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Published in: Drugs & Aging 2/2023

06-02-2023 | Status Epilepticus | Leading Article

Status Epilepticus in Older Adults: Diagnostic and Treatment Considerations

Authors: Gamaleldin M. Osman, Sara E. Hocker

Published in: Drugs & Aging | Issue 2/2023

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Abstract

Status epilepticus (SE) is one of the leading life-threatening neurological emergencies in the elderly population, with significant morbidity and mortality. SE presents unique diagnostic and therapeutic challenges in the older population given overlap with other causes of encephalopathy, complicating diagnosis, and the common occurrence of multiple comorbid diseases complicates treatment. First-line therapy involves the use of rescue benzodiazepine in the form of intravenous lorazepam or diazepam, intramuscular or intranasal midazolam and rectal diazepam. Second-line therapies include parenteral levetiracetam, fosphenytoin, valproate and lacosamide, and underlying comorbidities guide the choice of appropriate medication, while third-line therapies may be influenced by the patient’s code status as well as the cause and type of SE. The standard of care for convulsive SE is treatment with an intravenous anesthetic, including midazolam, propofol, ketamine and pentobarbital. There is currently limited evidence guiding appropriate therapy in patients failing third-line therapies. Adjunctive strategies may include immunomodulatory treatments, non-pharmacological strategies such as ketogenic diet, neuromodulation therapies and surgery in select cases. Surrogate decision makers should be updated early and often in refractory episodes of SE and informed of the high morbidity and mortality associated with the disease as well as the high probability of subsequent epilepsy among survivors.
Literature
1.
go back to reference DeLorenzo RJ, Pellock JM, Towne AR, Boggs JG. Epidemiology of status epilepticus. J Clin Neurophysiol. 1995;12(4):316–25.PubMedCrossRef DeLorenzo RJ, Pellock JM, Towne AR, Boggs JG. Epidemiology of status epilepticus. J Clin Neurophysiol. 1995;12(4):316–25.PubMedCrossRef
2.
go back to reference Hesdorffer DC, Logroscino G, Cascino G, Annegers JF, Hauser WA. Incidence of status epilepticus in Rochester, Minnesota, 1965–1984. Neurology. 1998;50(3):735–41.PubMedCrossRef Hesdorffer DC, Logroscino G, Cascino G, Annegers JF, Hauser WA. Incidence of status epilepticus in Rochester, Minnesota, 1965–1984. Neurology. 1998;50(3):735–41.PubMedCrossRef
4.
go back to reference Sheth RD, Drazkowski JF, Sirven JI, Gidal BE, Hermann BP. Protracted ictal confusion in elderly patients. Arch Neurol. 2006;63(4):529–32.PubMedCrossRef Sheth RD, Drazkowski JF, Sirven JI, Gidal BE, Hermann BP. Protracted ictal confusion in elderly patients. Arch Neurol. 2006;63(4):529–32.PubMedCrossRef
5.
go back to reference Terzano MG, Parrino L, Mazzucchi A, Moretti G. Confusional states with periodic lateralized epileptiform discharges (PLEDs): a peculiar epileptic syndrome in the elderly. Epilepsia. 1986;27(4):446–57.PubMedCrossRef Terzano MG, Parrino L, Mazzucchi A, Moretti G. Confusional states with periodic lateralized epileptiform discharges (PLEDs): a peculiar epileptic syndrome in the elderly. Epilepsia. 1986;27(4):446–57.PubMedCrossRef
6.
go back to reference Logroscino G, Hesdorffer DC, Cascino G, Annegers JF, Hauser WA. Short-term mortality after a first episode of status epilepticus. Epilepsia. 1997;38(12):1344–9.PubMedCrossRef Logroscino G, Hesdorffer DC, Cascino G, Annegers JF, Hauser WA. Short-term mortality after a first episode of status epilepticus. Epilepsia. 1997;38(12):1344–9.PubMedCrossRef
7.
go back to reference DeLorenzo RJ, Towne AR, Pellock JM, Ko D. Status epilepticus in children, adults, and the elderly. Epilepsia. 1992;33(Suppl 4):S15-25.PubMedCrossRef DeLorenzo RJ, Towne AR, Pellock JM, Ko D. Status epilepticus in children, adults, and the elderly. Epilepsia. 1992;33(Suppl 4):S15-25.PubMedCrossRef
8.
go back to reference Hui AC, Lam AK, Wong A, Chow KM, Chan EL, Choi SL, et al. Generalized tonic-clonic status epilepticus in the elderly in China. Epileptic Disord. 2005;7(1):27–31.PubMed Hui AC, Lam AK, Wong A, Chow KM, Chan EL, Choi SL, et al. Generalized tonic-clonic status epilepticus in the elderly in China. Epileptic Disord. 2005;7(1):27–31.PubMed
9.
go back to reference Vilella L, González Cuevas M, Quintana Luque M, Toledo M, Sueiras Gil M, Guzmán L, et al. Prognosis of status epilepticus in elderly patients. Acta Neurol Scand. 2018;137(3):321–8.PubMedCrossRef Vilella L, González Cuevas M, Quintana Luque M, Toledo M, Sueiras Gil M, Guzmán L, et al. Prognosis of status epilepticus in elderly patients. Acta Neurol Scand. 2018;137(3):321–8.PubMedCrossRef
10.
go back to reference Kilbride RD, Reynolds AS, Szaflarski JP, Hirsch LJ. Clinical outcomes following prolonged refractory status epilepticus (PRSE). Neurocrit Care. 2013;18(3):374–85.PubMedCrossRef Kilbride RD, Reynolds AS, Szaflarski JP, Hirsch LJ. Clinical outcomes following prolonged refractory status epilepticus (PRSE). Neurocrit Care. 2013;18(3):374–85.PubMedCrossRef
11.
go back to reference Arnautova EN, Nesmeianova TN. A proposed international classification of epileptic seizures. Epilepsia. 1964;5:297–306.PubMedCrossRef Arnautova EN, Nesmeianova TN. A proposed international classification of epileptic seizures. Epilepsia. 1964;5:297–306.PubMedCrossRef
12.
go back to reference Treatment of convulsive status epilepticus. Recommendations of the Epilepsy Foundation of America’s Working Group on Status Epilepticus. JAMA. 1993;270(7):854–9.CrossRef Treatment of convulsive status epilepticus. Recommendations of the Epilepsy Foundation of America’s Working Group on Status Epilepticus. JAMA. 1993;270(7):854–9.CrossRef
13.
