Efficacy and safety of subconjunctival bevacizumab for recurrent pterygium

Purpose: To evaluate the clinical outcome(s) and complication(s) of subconjunctival bevacizumab treatment in patients with recurrent pterygium. Methods: This prospective case series included patients who had undergone pterygium surgery and were diagnosed with recurrent pterygium. All patients received one subconjunctival injection of 0.5 mL of bevacizumab (2.5 mg/0.1 mL). The main outcome was the change in size and clinical appearance. The clinical appearance of the pterygium was graded according to Tan and colleagues. The horizontal size of the pterygium (from limbus to apex) was recorded from baseline to 2 months after injection. Treatment-related complications and adverse events were reported. Results: We included 36 eyes of 36 patients (18 males) with a mean age of 58.75 ± 10.98 years. Totally, 30.6% patients developed recurrent pterygium in both eyes (only the worst eye was treated), with 47.2% developing it in the left eye and 22.2% in the right eye. More than half the patients (58.3%) had a family history of pterygium. There was a significant difference in the size of pterygium at different intervals (P<0.05). Approximately two-thirds (66.7%) of patients presented with hyposphagma on the 2nd day after subconjunctival application; this value decreased to 30.6% by day 7 and to 0% at 1 month. Most patients (69.4%) exhibited amelioration of irritative symptoms within 2 days, 88.9% after 7 days, and 97.2% after 1 month. Conclusions: Subconjunctival bevacizumab injection is useful for the management of patients with recurrent pterygium, with no significant local or systemic adverse effects.

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Main Authors: Stival,Larissa Rossana Souza, Lago,Anelise Medeiros, Figueiredo,Marisa Novaes Falleiro Chaves de, Bittar,Ricardo Henrique Goulart, Machado,Márcia Leite, Nassaralla Junior,João Jorge
Format: Digital revista
Language:English
Published: Conselho Brasileiro de Oftalmologia 2014
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492014000100004
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spelling oai:scielo:S0004-274920140001000042014-07-22Efficacy and safety of subconjunctival bevacizumab for recurrent pterygiumStival,Larissa Rossana SouzaLago,Anelise MedeirosFigueiredo,Marisa Novaes Falleiro Chaves deBittar,Ricardo Henrique GoulartMachado,Márcia LeiteNassaralla Junior,João Jorge Pterygium Recurrence Antibodies, monoclonal/therapeutic use Angiogenesis inhibitors/administration &amp; dosage Injections Purpose: To evaluate the clinical outcome(s) and complication(s) of subconjunctival bevacizumab treatment in patients with recurrent pterygium. Methods: This prospective case series included patients who had undergone pterygium surgery and were diagnosed with recurrent pterygium. All patients received one subconjunctival injection of 0.5 mL of bevacizumab (2.5 mg/0.1 mL). The main outcome was the change in size and clinical appearance. The clinical appearance of the pterygium was graded according to Tan and colleagues. The horizontal size of the pterygium (from limbus to apex) was recorded from baseline to 2 months after injection. Treatment-related complications and adverse events were reported. Results: We included 36 eyes of 36 patients (18 males) with a mean age of 58.75 ± 10.98 years. Totally, 30.6% patients developed recurrent pterygium in both eyes (only the worst eye was treated), with 47.2% developing it in the left eye and 22.2% in the right eye. More than half the patients (58.3%) had a family history of pterygium. There was a significant difference in the size of pterygium at different intervals (P<0.05). Approximately two-thirds (66.7%) of patients presented with hyposphagma on the 2nd day after subconjunctival application; this value decreased to 30.6% by day 7 and to 0% at 1 month. Most patients (69.4%) exhibited amelioration of irritative symptoms within 2 days, 88.9% after 7 days, and 97.2% after 1 month. Conclusions: Subconjunctival bevacizumab injection is useful for the management of patients with recurrent pterygium, with no significant local or systemic adverse effects. info:eu-repo/semantics/openAccessConselho Brasileiro de OftalmologiaArquivos Brasileiros de Oftalmologia v.77 n.1 20142014-02-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492014000100004en10.5935/0004-2749.20140003
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libraryname SciELO
language English
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author Stival,Larissa Rossana Souza
Lago,Anelise Medeiros
Figueiredo,Marisa Novaes Falleiro Chaves de
Bittar,Ricardo Henrique Goulart
Machado,Márcia Leite
Nassaralla Junior,João Jorge
spellingShingle Stival,Larissa Rossana Souza
Lago,Anelise Medeiros
Figueiredo,Marisa Novaes Falleiro Chaves de
Bittar,Ricardo Henrique Goulart
Machado,Márcia Leite
Nassaralla Junior,João Jorge
Efficacy and safety of subconjunctival bevacizumab for recurrent pterygium
author_facet Stival,Larissa Rossana Souza
Lago,Anelise Medeiros
Figueiredo,Marisa Novaes Falleiro Chaves de
Bittar,Ricardo Henrique Goulart
Machado,Márcia Leite
Nassaralla Junior,João Jorge
author_sort Stival,Larissa Rossana Souza
title Efficacy and safety of subconjunctival bevacizumab for recurrent pterygium
title_short Efficacy and safety of subconjunctival bevacizumab for recurrent pterygium
title_full Efficacy and safety of subconjunctival bevacizumab for recurrent pterygium
title_fullStr Efficacy and safety of subconjunctival bevacizumab for recurrent pterygium
title_full_unstemmed Efficacy and safety of subconjunctival bevacizumab for recurrent pterygium
title_sort efficacy and safety of subconjunctival bevacizumab for recurrent pterygium
description Purpose: To evaluate the clinical outcome(s) and complication(s) of subconjunctival bevacizumab treatment in patients with recurrent pterygium. Methods: This prospective case series included patients who had undergone pterygium surgery and were diagnosed with recurrent pterygium. All patients received one subconjunctival injection of 0.5 mL of bevacizumab (2.5 mg/0.1 mL). The main outcome was the change in size and clinical appearance. The clinical appearance of the pterygium was graded according to Tan and colleagues. The horizontal size of the pterygium (from limbus to apex) was recorded from baseline to 2 months after injection. Treatment-related complications and adverse events were reported. Results: We included 36 eyes of 36 patients (18 males) with a mean age of 58.75 ± 10.98 years. Totally, 30.6% patients developed recurrent pterygium in both eyes (only the worst eye was treated), with 47.2% developing it in the left eye and 22.2% in the right eye. More than half the patients (58.3%) had a family history of pterygium. There was a significant difference in the size of pterygium at different intervals (P<0.05). Approximately two-thirds (66.7%) of patients presented with hyposphagma on the 2nd day after subconjunctival application; this value decreased to 30.6% by day 7 and to 0% at 1 month. Most patients (69.4%) exhibited amelioration of irritative symptoms within 2 days, 88.9% after 7 days, and 97.2% after 1 month. Conclusions: Subconjunctival bevacizumab injection is useful for the management of patients with recurrent pterygium, with no significant local or systemic adverse effects.
publisher Conselho Brasileiro de Oftalmologia
publishDate 2014
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0004-27492014000100004
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