We hypothesize that without continuous EEG registration, subclinical electrographic seizures will be missed. Repetive ictal seizures and a sublcinical status epilepticus may be deleterious to the immature brain. On the other hand the use of…
ID
Bron
Verkorte titel
Aandoening
neonatal seizures in fullterm infants following perinatal asphyxia
Ondersteuning
Dutch Epilepsy Foundation
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1. What is the number of electrographic seizure discharges missed if you do not monitor continuously; <br>
2. Does instantaneous treatment of electrographical seizures lead to: <br>
a. A reduction of seizure discharges; <br>
b. Less damage on the neonatal MRI.
Achtergrond van het onderzoek
Neonatal seizures are commonly seen following perinatal asphixia. Since the introduction of the continuous bedside simplified EEG monitoring devices, it has become clear that subclinical seizures occur in about 50-60% of all neonatal seizures.
As yet it is not known whether treatment of these subclinical seizures is necessary and will improve longterm outcome.
Treatment of neonatal seizures is a challenge and the most commonly used anti-epileptic drugs are only effective in about 50% of the cases.
To resolve the problem whether treatment of subclinical seizures is required or unnecessary and maybe even deleterious to the developing brain, a randomised controlled trial (RCT) is performed.
In the randomised trial infants will be either treated with antiepileptic drugs when they have clinical as well as subclinical seizures, as detetected on the amplitude integrated EEG.
In the other arm, only clinical seizures will be treated and the aEEG will record but will be blinded.
Doel van het onderzoek
We hypothesize that without continuous EEG registration, subclinical electrographic seizures will be missed. Repetive ictal seizures and a sublcinical status epilepticus may be deleterious to the immature brain. On the other hand the use of antiepileptic drugs may also have adverse effects, especially to the developing brain.
Onderzoeksopzet
N/A
Onderzoeksproduct en/of interventie
Following initiation of aEEG registration and the occurrence of the first subclinical seizure, and following parental consent, the infant will be randomised to group A (treatment of clinical as well subclinical seizures as detetected on the aEEG) or group B (the aEEG will be blinded, and only clinical seizures will be treated;
Intermittent standard EEG can be performed and in case the EEG shows a status epilepticus this can be treated, but in case a subclinical seizure is seen on the standard EEG, this will not be treated with anti-epileptic drugs).
Publiek
P.O. Box 85090
L.S. Vries, de
Utrecht 3508 AB
The Netherlands
l.devries@wkz.azu.nl
Wetenschappelijk
P.O. Box 85090
L.S. Vries, de
Utrecht 3508 AB
The Netherlands
l.devries@wkz.azu.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
Fullterm infants admitted to the neonatal intensive care unit, within the first 24 hours after birth with subclinical seizures on the aEEG, in 8 Dutch and 3 Belgium centres.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
Preterm infants (<37 wks GA) and fullterm infants with neonatal seizures admitted after the first 24 hours after birth. Infants with chromosomal disorders, congenital anomalies and meningitis.
Opzet
Deelname
Opgevolgd door onderstaande (mogelijk meer actuele) registratie
Geen registraties gevonden.
Andere (mogelijk minder actuele) registraties in dit register
Geen registraties gevonden.
In overige registers
Register | ID |
---|---|
NTR-new | NL268 |
NTR-old | NTR306 |
Ander register | : N/A |
ISRCTN | ISRCTN61541169 |
Samenvatting resultaten
<br>
van Rooij LG, Toet MC, Osredkar D, van Huffelen AC, Groenendaal F, de Vries LS.Recovery of amplitude integrated electroencephalographic background patterns within 24 hours of perinatal asphyxia.Arch Dis Child Fetal Neonatal Ed. 2005;90:F245-51.
<br>
Toet MC, Groenendaal F, Osredkar D, van Huffelen AC, de Vries LS.Postneonatal epilepsy following amplitude-integrated EEG-detected neonatal seizures Pediatr Neurol 2005; 32:241-7