Evidence map›Paper›PMID 36138616›Full record

ArticleChildren (Basel, Switzerland)2022

Optical Coherence Tomography Significance in Managing Early Onset of Optic Pathway Gliomas in Children Younger than 5 Years of Age-A Retrospective Study.

Rossana Pavone, Carla Fonte, Iacopo Sardi, Roberto Caputo, Elisa Marziali, Fabio Mazzeo, Jacopo Secci, Alessia Bergamini, Salvatore De Masi, Maria Carmela Leo and 2 more

Open access · goldAbstract read
In one paragraph

Article in Children (Basel, Switzerland), 2022. 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
0.1field-weighted citation impact, top 51% 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, 1 citations in OpenAlex.

  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

12 authors at 2 institutions in 1 country.

Rossana PavoneNeuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's Hospital, 50134 Florence, Italy.
Carla FonteNeuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's Hospital, 50134 Florence, Italy.
Iacopo SardiNeuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's Hospital, 50134 Florence, Italy.ORCID 0000-0002-8763-6524
Roberto CaputoPediatric Ophthalmology Unit, Meyer Children's Hospital, Viale Pieraccini 24, 50134 Florence, Italy.
Elisa MarzialiPediatric Ophthalmology Unit, Meyer Children's Hospital, Viale Pieraccini 24, 50134 Florence, Italy.ORCID 0000-0002-6676-9379
Fabio MazzeoPediatric Ophthalmology Unit, Meyer Children's Hospital, Viale Pieraccini 24, 50134 Florence, Italy.
Jacopo SecciPediatric Ophthalmology Unit, Meyer Children's Hospital, Viale Pieraccini 24, 50134 Florence, Italy.
Alessia BergaminiPediatric Ophthalmology Unit, Meyer Children's Hospital, Viale Pieraccini 24, 50134 Florence, Italy.
Salvatore De MasiClinical Trial Center, Careggi Hospital, 50134 Florence, Italy.ORCID 0000-0001-5889-9280
Maria Carmela LeoClinical Research and Study Design Office, Meyer Children's Hospital, 50134 Florence, Italy.
Maria Luigia CensulloNeuro-Oncology Unit, Department of Pediatric Oncology, Meyer Children's Hospital, 50134 Florence, Italy.
Giacomo Maria BacciPediatric Ophthalmology Unit, Meyer Children's Hospital, Viale Pieraccini 24, 50134 Florence, Italy.ORCID 0000-0002-8741-4833
Meyer Children's Hospital · ITAzienda Ospedaliero-Universitaria Careggi · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We aimed to investigate the significance of optical coherence tomography (SD-OCT) in managing pediatric optic pathway gliomas (OPGs) in children younger than 5 years of age. A retrospective monocentric study was conducted. SD-OCT scans were obtained using the handheld iVue system to assess peripapillary retinal nerve fibre layer (pRNFL) thickness at three time points: baseline (OCT1), end of treatment (OCT2), and at last follow-up (OCT3). We compared the median value of pRNFL (and interquartile range-IQR) at different follow-up times and in different sub-groups (stable disease-SD, partial response-PR, and progression disease-PD). Thirteen children younger than 5 years of age were included. The Median follow-up time was 3.9 years (IQR 1.2). Six patients showed a pRNFL change of more than 10% during follow-up. Seven patients showed PD during follow-up. Median pRNFL at baseline was 81.5 µm (IQR 31.5); median pRNFL at the end of treatment was 73 µm (IQR 33); median pRNFL at last follow-up was 72 µm (IQR 38.5). The mean pRNFL at baseline was significantly lower than the mean normative values. Only subjects with PD showed pRNFL change close to statistical significance. This study confirms the role of SD-OCT in managing OPGs for therapeutic decisions and strategy planning of visual rehabilitation.

Indexed as

neurofibromatosisOPGoptical coherence tomographyoptic pathway gliomapRNFLSD-OCT

Identifiers

PMID36138616
PMCPMC9497564
OpenAlexW4293659869

What OpenQuestion holds

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LicenceCC BY
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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.