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==Overview==
==Overview==
A seizure is a transient event that is due to excessive or synchronous [[neuronal]] activity in the [[brain]]. Seizures may be provoked (by hypoglycemia or alcohol withdrawal, etc) or spontaneous (by underlying [[epilepsy]]). [[Signs]] and [[symptoms]] of seizures depend on the area of the brain that is the origin and may include loss of [[consciousness]], [[confusion]], [[visual]] or other [[sensory]] symptoms, body shaking, limb jerking, or a brief loss of awareness. [[Diagnosis]] of seizure is done by taking the patient's history, [[physical examination]], [[EEG]], and brain [[imaging]]. In the acute setting, seizures are initially treated with [[benzodiazepines]] ([[lorazepam]] or [[midazolam]]), followed by [[phenytoin]] or [[phenobarbital]]. Treatment with [[antiepileptic drugs |antiepileptic drugs (AEDs)]] may be required in some patients.
A seizure is a transient event that is due to excessive or synchronous [[neuronal]] activity in the [[brain]]. The term 'seizure' is derived from a [[Greek]] word that means 'to take hold'. In 2017, the [[International League Against Epilepsy]] (ILAE) classified [[seizure]] by its onsets as focal (aware/impaired awareness, motor, nonmotor, focal to tonic-clonic seizures), generalized (motor, nonmotor), and unknown (motor, nonmotor, and unclassified). Seizures may be provoked (by [[hypoglycemia]] or [[alcohol withdrawal]], etc) or spontaneous (by underlying [[epilepsy]]). It is estimated that 11% of the [[population]] experience a seizure in their life compared to the estimation of 3% for [[epilepsy]]. [[Risk factors]] that can precipitate or provoke seizure include, excessive [[sleep deprivation]], [[alcohol]] use, illicit [[drug]] use, some [[medications]] that reduce the seizure [[threshold]], [[toxins]], [[homeostasis]] abnormality due to [[organ failure]], [[metabolic]] abnormalities, and [[medical]] and [[surgical]] histories that may be important in assessing the [[patient’s]] risk for future seizures. Some of the causes of seizure include, [[brain]] [[injury]], [[brain]] [[hemorrhage]], [[encephalitis]], high [[fever]], [[chronic]] [[alcohol]] use, [[chronic]] [[sleep deprivation]], [[medications]], [[metabolic]] [[abnormalities]], [[withdrawal]] from [[alcohol]] or [[drugs]]. [[Signs]] and [[symptoms]] of seizures depend on the area of the [[brain]] that it originates from. Seizure can be associated with loss of [[consciousness]], [[confusion]], [[visual]] or other [[sensory]] symptoms, [[body]] shaking, [[limb]] jerking, or a brief loss of awareness. [[Diagnosis]] of seizure is done by taking the patient's history, [[physical examination]], laboratory investigation,  [[EEG]], and [[brain]] [[imaging]]. In the acute setting, seizures are initially treated with [[benzodiazepines]] ([[lorazepam]] or [[midazolam]]), followed by [[phenytoin]] or [[phenobarbital]]. Treatment with [[antiepileptic drugs |antiepileptic drugs (AEDs)]] may be required in some [[patients]].
[[Prevention]] is based on controlling the [[risk factors]] that may provoke a seizure.


==Historical Perspective==
==Historical Perspective==
The term 'seizure' is derived from a [[Greek]] word meaning, 'to take hold'. Different words have been used interchangeably in historical texts, such as [[epilepsy]], [[epileptic]] [[seizure]], attack, or [[convulsion]]. [[Epilepsy]] has been mentioned in many documents and texts throughout history including ancient Babylonians, Egyptians, Greeks, Indian (Ayurveda), Persian (Avicenna), and Chinese. [[Epilepsy]] was first described by Hippocrates in Ancient Greece (460–377 B.C.). Until the 18th century, [[epilepsy]] was considered an idiopathic [[disease]] originating in the [[brain]]. The foundation of the modern knowledge of epilepsy was through the work of William Cullen and Samuel A. Tissot. In the 19th century, the understanding of [[epilepsy]] increased. [[Electroencephalography |Electroencephalography (EEG)]] started to gain attention in the late 19th century. In the 20th century, rapid development in medical knowledge happened ([[brain]] [[computed tomography |CT]], [[brain]] [[magnetic resonance imaging |MRI]], and [[PET scan]].
The term 'seizure' is derived from a [[Greek]] word that means 'to take hold'. [[Epilepsy]] was first described by Hippocrates in Ancient Greece (460–377 B.C.). Until the 18th century, [[epilepsy]] was considered an [[idiopathic disease]] originating in the [[brain]]. The foundation of the modern knowledge of [[epilepsy]] was through the work of William Cullen and Samuel A. In the 20th century, rapid development in medical [[imaging]] occurred with development in [[brain]] [[computed tomography |CT]], [[brain]] [[magnetic resonance imaging |MRI]], and [[PET scan]].


==Classification==
==Classification==
In 2017, the [[International League Against Epilepsy]] (ILAE) classified [[seizures]] by their onsets as focal (aware/impaired awareness, motor, nonmotor, focal to tonic-clonic seizures), generalized (motor, nonmotor), and unknown (motor, nonmotor, and unclassified). In 1981, the [[International League Against Epilepsy]] (ILAE) classified epileptic [[seizures]] as [[Focal seizures|partial seizures]] ([[simple partial seizure]]s, [[complex partial seizure]]s, and [[partial seizures]] evolving to secondarily [[generalized seizures]]), [[Generalised epilepsy|generalized seizures]] ([[absence seizure]]s, [[myoclonic seizure]]s, [[clonic seizure]]s, [[Tonic |tonic]] seizures, [[tonic-clonic seizure]]s (grand mal), and [[atonic seizure]]s), and unclassified epileptic seizures.
In 2017, the [[International League Against Epilepsy]] (ILAE) classified [[seizure]] by its onsets as focal (aware/impaired awareness, motor, nonmotor, focal to tonic-clonic seizures), generalized (motor, nonmotor), and unknown (motor, nonmotor, and unclassified). In 1981, the [[International League Against Epilepsy]] (ILAE) classified epileptic [[seizures]] as [[Focal seizures|partial seizures]] ([[simple partial seizure]]s, [[complex partial seizure]]s, and [[partial seizures]] evolving to secondarily [[generalized seizures]]), [[Generalised epilepsy|generalized seizures]] ([[absence seizure]]s, [[myoclonic seizure]]s, [[clonic seizure]]s, [[Tonic |tonic]] seizures, [[tonic-clonic seizure]]s (grand mal), and [[atonic seizure]]s), and unclassified [[epileptic seizures]].


