Medicine:Sudden unexpected death in epilepsy

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Short description: Fatal complication of epilepsy
Sudden unexpected death in epilepsy
SpecialtyNeurology

Sudden unexpected death in epilepsy (SUDEP) is a fatal complication of epilepsy.[1] It is defined as the sudden and unexpected, non-traumatic and non-drowning death of a person with epilepsy, without a toxicological or anatomical cause of death detected during the post-mortem examination.[2][3]

While the mechanisms underlying SUDEP are still poorly understood, it is possibly the most common cause of death as a result of complications from epilepsy, accounting for between 7.5 and 17% of all epilepsy-related deaths[2] and 50% of all deaths in refractory epilepsy.[4][5] The causes of SUDEP seem to be multifactorial[2] and include respiratory, cardiac, and cerebral factors as well as the severity of epilepsy and seizures.[5] Proposed pathophysiological mechanisms include seizure-induced cardiac and respiratory arrests.[4]

Among epileptics, SUDEP occurs in about 1 in 1,000 adults and 1 in 4,500 children annually.[6] Rates of death as a result of prolonged seizures (status epilepticus) are not classified as SUDEP.[7]

Categories

The overarching term SUDEP can be subdivided into four different categories: Definite, Probably, Possible, and Unlikely.[8]

  1. Definite SUDEP: a non-traumatic and non-drowning death in an individual with epilepsy, without a cause of death after postmortem examination.
    • Definite SUDEP Plus: includes the presence of a concomitant condition other than epilepsy, where death may be due to the combined effects of both epilepsy and the other condition.
  2. Probably SUDEP: all the same criteria for Definite SUDEP are met, but no postmortem examination is performed.
  3. Possible SUDEP: insufficient information is available regarding the death, with no postmortem examination.
  4. Unlikely SUDEP: an alternate cause of death has been determined, ruling out the possibility of SUDEP being the cause.

Risk factors

Consistent risk factors include:

  • Severity of seizures, increased refractoriness of epilepsy and presence of generalized tonic–clonic seizures:[4] the most consistent risk factor is an increased frequency of tonic–clonic seizures.[5]
  • Poor compliance.[4] Lack of therapeutic levels of anti-epileptic drugs, non-adherence to treatment regimens and frequent changes in regimens are risk factors for sudden death.[5]
  • Young age and early age of seizures onset[4]
  • Male sex[9]
  • Being asleep during a seizure is likely to favour SUDEP occurrence.[10]

Genetic mutations have been identified that increase a person's risk for SUDEP (some are discussed below), but ultimately their genetic risk is determined by the function of multiple genes that is not yet well understood. Overlap is seen between these ion channel genes and the different sudden death disorders, including SUDEP,[11] SIDS,[12] sudden unexpected death (SUD),[13] and sudden unexplained death in childhood (SUDC).[14] Many of the genes are involved in long QT syndrome.

  • Mutations in the KCNQ1 gene that codes for the voltage-gated potassium channel KV7.1 have been implicated in cardiac arrhythmias, such as long QT syndrome 1 (LQT1), and epilepsy.[11][12]
  • Mutations in potassium channel gene KCNH2 have been identified with LQT2.[12][11]
  • Mutations in sodium channel gene SCN5A have been identified with LQT3.[11][12]
  • Mutations in potassium channel gene KCNJ2 have been identified with LQT7.[11][12]
  • Mutations in calcium channel gene CACNA1C have been identified with LQT8.[11]
  • The sodium ion channel genes SCN1A, SCN1B, SCN2A, and SCN8A and the potassium channel KCNA1 have been implicated in both epilepsy and SUDEP.[15][11]

Mechanism

The mechanisms underlying SUDEP are not well understood but probably involve several pathophysiological mechanisms and circumstances. The most commonly involved are seizure-induced hypoventilation and cardiac arrhythmias, but different mechanisms may be involved in different individuals, and more than one mechanism may be involved in any one individual.[16]