go back to reference Lowenstein DH, Bleck T, Macdonald RL. It’s time to revise the definition of status epilepticus. Epilepsia. 1999;40(1):120–2.PubMedCrossRef Lowenstein DH, Bleck T, Macdonald RL. It’s time to revise the definition of status epilepticus. Epilepsia. 1999;40(1):120–2.PubMedCrossRef
14.
go back to reference Brophy G, Bell R, Claassen J, Alldredge B, Bleck T, Glauser T, et al. Guidelines for the evaluation and management of status epilepticus. Neurocrit Care. 2012;17(1):3–23.PubMedCrossRef Brophy G, Bell R, Claassen J, Alldredge B, Bleck T, Glauser T, et al. Guidelines for the evaluation and management of status epilepticus. Neurocrit Care. 2012;17(1):3–23.PubMedCrossRef
15.
go back to reference Trinka E, Cock H, Hesdorffer D, Rossetti AO, Scheffer IE, Shinnar S, et al. A definition and classification of status epilepticus – Report of the ILAE Task Force on Classification of Status Epilepticus. Epilepsia. 2015;56(10):1515–23.PubMedCrossRef Trinka E, Cock H, Hesdorffer D, Rossetti AO, Scheffer IE, Shinnar S, et al. A definition and classification of status epilepticus – Report of the ILAE Task Force on Classification of Status Epilepticus. Epilepsia. 2015;56(10):1515–23.PubMedCrossRef
16.
go back to reference Hirsch LJ, Gaspard N, van Baalen A, Nabbout R, Demeret S, Loddenkemper T, et al. Proposed consensus definitions for new-onset refractory status epilepticus (NORSE), febrile infection-related epilepsy syndrome (FIRES), and related conditions. Epilepsia. 2018;59(4):739–44.PubMedCrossRef Hirsch LJ, Gaspard N, van Baalen A, Nabbout R, Demeret S, Loddenkemper T, et al. Proposed consensus definitions for new-onset refractory status epilepticus (NORSE), febrile infection-related epilepsy syndrome (FIRES), and related conditions. Epilepsia. 2018;59(4):739–44.PubMedCrossRef
18.
go back to reference Knake S, Rosenow F, Vescovi M, Oertel WH, Mueller HH, Wirbatz A, et al. Incidence of status epilepticus in adults in Germany: a prospective, population-based study. Epilepsia. 2001;42(6):714–8.PubMedCrossRef Knake S, Rosenow F, Vescovi M, Oertel WH, Mueller HH, Wirbatz A, et al. Incidence of status epilepticus in adults in Germany: a prospective, population-based study. Epilepsia. 2001;42(6):714–8.PubMedCrossRef
19.
go back to reference Govoni V, Fallica E, Monetti VC, Guerzoni F, Faggioli R, Casetta I, et al. Incidence of status epilepticus in southern Europe: a population study in the health district of Ferrara, Italy. Eur Neurol. 2008;59(3–4):120–6.PubMedCrossRef Govoni V, Fallica E, Monetti VC, Guerzoni F, Faggioli R, Casetta I, et al. Incidence of status epilepticus in southern Europe: a population study in the health district of Ferrara, Italy. Eur Neurol. 2008;59(3–4):120–6.PubMedCrossRef
20.
go back to reference Yoshimura H, Matsumoto R, Ueda H, Ariyoshi K, Ikeda A, Takahashi R, et al. Status epilepticus in the elderly: comparison with younger adults in a comprehensive community hospital. Seizure Eur J Epilepsy. 2018;61:23–9.CrossRef Yoshimura H, Matsumoto R, Ueda H, Ariyoshi K, Ikeda A, Takahashi R, et al. Status epilepticus in the elderly: comparison with younger adults in a comprehensive community hospital. Seizure Eur J Epilepsy. 2018;61:23–9.CrossRef
21.
go back to reference Rohracher A, Reiter DP, Brigo F, Kalss G, Thomschewski A, Novak H, et al. Status epilepticus in the elderly—a retrospective study on 120 patients. Epilepsy Res. 2016;127:317–23.PubMedCrossRef Rohracher A, Reiter DP, Brigo F, Kalss G, Thomschewski A, Novak H, et al. Status epilepticus in the elderly—a retrospective study on 120 patients. Epilepsy Res. 2016;127:317–23.PubMedCrossRef
22.
go back to reference Sadeghi M, Eshraghi M, Akers KG, Hadidchi S, Kakara M, Nasseri M, et al. Outcomes of status epilepticus and their predictors in the elderly—a systematic review. Seizure Eur J Epilepsy. 2020;81:210–21.CrossRef Sadeghi M, Eshraghi M, Akers KG, Hadidchi S, Kakara M, Nasseri M, et al. Outcomes of status epilepticus and their predictors in the elderly—a systematic review. Seizure Eur J Epilepsy. 2020;81:210–21.CrossRef
23.
go back to reference Martin Y, Artaz MA, Bornand-Rousselot A. Nonconvulsive status epilepticus in the elderly. J Am Geriatr Soc. 2004;52(3):476–7.PubMedCrossRef Martin Y, Artaz MA, Bornand-Rousselot A. Nonconvulsive status epilepticus in the elderly. J Am Geriatr Soc. 2004;52(3):476–7.PubMedCrossRef
24.
go back to reference Kantanen AM, Reinikainen M, Parviainen I, Ruokonen E, Ala-Peijari M, Bäcklund T, et al. Incidence and mortality of super-refractory status epilepticus in adults. Epilepsy Behav. 2015;49:131–4.PubMedCrossRef Kantanen AM, Reinikainen M, Parviainen I, Ruokonen E, Ala-Peijari M, Bäcklund T, et al. Incidence and mortality of super-refractory status epilepticus in adults. Epilepsy Behav. 2015;49:131–4.PubMedCrossRef
25.
go back to reference Hocker SE, Britton JW, Mandrekar JN, Wijdicks EF, Rabinstein AA. Predictors of outcome in refractory status epilepticus. JAMA Neurol. 2013;70(1):72–7.PubMedCrossRef Hocker SE, Britton JW, Mandrekar JN, Wijdicks EF, Rabinstein AA. Predictors of outcome in refractory status epilepticus. JAMA Neurol. 2013;70(1):72–7.PubMedCrossRef
26.
go back to reference Mayer SA, Claassen J, Lokin J, Mendelsohn F, Dennis LJ, Fitzsimmons B-F. Refractory status epilepticus: frequency, risk factors, and impact on outcome. Arch Neurol. 2002;59(2):205–10.PubMedCrossRef Mayer SA, Claassen J, Lokin J, Mendelsohn F, Dennis LJ, Fitzsimmons B-F. Refractory status epilepticus: frequency, risk factors, and impact on outcome. Arch Neurol. 2002;59(2):205–10.PubMedCrossRef
27.
go back to reference Nandal S, Castles A, Asrar Ul Haq M, van Gaal W. Takotsubo cardiomyopathy triggered by status epilepticus: case report and literature review. BMJ Case Rep. 2019;12(1). Nandal S, Castles A, Asrar Ul Haq M, van Gaal W. Takotsubo cardiomyopathy triggered by status epilepticus: case report and literature review. BMJ Case Rep. 2019;12(1).
