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DOI: 10.1055/s-0043-1767764
Specificity and sensitivity of the SeLECT score in predicting late seizures in patients undergoing intravenous thrombolytic treatment and the effect of diabetes mellitus and leukoaraiosis
Especificidade e sensibilidade do escore SeLECT na predição de convulsões tardias em pacientes submetidos a tratamento trombolítico intravenoso e o efeito do diabetes mellitus e leucoaraioseAbstract
Background Seizures after stroke can negatively affect the prognosis of ischemic stroke and cause a decrease in quality of life. The efficacy of intravenous (IV) recombinant tissue plasminogen activator (rt-PA) treatment in acute ischemic stroke has been demonstrated in many studies, and IV rt-PA treatment has been increasingly used around the world. The SeLECT score is a useful score for the prediction of late seizures after stroke and includes the severity of stroke (Se), large artery atherosclerosis (L), early seizure (E), cortical involvement (C), and the territory of the middle cerebral artery (T). However, the specificity and sensitivity of the SeLECT score have not been studied in acute ischemic stroke patients that received IV rt-PA treatment.
Objective In the present study, we aimed to validate and develop the SeLECT score in acute ischemic stroke patients receiving IV rt-PA treatment.
Methods The present study included 157 patients who received IV thrombolytic treatment in our third-stage hospital. The 1-year seizure rates of the patients were detected. SeLECT scores were calculated.
Results In our study, we found that the SeLECT score had low sensitivity but high specificity for predicting the likelihood of late seizure after stroke in patients administered IV rt-PA therapy. In addition to the SeLECT score, we found that the specificity and sensitivity were higher when we evaluated diabetes mellitus (DM) and leukoaraiosis.
Conclusion We found that DM was an independent risk factor for late seizures after stroke in a patient group receiving thrombolytic therapy, and late seizures after stroke were less frequent in patients with leukoaraiosis.
Resumo
Antecedentes As convulsões após o AVC podem afetar negativamente o prognóstico do AVC isquêmico e causar uma diminuição na qualidade de vida. A eficácia do tratamento com ativador do plasminogênio tecidual recombinante (rt-PA) intravenoso (IV) no AVC isquêmico agudo foi demonstrada em muitos estudos, e o tratamento com rt-PA IV tem sido cada vez mais usado em todo o mundo. A pontuação SeLECT é uma pontuação útil para a previsão de convulsões tardias após AVC e inclui a gravidade do AVC (Se), aterosclerose de grandes artérias (L), convulsão precoce (E), envolvimento cortical (C) e o território do meio artéria cerebral (T). No entanto, a especificidade e a sensibilidade do escore SeLECT não foram estudadas em pacientes com AVC isquêmico agudo que receberam tratamento IV com rt-PA.
Objetivo No presente estudo, objetivamos validar e desenvolver o escore SeLECT em pacientes com AVC isquêmico agudo recebendo tratamento IV com rt-PA.
Métodos O presente estudo incluiu 157 pacientes que receberam tratamento trombolítico IV em nosso hospital de terceiro estágio. As taxas de convulsão de 1 ano dos pacientes foram detectadas. Os escores SeLECT foram calculados.
Resultados Em nosso estudo, descobrimos que o escore SeLECT apresentou baixa sensibilidade, mas alta especificidade para prever a probabilidade de convulsão tardia após AVC em pacientes que receberam terapia IV com rt-PA. Além do escore SeLECT, descobrimos que a especificidade e a sensibilidade foram maiores quando avaliamos diabetes mellitus (DM) e leucoaraiose.
Conclusão Descobrimos que DM foi um fator de risco independente para convulsões tardias após AVC em um grupo de pacientes recebendo terapia trombolítica, e convulsões tardias após AVC foram menos frequentes em pacientes com leucoaraiose.
Palavras-chave
Acidente Vascular Cerebral - Convulsões - Administração Intravenosa - Ativador de Plasminogênio TecidualAuthors' Contributions
YD: concepts, design, clinical studies, data acquisition, manuscript preparation, guarantor; MB, YD: definition of intellectual content, manuscript review; YD, ABD: literature search; YD, GÖ: data analysis; GÖ: statistical analysis; MB, ABD: manuscript editing.