==Pathophysiology==
==Pathophysiology==
Normally, seizures do not happen because the [[membrane]] stability of [[neurons]] is maintained, and the discharges that lead to seizures are prevented from transferring.<ref name="pmid21109098">{{cite journal| author=Huff JS, Fountain NB| title=Pathophysiology and definitions of seizures and status epilepticus. | journal=Emerg Med Clin North Am | year= 2011 | volume= 29 | issue= 1 | pages= 1-13 | pmid=21109098 | doi=10.1016/j.emc.2010.08.001 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21109098  }} </ref>
Normally, seizures do not occur because the [[membrane]] stability of [[neurons]] is maintained, and the discharges that lead to seizures are prevented from transferring. In a normal [[brain]],  some circumstances can provoke seizures, such as: [[hyponatremia]], drug [[withdrawal]], and [[hypoglycemia]]. [[Abnormalities]] in different parts of the [[nervous system]] may cause seizure, such as: [[brain]] regions, [[cells]], [[ions]], networks, and [[receptors]]. The imbalance of excessive [[excitation]] and reduced [[inhibition]] can [[cause]] seizures and is also responsible for prolonging it if the imbalance persists. [[Glutamate]] is the most common [[excitatory]] [[neurotransmitter]] and acts on the [[N-methyl-D-aspartate receptor|N-methyl-D-aspartate (NMDA) receptor]]. However, [[NMDA antagonist]] [[drugs]] have not been [[clinically]] successful. [[Gamma aminobutyric acid |Gamma-aminobutyric acid (GABA)]] is the most common [[inhibition neurotransmitter]]. [[GABA]] inhibits excess [[excitation]] of the [[neurons]] by activating the [[GABAA receptor]]. Increasing the [[inhibition]] of [[GABA]] (even if the inhibition is not damaged) may be helpful in a seizure, since it may overwhelm the excess [[excitation]] of the seizure. Examples of [[GABA]]-enhancing [[drugs]] are [[benzodiazepines]], [[barbiturates]], [[propofol]], and some [[anesthetics]]. However, these [[drugs]] are not suitable for long term [[therapy]] since [[patients]] usually become tolerant to their effect.
 
In a normal [[brain]],  some circumstances can provoke seizures, such as:<ref name="pmid21109098">{{cite journal| author=Huff JS, Fountain NB| title=Pathophysiology and definitions of seizures and status epilepticus. | journal=Emerg Med Clin North Am | year= 2011 | volume= 29 | issue= 1 | pages= 1-13 | pmid=21109098 | doi=10.1016/j.emc.2010.08.001 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21109098  }} </ref>
* [[Hyponatremia]]: by disrupting the electrochemical gradients across [[cell]] membranes and causing instability
* Drug [[withdrawal]] ([[benzodiazepines]], [[barbiturates]], and [[alcohol]]): may sensitize inhibitory [[GABAA]] receptors and stimulate a seizure
* [[Hypoglycemia]]: by changing the [[metabolism]] of [[cells]]
 
Abnormalities in different parts of the [[nervous system]] may cause seizure, such as [[brain]] regions, [[cells]], [[ions]], networks, and [[receptors]].<ref name="pmid21109098">{{cite journal| author=Huff JS, Fountain NB| title=Pathophysiology and definitions of seizures and status epilepticus. | journal=Emerg Med Clin North Am | year= 2011 | volume= 29 | issue= 1 | pages= 1-13 | pmid=21109098 | doi=10.1016/j.emc.2010.08.001 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21109098  }} </ref>
 
The imbalance of excessive [[excitation]] and reduced [[inhibition]] that causes and keeps the seizure going on.<ref name="pmid7560021">{{cite journal| author=Fountain NB, Lothman EW| title=Pathophysiology of status epilepticus. | journal=J Clin Neurophysiol | year= 1995 | volume= 12 | issue= 4 | pages= 326-42 | pmid=7560021 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7560021  }} </ref>
 
'''N-methyl-D-aspartate (NMDA) Receptor'''
* [[Glutamate]] is the most common [[excitation neurotransmitter]] and affects by the [[N-methyl-D-aspartate receptor|N-methyl-D-aspartate (NMDA) receptor]].
* However, [[NMDA antagonist]] drugs have not been clinically successful, probably due to their effects on learning and [[memory]].
 
'''Gamma aminobutyric acid (GABA) Receptor'''
* [[Gamma aminobutyric acid |Gamma-aminobutyric acid (GABA)]] is the most common [[inhibition neurotransmitter]].<ref name="pmid7560021">{{cite journal| author=Fountain NB, Lothman EW| title=Pathophysiology of status epilepticus. | journal=J Clin Neurophysiol | year= 1995 | volume= 12 | issue= 4 | pages= 326-42 | pmid=7560021 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7560021  }} </ref>
* [[GABA]] inhibits excess [[excitation]] of the neurons by activating the [[GABAA receptor]].  
* Increasing the inhibition of GABA (even if the inhibition is not damaged) may be helpful in a seizure, since it may overwhelm the excess excitation of the seizure.
** Examples of [[GABA]]-enhancing drugs are [[benzodiazepines]], [[barbiturates]], [[propofol]], and some [[anesthetics]].  
*** However, these drugs are not suitable for long term therapy since patients usually become tolerant to their effect.


==Causes==
==Causes==
Some of the causes of seizure include:<ref name="pmid27720347">{{cite journal| author=Legg KT, Newton M| title=Counselling adults who experience a first seizure. | journal=Seizure | year= 2017 | volume= 49 | issue=  | pages= 64-68 | pmid=27720347 | doi=10.1016/j.seizure.2016.09.012 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27720347  }} </ref>
Some of the causes of seizure include, [[brain]] [[injury]], [[brain]] [[hemorrhage]], [[encephalitis]], high [[fever]], [[chronic]] [[alcohol]] use, [[chronic]] [[sleep deprivation]], [[medications]], [[metabolic]] [[abnormalities]], [[withdrawal]] from [[alcohol]] or [[drugs]].
* [[Brain]] injury (such as a [[tumor]], [[vascular]], [[traumatic]], and developmental)
* Brain [[hemorrhage]]
* [[Encephalitis]]
* High [[fever]]
* Excessive [[alcohol]] use
* Excessive [[sleep deprivation]]
* [[Medications]]
* [[Metabolic]] abnormalities
* [[Withdrawal]] from [[alcohol]] or [[drugs]]


==Differentiating Seizure from Other Diseases==
==Differentiating Seizure from Other Diseases==
[[Differential diagnosis]] of epileptic seizures may include:<ref name="pmid30704683">{{cite journal| author=Johnson EL| title=Seizures and Epilepsy. | journal=Med Clin North Am | year= 2019 | volume= 103 | issue= 2 | pages= 309-324 | pmid=30704683 | doi=10.1016/j.mcna.2018.10.002 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30704683  }} </ref>
[[Differential diagnosis]] of epileptic seizures may include, [[concussion]], [[drug]] [[intoxication]] or [[withdrawal]], [[migraine]], [[psychogenic]] non-[[epileptic]] events, [[panic attacks]], [[sleep disorders]], [[syncope]], [[transient global amnesia]], [[transient ischemic attack|transient ischemic attack (TIA)]].
* [[Concussion]]
* Drug [[intoxication]] or [[withdrawal]]
* [[Migraine]]
* [[Psychogenic]] nonepileptic events
* [[Panic attacks]]
* [[Sleep disorders]]
* [[Syncope]]
* [[Transient global amnesia]]
* [[Transient ischemic attack|Transient ischemic attack (TIA)]]


