eMedicine Specialties > Neurology > Seizures and Epilepsy
Posttraumatic Epilepsy: Follow-up
Updated: Oct 22, 2009
Follow-up
Further Outpatient Care
Regular follow-up should be performed for a review of medications; for neuropsychological assessment; and for monitoring of adverse effects, drug levels if indicated, and the patient's neurologic status.
Inpatient & Outpatient Medications
- Prophylaxis
- Findings of the latest Cochrane Review are that prophylactic treatment in the acute phase does not reduce death or disability rates.
- Treatment of early PTS does not decrease the risk of late PTS.
- Treatment
- Early PTS: The recommendation is that early PTS should be treated promptly, as seizure activity is likely to further damage the already-compromised brain. IV phenytoin and sodium valproate are the drugs of choice and usually effective in stopping the seizure.
- Late PTS: Treatment is not mandatory, as some patients with a low frequency of seizures may choose not to take regular medication. Compliance with long-term treatment is often poor in this group of patients. The anticonvulsant usually prescribed is sodium valproate, phenytoin, or carbamazepine. Among the newer anticonvulsants, levetiracetam has been used successfully after craniotomy.
Deterrence/Prevention
- A large percentage of PTEs should be viewed as preventable. Encourage preventive strategies, such as use of child seats and the use of helmets when cycling.
- Current evidence suggests that the treatment of early PTS does not influence the incidence of PTE. Routine preventive anticonvulsants are not indicated for patients with head injuries.
- Some have proposed the existence of a therapeutic window of opportunity of about 1 hour after traumatic brain injury. During this period, an agent (eg, sodium valproate), if delivered, may prevent or abort the epileptogenic process. Studies to explore such treatment are underway.
Complications
- Posttraumatic status epilepticus, which is more common in children than adults, is a complication of PTE.
- Psychological problems related to social isolation and the stigma of epilepsy are common and must be addressed.
Prognosis
- The risk of PTS decreases with time and reaches the normal value for the population at 5 years after the head injury.
- About half the patients who develop late PTS have 3 or fewer seizures and go into spontaneous remission thereafter.
Patient Education
- As in any seizure disorder, patients must be warned to exercise caution during bathing, swimming, and climbing heights. They should never be alone during these activities. In all situations, appropriate steps should be taken to ensure the safety of the person if a seizure occurs.
- Patients must also be counseled about the limitations in obtaining a driver's license.
- For excellent patient education resources, visit eMedicine's Brain and Nervous System Center. Also, see eMedicine's patient education article Epilepsy.
Miscellaneous
Medicolegal Pitfalls
- The medical/legal aspect is an important issue in cases of PTE, as some patients pursue legal actions against various authorities and individuals responsible for the circumstances of the accident.
- Clinicians are often asked to estimate the risk of a patient developing PTE in the future as a result of sustained brain injury. This is a difficult task and should be left to an experienced senior specialist.
Special Concerns
- Many patients are not able to obtain a driving license.
More on Posttraumatic Epilepsy |
| Overview: Posttraumatic Epilepsy |
| Differential Diagnoses & Workup: Posttraumatic Epilepsy |
| Treatment & Medication: Posttraumatic Epilepsy |
Follow-up: Posttraumatic Epilepsy |
| References |
| « Previous Page |
References
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Skandsen T, Ivar Lund T, Fredriksli O, Vik A. Global outcome, productivity and epilepsy 3--8 years after severe head injury. The impact of injury severity. Clin Rehabil. Jul 2008;22(7):653-62. [Medline].
Hudak AM, Trivedi K, Harper CR, Booker K, Caesar RR, Agostini M, et al. Evaluation of seizure-like episodes in survivors of moderate and severe traumatic brain injury. J Head Trauma Rehabil. Jul-Aug 2004;19(4):290-5. [Medline].
Temkin NR, Dikmen SS, Wilensky AJ. A randomized, double-blind study of phenytoin for the prevention of post-traumatic seizures. N Engl J Med. Aug 23 1990;323(8):497-502. [Medline].
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Chang BS, Lowenstein DH. Practice parameter: antiepileptic drug prophylaxis in severe traumatic brain injury: report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. Jan 14 2003;60(1):10-6. [Medline].
Chang BS, Lowenstein DH. Practice parameter: antiepileptic drug prophylaxis in severe traumatic brain injury: report of the Quality Standards Subcommittee of the American Academy of Neurology. Neurology. Jan 14 2003;60(1):10-6. [Medline].
D'Ambrosio R, Perucca E. Epilepsy after head injury. Curr Opin Neurol. Dec 2004;17(6):731-5. [Medline].
Frey LC. Epidemiology of posttraumatic epilepsy: a critical review. Epilepsia. 2003;44 Suppl 10:11-7. [Medline].
Garga N, Lowenstein DH. Posttraumatic epilepsy: a major problem in desperate need of major advances. Epilepsy Curr. Jan-Feb 2006;6(1):1-5. [Medline].
Schierhout G, Roberts I. Anti-epileptic drugs for preventing seizures following acute traumatic brain injury. Cochrane Database Syst Rev. 2001;CD000173. [Medline].
Temkin NR. Prophylactic Anticonvulsants After Neurosurgery. Epilepsy Curr. Jul 2002;2(4):105-107. [Medline].
Temkin NR, Dikmen SS, Anderson GD, et al. Valproate therapy for prevention of posttraumatic seizures: a randomized trial. J Neurosurg. Oct 1999;91(4):593-600. [Medline].
Further Reading
Keywords
PTE, head injury, head trauma, posttraumatic seizure, PTS, traumatic brain injury, TBI
Follow-up: Posttraumatic Epilepsy