Publication History
Received: 02 June 2022
Accepted: 14 November 2022
Article published online:
14 April 2023
© 2023. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)
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References
- 1 Seshadri S, Wolf PA. Lifetime risk of stroke and dementia: current concepts, and estimates from the Framingham Study. Lancet Neurol 2007; 6 (12) 1106-1114
- 2 Hauser WA, Annegers JF, Kurland LT. Incidence of epilepsy and unprovoked seizures in Rochester, Minnesota: 1935-1984. Epilepsia 1993; 34 (03) 453-468
- 3 Huang CW, Saposnik G, Fang J, Steven DA, Burneo JG. Influence of seizures on stroke outcomes: a large multicenter study. Neurology 2014; 82 (09) 768-776
- 4 Kim JS, Choi-Kwon S, Kwon SU, Lee HJ, Park K-A, Seo YS. Factors affecting the quality of life after ischemic stroke: young versus old patients. J Clin Neurol 2005; 1 (01) 59-68
- 5 Guekht A, Mizinova M, Ershov A. et al. In-hospital costs in patients with seizures and epilepsy after stroke. Epilepsia 2015; 56 (08) 1309-1313
- 6 National Institute of Neurological Disorders and Stroke rt-PA Stroke Study Group. Tissue plasminogen activator for acute ischemic stroke. N Engl J Med 1995; 333 (24) 1581-1587
- 7 Hacke W, Kaste M, Bluhmki E. et al; ECASS Investigators. Thrombolysis with alteplase 3 to 4.5 hours after acute ischemic stroke. N Engl J Med 2008; 359 (13) 1317-1329
- 8 Yepes M, Roussel BD, Ali C, Vivien D. Tissue-type plasminogen activator in the ischemic brain: more than a thrombolytic. Trends Neurosci 2009; 32 (01) 48-55
- 9 Qian Z, Gilbert ME, Colicos MA, Kandel ER, Kuhl D. Tissue-plasminogen activator is induced as an immediate-early gene during seizure, kindling and long-term potentiation. Nature 1993; 361 (6411): 453-457
- 10 Yepes M, Sandkvist M, Coleman TA. et al. Regulation of seizure spreading by neuroserpin and tissue-type plasminogen activator is plasminogen-independent. J Clin Invest 2002; 109 (12) 1571-1578
- 11 Tsirka SE, Gualandris A, Amaral DG, Strickland S. Excitotoxin-induced neuronal degeneration and seizure are mediated by tissue plasminogen activator. Nature 1995; 377 (6547): 340-344
- 12 Naylor J, Thevathasan A, Churilov L. et al. Association between different acute stroke therapies and development of post stroke seizures. BMC Neurol 2018; 18 (01) 61
- 13 Belcastro V, Brigo F, Ferlazzo E. et al. Incidence of early poststroke seizures during reperfusion therapies in patients with acute ischemic stroke: An observational prospective study: (TESI study: “Trombolisi/Trombectomia e crisi Epilettiche precoci nello Stroke Ischemico”). Epilepsy Behav 2020; 104 (Pt B): 106476
- 14 Burneo JG, Antaya TC, Allen BN, Belisle A, Shariff SZ, Saposnik G. The risk of new-onset epilepsy and refractory epilepsy in older adult stroke survivors. Neurology 2019; 93 (06) e568-e577
- 15 Dinç Y, Uzuner GT, Emir B. Evaluation of Seizure After Stroke in Stroke Unit. Turk J Neurol 2018; 24: 153-158
- 16 Beghi E, Carpio A, Forsgren L. et al. Recommendation for a definition of acute symptomatic seizure. Epilepsia 2010; 51 (04) 671-675
- 17 Fisher RS, Acevedo C, Arzimanoglou A. et al. ILAE official report: a practical clinical definition of epilepsy. Epilepsia 2014; 55 (04) 475-482
- 18 Galovic M, Döhler N, Erdélyi-Canavese B. et al. Prediction of late seizures after ischaemic stroke with a novel prognostic model (the SeLECT score): a multivariable prediction model development and validation study. Lancet Neurol 2018; 17 (02) 143-152
- 19 Larrue V, von Kummer R R, Müller A, Bluhmki E. Risk factors for severe hemorrhagic transformation in ischemic stroke patients treated with recombinant tissue plasminogen activator: a secondary analysis of the European-Australasian Acute Stroke Study (ECASS II). Stroke 2001; 32 (02) 438-441
- 20 Cuadrado-Godia E. Early neurological deterioration, easy methods to detect it. Indian J Med Res 2015; 141 (03) 266-268