28.
go back to reference Malter MP, Nass RD, Kaluschke T, Fink GR, Burghaus L, Dohmen C. New onset status epilepticus in older patients: clinical characteristics and outcome. Seizure. 2017;51:114–20.PubMedCrossRef Malter MP, Nass RD, Kaluschke T, Fink GR, Burghaus L, Dohmen C. New onset status epilepticus in older patients: clinical characteristics and outcome. Seizure. 2017;51:114–20.PubMedCrossRef
29.
go back to reference Oono M, Uno H, Umesaki A, Nagatsuka K, Kinoshita M, Naritomi H. Severe and prolonged ictal paresis in an elderly patient. Epilepsy Behav Case Rep. 2014;2:105–7.PubMedPubMedCentralCrossRef Oono M, Uno H, Umesaki A, Nagatsuka K, Kinoshita M, Naritomi H. Severe and prolonged ictal paresis in an elderly patient. Epilepsy Behav Case Rep. 2014;2:105–7.PubMedPubMedCentralCrossRef
30.
go back to reference Ericson EJ, Gerard EE, Macken MP, Schuele SU. Aphasic status epilepticus: electroclinical correlation. Epilepsia. 2011;52(8):1452–8.PubMedCrossRef Ericson EJ, Gerard EE, Macken MP, Schuele SU. Aphasic status epilepticus: electroclinical correlation. Epilepsia. 2011;52(8):1452–8.PubMedCrossRef
31.
go back to reference Azman F, Tezer FI, Saygi S. Aphasic status epilepticus in a tertiary referral center in Turkey: clinical features, etiology, and outcome. Epilepsy Res. 2020;167:106479.PubMedCrossRef Azman F, Tezer FI, Saygi S. Aphasic status epilepticus in a tertiary referral center in Turkey: clinical features, etiology, and outcome. Epilepsy Res. 2020;167:106479.PubMedCrossRef
32.
go back to reference Barry E, Sussman NM, Bosley TM, Harner RN. Ictal blindness and status epilepticus amauroticus. Epilepsia. 1985;26(6):577–84.PubMedCrossRef Barry E, Sussman NM, Bosley TM, Harner RN. Ictal blindness and status epilepticus amauroticus. Epilepsia. 1985;26(6):577–84.PubMedCrossRef
33.
go back to reference Shaw S, Kim P, Millett D. Status epilepticus amauroticus revisited: ictal and peri-ictal homonymous hemianopsia. Arch Neurol. 2012;69(11):1504–7.PubMedCrossRef Shaw S, Kim P, Millett D. Status epilepticus amauroticus revisited: ictal and peri-ictal homonymous hemianopsia. Arch Neurol. 2012;69(11):1504–7.PubMedCrossRef
34.
go back to reference Leitinger M, Beniczky S, Rohracher A, Gardella E, Kalss G, Qerama E, et al. Salzburg consensus criteria for non-convulsive status epilepticus–approach to clinical application. Epilepsy Behav. 2015;49:158–63.PubMedCrossRef Leitinger M, Beniczky S, Rohracher A, Gardella E, Kalss G, Qerama E, et al. Salzburg consensus criteria for non-convulsive status epilepticus–approach to clinical application. Epilepsy Behav. 2015;49:158–63.PubMedCrossRef
35.
36.
go back to reference Osman GM, Araújo DF, Maciel CB. Ictal interictal continuum patterns. Curr Treat Options Neurol. 2018;20(5):15.PubMedCrossRef Osman GM, Araújo DF, Maciel CB. Ictal interictal continuum patterns. Curr Treat Options Neurol. 2018;20(5):15.PubMedCrossRef
37.
go back to reference Zafar SF, Subramaniam T, Osman G, Herlopian A, Struck AF. Electrographic seizures and ictal-interictal continuum (IIC) patterns in critically ill patients. Epilepsy Behav. 2020;106:107037.PubMedCrossRef Zafar SF, Subramaniam T, Osman G, Herlopian A, Struck AF. Electrographic seizures and ictal-interictal continuum (IIC) patterns in critically ill patients. Epilepsy Behav. 2020;106:107037.PubMedCrossRef
38.
go back to reference Jirsch J, Hirsch LJ. Nonconvulsive seizures: developing a rational approach to the diagnosis and management in the critically ill population. Clin Neurophysiol. 2007;118(8):1660–70.PubMedCrossRef Jirsch J, Hirsch LJ. Nonconvulsive seizures: developing a rational approach to the diagnosis and management in the critically ill population. Clin Neurophysiol. 2007;118(8):1660–70.PubMedCrossRef
39.
go back to reference O'Rourke D, Chen PM, Gaspard N, Foreman B, McClain L, Karakis I, et al. Response Rates to Anticonvulsant Trials in Patients with Triphasic-Wave EEG Patterns of Uncertain Significance. Neurocrit Care. 2015. O'Rourke D, Chen PM, Gaspard N, Foreman B, McClain L, Karakis I, et al. Response Rates to Anticonvulsant Trials in Patients with Triphasic-Wave EEG Patterns of Uncertain Significance. Neurocrit Care. 2015.
