Evidence map›Paper›PMID 41303411›Full record

ArticleInternational journal of molecular sciences2025

Evaluation of the Duration of Good Visual Acuity During Anti-VEGF Therapy for Age-Related Macular Degeneration in Routine Clinical Practice.

Andrea Gyenes, Lilla István, András Papp, Miklós Resch, Zsuzsa Récsán, Mónika Ecsedy, Zsuzsanna Szepessy, Antal Szabó, Balázs Lesch, György Barcsay and 4 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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
–field-weighted citation impact
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.

  1. Special Issue: Molecular Mechanisms and Treatment of Retinal Diseases.International journal of molecular sciences · 2026
    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

14 authors.

Andrea GyenesDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Lilla IstvánDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
András PappDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Miklós ReschDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Zsuzsa RécsánDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Mónika EcsedyDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Zsuzsanna SzepessyDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Antal SzabóDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Balázs LeschDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
György BarcsayDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Ágnes BorbándyDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Gábor László SándorDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Zoltán Z NagyDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.
Illés KovácsDepartment of Ophthalmology, Semmelweis University, 1085 Budapest, Hungary.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to analyse data from a clinical database using a novel visual acuity parameter to determine whether anti-VEGF molecules that target multiple domains involved in neovascularisation are more likely to achieve good visual acuity than agents that solely inhibit VEGF. This retrospective study analysed data from patients treated with anti-VEGF injections between 2015 and 2023. We set an ETDRS score threshold of 70 (equivalent to 20/40 Snellen acuity) to calculate 'time in range' (TIR). TIR is defined as 'time spent with best-corrected visual acuity (BCVA) better than 20/40' and can highlight significant variations in the time individuals spend above the threshold during their AMD treatment. Over nine years, 30,209 aflibercept and 10,876 ranibizumab injections were administered to 6043 patients. Patients received an average of 6.8 injections. The mean BCVA at the first injection was 57.00 ± 16.15 ETDRS letters for ranibizumab patients and 58.75 ± 15.82 for aflibercept patients, with a statistically significant difference (

Indexed as

Angiogenesis InhibitorsMacular DegenerationRanibizumabRecombinant Fusion ProteinsVascular Endothelial Growth Factor AVisual AcuityAgedAged, 80 and overFemaleHumansIntravitreal InjectionsMaleMiddle AgedReceptors, Vascular Endothelial Growth FactorRetrospective StudiesTreatment OutcomeafliberceptAngiogenesis InhibitorsRanibizumabReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsVascular Endothelial Growth Factor Aafliberceptanti-VEGFnAMDranibizumabthreshold‘time in range’

Identifiers

PMID41303411
PMCPMC12652666

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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.