Please use this identifier to cite or link to this item: http://localhost:80/xmlui/handle/123456789/1322
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dc.contributor.authorFarooq, Omer-
dc.contributor.authorHabib, Asad-
dc.contributor.authorShah, Masood Alam-
dc.contributor.authorAhmed, Najia-
dc.date.accessioned2019-11-15T06:23:55Z-
dc.date.available2019-11-15T06:23:55Z-
dc.date.issued2019-01-01-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/1322-
dc.description.abstractObjective: To determine the efficacy of oral eplerenone in anatomical and functional improvement in patients with chronic central serous chorioretinopathy (CSCR). Methods: This quasi experimental study was performed at PNS Shifa Hospital Karachi from September 2018 to February 2019. Study included 23 patients. Patients were included using consecutive sampling technique and informed consent was taken from all patients before staring treatment. 50 mg of oral eplerenone per day was given for three months. Subretinal fluid (SRF) height and visual acuity (VA) were noted at baseline, one month and three month follow-up. Structured Study performa was used for data collection. Data was analysed and assessed with SPSS version 23. P value of <0.05 was considered statistically significant. Results: Mean age of patients was 40.7±7 years and mean duration of disease before treatment was 3.7±0.76 months. Mean baseline BCVA and SRF height was 0.39±0.02 logMAR and 123±12.5 μm respectively. Sixty-five percent patients responded at one month and 80% at three months with reduction in SRF height. Improvement in visual acuity was also statistically significant at 3 months (p<0.05). Conclusion: Use of eplerenone in chronic CSCR resulted in significant improvement in vision and decrease in mean SRF height.en_US
dc.language.isoen_USen_US
dc.publisherPak J Med Scien_US
dc.subjectMedical and Health Sciencesen_US
dc.subjectCentral serous retinopathyen_US
dc.subjectEplerenoneen_US
dc.subjectMineralocorticoidsen_US
dc.subjectSubretinal fluiden_US
dc.titleEffect of oral eplerenone in anatomical and functional improvement in patients with chronic central serous chorioretinopathyen_US
dc.typeArticleen_US
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