==Epidemiology and Demographics==
==Epidemiology and Demographics==
It is estimated that 11% of the [[population]] experience a seizure in their life compared to the estimation of 3% for [[epilepsy]]. In the US, seizure is estimated to account for 1 million or 1% of [[Emergency department|emergency department (ED)]] visits annually. The [[incidence]] of [[acute]] [[symptomatic]] seizures is estimated to be 39 cases per 100,000 individuals in the US. Seizures are more common among [[males]] and the Black race.
It is estimated that 11% of the [[population]] experience a seizure in their life compared to the estimation of 3% for [[epilepsy]]. In the US, seizure is estimated to account for 1 million or 1% of [[Emergency department|emergency department (ED)]] visits annually. The [[incidence]] of [[acute]] [[symptomatic]] seizures is estimated to be 39 cases per 100,000 individuals in the US. Seizures are more common among [[males]] and people of African descent.


==Risk Factors==
==Risk Factors==
[[Risk factors]] that can precipitate or provoke seizure include: excessive [[sleep deprivation]], [[alcohol]] use, illicit [[drug]] use, some [[medications]] that reduce the seizure [[threshold]], [[toxins]], [[homeostasis]] abnormality due to [[organ failure]], [[metabolic]] abnormalities, and [[medical]] and [[surgical]] histories that may be important in assessing the [[patient’s]] risk for future seizures.
[[Risk factors]] that can precipitate or provoke seizure include, excessive [[sleep deprivation]], [[alcohol]] use, illicit [[drug]] use, some [[medications]] that reduce the seizure [[threshold]], [[toxins]], [[homeostasis]] abnormality due to [[organ failure]], [[metabolic]] abnormalities, and [[medical]] and [[surgical]] histories that may be important in assessing the [[patient’s]] risk for future seizures.


==Screening==
==Screening==
The [[EEG]] monitoring has been recommended in [[neonates]] with known or suspected acute [[brain injury]] combined with [[encephalopathy]], [[differential diagnosis]] of abnormal paroxysmal events, and in high-risk populations.
The [[EEG]] monitoring has been recommended in [[neonates]] with known or suspected [[acute]] [[brain injury]] combined with [[encephalopathy]], [[diseases]] associated with abnormal [[paroxysmal]] events, and in high-risk [[population]].


==Natural History, Complications, and Prognosis==
==Natural History, Complications, and Prognosis==
* The recurrence rate of seizure within 2 years is 35% to 40% in patients with a first-time unprovoked seizure.<ref name="pmid8827178">{{cite journal| author=Berg AT, Testa FM, Levy SR, Shinnar S| title=The epidemiology of epilepsy. Past, present, and future. | journal=Neurol Clin | year= 1996 | volume= 14 | issue= 2 | pages= 383-98 | pmid=8827178 | doi=10.1016/s0733-8619(05)70263-2 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8827178  }} </ref>
The recurrence rate of seizure within two years is 35% to 40% in [[patients]] with a first-time unprovoked seizure. [[Status epilepticus]] occurs in about 6%-7% of the [[patients]] with seizure in the [[emergency department|emergency department (ED)]]. The overall [[mortality rate]] of [[status epilepticus]] is approximately 22% (3% in [[pediatric]] patients to 26% in adults). Simple [[febrile seizure|febrile seizures]] are considered normal in childhood and the [[prognosis]] is generally excellent. The recurrence rate is about 12% in [[children]] that have their first [[febrile seizure]] in [[infancy]] and about 50% in those who have their first [[febrile seizure]] later.
* [[Status epilepticus]] occurs in about 6%-7% of the patients with seizure in the [[emergency department|emergency department (ED)]].<ref name="pmid11388937">{{cite journal| author=Huff JS, Morris DL, Kothari RU, Gibbs MA, Emergency Medicine Seizure Study Group| title=Emergency department management of patients with seizures: a multicenter study. | journal=Acad Emerg Med | year= 2001 | volume= 8 | issue= 6 | pages= 622-8 | pmid=11388937 | doi=10.1111/j.1553-2712.2001.tb00175.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11388937  }} </ref><ref name="pmid2924743">{{cite journal| author=Krumholz A, Grufferman S, Orr ST, Stern BJ| title=Seizures and seizure care in an emergency department. | journal=Epilepsia | year= 1989 | volume= 30 | issue= 2 | pages= 175-81 | pmid=2924743 | doi=10.1111/j.1528-1157.1989.tb05451.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=2924743  }} </ref><ref name="pmid1883923">{{cite journal| author=Brinar V, Bozicević D, Zurak N, Gubarev N, Djaković V| title=Epileptic seizures as a symptom of various neurological diseases. | journal=Neurol Croat | year= 1991 | volume= 40 | issue= 2 | pages= 93-101 | pmid=1883923 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1883923  }} </ref>
* Some [[complications]] that have been suggested in seizure include:<ref name="pmid30948624">{{cite journal| author=Foster E, Carney P, Liew D, Ademi Z, O'Brien T, Kwan P| title=First seizure presentations in adults: beyond assessment and treatment. | journal=J Neurol Neurosurg Psychiatry | year= 2019 | volume= 90 | issue= 9 | pages= 1039-1045 | pmid=30948624 | doi=10.1136/jnnp-2018-320215 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30948624  }} </ref>
** Accidents and [[injuries]]: mostly [[cranial]] soft tissue [[contusions]] or [[lacerations]]
** Lifestyle and [[psychosocial]] impact: financial, social, and relationship problems such as driving, work-related activities, reduced productivity, stigma in society
** [[Comorbidities]]
*** [[Medical]]: [[stroke]], [[ischaemic heart disease]], [[cancer]], [[migraine]], [[vertigo]], and [[sleep disorders]]
*** [[Psychiatric]]: [[depression]] and anxiety
*** [[Neurodegenerative]] diseases: [[dementia]] and [[Alzheimer disease |Alzheimer disease (AD)]]
** [[Death]]
* The overall mortality rate of [[status epilepticus]] is approximately 22% (3% in [[pediatric]] patients to 26% in adults).<ref name="pmid8780085">{{cite journal| author=DeLorenzo RJ, Hauser WA, Towne AR, Boggs JG, Pellock JM, Penberthy L | display-authors=etal| title=A prospective, population-based epidemiologic study of status epilepticus in Richmond, Virginia. | journal=Neurology | year= 1996 | volume= 46 | issue= 4 | pages= 1029-35 | pmid=8780085 | doi=10.1212/wnl.46.4.1029 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8780085  }} </ref>
* Simple [[febrile seizure|febrile seizures]] are considered normal in childhood and the prognosis is generally excellent.
** The recurrence rate is about 12% in children that have their first [[febrile seizure]] in infancy and about 50% in those who have their first [[febrile seizure]] later.<ref name="pmid1603702">{{cite journal| author=Kenney RD, Taylor JA| title=Absence of serum chemistry abnormalities in pediatric patients presenting with seizures. | journal=Pediatr Emerg Care | year= 1992 | volume= 8 | issue= 2 | pages= 65-6 | pmid=1603702 | doi=10.1097/00006565-199204000-00001 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=1603702  }} </ref><ref name="pmid10969121">{{cite journal| author=Walton DM, Thomas DC, Aly HZ, Short BL| title=Morbid hypocalcemia associated with phosphate enema in a six-week-old infant. | journal=Pediatrics | year= 2000 | volume= 106 | issue= 3 | pages= E37 | pmid=10969121 | doi=10.1542/peds.106.3.e37 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=10969121  }} </ref>


