Diagnosing nonconvulsive status epilepticus: Defining electroencephalographic and clinical response to diagnostic intravenous antiseizure medication trials

Author:

Leitinger Markus12ORCID,Gaspard Nicolas34ORCID,Hirsch Lawrence J.5ORCID,Beniczky Sándor678ORCID,Kaplan Peter W.9,Husari Khalil9,Trinka Eugen1210ORCID

Affiliation:

1. Department of Neurology, member of European Reference Network EpiCARE, Center for Cognitive Neuroscience Christian Doppler University Hospital, Paracelsus Medical University Salzburg Austria

2. Neuroscience Institute, Center for Cognitive Neuroscience Christian Doppler University Hospital, Paracelsus Medical University Salzburg Austria

3. Hôpital Universitaire de Bruxelles–Hôpital Erasme Brussels Belgium

4. Université Libre de Bruxelles Brussels Belgium

5. Comprehensive Epilepsy Center, Department of Neurology Yale University School of Medicine New Haven Connecticut USA

6. Department of Clinical Neurophysiology Danish Epilepsy Center Dianalund Denmark

7. Department of Clinical Neurophysiology Aarhus University Hospital and Department of Clinical Medicine, Aarhus University Aarhus Denmark

8. Department of Clinical Medicine Aarhus University Aarhus Denmark

9. Department of Neurology Johns Hopkins University School of Medicine, Johns Hopkins Bayview Medical Center Baltimore Maryland USA

10. Institute of Public Health, Medical Decision Making and Health Technology Assessment University for Health Sciences, Medical Informatics, and Technology Hall in Tyrol Austria

Abstract

AbstractObjectiveThe Salzburg criteria for nonconvulsive status epilepticus (NCSE) and the American Clinical Neurophysiology Society (ACNS) Standardized Critical Care EEG Terminology 2021 include a diagnostic trial with intravenous (IV) antiseizure medications (ASMs) to assess electroencephalographic (EEG) and clinical response as a diagnostic criterion for definite NCSE and possible NCSE. However, how to perform this diagnostic test and assessing the EEG and clinical responses have not been operationally defined.MethodsWe performed a Delphi process involving six experts to standardize the diagnostic administration of IV ASM and propose operational criteria for EEG and clinical response.ResultsEither benzodiazepines (BZDs) or non‐BZD ASMs can be used as first choice for a diagnostic IV ASM trial. However, non‐BZDs should be considered in patients who already have impaired alertness or are at risk of respiratory depression. Levetiracetam, valproate, lacosamide, brivaracetam, or (if the only feasible drug) fosphenytoin or phenobarbital were deemed appropriate for a diagnostic IV trial. The starting dose should be approximately two thirds to three quarters of the full loading dose recommended for treatment of status epilepticus, with an additional smaller dose if needed. ASMs should be administered during EEG recording under supervision. A monitoring time of at least 15 min is recommended. If there is no response, a second trial with another non‐BDZ or BDZs may be considered. A positive EEG response is defined as the resolution of the ictal–interictal continuum pattern for at least three times the longest previously observed spontaneous interval of resolution (if any), but minimum of one continuous minute. For a clinical response, physicians should use a standardized examination before and after IV ASM administration. We suggest a definite time‐locked improvement in a focal deficit or at least one‐step improvement on a new dedicated one‐domain 10‐level NCSE response scale.SignificanceThe proposed standardized approach of a diagnostic IV ASM trial further refines the ACNS and Salzburg diagnostic criteria for NCSE.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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