TY - JOUR
T1 - Development and Validation of a Clinical Score to Predict Epilepsy after Cerebral Venous Thrombosis
AU - Lindgren, Erik
AU - Shu, Liqi
AU - Simaan, Naaem
AU - Krzywicka, Katarzyna
AU - De Winter, Maria A.
AU - Sánchez Van Kammen, Mayte
AU - Molad, Jeremy
AU - Klein, Piers
AU - Hallevi, Hen
AU - Barnea, Rani
AU - Heldner, Mirjam R.
AU - Hiltunen, Sini
AU - De Sousa, Diana Aguiar
AU - Ferro, José M.
AU - Arauz, Antonio
AU - Putaala, Jukka
AU - Arnold, Marcel
AU - Nguyen, Thanh N.
AU - Stretz, Christoph
AU - Tatlisumak, Turgut
AU - Jood, Katarina
AU - Yaghi, Shadi
AU - Leker, Ronen R.
AU - Coutinho, Jonathan M.
AU - Mansour, Maryam
AU - Canhão, Patrícia
AU - Ekizoglu, Esme
AU - Rodrigues, Miguel
AU - Silva, Elisa M.
AU - Garcia-Esperon, Carlos
AU - Arnao, Valentina
AU - Aladin, Shorooq
AU - Mendel, Rom
AU - Aridon, Paolo
AU - Sezgin, Mine
AU - Alasheev, Andrey
AU - Smolkin, Andrey
AU - Guisado-Alonso, Daniel
AU - Yesilot, Nilufer
AU - Barboza, Miguel A.
AU - Ghiasian, Masoud
AU - Silvis, Suzanne M.
AU - Fang, Ton
AU - Siegler, James E.
AU - Wu, Teddy
AU - Wilson, Duncan
AU - Asad, Syed Daniyal
AU - Al Kasab, Sami
AU - Almallouhi, Eyad
AU - Frontera, Jennifer
AU - Rothstein, Aaron
AU - Bakradze, Ekaterina
AU - Omran, Setareh Salehi
AU - Henninger, Nils
AU - Kuohn, Lindsey
AU - Zubair, Adeel
AU - Sharma, Richa
AU - Kerrigan, Deborah
AU - Aziz, Yasmin
AU - Mistry, Eva
AU - Zuurbier, Susanna M.
N1 - Publisher Copyright:
© 2024 American Medical Association. All rights reserved.
PY - 2024/12/1
Y1 - 2024/12/1
N2 - Importance: One of 10 patients develop epilepsy in the late phase after cerebral venous thrombosis (CVT) diagnosis but predicting the individual risk is difficult. Objective: To develop and externally validate a prognostic score to estimate the individual risk of post-CVT epilepsy. Design, Setting, and Participants: This observational cohort study included both retrospective and prospective patients enrolled from 1994 through 2022. For development of the DIAS3 score, data from the International CVT Consortium (n = 1128), a large international hospital-based multicenter CVT cohort, were used. For validation, data from 2 independent multicenter cohorts, the ACTION-CVT (n = 543) and the Israel CVT study (n = 556), were used. Of 2937 eligible, consecutively enrolled adult patients with radiologically verified CVT, 710 patients with a history of epilepsy prior to CVT, follow-up less than 8 days, and missing late seizure status were excluded. Exposure: The prediction score (DIAS3) was developed based on available literature and clinical plausibility and consisted of 6 readily available clinical variables collected during the acute phase: decompressive hemicraniectomy, intracerebral hemorrhage at presentation, age, seizure(s) in the acute phase (excluding status epilepticus), status epilepticus in the acute phase, and subdural hematoma at presentation. Main Outcome and Measure: Time to a first late seizure, defined as occurring more than 7 days after diagnosis of CVT. Results: Of 1128 patients included in the derivation cohort (median age, 41 [IQR, 30-53] years; 805 women [71%]), 128 (11%) developed post-CVT epilepsy during a median follow-up of 12 (IQR, 3-26) months. According to the DIAS3 score, the predicted 1-year and 3-year risk of epilepsy in individual patients ranged from 7% to 68% and 10% to 83%, respectively. Internal and external validation showed adequate discrimination in the derivation cohort (1 year and 3 years: C statistic, 0.74; 95% CI, 0.70-0.79) and the 2 independent validation cohorts, (ACTION-CVT) 1 year: C statistic, 0.76; 95% CI, 0.67-0.84; 3 years: C statistic, 0.77; 95% CI, 0.66-0.84; and Israel CVT study 1 year: C statistic, 0.80; 95% CI, 0.75-0.86. Calibration plots indicated adequate agreement between predicted and observed risks. Conclusions and Relevance: The DIAS3 score (freely available online) is a simple tool that can help predict the risk of post-CVT epilepsy in individual patients. The model can improve opportunities for personalized medicine and may aid in decision-making regarding antiseizure medication, patient counseling, and facilitation of research on epileptogenesis in CVT.