40.
go back to reference Engelhorn T, Weise J, Hammen T, Bluemcke I, Hufnagel A, Doerfler A. Early diffusion-weighted MRI predicts regional neuronal damage in generalized status epilepticus in rats treated with diazepam. Neurosci Lett. 2007;417(3):275–80.PubMedCrossRef Engelhorn T, Weise J, Hammen T, Bluemcke I, Hufnagel A, Doerfler A. Early diffusion-weighted MRI predicts regional neuronal damage in generalized status epilepticus in rats treated with diazepam. Neurosci Lett. 2007;417(3):275–80.PubMedCrossRef
41.
go back to reference González-Cuevas M, Coscojuela P, Santamarina E, Pareto D, Quintana M, Sueiras M, et al. Usefulness of brain perfusion CT in focal-onset status epilepticus. Epilepsia. 2019;60(7):1317–24.PubMedCrossRef González-Cuevas M, Coscojuela P, Santamarina E, Pareto D, Quintana M, Sueiras M, et al. Usefulness of brain perfusion CT in focal-onset status epilepticus. Epilepsia. 2019;60(7):1317–24.PubMedCrossRef
42.
go back to reference Venkatraman A, Khawaja A, Bag AK, Mirza M, Szaflarski JP, Pati SBB. Perfusion MRI can impact treatment decision in ictal-interictal continuum. J Clin Neurophysiol. 2017;34(4):e15–8.PubMedCrossRef Venkatraman A, Khawaja A, Bag AK, Mirza M, Szaflarski JP, Pati SBB. Perfusion MRI can impact treatment decision in ictal-interictal continuum. J Clin Neurophysiol. 2017;34(4):e15–8.PubMedCrossRef
43.
go back to reference Assal F, Papazyan JP, Slosman DO, Jallon P, Goerres GW. SPECT in periodic lateralized epileptiform discharges (PLEDs): a form of partial status epilepticus? Seizure. 2001;10(4):260–5.PubMedCrossRef Assal F, Papazyan JP, Slosman DO, Jallon P, Goerres GW. SPECT in periodic lateralized epileptiform discharges (PLEDs): a form of partial status epilepticus? Seizure. 2001;10(4):260–5.PubMedCrossRef
44.
go back to reference Struck AF, Westover MB, Hall LT, Deck GM, Cole AJ, Rosenthal ES. Metabolic correlates of the ictal-interictal continuum: FDG-PET during continuous EEG. Neurocrit Care. 2016;24(3):324–31.PubMedPubMedCentralCrossRef Struck AF, Westover MB, Hall LT, Deck GM, Cole AJ, Rosenthal ES. Metabolic correlates of the ictal-interictal continuum: FDG-PET during continuous EEG. Neurocrit Care. 2016;24(3):324–31.PubMedPubMedCentralCrossRef
45.
go back to reference Young GB, Kreeft JH, McLachlan RS, Demelo J. EEG and clinical associations with mortality in comatose patients in a general intensive care unit. J Clin Neurophysiol. 1999;16. Young GB, Kreeft JH, McLachlan RS, Demelo J. EEG and clinical associations with mortality in comatose patients in a general intensive care unit. J Clin Neurophysiol. 1999;16.
46.
go back to reference Drislane FW, Blum AS, Lopez MR, Gautam S, Schomer DL. Duration of refractory status epilepticus and outcome: loss of prognostic utility after several hours. Epilepsia. 2009;50(6):1566–71.PubMedCrossRef Drislane FW, Blum AS, Lopez MR, Gautam S, Schomer DL. Duration of refractory status epilepticus and outcome: loss of prognostic utility after several hours. Epilepsia. 2009;50(6):1566–71.PubMedCrossRef
47.
go back to reference Glauser T, Shinnar S, Gloss D, Alldredge B, Arya R, Bainbridge J, et al. Evidence-based guideline: treatment of convulsive status epilepticus in children and adults: report of the Guideline Committee of the American Epilepsy Society. Epilepsy Curr. 2016;16(1):48–61.PubMedPubMedCentralCrossRef Glauser T, Shinnar S, Gloss D, Alldredge B, Arya R, Bainbridge J, et al. Evidence-based guideline: treatment of convulsive status epilepticus in children and adults: report of the Guideline Committee of the American Epilepsy Society. Epilepsy Curr. 2016;16(1):48–61.PubMedPubMedCentralCrossRef
48.
go back to reference Treiman DM, Meyers PD, Walton NY, Collins JF, Colling C, Rowan AJ, et al. A comparison of four treatments for generalized convulsive status epilepticus. Veterans Affairs Status Epilepticus Cooperative Study Group. N Engl J Med. 1998;339(12):792–8.PubMedCrossRef Treiman DM, Meyers PD, Walton NY, Collins JF, Colling C, Rowan AJ, et al. A comparison of four treatments for generalized convulsive status epilepticus. Veterans Affairs Status Epilepticus Cooperative Study Group. N Engl J Med. 1998;339(12):792–8.PubMedCrossRef
49.
go back to reference Alldredge BK, Gelb AM, Isaacs SM, Corry MD, Allen F, Ulrich S, et al. A comparison of lorazepam, diazepam, and placebo for the treatment of out-of-hospital status epilepticus. N Engl J Med. 2001;345(9):631–7.PubMedCrossRef Alldredge BK, Gelb AM, Isaacs SM, Corry MD, Allen F, Ulrich S, et al. A comparison of lorazepam, diazepam, and placebo for the treatment of out-of-hospital status epilepticus. N Engl J Med. 2001;345(9):631–7.PubMedCrossRef
50.
go back to reference Silbergleit R, Durkalski V, Lowenstein D, Conwit R, Pancioli A, Palesch Y, et al. Intramuscular versus intravenous therapy for prehospital status epilepticus. N Engl J Med. 2012;366(7):591–600.PubMedPubMedCentralCrossRef Silbergleit R, Durkalski V, Lowenstein D, Conwit R, Pancioli A, Palesch Y, et al. Intramuscular versus intravenous therapy for prehospital status epilepticus. N Engl J Med. 2012;366(7):591–600.PubMedPubMedCentralCrossRef
51.
go back to reference The Treatment of Epilepsy. 4th. edition. Oxford: Wiley Blackwell; 2015. The Treatment of Epilepsy. 4th. edition. Oxford: Wiley Blackwell; 2015.
53.
go back to reference Kay L, Merkel N, von Blomberg A, Willems LM, Bauer S, Reif PS, et al. Intranasal midazolam as first-line inhospital treatment for status epilepticus: a pharmaco-EEG cohort study. Ann Clin Transl Neurol. 2019;6(12):2413–25.PubMedPubMedCentralCrossRef Kay L, Merkel N, von Blomberg A, Willems LM, Bauer S, Reif PS, et al. Intranasal midazolam as first-line inhospital treatment for status epilepticus: a pharmaco-EEG cohort study. Ann Clin Transl Neurol. 2019;6(12):2413–25.PubMedPubMedCentralCrossRef
54.
go back to reference Inokuchi R, Ohashi-Fukuda N, Nakamura K, Wada T, Gunshin M, Kitsuta Y, et al. Comparison of intranasal and intravenous diazepam on status epilepticus in stroke patients: a retrospective cohort study. Medicine (Baltimore). 2015;94(7):e555-e. Inokuchi R, Ohashi-Fukuda N, Nakamura K, Wada T, Gunshin M, Kitsuta Y, et al. Comparison of intranasal and intravenous diazepam on status epilepticus in stroke patients: a retrospective cohort study. Medicine (Baltimore). 2015;94(7):e555-e.