==Diagnosis==
==Diagnosis==
===Diagnostic Study of Choice===
The basis of seizure investigation and [[diagnosis]] depends upon, a detailed history of any event before and after a seizure episode, investigation of co-existing conditions, a focused [[physical examination]], laboratory evaluation, and [[brain]] [[imaging]].
===History and Symptoms===
===History and Symptoms===
The main part of the seizure [[history]] should be about the [[patient]]’s awareness, experience, and remembrance of the seizure. [[Symptoms]] of seizure include, [[aura]], [[staring spells]], [[myoclonic]] jerks, impaired awareness, [[paresthesias]], lost of [[consciousness]], [[Déjà vu]] experiences and [[confusion]].
The main part of the seizure [[history]] should be about the [[patient]]’s awareness, experience, and remembrance of the seizure. [[Symptoms]] of seizure include, [[aura]], [[staring spells]], [[myoclonic]] jerks, impaired awareness, [[paresthesias]], lost of [[consciousness]], [[Déjà vu]] experiences and [[confusion]].


===Physical Examination===
===Physical Examination===
The [[physical examination]] of patients with seizure may reveal:<ref name="pmid28027373">{{cite journal| author=Gavvala JR, Schuele SU| title=New-Onset Seizure in Adults and Adolescents: A Review. | journal=JAMA | year= 2016 | volume= 316 | issue= 24 | pages= 2657-2668 | pmid=28027373 | doi=10.1001/jama.2016.18625 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28027373  }} </ref><ref name="pmid23041172">{{cite journal| author=Brigo F, Storti M, Lochner P, Tezzon F, Fiaschi A, Bongiovanni LG | display-authors=etal| title=Tongue biting in epileptic seizures and psychogenic events: an evidence-based perspective. | journal=Epilepsy Behav | year= 2012 | volume= 25 | issue= 2 | pages= 251-5 | pmid=23041172 | doi=10.1016/j.yebeh.2012.06.020 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23041172  }} </ref><ref name="pmid11297707">{{cite journal| author=Browne TR, Holmes GL| title=Epilepsy. | journal=N Engl J Med | year= 2001 | volume= 344 | issue= 15 | pages= 1145-51 | pmid=11297707 | doi=10.1056/NEJM200104123441507 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=11297707  }} </ref><ref name="pmid15101468">{{cite journal| author=Ahmed SN, Spencer SS| title=An approach to the evaluation of a patient for seizures and epilepsy. | journal=WMJ | year= 2004 | volume= 103 | issue= 1 | pages= 49-55 | pmid=15101468 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=15101468  }} </ref><ref name="pmid30743294">{{cite journal| author=Bank AM, Bazil CW| title=Emergency Management of Epilepsy and Seizures. | journal=Semin Neurol | year= 2019 | volume= 39 | issue= 1 | pages= 73-81 | pmid=30743294 | doi=10.1055/s-0038-1677008 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30743294  }} </ref>
The [[physical examination]] of [[patients]] with seizure may reveal: lateral [[tongue]] bites, [[nuchal rigidity]] or [[asterixis]], [[bruises]] or [[scrapes]] on the [[body]] after falls, [[signs]] of a [[neurocutaneous syndrome]] associated with [[epilepsy]] on the [[skin]], [[back pain]], transient or persistent focal [[weakness]] or asymmetry, and [[urinary incontinence]].
* Lateral tongue bites
* [[Nuchal rigidity]] or [[asterixis]] (may suggest an underlying systemic disorder)
* [[Bruises]] or scrapes on the body after falls
* [[Signs]] of a [[neurocutaneous syndrome]] associated with [[epilepsy]] on the [[skin]] (such as [[neurofibromatosis]], [[tuberous sclerosis]], and [[Sturge-Weber syndrome]])
* [[Back pain]] (may suggest a vertebral [[compression fracture]])
* Transient or persistent focal [[weakness]] or asymmetry (May suggest the area of the [[brain]] abnormality that may have caused the seizure)
* [[Urinary incontinence]]


===Laboratory Findings===
===Laboratory Findings===
The [[laboratory]] tests for patients with seizure may include checking for:<ref name="pmid28027373">{{cite journal| author=Gavvala JR, Schuele SU| title=New-Onset Seizure in Adults and Adolescents: A Review. | journal=JAMA | year= 2016 | volume= 316 | issue= 24 | pages= 2657-2668 | pmid=28027373 | doi=10.1001/jama.2016.18625 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28027373  }} </ref><ref name="pmid28288363">{{cite journal| author=Nass RD, Sassen R, Elger CE, Surges R| title=The role of postictal laboratory blood analyses in the diagnosis and prognosis of seizures. | journal=Seizure | year= 2017 | volume= 47 | issue=  | pages= 51-65 | pmid=28288363 | doi=10.1016/j.seizure.2017.02.013 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28288363  }} </ref><ref name="pmid28288363">{{cite journal| author=Nass RD, Sassen R, Elger CE, Surges R| title=The role of postictal laboratory blood analyses in the diagnosis and prognosis of seizures. | journal=Seizure | year= 2017 | volume= 47 | issue=  | pages= 51-65 | pmid=28288363 | doi=10.1016/j.seizure.2017.02.013 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28288363  }} </ref>
The [[laboratory]] tests for [[patients]] with seizure may include, [[hypoglycemia]], [[hyponatremia]], [[uremia]], [[drug intoxication]], [[ammonia]] levels, [[creatine kinase|creatine kinase (CK)]] levels, [[lactate]] levels, [[prolactin]] levels. Elevated [[prolactin]] level may be helpful in differentiating generalized [[tonic-clonic]] or complex partial seizure from [[psychogenic]] non-[[epileptic]] seizures, only if the [[patient]]’s [[prolactin]] level is measured 10 to 20 minutes after a suspected seizure event. Analysis of the serum [[prolactin]] level is not effective in distinguishing a seizure from [[syncope]]. No conclusion could be established regarding [[serum]] [[prolactin]] changes following [[status epilepticus]], repetitive seizures, and [[neonatal]] seizures.
* [[Hypoglycemia]]
 
