Laser versus Anti-VEGF: A Paradigm Shift for Treatment-Warranted Retinopathy of Prematurity
- PMID: 37337024
- PMCID: PMC10442041
- DOI: 10.1007/s40123-023-00744-7
Laser versus Anti-VEGF: A Paradigm Shift for Treatment-Warranted Retinopathy of Prematurity
Abstract
Retinopathy of prematurity (ROP), a leading cause of childhood blindness, has historically been associated with blindness from overgrowth of blood vessels from the retina into the vitreous that lead to complex retinal detachments. Our understanding of ROP has evolved with the survival of extremely low-birthweight infants and includes not only overgrowth of blood vessels, but also insufficient developmental retinal vascular growth in early phases of the disease. Our current treatments of ROP have focused on methods to improve perinatal and prenatal care, reduce premature birth, and prevent early phases of ROP. Nonetheless, addressing vasoproliferation in treatment-warranted eyes remains the mainstay of management. Two main treatment strategies co-exist today: laser treatment, which has been the standard of care since the 1990s, and anti-VEGF injections, which have been used since early reports in 2007 (Travassos et al. in Ophthalmic Surg Lasers Imaging, 38:233-237, https://doi.org/10.3928/15428877-20070501-09 , 2007, Shah et al. in Indian J Ophthalmol 55:75-76, https://doi.org/10.4103/0301-4738.29505 , 2007, Quiroz-Mercado et al. in Semin Ophthalmol 22:109-125, https://doi.org/10.1080/08820530701420082 , 2007).
Keywords: Anti-VEGF; Laser; ROP; Retinopathy of prematurity; Vitreoretinal surgery.
© 2023. The Author(s).
Conflict of interest statement
Mary Elizabeth Hartnett is PI for NEI/NIH support for R01EY107011 and R01EY105130, R21EY033579 and receives partial salary support. She receives departmental support from Research to Prevent Blindness. Mary Elizabeth Hartnett serves on the Scientific Advisory Boards for nonprofit Knights Templar Eye Foundation, and as chair of the Macula Society and the Jack McGovern Coats’ Disease Foundation. Mary Elizabeth Hartnett’s institution received financial support for the Regeneron BUTTERFLEYE study for IRB development. Otherwise there is no support from commercial sponsors. Andreas Stahl is a Speaker for Allergan, Bayer, and Novartis and is on the following Scientific advisory boards: Bayer, Novartis, and Roche. Andreas Stahl receives Research grants from Bayer and Novartis and performs Clinical trials for Bayer and Novartis. Andreas Stahl is on the Board of Directors: SemaThera Inc.
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