eMedicine Specialties > Neurology > Pediatric Neurology
Epileptic and Epileptiform Encephalopathies: Follow-up
Updated: Jul 29, 2009
Follow-up
Further Inpatient Care
- The evaluation and management of epileptic and epileptiform encephalopathies usually are performed on an outpatient basis, although the initial long-term EEG and evaluation may be performed in the hospital.
- Patients with intractable seizures may need hospitalization at times for seizure control.
Complications
- The complications of epileptic and epileptiform encephalopathies usually are secondary to the treatment, especially with antiepileptic drugs (AEDs) or high-dose steroids. However, the psychiatric and psychological problems associated with a neurological handicap, especially a neurodegenerative process, can have a great impact on both the child and the family. In Landau-Kleffner syndrome (LKS), behavioral and emotional disturbances are the major problems encountered.
Prognosis
- The prognosis is related to the underlying disorder.
Patient Education
- Input from a neurologist, developmental pediatrician, psychologist, neuropsychologist, audiologist, or speech pathologist is needed to determine the proper educational program.
- For excellent patient education resources, visit eMedicine's Brain and Nervous System Center. Also, see eMedicine's patient education article Epilepsy.
Miscellaneous
Medicolegal Pitfalls
- In any neurological disorder, determining the etiology is important, since specific etiologies may require specific treatments. Excluding an underlying structural or metabolic disorder is especially important when regression in intellectual or motor milestones has occurred. A thorough evaluation, including appropriate laboratory studies, neuroimaging, and consultations, should be performed as indicated by the history and examination.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous authors Stavros M Hadjiloizou, MD, and James J Riviello Jr, MD, to the development and writing of this article.
More on Epileptic and Epileptiform Encephalopathies |
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| Differential Diagnoses & Workup: Epileptic and Epileptiform Encephalopathies |
| Treatment & Medication: Epileptic and Epileptiform Encephalopathies |
Follow-up: Epileptic and Epileptiform Encephalopathies |
| Multimedia: Epileptic and Epileptiform Encephalopathies |
| References |
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Further Reading
Keywords
epileptic encephalopathy, epileptic encephalopathies, epileptiform encephalopathy, epileptiform encephalopathies, catastrophic epilepsy, catastrophic epilepsies, epileptiform aphasia, malignant epilepsy, malignant epilepsies, early myoclonic encephalopathy, early infantile epileptic encephalopathy, Ohtahara syndrome, migrating partial epilepsy, migrating partial epilepsy in infancy, West syndrome, infantile spasms, severe myoclonic epilepsy in infancy, Dravet syndrome, myoclonic status, myoclonic status in non-progressive syndromes, myoclonic astatic epilepsy, Doose syndrome, Lennox-Gastaut syndrome, Landau-Kleffner syndrome, LKS, acquired epileptiform aphasia, verbal auditory agnosia, language regression, word deafness, continuous spikes and waves during slow wave sleep, electrical status epilepticus of sleep, autism, autistic spectrum disorders, pervasive development disorder, PDD, transient cognitive impairment, benign childhood epilepsy with centro-temporal spikes, BCECTS, benignrolandic epilepsy
Follow-up: Epileptic and Epileptiform Encephalopathies