TY - JOUR
T1 - Validation of a risk score to differentiate autoimmune and viral encephalitis
T2 - a Nationwide Cohort Study in Denmark
AU - Fjordside, Lasse
AU - Nissen, Mette Scheller
AU - Florescu, Anna Maria
AU - Storgaard, Merete
AU - Larsen, Lykke
AU - Wiese, Lothar
AU - von Lüttichau, Hans Rudolf
AU - Jepsen, Micha Phill Grønholm
AU - Hansen, Birgitte Rønde
AU - Andersen, Christian Østergaard
AU - Bodilsen, Jacob
AU - Nielsen, Henrik
AU - Blaabjerg, Morten
AU - Lebech, Anne-Mette
AU - Mens, Helene
N1 - © 2024. The Author(s).
PY - 2024/8
Y1 - 2024/8
N2 - 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.
AB - 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.
KW - Adult
KW - Aged
KW - Aged, 80 and over
KW - Autoimmune Diseases/epidemiology
KW - Cohort Studies
KW - Denmark/epidemiology
KW - Diagnosis, Differential
KW - Encephalitis, Viral/diagnosis
KW - Encephalitis/diagnosis
KW - Female
KW - Humans
KW - Male
KW - Middle Aged
KW - Retrospective Studies
KW - Risk Assessment/methods
KW - Young Adult
UR - http://www.scopus.com/inward/record.url?scp=85193820634&partnerID=8YFLogxK
U2 - 10.1007/s00415-024-12392-3
DO - 10.1007/s00415-024-12392-3
M3 - Journal article
C2 - 38761191
SN - 0340-5354
VL - 271
SP - 4972
EP - 4981
JO - Journal of Neurology
JF - Journal of Neurology
IS - 8
ER -