Evidence map›Paper›PMID 41312349›Full record

ArticleFrontiers in neurology2025

Benzodiazepines versus non-benzodiazepine antiseizure medications as first-line agents for status epilepticus: analysis of real word data from a 9-years prospective cohort.

Francesco Brigo, Gianni Turcato, Giada Giovannini, Simona Lattanzi, Arian Zaboli, Niccolò Orlandi, Margherita Burani, Lisa Taruffi, Leonardo Affronte, Stefano Meletti

Abstract read
In one paragraph

Article in Frontiers in neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Francesco BrigoInnovation, Research and Teaching Service (SABES-ASDAA), Bolzano, Italy.
Gianni TurcatoDepartment of Internal Medicine, Hospital of Santorso (AULSS-7), Santorso, Italy.
Giada GiovanniniNeurophysiology Unit and Epilepsy Center, Azienda Ospedaliera-Universitaria di Modena, Modena, Italy.
Simona LattanziDepartment of Experimental and Clinical Medicine, Neurological Clinic, Marche Polytechnic University, Ancona, Italy.
Arian ZaboliInnovation, Research and Teaching Service (SABES-ASDAA), Bolzano, Italy.
Niccolò OrlandiNeurophysiology Unit and Epilepsy Center, Azienda Ospedaliera-Universitaria di Modena, Modena, Italy.
Margherita BuraniNeurophysiology Unit and Epilepsy Center, Azienda Ospedaliera-Universitaria di Modena, Modena, Italy.
Lisa TaruffiNeurophysiology Unit and Epilepsy Center, Azienda Ospedaliera-Universitaria di Modena, Modena, Italy.
Leonardo AffronteNeurophysiology Unit and Epilepsy Center, Azienda Ospedaliera-Universitaria di Modena, Modena, Italy.
Stefano MelettiNeurophysiology Unit and Epilepsy Center, Azienda Ospedaliera-Universitaria di Modena, Modena, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and objectives: The treatment of status epilepticus (SE) follows a stepwise approach, with benzodiazepines (BDZ) being the first-line therapy. This study analyzed real-word data on use of BDZ and non-BDZ antiseizure medications (ASMs) in SE treatment over 9-years to evaluate whether non-BDZ given as a first-line treatment affect 30-day mortality and other outcomes. Methods: We included SE cases in patients aged ≥14 years who were prospectively registered at Baggiovara Civil Hospital (Modena, Italy) between September 1, 2013, and October 31, 2021. First-line treatment choices were dichotomized as: (i) i.v. BDZ; (ii) other ASMs. A multivariate model with logistic regression and an adjusted stepwise method for variables was used. Then, a propensity-score matched analysis was performed with clinical variables unevenly distributed between the two groups to evaluate the independent association between first-line therapy and 30-day mortality and secondary outcomes. Results: Six hundred and thirty patients were included: 73.5% (463/630) received a BDZ as first-line therapy and 26.5% (167/630) were treated with non-BDZ. In the primary analyses of the whole cohort, 30-day mortality was 25.9 and 35.3% in patients receiving BDZ and non-BDZ, respectively ( Conclusion: The use of non-BDZ first-line treatment was found to be frequent, approaching 25%. Our propensity-score matching analysis shows that in some patients, mainly with NCSE, the overall prognosis of SE was not affected by first-line use of non-BDZ drugs. In these cases, SE prognosis might only be partially dependent on the first medications administered and could be more influenced by other biological variables.

Indexed as

benzodiazepinesmortalityprognosispropensity scorestatus epilepticus

Identifiers

PMID41312349
PMCPMC12649711

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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.