Evidence map›Paper›PMID 29030796›Full record

ArticleInternational ophthalmology2018

Classification and characterization of acute macular neuroretinopathy with spectral domain optical coherence tomography.

Katerina Hufendiek, Maria-Andreea Gamulescu, Karsten Hufendiek, Horst Helbig, David Märker

Abstract readCase Reports
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In one paragraph

Article in International ophthalmology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 33% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Optical coherence tomography angiography suggests choriocapillaris perfusion deficit as etiology of acute macular neuroretinopathy.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2024
    Article
  2. Article
  3. Paracentral Acute Middle MaculopathyTurkish journal of ophthalmology · 2020
    Article
  4. 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

5 authors at 2 institutions in 1 country.

Katerina HufendiekDepartment of Ophthalmology, University Medical Center Regensburg, Regensburg, Germany. hufendiek.katerina@mh-hannover.de.
Maria-Andreea GamulescuDepartment of Ophthalmology, University Medical Center Regensburg, Regensburg, Germany.
Karsten HufendiekDepartment of Ophthalmology, University Medical Center Regensburg, Regensburg, Germany.
Horst HelbigDepartment of Ophthalmology, University Medical Center Regensburg, Regensburg, Germany.
David MärkerDepartment of Ophthalmology, University Medical Center Regensburg, Regensburg, Germany.
University Hospital Regensburg · DEMedizinische Hochschule Hannover · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo classify and characterize AMN lesions with SD-OCT during a follow-up as long as 5 years.

methodsRetrospective study of 14 patients (18 eyes) with special focus on SD-OCT. We measured thickness of inner nuclear layer (INL), outer retinal layer (ONL), and hyperreflective band at baseline and during follow-up. AMN lesions were classified as type 1 and type 2.

resultsOf 14 patients (six males, eight females, mean age 29.7 years), three patients (four eyes) had type 1 and nine (12 eyes) had type 2. Two patients did not meet the criteria for AMN type 1 or 2 and were therefore classified as new subtype of AMN. In all patients, statistically significant thinning of ONL and INL was observable. Mean ONL of all patients was 90.2 ± 7.81 and 72.3 ± 15.64 μm (p < 0.05) during follow-up; mean INL was 54.4 ± 10.71 and 37.5 ± 6.18 μm (p < 0.05) in the course. In the subgroup analysis in AMN type 2, the thinning of both ONL and INL was also statistically significant (mean ONL: 87.4 ± 6.02 and 71.6 ± 12.7 μm (p < 0.05); mean INL: 48.5 ± 5.04 and 38.5 ± 5.6 μm (p < 0.05)) in the course.

conclusionSD-OCT allows for classification, characterization, and further understanding of AMN lesions. Up to now, this is one of the largest AMN case series differentiating into different subtypes and following up for up to 5 years. Furthermore, we describe a new AMN subtype characterized by initially clinically visible yellowish parafoveal lesions, subtle pigmentary changes at late stage, lack of classic dark appearance on IR reflectance, involvement of RPE/Bruch's complex, and disruption of ellipsoid zone and interdigitation zone. The patients suffered from a prolonged visual impairment and paracentral scotomata. We propose the term AMN type 3 or "paracentral acute outer maculopathy."

Indexed as

AdultFemaleHumansMacula LuteaMaleMiddle AgedRetinal DiseasesRetrospective StudiesTomography, Optical CoherenceYoung AdultAMNCharacterizationClassificationFollow-upSD-OCT

Identifiers

PMID29030796
OpenAlexW2760895141

What OpenQuestion holds

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Registered trials

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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.