Efficacy of Intravitreal Bevacizumab in Chronic Central Serous Chorioretinopathy in Terms of Mean Reduction of Central Macular Thickness in Pakistani Patients

Huzaifa Akhlaq, Minnie Malik, Ejaz Ahmad Javed, I. Ahmad, Shahzad Hassan
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Abstract

Background: Central serous chorioretinopathy (CSCR) is an idiopathic condition described by serous neurosensory retinal detachment at the posterior pole, usually associated with serous retinal pigment epithelial detachment (PED). CSCR patients as a rule have good visual prognosis. In most of the patients, CSCR is self-limiting and patients regain the last visual acuity. However, some patients may have visual disability due to permanent RPE and photoreceptor damage. Objective: The objective of the study is to determine the effect of intravitreal Bevacizumab in cases of chronic central serous chorioretinopathy in terms of mean change in central macular thickness. Study Design: Interventional experimental study. Settings: The study was conducted in Department of Ophthalmology, Allied Hospital, Faisalabad Pakistan. Duration: 2 years from January 2017 to December 2018. Methodology: An aggregate of 95 cases were recruited for the study. Study included both male and female patients with diagnosis of chronic CSCR (at least 6month duration). Best corrected visual acuity, Intra Ocular Pressure on Goldman applanation Tonometer and Optical coherence tomography on Optovue were recorded of both eye of all patients. Before starting the treatment, informed consent was signed by every patient and they were called on the day of injection. Intravitreal off label Bevacizumab (1.25/0.05ml) was given through pars plana in operation theater under aseptic conditions. After injection topical antibiotic drops were given to patients for one week and patients called for follow up after one week, one month, 2 month and 3 months. Same parameters BCVA, IOP, Dilated fundus examine and OCT was recorded on every visit. The final outcome i.e., change in central macular thickness was recorded. Results: In this study, out of 95 cases, 53.68%(n=51) were between 30-45 years of age while 46.32%(n=44) were between 46-60 years of age, mean ± SD was calculated as 46.83+7.82 years, 74.74%(n=71) were male and 25.26%(n=24) were females. Pre-treatment mean central macular thickness was recorded as 344.77+14.61µ which reduced to 154.57+16.57 µ, mean difference was recorded as 190.2+21.46 µ, p value was 0.0001 showing a significant difference. Conclusion: We concluded that intravitreal Bevacizumab significantly reduced central macular thickness in cases of chronic central serous chorioretinopathy.
玻璃体内贝伐单抗治疗慢性中枢性浆液性脉络膜视网膜病变在巴基斯坦患者中枢性黄斑厚度平均减少方面的疗效
背景:中枢性浆液性脉络膜视网膜病变(CSCR)是一种以后极浆液性神经感觉视网膜脱离为特征的特发性疾病,通常伴有浆液性视网膜色素上皮脱离(PED)。CSCR患者通常有良好的视力预后。在大多数患者中,CSCR是自限性的,患者可以恢复最后的视力。然而,一些患者可能由于永久性RPE和光感受器损伤而出现视力障碍。目的:本研究的目的是确定玻璃体内贝伐单抗治疗慢性中枢性浆液性脉络膜视网膜病变对中枢性黄斑厚度平均变化的影响。研究设计:介入性实验研究。背景:本研究在巴基斯坦费萨拉巴德联合医院眼科进行。工期:2年,2017年1月至2018年12月。研究方法:共纳入95例病例。研究包括诊断为慢性CSCR(病程至少6个月)的男性和女性患者。记录两眼最佳矫正视力、Goldman眼压计眼压和Optovue光学相干断层扫描。在开始治疗前,每位患者都签署了知情同意书,并在注射当天进行了电话访谈。无菌条件下,在手术室通过平面pars给药,玻璃体内给予超说明书贝伐单抗(1.25/0.05ml)。注射后给予局部抗生素滴剂1周,1周、1个月、2个月、3个月后随访。每次就诊均记录BCVA、IOP、眼底扩张检查、OCT等相同参数。记录最终结果,即黄斑中央厚度的变化。结果:本组95例患者中,年龄在30 ~ 45岁之间的占53.68%(n=51), 46 ~ 60岁之间的占46.32%(n=44),平均±SD为46.83+7.82岁,其中男性占74.74%(n=71),女性占25.26%(n=24)。治疗前黄斑中央厚度均值为344.77+14.61µ,治疗前均值为154.57+16.57µ,治疗前均值为190.2+21.46µ,p值为0.0001,差异有统计学意义。结论:我们的结论是,玻璃体内贝伐单抗可显著降低慢性中枢性浆液性脉络膜视网膜病变患者的中枢性黄斑厚度。
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