Evidence map›Paper›PMID 39306616›Full record

ArticleEye (London, England)2024

Fight Retinal Blindness SPAIN. Report 3: clinical outcomes of vascular endothelial growth factor inhibitors in low vision eyes with neovascular age-related macular degeneration. A national database study.

Martín Puzo, Pilar Calvo-Perez, Francisco Bartol-Puyal, Jorge Sanchez-Monroy, Ruben Martin-Pinardel, Alba Parrado-Carrillo, Aina Moll-Udina, Carolina Bernal-Morales, Laura Sanchez-Vela, Laura Sararols-Ramsay and 16 more

Abstract readMulticenter Study
In one paragraph

Article in Eye (London, England), 2024. 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
–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

4 citing papers in PubMed.

  1. Article
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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

26 authors.

Martín Puzo *Miguel Servet Ophthalmology Research Group (GIMSO), Miguel Servet University Hospital, Aragón Institute for Health Research (IIS-Aragón), Universidad de Zaragoza, Zaragoza, Spain. martinpuzo@hotmail.com.ORCID http://orcid.org/0000-0002-5048-4846
Pilar Calvo-Perez *Miguel Servet Ophthalmology Research Group (GIMSO), Miguel Servet University Hospital, Aragón Institute for Health Research (IIS-Aragón), Universidad de Zaragoza, Zaragoza, Spain.
Francisco Bartol-PuyalMiguel Servet Ophthalmology Research Group (GIMSO), Miguel Servet University Hospital, Aragón Institute for Health Research (IIS-Aragón), Universidad de Zaragoza, Zaragoza, Spain.ORCID http://orcid.org/0000-0002-4476-6003
Jorge Sanchez-MonroyMiguel Servet Ophthalmology Research Group (GIMSO), Miguel Servet University Hospital, Aragón Institute for Health Research (IIS-Aragón), Universidad de Zaragoza, Zaragoza, Spain.ORCID http://orcid.org/0000-0001-5743-1520
Ruben Martin-PinardelFundació de Recerca Clínic Barcelona-Institut de Investigacions Biomediques August Pi i Sunyer (FRCB-IDIBAPS), Barcelona, Spain.
Alba Parrado-CarrilloHospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.
Aina Moll-UdinaHospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.
Carolina Bernal-MoralesHospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.ORCID http://orcid.org/0000-0001-5469-3963
Laura Sanchez-VelaHospital Universitari Vall de Hebrón, Barcelona, Spain.
Laura Sararols-RamsayFundació Privada Hospital Asil Granollers, Granollers, Spain.
Gonzaga Garay-AramburuOSI Araba, Vitoria-Gasteiz, Spain.ORCID http://orcid.org/0000-0001-5255-8426
Carolina ArruabarrenaHospital Universitario Principe de Asturias, Madrid, Spain.ORCID http://orcid.org/0000-0002-5312-8900
José García-ArumíHospital Universitari Vall de Hebrón, Barcelona, Spain.
Maximino AbraldesHospital de Conxo, Santiago de Compostela, Spain.
José María Ruiz-MorenoHospital Universitario Puerta del Hierro, Madrid, Spain.ORCID http://orcid.org/0000-0001-9636-0788
Xavier ValldeperasHospital Universitari Germans Trias i Pujol, Badalona, Spain.
Daniel Velázquez-VilloriaClínica Villoria, Pontevedra, Spain.ORCID http://orcid.org/0000-0002-8677-6859
José Juan Escobar-BarrancoHospital Dos de Maig, Barcelona, Spain.
Roberto Gallego-PinazoOftalvist Valencia, Valencia, Spain.
Marta S FigueroaHospital Universitario Ramon y Cajal, Madrid, Spain.
Marc Figueras-RocaHospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.
Daniel BarthelmesUniversity Hospital Zurich, University of Zurich, Zurich, Switzerland.
Mark C GilliesSave Sight Institute, Sydney Medical School, University of Sydney, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0001-8580-0274
Ricardo P Casaroli-MaranoHospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.
Javier Zarranz-VenturaHospital Clínic de Barcelona, Universitat de Barcelona, Barcelona, Spain.ORCID http://orcid.org/0000-0003-2338-8143
from the writing committee of the Fight Retinal Blindness Spain (FRB! Spain) Users Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo compare visual outcomes for low vision eyes (LVE) (<35 letters LogMAR or <20/200 Snellen) versus non-low vision eyes (NLVE) (>35 letters LogMAR or >20/200 Snellen) at the time of the first injection in a clinical practice setting.

methodsSubgroup analysis of a multicenter national database of treatment- naïve eyes neovascular age related macular degeneration (nAMD) treated with anti-VEGF intravitreal injections divided into LVE and NLVE. Demographics, visual acuity (VA) at baseline and subsequent timepoints (12, 24, and 36 months), number of injections and visits data were collected using a validated web-based tool (Fight Retinal Blindness!).

results3138 eyes were included, 705 LVE and 2433 NLVE. The LVE group had the greatest VA gain (p < 0.001), at 12, 24, and 36 months (+15, +15, and +13 letters respectively). The proportion of patients with VA loss (-5 letters) differed between groups at 12, 24, and 36 and was significantly greater (p < 0.001) in NLVE. The proportion of patients with VA gain (+5 letters) was significantly higher (p < 0.001) in LVE in all timeframes. The proportions of LVE that still had VA ≤ 35 letters at 12, 24, and 36 months were 54%, 54%, and 57%. Conversely, 8%, 9%, and 8% of LVE achieved VA ≥ 70 letters at 12, 24, and 36 months. LVE received fewer intravitreal injections than NLVE throughout follow-up (6, 9, 12 vs 7, 11, 15).

conclusionFindings of this study support the need for ongoing therapy in patients with initial visual acuity less than 35 letters since sustained visual improvements can be achieved and maintained for the first 3 years of treatment.

Indexed as

Angiogenesis InhibitorsDatabases, FactualIntravitreal InjectionsRanibizumabVascular Endothelial Growth Factor AVision, LowVisual AcuityWet Macular DegenerationAgedAged, 80 and overBevacizumabFemaleHumansMaleReceptors, Vascular Endothelial Growth FactorRetrospective StudiesAngiogenesis InhibitorsBevacizumabRanibizumabReceptors, Vascular Endothelial Growth FactorVascular Endothelial Growth Factor AVEGFA protein, human

Identifiers

PMID39306616
PMCPMC11621359

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.