Background <p>A febrile seizure (FS) is the most common type of seizure without underlying neurological disease in pediatrics. Due to their sudden onset and striking symptoms, FS cause uncertainty among parents and medical staff. This leads to high demand on the healthcare system and, not infrequently, to “overdiagnosis.”</p> Objective, material and methods <p>Practical instructions were elaborated based on review articles and guidelines on this topic.</p> Results and discussion <p>The recommendations on acute management in the current literature are consistent. Priority is given to interruption of the seizure and stabilization of the vital parameters. With respect to the decision for subsequent diagnostics, the differentiation between simple and complex FS as well as the recognition of red flags as indications are highlighted; however, there is no consistent definition of which diagnostic tool should be implemented at which point in time. There are predictive risk factors for the prognosis of further FS or the manifestation of an epilepsy over time. Long-term cognitive development disorders have not been reported for simple FS.</p>

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Fieberkrämpfe in der Pädiatrie

  • Katja Steinbrücker,
  • Johannes Koch

摘要

Background

A febrile seizure (FS) is the most common type of seizure without underlying neurological disease in pediatrics. Due to their sudden onset and striking symptoms, FS cause uncertainty among parents and medical staff. This leads to high demand on the healthcare system and, not infrequently, to “overdiagnosis.”

Objective, material and methods

Practical instructions were elaborated based on review articles and guidelines on this topic.

Results and discussion

The recommendations on acute management in the current literature are consistent. Priority is given to interruption of the seizure and stabilization of the vital parameters. With respect to the decision for subsequent diagnostics, the differentiation between simple and complex FS as well as the recognition of red flags as indications are highlighted; however, there is no consistent definition of which diagnostic tool should be implemented at which point in time. There are predictive risk factors for the prognosis of further FS or the manifestation of an epilepsy over time. Long-term cognitive development disorders have not been reported for simple FS.