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光学相干断层扫描参数作为中心性浆液性脉络膜视网膜病变中依普利酮治疗反应的预测指标

Optical Coherence Tomography Parameters as Predictors of Treatment Response to Eplerenone in Central Serous Chorioretinopathy.

作者信息

Borrelli Enrico, Zuccaro Biancamaria, Zucchiatti Ilaria, Parravano Mariacristina, Querques Lea, Costanzo Eliana, Sacconi Riccardo, Prascina Francesco, Scarinci Fabio, Bandello Francesco, Querques Giuseppe

机构信息

Department of Ophthalmology, University Vita-Salute, IRCCS Ospedale San Raffaele, Milan 20132, Italy.

IRCCS-Fondazione Bietti, Rome 00198, Italy.

出版信息

J Clin Med. 2019 Aug 22;8(9):1271. doi: 10.3390/jcm8091271.

DOI:10.3390/jcm8091271
PMID:31443376
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6781176/
Abstract

: To present data on clinical response to eplerenone over a 1-year period in patients with central serous chorioretinopathy (CSC), and to evaluate optical coherence tomography (OCT) variables as predictors of treatment response at 3- and 12-month follow-up visits. : Patients with acute or chronic CSC treated with eplerenone were retrospectively included. Clinical and imaging characteristics were recorded at baseline and at the 3-month and 12-month follow-up visits. Changes from baseline in quantitative measurements were calculated at each follow-up. Logistic regression analysis was computed to correlate clinical and OCT parameters at baseline with response to treatment at 3 and 12 months of follow-up. : A total of 50 eyes of 50 patients were included in the study. Mean ± SD best corrected visual acuity (BCVA) was 0.20 ± 0.14 Logarithm of the Minimum Angle of Resolution (LogMAR) at baseline and significantly improved at both the 3-month (0.12 ± 0.13 LogMAR, < 0.0001) and 12-month (0.10 ± 0.12 LogMAR, < 0.0001) follow-up visits. At the 3-month follow-up visit, 25 out of 50 eyes (50.0%) demonstrated macular complete subretinal fluid (SRF) resolution, while 13 eyes (26.0%) showed macular partial SRF resolution, and 12 eyes (24%) had neither partial nor complete macular SRF resolution. Among those patients with macular partial or complete SRF resolution at 3 months and thus not shifted to photodynamic therapy, 36 out of 38 cases had macular complete SRF resolution at the 12-month follow-up visit. There was a significant change from baseline at both follow-up visits in all anatomical OCT parameters (except for reduction in choroidal thickness that did not reach the statistical significance at the 12-month follow-up visit). Several OCT parameters at baseline were independently significant predictors for macular subretinal fluid complete resolution at 3 months, including (i) a thicker subfoveal choroidal thickness; (ii) a smaller subretinal fluid maximum diameter; (iii) a lower number of serous pigment epithelium detachments; and (iv) a lower number of intraretinal hyperreflective foci. : Treatment with eplerenone in CSC patients is confirmed to be beneficial for both anatomical and functional outcomes. We identified attractive OCT metrics that could potentially be used as a tool to select patients who might mainly benefit from this treatment.

摘要

目的

呈现依普利酮治疗中心性浆液性脉络膜视网膜病变(CSC)患者1年期间的临床反应数据,并评估光学相干断层扫描(OCT)变量作为3个月和12个月随访时治疗反应的预测指标。

方法

回顾性纳入接受依普利酮治疗的急性或慢性CSC患者。在基线以及3个月和12个月随访时记录临床和影像学特征。每次随访时计算定量测量相对于基线的变化。进行逻辑回归分析,以关联基线时的临床和OCT参数与随访3个月和12个月时的治疗反应。

结果

本研究共纳入50例患者的50只眼。基线时平均最佳矫正视力(BCVA)±标准差为0.20±0.14最小分辨角对数(LogMAR),在3个月(0.12±0.13 LogMAR,P<0.0001)和12个月(0.10±0.12 LogMAR,P<0.0001)随访时均显著改善。在3个月随访时,50只眼中有25只(50.0%)黄斑区视网膜下液(SRF)完全吸收,13只眼(26.0%)黄斑区SRF部分吸收,12只眼(24%)黄斑区SRF既无部分吸收也无完全吸收。在3个月时黄斑区SRF部分或完全吸收且未转向光动力治疗的患者中,38例中有36例在12个月随访时黄斑区SRF完全吸收。在两次随访时,所有解剖学OCT参数相对于基线均有显著变化(12个月随访时脉络膜厚度减小未达到统计学显著性除外)。基线时的几个OCT参数是3个月时黄斑区视网膜下液完全吸收的独立显著预测指标,包括:(i)黄斑中心凹下脉络膜厚度较厚;(ii)视网膜下液最大直径较小;(iii)浆液性色素上皮脱离数量较少;(iv)视网膜内高反射灶数量较少。

结论

依普利酮治疗CSC患者对解剖和功能结局均有益。我们确定了有吸引力的OCT指标,这些指标可能用作选择可能主要从该治疗中获益的患者的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/171fb9269c63/jcm-08-01271-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/f3b88d324bd3/jcm-08-01271-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/5622dabaa4da/jcm-08-01271-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/12391b8a291b/jcm-08-01271-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/b601613c7a59/jcm-08-01271-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/171fb9269c63/jcm-08-01271-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/f3b88d324bd3/jcm-08-01271-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/5622dabaa4da/jcm-08-01271-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/12391b8a291b/jcm-08-01271-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/b601613c7a59/jcm-08-01271-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ea65/6781176/171fb9269c63/jcm-08-01271-g005.jpg

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