  • Cardiac factors: cardiac arrhythmias and other cardiac events are known to be involved in some cases of SUDEP.[5] Such arrhythmias are defined as ictal arrhythmias and include the ictal asystole, which is a rare occurrence mostly in people that have temporal lobe epilepsy.[17][18]
  • Respiratory factors: impaired respiration and seizure-induced pulmonary dysfunction as well as central apnea as a result of brain-stem respiratory centers suppression is known to play a role in some cases of SUDEP.[5]
  • Cerebral and autonomic nervous system dysregulation: cardiac arrhythmia and respiratory failure as a result of seizure-related changes to brain function and dysfunction of the autonomic nervous system have been described in cases of SUDEP. These include cases of post-ictal generalized EEG suppression described as cerebral shutdown, but its significance remains unclear.[19]
  • Genetic factors: mutations in several genes have been associated with an increased susceptibility to SUDEP. Over 33% of these are related to mutations which lead to increased susceptibility for arrhythmia. Genes involved include the hyperpolarization-activated cyclic nucleotide-gated channels genes (HCN1, HCN2, HCN3 and HCN4).[2]
  • Anti epileptic drugs: most evidence suggests that antiepileptic drugs are not associated with an increased risk for SUDEP, but rather reduce its incidence.[20] Some studies however indicate that some antiepileptic drugs such as lamotrigine and carbamazepine, may increase the risk of SUDEP in females and certain individuals.[21][22] It is unclear if this is because of the potential cardio-respiratory adverse effects such as lengthening of the QT interval and reduction of heart rate known to be associated with these drugs under certain circumstances,[16] or because a high drug dosage could be a surrogate marker for poor seizure control.[23]
  • Vagal nerve stimulation: concerns have been raised that vagal nerve stimulation may induce bradycardia or cardiac arrest and may exacerbate sleep apnoea common in people with epilepsy.[16]

Management

Currently, the most effective strategy to protect against SUDEP in childhood epilepsy is seizure control, but this approach is not completely effective and is particularly challenging in cases of intractable epilepsy. The lack of generally recognized clinical recommendations available are a reflection of the dearth of data on the effectiveness of any particular clinical strategy,[16] but based on present evidence, the following may be relevant:

  • Epileptic seizure control with the appropriate use of medication and lifestyle counseling is the focus of prevention.[5]
  • Detection of seizures using wristbands which can alert carers in case the wearer has stopped breathing or has a heart problem.[24][25]
  • Reduction of stress, participation in physical exercises, and night supervision might minimize the risk of SUDEP.[2]
  • Knowledge of how to perform the appropriate first-aid responses to seizure by persons who live with epileptic people may prevent death.[5]
  • People with arrhythmias associated with seizures should be submitted to extensive cardiac investigation[2] to determine the indication for on-demand cardiac pacing.[16]
  • Successful epilepsy surgery may reduce the risk of SUDEP, but this depends on the outcome in terms of seizure control.[16]
  • The use of anti-suffocation pillows has been advocated by some practitioners to improve respiration while sleeping, but their effects remain unproven because experimental studies are lacking.[5]
  • Providing information to individuals and relatives about SUDEP is beneficial.[19][26]
  • Night time supervision[9]

Epidemiology

  • In the US, prevalence of SUDEP is approximately 1.16 cases for every 1000 people with epilepsy per year.[27] In comparison, a study in Denmark found that among 1-35 year old individuals, the incidence of sudden cardiac death (SCD) was 1.9 cases per 100,000 person-years,[28] while 1 in 2000 infants in the Western world will die from SIDS in the first year of life.[29] This means that sudden, unexpected death is more common among individuals with epilepsy when compared to infants or the general population.
  • SUDEP accounts for 8–17% of deaths in people with epilepsy.[30]
  • The risk of sudden death in young adults with epilepsy is increased 20-40-fold compared to the general population.[31][32][19]
  • SUDEP is the number one cause of epilepsy-related death in people with pharmacoresistant epilepsy.[19]
  • Children with epilepsy have a cumulative risk of dying suddenly of 7% within 40 years.[19]
  • Within the pediatric population, SUDEP accounts for 30-50% of the deaths in severe early onset epilepsies, affecting between 1 in 500 and 1 in 1000 epilepsy patients yearly.[33][34]

