Subconjunctival Bevacizumab for Primary Pterygium Excision; a Randomized Clinical Trial

Purpose: To evaluate the safety of local bevacizumab and its effect on recurrence of primary pterygium excision. Methods: This randomized, placebo-controlled clinical trial was conducted on 44 eyes of 44 patients randomized to Group 1 (bevacizumab) and Group 2 (balanced salt solution). Group 1 unde...

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Main Authors: Mohammad-Reza Razeghinejad, Mohammad Banifatemi
Format: Article
Language:English
Published: Knowledge E 2014-01-01
Series:Journal of Ophthalmic & Vision Research
Subjects:
Online Access:http://www.jovr.org/article.asp?issn=2008-322X;year=2014;volume=9;issue=1;spage=22;epage=30;aulast=Razeghinejad
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author Mohammad-Reza Razeghinejad
Mohammad Banifatemi
author_facet Mohammad-Reza Razeghinejad
Mohammad Banifatemi
author_sort Mohammad-Reza Razeghinejad
collection DOAJ
description Purpose: To evaluate the safety of local bevacizumab and its effect on recurrence of primary pterygium excision. Methods: This randomized, placebo-controlled clinical trial was conducted on 44 eyes of 44 patients randomized to Group 1 (bevacizumab) and Group 2 (balanced salt solution). Group 1 underwent pterygium excision with a rotational conjunctival flap and received a total of 7.5 mg subconjunctival bevacizumab (5 mg/0.2 mL on the day of surgery and 2.5 mg/0.1 mL on the fourth day after surgery). Group 2 received balanced salt solution in the same manner. Recurrence, defined as any fibrovascular tissue crossing the limbus, and the number of patients with >1.5 mm fibrovascular overgrowth on the cornea were compared between the study groups. Results: There was no statistically significant difference between the study groups in terms of demographics, pterygium size, daily sun exposure, preoperative visual acuity, keratomeric readings, corneal astigmatism, or IOP (P>0.05). Three and four patients in each group at the three- and six-month visits, respectively, had more than 1.5 mm fibrovascular tissue overgrowth on the cornea (P=1 and 0.62, respectively). At the three-month visit, 3 patients in Group 1 versus 7 patients in Group 2 (P=0.13), and at the six-month visit 4 patients in Group 1 versus 8 patients in Group 2 (P=0.17) had fibrovascular tissue crossing the limbus. Patients in Group 1 experienced a statistically significant rise in IOP at the one-week visit (P=0.007). Conclusion: Bevacizumab had no significant effect on the recurrence rate of pterygium. Although the frequency of fibrovascular tissue crossing the limbus in the bevacizumab group was half that of the BSS group, the difference failed to reach a statistically significant level.
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spelling doaj.art-d276940492e64edab080e64269f650cc2022-12-22T02:44:06ZengKnowledge EJournal of Ophthalmic & Vision Research2008-322X2014-01-01912230Subconjunctival Bevacizumab for Primary Pterygium Excision; a Randomized Clinical TrialMohammad-Reza RazeghinejadMohammad BanifatemiPurpose: To evaluate the safety of local bevacizumab and its effect on recurrence of primary pterygium excision. Methods: This randomized, placebo-controlled clinical trial was conducted on 44 eyes of 44 patients randomized to Group 1 (bevacizumab) and Group 2 (balanced salt solution). Group 1 underwent pterygium excision with a rotational conjunctival flap and received a total of 7.5 mg subconjunctival bevacizumab (5 mg/0.2 mL on the day of surgery and 2.5 mg/0.1 mL on the fourth day after surgery). Group 2 received balanced salt solution in the same manner. Recurrence, defined as any fibrovascular tissue crossing the limbus, and the number of patients with >1.5 mm fibrovascular overgrowth on the cornea were compared between the study groups. Results: There was no statistically significant difference between the study groups in terms of demographics, pterygium size, daily sun exposure, preoperative visual acuity, keratomeric readings, corneal astigmatism, or IOP (P>0.05). Three and four patients in each group at the three- and six-month visits, respectively, had more than 1.5 mm fibrovascular tissue overgrowth on the cornea (P=1 and 0.62, respectively). At the three-month visit, 3 patients in Group 1 versus 7 patients in Group 2 (P=0.13), and at the six-month visit 4 patients in Group 1 versus 8 patients in Group 2 (P=0.17) had fibrovascular tissue crossing the limbus. Patients in Group 1 experienced a statistically significant rise in IOP at the one-week visit (P=0.007). Conclusion: Bevacizumab had no significant effect on the recurrence rate of pterygium. Although the frequency of fibrovascular tissue crossing the limbus in the bevacizumab group was half that of the BSS group, the difference failed to reach a statistically significant level.http://www.jovr.org/article.asp?issn=2008-322X;year=2014;volume=9;issue=1;spage=22;epage=30;aulast=RazeghinejadAngiogenesis; Bevacizumab; Pterygium; Pterygium Recurrence
spellingShingle Mohammad-Reza Razeghinejad
Mohammad Banifatemi
Subconjunctival Bevacizumab for Primary Pterygium Excision; a Randomized Clinical Trial
Journal of Ophthalmic & Vision Research
Angiogenesis; Bevacizumab; Pterygium; Pterygium Recurrence
title Subconjunctival Bevacizumab for Primary Pterygium Excision; a Randomized Clinical Trial
title_full Subconjunctival Bevacizumab for Primary Pterygium Excision; a Randomized Clinical Trial
title_fullStr Subconjunctival Bevacizumab for Primary Pterygium Excision; a Randomized Clinical Trial
title_full_unstemmed Subconjunctival Bevacizumab for Primary Pterygium Excision; a Randomized Clinical Trial
title_short Subconjunctival Bevacizumab for Primary Pterygium Excision; a Randomized Clinical Trial
title_sort subconjunctival bevacizumab for primary pterygium excision a randomized clinical trial
topic Angiogenesis; Bevacizumab; Pterygium; Pterygium Recurrence
url http://www.jovr.org/article.asp?issn=2008-322X;year=2014;volume=9;issue=1;spage=22;epage=30;aulast=Razeghinejad
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AT mohammadbanifatemi subconjunctivalbevacizumabforprimarypterygiumexcisionarandomizedclinicaltrial