Treatment and prognostic factors for long-term outcome in patients with anti-NMDA receptor encephalitis: an observational cohort study

被引:2307
作者
Titulaer, Maarten J. [1 ,2 ,3 ]
McCracken, Lindsey [1 ,2 ]
Gabilondo, Inigo [3 ]
Armangue, Thais [3 ]
Glaser, Carol [4 ]
Iizuka, Takahiro [5 ]
Honig, Lawrence S. [6 ]
Benseler, Susanne M. [7 ]
Kawachi, Izumi [8 ]
Martinez-Hernandez, Eugenia [1 ,2 ,9 ]
Aguilar, Esther [3 ]
Gresa-Arribas, Nuria [3 ]
Ryan-Florance, Nicole [10 ]
Torrents, Abiguei [11 ]
Saiz, Albert [3 ]
Rosenfeld, Myrna R. [1 ,2 ,3 ]
Balice-Gordon, Rita [1 ,2 ]
Graus, Francesc
Dalmau, Josep [1 ,2 ,3 ,12 ]
机构
[1] Hosp Univ Penn, Dept Neurol, Perelman Sch Med, Philadelphia, PA 19104 USA
[2] Hosp Univ Penn, Dept Neurosci, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Univ Barcelona Invest Biomed August Pi & Sunyer I, Dept Neurol, Hosp Clin, Barcelona, Spain
[4] Calif Dept Publ Hlth, Richmond, CA USA
[5] Kitasato Univ, Sch Med, Dept Neurol, Sagamihara, Kanagawa 228, Japan
[6] Columbia Univ, Dept Neurol, New York, NY USA
[7] Univ Toronto, Dept Rheumatol, Hosp Sick Children, Toronto, ON M5S 1A1, Canada
[8] Niigata Univ, Brain Res Inst, Dept Neurol, Niigata 95021, Japan
[9] Univ Autonoma Barcelona, Dept Neurol, Hosp St Pau, Barcelona, Spain
[10] Univ Penn, Dept Neurol, Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[11] Hosp Clin Barcelona, IDIBAPS, Barcelona, Spain
[12] ICREA, Barcelona, Spain
基金
美国国家卫生研究院;
关键词
PATHOGENESIS; DISORDERS;
D O I
10.1016/S1474-4422(12)70310-1
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background Anti-NMDA receptor (NMDAR) encephalitis is an autoimmune disorder in which the use of immunotherapy and the long-term outcome have not been defined. We aimed to assess the presentation of the disease, the spectrum of symptoms, immunotherapies used, timing of improvement, and long-term outcome. Methods In this multi-institutional observational study, we tested for the presence of NMDAR antibodies in serum or C SF samples of patients with encephalitis between Jan 1,2007, and Jan 1, 2012. All patients who tested positive for NMDAR antibodies were included in the study; patients were assessed at symptom onset and at months 4,8,12,18, and 24, by use of the modified Rankin scale (mRS). Treatment included first-line immunotherapy (steroids, intravenous immunoglobulin, plasmapheresis), second-line immunotherapy (ritincimab, cydophosphamide), and tumour removal. Predictors of outcome were determined at the Universities of Pennsylvania (PA, USA) and Barcelona (Spain) by use of a generalised linear mixed model with binary distribution. Results We enrolled 577 patients (median age 21 years, range 8 months to 85 years), 211 of whom were children (<18 years). Treatment effects and outcome were assessable in 501 (median follow-up 24 months, range 4-186): 472 (94%) underwent first-line immunotherapy or tumour removal, resulting in improvement within 4 weeks in 251 (53%). Of 221 patients who did not improve with first-line treatment, 125 (57%) received second-line immunotherapy that resulted in a better outcome (mRS 0-2) than those who did not (odds ratio [OR] 2.69, CI 1-24-5.80; p=0.012). During the first 24 months, 394 of 501 patients achieved a good outcome (mRS 0-2; median 6 months, IQR 2-12) and 30 died. At 24 months' follow-up, 203 (81%) of 252 patients had good outcome. Outcomes continued to improve for up to 18 months after symptom onset. Predictors of good outcome were early treatment (0.62,0.50-0.76; p<0.0001) and no admission to an intensive care unit (0.12,0.06-0-22; p<0.0001). 45 patients had one or multiple relapses (representing a 12% risk within 2 years); 46 (67%) of 69 relapses were less severe than initial episodes (p<0.0001). In 177 children, predictors of good outcome and the magnitude of effect of second-line immunotherapy were similar to those of the entire cohort. Interpretation Most patients with anti-NMDAR encephalitis respond to immunotherapy. Second-line immunotherapy is usually effective when first-line treatments fail. In this cohort, the recovery of some patients took up to 18 months.
引用
收藏
页码:157 / 165
页数:9
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