- 21 Mazya M, Egido JA, Ford GA. et al; SITS Investigators. Predicting the risk of symptomatic intracerebral hemorrhage in ischemic stroke treated with intravenous alteplase: safe Implementation of Treatments in Stroke (SITS) symptomatic intracerebral hemorrhage risk score. Stroke 2012; 43 (06) 1524-1531
- 22 van Swieten JC, Hijdra A, Koudstaal PJ, van Gijn J. Grading white matter lesions on CT and MRI: a simple scale. J Neurol Neurosurg Psychiatry 1990; 53 (12) 1080-1083
- 23 Shen L, Yang J, Tang Y. Predictive Values of the SeLECT Score and IL-1β for Post-Stroke Epilepsy. Neuropsychiatr Dis Treat 2021; 17: 2465-2472
- 24 Krakow K, Sitzer M, Rosenow F, Steinmetz H, Foerch C. Arbeitsgruppe Schlaganfall Hessen. Predictors of acute poststroke seizures. Cerebrovasc Dis 2010; 30 (06) 584-589
- 25 Adelöw C, Andersson T, Ahlbom A, Tomson T. Prior hospitalization for stroke, diabetes, myocardial infarction, and subsequent risk of unprovoked seizures. Epilepsia 2011; 52 (02) 301-307
- 26 Uchino H, Smith ML, Bengzon J, Lundgren J, Siesjö BK. Characteristics of postischemic seizures in hyperglycemic rats. J Neurol Sci 1996; 139 (01) 21-27
- 27 Maheandiran M, Mylvaganam S, Wu C. et al. Severe hypoglycemia in a juvenile diabetic rat model: presence and severity of seizures are associated with mortality. PLoS One 2013; 8 (12) e83168
- 28 Schwechter EM, Velísková J, Velísek L. Correlation between extracellular glucose and seizure susceptibility in adult rats. Ann Neurol 2003; 53 (01) 91-101
- 29 Vezzani A, French J, Bartfai T, Baram TZ. The role of inflammation in epilepsy. Nat Rev Neurol 2011; 7 (01) 31-40
- 30 Johnson MR, Behmoaras J, Bottolo L. et al. Systems genetics identifies Sestrin 3 as a regulator of a proconvulsant gene network in human epileptic hippocampus. Nat Commun 2015; 6: 6031
- 31 Sada N, Lee S, Katsu T, Otsuki T, Inoue T. Epilepsy treatment. Targeting LDH enzymes with a stiripentol analog to treat epilepsy. Science 2015; 347 (6228): 1362-1367
- 32 Tao R, Xiong X, Liangpunsakul S, Dong XC. Sestrin 3 protein enhances hepatic insulin sensitivity by direct activation of the mTORC2-Akt signaling. Diabetes 2015; 64 (04) 1211-1223
- 33 Shi Z, Lei Z, Wu F, Xia L, Ruan Y, Xu ZC. Increased Sestrin3 Contributes to Post-ischemic Seizures in the Diabetic Condition. Front Neurosci 2021; 14: 591207
- 34 Jennett B. Posttraumatic epilepsy. Adv Neurol 1979; 22: 137-147
- 35 Luhmann HJ, Mudrick-Donnon LA, Mittmann T, Heinemann U. Ischaemia-induced long-term hyperexcitability in rat neocortex. Eur J Neurosci 1995; 7 (02) 180-191
- 36 Stroemer RP, Kent TA, Hulsebosch CE. Neocortical neural sprouting, synaptogenesis, and behavioral recovery after neocortical infarction in rats. Stroke 1995; 26 (11) 2135-2144
- 37 Hachinski VC, Potter P, Merskey H. Leuko-araiosis. Arch Neurol 1987; 44 (01) 21-23
- 38 Steingart A, Hachinski VC, Lau C. et al. Cognitive and neurologic findings in demented patients with diffuse white matter lucencies on computed tomographic scan (leuko-araiosis). Arch Neurol 1987; 44 (01) 36-39
- 39 Hilal S, Sikking E, Shaik MA. et al. Cortical cerebral microinfarcts on 3T MRI: A novel marker of cerebrovascular disease. Neurology 2016; 87 (15) 1583-1590
- 40 Johnson EL, Krauss GL, Lee AK. et al. Association between white matter hyperintensities, cortical volumes, and late-onset epilepsy. Neurology 2019; 92 (09) e988-e995
- 41 Eryildiz ES, Özdemir A, Yılmaz D, Baş DF. The role of leukoaraiosis on outcomes and recombinant tissue-plasminogen activator-related symptomatic intracerebral hemorrhages in acute stroke. Neurol Sci Neurophysiol 2020; 37: 70-74
- 42 Wiszniewska M, Devuyst G, Bogousslavsky J, Ghika J, van Melle G. What is the significance of leukoaraiosis in patients with acute ischemic stroke?. Arch Neurol 2000; 57 (07) 967-973