Febrile seizures occur in 2-5% of the population and are typically limited to children between 3 months and 5 years-of-age. The pathophysiological link between increased body temperature and increased seizure susceptibility is unsolved in humans. In a mouse model it has been shown that young animals had a tendency to hyperventilate thereby causing intra-cerebral hypocapnia / alkalosis and a decrease of their seizure threshold. This effect was not observed in older animals. Redressing the pCO2 (carbon dioxide partial pressure) by breathing carbon dioxide enriched air instantly stopped the seizures. In this study the investigators want to investigate the respiratory physiology in children with febrile seizures and compare it to children who have fever but did not have febrile seizures. The investigators hypothesize that in children with febrile seizures the rising body temperature triggers a larger increase of respiratory rate (hyperventilation) and subsequent drop in pCO2 levels. This study could provide the basic physiological data for an interventional trial to test the efficacy of carbon dioxide inhalation to interrupt febrile seizures.
The aim of the study is the continuous non-invasive monitoring of * body temperature * respiratory rate * transcutaneous pCO2 * heart rate * pulsoxymetric SaO2 (arterial oxygen saturation) during a febrile illness * in children without febrile seizures and * in children who had suffered a febrile seizure during the actual febrile illness. Children will be recruited from the emergency units of the Charité University Hospital and a large Community Hospital, matched according to age, gender and the cause of their febrile illness and their data will enter final analysis if their body temperature rose at least once to or above 38.0 degree C and changed more than 1.0 degree C during the observational period.
Study Type
OBSERVATIONAL
Enrollment
100
Charité Universitätsmedizin Berlin
Berlin, Germany
Change of transcutaneous pCO2 per change of body temperature [mmHg/degree C]
The following parameters are continuously monitored in the sleeping child at night during febrile illness: body temperature, respiratory rate, transcutaneous pCO2, heart rate, pulsoxymetric SaO2
Time frame: First or second night of febrile illness
Change of respiratory rate per change of body temperature [1/sec * degree C]
The following parameters are continuously monitored in the sleeping child at night during febrile illness: body temperature, respiratory rate, transcutaneous pCO2, heart rate, pulsoxymetric SaO2
Time frame: First or second night of febrile illness
Change of transcutaneous pCO2 per change of respiratory rate [mmHg * sec]
The following parameters are continuously monitored in the sleeping child at night during febrile illness: body temperature, respiratory rate, transcutaneous pCO2, heart rate, pulsoxymetric SaO2
Time frame: First or second night of febrile illness
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