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1.
Eye (Lond) ; 34(9): 1592-1599, 2020 09.
Article in English | MEDLINE | ID: mdl-31784704

ABSTRACT

PURPOSE: To compare the efficacy and safety of subthreshold micropulse laser (SML) with threshold conventional laser (TCL) in central serous chorioretinopathy (CSC). METHODS: Prospective, randomized, double-masked, non-inferiority, 12-week clinical trial. Patients were randomly assigned 1:1 to SML group or TCL group. Patients in the SML group were treated with 577 nm micropulse laser. The spot size was 160 µm, the duty cycle was 5% and exposure time was 0.2 s. The power was 50% threshold tested. Patients in the TCL group were treated with 577 nm continuous laser. The power was 100% threshold tested. The primary outcome was the mean change in best-corrected visual acuity (BCVA) at week 12, with a non-inferiority limit of five letters on the Early Treatment Diabetic Retinopathy Study (ETDRS) visual acuity charts. RESULTS: Eighty-eight patients were enroled. Seventy-seven patients were male. Forty-four patients were in SML group and 44 in TCL group. At week 12, SML was equivalent to TCL with a gain of 6.23 ± 8.59 and 6.61 ± 6.35 letters, respectively, (SML-TCL difference: -0.38 letters; 95% confidence interval (CI):-3.58-2.81; Pnon-inferiority = 0.0026). There was no statistically significant difference between the two groups (t = 0.240, P = 0.811). At week 12, the proportion of patients whose SRF had been totally absorbed was 63.63 and 81.82% respectively for SML and TCL groups. There was no statistically significant difference between the two groups (χ2 = 3.67, P = 0.056). CONCLUSIONS: Both SML and TCL can improve visual acuity in CSC. SML was non-inferior to TCL in the improvement of BCVA.


Subject(s)
Central Serous Chorioretinopathy , Central Serous Chorioretinopathy/surgery , Female , Humans , Laser Coagulation , Lasers , Male , Prospective Studies , Treatment Outcome , Visual Acuity
2.
PLoS One ; 12(9): e0185070, 2017.
Article in English | MEDLINE | ID: mdl-28922378

ABSTRACT

PURPOSE: To measure visual acuity and metamorphopsia in patients with age-related macular degeneration (AMD) and to explore their relationship with macular lesions. METHODS: In this cross-sectional study, a total of 32 normal subjects (32 eyes) and 35 AMD patients (35 eyes) were recruited. They were categorized into 4 groups: normal, dry AMD, non-active wet AMD, and active wet AMD. Best-corrected visual acuity (BCVA) was measured using the Early Treatment Diabetic Retinopathy Study protocol. Metamorphopsia was quantified with the orientation discrimination threshold (ODT). Macular lesions, including drusen, sub-retinal fluid (SRF), intra-retinal fluid (IRF), pigmented epithelium detachment (PED), and scarring, were identified with spectral-domain optical coherence tomography (SD-OCT). A linear regression model was established to identify the relationships between the functional and structural changes. RESULTS: BCVA progressively worsened across the normal, dry AMD, non-active wet AMD, and active wet AMD groups (P < 0.001), and ODT increased across the groups (P < 0.001). The correlation between BCVA and ODT varied among the groups. The partial correlation between BCVA and ODT was -0.61 (P < 0.001). Linear regression showed that ODT significantly depended on IRF (ß = 0.61, P < 0.001), SRF (ß = 0.34, P = 0.003), and scarring (ß = 0.26, P = 0.050), while BCVA significantly depended only on scarring (ß = -0.52, P < 0.001), and IRF (ß = -0.36, P = 0.016). CONCLUSIONS: From dry AMD to active wet AMD, BCVA gradually worsened while ODT increased. The correlation between BCVA and ODT varied among these groups, indicating that AMD lesions affect them differently. ODT and BCVA should be used concurrently for better monitoring of the disease.


Subject(s)
Macular Degeneration , Retinal Pigment Epithelium , Tomography, Optical Coherence , Aged , Aged, 80 and over , Female , Humans , Macular Degeneration/classification , Macular Degeneration/diagnostic imaging , Macular Degeneration/metabolism , Male , Middle Aged , Retinal Pigment Epithelium/diagnostic imaging , Retinal Pigment Epithelium/metabolism
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