* [[Hyponatremia]]  
===Electrocardiogram===
* [[Uremia]]
An [[ECG]] in [[patient]]s presenting with seizure is very crucial to prevent sudden unexpected death in [[epilepsy]] (SUDEP). Important [[signs]] to look for are, [[ST depression]], [[T wave inversion]], [[heart block]], [[prolonged QT interval]], [[Brugada Syndrome]].
* [[Drug intoxication]]
* [[Ammonia]] levels
* [[Creatine kinase|Creatine kinase (CK)]] levels
* [[Lactate]] levels
* [[Prolactin]] levels


'''Serum Prolactin Level:''' <ref name="pmid16157897">{{cite journal| author=Chen DK, So YT, Fisher RS, Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology| title=Use of serum prolactin in diagnosing epileptic seizures: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. | journal=Neurology | year= 2005 | volume= 65 | issue= 5 | pages= 668-75 | pmid=16157897 | doi=10.1212/01.wnl.0000178391.96957.d0 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16157897  }} </ref>
===X-ray===
* Elevated [[prolactin]] level may be helpful in differentiating generalized tonic-clonic or complex partial seizure from [[psychogenic]] nonepileptic seizures, only if the patient’s [[prolactin]] level is measured 10 to 20 minutes after a suspected seizure event.
There are no [[x-ray]] findings associated with a seizure. [[CT]] [[scan]] and [[MRI]] are superior to [[x-ray]] for [[imaging]] findings associated with seizures.
* Analysis of the serum [[prolactin]] level is not effective in distinguishing a seizure from [[syncope]].
* No conclusion could be established regarding serum [[prolactin]] changes following [[status epilepticus]], repetitive seizures, and [[neonatal]] seizures.


===Electroencephalogram===
===Echocardiography and Ultrasound===
[[EEG]] should be performed as soon as possible and can detect: focal sharp waves or spikes ([[focal epilepsy]]) and bilateral/generalized epileptiform activity (generalized [[epilepsy]]).<ref name="pmid30704683">{{cite journal| author=Johnson EL| title=Seizures and Epilepsy. | journal=Med Clin North Am | year= 2019 | volume= 103 | issue= 2 | pages= 309-324 | pmid=30704683 | doi=10.1016/j.mcna.2018.10.002 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30704683  }} </ref>
There are no [[echocardiography]]/[[ultrasound]] findings associated with seizures. However, an [[echocardiogram]] may be helpful in preventing sudden unexpected death in [[epilepsy]] (SUDEP) by looking for any functional or structural [[abnormality]] of the [[heart]].


===CT===
===CT===
[[CT scan|Computed tomography scan (CT scan)]] in the [[emergency department]] is helpful in ruling out [[hemorrhage]] or other lesions.<ref name="pmid30743294">{{cite journal| author=Bank AM, Bazil CW| title=Emergency Management of Epilepsy and Seizures. | journal=Semin Neurol | year= 2019 | volume= 39 | issue= 1 | pages= 73-81 | pmid=30743294 | doi=10.1055/s-0038-1677008 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30743294  }} </ref>
[[CT scan|Computed tomography scan (CT scan)]] in the [[emergency department]] is helpful in ruling out [[hemorrhage]] or other [[lesions]].


===MRI===
===MRI===
* [[MRI scan]] (preferably 3 tesla) should be performed in order to detect epileptogenic lesions.<ref name="pmid30743294">{{cite journal| author=Bank AM, Bazil CW| title=Emergency Management of Epilepsy and Seizures. | journal=Semin Neurol | year= 2019 | volume= 39 | issue= 1 | pages= 73-81 | pmid=30743294 | doi=10.1055/s-0038-1677008 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30743294  }} </ref>
[[MRI scan]] (preferably 3 teslas) should be performed in order to detect epileptogenic [[lesions]]. [[MRI]] is more sensitive in detecting some findings related to seizures such as [[hippocampal sclerosis]] and [[cortical dysplasia]].
* [[MRI]] is more sensitive in detecting some findings compared to [[CT scan]].<ref name="pmid8001611">{{cite journal| author=Radue EW, Scollo-Lavizzari G| title=Computed tomography and magnetic resonance imaging in epileptic seizures. | journal=Eur Neurol | year= 1994 | volume= 34 Suppl 1 | issue=  | pages= 55-7 | pmid=8001611 | doi=10.1159/000119510 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=8001611  }} </ref>


===Other Imaging Findings===
===Other Imaging Findings===
3-T [[MRI]] may be helpful in patients with [[epilepsy]] and negative 1.5-T [[MRI]].<ref name="pmid27408997">{{cite journal| author=Ladino LD, Balaguera P, Rascovsky S, Delgado J, Llano J, Hernández-Ronquillo L | display-authors=etal| title=Clinical Benefit of 3 Tesla Magnetic Resonance Imaging Rescanning in Patients With Focal Epilepsy and Negative 1.5 Tesla Magnetic Resonance Imaging. | journal=Rev Invest Clin | year= 2016 | volume= 68 | issue= 3 | pages= 112-8 | pmid=27408997 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27408997  }} </ref><ref name="pmid16217054">{{cite journal| author=Knake S, Triantafyllou C, Wald LL, Wiggins G, Kirk GP, Larsson PG | display-authors=etal| title=3T phased array MRI improves the presurgical evaluation in focal epilepsies: a prospective study. | journal=Neurology | year= 2005 | volume= 65 | issue= 7 | pages= 1026-31 | pmid=16217054 | doi=10.1212/01.wnl.0000179355.04481.3c | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=16217054  }} </ref>
3-T [[MRI]] may be helpful in patients with [[epilepsy]] and negative 1.5-T [[MRI]].


