Ketamine as advanced second‐line treatment in benzodiazepine‐refractory convulsive status epilepticus in children

Author:

Buratti Silvia1ORCID,Giacheri Emanuele2ORCID,Palmieri Antonella3ORCID,Tibaldi Jessica3ORCID,Brisca Giacomo2ORCID,Riva Antonella4ORCID,Striano Pasquale45ORCID,Mancardi Maria Margherita6ORCID,Nobili Lino46ORCID,Moscatelli Andrea1ORCID

Affiliation:

1. Neonatal and Pediatric Intensive Care Unit, Emergency Department IRCCS Istituto Giannina Gaslini Genoa Italy

2. Intermediate Care Unit, Emergency Department IRCCS Istituto Giannina Gaslini Genoa Italy

3. Emergency Medicine Unit, Emergency Department IRCCS Istituto Giannina Gaslini Genoa Italy

4. Department of Neuroscience (DINOGMI) University of Genoa Genoa Italy

5. Pediatric Neurology and Muscular Disease Unit IRCCS Istituto Giannina Gaslini Genoa Italy

6. Child Neuropsychiatry Unit IRCCS Istituto Giannina Gaslini Genoa Italy

Abstract

AbstractStatus epilepticus (SE) is one of the most common neurological emergencies in children. To date, there is no definitive evidence to guide treatment of SE refractory to benzodiazepines. The main objectives of treatment protocols are to expedite therapeutic decisions and to use fast‐ and short‐acting medications without significant adverse effects. Protocols differ among institutions, and most frequently valproate, phenytoin, and levetiracetam are used as second‐line treatment. After failure of first‐ and second‐line medications, admission to the intensive care unit and continuous infusion of anesthetics are usually indicated. Ketamine is a noncompetitive N‐methyl‐D‐aspartate receptor antagonist that has been safely used for the treatment of refractory SE in adults and children. In animal models of SE, ketamine demonstrated antiepileptic and neuroprotective properties and synergistic effects with other antiseizure medications. We reviewed the literature to demonstrate the potential role of ketamine as an advanced second‐line agent in the treatment of SE. Pharmacological targets, pathophysiology of SE, and the receptor trafficking hypothesis are reviewed and presented. The pharmacology of ketamine is outlined with related properties, advantages, and side effects. We summarize the most recent and relevant publications on experimental and clinical studies on ketamine in SE. Key expert opinion is also reported. Considering the current knowledge on SE pathophysiology, early sequential polytherapy should include ketamine for its wide range of positive assets. Future research and clinical trials on SE pharmacotherapy should focus on the role of ketamine as second‐line medication.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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