Evidence map›Paper›PMID 35206485›Full record

ArticleInternational journal of environmental research and public health2022

The Effectiveness of Brolucizumab and Aflibercept in Patients with Neovascular Age-Related Macular Degeneration.

Magdalena Musiał-Kopiejka, Katarzyna Polanowska, Dariusz Dobrowolski, Katarzyna Krysik, Edward Wylęgała, Beniamin Oskar Grabarek, Anita Lyssek-Boroń

Open access · goldAbstract read
In one paragraph

Article in International journal of environmental research and public health, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
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  5. Escherichia coli in the production of biopharmaceuticals.Biotechnology and applied biochemistry · 2025
    Review
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  7. Article
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  9. Article
  10. Interaction of High-Molecular Weight Fucoidan fromInternational journal of molecular sciences · 2023
    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

7 authors at 2 institutions in 1 country.

Magdalena Musiał-KopiejkaTrauma Centre, Department of Ophthalmology, St. Barbara Hospital, 41-200 Sosnowiec, Poland.
Katarzyna PolanowskaTrauma Centre, Department of Ophthalmology, St. Barbara Hospital, 41-200 Sosnowiec, Poland.
Dariusz DobrowolskiTrauma Centre, Department of Ophthalmology, St. Barbara Hospital, 41-200 Sosnowiec, Poland.ORCID 0000-0002-8768-1691
Katarzyna KrysikTrauma Centre, Department of Ophthalmology, St. Barbara Hospital, 41-200 Sosnowiec, Poland.ORCID 0000-0001-9737-5391
Edward WylęgałaChair and Clinical Department of Ophthalmology, Division of Medical Science in Zabrze, Medical University of Silesia in Katowice, 40-760 Katowice, Poland.ORCID 0000-0002-6707-5790
Beniamin Oskar GrabarekDepartment of Histology, Cytophysiology and Embryology, Faculty of Medicine, University of Technology, Academy of Silesia in Katowice, 41-800 Zabrze, Poland.ORCID 0000-0003-1633-7145
Anita Lyssek-BorońTrauma Centre, Department of Ophthalmology, St. Barbara Hospital, 41-200 Sosnowiec, Poland.ORCID 0000-0003-4405-8020
Instytut Kolejnictwa · PLUniversity of Silesia in Katowice · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is a progressive, chronic disease of the central area of the retina, which, if untreated, leads to blindness. This study aimed to compare the effectiveness of therapy using anti-VEGF drugs, namely brolucizumab and aflibercept, in patients with neovascular AMD (nAMD) during a monitoring period lasting around 20 weeks. The analysis consisted of 40 patients diagnosed with neovascular age-related macular degeneration, with 20 patients receiving aflibercept (Eylea, Bayer) at a dose of 2 mg/50 µL into the vitreous chamber at the following intervals-3 doses, 4 weeks apart, followed by a fourth dose after 8 weeks. The remaining 20 patients received brolucizumab (Beovu, Novartis) at a dose of 6 mg/50 µL, administered in the following schedule-3 initial doses, 4 weeks apart, with the administration of a fourth dose decided for each patient individually by the doctor, depending on disease activity, assessed through imaging tests. To evaluate treatment effectiveness, the following measurements were used: 'read distance and near visual acuity' for each eye separately using the Snellen chart; and non-invasive retinal imaging techniques-optical coherence tomography (OCT) and OCT angiography (OCTA). In patients treated using brolucizumab, during the observation period, statistically significant differences were found in the following parameters: flow area (

Indexed as

Angiogenesis InhibitorsWet Macular DegenerationAntibodies, Monoclonal, HumanizedFollow-Up StudiesHumansInfantReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsTreatment OutcomeVascular Endothelial Growth Factor AVisual AcuityafliberceptAngiogenesis InhibitorsAntibodies, Monoclonal, HumanizedbrolucizumabReceptors, Vascular Endothelial Growth FactorRecombinant Fusion ProteinsVascular Endothelial Growth Factor Aafliberceptage-related macular degenerationbrolucizumabchoroidal neovascularizationflow areaFOVEAneovascular age-related macular degenerationretinal pigment epitheliumselect areaVEGFvisus

Identifiers

PMID35206485
PMCPMC8872595
OpenAlexW4213107959

What OpenQuestion holds

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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.