===Other Diagnostic Studies===
===Other Diagnostic Studies===
* [[EEG]] with [[sleep deprivation]] is helpful when standard [[EEG]] does not detect any epileptiform changes.<ref name="pmid14521275">{{cite journal| author=Schreiner A, Pohlmann-Eden B| title=Value of the early electroencephalogram after a first unprovoked seizure. | journal=Clin Electroencephalogr | year= 2003 | volume= 34 | issue= 3 | pages= 140-4 | pmid=14521275 | doi=10.1177/155005940303400307 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14521275  }} </ref>
[[EEG]] with [[sleep deprivation]] is helpful when standard [[EEG]] does not detect any epileptiform changes. [[Lumbar puncture |Lumbar puncture (LP)]] should be considered in those [[patients]] suspected of [[meningitis]], [[encephalitis]], [[subarachnoid hemorrhage]].
* [[Lumbar puncture |Lumbar puncture (LP)]] should be considered in those patients suggesting the following causes:<ref name="pmid28027373">{{cite journal| author=Gavvala JR, Schuele SU| title=New-Onset Seizure in Adults and Adolescents: A Review. | journal=JAMA | year= 2016 | volume= 316 | issue= 24 | pages= 2657-2668 | pmid=28027373 | doi=10.1001/jama.2016.18625 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28027373  }} </ref>
** [[Meningitis]]
** [[Encephalitis]]
** [[Subarachnoid hemorrhage]]


==Treatment==
==Treatment==
===Medical Therapy===
===Medical Therapy===
* In the acute setting, seizures are initially treated with [[benzodiazepines]] ([[lorazepam]] or [[midazolam]]), followed by [[phenytoin]] or [[phenobarbital]].<ref name="pmid26900382">{{cite journal| author=Glauser T, Shinnar S, Gloss D, Alldredge B, Arya R, Bainbridge J | display-authors=etal| title=Evidence-Based Guideline: Treatment of Convulsive Status Epilepticus in Children and Adults: Report of the Guideline Committee of the American Epilepsy Society. | journal=Epilepsy Curr | year= 2016 | volume= 16 | issue= 1 | pages= 48-61 | pmid=26900382 | doi=10.5698/1535-7597-16.1.48 | pmc=4749120 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=26900382  }} </ref>
In the [[acute]] setting, seizures are initially treated with [[benzodiazepines]] ([[lorazepam]] or [[midazolam]]), followed by [[phenytoin]] or [[phenobarbital]][[Antiepileptic drugs |Antiepileptic drugs (AEDs)]] are commonly used in treating focal and generalized [[epilepsies]].
 
* [[Antiepileptic drugs |Antiepileptic drugs (AEDs)]] are commonly used in treating focal and generalized [[epilepsies]].<ref name="pmid30704683">{{cite journal| author=Johnson EL| title=Seizures and Epilepsy. | journal=Med Clin North Am | year= 2019 | volume= 103 | issue= 2 | pages= 309-324 | pmid=30704683 | doi=10.1016/j.mcna.2018.10.002 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30704683  }} </ref>


===Surgery===  
===Surgery===  
* [[Surgery]] may be helpful in patients with [[focal epilepsy]] if there is no seizure control after two or more [[antiepileptic drugs |antiepileptic drugs (AEDs)]].
[[Surgery]] may be helpful in [[patients]] with [[focal epilepsy]] if there is no seizure control after two or more [[antiepileptic drugs |antiepileptic drugs (AEDs)]].
* [[Laser]] interstitial [[thermal ablation]] and neurostimulation may be helpful as alternative therapies to [[surgery]] in some patients.<ref name="pmid30704683">{{cite journal| author=Johnson EL| title=Seizures and Epilepsy. | journal=Med Clin North Am | year= 2019 | volume= 103 | issue= 2 | pages= 309-324 | pmid=30704683 | doi=10.1016/j.mcna.2018.10.002 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30704683  }} </ref>
[[Laser]] interstitial [[thermal ablation]] and neurostimulation may be helpful as alternative therapies to [[surgery]] in some [[patients]].


===Primary Prevention===
===Primary Prevention===
* Some of the preventable [[etiologies]] for [[epilepsy]] that should be considered in [[primary prevention]] include [[Central nervous system |central nervous system (CNS)]] infection, [[CNS]] [[parasitosis]], pre- and [[perinatal]] [[brain]] insults, [[stroke]], and [[Traumatic brain injury|traumatic brain injury (TBI)]].<ref name="pmid29637551">{{cite journal| author=Thurman DJ, Begley CE, Carpio A, Helmers S, Hesdorffer DC, Mu J | display-authors=etal| title=The primary prevention of epilepsy: A report of the Prevention Task Force of the International League Against Epilepsy. | journal=Epilepsia | year= 2018 | volume= 59 | issue= 5 | pages= 905-914 | pmid=29637551 | doi=10.1111/epi.14068 | pmc=7004820 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=29637551  }} </ref>
Some of the preventable [[etiologies]] for [[epilepsy]] that should be considered in [[primary prevention]] include [[Central nervous system |central nervous system (CNS)]] [[infection]], [[CNS]] [[parasitosis]], [[prenatal]] and [[perinatal]] [[brain]] insults, [[stroke]], and [[Traumatic brain injury|traumatic brain injury (TBI)]]. Factors that can precipitate or provoke seizure may include [[chronic]] [[sleep deprivation]], [[alcohol]] use, illicit [[drug]] use, some [[medications]] that reduce the seizure [[threshold]], [[toxins]], [[homeostasis]] [[abnormalities]] due to [[organ failure]], [[metabolic]] [[abnormalities]], and [[medical]] and [[surgical]] histories that may be important in assessing the [[patient]]’s risk for future seizures.
 
* Some factors that can perticipate or provoke seizure may include excessive [[sleep deprivation]], alcohol use, illicit drug use, some [[medications]] that reduce the seizure threshold, [[toxins]], [[homeostasis]] abnormality due to [[organ failure]], [[metabolic]] abnormalities, and [[medical]] and [[surgical]] histories that may be important in assessing the patient’s risk for future seizures.<ref name="Pohlmann-Eden Legg 2013 pp. 61–67">{{cite journal | last=Pohlmann-Eden | first=Bernd | last2=Legg | first2=Karen T. | title=Treatment of first seizure in adults: A comprehensive approach integrating 10 key principles | journal=Epileptology | publisher=Elsevier BV | volume=1 | issue=1 | year=2013 | issn=2212-8220 | doi=10.1016/j.epilep.2013.01.005 | pages=61–67}}</ref><ref name="pmid9717943">{{cite journal| author=Delanty N, Vaughan CJ, French JA| title=Medical causes of seizures. | journal=Lancet | year= 1998 | volume= 352 | issue= 9125 | pages= 383-90 | pmid=9717943 | doi=10.1016/S0140-6736(98)02158-8 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9717943  }} </ref><ref name="pmid28027373">{{cite journal| author=Gavvala JR, Schuele SU| title=New-Onset Seizure in Adults and Adolescents: A Review. | journal=JAMA | year= 2016 | volume= 316 | issue= 24 | pages= 2657-2668 | pmid=28027373 | doi=10.1001/jama.2016.18625 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=28027373  }} </ref>


