Evidence map›Paper›PMID 31723247›Full record

ArticleEye (London, England)2020

Macular ganglion cell complex thinning in children with visual field defects due to central nervous system pathology.

S Noval, M A Henríquez-Recine, I Contreras, M Galdós, B Zafra, J Barrio-Barrio, F Carceller

Open access · bronzeAbstract read
In one paragraph

Article in Eye (London, England), 2020. 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
1.1field-weighted citation impact, top 23% 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.

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, 7 citations in OpenAlex.

  1. Intraocular pressure and optical coherence tomography parameters in pediatric hydrocephalus: a comparative analysis of patients with and without shunts versus healthy controls.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
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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 at 4 institutions in 1 country.

S NovalDepartment of Ophthalmology, Hospital Universitario La Paz, IdiPaz, Madrid, Spain.
M A Henríquez-RecineDepartment of Ophthalmology, Hospital Universitario La Paz, IdiPaz, Madrid, Spain. maria.angelica.h@gmail.com.ORCID http://orcid.org/0000-0003-0546-2012
I ContrerasDepartment of Ohthalmology, Hospital Universitario Ramón y Cajal. Clínica Rementería, Madrid, Spain.
M GaldósDepartment of Ophthalmology, Hospital de Cruces, Bilbao, Spain.
B ZafraDepartment of Ophthalmology, Hospital Universitario La Paz, IdiPaz, Madrid, Spain.
J Barrio-BarrioDepartment of Ophthalmology, Clínica Universidad de Navarra, Pamplona, Spain.ORCID http://orcid.org/0000-0002-0654-0249
F CarcellerDepartment of Neurosurgery, Hospital Universitario La Paz, IdiPaz, Madrid, Spain.
Hospital Universitario La Paz · ESClínica Rementería · ESClinica Universidad de Navarra · ESHospital de Cruces · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo study the relationship between macular ganglion cell complex (GCC) thickness and visual field defects (VFD) caused by central nervous system (CNS) lesions in children and evaluate the possibility of predicting VFD according to GCC maps.

methodsThe GCC maps of a group of children with VFD due to CNS lesions with respect of the vertical meridian in at least one eye (study group), as well as of children with other neuro-ophthalmological problems and healthy children were presented to two masked evaluators, who were asked to predict the patients' VFD on the basis of GCC damage: the evaluators classified VFD as normal, hemianopia (homonymous or heteronymous) or diffuse.

resultsSeventeen patients were included in the study group, with a median age of 12 years. Fifteen had brain tumours and two epilepsy. The mean MD of the affected hemifields was -26.00 dB (SD 7.89 dB) versus -5.51 dB (SD 3.52 dB) for the nonaffected hemifields, p < 0.001. The mean GCC thickness was of 56.04 μm (SD 11.95 μm) in the affected hemiretinas versus 74.31 μm (SD 10.64 μm) for the non-affected, p < 0.001. Kappa coefficients between VFD and those estimated by the evaluators were 0.705 and 0.658 (p < 0.001) for evaluators 1 and 2.

conclusionsGCC thickness can reflect damage to the visual pathway and GCC maps may be useful to identify chiasmal and retrochiasmal lesions, since GCC atrophy in most of these cases respects the vertical meridian. GCC maps might be used as a surrogate marker for visual damage in patients unable to perform perimetry.

Indexed as

Visual FieldsVisual Field TestsCentral Nervous SystemChildHumansRetinal Ganglion CellsTomography, Optical Coherence

Identifiers

PMID31723247
PMCPMC7608095
OpenAlexW2984665042

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.