TY - JOUR
T1 - Implications for driving based on the risk of seizures after ischaemic stroke
AU - Schubert, Kai Michael
AU - Bicciato, Giulio
AU - Sinka, Lucia
AU - Abraira, Laura
AU - Santamarina, Estevo
AU - Álvarez-Sabín, José
AU - Ferreira-Atuesta, Carolina
AU - Katan, Mira
AU - Scherrer, Natalie
AU - Terziev, Robert
AU - Döhler, Nico
AU - Erdélyi-Canavese, Barbara
AU - Felbecker, Ansgar
AU - Siebel, Philip
AU - Winklehner, Michael
AU - Von Oertzen, Tim J.
AU - Wagner, Judith N.
AU - Gigli, Gian Luigi
AU - Nilo, Annacarmen
AU - Janes, Francesco
AU - Merlino, Giovanni
AU - Valente, Mariarosaria
AU - Zafra-Sierra, María Paula
AU - Mayor-Romero, Luis Carlos
AU - Conrad, Julian
AU - Evers, S.
AU - Lochner, Piergiorgio
AU - Roell, Frauke
AU - Brigo, Francesco
AU - Bentes, Carla
AU - Peralta, Rita
AU - Pinho E Melo, Teresa
AU - Keezer, Mark R.
AU - Duncan, John Sidney
AU - Sander, Josemir W.
AU - Tettenborn, Barbara
AU - Koepp, Matthias
AU - Galovic, Marian
N1 - Publisher Copyright:
© 2024 Author(s). Published by BMJ.
PY - 2024
Y1 - 2024
N2 - Background: In addition to other stroke-related deficits, the risk of seizures may impact driving ability after stroke. Methods: We analysed data from a multicentre international cohort, including 4452 adults with acute ischaemic stroke and no prior seizures. We calculated the Chance of Occurrence of Seizure in the next Year (COSY) according to the SeLECT2.0 prognostic model. We considered COSY<20% safe for private and <2% for professional driving, aligning with commonly used cut-offs. Results: Seizure risks in the next year were mainly influenced by the baseline risk-stratified according to the SeLECT2.0 score and, to a lesser extent, by the poststroke seizure-free interval (SFI). Those without acute symptomatic seizures (SeLECT2.0 0-6 points) had low COSY (0.7%-11%) immediately after stroke, not requiring an SFI. In stroke survivors with acute symptomatic seizures (SeLECT2.0 3-13 points), COSY after a 3-month SFI ranged from 2% to 92%, showing substantial interindividual variability. Stroke survivors with acute symptomatic status epilepticus (SeLECT2.0 7-13 points) had the highest risk (14%-92%). Conclusions: Personalised prognostic models, such as SeLECT2.0, may offer better guidance for poststroke driving decisions than generic SFIs. Our findings provide practical tools, including a smartphone-based or web-based application, to assess seizure risks and determine appropriate SFIs for safe driving.
AB - Background: In addition to other stroke-related deficits, the risk of seizures may impact driving ability after stroke. Methods: We analysed data from a multicentre international cohort, including 4452 adults with acute ischaemic stroke and no prior seizures. We calculated the Chance of Occurrence of Seizure in the next Year (COSY) according to the SeLECT2.0 prognostic model. We considered COSY<20% safe for private and <2% for professional driving, aligning with commonly used cut-offs. Results: Seizure risks in the next year were mainly influenced by the baseline risk-stratified according to the SeLECT2.0 score and, to a lesser extent, by the poststroke seizure-free interval (SFI). Those without acute symptomatic seizures (SeLECT2.0 0-6 points) had low COSY (0.7%-11%) immediately after stroke, not requiring an SFI. In stroke survivors with acute symptomatic seizures (SeLECT2.0 3-13 points), COSY after a 3-month SFI ranged from 2% to 92%, showing substantial interindividual variability. Stroke survivors with acute symptomatic status epilepticus (SeLECT2.0 7-13 points) had the highest risk (14%-92%). Conclusions: Personalised prognostic models, such as SeLECT2.0, may offer better guidance for poststroke driving decisions than generic SFIs. Our findings provide practical tools, including a smartphone-based or web-based application, to assess seizure risks and determine appropriate SFIs for safe driving.
KW - Activities of Daily Living
KW - CLINICAL NEUROLOGY
KW - EPILEPSY
KW - STROKE
UR - http://www.scopus.com/inward/record.url?scp=85193946450&partnerID=8YFLogxK
U2 - 10.1136/jnnp-2024-333505
DO - 10.1136/jnnp-2024-333505
M3 - Article
AN - SCOPUS:85193946450
SN - 0022-3050
JO - Journal of Neurology, Neurosurgery and Psychiatry
JF - Journal of Neurology, Neurosurgery and Psychiatry
M1 - jnnp-2024-333505
ER -