57.
go back to reference French J, Biton V, Dave H, Detyniecki K, Gelfand MA, Gong H, et al. A randomized Phase 2b efficacy study in patients with seizure episodes with a predictable pattern using Staccato® alprazolam for rapid seizure termination. Epilepsia. 2022. French J, Biton V, Dave H, Detyniecki K, Gelfand MA, Gong H, et al. A randomized Phase 2b efficacy study in patients with seizure episodes with a predictable pattern using Staccato® alprazolam for rapid seizure termination. Epilepsia. 2022.
58.
go back to reference Claassen J, How I. Treat patients with EEG patterns on the ictal-interictal continuum in the neuro ICU. Neurocrit Care. 2009;11(3):437–44.PubMedCrossRef Claassen J, How I. Treat patients with EEG patterns on the ictal-interictal continuum in the neuro ICU. Neurocrit Care. 2009;11(3):437–44.PubMedCrossRef
59.
go back to reference Hopp JL, Sanchez A, Krumholz A, Hart G, Barry E. Nonconvulsive status epilepticus: value of a benzodiazepine trial for predicting outcomes. Neurologist. 2011;17(6):325–9.PubMedCrossRef Hopp JL, Sanchez A, Krumholz A, Hart G, Barry E. Nonconvulsive status epilepticus: value of a benzodiazepine trial for predicting outcomes. Neurologist. 2011;17(6):325–9.PubMedCrossRef
60.
go back to reference Kapur J, Elm J, Chamberlain JM, Barsan W, Cloyd J, Lowenstein D, et al. Randomized trial of three anticonvulsant medications for status epilepticus. N Engl J Med. 2019;381(22):2103–13.PubMedPubMedCentralCrossRef Kapur J, Elm J, Chamberlain JM, Barsan W, Cloyd J, Lowenstein D, et al. Randomized trial of three anticonvulsant medications for status epilepticus. N Engl J Med. 2019;381(22):2103–13.PubMedPubMedCentralCrossRef
61.
go back to reference Chamberlain JM, Kapur J, Shinnar S, Elm J, Holsti M, Babcock L, et al. Efficacy of levetiracetam, fosphenytoin, and valproate for established status epilepticus by age group (ESETT): a double-blind, responsive-adaptive, randomised controlled trial. Lancet. 2020;395(10231):1217–24.PubMedPubMedCentralCrossRef Chamberlain JM, Kapur J, Shinnar S, Elm J, Holsti M, Babcock L, et al. Efficacy of levetiracetam, fosphenytoin, and valproate for established status epilepticus by age group (ESETT): a double-blind, responsive-adaptive, randomised controlled trial. Lancet. 2020;395(10231):1217–24.PubMedPubMedCentralCrossRef
62.
go back to reference Nakamura K, Marushima A, Takahashi Y, Mochizuki M, Kimura A, Fukuda Y, et al. Levetiracetam versus fosphenytoin as a second-line treatment after diazepam for adult convulsive status epilepticus: a multicentre non-inferiority randomised control trial. Journal of Neurology, Neurosurgery & Psychiatry. 2022:jnnp-2022-329485. Nakamura K, Marushima A, Takahashi Y, Mochizuki M, Kimura A, Fukuda Y, et al. Levetiracetam versus fosphenytoin as a second-line treatment after diazepam for adult convulsive status epilepticus: a multicentre non-inferiority randomised control trial. Journal of Neurology, Neurosurgery & Psychiatry. 2022:jnnp-2022-329485.
63.
go back to reference Müller A, Schmiedeknecht A, Mende M, Awissus C, Rosenow F, Hamer H, et al. Treatment of established status epilepticus in the elderly - a study protocol for a prospective multicenter double-blind comparative effectiveness trial (ToSEE). BMC Neurol. 2020;20(1):438.PubMedPubMedCentralCrossRef Müller A, Schmiedeknecht A, Mende M, Awissus C, Rosenow F, Hamer H, et al. Treatment of established status epilepticus in the elderly - a study protocol for a prospective multicenter double-blind comparative effectiveness trial (ToSEE). BMC Neurol. 2020;20(1):438.PubMedPubMedCentralCrossRef
64.
go back to reference O’Brien TJ, Cascino GD, So EL, Hanna DR. Incidence and clinical consequence of the purple glove syndrome in patients receiving intravenous phenytoin. Neurology. 1998;51(4):1034–9.PubMedCrossRef O’Brien TJ, Cascino GD, So EL, Hanna DR. Incidence and clinical consequence of the purple glove syndrome in patients receiving intravenous phenytoin. Neurology. 1998;51(4):1034–9.PubMedCrossRef
65.
go back to reference Status Epilepticus: A clinical perspective. 2nd edition ed. Cham, Switzerland: Springer; 2018. Status Epilepticus: A clinical perspective. 2nd edition ed. Cham, Switzerland: Springer; 2018.
66.
go back to reference Josephson CB, Wiebe S, Delgado-Garcia G, Gonzalez-Izquierdo A, Denaxas S, Sajobi TT, et al. Association of enzyme-inducing antiseizure drug use with long-term cardiovascular disease. JAMA Neurol. 2021;78(11):1367–74.PubMedCrossRef Josephson CB, Wiebe S, Delgado-Garcia G, Gonzalez-Izquierdo A, Denaxas S, Sajobi TT, et al. Association of enzyme-inducing antiseizure drug use with long-term cardiovascular disease. JAMA Neurol. 2021;78(11):1367–74.PubMedCrossRef
67.
go back to reference Rowan AJ, Ramsay RE, Collins JF, Pryor F, Boardman KD, Uthman BM, et al. New onset geriatric epilepsy: a randomized study of gabapentin, lamotrigine, and carbamazepine. Neurology. 2005;64(11):1868–73.PubMedCrossRef Rowan AJ, Ramsay RE, Collins JF, Pryor F, Boardman KD, Uthman BM, et al. New onset geriatric epilepsy: a randomized study of gabapentin, lamotrigine, and carbamazepine. Neurology. 2005;64(11):1868–73.PubMedCrossRef
68.
go back to reference French JA, Perucca E, Sander JW, Bergfeldt L, Baulac M, Auerbach DS, et al. FDA safety warning on the cardiac effects of lamotrigine: an advisory from the Ad Hoc ILAE/AES Task Force. Epilepsia Open. 2021;6(1):45–8.PubMedPubMedCentralCrossRef French JA, Perucca E, Sander JW, Bergfeldt L, Baulac M, Auerbach DS, et al. FDA safety warning on the cardiac effects of lamotrigine: an advisory from the Ad Hoc ILAE/AES Task Force. Epilepsia Open. 2021;6(1):45–8.PubMedPubMedCentralCrossRef
69.
