. Acquired neuromyotonia: evidence for autoantibodies directed against K+ channels of peripheral nerves. Ann Neurol 1995; 38 (05) 714-722
- 51 Lai M, Huijbers MG, Lancaster E. et al. Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series. Lancet Neurol 2010; 9 (08) 776-785
- 52 Irani SR, Alexander S, Waters P. et al. Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan's syndrome and acquired neuromyotonia. Brain 2010; 133 (09) 2734-2748
- 53 van Sonderen A, Schreurs MW, de Bruijn MA. et al. The relevance of VGKC positivity in the absence of LGI1 and Caspr2 antibodies. Neurology 2016; 86 (18) 1692-1699
- 54 Armangue T, Olivé-Cirera G, Martínez-Hernandez E. et al; Spanish Pediatric anti-MOG Study Group. Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study. Lancet Neurol 2020; 19 (03) 234-246
- 55 Han JY, Kim SY, Kim H. et al. Clinico-radiological characteristics of anti-myelin oligodendrocyte glycoprotein antibody-associated autoimmune encephalitis in children. Dev Med Child Neurol 2022; 64 (08) 998-1007
- 56 Kang Q, Liao H, Yang L, Fang H, Hu W, Wu L. Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort Study. Front Pediatr 2022; 10: 880693
- 57 de Bruijn MAAM, Bruijstens AL, Bastiaansen AEM. et al; CHANCE Study Group. Pediatric autoimmune encephalitis: Recognition and diagnosis. Neurol Neuroimmunol Neuroinflamm 2020; 7 (03) e682
- 58 Hennes EM, Baumann M, Schanda K. et al; BIOMARKER Study Group. Prognostic relevance of MOG antibodies in children with an acquired demyelinating syndrome. Neurology 2017; 89 (09) 900-908
- 59 Huda S, Whittam D, Jackson R. et al. Predictors of relapse in MOG antibody associated disease: a cohort study. BMJ Open 2021; 11 (11) e055392
- 60 Di Pauli F, Mader S, Rostasy K. et al. Temporal dynamics of anti-MOG antibodies in CNS demyelinating diseases. Clin Immunol 2011; 138 (03) 247-254
- 61 Balu R, McCracken L, Lancaster E, Graus F, Dalmau J, Titulaer MJ. A score that predicts 1-year functional status in patients with anti-NMDA receptor encephalitis. Neurology 2019; 92 (03) e244-e252
- 62 Zuliani L, Nosadini M, Gastaldi M. et al. Management of antibody-mediated autoimmune encephalitis in adults and children: literature review and consensus-based practical recommendations. Neurol Sci 2019; 40 (10) 2017-2030
- 63 Hahn C, Budhram A, Alikhani K. et al. Canadian Consensus Guidelines for the Diagnosis and Treatment of Autoimmune Encephalitis in Adults. Can J Neurol Sci 2024; •••: 1-21
- 64 Dubey D, Britton J, McKeon A. et al. Randomized Placebo-Controlled Trial of Intravenous Immunoglobulin in Autoimmune LGI1/CASPR2 Epilepsy. Ann Neurol 2020; 87 (02) 313-323
- 65 Alkabie S, Budhram A. Prolonged Corticosteroids Without Maintenance Immunotherapy for Treatment of Anti-LGI1 Encephalitis: Analysis of Outcomes and Relapse Rate. Neurol Neuroimmunol Neuroinflamm 2023; 10 (03) e200115
- 66 Rodriguez A, Klein CJ, Sechi E. et al. LGI1 antibody encephalitis: acute treatment comparisons and outcome. J Neurol Neurosurg Psychiatry 2022; 93 (03) 309-315
