Evidence map›Paper›PMID 32141037›Full record

ReviewOphthalmology and therapy2020

Reviewing the Role of Ultra-Widefield Imaging in Inherited Retinal Dystrophies.

Maria Vittoria Cicinelli, Alessandro Marchese, Alessandro Bordato, Maria Pia Manitto, Francesco Bandello, Maurizio Battaglia Parodi

Open access · goldAbstract readReview
In one paragraph

Review in Ophthalmology and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Structural evaluation in inherited retinal diseases.The British journal of ophthalmology · 2021
    Review
  9. Article
  10. Imaging the pediatric retina: An overview.Indian journal of ophthalmology · 2021
    Review
  11. Review
  12. Article
  13. Article
  14. 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 at 1 institution in 1 country.

Maria Vittoria CicinelliDepartment of Ophthalmology, San Raffaele Vita-Salute University, Ospedale San Raffaele, Milan, Italy. cicinelli.mariavittoria@hsr.it.
Alessandro MarcheseDepartment of Ophthalmology, San Raffaele Vita-Salute University, Ospedale San Raffaele, Milan, Italy.
Alessandro BordatoDepartment of Ophthalmology, San Raffaele Vita-Salute University, Ospedale San Raffaele, Milan, Italy.
Maria Pia ManittoDepartment of Ophthalmology, San Raffaele Vita-Salute University, Ospedale San Raffaele, Milan, Italy.
Francesco BandelloDepartment of Ophthalmology, San Raffaele Vita-Salute University, Ospedale San Raffaele, Milan, Italy.
Maurizio Battaglia ParodiDepartment of Ophthalmology, San Raffaele Vita-Salute University, Ospedale San Raffaele, Milan, Italy.
IRCCS Ospedale San Raffaele · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inherited retinal dystrophies (IRD) are a heterogeneous group of rare chronic disorders caused by genetically determined degeneration of photoreceptors and retinal pigment epithelium cells. Ultra-widefield (UWF) imaging is a useful diagnostic tool for evaluating retinal integrity in IRD, including Stargardt disease, retinitis pigmentosa, cone dystrophies, and Best vitelliform dystrophy. Color or pseudocolor and fundus autofluorescence images obtained with UWF provide previously unavailable information on the retinal periphery, which correlates well with visual field measurement or electroretinogram. Despite unavoidable artifacts of the UWF device, the feasibility of investigations in infants and in patients with poor fixation makes UWF imaging a precious resource in the diagnostic armamentarium for IRD.

Indexed as

Best vitelliform diseaseFundus autofluorescenceInherited retinal dystrophyRetinitis pigmentosaStargardt dystrophyUltra-widefield imaging

Identifiers

PMID32141037
PMCPMC7196101
OpenAlexW3009208587

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.