Evidence map›Paper›PMID 28104417›Full record

Trial reportAmerican journal of ophthalmology2017

The Longitudinal Idiopathic Intracranial Hypertension Trial: Outcomes From Months 6-12.

Michael Wall, Mark J Kupersmith, Matthew J Thurtell, Heather E Moss, Elizabeth Ann Moss, Peggy Auinger, NORDIC Idiopathic Intracranial Hypertension Study Group

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in American journal of ophthalmology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
–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

12 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Observational
  6. Article
  7. Article
  8. New Options (or not) for Treatment of Idiopathic Intracranial Hypertension.Current neurology and neuroscience reports · 2022
    Review
  9. Review
  10. Article
  11. Review
  12. 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

7 authors.

Michael WallDepartment of Neurology, University of Iowa, Iowa City, Iowa; Department of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, Iowa. Electronic address: michael-wall@uiowa.edu.
Mark J KupersmithMount Sinai West and New York Eye and Ear Infirmary, New York, New York.
Matthew J ThurtellDepartment of Ophthalmology and Visual Sciences, University of Iowa, Iowa City, Iowa.
Heather E MossIllinois Eye and Ear Infirmary, Chicago, Illinois.
Elizabeth Ann MossMount Sinai West and New York Eye and Ear Infirmary, New York, New York.
Peggy AuingerCenter for Human Experimental Therapeutics, University of Rochester, Rochester, New York.
NORDIC Idiopathic Intracranial Hypertension Study Group

Funding

Neuro-Ophthalmology Research Disease Investigator Consortium (NORDIC) NetworkU10EY017281 · NEI · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI KUPERSMITH, MARK J · 2009 to 2014
$10.2M
Physiologically Based Markers of Idiopathic Intracranial HypertensionK23EY024345 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MOSS, HEATHER ELSPETH · 2014 to 2018
$1.1M
NEI NIH HHS K23 EY024345NEI NIH HHS U10 EY017281
6 · The paper itself

Abstract

purposeTo determine whether the beneficial effects of acetazolamide (ACZ) in improving vision at 6 months continues to month 12 in participants of the Idiopathic Intracranial Hypertension Treatment Trial (IIHTT).

designNonrandomized clinical study.

methodsIn the IIHTT, subjects were randomly assigned to placebo-plus-diet or maximally tolerated dosage of acetazolamide-plus-diet. At 6 months subjects transitioned from study drug to ACZ. This resulted in the following groups: (1) ACZ to ACZ; n = 34; (2) placebo to ACZ; n = 35; (3) ACZ to no treatment; n = 16; and (4) placebo to no treatment; n = 11. Ninety-six IIHTT subjects had evaluations at 6 and 12 months. Our main outcome measure was change from month 6 to month 12 in visual field mean deviation (MD) with secondary measures being change in papilledema grade, ETDRS scores, and quality-of-life (QoL) measures.

resultsThe ACZ to ACZ group improved 0.35 dB, P = .05; placebo subjects with no ACZ improved 0.81 dB MD, P = .07 at 12 months. The other groups improved 0.35-0.46 dB MD. Mean improvements in papilledema grade occurred most markedly in the group that exchanged placebo for ACZ (0.91 units, P < .001). QoL and headache disability scores showed significant improvements in the placebo group with added ACZ.

conclusionImprovements in MD continued from month 6 to month 12 of the IIHTT in all treatment groups, most marked in the placebo group tapered off study drug. Adding ACZ to the placebo group significantly improved papilledema grade, headache, and QoL measures.

Indexed as

AcetazolamideAdministration, OralAdultCarbonic Anhydrase InhibitorsDose-Response Relationship, DrugFemaleFollow-Up StudiesHumansMalePapilledemaPseudotumor CerebriQuality of LifeTime FactorsTreatment OutcomeVisual FieldsAcetazolamideCarbonic Anhydrase Inhibitors

Identifiers

PMID28104417
PMCPMC5376520

What OpenQuestion holds

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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.