Evidence map›Paper›PMID 37634060›Full record

ArticleAnnals of medicine2023

Characterising the diagnosis of genetic maculopathies in a real-world private tertiary retinal practice in Australia: protocol for a retrospective clinical audit.

Alexis Ceecee Britten-Jones, Demi Markakis, Robyn H Guymer, Ming-Lee Lin, Simon Skalicky, Lauren N Ayton, Heather G Mack

Open access · goldAbstract read
In one paragraph

Article in Annals of medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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 at 2 institutions in 1 country.

Alexis Ceecee Britten-JonesOphthalmology, Department of Surgery, University of Melbourne, Melbourne, Australia.ORCID 0000-0002-1101-2870
Demi MarkakisCabrini Hospital, Malvern, Australia.ORCID 0000-0002-8266-3769
Robyn H GuymerOphthalmology, Department of Surgery, University of Melbourne, Melbourne, Australia.ORCID 0000-0002-9441-4356
Ming-Lee LinEye Surgery Associates, East Melbourne, Australia.
Simon SkalickyOphthalmology, Department of Surgery, University of Melbourne, Melbourne, Australia.ORCID 0000-0001-8022-8002
Lauren N AytonOphthalmology, Department of Surgery, University of Melbourne, Melbourne, Australia.ORCID 0000-0001-9907-084X
Heather G MackOphthalmology, Department of Surgery, University of Melbourne, Melbourne, Australia.ORCID 0000-0001-9756-1098
The University of Melbourne · AUCabrini Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAccurate diagnosis of macular atrophy is paramount to enable appropriate treatment when novel treatments for geographic atrophy and macular dystrophies become available. Genetic testing is useful in distinguishing between the two conditions but is not feasible for the majority of patients in real-world clinical practice. Therefore, we aimed to investigate the potential misdiagnosis of inherited macular dystrophy as age-related macular degeneration (AMD) in real-world ophthalmic practice to assist in the development of guidelines to improve diagnostic accuracy while minimizing genetic testing for targeted patients.

methodsRetrospective review of the medical records of patients diagnosed with AMD, which included imaging, between 1995 and 2023 from a large multidisciplinary private ophthalmic practice in Australia. We will use a stepwise method to screen for probable cases of macular dystrophy, followed by a consensus review by an expert panel. The outcomes are (1) to determine the potential misdiagnosis rate of macular dystrophy as atrophic AMD by retinal specialists and general ophthalmologists; (2) to identify clinical imaging modalities that are most useful for differentiating macular dystrophy from atrophic AMD; and (3) to establish preliminary guidance for clinicians to improve the diagnosis of macular atrophy from AMD in practice, and thereby target cost-efficient genetic testing. DISCUSSION: Improving the diagnostic accuracy of both AMD and macular dystrophy, while ensuring cost-efficient genetic testing, will improve the targeted treatment of macular diseases when emerging treatments become available.

Indexed as

Macular DegenerationAtrophyAustraliaClinical AuditHumansRetrospective StudiesAge-related macular degenerationfundus autofluorescenceinherited macular diseaseinherited retinal diseasemacular dystrophyretrospective clinical review

Identifiers

PMID37634060
PMCPMC10461509
OpenAlexW4386201160

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.