See also

  • Martha Parke Custis
  • Cameron Boyce

References

  1. ↑ Ryvlin, P; Nashef, L; Tomson, T (May 2013). "Prevention of sudden unexpected death in epirealistic goal?". Epilepsia 54 Suppl 2: 23–8. doi:10.1111/epi.12180. PMID 23646967. 
  2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 Terra, VC; Cysneiros, R; Cavalheiro, EA; Scorza, FA (Mar 2013). "Sudden unexpected death in epilepsy: from the lab to the clinic setting.". Epilepsy & Behavior 26 (3): 415–20. doi:10.1016/j.yebeh.2012.12.018. PMID 23402930. 
  3. ↑ Nashef, L; So, EL; Ryvlin, P; Tomson, T (Feb 2012). "Unifying the definitions of sudden unexpected death in epilepsy.". Epilepsia 53 (2): 227–33. doi:10.1111/j.1528-1167.2011.03358.x. PMID 22191982. 
  4. ↑ 4.0 4.1 4.2 4.3 4.4 Tolstykh, GP; Cavazos, JE (Mar 2013). "Potential mechanisms of sudden unexpected death in epilepsy.". Epilepsy & Behavior 26 (3): 410–4. doi:10.1016/j.yebeh.2012.09.017. PMID 23305781. 
  5. ↑ 5.0 5.1 5.2 5.3 5.4 5.5 5.6 5.7 5.8 Devinsky, Orrin (10 November 2011). "Sudden, Unexpected Death in Epilepsy". New England Journal of Medicine 365 (19): 1801–1811. doi:10.1056/NEJMra1010481. PMID 22070477. 
  6. ↑ Harden, C; Tomson, T; Gloss, D; Buchhalter, J; Cross, JH; Donner, E; French, JA; Gil-Nagel, A et al. (25 April 2017). "Practice guideline summary: Sudden unexpected death in epilepsy incidence rates and risk factors: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the American Epilepsy Society.". Neurology 88 (17): 1674–1680. doi:10.1212/WNL.0000000000003685. PMID 28438841. 
  7. ↑ "Sudden unexpected death in epilepsy: current knowledge and future directions". Lancet Neurology 7 (11): 1021–31. November 2008. doi:10.1016/S1474-4422(08)70202-3. PMID 18805738. 
  8. ↑ Nashef, Lina; So, Elson L.; Ryvlin, Philippe; Tomson, Torbjörn (February 2012). "Unifying the definitions of sudden unexpected death in epilepsy". Epilepsia 53 (2): 227–233. doi:10.1111/j.1528-1167.2011.03358.x. ISSN 1528-1167. PMID 22191982. 
  9. ↑ 9.0 9.1 Maguire, Melissa J.; Jackson, Cerian F.; Marson, Anthony G.; Nevitt, Sarah J. (2 April 2020). "Treatments for the prevention of Sudden Unexpected Death in Epilepsy (SUDEP)". The Cochrane Database of Systematic Reviews 2020 (4): CD011792. doi:10.1002/14651858.CD011792.pub3. ISSN 1469-493X. PMID 32239759. 
  10. ↑ Nobili, L; Proserpio, P; Rubboli, G; Montano, N; Didato, G; Tassinari, CA (Aug 2011). "Sudden unexpected death in epilepsy (SUDEP) and sleep.". Sleep Medicine Reviews 15 (4): 237–46. doi:10.1016/j.smrv.2010.07.006. PMID 20951616. 
  11. ↑ 11.0 11.1 11.2 11.3 11.4 11.5 11.6 Johnson, Jonathan N.; Tester, David J.; Bass, Nancy E.; Ackerman, Michael J. (July 2010). "Cardiac channel molecular autopsy for sudden unexpected death in epilepsy". Journal of Child Neurology 25 (7): 916–921. doi:10.1177/0883073809343722. ISSN 1708-8283. PMID 20395638. 
  12. ↑ 12.0 12.1 12.2 12.3 12.4 Van Niekerk, Chantal; Van Deventer, Barbara Ströh; du Toit-Prinsloo, Lorraine (September 2017). "Long QT syndrome and sudden unexpected infant death". Journal of Clinical Pathology 70 (9): 808–813. doi:10.1136/jclinpath-2016-204199. ISSN 1472-4146. PMID 28663329. 
