Intravitreal Ziv-Aflibercept for Diabetic Macular Edema : 48-Week Outcomes

Copyright 2018, SLACK Incorporated.

Détails bibliographiques
Publié dans:Ophthalmic surgery, lasers & imaging retina. - 2013. - 49(2018), 4 vom: 01. Apr., Seite 245-250
Auteur principal: de Andrade, Gabriel Costa (Auteur)
Autres auteurs: de Oliveira Dias, João Rafael, Maia, André, Farah, Michel Eid, Meyer, Carsten H, Rodrigues, Eduardo Buchele
Format: Article en ligne
Langue:English
Publié: 2018
Accès à la collection:Ophthalmic surgery, lasers & imaging retina
Sujets:Clinical Trial Journal Article Research Support, Non-U.S. Gov't Recombinant Fusion Proteins aflibercept 15C2VL427D Receptors, Vascular Endothelial Growth Factor EC 2.7.10.1
Description
Résumé:Copyright 2018, SLACK Incorporated.
BACKGROUND AND OBJECTIVE: To study the safety and efficacy of intravitreal injections of ziv-aflibercept (IVI-ZA) (Zaltrap; Sanofi-Aventis and Regeneron Pharmaceuticals, Tarrytown, NY) during a period of 48 weeks in patients with diabetic macular edema (DME)
PATIENTS AND METHODS: Seven consecutive patients with DME were enrolled and submitted to 12 consecutive IVI-ZA with a 4-week interval. The safety parameters included changes in full-field electroretinogram (ERG) and systemic or ocular complications, and the efficacy parameters were the mean change from baseline in best-corrected visual acuity (BCVA) and central retinal thickness (CRT)
RESULTS: No significant differences were found in any ERG component after IVI-ZA, and no systemic or ocular complication was observed. The improvement of BCVA was most significant after the first IVI-ZA and remained until week 48 (P < .05). The CRT significantly decreased during the course of 48 weeks
CONCLUSION: The 48-week results are consistent with our previous 24-week findings, supporting IVI-ZA as a safe, efficient, and well-tolerated therapy for patients with DME. [Ophthalmic Surg Lasers Imaging Retina. 2018;49:245-250.]
Description:Date Completed 11.03.2019
Date Revised 11.03.2019
published: Print
Citation Status MEDLINE
ISSN:2325-8179
DOI:10.3928/23258160-20180329-06