go back to reference Limdi NA, Knowlton RK, Cofield SS, Ver Hoef LW, Paige AL, Dutta S, et al. Safety of rapid intravenous loading of valproate. Epilepsia. 2007;48(3):478–83.PubMedCrossRef Limdi NA, Knowlton RK, Cofield SS, Ver Hoef LW, Paige AL, Dutta S, et al. Safety of rapid intravenous loading of valproate. Epilepsia. 2007;48(3):478–83.PubMedCrossRef
70.
go back to reference Lind J, Nordlund P. Intravenous use of valproic acid in status epilepticus is associated with high risk of hyperammonemia. Seizure. 2019;69:20–4.PubMedCrossRef Lind J, Nordlund P. Intravenous use of valproic acid in status epilepticus is associated with high risk of hyperammonemia. Seizure. 2019;69:20–4.PubMedCrossRef
71.
go back to reference Habhab SF, Ulvin LB, Taubøll E, Svalheim S, Olsen KB, Horn MA, et al. Influence of valproate-induced hyperammonemia on treatment decision in an adult status epilepticus cohort. Epilepsy Behav. 2020;111:107193.PubMedCrossRef Habhab SF, Ulvin LB, Taubøll E, Svalheim S, Olsen KB, Horn MA, et al. Influence of valproate-induced hyperammonemia on treatment decision in an adult status epilepticus cohort. Epilepsy Behav. 2020;111:107193.PubMedCrossRef
72.
go back to reference Smith KM, Britton JW, Hocker SE, Toledano M. Hyperammonemia in patients with status epilepticus treated with or without valproic acid. Neurologist. 2021;26(3):80–2.PubMedCrossRef Smith KM, Britton JW, Hocker SE, Toledano M. Hyperammonemia in patients with status epilepticus treated with or without valproic acid. Neurologist. 2021;26(3):80–2.PubMedCrossRef
73.
go back to reference Werhahn KJ, Klimpe S, Balkaya S, Trinka E, Krämer G. The safety and efficacy of add-on levetiracetam in elderly patients with focal epilepsy: a one-year observational study. Seizure. 2011;20(4):305–11.PubMedCrossRef Werhahn KJ, Klimpe S, Balkaya S, Trinka E, Krämer G. The safety and efficacy of add-on levetiracetam in elderly patients with focal epilepsy: a one-year observational study. Seizure. 2011;20(4):305–11.PubMedCrossRef
74.
go back to reference Husain AM, Lee JW, Kolls BJ, Hirsch LJ, Halford JJ, Gupta PK, et al. Randomized trial of lacosamide versus fosphenytoin for nonconvulsive seizures. Ann Neurol. 2018;83(6):1174–85.PubMedPubMedCentralCrossRef Husain AM, Lee JW, Kolls BJ, Hirsch LJ, Halford JJ, Gupta PK, et al. Randomized trial of lacosamide versus fosphenytoin for nonconvulsive seizures. Ann Neurol. 2018;83(6):1174–85.PubMedPubMedCentralCrossRef
75.
go back to reference Belcastro V, Vidale S, Pierguidi L, Sironi L, Tancredi L, Striano P, et al. Intravenous lacosamide as treatment option in post-stroke non convulsive status epilepticus in the elderly: a proof-of-concept, observational study. Seizure. 2013;22(10):905–7.PubMedCrossRef Belcastro V, Vidale S, Pierguidi L, Sironi L, Tancredi L, Striano P, et al. Intravenous lacosamide as treatment option in post-stroke non convulsive status epilepticus in the elderly: a proof-of-concept, observational study. Seizure. 2013;22(10):905–7.PubMedCrossRef
76.
go back to reference Strzelczyk A, Zöllner JP, Willems LM, Jost J, Paule E, Schubert-Bast S, et al. Lacosamide in status epilepticus: systematic review of current evidence. Epilepsia. 2017;58(6):933–50.PubMedCrossRef Strzelczyk A, Zöllner JP, Willems LM, Jost J, Paule E, Schubert-Bast S, et al. Lacosamide in status epilepticus: systematic review of current evidence. Epilepsia. 2017;58(6):933–50.PubMedCrossRef
77.
go back to reference Nizam A, Mylavarapu K, Thomas D, Briskin K, Wu B, Saluja D, et al. Lacosamide-induced second-degree atrioventricular block in a patient with partial epilepsy. Epilepsia. 2011;52(10):e153–5.PubMedCrossRef Nizam A, Mylavarapu K, Thomas D, Briskin K, Wu B, Saluja D, et al. Lacosamide-induced second-degree atrioventricular block in a patient with partial epilepsy. Epilepsia. 2011;52(10):e153–5.PubMedCrossRef
78.
go back to reference Kang BS, Jung KH, Shin JW, Moon JS, Byun JI, Lim JA, et al. Induction of burst suppression or coma using intravenous anesthetics in refractory status epilepticus. J Clin Neurosci. 2015;22(5):854–8.PubMedCrossRef Kang BS, Jung KH, Shin JW, Moon JS, Byun JI, Lim JA, et al. Induction of burst suppression or coma using intravenous anesthetics in refractory status epilepticus. J Clin Neurosci. 2015;22(5):854–8.PubMedCrossRef
79.
go back to reference Rossetti AO, Logroscino G, Bromfield EB. Refractory status epilepticus: effect of treatment aggressiveness on prognosis. Arch Neurol. 2005;62(11):1698–702.PubMedCrossRef Rossetti AO, Logroscino G, Bromfield EB. Refractory status epilepticus: effect of treatment aggressiveness on prognosis. Arch Neurol. 2005;62(11):1698–702.PubMedCrossRef
80.
go back to reference Sutter R, Marsch S, Fuhr P, Kaplan PW, Ruegg S. Anesthetic drugs in status epilepticus: risk or rescue? A 6-year cohort study. Neurology. 2014;82(8):656–64.PubMedPubMedCentralCrossRef Sutter R, Marsch S, Fuhr P, Kaplan PW, Ruegg S. Anesthetic drugs in status epilepticus: risk or rescue? A 6-year cohort study. Neurology. 2014;82(8):656–64.PubMedPubMedCentralCrossRef
81.
