Evaluation of a First Seizure



FREE PREVIEW Log in or buy this issue to read the full article. AAFP members and paid subscribers get free access to all articles. Subscribe now.


FREE PREVIEW Subscribe or buy this issue. AAFP members and paid subscribers get free access to all articles.

Am Fam Physician. 2007 May 1;75(9):1342-1347.

  Patient information: See related handout on seizures, written by the authors of this article.

Seizure is a common presentation in the emergency care setting, and new-onset epilepsy is the most common cause of unprovoked seizures. The patient history and physical examination should direct the type and timing of laboratory and imaging studies. No single sign, symptom, or test clearly differentiates a seizure from a nonseizure event (e.g., syncope, pseudoseizure). Electroencephalography is recommended for patients presenting with a first seizure, and neuroimaging is recommended for adults. Neuroimaging also should be performed in children with risk factors such as head trauma, focal neurologic deficits, or a history of malignancy. Magnetic resonance imaging is preferred over computed tomography except when acute intracranial bleeding is suspected. The most common laboratory findings associated with a seizure are abnormal sodium and glucose levels. Patients with a normal neurologic examination, normal test results, and no structural brain disease do not require hospitalization or antiepileptic medications. Treatment with antiepileptic medications reduces the one- to two-year risk of recurrent seizures but does not reduce the long-term risk of recurrence and does not affect remission rates. Regardless of etiology, a seizure diagnosis severely limits a patient's driving privileges, although laws vary by state.

About 2 to 5 percent of Americans experience an afebrile seizure, and seizures account for approximately 1 to 2 percent of all emergency department visits.1 The self-reported prevalence of epilepsy is 1.1 to 2.2 percent in the United States.2 Most patients (57 percent) who present with a first seizure are younger than 25 years, and 71 percent of this subset is 15 years or younger; 58 percent of patients with a first seizure are men.3

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendation Evidence rating References

Neuroimaging is recommended for adults presenting with a first unprovoked seizure and for children with risk factors.

C

1,7,17,20

Immediate neuroimaging is recommended for patients who have an increased risk of acute intracranial pathology.

C

1,7

Routine laboratory tests in adults should include glucose and sodium measurements and a pregnancy test if applicable; immunocompromised patients should receive a lumbar puncture.

C

1

Electroencephalography is recommended for patients presenting with a first seizure.

C

1,7,21

Magnetic resonance imaging is preferred over computed tomography unless acute intracranial bleeding is suspected.

C

7,16

Patients with a normal neurologic examination and no known structural brain disease or comorbidities do not require hospitalization or antiepileptic medication.

C

1,7


A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, see page 1289 or http://www.aafp.org/afpsort.xml.

SORT: KEY RECOMMENDATIONS FOR PRACTICE

View Table

SORT: KEY RECOMMENDATIONS FOR PRACTICE

Clinical recommendation Evidence rating References

Neuroimaging is recommended for adults presenting with a first unprovoked seizure and for children with risk factors.

C

1,7,17,20

Immediate neuroimaging is recommended for patients who have an increased risk of acute intracranial pathology.

C

1,7

Routine laboratory tests in adults should include glucose and sodium measurements and a pregnancy test if applicable; immunocompromised patients should receive a lumbar puncture.

C

1

Electroencephalography is recommended for patients presenting with a first seizure.

C

1,7,21

Magnetic resonance imaging is preferred over computed tomography unless acute intracranial bleeding is suspected.

C

7,16

Patients with a normal neurologic examination and no known structural brain disease or comorbidities do not require hospitalization or antiepileptic medication.

C

1,7


A = consistent, good-quality patient-oriented evidence; B = inconsistent or limited-quality patient-oriented evidence; C = consensus, disease-oriented evidence, usual practice, expert opinion, or case series. For information about the SORT evidence rating system, see page 1289 or http://www.aafp.org/afpsort.xml.

Seizure Types

Seizures are categorized based on presentation and etiology. A generalized seizure involves all areas of the brain (both hemispheres), whereas a partial (focal) seizure involves only one area of the brain. A first seizure is twice as likely to be a generalized seizure as a partial seizure. Most generalized seizures occur when the patient is awake, but one in four occurs during sleep.3 Partial seizures can be further classified as simple (i.e., no loss of consciousness) or complex (i.e., loss of consciousness).

