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Comparison of Pterygium Recurrence with and without Using Postsurgical Topical Cyclosporin A 0.05%: A Randomized
Yousef Alizadeh1, Mitra Akbari1, Reza Soltani Moghadam1
1Eye Research Center, Department of Eye, Amiralmomenin Hospital, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran.
Journal of Current Ophthalmology
|September 23, 2022
Summary
Topical cyclosporin A (CsA) 0.05% did not improve outcomes after pterygium surgery. This study found no significant difference in recurrence, inflammation, or complications between CsA and control groups.
Area of Science:
- Ophthalmology
- Surgical Innovation
- Clinical Trials
Background:
- Pterygium surgery, often using mitomycin C (MMC) and conjunctival flaps, aims to prevent recurrence.
- Postoperative inflammation and recurrence remain challenges in pterygium management.
Purpose of the Study:
- To assess the efficacy of 3-month topical cyclosporin A (CsA) 0.05% in preventing pterygium recurrence post-surgery.
- To evaluate the impact of CsA on postoperative inflammation and complications.
Main Methods:
- A randomized, single-blind clinical trial involving 78 patients undergoing pterygium surgery with the rotational conjunctival flap technique and MMC.
- Patients were allocated to either a control group or a case group receiving CsA 0.05% for 3 months.
- Outcomes including visual acuity, intraocular pressure, inflammation, complications, and recurrence were monitored up to 6 months postoperatively.
Main Results:
- No significant differences were observed in clinical inflammation between the CsA and control groups at 1 and 3 months postoperatively (P = 0.108 and P = 0.780).
- Complication rates were similar between the groups (P = 0.99), with no serious adverse events reported.
- The pterygium recurrence rate was comparable: 5.1% in the CsA group versus 7.7% in the control group (P = 0.99).
Conclusions:
- Three-month administration of topical CsA 0.05% demonstrated no significant benefit in preventing pterygium recurrence after surgery.
- CsA 0.05% did not show a priority for improving postoperative outcomes, including inflammation and complication rates, in this surgical technique.
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