AB - Importance: One of 10 patients develop epilepsy in the late phase after cerebral venous thrombosis (CVT) diagnosis but predicting the individual risk is difficult. Objective: To develop and externally validate a prognostic score to estimate the individual risk of post-CVT epilepsy. Design, Setting, and Participants: This observational cohort study included both retrospective and prospective patients enrolled from 1994 through 2022. For development of the DIAS3 score, data from the International CVT Consortium (n = 1128), a large international hospital-based multicenter CVT cohort, were used. For validation, data from 2 independent multicenter cohorts, the ACTION-CVT (n = 543) and the Israel CVT study (n = 556), were used. Of 2937 eligible, consecutively enrolled adult patients with radiologically verified CVT, 710 patients with a history of epilepsy prior to CVT, follow-up less than 8 days, and missing late seizure status were excluded. Exposure: The prediction score (DIAS3) was developed based on available literature and clinical plausibility and consisted of 6 readily available clinical variables collected during the acute phase: decompressive hemicraniectomy, intracerebral hemorrhage at presentation, age, seizure(s) in the acute phase (excluding status epilepticus), status epilepticus in the acute phase, and subdural hematoma at presentation. Main Outcome and Measure: Time to a first late seizure, defined as occurring more than 7 days after diagnosis of CVT. Results: Of 1128 patients included in the derivation cohort (median age, 41 [IQR, 30-53] years; 805 women [71%]), 128 (11%) developed post-CVT epilepsy during a median follow-up of 12 (IQR, 3-26) months. According to the DIAS3 score, the predicted 1-year and 3-year risk of epilepsy in individual patients ranged from 7% to 68% and 10% to 83%, respectively. Internal and external validation showed adequate discrimination in the derivation cohort (1 year and 3 years: C statistic, 0.74; 95% CI, 0.70-0.79) and the 2 independent validation cohorts, (ACTION-CVT) 1 year: C statistic, 0.76; 95% CI, 0.67-0.84; 3 years: C statistic, 0.77; 95% CI, 0.66-0.84; and Israel CVT study 1 year: C statistic, 0.80; 95% CI, 0.75-0.86. Calibration plots indicated adequate agreement between predicted and observed risks. Conclusions and Relevance: The DIAS3 score (freely available online) is a simple tool that can help predict the risk of post-CVT epilepsy in individual patients. The model can improve opportunities for personalized medicine and may aid in decision-making regarding antiseizure medication, patient counseling, and facilitation of research on epileptogenesis in CVT.
UR - http://www.scopus.com/inward/record.url?scp=85209633642&partnerID=8YFLogxK
U2 - 10.1001/jamaneurol.2024.3481
DO - 10.1001/jamaneurol.2024.3481
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C2 - 39432281
AN - SCOPUS:85209633642
SN - 2168-6149
VL - 81
JO - JAMA Neurology
JF - JAMA Neurology
IS - 12
ER -