Oral Eplerenone Versus Observation in the Management of Acute Central Serous Chorioretinopathy: A Prospective, Randomized Comparative Study

In this prospective, interventional case-control study, 58 patients with unilateral acute central serous chorioretinopathy (CSCR) were recruited. Patients ≥ 18 years age, presenting with first episodes of acute CSCR, were included. Acute CSCR was defined by the presence of subretinal fluid (SRF) and...

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Main Authors: Ramesh Venkatesh (Author), Arpitha Pereira (Author), Chaitra Jayadev (Author), Vishma Prabhu (Author), Aditya Aseem (Author), Kushagra Jain (Author), Bharathi Bavaharan (Author), Naresh Kumar Yadav (Author), Jay Chhablani (Author)
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Published: MDPI AG, 2020-07-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Ramesh Venkatesh  |e author 
700 1 0 |a Arpitha Pereira  |e author 
700 1 0 |a Chaitra Jayadev  |e author 
700 1 0 |a Vishma Prabhu  |e author 
700 1 0 |a Aditya Aseem  |e author 
700 1 0 |a Kushagra Jain  |e author 
700 1 0 |a Bharathi Bavaharan  |e author 
700 1 0 |a Naresh Kumar Yadav  |e author 
700 1 0 |a Jay Chhablani  |e author 
245 0 0 |a Oral Eplerenone Versus Observation in the Management of Acute Central Serous Chorioretinopathy: A Prospective, Randomized Comparative Study 
260 |b MDPI AG,   |c 2020-07-01T00:00:00Z. 
500 |a 10.3390/ph13080170 
500 |a 1424-8247 
520 |a In this prospective, interventional case-control study, 58 patients with unilateral acute central serous chorioretinopathy (CSCR) were recruited. Patients ≥ 18 years age, presenting with first episodes of acute CSCR, were included. Acute CSCR was defined by the presence of subretinal fluid (SRF) and symptoms for <12 weeks duration with no clinical or imaging features of chronicity. Patients were alternately divided into treatment (Table Eplerenone 50 mg/day for minimum 1 month) and observation groups. Vision, SRF height and subfoveal choroidal thickness (SFCT) were checked at 1-, 2- and 3-months in both eyes of each group. Each group had 29 eyes. Mean age was 40.4 ± 7.1 and 43.3 ± 8.34 years in treatment and observation group, respectively. Mean symptom duration was 6.46 ± 1.45 and 5.87 ± 2.09 weeks, respectively. Vision improvement to 6/6 was seen in 92%, 100% and 100% cases in treatment group and 74%, 86% and 100% in control group at each visit, respectively. Complete SRF resolution in the treatment group was noted in 45%, 55% and 62% cases at each respective monthly visit. In the observation group, complete SRF resolution was noted in 10%, 21% and 31% at 1-, 2- and 3-month visits, respectively. SRF (<i>p</i> < 0.001) and SFCT (<i>p</i> < 0.001) reduction was noted in the affected eye of both groups. SFCT was reduced in the fellow eye after treatment (<i>p</i> = 0.005) compared to the observation group (<i>p</i> = 0.276). In conclusion, oral eplerenone achieves faster SRF resolution and vision improvement in acute CSCR. Additionally, it shows beneficial effects on the fellow eye. 
546 |a EN 
690 |a acute 
690 |a central serous chorioretinopathy 
690 |a eplerenone 
690 |a contralateral eye 
690 |a Medicine 
690 |a R 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceuticals, Vol 13, Iss 8, p 170 (2020) 
787 0 |n https://www.mdpi.com/1424-8247/13/8/170 
787 0 |n https://doaj.org/toc/1424-8247 
856 4 1 |u https://doaj.org/article/4aafa33d1b5b43dfb91f378e0069a7d6  |z Connect to this object online.