Symptomatic seizures are those that have a recognizable cause (e.g., head injury, brain tumor), and idiopathic seizures are those for which no abnormality is found. Acute symptomatic seizures are caused by a recent or current event, whereas remote symptomatic seizures are caused by a chronic abnormality such as an old stroke. A provoked seizure is caused by an identifiable transient disturbance such as an electrolyte abnormality (e.g., hypocalcemia). In the year following an acute symptomatic seizure diagnosis, patients have a higher risk of death than those without this diagnosis. Idiopathic seizures are not associated with increased risk of death.4

Etiology

There are multiple causes of seizure (Table 15), but new-onset epilepsy is the most common cause of a first seizure.3 One in six patients who present with a single seizure will have an identifiable potential cause such as pre- or perinatal brain injury (4.4 percent), cerebrovascular disease (3.9 percent), head injury (3.2 percent), brain tumor (1.7 percent), or alcohol use (0.3 percent).3

Table 1

Selected Causes of Seizure

Alcohol use and withdrawal

Brain injury or abnormality

Brain tumor

Cerebral dysgenesis

Cerebrovascular, degenerative, inflammatory/autoimmune diseases

Genetic disorders

Head trauma

Peri- or prenatal brain injury

Central nervous system infections

Cysticercosis

Encephalitis

Meningitis

Contrast agents

Epilepsy

Fever (children)

Illicit drug use and withdrawal

Medications

Analgesics (e.g., local anesthetics, meperidine [Demerol], tramadol [Ultram])

Antibiotics (e.g., beta-lactam antibiotics, isoniazid [INH; Nydrazid], quinolones, some human immunodeficiency virus medications)

Immunomodulators (e.g., cyclosporine [Sandimmune], interferons, tacrolimus [Prograf])

Psychotropics (e.g., antidepressants, antipsychotics, lithium, stimulants)

Theophylline

Metabolic disorders

Electrolyte abnormalities

Inborn errors of metabolism

Liver or kidney failure

Pyridoxine deficiency


Information from reference 5.

Table 1   Selected Causes of Seizure

View Table

Table 1

Selected Causes of Seizure

Alcohol use and withdrawal

Brain injury or abnormality

Brain tumor

Cerebral dysgenesis

Cerebrovascular, degenerative, inflammatory/autoimmune diseases

Genetic disorders

Head trauma

Peri- or prenatal brain injury

Central nervous system infections

Cysticercosis

Encephalitis

Meningitis

Contrast agents

Epilepsy

Fever (children)

Illicit drug use and withdrawal

Medications

Analgesics (e.g., local anesthetics, meperidine [Demerol], tramadol [Ultram])

Antibiotics (e.g., beta-lactam antibiotics, isoniazid [INH; Nydrazid], quinolones, some human immunodeficiency virus medications)

Immunomodulators (e.g., cyclosporine [Sandimmune], interferons, tacrolimus [Prograf])

Psychotropics (e.g., antidepressants, antipsychotics, lithium, stimulants)

Theophylline

Metabolic disorders

Electrolyte abnormalities

Inborn errors of metabolism

Liver or kidney failure

Pyridoxine deficiency


Information from reference 5.

Evaluation

When evaluating a patient who has just experienced a seizure, the physician should first verify that the patient has normal vital signs and adequate oxygenation and that there is no further seizure activity. There is no standardized algorithm for the evaluation of every patient with a first seizure. Instead, a careful history and physical examination should determine imaging and laboratory testing decisions.6

The history should initially focus on determining whether a seizure actually occurred and evaluating the circumstances and characteristics of the event. The behaviors of the patient during the event and evidence of partial onset may be important in identifying a specific form of epilepsy. A history of trauma or symptoms of infection (e.g., stiff neck, fever, headache) also helps direct the evaluation. The patient should be asked about medication, illicit drug, and alcohol use. A history of neurologic or developmental disorders or a family history of epilepsy may help narrow the differential diagnosis. The physical examination should include a thorough neurologic and mental status evaluation.