- 67 Stingl C, Cardinale K, Van Mater H. An Update on the Treatment of Pediatric Autoimmune Encephalitis. Curr Treatm Opt Rheumatol 2018; 4 (01) 14-28
- 68 Dale RC, Brilot F, Duffy LV. et al. Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS disease. Neurology 2014; 83 (02) 142-150
- 69 Dou X, Li D, Wu Y. et al. Efficacy and Safety of Rituximab in Chinese Children With Refractory Anti-NMDAR Encephalitis. Front Neurol 2020; 11: 606923
- 70 Ellul MA, Wood G, Tooren HVD, Easton A, Babu A, Michael BD. Update on the diagnosis and management of autoimmune encephalitis. Clin Med (Lond) 2020; 20 (04) 389-392
- 71 Nosadini M, Mohammad SS, Ramanathan S, Brilot F, Dale RC. Immune therapy in autoimmune encephalitis: a systematic review. Expert Rev Neurother 2015; 15 (12) 1391-1419
- 72 Ciano-Petersen NL, Muñiz-Castrillo S, Vogrig A, Joubert B, Honnorat J. Immunomodulation in the acute phase of autoimmune encephalitis. Rev Neurol (Paris) 2022; 178 (1-2): 34-47
- 73 Dinoto A, Ferrari S, Mariotto S. Treatment Options in Refractory Autoimmune Encephalitis. CNS Drugs 2022; 36 (09) 919-931
- 74 Bien CG. Management of autoimmune encephalitis. Curr Opin Neurol 2021; 34 (02) 166-171
- 75 Lee WJ, Lee ST, Byun JI. et al. Rituximab treatment for autoimmune limbic encephalitis in an institutional cohort. Neurology 2016; 86 (18) 1683-1691
- 76 Nepal G, Shing YK, Yadav JK. et al. Efficacy and safety of rituximab in autoimmune encephalitis: A meta-analysis. Acta Neurol Scand 2020; 142 (05) 449-459
- 77 Du Y, Zhao C, Liu J. et al. Simplified regimen of combined low-dose rituximab for autoimmune encephalitis with neuronal surface antibodies. J Neuroinflammation 2022; 19 (01) 259
- 78 Lee WJ, Lee ST, Shin YW. et al. Teratoma Removal, Steroid, IVIG, Rituximab and Tocilizumab (T-SIRT) in Anti-NMDAR Encephalitis. Neurotherapeutics 2021; 18 (01) 474-487
- 79 Nguyen L, Wang C. Anti-NMDA Receptor Autoimmune Encephalitis: Diagnosis and Management Strategies. Int J Gen Med 2023; 16: 7-21
- 80 Smets I, Titulaer MJ. Antibody Therapies in Autoimmune Encephalitis. Neurotherapeutics 2022; 19 (03) 823-831
- 81 Wang B, Wang C, Feng J, Hao M, Guo S. Clinical Features, Treatment, and Prognostic Factors in Neuronal Surface Antibody-Mediated Severe Autoimmune Encephalitis. Front Immunol 2022; 13: 890656
- 82 Behrendt V, Krogias C, Reinacher-Schick A, Gold R, Kleiter I. Bortezomib Treatment for Patients With Anti-N-Methyl-d-Aspartate Receptor Encephalitis. JAMA Neurol 2016; 73 (10) 1251-1253
- 83 Dinoto A, Cheli M, Bratina A, Sartori A, Manganotti P. Bortezomib in anti-N-Methyl-d-Aspartate-Receptor (NMDA-R) encephalitis: A systematic review. J Neuroimmunol 2021; 356: 577586
- 84 Li YH, Jiang L. Recent research on immunotherapy for anti-N-methyl-D-aspartate receptor encephalitis. Zhongguo Dang Dai Er Ke Za Zhi 2022; 24 (08) 948-953
- 85 Scheibe F, Prüss H, Mengel AM. et al. Bortezomib for treatment of therapy-refractory anti-NMDA receptor encephalitis. Neurology 2017; 88 (04) 366-370
- 86 Schwarz L, Akbari N, Prüss H, Meisel A, Scheibe F. Clinical characteristics, treatments, outcome, and prognostic factors of severe autoimmune encephalitis in the intensive care unit: Standard treatment and the value of additional plasma cell-depleting escalation therapies for treatment-refractory patients. Eur J Neurol 2023; 30 (02) 474-489
