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Background: Combined first-line therapies have been frequently adopted for patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR) encephalitis. Plasma exchange (PE) or immunoadsorption (IA) was used as an add-on option following initial immunotherapies, including high-dose steroids and intravenous immunoglobulin (IVIG). However, whether a shorter delay of PE or IA can improve the early recovery prognosis of patients with anti-NMDAR encephalitis remains largely unknown.
Objective: To compare short-term clinical improvement between patients with early and late initiation of PE or IA in anti-NMDAR encephalitis.
Design: A retrospective study was conducted for patients admitted with anti-NMDAR encephalitis between January 2015 and December 2023 ( = 29), including 21 patients who received PE or IA as synergistic therapies.
Methods: The clinical prognosis was compared between the early PE/IA group and the late PE/IA group in the research. Primary outcome included changes in the Clinical Assessment Scale for Autoimmune Encephalitis (∆CASE) at 90 and 120 days after encephalitis onset. Secondary outcomes included changes in the modified Rankin scale (∆mRS) after 90 and 120 days from encephalitis onset, and the length of intensive care unit (ICU) stay for patients with severe anti-NMDAR encephalitis.
Results: The ∆CASE scores after 90 and 120 days from encephalitis onset revealed a significant difference between patients with early and late initiation of PE or IA ( ⩽ 0.05). A significant difference in the ∆mRS was also found between patients with early and late initiation of PE or IA in severe encephalitis ( ⩽ 0.05). No significant difference was found in the length of ICU admission ( = 0.101).
Conclusion: Our findings emphasize the importance of considering PE or IA as early as feasible for patients with anti-NMDAR encephalitis, even when steroids and IVIG are in use.
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http://dx.doi.org/10.1177/17562864241276208 | DOI Listing |
Pediatr Neurol
August 2025
Division of Pediatric Neurology and Developmental Neuroscience, Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas; Center for Human Immunobiology, Department of Pediatrics, Baylor College of Medicine and Texas Children's Hospital, Houston, Texas. Elec
Background: Pediatric N-methyl-d-aspartate receptor (NMDAR) encephalitis (pNMDARE) is characterized by severe neuropsychiatric symptoms and prolonged hospitalization and recovery. Early pNMDARE diagnosis is complicated by neuropsychiatric mimickers requiring strong clinical suspicion to escalate to the required lumbar puncture (LP), delaying diagnosis and treatment. Since autonomic dysfunction is a cardinal feature of pNMDARE, we hypothesized that early vital signs serve as a potential noninvasive biomarker to screen for appropriate escalation of pNMDARE evaluation.
View Article and Find Full Text PDFNeurol Sci
September 2025
Department of Neurology, JIPMER, 605006, Puducherry, India.
J Craniofac Surg
September 2025
Department of Neurosurgery, The Sixth Affiliated Hospital, School of Medicine, South China University of Technology, Foshan, Guangdong, China.
This case report highlights a rare association between anti-NMDAR encephalitis and meningioma, where the patient developed typical autoimmune encephalitis symptoms shortly after tumor resection. Unlike the well-established link with ovarian teratomas, meningioma-associated cases may involve indirect immune mechanisms, such as molecular mimicry or bystander activation, rather than direct antigen exposure. The findings emphasize the need for postoperative autoimmune screening in neurosurgical patients with unexplained neuropsychiatric symptoms.
View Article and Find Full Text PDFQuant Imaging Med Surg
September 2025
Department of Neurology, The First Affiliated Hospital of Dalian Medical University, Dalian, China.
Background: Imaging, particularly multimodal magnetic resonance imaging (MRI), serves as an essential auxiliary examination for diagnosing autoimmune encephalitis (AE). The diversity of autoantibodies complicates the imaging presentation of AE, exhibiting both common and individual features across different subtypes of AE. Currently, there is a lack of comprehensive studies on the imaging features of different subtypes of AE.
View Article and Find Full Text PDFBMC Neurol
August 2025
Department of Clinical Pediatrics Sciences, Unit of Child Neuropsychiatry, Member of the ERN Epicare Network, IRCCS Istituto Giannina Gaslini, Via G Gaslini 5, Genova, 16100, Italy.
Background: Herpes simplex virus 1 (HSV-1) encephalitis may result in relapsing neurological symptoms secondary to immune-mediated processes, including anti-N-methyl-D-aspartate receptor (NMDAR) encephalitis. Refractory status dyskineticus (RSD), a severe subset of status dystonicus, is characterized by a hyperkinetic movement disorder phenotype alongside dystonic features. This critical condition presents substantial challenges in neurocritical care.
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