Evidence map›Paper›PMID 42397688›Full record

Trial reportEpilepsia2026

Factors associated with rapid pediatric acute seizure emergency treatment: Quality Improvement in Time to Treat Status Epilepticus baseline cohort.

Adam P Ostendorf, Gabrielle Brown-Mitchell, Tobias Loddenkemper, Lindsey A Morgan, Brian Appavu, Raquel Farias-Moeller, Dana Harrar, Craig Press, Janette Mailo, Nicholas S Abend and 7 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Epilepsia, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Adam P OstendorfNationwide Children's Hospital and Ohio State University, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0002-9994-6650
Gabrielle Brown-MitchellNationwide Children's Hospital and Ohio State University, Columbus, Ohio, USA.
Tobias LoddenkemperBoston Children's Hospital, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0003-2074-0674
Lindsey A MorganSeattle Children's Hospital and University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-2206-5561
Brian AppavuHonor Health Neurology, Bob Bove Neuroscience Institute, Scottsdale, Arizona, USA.ORCID https://orcid.org/0000-0002-5396-2559
Raquel Farias-MoellerDivision of Pediatric Neurology, Department of Neurology, Children's Wisconsin and Medical College of Wisconsin, Milwaukee, Wisconsin, USA.ORCID https://orcid.org/0000-0001-8717-7703
Dana HarrarCenter for Neuroscience and Behavioral Health, Children's National Hospital, George Washington University, Washington, District of Columbia, USA.ORCID https://orcid.org/0000-0001-6382-8479
Craig PressDepartments of Neurology and Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID https://orcid.org/0000-0003-4435-206X
Janette MailoDivision of Neurology, Department of Neuroscience, Barrow Neurological Institute at Phoenix Children's Hospital, Phoenix, Arizona, USA.ORCID https://orcid.org/0000-0002-3586-7080
Nicholas S AbendDepartments of Neurology and Pediatrics, Children's Hospital of Philadelphia, University of Pennsylvania, Philadelphia, Pennsylvania, USA.ORCID https://orcid.org/0000-0001-6166-2663
William D GaillardCenter for Neuroscience and Behavioral Health, Children's National Hospital, George Washington University, Washington, District of Columbia, USA.ORCID https://orcid.org/0000-0001-5709-0033
Shasha BaiEmory University School of Medicine, Atlanta, Georgia, USA.ORCID https://orcid.org/0000-0003-4999-327X
Mariah EisnerBiostatics Resource, Nationwide Children's Hospital, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0002-4703-4342
Emily KroshusDepartment of Pediatrics, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0002-7484-2601
Kathryn VannattaNationwide Children's Hospital and Ohio State University, Columbus, Ohio, USA.ORCID https://orcid.org/0000-0002-9218-2352
Howard P GoodkinDepartment of Pediatrics, University of Washington, Seattle, Washington, USA.ORCID https://orcid.org/0000-0003-0528-4949
QuITT‐SE Study Group

Funding

Quality Improvement in time to Treatment of Status Epilepticus (QuITT-SE)R01NS133037 · NINDS · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI ADAM P. OSTENDORF · 2023 to 2026
$2.7M
NIH HHS R01NS133037NINDS NIH HHS R01 NS133037
6 · The paper itself

Abstract

objectiveStatus epilepticus (SE) treatment is more effective when benzodiazepines (BZDs) are given soon after SE diagnosis. The Quality Improvement in Time to Treat Status Epilepticus (QuITT-SE) trial is a multicenter, randomized, stepped-wedge effectiveness-implementation hybrid study aimed at improving time to SE treatment. We report the QuITT-SE baseline cohort and test the hypothesis that acute seizure emergency episodes treated promptly differ in clinical and demographic features from those with delayed treatment.

methodsData were summarized from 371 consecutive acute seizures episodes treated with a BZD in the inpatient, non-intensive care unit (ICU) setting from 207 individual patients across eight centers per the QuITT-SE protocol. To test our hypothesis, we utilized a multivariable negative binomial mixed effects model with random intercepts to estimate the incidence rate ratios for variables of interest for time to BZD treatment.

resultsThe median age was 7 years (IQR = 3-12). Nonelective ICU transfers occurred with 26% of episodes, including 13% within 6 h of the episode. The median time from seizure onset to BZD treatment was 6 min (IQR = 4-10), with 74% of all episodes and 63% of SE treated within 10 min. BZD administration was faster when nurses made the treatment decision, when the intranasal (IN) route was used, when the patient received prior rescue medication within 24 h, or with certain elective admission types. Seizures were shorter when BZD administration was faster or when treatment was with IN midazolam versus intravenous lorazepam (median = 8 min [IQR = 6-15] vs. 10 min [IQR = 7-17], p = .04). Patients were less likely to be transferred to the ICU if they received IN midazolam (odds ratio = .3, p = .007). SIGNIFICANCE: Delayed BZD administration occurs in one third of SE treatment. Prolonged seizures and ICU transfers are associated with modifiable risk factors. Baseline drivers of delayed acute seizure treatment may be addressed using the QuITT-SE interventions, the study of which is currently ongoing.

Indexed as

AnticonvulsantsBenzodiazepinesQuality ImprovementSeizuresStatus EpilepticusTime-to-TreatmentChildChild, PreschoolCohort StudiesFemaleHumansLorazepamMaleMidazolamTime FactorsTreatment OutcomeAnticonvulsantsBenzodiazepinesLorazepamMidazolambenzodiazepinepediatricseizurestatus epilepticustreatment delay

Identifiers

PMID42397688
PMCPMC13592489

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.