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content:neonatal_seizures [2020/02/23 13:54] – [Management] icna | content:neonatal_seizures [2020/02/23 15:39] – [Neonatal seizures] icna | ||
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* Neonatal epileptic seizures occur from birth to the end of the neonatal period. | * Neonatal epileptic seizures occur from birth to the end of the neonatal period. | ||
* The neonatal period is defined as the first 28 days of life of a full-term infant. | * The neonatal period is defined as the first 28 days of life of a full-term infant. | ||
- | * Most neonatal seizures are acute (pro-voked, occasional, reactive) | + | * Most neonatal seizures are acute symptomatic seizures caused by an acute illness such as hypoxic–ischaemic encephalopathy, |
* seizures are the most common and important sign of acute neonatal encephalopathy | * seizures are the most common and important sign of acute neonatal encephalopathy | ||
* neonatal seizures are a major risk for death or subsequent neurological disability and, by themselves, may contribute to an adverse neuro-developmental outcome. | * neonatal seizures are a major risk for death or subsequent neurological disability and, by themselves, may contribute to an adverse neuro-developmental outcome. | ||
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* ‘decoupling response’ - commonly seen after starting AEDs where AEDs may suppress the clinical manifestations of seizures but not the EEG ictal discharge | * ‘decoupling response’ - commonly seen after starting AEDs where AEDs may suppress the clinical manifestations of seizures but not the EEG ictal discharge | ||
* may arise from foci not consistently echoed by surface electrodes[(: | * may arise from foci not consistently echoed by surface electrodes[(: | ||
+ | ==== Differential diagnosis ==== | ||
+ | * [[hyperekplexia]] | ||
+ | * [[benign neonatal sleep myoclonus]] | ||
+ | * [[Benign Non-Epileptic Myoclonus of Early Infancy]] ([[benign non-epileptic infantile spasms]]) | ||
+ | * paroxysmal, non-epileptic movement disorder of otherwise healthy infants who have normal EEG and development[(: | ||
+ | * ‘benign non-epileptic infantile spasms’ is descriptively more accurate than myoclonus[(: | ||
+ | * thought to be the same condition as ‘shuddering attacks’[(: | ||
==== Prognosis ==== | ==== Prognosis ==== | ||
* depends on the underlying cause[(: | * depends on the underlying cause[(: | ||
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* often recommended as first-line treatment[(: | * often recommended as first-line treatment[(: | ||
* recommended as first line treatment in the UK[(: | * recommended as first line treatment in the UK[(: | ||
- | * included in the only RCT of first-line treatment of neonatal seizure | + | * included in RCTs of first-line treatment of neonatal seizure |
* most studied anti-epileptic medication in animals | * most studied anti-epileptic medication in animals | ||
* historical precedence as the first-line antiepileptic drug for neonates | * historical precedence as the first-line antiepileptic drug for neonates | ||
* extremely limited evidence on the effect of phenobarbital on long-term neonatal neurodevelopment | * extremely limited evidence on the effect of phenobarbital on long-term neonatal neurodevelopment | ||
* U.S. Food and Drug Administration (FDA) has never approved phenobarbital for use in any patient population[(: | * U.S. Food and Drug Administration (FDA) has never approved phenobarbital for use in any patient population[(: | ||
+ | * animal studies have raised concerns that neonatal phenobarbital exposure induces neuronal apoptosis, disruption of synaptic development in the striatum, and other behavioral deficits[(: | ||
* **Levetiracetam** | * **Levetiracetam** | ||
* effective as second-line treatments for neonatal seizures that are unresponsive to phenobarbital | * effective as second-line treatments for neonatal seizures that are unresponsive to phenobarbital | ||
* FDA-approved for children as young as one-month of age[(: | * FDA-approved for children as young as one-month of age[(: | ||
* efficacy and safety profile has not been adequately studied in term or preterm neonates within the first month of life | * efficacy and safety profile has not been adequately studied in term or preterm neonates within the first month of life | ||
- | * dosing of 40–50mg/ | + | |
+ | | ||
* a recent open labelled RCT (Level III neonatal unit; 100 neonates) used Levetiracetam (20 mg/kg) or Phenobarbitone (20 mg/kg) intravenously and concluded that Levetiracetam achieves better control than Phenobarbitone for neonatal clinical seizures when used as first-line antiepileptic drug, and is not associated with adverse drug reactions[(: | * a recent open labelled RCT (Level III neonatal unit; 100 neonates) used Levetiracetam (20 mg/kg) or Phenobarbitone (20 mg/kg) intravenously and concluded that Levetiracetam achieves better control than Phenobarbitone for neonatal clinical seizures when used as first-line antiepileptic drug, and is not associated with adverse drug reactions[(: | ||
* phenytoin/ | * phenytoin/ | ||
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* consider pyridoxine challenge when other antiepileptics provide no response | * consider pyridoxine challenge when other antiepileptics provide no response | ||
* minimal data for many antiepileptics including topiramate, which is being increasingly used in neonates | * minimal data for many antiepileptics including topiramate, which is being increasingly used in neonates | ||
- | * steroids and / or vigabatrin are considered in epileptic spasms | + | * steroids and / or [[vigabatrin]] are considered in epileptic spasms |
- | * tonic seizures related to benign familial neonatal | + | * Low-dose carbamazepine (CBZ) should be considered as first-line treatment for benign familial neonatal |
* there is equipoise on levetiracetam vs phenobarbitone as first line treatment[(: | * there is equipoise on levetiracetam vs phenobarbitone as first line treatment[(: | ||
+ | * The 2011 World Health Organization (WHO) guidelines for neonatal seizures[(: | ||