go back to reference Marchi NA, Novy J, Faouzi M, Stahli C, Burnand B, Rossetti AO. Status epilepticus: impact of therapeutic coma on outcome. Crit Care Med. 2015;43(5):1003–9.PubMedCrossRef Marchi NA, Novy J, Faouzi M, Stahli C, Burnand B, Rossetti AO. Status epilepticus: impact of therapeutic coma on outcome. Crit Care Med. 2015;43(5):1003–9.PubMedCrossRef
82.
go back to reference Kowalski RG, Ziai WC, Rees RN, Werner JKJ, Kim G, Goodwin H, et al. Third-line antiepileptic therapy and outcome in status epilepticus: The impact of vasopressor use and prolonged mechanical ventilation*. Crit Care Med. 2012;40(9):2677–84.PubMedCrossRef Kowalski RG, Ziai WC, Rees RN, Werner JKJ, Kim G, Goodwin H, et al. Third-line antiepileptic therapy and outcome in status epilepticus: The impact of vasopressor use and prolonged mechanical ventilation*. Crit Care Med. 2012;40(9):2677–84.PubMedCrossRef
83.
go back to reference Hocker SE, Sutter R, Shorvon S. Anesthetic drugs in status epilepticus: Risk or rescue? A 6-year cohort study. Neurology. 2014;83(9):866.PubMedCrossRef Hocker SE, Sutter R, Shorvon S. Anesthetic drugs in status epilepticus: Risk or rescue? A 6-year cohort study. Neurology. 2014;83(9):866.PubMedCrossRef
84.
go back to reference Fernandez A, Lantigua H, Lesch C, Shao B, Foreman B, Schmidt JM, et al. High-dose midazolam infusion for refractory status epilepticus. Neurology. 2014;82(4):359–65.PubMedPubMedCentralCrossRef Fernandez A, Lantigua H, Lesch C, Shao B, Foreman B, Schmidt JM, et al. High-dose midazolam infusion for refractory status epilepticus. Neurology. 2014;82(4):359–65.PubMedPubMedCentralCrossRef
85.
go back to reference Muhlhofer WG, Layfield S, Lowenstein D, Lin CP, Johnson RD, Saini S, et al. Duration of therapeutic coma and outcome of refractory status epilepticus. Epilepsia. 2019;60(5):921–34.PubMedPubMedCentralCrossRef Muhlhofer WG, Layfield S, Lowenstein D, Lin CP, Johnson RD, Saini S, et al. Duration of therapeutic coma and outcome of refractory status epilepticus. Epilepsia. 2019;60(5):921–34.PubMedPubMedCentralCrossRef
86.
go back to reference Gaspard N, Foreman B, Judd LM, Brenton JN, Nathan BR, McCoy BM, et al. Intravenous ketamine for the treatment of refractory status epilepticus: a retrospective multicenter study. Epilepsia. 2013;54(8):1498–503.PubMedPubMedCentralCrossRef Gaspard N, Foreman B, Judd LM, Brenton JN, Nathan BR, McCoy BM, et al. Intravenous ketamine for the treatment of refractory status epilepticus: a retrospective multicenter study. Epilepsia. 2013;54(8):1498–503.PubMedPubMedCentralCrossRef
87.
go back to reference Rosati A, De Masi S, Guerrini R. Ketamine for refractory status epilepticus: a systematic review. CNS Drugs. 2018;32(11):997–1009.PubMedCrossRef Rosati A, De Masi S, Guerrini R. Ketamine for refractory status epilepticus: a systematic review. CNS Drugs. 2018;32(11):997–1009.PubMedCrossRef
88.
go back to reference Fechner A, Hubert K, Jahnke K, Knake S, Konczalla J, Menzler K, et al. Treatment of refractory and superrefractory status epilepticus with topiramate: a cohort study of 106 patients and a review of the literature. Epilepsia. 2019;60(12):2448–58.PubMedCrossRef Fechner A, Hubert K, Jahnke K, Knake S, Konczalla J, Menzler K, et al. Treatment of refractory and superrefractory status epilepticus with topiramate: a cohort study of 106 patients and a review of the literature. Epilepsia. 2019;60(12):2448–58.PubMedCrossRef
90.
go back to reference Brigo F, Lattanzi S, Rohracher A, Russo E, Meletti S, Grillo E, et al. Perampanel in the treatment of status epilepticus: a systematic review of the literature. Epilepsy Behav. 2018;86:179–86.PubMedCrossRef Brigo F, Lattanzi S, Rohracher A, Russo E, Meletti S, Grillo E, et al. Perampanel in the treatment of status epilepticus: a systematic review of the literature. Epilepsy Behav. 2018;86:179–86.PubMedCrossRef
91.
go back to reference Zeiler FA, Zeiler KJ, Teitelbaum J, Gillman LM, West M. Modern inhalational anesthetics for refractory status epilepticus. Can J Neurol Sci. 2015;42(2):106–15.PubMedCrossRef Zeiler FA, Zeiler KJ, Teitelbaum J, Gillman LM, West M. Modern inhalational anesthetics for refractory status epilepticus. Can J Neurol Sci. 2015;42(2):106–15.PubMedCrossRef
92.
go back to reference Suga H, Yanagida A, Kanazawa N, Ohara H, Kitagawa T, Hayashi M, et al. Status epilepticus suspected autoimmune: neuronal surface antibodies and main clinical features. Epilepsia. 2021;62(11):2719–31.PubMedCrossRef Suga H, Yanagida A, Kanazawa N, Ohara H, Kitagawa T, Hayashi M, et al. Status epilepticus suspected autoimmune: neuronal surface antibodies and main clinical features. Epilepsia. 2021;62(11):2719–31.PubMedCrossRef
93.
go back to reference Gaspard N, Foreman BP, Alvarez V, Cabrera Kang C, Probasco JC, Jongeling AC, et al. New-onset refractory status epilepticus: etiology, clinical features, and outcome. Neurology. 2015;85(18):1604–13.PubMedPubMedCentralCrossRef Gaspard N, Foreman BP, Alvarez V, Cabrera Kang C, Probasco JC, Jongeling AC, et al. New-onset refractory status epilepticus: etiology, clinical features, and outcome. Neurology. 2015;85(18):1604–13.PubMedPubMedCentralCrossRef
94.
go back to reference Dubey D, Singh J, Britton JW, Pittock SJ, Flanagan EP, Lennon VA, et al. Predictive models in the diagnosis and treatment of autoimmune epilepsy. Epilepsia. 2017;58(7):1181–9.PubMedCrossRef Dubey D, Singh J, Britton JW, Pittock SJ, Flanagan EP, Lennon VA, et al. Predictive models in the diagnosis and treatment of autoimmune epilepsy. Epilepsia. 2017;58(7):1181–9.PubMedCrossRef
95.