  13. ↑ Wang, Dawei; Shah, Krunal R.; Um, Sung Yon; Eng, Lucy S.; Zhou, Bo; Lin, Ying; Mitchell, Adele A.; Nicaj, Leze et al. (April 2014). "Cardiac channelopathy testing in 274 ethnically diverse sudden unexplained deaths". Forensic Science International 237: 90–99. doi:10.1016/j.forsciint.2014.01.014. ISSN 1872-6283. PMID 24631775. 
  14. ↑ Winkel, Bo Gregers; Larsen, Maiken Kudahl; Berge, Knut Erik; Leren, Trond Paul; Nissen, Peter Henrik; Olesen, Morten Salling; Hollegaard, Mads Vilhelm; Jespersen, Thomas et al. (October 2012). "The prevalence of mutations in KCNQ1, KCNH2, and SCN5A in an unselected national cohort of young sudden unexplained death cases". Journal of Cardiovascular Electrophysiology 23 (10): 1092–1098. doi:10.1111/j.1540-8167.2012.02371.x. ISSN 1540-8167. PMID 22882672. 
  15. ↑ Klassen, Tara L.; Bomben, Valerie C.; Patel, Ankita; Drabek, Janice; Chen, Tim T.; Gu, Wenli; Zhang, Feng; Chapman, Kevin et al. (February 2014). "High-resolution molecular genomic autopsy reveals complex sudden unexpected death in epilepsy risk profile". Epilepsia 55 (2): e6–12. doi:10.1111/epi.12489. ISSN 1528-1167. PMID 24372310. 
  16. ↑ 16.0 16.1 16.2 16.3 16.4 16.5 Shorvon, S; Tomson, T (Dec 10, 2011). "Sudden unexpected death in epilepsy.". Lancet 378 (9808): 2028–38. doi:10.1016/S0140-6736(11)60176-1. PMID 21737136. 
  17. ↑ So, N. K.; Sperling, M. R. (31 July 2007). "Ictal asystole and SUDEP". Neurology 69 (5): 423–424. doi:10.1212/01.wnl.0000268698.04032.bc. PMID 17664399. 
  18. ↑ Schuele, SU; Bermeo, AC; Alexopoulos, AV; Locatelli, ER; Burgess, RC; Dinner, DS; Foldvary-Schaefer, N (Jul 31, 2007). "Video-electrographic and clinical features in patients with ictal asystole.". Neurology 69 (5): 434–41. doi:10.1212/01.wnl.0000266595.77885.7f. PMID 17664402. 
  19. ↑ 19.0 19.1 19.2 19.3 19.4 Surges, R; Sander, JW (Apr 2012). "Sudden unexpected death in epilepsy: mechanisms, prevalence, and prevention.". Current Opinion in Neurology 25 (2): 201–7. doi:10.1097/WCO.0b013e3283506714. PMID 22274774. 
  20. ↑ Ryvlin, P; Cucherat, M; Rheims, S (Nov 2011). "Risk of sudden unexpected death in epilepsy in patients given adjunctive antiepileptic treatment for refractory seizures: a meta-analysis of placebo-controlled randomised trials.". Lancet Neurology 10 (11): 961–8. doi:10.1016/S1474-4422(11)70193-4. PMID 21937278. 
  21. ↑ Hesdorffer, DC; Tomson, T (Feb 2013). "Sudden unexpected death in epilepsy. Potential role of antiepileptic drugs.". CNS Drugs 27 (2): 113–9. doi:10.1007/s40263-012-0006-1. PMID 23109241. 
  22. ↑ Aurlien, Dag; Larsen, Jan Petter; Gjerstad, Leif; Taubøll, Erik (February 2012). "Increased risk of sudden unexpected death in epilepsy in females using lamotrigine: a nested, case-control study". Epilepsia 53 (2): 258–266. doi:10.1111/j.1528-1167.2011.03334.x. ISSN 1528-1167. PMID 22126371. 
  23. ↑ Surges, R; Thijs, RD; Tan, HL; Sander, JW (Sep 2009). "Sudden unexpected death in epilepsy: risk factors and potential pathomechanisms.". Nature Reviews. Neurology 5 (9): 492–504. doi:10.1038/nrneurol.2009.118. PMID 19668244. 
  24. ↑ "New sleep seizure detection device may help against sudden unexpected death in epilepsy (SUDEP)". Epilepsy Action. 19 Nov 2018. https://www.epilepsy.org.uk/news/news/new-sleep-seizure-detection-device-may-help-against-sudden-unexpected-death-epilepsy-sudep. 
