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Published on: January 26, 2018
Micropulse Transscleral Cyclophotocoagulation for the Management of Diverse Glaucoma Types: A Multicenter Short-Term
Núbia Vanessa Dos Anjos Lima1, Nara Lidia Vieira Lopes2, Heloisa Andrade Maestrini3
1Department of Ophthalmology, UniCeub - Brasília, Brasília, DF, Brazil.
Purpose:
To evaluate the safety and effectiveness of micropulse transscleral cyclophotocoagulation (MP-TSCPC) in patients with various types of glaucoma by assessing intraocular pressure (IOP) reduction, medication burden, and the potential influence of diagnosis, prior surgeries, or comorbidities on treatment success.
Patients And Methods:
This retrospective, multicenter study included 101 eyes treated with MP-TSCPC using the IRIDEX Cyclo G6 MP3 laser. Follow-up was performed for at least 12 months. The primary outcomes were IOP reduction and changes in the number of hypotensive medications. The secondary outcomes included complication rates and visual acuity stability. Success was defined as IOP reduction ≥20% or IOP between 6 and 21 mmHg, with or without medication. Statistical analyses included paired t-tests and Cox regression to assess subgroup influence.
Results:
Baseline intraocular pressure (IOP) was 26.19 ± 6.77 mmHg and decreased to 14.40 ± 6.10 mmHg at 12 months (Δ = -11.76 ± 8.03 mmHg; ≈ -45%; p<0.0001). Mean logMAR visual acuity changed from 0.53 ± 0.64 preoperatively to 0.63 ± 0.72 postoperatively (p < 0.001). No significant differences in treatment success were found among the glaucoma subtypes, previous ocular surgeries, or comorbidities (all p > 0.05). Visual acuity remained stable in most patients, with only two cases of loss of light perception. Severe complications were rare, and no cases of phthisis bulbi or hypotony were observed.
Conclusion:
MP-TSCPC safely provides sustained IOP control and medication reduction across diverse glaucoma types, supporting its role as a versatile alternative for both refractory and functional eyes with glaucoma. The real-world, multicenter nature of this study enhances its external validity, although its retrospective design and 12-month follow-up limit long-term generalizability.
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