Routine Clinical Practice Treatment Outcomes of Eplerenone in Acute and Chronic Central Serous Chorioretinopathy

Purpose: To evaluate efficacy of eplerenone therapy vs. observation on resolution of subretinal fluid (SRF) in patients with acute and chronic central serous chorioretinopathy (CSCR) in routine clinical practice.Methods: Retrospective comparative case series of eyes diagnosed with CSCR treated with...

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Main Authors: Katrin Fasler, Jeanne M. Gunzinger, Daniel Barthelmes, Sandrine A. Zweifel
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-05-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2021.675295/full
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author Katrin Fasler
Katrin Fasler
Jeanne M. Gunzinger
Jeanne M. Gunzinger
Daniel Barthelmes
Daniel Barthelmes
Daniel Barthelmes
Sandrine A. Zweifel
Sandrine A. Zweifel
author_facet Katrin Fasler
Katrin Fasler
Jeanne M. Gunzinger
Jeanne M. Gunzinger
Daniel Barthelmes
Daniel Barthelmes
Daniel Barthelmes
Sandrine A. Zweifel
Sandrine A. Zweifel
author_sort Katrin Fasler
collection DOAJ
description Purpose: To evaluate efficacy of eplerenone therapy vs. observation on resolution of subretinal fluid (SRF) in patients with acute and chronic central serous chorioretinopathy (CSCR) in routine clinical practice.Methods: Retrospective comparative case series of eyes diagnosed with CSCR treated with eplerenone or observation. Primary outcome measure was maximum height of SRF at 12 months. Secondary outcome was percentage of eyes with complete resolution of SRF, percentage of eyes with reduction of SRF ≥50%, and best corrected visual acuity (VA) at 12 months. Separate analysis was conducted for eyes with acute and chronic CSCR.Results: Sixty-eight eyes of 60 patients (82% male) were included. Eleven of the 38 eyes with acute CSCR, and seven of the 30 eyes with chronic CSCR, received eplerenone. Subretinal fluid decreased from baseline to 12 months in acute (287 ± 221 to 31 ± 63 µm) and chronic (148 ± 134 to 40 ± 42 µm) CSCR. Kaplan-Meier curves were similar for treated and observed eyes and COX regression analysis did not show a significant difference in SRF resolution in treated vs. observed eyes (p = 0.6 for acute, p = 0.2 for chronic CSCR).Conclusion: This routine clinical practice outcome study did not show evidence of efficacy of eplerenone on resolution of SRF in acute nor chronic CSCR.
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spelling doaj.art-5b00d771b9b44ee994d7c340b2730f2c2022-12-21T21:27:01ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122021-05-011210.3389/fphar.2021.675295675295Routine Clinical Practice Treatment Outcomes of Eplerenone in Acute and Chronic Central Serous ChorioretinopathyKatrin Fasler0Katrin Fasler1Jeanne M. Gunzinger2Jeanne M. Gunzinger3Daniel Barthelmes4Daniel Barthelmes5Daniel Barthelmes6Sandrine A. Zweifel7Sandrine A. Zweifel8Department of Ophthalmology, University Hospital Zurich, Zurich, SwitzerlandUniversity of Zurich, Zurich, SwitzerlandDepartment of Ophthalmology, University Hospital Zurich, Zurich, SwitzerlandUniversity of Zurich, Zurich, SwitzerlandDepartment of Ophthalmology, University Hospital Zurich, Zurich, SwitzerlandUniversity of Zurich, Zurich, SwitzerlandSave Sight Institute, The University of Sydney, Sydney, NSW, AustraliaDepartment of Ophthalmology, University Hospital Zurich, Zurich, SwitzerlandUniversity of Zurich, Zurich, SwitzerlandPurpose: To evaluate efficacy of eplerenone therapy vs. observation on resolution of subretinal fluid (SRF) in patients with acute and chronic central serous chorioretinopathy (CSCR) in routine clinical practice.Methods: Retrospective comparative case series of eyes diagnosed with CSCR treated with eplerenone or observation. Primary outcome measure was maximum height of SRF at 12 months. Secondary outcome was percentage of eyes with complete resolution of SRF, percentage of eyes with reduction of SRF ≥50%, and best corrected visual acuity (VA) at 12 months. Separate analysis was conducted for eyes with acute and chronic CSCR.Results: Sixty-eight eyes of 60 patients (82% male) were included. Eleven of the 38 eyes with acute CSCR, and seven of the 30 eyes with chronic CSCR, received eplerenone. Subretinal fluid decreased from baseline to 12 months in acute (287 ± 221 to 31 ± 63 µm) and chronic (148 ± 134 to 40 ± 42 µm) CSCR. Kaplan-Meier curves were similar for treated and observed eyes and COX regression analysis did not show a significant difference in SRF resolution in treated vs. observed eyes (p = 0.6 for acute, p = 0.2 for chronic CSCR).Conclusion: This routine clinical practice outcome study did not show evidence of efficacy of eplerenone on resolution of SRF in acute nor chronic CSCR.https://www.frontiersin.org/articles/10.3389/fphar.2021.675295/fullaldosterone antagonistscentral serous chorioretinopathyeplerenonemedical retinaretinal disease
spellingShingle Katrin Fasler
Katrin Fasler
Jeanne M. Gunzinger
Jeanne M. Gunzinger
Daniel Barthelmes
Daniel Barthelmes
Daniel Barthelmes
Sandrine A. Zweifel
Sandrine A. Zweifel
Routine Clinical Practice Treatment Outcomes of Eplerenone in Acute and Chronic Central Serous Chorioretinopathy
Frontiers in Pharmacology
aldosterone antagonists
central serous chorioretinopathy
eplerenone
medical retina
retinal disease
title Routine Clinical Practice Treatment Outcomes of Eplerenone in Acute and Chronic Central Serous Chorioretinopathy
title_full Routine Clinical Practice Treatment Outcomes of Eplerenone in Acute and Chronic Central Serous Chorioretinopathy
title_fullStr Routine Clinical Practice Treatment Outcomes of Eplerenone in Acute and Chronic Central Serous Chorioretinopathy
title_full_unstemmed Routine Clinical Practice Treatment Outcomes of Eplerenone in Acute and Chronic Central Serous Chorioretinopathy
title_short Routine Clinical Practice Treatment Outcomes of Eplerenone in Acute and Chronic Central Serous Chorioretinopathy
title_sort routine clinical practice treatment outcomes of eplerenone in acute and chronic central serous chorioretinopathy
topic aldosterone antagonists
central serous chorioretinopathy
eplerenone
medical retina
retinal disease
url https://www.frontiersin.org/articles/10.3389/fphar.2021.675295/full
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