  25. ↑ Picard, Rosalind (5 April 2019). "An AI smartwatch that detects seizures". https://www.ted.com/talks/rosalind_picard_an_ai_smartwatch_that_detects_seizures/transcript?language=en. 
  26. ↑ Gutiérrez-Viedma, Álvaro; Sanz-Graciani, Isabel; Romeral-Jiménez, María; Parejo-Carbonell, Beatriz; Serrano-García, Irene; Cuadrado, María-Luz; Aledo-Serrano, Ángel; Gil-Nagel, Antonio et al. (2019-10-01). "Patients' knowledge on epilepsy and SUDEP improves after a semi-structured health interview" (in en). Epilepsy & Behavior 99: 106467. doi:10.1016/j.yebeh.2019.106467. ISSN 1525-5050. PMID 31421520. https://www.epilepsybehavior.com/article/S1525-5050(19)30619-5/abstract. 
  27. ↑ Thurman, David J.; Hesdorffer, Dale C.; French, Jacqueline A. (October 2014). "Sudden unexpected death in epilepsy: assessing the public health burden". Epilepsia 55 (10): 1479–1485. doi:10.1111/epi.12666. ISSN 1528-1167. PMID 24903551. 
  28. ↑ Lynge, Thomas Hadberg; Jeppesen, Alexander Gade; Winkel, Bo Gregers; Glinge, Charlotte; Schmidt, Michael Rahbek; Søndergaard, Lars; Risgaard, Bjarke; Tfelt-Hansen, Jacob (June 2018). "Nationwide Study of Sudden Cardiac Death in People With Congenital Heart Defects Aged 0 to 35 Years". Circulation: Arrhythmia and Electrophysiology 11 (6): e005757. doi:10.1161/CIRCEP.117.005757. ISSN 1941-3084. PMID 29858381. 
  29. ↑ Goldstein, Richard D.; Trachtenberg, Felicia L.; Sens, Mary Ann; Harty, Brian J.; Kinney, Hannah C. (January 2016). "Overall Postneonatal Mortality and Rates of SIDS". Pediatrics 137 (1): e20152298. doi:10.1542/peds.2015-2298. ISSN 1098-4275. PMID 26634772. 
  30. ↑ Nouri, Shahin (December 3, 2015). "Sudden Unexpected Death in Epilepsy". Medscape. https://emedicine.medscape.com/article/1187111-overview. 
  31. ↑ Shorvon, Simon; Tomson, Torbjorn (2011-12-10). "Sudden unexpected death in epilepsy". Lancet 378 (9808): 2028–2038. doi:10.1016/S0140-6736(11)60176-1. ISSN 1474-547X. PMID 21737136. 
  32. ↑ Annegers, J. F.; Coan, S. P. (September 1999). "SUDEP: overview of definitions and review of incidence data". Seizure 8 (6): 347–352. doi:10.1053/seiz.1999.0306. ISSN 1059-1311. PMID 10512776. 
  33. ↑ Scorza, Fulvio Alexandre; Cysneiros, Roberta Monterazzo; de Albuquerque, Marly; Scattolini, Marcello; Arida, Ricardo Mario (June 2011). "Sudden unexpected death in epilepsy: an important concern". Clinics 66 (Suppl 1): 65–69. doi:10.1590/S1807-59322011001300008. ISSN 1807-5932. PMID 21779724. 
  34. ↑ "Epilepsy Facts". Citizens United for Research in Epilepsy. http://www.cureepilepsy.org/aboutepilepsy/facts.asp. 

External links

  • Harden, C; Tomson, T; Gloss, D; Buchhalter, J; Cross, JH; Donner, E; French, JA; Gil-Nagel, A et al. (25 April 2017). "Practice guideline summary: Sudden unexpected death in epilepsy incidence rates and risk factors: Report of the Guideline Development, Dissemination, and Implementation Subcommittee of the American Academy of Neurology and the American Epilepsy Society.". Neurology 88 (17): 1674–1680. doi:10.1212/WNL.0000000000003685. PMID 28438841. 



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