===Secondary Prevention===
===Secondary Prevention===
* Patients that have has first seizures should be counseled for their seizure and the possible etiology, lifestyle considerations (safety measures and avoidance of the factors that can lower the seizure threshold and predispose to recurrences, such as [[sleep deprivation]], use of [[alcohol]], and illicit drugs), driving, [[antiepileptic drugs|antiepileptic drugs (AED)]] and their [[side effects]], and follow-up.<ref name="pmid27720347">{{cite journal| author=Legg KT, Newton M| title=Counselling adults who experience a first seizure. | journal=Seizure | year= 2017 | volume= 49 | issue=  | pages= 64-68 | pmid=27720347 | doi=10.1016/j.seizure.2016.09.012 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27720347  }} </ref>
[[Patients]] that have had a first seizure should be counseled for their seizure episode and the possible [[etiology]], lifestyle modifications (safety measures and avoidance of the factors that can lower the seizure threshold and predispose to recurrences, such as [[sleep deprivation]], use of [[alcohol]], and illicit [[drugs]]), driving, [[antiepileptic drugs|antiepileptic drugs (AED)]] and their [[side effects]], and follow-up. [[Patients]], family members, friends, and co-workers should be counseled for seizure first aid during a seizure event such as removal of harmful objects, repositioning the [[patient]] in order to support [[breathing]], timing the seizure, calling for help, not restraining or holding the [[patient]] down, and not putting anything in the [[patient]]'s mouth.
* Patients, family members, friends, and co-workers should be counseled for seizure first aid during a seizure event such as removal of harmful objects, repositioning the patient in order to support [[breathing]], timing the seizure, calling for help, not restraining or holding the patient down, and not putting anything in the patient's mouth.<ref name="pmid27720347">{{cite journal| author=Legg KT, Newton M| title=Counselling adults who experience a first seizure. | journal=Seizure | year= 2017 | volume= 49 | issue=  | pages= 64-68 | pmid=27720347 | doi=10.1016/j.seizure.2016.09.012 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27720347  }} </ref>


===Cost-Effectiveness of Therapy===
===Cost-Effectiveness of Therapy===
The national economical impact of [[epilepsy]] is estimated at $9.6 billion per year in the United States.<ref name="pmid19508694">{{cite journal| author=Yoon D, Frick KD, Carr DA, Austin JK| title=Economic impact of epilepsy in the United States. | journal=Epilepsia | year= 2009 | volume= 50 | issue= 10 | pages= 2186-91 | pmid=19508694 | doi=10.1111/j.1528-1167.2009.02159.x | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19508694  }} </ref>
The national economical impact of [[epilepsy]] is estimated at $9.6 billion per year in the United States.


===Future or Investigational Therapies===
===Future or Investigational Therapies===
Further studies are required for producing new [[drugs]] with novel [[mechanisms of action]] and finding new [[treatments]] by increasing the knowledge of the mechanisms of [[dietary]] therapy in [[epilepsy]] and the role that neurosteroid [[hormones]] have in exacerbating [[epilepsy]].<ref name="pmid30704683">{{cite journal| author=Johnson EL| title=Seizures and Epilepsy. | journal=Med Clin North Am | year= 2019 | volume= 103 | issue= 2 | pages= 309-324 | pmid=30704683 | doi=10.1016/j.mcna.2018.10.002 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=30704683  }} </ref>
Further studies are required for producing new [[drugs]] with novel [[mechanisms of action]] and finding new [[treatments]] by increasing the knowledge of the mechanisms of [[dietary]] therapy in [[epilepsy]] and the role that neurosteroid [[hormones]] have in exacerbating [[epilepsy]].


==References==
==References==

Latest revision as of 00:09, 22 April 2021

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Shakiba Hassanzadeh, MD[2]

Overview

A seizure is a transient event that is due to excessive or synchronous neuronal activity in the brain. The term 'seizure' is derived from a Greek word that means 'to take hold'. In 2017, the International League Against Epilepsy (ILAE) classified seizure by its onsets as focal (aware/impaired awareness, motor, nonmotor, focal to tonic-clonic seizures), generalized (motor, nonmotor), and unknown (motor, nonmotor, and unclassified). Seizures may be provoked (by hypoglycemia or alcohol withdrawal, etc) or spontaneous (by underlying epilepsy). It is estimated that 11% of the population experience a seizure in their life compared to the estimation of 3% for epilepsy. Risk factors that can precipitate or provoke seizure include, excessive sleep deprivation, alcohol use, illicit drug use, some medications that reduce the seizure threshold, toxins, homeostasis abnormality due to organ failure, metabolic abnormalities, and medical and surgical histories that may be important in assessing the patient’s risk for future seizures. Some of the causes of seizure include, brain injury, brain hemorrhage, encephalitis, high fever, chronic alcohol use, chronic sleep deprivation, medications, metabolic abnormalities, withdrawal from alcohol or drugs. Signs and symptoms of seizures depend on the area of the brain that it originates from. Seizure can be associated with loss of consciousness, confusion, visual or other sensory symptoms, body shaking, limb jerking, or a brief loss of awareness. Diagnosis of seizure is done by taking the patient's history, physical examination, laboratory investigation, EEG, and brain imaging. In the acute setting, seizures are initially treated with benzodiazepines (lorazepam or midazolam), followed by phenytoin or phenobarbital. Treatment with antiepileptic drugs (AEDs) may be required in some patients. Prevention is based on controlling the risk factors that may provoke a seizure.

Historical Perspective

The term 'seizure' is derived from a Greek word that means 'to take hold'. Epilepsy was first described by Hippocrates in Ancient Greece (460–377 B.C.). Until the 18th century, epilepsy was considered an idiopathic disease originating in the brain. The foundation of the modern knowledge of epilepsy was through the work of William Cullen and Samuel A. In the 20th century, rapid development in medical imaging occurred with development in brain CT, brain MRI, and PET scan.

Classification

In 2017, the International League Against Epilepsy (ILAE) classified seizure by its onsets as focal (aware/impaired awareness, motor, nonmotor, focal to tonic-clonic seizures), generalized (motor, nonmotor), and unknown (motor, nonmotor, and unclassified). In 1981, the International League Against Epilepsy (ILAE) classified epileptic seizures as partial seizures (simple partial seizures, complex partial seizures, and partial seizures evolving to secondarily generalized seizures), generalized seizures (absence seizures, myoclonic seizures, clonic seizures, tonic seizures, tonic-clonic seizures (grand mal), and atonic seizures), and unclassified epileptic seizures.

Pathophysiology

Normally, seizures do not occur because the membrane stability of neurons is maintained, and the discharges that lead to seizures are prevented from transferring. In a normal brain, some circumstances can provoke seizures, such as: hyponatremia, drug withdrawal, and hypoglycemia. Abnormalities in different parts of the nervous system may cause seizure, such as: brain regions, cells, ions, networks, and receptors. The imbalance of excessive excitation and reduced inhibition can cause seizures and is also responsible for prolonging it if the imbalance persists. Glutamate is the most common excitatory neurotransmitter and acts on the N-methyl-D-aspartate (NMDA) receptor. However, NMDA antagonist drugs have not been clinically successful. Gamma-aminobutyric acid (GABA) is the most common inhibition neurotransmitter. GABA inhibits excess excitation of the neurons by activating the GABAA receptor. Increasing the inhibition of GABA (even if the inhibition is not damaged) may be helpful in a seizure, since it may overwhelm the excess excitation of the seizure. Examples of GABA-enhancing drugs are benzodiazepines, barbiturates, propofol, and some anesthetics. However, these drugs are not suitable for long term therapy since patients usually become tolerant to their effect.

