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Patterns of benzodiazepine underdosing in the Established Status Epilepticus Treatment Trial

Sathe, AG; Underwood, E; Coles, LD; Elm, JJ; Silbergleit, R; Chamberlain, JM; Kapur, J; Cock, HR; Fountain, NB; Shinnar, S; et al. Sathe, AG; Underwood, E; Coles, LD; Elm, JJ; Silbergleit, R; Chamberlain, JM; Kapur, J; Cock, HR; Fountain, NB; Shinnar, S; Lowenstein, DH; Rosenthal, ES; Conwit, RA; Bleck, TP; Cloyd, JC (2021) Patterns of benzodiazepine underdosing in the Established Status Epilepticus Treatment Trial. Epilepsia, 62 (3). pp. 795-806. ISSN 0013-9580 https://doi.org/10.1111/epi.16825
SGUL Authors: Cock, Hannah Rutherford

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Abstract

Objective This study was undertaken to describe patterns of benzodiazepine use as first‐line treatment of status epilepticus (SE) and test the association of benzodiazepine doses with response to second‐line agents in patients enrolled in the Established Status Epilepticus Treatment Trial (ESETT). Methods Patients refractory to an adequate dose of benzodiazepines for the treatment of SE were enrolled in ESETT. Choice of benzodiazepine, doses given prior to administration of second‐line agent, route of administration, setting, and patient weight were characterized. These were compared with guideline‐recommended dosing. Logistic regression was used to determine the association of the first dose of benzodiazepine and the cumulative benzodiazepine dose with the response to second‐line agent. Results Four hundred sixty patients were administered 1170 doses of benzodiazepines (669 lorazepam, 398 midazolam, 103 diazepam). Lorazepam was most frequently administered intravenously in the emergency department, midazolam intramuscularly or intravenously by the emergency medical services personnel, and diazepam rectally prior to ambulance arrival. The first dose of the first benzodiazepine (N = 460) was lower than guideline recommendations in 76% of midazolam administrations and 81% of lorazepam administrations. Among all administrations, >85% of midazolam and >76% of lorazepam administrations were lower than recommended. Higher first or cumulative benzodiazepine doses were not associated with better outcomes or clinical seizure cessation in response to second‐line medications in these benzodiazepine‐refractory seizures. Significance Benzodiazepines as first‐line treatment of SE, particularly midazolam and lorazepam, are frequently underdosed throughout the United States. This broad and generalizable cohort confirms prior single site reports that underdosing is both pervasive and difficult to remediate. (ESETT ClinicalTrials.gov identifier: NCT01960075.)

Item Type: Article
Additional Information: This is the peer reviewed version of the following article: Sathe, A.G., Underwood, E., Coles, L.D., Elm, J.J., Silbergleit, R., Chamberlain, J.M., Kapur, J., Cock, H.R., Fountain, N.B., Shinnar, S., Lowenstein, D.H., Rosenthal, E.S., Conwit, R.A., Bleck, T.P. and Cloyd, J.C. (2021), Patterns of benzodiazepine underdosing in the Established Status Epilepticus Treatment Trial. Epilepsia, 62: 795-806, which has been published in final form at https://doi.org/10.1111/epi.16825. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Keywords: 1103 Clinical Sciences, 1109 Neurosciences, Neurology & Neurosurgery
SGUL Research Institute / Research Centre: Academic Structure > Institute of Medical & Biomedical Education (IMBE)
Academic Structure > Institute of Medical & Biomedical Education (IMBE) > Centre for Clinical Education (INMECE )
Journal or Publication Title: Epilepsia
ISSN: 0013-9580
Language: en
Dates:
DateEvent
5 March 2021Published
10 February 2021Published Online
5 January 2021Accepted
Publisher License: Publisher's own licence
Projects:
Project IDFunderFunder ID
U01NS088034National Institute of Neurological Disorders and Strokehttp://dx.doi.org/10.13039/100000065
U01NS088023National Institute of Neurological Disorders and Strokehttp://dx.doi.org/10.13039/100000065
U01NS056975National Institute of Neurological Disorders and Strokehttp://dx.doi.org/10.13039/100000065
U01NS059041National Institute of Neurological Disorders and Strokehttp://dx.doi.org/10.13039/100000065
R01NS099653National Institute of Neurological Disorders and Strokehttp://dx.doi.org/10.13039/100000065
URI: https://openaccess.sgul.ac.uk/id/eprint/112940
Publisher's version: https://doi.org/10.1111/epi.16825

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