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Abstract Details

Exploring the Impact of Need for a Second Dose of Rescue Therapy for Seizure Episodes on Healthcare Utilization
Epilepsy/Clinical Neurophysiology (EEG)
Epilepsy/Clinical Neurophysiology (EEG) Posters (7:00 AM-5:00 PM)
132

Proportions of seizure episodes requiring a second dose of rescue medication and the impact those second doses had on healthcare utilization are reported.

Seizure clusters may last up to 24 hours. Approved outpatient rescue therapies have differing profiles that may affect multiple aspects of healthcare utilization.

For 3 large, long-term studies of approved seizure-cluster treatments (ie, rectal diazepam, intranasal midazolam, diazepam nasal spray), percentage of episodes controlled by the initial dose was compared with those requiring a second dose before 6 or 12 hours. Hospitalization data after second doses were collected.

For rectal diazepam seizure control ≤12 hours after treatment, 77% of administrations (1215/1578) prevented further seizures (second doses not reported). For intranasal midazolam, measuring seizure control 10 minutes to 6 hours after treatment, 55.5% (1108/1998) of seizure-cluster episodes were successfully treated; second doses were not administered in 61.4% of seizure episodes (1226/1998). For diazepam nasal spray, no second dose was administered in 94.5% (3829/4053) of seizure episodes within 6 hours of the initial dose and 92.2% (3735/4053) within 12 hours.

For diazepam rectal gel, 16 of 363 seizure clusters were subsequently treated in the emergency department. For intranasal midazolam, 4 patients had 1 serious adverse event (SAE) possibly treatment related (association with second dose not reported). For diazepam nasal spray, no SAEs were considered treatment related; 3 SAEs occurred the day of/day after a second dose. None required a dose change; all resolved.

Across these noncomparative open-label studies, need for a second dose ranged from <10% to <40% at 6 and 12 hours. Differences among approved therapies appear to have the potential to impact healthcare burden and should be considered when selecting rescue therapy for seizure clusters.
Authors/Disclosures

PRESENTER
No disclosure on file
R E. Faught, Jr., MD, FÂé¶¹´«Ã½Ó³»­ (Emory University) Dr. Faught has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Neurelis. Dr. Faught has received personal compensation in the range of $500-$4,999 for serving as a Consultant for LivaNova. Dr. Faught has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for SK Life Science. Dr. Faught has received personal compensation in the range of $500-$4,999 for serving as an Expert Witness for Gideon, Essary, Tardio and Carter PLC, Nashville TN TN law firm. Dr. Faught has received personal compensation in the range of $5,000-$9,999 for serving as an Expert Witness for Friedman Dazio and Zulanas Law Firm Birmingham AL. The institution of Dr. Faught has received research support from UCB Pharma. The institution of Dr. Faught has received research support from Cognizance.
Dave F. Cook No disclosure on file
Enrique Carrazana (Neurelis, Inc.) Enrique Carrazana has received personal compensation for serving as an employee of Neurelis. Enrique Carrazana has received personal compensation in the range of $10,000-$49,999 for serving as an officer or member of the Board of Directors for Hawaii-Biotech, CND Life Sciences, Apex Labs. Enrique Carrazana has stock in Neurelis, CND, Apex.