Evidence map›Paper›PMID 38667534›Full record

ArticleDiseases (Basel, Switzerland)2024

Efficacy and Safety of Plasma Rich in Growth Factor in Patients with Congenital Aniridia and Dry Eye Disease.

Javier Lozano-Sanroma, Alberto Barros, Ignacio Alcalde, Rosa Alvarado-Villacorta, Ronald M Sánchez-Ávila, Juan Queiruga-Piñeiro, Luis Fernández-Vega-Cueto, Eduardo Anitua, Jesús Merayo-Lloves

Abstract read
In one paragraph

Article in Diseases (Basel, Switzerland), 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. Blood Derivatives in the Therapy of Ocular Surface Diseases.International journal of molecular sciences · 2025
    Review
  2. Article
  3. Article
  4. Review
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

9 authors.

Javier Lozano-SanromaInstituto Universitario Fernández-Vega, Fundación de Investigación Oftalmológica, 33012 Oviedo, Spain.ORCID 0000-0001-5306-1921
Alberto BarrosInstituto Universitario Fernández-Vega, Fundación de Investigación Oftalmológica, 33012 Oviedo, Spain.ORCID 0000-0002-4976-3792
Ignacio AlcaldeInstituto Universitario Fernández-Vega, Fundación de Investigación Oftalmológica, 33012 Oviedo, Spain.ORCID 0000-0001-6051-9240
Rosa Alvarado-VillacortaInstituto Universitario Fernández-Vega, Fundación de Investigación Oftalmológica, 33012 Oviedo, Spain.ORCID 0000-0003-1885-2335
Ronald M Sánchez-ÁvilaRegenerative Medicine Laboratory, Biotechnology Institute (BTI), 01007 Vitoria, Spain.
Juan Queiruga-PiñeiroInstituto Universitario Fernández-Vega, Fundación de Investigación Oftalmológica, 33012 Oviedo, Spain.ORCID 0000-0002-4009-7228
Luis Fernández-Vega-CuetoInstituto Universitario Fernández-Vega, Fundación de Investigación Oftalmológica, 33012 Oviedo, Spain.
Eduardo AnituaRegenerative Medicine Laboratory, Biotechnology Institute (BTI), 01007 Vitoria, Spain.ORCID 0000-0002-8386-5303
Jesús Merayo-LlovesInstituto Universitario Fernández-Vega, Fundación de Investigación Oftalmológica, 33012 Oviedo, Spain.ORCID 0000-0003-3740-3754

Funding

Asociación Española de Aniridia AEA-FIO-010322Fundación de Investigación Oftalmológica FIO-24001Fundación Eduardo Anitua BTI23002Instituto de Salud Carlos III FISS-21-RD21/0002/0041
6 · The paper itself

Abstract

Congenital aniridia is a rare bilateral ocular malformation characterized by the partial or complete absence of the iris and is frequently associated with various anomalies, including keratopathy, cataract, glaucoma, and foveal and optic nerve hypoplasia. Additionally, nearly 50% of individuals with congenital aniridia experience symptoms of ocular dryness. Traditional treatment encompasses artificial tears and autologous serum. This study aimed to assess the effectiveness and safety of using platelet rich in growth factors (PRGF) plasma in patients with congenital aniridia and ocular dryness symptoms.

methodsThe included patients underwent two cycles of a 3-month PRGF treatment. At 6 months, symptomatology was evaluated using the OSDI and SANDE questionnaires, and ocular surface parameters were analyzed.

resultsThe OSDI and SANDE values for frequency and severity demonstrated statistically significant improvements (

conclusionThe use of PRGF in patients with congenital aniridia and ocular dryness symptoms led to significant improvements in symptomatology, ocular redness, and ocular damage. No adverse effects were observed during the use of PRGF.

Indexed as

congenital aniridiaDEDocular rednessplasma rich in growth factorsPRGF

Identifiers

PMID38667534
PMCPMC11048876

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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.