Validation of a risk score to differentiate autoimmune and viral encephalitis: a Nationwide Cohort Study in Denmark

医学 队列 自身免疫性脑炎 接收机工作特性 脑炎 内科学 队列研究 病因学 回顾性队列研究 曲线下面积 人口 儿科 免疫学 病毒 环境卫生
作者
Lasse Fjordside,Mette Scheller Nissen,Anna Maria Florescu,Merete Storgaard,Lykke Larsen,Lothar Wiese,Hans R. Lüttichau,Micha Phill Grønholm Jepsen,Birgitte Rønde Hansen,Christian Østergaard Andersen,Jacob Bodilsen,Henrik Nielsen,Morten Blaabjerg,Anne‐Mette Lebech,Helene Mens
出处
期刊:Journal of Neurology [Springer Science+Business Media]
标识
DOI:10.1007/s00415-024-12392-3
摘要

Abstract Background A score to differentiate autoimmune (AE) and viral encephalitis (VE) early upon admission has recently been developed but needed external validation. The objective of this study was to evaluate the performance of the score in a larger and more diagnostically diverse patient cohort. Methods We conducted a retrospective nationwide and population-based cohort study including all adults with encephalitis of definite viral (2015–2022) or autoimmune aetiology (2009–2022) in Denmark. Variables included in the score-model were extracted from patient records and individual risk scores were assessed. The performance of the score was assessed by receiver-operating characteristics (ROC) curve analyses and calculation of the area under the curve (AUC). Results A total of 496 patients with encephalitis [AE n = 90, VE n = 287 and presumed infectious encephalitis (PIE) n = 119] were included in the study. The score was highly accurate in predicting cases of AE reaching an AUC of 0.94 (95% CI 0.92–0.97). Having a score ≥ 3 predicted AE with a PPV of 87% and an NPV of 91%. The risk score was found to perform well across aetiological subgroups and applied to the PIE cohort resulted in an AUC of 0.88 (95% CI 0.84–0.93). Conclusion The excellent performance of the score as reported in the development study was confirmed in this significantly larger and more diverse cohort of patients with encephalitis in Denmark. These results should prompt further prospective testing with wider inclusion criteria.
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