Evidence map›Paper›PMID 40452235›Full record

ArticleEuropean journal of neurology2025

Fulminant Idiopathic Intracranial Hypertension-Clinical Characteristics and Continuous Drainage as a Novel Treatment Approach.

Yoel Schwartzmann, Samuel Moscovici, Dana Ekstein, Hamza Jubran, Tamir Ben-Hur, Joshua M Kruger

Abstract read
In one paragraph

Article in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

6 authors.

Yoel SchwartzmannDepartment of Neurology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.ORCID 0000-0003-4459-6996
Samuel MoscoviciThe Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Dana EksteinDepartment of Neurology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.ORCID 0000-0002-3860-6054
Hamza JubranDepartment of Neurology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Tamir Ben-HurDepartment of Neurology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
Joshua M KrugerThe Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFulminant idiopathic intracranial hypertension (fIIH) is a severe condition which causes rapid visual loss. Conventional fIIH management involves surgical interventions, but their effectiveness and safety remain uncertain. The use of temporary continuous CSF drainage (CD) for fIIH has not been fully explored in the adult population. We present the results of CD treatment in severe IIH cases.

methodIIH Patients treated with CD were compared to control groups of extreme CSF opening pressure (> 45 cm H

resultsEighteen female patients underwent CD treatment. Indications for CD treatment were acute visual deterioration or development of a VI nerve palsy and severe papilledema (despite acetazolamide treatment). All patients stabilized after CD treatment. Four patients had acute complications that fully resolved. Visual acuity (VA) in fIIH patients was significantly reduced prior to treatment (mean 6/15 ± 6/19 vs. 6/7.5 ± 6/30, p < 0.01). CD treatment resulted in marked long-term improvement in VA (mean 6/7.5 ± 6/19 vs. 6/7 ± 6/38, p = 0.12 and 6/7 ± 6/48, p = 0.05). Compared to the extreme CSF opening pressure group, female sex, obesity, and TVO's were more common in the CD group. Compared to the general IIH group, female sex, obesity, endocrinopathy, and CSF opening pressure were higher in the CD group.

conclusionIIH patients with very high CSF opening pressure and the presence of obesity and endocrinopathy may be at higher risk to develop fIIH. CD treatment is an extremely effective and safe treatment option for severe cases of IIH.

Indexed as

DrainagePseudotumor CerebriAdultFemaleHumansMaleMiddle AgedTreatment OutcomeVisual AcuityYoung Adultcontinuous drainagefulminant idiopathic intracranial hypertensionidiopathic intracranial hypertension

Identifiers

PMID40452235
PMCPMC12127567

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