Causes

Some of the causes of seizure include, brain injury, brain hemorrhage, encephalitis, high fever, chronic alcohol use, chronic sleep deprivation, medications, metabolic abnormalities, withdrawal from alcohol or drugs.

Differentiating Seizure from Other Diseases

Differential diagnosis of epileptic seizures may include, concussion, drug intoxication or withdrawal, migraine, psychogenic non-epileptic events, panic attacks, sleep disorders, syncope, transient global amnesia, transient ischemic attack (TIA).

Epidemiology and Demographics

It is estimated that 11% of the population experience a seizure in their life compared to the estimation of 3% for epilepsy. In the US, seizure is estimated to account for 1 million or 1% of emergency department (ED) visits annually. The incidence of acute symptomatic seizures is estimated to be 39 cases per 100,000 individuals in the US. Seizures are more common among males and people of African descent.

Risk Factors

Risk factors that can precipitate or provoke seizure include, excessive sleep deprivation, alcohol use, illicit drug use, some medications that reduce the seizure threshold, toxins, homeostasis abnormality due to organ failure, metabolic abnormalities, and medical and surgical histories that may be important in assessing the patient’s risk for future seizures.

Screening

The EEG monitoring has been recommended in neonates with known or suspected acute brain injury combined with encephalopathy, diseases associated with abnormal paroxysmal events, and in high-risk population.

Natural History, Complications, and Prognosis

The recurrence rate of seizure within two years is 35% to 40% in patients with a first-time unprovoked seizure. Status epilepticus occurs in about 6%-7% of the patients with seizure in the emergency department (ED). The overall mortality rate of status epilepticus is approximately 22% (3% in pediatric patients to 26% in adults). Simple febrile seizures are considered normal in childhood and the prognosis is generally excellent. The recurrence rate is about 12% in children that have their first febrile seizure in infancy and about 50% in those who have their first febrile seizure later.

Diagnosis

Diagnostic Study of Choice

The basis of seizure investigation and diagnosis depends upon, a detailed history of any event before and after a seizure episode, investigation of co-existing conditions, a focused physical examination, laboratory evaluation, and brain imaging.

History and Symptoms

The main part of the seizure history should be about the patient’s awareness, experience, and remembrance of the seizure. Symptoms of seizure include, aura, staring spells, myoclonic jerks, impaired awareness, paresthesias, lost of consciousness, Déjà vu experiences and confusion.

Physical Examination

The physical examination of patients with seizure may reveal: lateral tongue bites, nuchal rigidity or asterixis, bruises or scrapes on the body after falls, signs of a neurocutaneous syndrome associated with epilepsy on the skin, back pain, transient or persistent focal weakness or asymmetry, and urinary incontinence.

Laboratory Findings

The laboratory tests for patients with seizure may include, hypoglycemia, hyponatremia, uremia, drug intoxication, ammonia levels, creatine kinase (CK) levels, lactate levels, prolactin levels. Elevated prolactin level may be helpful in differentiating generalized tonic-clonic or complex partial seizure from psychogenic non-epileptic seizures, only if the patient’s prolactin level is measured 10 to 20 minutes after a suspected seizure event. Analysis of the serum prolactin level is not effective in distinguishing a seizure from syncope. No conclusion could be established regarding serum prolactin changes following status epilepticus, repetitive seizures, and neonatal seizures.

Electrocardiogram

An ECG in patients presenting with seizure is very crucial to prevent sudden unexpected death in epilepsy (SUDEP). Important signs to look for are, ST depression, T wave inversion, heart block, prolonged QT interval, Brugada Syndrome.

X-ray

There are no x-ray findings associated with a seizure. CT scan and MRI are superior to x-ray for imaging findings associated with seizures.

Echocardiography and Ultrasound

There are no echocardiography/ultrasound findings associated with seizures. However, an echocardiogram may be helpful in preventing sudden unexpected death in epilepsy (SUDEP) by looking for any functional or structural abnormality of the heart.

CT

Computed tomography scan (CT scan) in the emergency department is helpful in ruling out hemorrhage or other lesions.

MRI

MRI scan (preferably 3 teslas) should be performed in order to detect epileptogenic lesions. MRI is more sensitive in detecting some findings related to seizures such as hippocampal sclerosis and cortical dysplasia.

Other Imaging Findings

3-T MRI may be helpful in patients with epilepsy and negative 1.5-T MRI.

Other Diagnostic Studies

EEG with sleep deprivation is helpful when standard EEG does not detect any epileptiform changes. Lumbar puncture (LP) should be considered in those patients suspected of meningitis, encephalitis, subarachnoid hemorrhage.

Treatment

Medical Therapy

In the acute setting, seizures are initially treated with benzodiazepines (lorazepam or midazolam), followed by phenytoin or phenobarbitalAntiepileptic drugs (AEDs) are commonly used in treating focal and generalized epilepsies.

Surgery

Surgery may be helpful in patients with focal epilepsy if there is no seizure control after two or more antiepileptic drugs (AEDs). Laser interstitial thermal ablation and neurostimulation may be helpful as alternative therapies to surgery in some patients.

Primary Prevention

Some of the preventable etiologies for epilepsy that should be considered in primary prevention include central nervous system (CNS) infection, CNS parasitosis, prenatal and perinatal brain insults, stroke, and traumatic brain injury (TBI). Factors that can precipitate or provoke seizure may include chronic sleep deprivation, alcohol use, illicit drug use, some medications that reduce the seizure threshold, toxins, homeostasis abnormalities due to organ failure, metabolic abnormalities, and medical and surgical histories that may be important in assessing the patient’s risk for future seizures.

Secondary Prevention

Patients that have had a first seizure should be counseled for their seizure episode and the possible etiology, lifestyle modifications (safety measures and avoidance of the factors that can lower the seizure threshold and predispose to recurrences, such as sleep deprivation, use of alcohol, and illicit drugs), driving, antiepileptic drugs (AED) and their side effects, and follow-up. Patients, family members, friends, and co-workers should be counseled for seizure first aid during a seizure event such as removal of harmful objects, repositioning the patient in order to support breathing, timing the seizure, calling for help, not restraining or holding the patient down, and not putting anything in the patient's mouth.

Cost-Effectiveness of Therapy

The national economical impact of epilepsy is estimated at $9.6 billion per year in the United States.

Future or Investigational Therapies

Further studies are required for producing new drugs with novel mechanisms of action and finding new treatments by increasing the knowledge of the mechanisms of dietary therapy in epilepsy and the role that neurosteroid hormones have in exacerbating epilepsy.

References


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