Differential Diagnosis

No sign, symptom, or test clearly differentiates a seizure from a nonseizure event (e.g., syncope, pseudoseizure).7 Up to 20 percent of patients diagnosed with epilepsy actually have pseudoseizures. Eye closure throughout the event is rare in true seizures but common in pseudoseizures, and a history of fibromyalgia or chronic pain syndrome is predictive of pseudoseizures.8

In older children and adults, a serum prolactin measurement, if obtained within 10 to 20 minutes of the event, is useful in differentiating a generalized tonic-clonic seizure or complex partial seizure from a pseudoseizure. The sensitivity of an elevated prolactin level is 60 percent for generalized tonic-clonic seizures and 46 percent for complex partial seizures.9

Syncope may be difficult to differentiate from seizures, particularly if the event was unwitnessed. Up to 90 percent of patients with syncope have myoclonic or other seizure-like movements while unconscious.10 Historic features suggestive of seizure include tongue biting, presence of an aura, sensation of epigastric fullness, postictal confusion, and focal neurologic signs. Tongue biting, especially lateral, is highly specific but not sensitive for generalized seizures.11 Events precipitated by an emotionally stressful event or preceded by light-headedness, sweating, prolonged standing, chest pain, palpitations, or slow heart rate are more likely to be syncopal.12

Diagnostic Testing

Adults who present to the emergency department after an unprovoked first seizure should receive immediate neuroimaging of the brain if feasible, although testing at a later date may be acceptable in certain patients if follow-up is reliable.1  Patients at an increased risk of acute intracranial pathology (Table 213) need immediate neuroimaging.1,7 Current practice guidelines allow a well-appearing child without risk factors to be discharged from the emergency department without emergent neuroimaging.7

Table 2

Risk Factors for Acute Intracranial Pathology in Adults with a First Unprovoked Seizure

Acquired immunodeficiency syndrome

Acute head trauma

Age older than 40 years

Fever

History of anticoagulation

History of malignancy

New focal neurologic deficit

Partial (focal) seizure

Persistent altered mental status

Persistent headache


note: Immediate neuroimaging is important if there is an increased risk of acute intracranial pathology.

Information from reference 13.

Table 2   Risk Factors for Acute Intracranial Pathology in Adults with a First Unprovoked Seizure

View Table

Table 2

Risk Factors for Acute Intracranial Pathology in Adults with a First Unprovoked Seizure

Acquired immunodeficiency syndrome

Acute head trauma

Age older than 40 years

Fever

History of anticoagulation

History of malignancy

New focal neurologic deficit

Partial (focal) seizure

Persistent altered mental status

Persistent headache


note: Immediate neuroimaging is important if there is an increased risk of acute intracranial pathology.

Information from reference 13.

A lumbar puncture is indicated for patients with a history or examination results suggestive of central nervous system infection and in patients who are immunocompromised. New-onset seizures may be the only symptom of central nervous system infection in patients with human immunodeficiency virus.14 Lumbar puncture is not routinely recommended in afebrile children but should be considered in children younger than six months and in those who have persistently altered mental status or meningeal signs.7

Glucose abnormalities and hyponatremia are the most common laboratory findings associated with seizures.1 Practice guidelines recommend testing children based on individual clinical circumstances and routinely measuring serum glucose and sodium levels in adults. Pregnancy testing should be performed in premenopausal women, and toxicology testing should be performed when substance abuse is suspected.1,7 Infants with new-onset seizures should be tested for electrolyte abnormalities.

Electroencephalography (EEG) is recommended for all patients with new-onset seizures.1,7 Emergent EEG testing is indicated if there is concern about status epilepticus. Nonconvulsive or subtle convulsive status epilepticus may be difficult to diagnose clinically and may be mistaken for a prolonged postictal state. One fourth of patients with treated status epilepticus who appear to be seizure-free continue to have seizure activity that is only detectable with EEG. Patients who have had a seizure and are in a drug-induced coma or who have received a long-acting paralytic agent also should receive immediate EEG testing.1

Most other patients with a first seizure can receive EEG testing at a scheduled follow-up visit. Although EEG within 24 to 48 hours of a seizure is more likely to show an abnormality, some early abnormalities, such as postictal slowing, may not be significant.7

Neuroimaging

The recommendations for imaging after a first seizure depend on patient age, seizure type, and associated risk factors.

