Zhou S M, Guan H Z, Zhao M S, Huang F J, Wei Y, Wang J, Liu J P, Zhao X L, Ren H T, Fan S Y, Peng B, Qiao L Y
Department of Neurology, Yuquan Hospital, Tsinghua University, Beijing 100040, China.
Department of Neurology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China.
Zhonghua Yi Xue Za Zhi. 2020 Jul 7;100(25):1937-1941. doi: 10.3760/cma.j.cn112137-20191219-02776.
To study the clinical features, continuous care and prognosis of the patients with severe and refractory anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis after intensive care unit (ICU). Clinical data of patients with severe and refractory anti-NMDAR encephalitis, who were transferred from ICU to general ward of neurology between December 2015 and October 2019, were retrospectively reviewed and analyzed in the study. Twenty patients (11 females and 9 males) were enrolled in the study. The median course of disease when patients were transferred to general ward was 4.4 (2.0, 6.0) months. Six cases were alert, 6 cases were in a coma, 5 were in the early recovery phase and 3 were in the late recovery phase. Severe malnutrition, pneumonia, urinary tract infections, bedsores and leukocytopenia were common complications. Seven out of 18 patients were tested positive for cerebrospinal fluid anti-NMDAR antibodies with high titers (≥1∶100). During this continuous therapy stage,10 patients were treated with intravenous immunoglobulin (IVIg), 1 with methylprednisolone, 2 with rituximab, 1 with intrathecal methotrexate and 1 received intravenous cyclophosphamide. All Patients were prescribed a long-term immunotherapy (mycophenolate mofetil 1.5-3.0 g/d). Sixteen patients (80%) had good prognosis (modified Rankin Scale (mRS)≤2), and the mortality was 10%, with follow-up time of 17.0 (8.0, 27.0) months. Patients with anti-NMDAR encephalitis, who are transferred from ICU, have severely impaired neurologic function. These patients need long-term individualized immunotherapy and continuous neurological care. Good outcomes can be achieved in most patients.
研究重症监护病房(ICU)后严重难治性抗N-甲基-D-天冬氨酸受体(NMDAR)脑炎患者的临床特征、持续护理及预后。本研究回顾性分析了2015年12月至2019年10月间从ICU转入神经内科普通病房的严重难治性抗NMDAR脑炎患者的临床资料。纳入研究的患者共20例(女性11例,男性9例)。患者转入普通病房时的疾病中位病程为4.4(2.0,6.0)个月。6例清醒,6例昏迷,5例处于早期恢复期,3例处于晚期恢复期。严重营养不良、肺炎、尿路感染、压疮和白细胞减少是常见并发症。18例患者中有7例脑脊液抗NMDAR抗体检测呈高滴度阳性(≥1∶100)。在这个持续治疗阶段,10例患者接受静脉注射免疫球蛋白(IVIg)治疗,1例接受甲泼尼龙治疗,2例接受利妥昔单抗治疗,1例接受鞘内注射甲氨蝶呤治疗,1例接受静脉注射环磷酰胺治疗。所有患者均接受长期免疫治疗(霉酚酸酯1.5 - 3.0 g/d)。16例患者(80%)预后良好(改良Rankin量表(mRS)≤2),死亡率为10%,随访时间为17.0(8.0,27.0)个月。从ICU转出的抗NMDAR脑炎患者神经功能严重受损。这些患者需要长期个体化免疫治疗和持续的神经护理。大多数患者可取得良好预后。