PURPOSE: To investigate whether patients who developed chronic central serous chorioretinopathy (cCSC) in association with corticosteroid treatment respond differently to photodynamic therapy (PDT) as compared to patients who have not used corticosteroids. METHODS: Clinical evaluation included visual acuity (VA), fundoscopy, optical coherence tomography (OCT), fluorescein and indocyanine green angiography. The main outcome measure was a complete resolution of subretinal fluid (SRF) on OCT after PDT. RESULTS: One hundred and twenty-three eyes (117 patients), including 35 steroid-associated cases (29%), who received PDT treatment with reduced settings for active cCSC were included. Complete resolution of SRF on OCT was seen in 69% of the ster...
PURPOSE: To compare the short-term therapeutic efficacy of oral spironolactone treatment with that o...
PURPOSE: To compare the efficacy and safety of half-fluence vs half-dose photodynamic therapy (PDT) ...
Purpose: Comparing anatomic and functional efficacy and safety of primary treatment with either half...
Purpose: The aim of this study is to investigate the effect of half-fluence photodynamic therapy (PD...
Purpose: To compare the effects of half-dose photodynamic therapy (PDT) and high-density subthreshol...
PURPOSE: To evaluate the efficacy of low-fluence compared with standard-fluence rate photodynamic th...
Purpose: To describe a spectrum of severe chronic central serous chorioretinopathy (cCSC) cases and ...
Purpose: To study the early anatomic choroidal alterations in eyes with chronic central serous chori...
PURPOSE: To compare the effects of half-dose photodynamic therapy (PDT) and high-density subthreshol...
PURPOSE: To evaluate the outcome of a prospective protocol for the treatment of chronic central sero...
Masumi G Asahi,1 Andrew T Chon,1 Esmeralda Gallemore,1 Ron P Gallemore1,2 1Clinical Research Depart...
PURPOSE: To assess the short-term outcome of and possible temporary vision loss after half-dose vert...
BACKGROUND: Chronic central serous chorioretinopathy (cCSC) is an eye disease characterized by an ac...
Purpose: To identify characteristics of Caucasian chronic central serous chorioretinopathy (cCSC) pa...
AIM: To observe the clinical effect of half-dose verteporfin photodynamic therapy(PDT)in the treatme...
PURPOSE: To compare the short-term therapeutic efficacy of oral spironolactone treatment with that o...
PURPOSE: To compare the efficacy and safety of half-fluence vs half-dose photodynamic therapy (PDT) ...
Purpose: Comparing anatomic and functional efficacy and safety of primary treatment with either half...
Purpose: The aim of this study is to investigate the effect of half-fluence photodynamic therapy (PD...
Purpose: To compare the effects of half-dose photodynamic therapy (PDT) and high-density subthreshol...
PURPOSE: To evaluate the efficacy of low-fluence compared with standard-fluence rate photodynamic th...
Purpose: To describe a spectrum of severe chronic central serous chorioretinopathy (cCSC) cases and ...
Purpose: To study the early anatomic choroidal alterations in eyes with chronic central serous chori...
PURPOSE: To compare the effects of half-dose photodynamic therapy (PDT) and high-density subthreshol...
PURPOSE: To evaluate the outcome of a prospective protocol for the treatment of chronic central sero...
Masumi G Asahi,1 Andrew T Chon,1 Esmeralda Gallemore,1 Ron P Gallemore1,2 1Clinical Research Depart...
PURPOSE: To assess the short-term outcome of and possible temporary vision loss after half-dose vert...
BACKGROUND: Chronic central serous chorioretinopathy (cCSC) is an eye disease characterized by an ac...
Purpose: To identify characteristics of Caucasian chronic central serous chorioretinopathy (cCSC) pa...
AIM: To observe the clinical effect of half-dose verteporfin photodynamic therapy(PDT)in the treatme...
PURPOSE: To compare the short-term therapeutic efficacy of oral spironolactone treatment with that o...
PURPOSE: To compare the efficacy and safety of half-fluence vs half-dose photodynamic therapy (PDT) ...
Purpose: Comparing anatomic and functional efficacy and safety of primary treatment with either half...