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Review
. 2014 Jun;81(6):592-8.
doi: 10.1007/s12098-014-1457-9. Epub 2014 May 6.

Advances in management of neonatal seizures

Affiliations
Review

Advances in management of neonatal seizures

Zachary A Vesoulis et al. Indian J Pediatr. 2014 Jun.

Abstract

Seizures are more common in the neonatal period than any other time in the human lifespan. A high index of suspicion for seizures should be maintained for infants who present with encephalopathy soon after birth, have had a stroke, central nervous system (CNS) infection or intracranial hemorrhage or have a genetic or metabolic condition associated with CNS malformations. Complicating the matter, most neonatal seizures lack a clinical correlate with only subtle autonomic changes and often no clinical indication at all. Over the last three decades, several tools have been developed to enhance the detection and treatment of neonatal seizures. The use of electroencephalography (EEG) and the later development of amplitude-integrated EEG (aEEG), allows for Neurologists and non-Neurologists alike, to significantly increase the sensitivity of seizure detection. When applied to the appropriate clinical setting, time to diagnosis and start of therapy is greatly reduced. Phenobarbital maintains the status of first-line therapy in worldwide use. However, newer anti-epileptic agents such as, levetiracetam, bumetanide, and topiramate are increasingly being applied to the neonatal population, offering the potential for seizure treatment with a significantly better side-effect profile. Seizures in premature infants, continue to confound clinicians and researchers alike. Though the apparent seizure burden is significant and there is an association between seizures and adverse outcomes, the two are not cleanly correlated. Compounding the issue, GABA-ergic anti-epileptic drugs are not only less effective in this age group due to reversed neuronal ion gradients but may cause harm. Selecting an appropriate treatment group remains a challenge.

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Conflict of interest statement

Conflict of Interest

None

Figures

Figure 1
Figure 1
Screenshot of aEEG trace demonstrating seizures. The upper raw trace (10 s) demonstrates signal from the left (C3-P3-upper) and right (C4-P4- lower) channels. The lower compressed trace (3.5 h) demonstrates aEEG signal from the left and right channels. Seizures are depicted as sudden rise in the upper and lower margin of the aEEG trace. The red cursor on the aEEG shows the raw EEG trace at that moment. The orange bar on the raw trace is the activated seizure detection algorithm that is also seen on the aEEG.

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