go back to reference Dubey D, Kothapalli N, McKeon A, Flanagan EP, Lennon VA, Klein CJ, et al. Predictors of neural-specific autoantibodies and immunotherapy response in patients with cognitive dysfunction. J Neuroimmunol. 2018;323:62–72.PubMedCrossRef Dubey D, Kothapalli N, McKeon A, Flanagan EP, Lennon VA, Klein CJ, et al. Predictors of neural-specific autoantibodies and immunotherapy response in patients with cognitive dysfunction. J Neuroimmunol. 2018;323:62–72.PubMedCrossRef
96.
go back to reference Toledano M, Britton JW, McKeon A, Shin C, Lennon VA, Quek AML, et al. Utility of an immunotherapy trial in evaluating patients with presumed autoimmune epilepsy. Neurology. 2014;82(18):1578–86.PubMedPubMedCentralCrossRef Toledano M, Britton JW, McKeon A, Shin C, Lennon VA, Quek AML, et al. Utility of an immunotherapy trial in evaluating patients with presumed autoimmune epilepsy. Neurology. 2014;82(18):1578–86.PubMedPubMedCentralCrossRef
97.
go back to reference Zeiler FA, Matuszczak M, Teitelbaum J, Kazina CJ, Gillman LM. Plasmapheresis for refractory status epilepticus, part I: a scoping systematic review of the adult literature. Seizure Eur J Epilepsy. 2016;43:14–22.CrossRef Zeiler FA, Matuszczak M, Teitelbaum J, Kazina CJ, Gillman LM. Plasmapheresis for refractory status epilepticus, part I: a scoping systematic review of the adult literature. Seizure Eur J Epilepsy. 2016;43:14–22.CrossRef
98.
go back to reference Khawaja AM, DeWolfe JL, Miller DW, Szaflarski JP. New-onset refractory status epilepticus (NORSE)—the potential role for immunotherapy. Epilepsy Behav. 2015;47:17–23.PubMedCrossRef Khawaja AM, DeWolfe JL, Miller DW, Szaflarski JP. New-onset refractory status epilepticus (NORSE)—the potential role for immunotherapy. Epilepsy Behav. 2015;47:17–23.PubMedCrossRef
99.
go back to reference Iizuka T, Kanazawa N, Kaneko J, Tominaga N, Nonoda Y, Hara A, et al. Cryptogenic NORSE. Its distinctive clinical features and response to immunotherapy. 2017;4(6):e396 Iizuka T, Kanazawa N, Kaneko J, Tominaga N, Nonoda Y, Hara A, et al. Cryptogenic NORSE. Its distinctive clinical features and response to immunotherapy. 2017;4(6):e396
100.
go back to reference Kenney-Jung DL, Vezzani A, Kahoud RJ, LaFrance-Corey RG, Ho ML, Muskardin TW, et al. Febrile infection-related epilepsy syndrome treated with anakinra. Ann Neurol. 2016;80(6):939–45.PubMedPubMedCentralCrossRef Kenney-Jung DL, Vezzani A, Kahoud RJ, LaFrance-Corey RG, Ho ML, Muskardin TW, et al. Febrile infection-related epilepsy syndrome treated with anakinra. Ann Neurol. 2016;80(6):939–45.PubMedPubMedCentralCrossRef
101.
go back to reference Jun JS, Lee ST, Kim R, Chu K, Lee SK. Tocilizumab treatment for new onset refractory status epilepticus. Ann Neurol. 2018;84(6):940–5.PubMedCrossRef Jun JS, Lee ST, Kim R, Chu K, Lee SK. Tocilizumab treatment for new onset refractory status epilepticus. Ann Neurol. 2018;84(6):940–5.PubMedCrossRef
104.
go back to reference Cervenka MC, Hocker S, Koenig M, Bar B, Henry-Barron B, Kossoff EH, et al. Phase I/II multicenter ketogenic diet study for adult superrefractory status epilepticus. Neurology. 2017;88(10):938–43.PubMedPubMedCentralCrossRef Cervenka MC, Hocker S, Koenig M, Bar B, Henry-Barron B, Kossoff EH, et al. Phase I/II multicenter ketogenic diet study for adult superrefractory status epilepticus. Neurology. 2017;88(10):938–43.PubMedPubMedCentralCrossRef
105.
go back to reference Zeiler FA, Matuszczak M, Teitelbaum J, Gillman LM, Kazina CJ. Electroconvulsive therapy for refractory status epilepticus: a systematic review. Seizure. 2016;35:23–32.PubMedCrossRef Zeiler FA, Matuszczak M, Teitelbaum J, Gillman LM, Kazina CJ. Electroconvulsive therapy for refractory status epilepticus: a systematic review. Seizure. 2016;35:23–32.PubMedCrossRef
106.
go back to reference Sobstyl M, Stapińska-Syniec A, Rylski M. Deep brain stimulation for the treatment of refractory and super-refractory status epilepticus. Seizure Eur J Epilepsy. 2020;81:58–62.CrossRef Sobstyl M, Stapińska-Syniec A, Rylski M. Deep brain stimulation for the treatment of refractory and super-refractory status epilepticus. Seizure Eur J Epilepsy. 2020;81:58–62.CrossRef
107.
go back to reference Perucca E. Clinically relevant drug interactions with antiepileptic drugs. Br J Clin Pharmacol. 2006;61(3):246–55.PubMedCrossRef Perucca E. Clinically relevant drug interactions with antiepileptic drugs. Br J Clin Pharmacol. 2006;61(3):246–55.PubMedCrossRef
108.
go back to reference Leitinger M, Trinka E, Zimmermann G, Beniczky S. Salzburg criteria for nonconvulsive status epilepticus: details matter. Epilepsia. 2019;60(11):2334–6.PubMedPubMedCentralCrossRef Leitinger M, Trinka E, Zimmermann G, Beniczky S. Salzburg criteria for nonconvulsive status epilepticus: details matter. Epilepsia. 2019;60(11):2334–6.PubMedPubMedCentralCrossRef
Metadata
Title
Status Epilepticus in Older Adults: Diagnostic and Treatment Considerations
Authors
Gamaleldin M. Osman
Sara E. Hocker
Publication date
06-02-2023
Publisher
Springer International Publishing
Published in
Drugs & Aging / Issue 2/2023
Print ISSN: 1170-229X
Electronic ISSN: 1179-1969
DOI
https://doi.org/10.1007/s40266-022-00998-z

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