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Changes in Central Macular Thickness following Single Session Multispot Panretinal Photocoagulation
Nawat Watanachai1, Janejit Choovuthayakorn1, Direk Patikulsila1
1Department of Ophthalmology, Faculty of Medicine, Chiang Mai University, Chiang Mai 50200, Thailand.
Single session panretinal photocoagulation (PRP) for proliferative diabetic retinopathy caused temporary macular thickening and mild visual acuity changes. The treatment showed a low incidence of macular edema, suggesting it is a safe option.
Area of Science:
- Ophthalmology
- Retinal Diseases
- Diabetic Retinopathy
Background:
- Proliferative diabetic retinopathy (PDR) is a severe complication of diabetes that can lead to vision loss.
- Panretinal photocoagulation (PRP) is a standard treatment for PDR, aiming to reduce neovascularization.
- Understanding the impact of PRP on macular health is crucial for patient management.
Purpose of the Study:
- To evaluate changes in central subfield (CSF) macular thickness after single-session, multispot PRP.
- To assess the effect of this PRP treatment on best-corrected visual acuity (BCVA).
Main Methods:
- Thirty-three patients with newly diagnosed PDR underwent single-session, 20-millisecond, multispot PRP.
- Central macular thickness and BCVA were measured at baseline, 4 weeks, and 12 weeks post-treatment.
- Statistical analysis compared follow-up measurements to baseline values.
Main Results:
- A statistically significant increase in mean CSF thickness was observed at 4 weeks (+24.0 μm) and 12 weeks (+17.4 μm) post-PRP.
- Mean BCVA showed a mild, statistically significant increase at 4 weeks (+0.05 logMAR units), returning near baseline by 12 weeks (+0.02 logMAR units).
- Macular edema occurred in only 5% of eyes at the 12-week follow-up.
Conclusions:
- Single-session, 20-millisecond, multispot PRP leads to temporary macular thickening and minor BCVA fluctuations.
- The incidence of macular edema following this PRP protocol appears to be low.
- This PRP treatment modality is considered a safe option for managing proliferative diabetic retinopathy.
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