CHILDREN

There is insufficient evidence to recommend for or against routine neuroimaging in children who present only with a single unprovoked seizure, although unnecessary radiation exposure should be avoided. The estimated lifetime risk of death from radiation-induced malignancy caused by a single computed tomography (CT) scan of the head at one year of age is 0.07 percent.15

Neuroimaging should be performed in children with a postictal focal neurologic deficit that does not resolve or in children who do not return to baseline neurologic function within several hours. Neuroimaging also should be performed in children with head trauma or a history of malignancy. Nonurgent magnetic resonance imaging (MRI) should be seriously considered in children younger than one year and in children with any of the following characteristics: significant cognitive or motor impairment of unknown etiology, unexplained abnormalities on neurologic examination, partial onset of seizure with or without secondary generalization, or no evidence of benign partial epilepsy of childhood or primary generalized epilepsy on EEG.7 Seizures only provoked by the presence of fever (febrile seizures) do not require neuroimaging.16

ADULTS

Neuroimaging scans reveal abnormalities in 3 to 38 percent of patients with a first seizure, depending on patient demographics. A joint consensus statement from the American College of Emergency Physicians (ACEP), the American Academy of Neurology (AAN), and others states that immediate neuroimaging is indicated when a serious structural brain lesion is suspected and also should be considered for patients with partial-onset seizures and for those who are older than 40 years. Neuroimaging at a later date is acceptable for patients who have completely recovered from their seizures and when there is no clear etiology, although immediate imaging should be performed if follow-up cannot be guaranteed.17

MRI is the preferred imaging method because it has greater sensitivity for detecting abnormalities than CT.7,16 However, patients with acute seizures initially should undergo CT because it more accurately detects acute bleeding and is reasonably sensitive in detecting other abnormalities.7,16

Intracranial disease is commonly detected on neuroimaging scans even if a nonbrain etiology for the seizure is apparent. A study of unselected patients presenting to an urban emergency department after a first seizure related to alcohol withdrawal showed brain abnormalities that required intervention or change in therapy in 10 out of 259 patients (3.9 percent). History of trauma and neurologic examination findings did not predict these abnormalities.13

Treatment

When predicting future risk, all seizures occurring within 24 hours are considered a single seizure. Approximately one half of patients who have a first unprovoked seizure and three out of four who have multiple seizures will have another seizure within the next eight years.18 Risk factors for seizure recurrence in children presenting with a first unprovoked seizure include abnormal EEG test results; a history of febrile seizures; remote, symptomatic etiology; seizure that occurs during sleep; and Todd's paralysis.18

The decision to initiate treatment after a single unprovoked seizure is controversial. A randomized controlled trial showed that antiepileptic medications initiated at the occurrence of a first seizure reduced the incidence of additional seizures over the next one to two years but did not reduce the long-term recurrence risk or affect remission rates.19

An AAN practice guideline states that treatment with antiepileptic medications is not indicated in children for the purpose of preventing epilepsy, but treatment may be considered if the benefits of reducing the risk of a second seizure outweigh the risks of pharmacologic and psychosocial adverse effects.20 There is no guideline for adults.

ACEP policy states that patients evaluated in the emergency department for a seizure who have a normal neurologic examination, no known comorbidities, and no known structural brain abnormalities may be referred for outpatient follow-up without initiating an antiepileptic medication.1 Consultation with a subspecialist is indicated if uncertainty remains after evaluation.21 If an antiepileptic medication is initiated, acceptable choices include carbamazepine (Tegretol), phenytoin (Dilantin), valproic acid/divalproex (Depakene), phenobarbital, gabapentin (Neurontin), lamotrigine (Lamictal), oxcarbazepine (Trileptal), and topiramate (Topamax).22

Driving Limitations

Most states require a three-to 18-month seizure-free period before a patient may resume driving a private vehicle, although most states have an appeals process for driving restrictions.23 Some states require physicians to report patients who are diagnosed with epilepsy.23 State driving laws for patients with epilepsy are available at http://www.epilepsyfoundation.org; click the driving link under Quick Links.