- 87 Benucci M, Tramacere L, Infantino M. et al. Efficacy of Tocilizumab in Limbic Encephalitis with Anti-CASPR2 Antibodies. Case Rep Neurol Med 2020; 2020: 5697670
- 88 Dale RC. Interleukin-6 Blockade as Rescue Therapy in Autoimmune Encephalitis. Neurotherapeutics 2016; 13 (04) 821-823
- 89 Lee W-J, Lee S-T, Moon J. et al. Tocilizumab in Autoimmune Encephalitis Refractory to Rituximab: An Institutional Cohort Study. Neurotherapeutics 2016; 13 (04) 824-832
- 90 Randell RL, Adams AV, Van Mater H. Tocilizumab in Refractory Autoimmune Encephalitis: A Series of Pediatric Cases. Pediatr Neurol 2018; 86: 66-68
- 91 Irani SR, Bera K, Waters P. et al. N-methyl-D-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes. Brain 2010; 133 (Pt 6): 1655-1667
- 92 Hacohen Y, Absoud M, Hemingway C. et al. NMDA receptor antibodies associated with distinct white matter syndromes. Neurol Neuroimmunol Neuroinflamm 2014; 1 (01) e2
- 93 Rada A, Birnbacher R, Gobbi C. et al. Seizures associated with antibodies against cell surface antigens are acute symptomatic and not indicative of epilepsy: insights from long-term data. J Neurol 2021; 268 (03) 1059-1069
- 94 Vogrig A, Joubert B, André-Obadia N, Gigli GL, Rheims S, Honnorat J. Seizure specificities in patients with antibody-mediated autoimmune encephalitis. Epilepsia 2019; 60 (08) 1508-1525
- 95 Vogrig A, Gigli GL, Nilo A, Pauletto G, Valente M. Seizures, Epilepsy, and NORSE Secondary to Autoimmune Encephalitis: A Practical Guide for Clinicians. Biomedicines 2022; 11 (01) 44
- 96 Fisher RS, Acevedo C, Arzimanoglou A. et al. ILAE official report: a practical clinical definition of epilepsy. Epilepsia 2014; 55 (04) 475-482
- 97 Cabezudo-García P, Mena-Vázquez N, Villagrán-García M, Serrano-Castro PJ. Efficacy of antiepileptic drugs in autoimmune epilepsy: A systematic review. Seizure 2018; 59: 72-76
- 98 de Bruijn MAAM, van Sonderen A, van Coevorden-Hameete MH. et al. Evaluation of seizure treatment in anti-LGI1, anti-NMDAR, and anti-GABABR encephalitis. Neurology 2019; 92 (19) e2185-e2196
- 99 Ilyas-Feldmann M, Prüß H, Holtkamp M. Long-term seizure outcome and antiseizure medication use in autoimmune encephalitis. Seizure 2021; 86 (86) 138-143
- 100 Liu X, Guo K, Lin J. et al. Long-term seizure outcomes in patients with autoimmune encephalitis: A prospective observational registry study update. Epilepsia 2022; 63 (07) 1812-1821
- 101 Britton JW, Dalmau J. Recognizing autoimmune encephalitis as a cause of seizures: Treating cause and not effect. Neurology 2019; 92 (19) 877-878
- 102 Elkhider H, Sharma R, Kapoor N, Vattoth S, Shihabuddin B. Autoimmune encephalitis and seizures, cerebrospinal fluid, imaging, and EEG findings: a case series. Neurol Sci 2022; 43 (04) 2669-2680
- 103 Shen CH, Fang GL, Yang F. et al. Seizures and risk of epilepsy in anti-NMDAR, anti-LGI1, and anti-GABAB R encephalitis. Ann Clin Transl Neurol 2020; 7 (08) 1392-1399
