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Bevacizumab treatment of macular edema in CRVO and BRVO: long-term follow-up. (BERVOLT study: Bevacizumab for RVO long-term follow-up).
Kornhauser, Tom; Schwartz, Roy; Goldstein, Michaella; Neudorfer, Meira; Loewenstein, Anat; Barak, Adiel.
Afiliación
  • Kornhauser T; Department of Ophthalmology, The Soroka University Medical Center, Ben Gurion University of the Negev, Beer Sheva, Israel. tomchook@gmail.com.
  • Schwartz R; Tel Aviv Sourasky Medical Center and The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Goldstein M; Tel Aviv Sourasky Medical Center and The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Neudorfer M; Tel Aviv Sourasky Medical Center and The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Loewenstein A; Tel Aviv Sourasky Medical Center and The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
  • Barak A; Tel Aviv Sourasky Medical Center and The Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Graefes Arch Clin Exp Ophthalmol ; 254(5): 835-44, 2016 May.
Article en En | MEDLINE | ID: mdl-26269374
ABSTRACT

PURPOSE:

To assess the efficacy and safety of intraocular injections of bevacizumab in patients with macular edema (ME) following branch retinal vein occlusion (BRVO) and central retinal vein occlusion (CRVO).

METHODS:

Retrospective, non-comparative case series. Patients ≥18 years of age with ME secondary to BRVO or CRVO who received a minimum of one intravitreal injection of bevacizumab with a follow-up >3 months were included. Primary endpoints were mean change in best corrected visual acuity (BCVA) from baseline to 12 and 24 months, and mean change in central macular thickness (CMT) after 3 injections. Secondary endpoints were mean change in BCVA and CMT from baseline to end of follow-up, number of injections, and ocular adverse events.

RESULTS:

Eighty-seven eyes with BRVO and 65 eyes with CRVO were included. Mean follow-up time was 24.4 and 26.1 months in the BRVO and CRVO groups, respectively. The mean change in BCVA was 0.25 LogMAR in the BRVO group and -0.118 LogMAR in the CRVO group.

CONCLUSION:

Visual acuity outcomes in the CRVO group were poorer, especially in patients with low baseline BCVA.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oclusión de la Vena Retiniana / Edema Macular / Inhibidores de la Angiogénesis / Bevacizumab Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Graefes Arch Clin Exp Ophthalmol Año: 2016 Tipo del documento: Article País de afiliación: Israel

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Oclusión de la Vena Retiniana / Edema Macular / Inhibidores de la Angiogénesis / Bevacizumab Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies Límite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Graefes Arch Clin Exp Ophthalmol Año: 2016 Tipo del documento: Article País de afiliación: Israel