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Plasma Rich in Growth Factors as an Adjuvant Agent in Non-Penetrating Deep Sclerectomy.
Rodríguez-Calvo, Pedro P; Rodríguez-Uña, Ignacio; Fernández-Vega-Cueto, Andrés; Sánchez-Ávila, Ronald M; Anitua, Eduardo; Merayo-Lloves, Jesús.
Afiliação
  • Rodríguez-Calvo PP; Instituto Universitario Fernandez-Vega, Fundación de Investigación Oftalmológica, University of Oviedo, 33012 Oviedo, Spain.
  • Rodríguez-Uña I; Instituto de Investigación Sanitaria del Principado de Asturias, 33011 Oviedo, Spain.
  • Fernández-Vega-Cueto A; Instituto Universitario Fernandez-Vega, Fundación de Investigación Oftalmológica, University of Oviedo, 33012 Oviedo, Spain.
  • Sánchez-Ávila RM; Instituto de Investigación Sanitaria del Principado de Asturias, 33011 Oviedo, Spain.
  • Anitua E; Instituto Universitario Fernandez-Vega, Fundación de Investigación Oftalmológica, University of Oviedo, 33012 Oviedo, Spain.
  • Merayo-Lloves J; Instituto de Investigación Sanitaria del Principado de Asturias, 33011 Oviedo, Spain.
J Clin Med ; 12(10)2023 May 22.
Article em En | MEDLINE | ID: mdl-37240710
ABSTRACT

BACKGROUND:

The purpose of this study is to evaluate the utility and safety of plasma rich in growth factors immunosafe eye drops (is-ePRGF) in the postoperative treatment of non-penetrating deep sclerectomy (NPDS).

METHODS:

This is a case-control study in patients with open-angle glaucoma. Group one (control) was not treated with is-ePRGF, while group two (is-ePRGF) was treated (four times a day for four months). Postoperative evaluations were performed at one day, one month, three months and six months. The main outcomes were intraocular pressure (IOP), microcysts in blebs with AS-OCT and the number of hypotensive eye drops.

RESULTS:

Preoperatively, group one (n = 48 eyes) and group two (n = 47 eyes) were similar in age (71.5 ± 10.7 vs. 70.9 ± 10.0 years; p = 0.68), IOP (20.6 ± 10.2 vs. 23.0 ± 9.0 mmHg; p = 0.26) and number of hypotensive drugs (2.7 ± 0.8 vs. 2.8 ± 0.9; p = 0.40). The IOP at six months dropped to 15.0 ± 8.0 mmHg (IOP reduction -27.2%) and 10.9 ± 4.3 mmHg (IOP reduction -52.6%) for group one and group two, respectively (p < 0.01). At six months, blebs with microcysts were 62.5% (group one) and 76.7% (group two). Postoperative complications were observed in 12 eyes (25%) for group one and in 5 eyes (11%) for group two (p = 0.06). No specific complications related to the use of is-ePRGF were identified.

CONCLUSIONS:

Topical is-ePRGF seems to reduce IOP and the rate of complications in the medium term after NPDS, so it can be considered as a possible safe adjuvant to achieve surgical success.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article