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Comparisons of One to Three Monthly Injections of Aflibercept for Diabetic Macular Edema by Practical Protocol.
Hayashi, Yuko; Tatsumi, Tomoaki; Oshitari, Toshiyuki; Kaiho, Tomomi; Takatsuna, Yoko; Arai, Miyuki; Baba, Takayuki; Yamamoto, Shuichi.
Afiliação
  • Hayashi Y; Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Tatsumi T; Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Oshitari T; Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Kaiho T; Department of Ophthalmology, International University of Health and Welfare, Narita, Japan.
  • Takatsuna Y; Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Arai M; Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Baba T; Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chiba, Japan.
  • Yamamoto S; Department of Ophthalmology and Visual Science, Chiba University Graduate School of Medicine, Chiba, Japan.
J Diabetes Res ; 2021: 1374891, 2021.
Article em En | MEDLINE | ID: mdl-33628832
ABSTRACT
The purpose of this study was to compare the efficacies of one initial intravitreal injection of aflibercept followed by a pro re nata (PRN; 1+PRN) regimen to those of three consecutive monthly injections followed by the PRN (3+PRN) regimen for diabetic macular edema (DME) with practical protocols. The medical records of 95 eyes of 71 cases that were diagnosed with DME and had received intravitreal aflibercept (IVA) injections were reviewed. Fifty-seven eyes had received IVA with the 1+PRN regimen, and 38 eyes had received IVA with the 3+PRN regimen. The best-corrected visual acuity (BCVA) and the central macular thickness (CMT) were measured at the baseline and at 1, 3, 6, and 12 months after the IVA. The mean number of injections of the 1+PRN group was 2.9 ± 1.7, which was significantly fewer than that of the 3+PRN group at 4.6 ± 1.4 (P < 0.001). The change of the mean BCVA before and after the IVA at 12 months of the 3+PRN group was -0.14 ± 0.17 logMAR units which was significantly better than that of the 1+PRN group of -0.045 ± 0.25 logMAR units (P = 0.02). The change of the CMT before and after the IVA at 6 months of the 3+PRN group was -141.3 ± 152.4 µm which was significantly more than that of the 1+PRN group at -86.1 ± 117.8 µm (P = 0.013). Although the mean number of injections was more than that in the 1+PRN regimen, the 3+PRN regimen had better visual outcomes at 12 months. In a practical protocol, we recommend the 3+PRN regimen for patients with DME (IRB#3541).
Assuntos

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes de Fusão / Edema Macular / Inibidores da Angiogênese / Receptores de Fatores de Crescimento do Endotélio Vascular / Retinopatia Diabética / Macula Lutea Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Diabetes Res Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Temas: Geral Base de dados: MEDLINE Assunto principal: Proteínas Recombinantes de Fusão / Edema Macular / Inibidores da Angiogênese / Receptores de Fatores de Crescimento do Endotélio Vascular / Retinopatia Diabética / Macula Lutea Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies Limite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: J Diabetes Res Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Japão