Usually, patients with a history or current diagnosis of epilepsy may not hold a commercial driver's license. If a seizure is caused by a medical condition (e.g., drug reaction, high fever, acute infectious disease, dehydration, acute metabolic disturbance), the patient may be allowed to hold a commercial driver's license after full recovery from the condition.24 Drivers with a history of epilepsy or seizures who have not needed antiseizure medication and have been seizure-free for 10 years may reapply to operate a commercial vehicle in interstate commerce.24 Drivers with a history of a single unprovoked seizure may be qualified to drive a commercial vehicle if they have not needed antiseizure medication and have been seizure-free for at least five years.24

The Authors

STEPHEN M. ADAMS, MD, is an associate professor in the Department of Family Medicine at the University of Tennessee College of Medicine, Chattanooga Unit. Dr. Adams received his medical degree from the University of Tennessee College of Medicine, Memphis, and completed a family medicine residency at the University of Alabama, Huntsville.

PAUL D. KNOWLES, MD, is an assistant professor in the Department of Pediatrics at the University of Tennessee College of Medicine, Chattanooga Unit, and is director of pediatric neurology at T.C. Thompson Children's Hospital, Chattanooga. Dr. Knowles received his medical degree from Eastern Virginia Medical School, Norfolk, and completed a residency at Children's Hospital, Akron, Ohio.

Address correspondence to Stephen M. Adams, MD, University of Tennessee Health Science Center, 1100 E. Third St., Chattanooga, TN 37403 (e-mail: stephen. adams@erlanger.org). Reprints are not available from the authors.

Author disclosure: Dr. Knowles has served on the speakers' bureaus for Novartis (Trileptal), UCB Pharma (Keppra), and Abbott (Depakote). He has been approached by Valeant (Diastat) but has not yet signed an agreement with them.

REFERENCES

1. American College of Emergency Physicians Clinical Policies Committee, Clinical Policies Subcommittee on Seizures. Clinical policy: critical issues in the evaluation and management of adult patients presenting to the emergency department with seizures. Ann Emerg Med. 2004;43:605–25.

2. Centers for Disease Control and Prevention. Prevalence of epilepsy and health-related quality of life and disability among adults with epilepsy—South Carolina, 2003 and 2004. MMWR Morb Mortal Wkly Rep. 2005;54:1080–2.

3. Jallon P, Loiseau P, Loiseau J. Newly diagnosed unprovoked epileptic seizures: presentation at diagnosis in CAROLE study. Coordination Active du Reseau Observatoire Longitudinal de l'Epilepsie. Epilepsia. 2001;42:464–75.

4. Beghi E, Leone M, Solari A. Mortality in patients with a first unprovoked seizure. Epilepsia. 2005;46(suppl 11):40–2.

5. Lowenstein DH. Diseases of the central nervous system. In: Braunwald E, Fauci AS, Kasper DL, Hauser SL, Longo DL, Jameson JL, eds. Harrison's Principles of Internal Medicine. 15th ed. New York, N.Y.: McGraw-Hill, 2001:2354–69.

6. Freeman JM. Less testing is needed in the emergency room after a first afebrile seizure. Pediatrics. 2003;111:194–6.

7. Hirtz D, Ashwal S, Berg A, Bettis D, Camfield C, Camfield P, et al. Practice parameter: evaluating a first nonfebrile seizure in children: report of the quality standards subcommittee of the American Academy of Neurology, the Child Neurology Society, and the American Epilepsy Society. Neurology. 2000;55:616–23.

8. LaFrance WC Jr, Benbadis SR. Avoiding the costs of unrecognized psychological nonepileptic seizures. Neurology. 2006;66:1620–1.

9. Chen DK, So YT, Fisher RS. Use of serum prolactin in diagnosing epileptic seizures: report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. 2005;65:668–75.

10. Lempert T, Bauer M, Schmidt D. Syncope: a videometric analysis of 56 episodes of transient cerebral hypoxia. Ann Neurol. 1994;36:233–7.

11. Benbadis SR, Wolgamuth BR, Goren H, Brener S, Fouad-Tarazi F. Value of tongue biting in the diagnosis of seizures. Arch Intern Med. 1995;155:2346–9.

12. McKeon A, Vaughan C, Delanty N. Seizure versus syncope [Published correction appears in Lancet Neurol 2006;5:293]. Lancet Neurol. 2006;5:171–80.

13. Earnest MP, Feldman H, Marx JA, Harris JA, Biletch M, Sullivan LP. Intracranial lesions shown by CT scans in 259 cases of first alcohol-related seizures. Neurology. 1988;38:1561–5.

14. Pesola GR, Westfal RE. New-onset generalized seizures in patients with AIDS presenting to an emergency department. Acad Emerg Med. 1998;5:905–11.

15. Brenner D, Elliston C, Hall E, Berdon W. Estimated risks of radiation-induced fatal cancer from pediatric CT. AJR Am J Roentgenol. 2001;176:289–96.

16. Bernal B, Altman NR. Evidence-based medicine: neuroimaging of seizures. Neuroimaging Clin N Am. 2003;13:211–24.

17. American College of Emergency Physicians, American Academy of Neurology, American Association of Neurological Surgeons, American Society of Neuro-radiology. Practice parameter: neuroimaging in the emergency patient presenting with seizure (summary statement). Ann Emerg Med. 1996;28:114–8.

18. Shinnar S, Berg AT, Moshe SL, O'Dell C, Alemany M, Newstein D, et al. The risk of seizure recurrence after a first unprovoked afebrile seizure in childhood: an extended follow-up. Pediatrics. 1996;98(2 pt 1):216–25.

19. Marson A, Jacoby A, Johnson A, Kim L, Gamble C, Chadwick D, for the Medical Research Council MESS Study Group. Immediate versus deferred antiepileptic drug treatment for early epilepsy and single seizures: a randomisedcontrolled trial. Lancet. 2005;365:2007–13.

20. Hirtz D, Berg A, Bettis D, Camfield C, Camfield P, Crumrine P, et al. Practice parameter: treatment of the child with a first unprovoked seizure: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology. 2003;60:166–75.

21. Ross SD. Management of newly diagnosed patients with epilepsy: a systematic review of the literature. Rockville, Md.: Agency for Healthcare Research and Quality, 2001. AHRQ Publication No. 01–E038.

22. French JA, Kanner AM, Bautista J, Abou-Khalil B, Browne T, Harden CL, et al. Efficacy and tolerability of the new antiepileptic drugs I: treatment of new onset epilepsy: report of the Therapeutics and Technology Assessment Subcommittee and Quality Standards Subcommittee of the American Academy of Neurology and the American Epilepsy Society. Neurology. 2004;62:1252–60.

23. Epilepsy Foundation. Driver information by state. Accessed January 19, 2007, at: http://www.epilepsyfoundation.org/advocacy/transportation/driverlicensing.cfm.

24. Federal Motor Carrier Safety Administration. Part 391: qualifications of drivers and longer combination vehicle (LCV) driver instructors. Subpart E—physical qualifications and examinations. Physical qualifications for drivers. Accessed January 19, 2007, at: http://www.fmcsa.dot.gov/rules-regulations/administration/fmcsr/fmcsrruletext.asp?section=391.41.



Copyright © 2007 by the American Academy of Family Physicians.
This content is owned by the AAFP. A person viewing it online may make one printout of the material and may use that printout only for his or her personal, non-commercial reference. This material may not otherwise be downloaded, copied, printed, stored, transmitted or reproduced in any medium, whether now known or later invented, except as authorized in writing by the AAFP. Contact afpserv@aafp.org for copyright questions and/or permission requests.

Want to use this article elsewhere? Get Permissions


Article Tools

  • Download PDF
  • Print page
  • Share this page
  • AFP CME Quiz

Information From Industry

More in AFP

More in Pubmed

Navigate this Article