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Secondary glaucoma after bevacizumab injection in Type-1 retinopathy of prematurity.
Jones, Anthony A; Martin, Jacob S; Giangiacomo, Annette L; Costakos, Deborah M.
Afiliação
  • Jones AA; Department of Ophthalmology, Medical College of Wisconsin, 8701 W Watertown Plank Rd, Milwaukee, WI 53226, USA.
  • Martin JS; Department of Pediatric Ophthalmology, Children's Hospital Milwaukee, 8915 W Connell Ct, Milwaukee, WI 53226, USA.
  • Giangiacomo AL; Department of Ophthalmology, Medical College of Wisconsin, 8701 W Watertown Plank Rd, Milwaukee, WI 53226, USA.
  • Costakos DM; Department of Pediatric Ophthalmology, Children's Hospital Milwaukee, 8915 W Connell Ct, Milwaukee, WI 53226, USA.
Am J Ophthalmol Case Rep ; 36: 102131, 2024 Dec.
Article em En | MEDLINE | ID: mdl-39161378
ABSTRACT

Purpose:

The authors report three separate cases of type 1 retinopathy of prematurity (ROP) treated with intravitreal bevacizumab before, or at 34 weeks postmenstrual age (PMA), with subsequent development of secondary glaucoma. Observations All three cases involve patients born ≤24 weeks and meeting the American Academy of Pediatrics criteria for ROP screening. Prior to treatment, each patient was noted to have normal anterior chamber structures with no signs of glaucoma. Each patient developed type 1 ROP and was treated with intravitreal bevacizumab, which was administered at or before 34 weeks PMA. Following the administration of intravitreal anti-vascular endothelial growth factor (VEGF), each patient developed a suspected open-angle glaucoma (OAG) within an approximate 4-week time frame. In these cases, the presentation of glaucoma differed from those that have been previously reported in the literature. Conclusion and importance Based on similar timing of glaucoma development following intravitreal bevacizumab injections, we hypothesize that the administration of anti-VEGF agents to very premature infants (≤24 weeks) at or before 34 weeks PMA, may predispose them to the development of secondary glaucoma through an unknown and possibly novel pathway.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Ophthalmol Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Am J Ophthalmol Case Rep Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos