Evidence map›Paper›PMID 20878265›Full record

Trial reportNeurocritical care2011

A randomized trial for the treatment of refractory status epilepticus.

Andrea O Rossetti, Tracey A Milligan, Serge Vulliémoz, Costas Michaelides, Manuel Bertschi, Jong Woo Lee

Registry-linked trialOpen access · bronzeAbstract readComparative StudyRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Neurocritical care, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00265616 (A Randomized Clinical Trial for the Treatment of Refractory Status Epilepticus), which is not on this map. Cited by 77 papers, 7 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 7 pooled it
8.2field-weighted citation impact, top 2% of its field
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.

NCT00265616 phase3terminatednot on this map

A Randomized Clinical Trial for the Treatment of Refractory Status Epilepticus

TypeinterventionalSponsorBrigham and Women's HospitalRan2006 to 2010Enrolled23ConditionsStatus EpilepticusArmspropofol, thiopental/pentobarbital
3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 7 syntheses or guidelines pooled it, 227 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Anticonvulsant therapy for status epilepticus.The Cochrane database of systematic reviews · 2014
    Pooled it
  6. Guideline
  7. Guideline
  8. Trial
  9. Trial
  10. Trial
  11. Article
  12. Article
  13. Review
  14. Ketamine reduces seizure and interictal continuum activity in refractory status epilepticus: a multicenter in-person and teleneurocritical care study.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

17 more citing papers are in PubMed but not listed here.

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

6 authors at 4 institutions in 2 countries.

Andrea O RossettiDepartment of Neurology, CHUV et Université de Lausanne, Lausanne, Switzerland. andrea.rossetti@chuv.ch
Tracey A Milligan
Serge Vulliémoz
Costas Michaelides
Manuel Bertschi
Jong Woo Lee
Brigham and Women's Hospital · USMassachusetts General Hospital · USUniversity Hospital of Bern · CHUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRefractory status epilepticus (RSE) has a mortality of 16-39%; coma induction is advocated for its management, but no comparative study has been performed. We aimed to assess the effectiveness (RSE control, adverse events) of the first course of propofol versus barbiturates in the treatment of RSE.

methodsIn this randomized, single blind, multi-center trial studying adults with RSE not due to cerebral anoxia, medications were titrated toward EEG burst-suppression for 36-48 h and then progressively weaned. The primary endpoint was the proportion of patients with RSE controlled after a first course of study medication; secondary endpoints included tolerability measures.

resultsThe trial was terminated after 3 years, with only 24 patients recruited of the 150 needed; 14 subjects received propofol, 9 barbiturates. The primary endpoint was reached in 43% in the propofol versus 22% in the barbiturates arm (P = 0.40). Mortality (43 vs. 34%; P = 1.00) and return to baseline clinical conditions at 3 months (36 vs. 44%; P = 1.00) were similar. While infections and arterial hypotension did not differ between groups, barbiturate use was associated with a significantly longer mechanical ventilation (P = 0.03). A non-fatal propofol infusion syndrome was detected in one patient, while one subject died of bowel ischemia after barbiturates. DISCUSSION: Although undersampled, this trial shows significantly longer mechanical ventilation with barbiturates and the occurrence of severe treatment-related complications in both arms. We describe practical issues necessary for the success of future studies needed to improve the current unsatisfactory state of evidence.

Indexed as

AdolescentAdultAgedAged, 80 and overBarbituratesComaCritical CareFemaleHumansHypnotics and SedativesMaleMiddle AgedPropofolProspective StudiesStatus EpilepticusTreatment OutcomeBarbituratesHypnotics and SedativesPropofol

Identifiers

PMID20878265
OpenAlexW2045765644

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.