Literature DB >> 8980840

Febrile seizures--treatment and outcome.

F U Knudsen1.   

Abstract

Assessment of treatment strategies in febrile seizures should be based on short- and long-term outcomes, with and without acute, intermittent, or chronic medical intervention, as well as short- and long-term side effects. Febrile seizures are a benign condition with a normal neurological, motor, intellectual, and cognitive long-term outcome and have a low risk of later epilepsy in most cases. Even many complex febrile seizures have a benign outcome. Prophylaxis may or may not reduce the recurrence rate, but does not appear to improve the long-term outcome as compared to acute treatment of seizures in progress. All agree that chronic prophylaxis with anti-epileptic agents is justified only in highly selected cases, if at all. Treatment with benzodiazepines during febrile episodes appears to effectively reduce the recurrence rate, provided adequate doses are given and compliance problems minimized. A selective approach to intermittent diazepam prophylaxis seems rational, as the recurrence risk and response to treatment are highly variable. An attractive alternative is acute treatment at seizure onset with rectal diazepam in solution given by the parents at home in order to prevent prolonged recurrent seizures. This regimen has the potential of moving the first line of anti-convulsant defence close to the child. It appears to be effective, inexpensive, feasible even for non-professionals, has few side effects and is well accepted by the parents. A reasonable policy would be to treat simple febrile seizures solely with acute rectal diazepam in solution and reserve intermittent diazepam prophylaxis for selected cases including those with multiple or prolonged recurrences, several risk factors for recurrent febrile seizures and other special situations.

Entities:  

Mesh:

Year:  1996        PMID: 8980840     DOI: 10.1016/s0387-7604(96)00059-9

Source DB:  PubMed          Journal:  Brain Dev        ISSN: 0387-7604            Impact factor:   1.961


  9 in total

1.  Hyperthermia-induced seizures modify the GABAA and benzodiazepine receptor binding in immature rat brain.

Authors:  M González-Ramírez; S Orozco; H Salgado; A Feria; L Rocha
Journal:  Cell Mol Neurobiol       Date:  2005-09       Impact factor: 5.046

2.  Seizure-induced neuronal injury: vulnerability to febrile seizures in an immature rat model.

Authors:  Z Toth; X X Yan; S Haftoglou; C E Ribak; T Z Baram
Journal:  J Neurosci       Date:  1998-06-01       Impact factor: 6.167

Review 3.  Febrile seizures.

Authors:  Leena D Mewasingh
Journal:  BMJ Clin Evid       Date:  2014-01-31

Review 4.  Febrile seizures.

Authors:  Leena D Mewasingh
Journal:  BMJ Clin Evid       Date:  2010-11-24

Review 5.  Febrile seizures and mechanisms of epileptogenesis: insights from an animal model.

Authors:  Roland A Bender; Celine Dubé; Tallie Z Baram
Journal:  Adv Exp Med Biol       Date:  2004       Impact factor: 2.622

Review 6.  Is neuronal death required for seizure-induced epileptogenesis in the immature brain?

Authors:  Tallie Z Baram; Mariam Eghbal-Ahmadi; Roland A Bender
Journal:  Prog Brain Res       Date:  2002       Impact factor: 2.453

Review 7.  Febrile seizures.

Authors:  Leena D Mewasingh
Journal:  BMJ Clin Evid       Date:  2008-05-22

8.  Hyperthermia-induced seizures modify the GABA(A) and benzodiazepine receptor binding in immature rat brain.

Authors:  M González Ramírez; S Orozco Suárez; H Salgado Ceballos; A Feria Velasco; L Rocha
Journal:  Cell Mol Neurobiol       Date:  2006-06-27       Impact factor: 4.231

Review 9.  Febrile seizures.

Authors:  Sajun Chung
Journal:  Korean J Pediatr       Date:  2014-09-30
  9 in total

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