Patient-Reported Outcome Measures in NMDA Receptor Encephalitis.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Josephine Heine, Ole Jonas Boeken, Sophia Rekers, Katharina Wurdack, Harald Prüss, Carsten Finke
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引用次数: 0

Abstract

Background and objectives: The characteristics of persistent long-term symptoms and their contribution to subjective quality of life remain unclear in patients with NMDAR encephalitis. In this study, we aimed to evaluate postacute neuropsychiatric symptoms, subjective cognitive complaints, and disease coping mechanisms and identify predictors of health-related quality of life (HRQoL) after N-methyl-D-aspartate receptor (NMDAR) encephalitis.

Methods: This cross-sectional observational study investigated patients with NMDAR encephalitis in the postacute phase. Psychometric scales included assessment of neuropsychiatric symptoms (i.e., fatigue, sleep, anxiety, and depressive symptoms), HRQoL, everyday independence, metamemory (i.e., self-rated ability, satisfaction, and use of strategies), and coping strategies (i.e., self-efficacy, disease-related coping, and stress management).

Results: A total of 50 patients (mean age 26.0 ± 10.1 years, 86% female) participated at a median of 4.15 (range 0.3-30.3) years after symptom onset. Patients reported significantly increased levels of anxiety (Beck Anxiety Inventory: 10.5 ± 7.7 [mean ± SD], 95% CI [8.32-12.71], p < 0.001) and depressive (Beck Depression Inventory-II: 11.4 ± 7.7 [9.22-13.62], p = 0.001) symptoms compared with the normative population. Both sleep problems (Pittsburgh Sleep Quality Index: 5.8 ± 3.0 [4.98-6.66], p < 0.001) and motor and cognitive fatigue (Fatigue Scale for Motor and Cognitive Function: 50.5 ± 23.1 [42.5-58.4], p < 0.001) were significantly more prevalent. Moreover, lower self-rated memory ability (Multifactorial Memory Questionnaire score: 54.6 ± 8.5 [52.1-57.1], p = 0.004) was associated with greater reliance on compensatory strategies and memory aids (r = -0.41, p = 0.004). Patients used significantly fewer cognitive coping strategies, such as relativization (11.7 ± 4.7 [10.3-13.1], p = 0.001), while depressive coping prevailed (49.1 ± 15.5 [44.5-53.8], p < 0.001). It is important to note that HRQoL was predicted by self-reported affective symptoms, self-efficacy, and coping behaviors in multivariable regression analyses, but not by acute disease severity or postacute physical disability.

Discussion: Our findings show that persistent neuropsychiatric and subjective cognitive concerns explain a large part of the reduced quality of life in patients with NMDAR encephalitis. These findings have important implications for a patient-centered postacute care and the role of disease coping strategies in the neurorehabilitation of autoimmune encephalitis.

NMDA 受体脑炎的患者报告结果指标
背景和目的:NMDAR 脑炎患者长期持续症状的特征及其对主观生活质量的影响仍不清楚。在这项研究中,我们旨在评估 N-甲基-D-天冬氨酸受体(NMDAR)脑炎后的急性期神经精神症状、主观认知主诉和疾病应对机制,并确定健康相关生活质量(HRQoL)的预测因素:这项横断面观察性研究调查了急性期后的 NMDAR 脑炎患者。心理测量量表包括神经精神症状(即疲劳、睡眠、焦虑和抑郁症状)、HRQoL、日常独立性、元记忆(即自评能力、满意度和策略使用)和应对策略(即自我效能、疾病相关应对和压力管理)的评估:共有 50 名患者(平均年龄为 26.0 ± 10.1 岁,86% 为女性)参加了此次调查,中位数为发病后 4.15 年(0.3-30.3 年不等)。患者的焦虑程度明显增加(贝克焦虑量表:10.5 ± 7.7 [10.5±7.7]):与常模人群相比,患者的焦虑(贝克焦虑量表:10.5 ± 7.7 [平均值 ± 标码],95% CI [8.32-12.71],p < 0.001)和抑郁(贝克抑郁量表-II:11.4 ± 7.7 [9.22-13.62],p = 0.001)症状明显增加。睡眠问题(匹兹堡睡眠质量指数:5.8 ± 3.0 [4.98-6.66],p < 0.001)以及运动和认知疲劳(运动和认知功能疲劳量表:50.5 ± 23.1 [4.98-6.66],p < 0.001)均高于正常人群:50.5±23.1[42.5-58.4],p < 0.001)明显更普遍。此外,自评记忆能力较低(多因素记忆问卷得分:54.6 ± 8.5 [52.1-57.1],p = 0.004)与更依赖补偿策略和记忆辅助工具有关(r = -0.41,p = 0.004)。患者使用的认知应对策略(如相对化)明显较少(11.7 ± 4.7 [10.3-13.1], p = 0.001),而抑郁应对策略占主导地位(49.1 ± 15.5 [44.5-53.8], p < 0.001)。值得注意的是,在多变量回归分析中,自我报告的情感症状、自我效能感和应对行为可预测 HRQoL,而急性疾病严重程度或急性期后的身体残疾则无法预测 HRQoL:我们的研究结果表明,NMDAR脑炎患者生活质量下降的很大一部分原因是持续的神经精神和主观认知问题。这些发现对以患者为中心的急性期后护理以及疾病应对策略在自身免疫性脑炎神经康复中的作用具有重要意义。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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