- 104 Wesselingh R, Butzkueven H, Buzzard K, Tarlinton D, O'Brien TJ, Monif M. Seizures in autoimmune encephalitis: Kindling the fire. Epilepsia 2020; 61 (06) 1033-1044
- 105 Flammer J, Neziraj T, Rüegg S, Pröbstel AK. Immune Mechanisms in Epileptogenesis: Update on Diagnosis and Treatment of Autoimmune Epilepsy Syndromes. Drugs 2023; 83 (02) 135-158
- 106 Blum RA, Tomlinson AR, Jetté N, Kwon CS, Easton A, Yeshokumar AK. Assessment of long-term psychosocial outcomes in anti-NMDA receptor encephalitis. Epilepsy Behav 2020; 108: 107088
- 107 de Bruijn MAAM, Aarsen FK, van Oosterhout MP. et al; CHANCE Study Group. Long-term neuropsychological outcome following pediatric anti-NMDAR encephalitis. Neurology 2018; 90 (22) e1997-e2005
- 108 Guasp M, Rosa-Justicia M, Muñoz-Lopetegi A. et al; Spanish anti-NMDAR Encephalitis Study Group. Clinical characterisation of patients in the post-acute stage of anti-NMDA receptor encephalitis: a prospective cohort study and comparison with patients with schizophrenia spectrum disorders. Lancet Neurol 2022; 21 (10) 899-910
- 109 Nicolle DCM, Moses JL. A Systematic Review of the Neuropsychological Sequelae of People Diagnosed with Anti N-Methyl-D-Aspartate Receptor Encephalitis in the Acute and Chronic Phases. Arch Clin Neuropsychol 2018; 33 (08) 964-983
- 110 Abboud H, Briggs F, Buerki R. et al. Residual symptoms and long-term outcomes after all-cause autoimmune encephalitis in adults. J Neurol Sci 2022; 434: 120124
- 111 Ariño H, Armangué T, Petit-Pedrol M. et al. Anti-LGI1-associated cognitive impairment: Presentation and long-term outcome. Neurology 2016; 87 (08) 759-765
- 112 Finke C, Kopp UA, Prüss H, Dalmau J, Wandinger K-P, Ploner CJ. Cognitive deficits following anti-NMDA receptor encephalitis. J Neurol Neurosurg Psychiatry 2012; 83 (02) 195-198
- 113 Heine J, Kopp UA, Klag J, Ploner CJ, Prüss H, Finke C. Long-Term Cognitive Outcome in Anti-N-Methyl-D-Aspartate Receptor Encephalitis. Ann Neurol 2021; 90 (06) 949-961
- 114 Devenney E, Hodges JR. The Mini-Mental State Examination: pitfalls and limitations. Pract Neurol 2017; 17 (01) 79-80
- 115 Naugle RI, Kawczak K. Limitations of the Mini-Mental State Examination. Cleve Clin J Med 1989; 56 (03) 277-281
- 116 New PW, Buchbinder R. Critical appraisal and review of the Rankin scale and its derivatives. Neuroepidemiology 2006; 26 (01) 4-15
- 117 Kapoor A, Lanctôt KL, Bayley M. et al. “Good Outcome” Isn't Good Enough: Cognitive Impairment, Depressive Symptoms, and Social Restrictions in Physically Recovered Stroke Patients. Stroke 2017; 48 (06) 1688-1690
- 118 Zhou H, Deng Q, Yang Z. et al. Performance of the clinical assessment scale for autoimmune encephalitis in a pediatric autoimmune encephalitis cohort. Front Immunol 2022; 13: 915352
- 119 Cai MT, Lai QL, Zheng Y. et al. Validation of the Clinical Assessment Scale for Autoimmune Encephalitis: A Multicenter Study. Neurol Ther 2021; 10 (02) 985-1000
- 120 Zhang Y, Tu E, Yao C, Liu J, Lei Q, Lu W. Validation of the Clinical Assessment Scale in Autoimmune Encephalitis in Chinese Patients. Front Immunol 2021; 12: 796965