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黄斑水肿患者玻璃体内同时注射地塞米松植入剂与抗血管生成药物:一项回顾性队列研究

Concurrent injection of dexamethasone intravitreal implant and anti-angiogenic agent in patients with macular edema: A retrospective cohort study.

作者信息

Lin Hung-Yu, Lee Chia-Yi, Huang Jing-Yang, Yang Shun-Fa, Chao Shih-Chun

机构信息

Department of Ophthalmology, Show Chwan Memorial Hospital, Changhua Institute of Medicine Department of Optometry, Chung Shan Medical University, Taichung Department of Optometry, Yuanpei University of Medical Technology, Hsinchu Department of Medical Research, Chung Shan Medical University Hospital, Taichung Department of Electrical and Computer Engineering, National Chiao Tung University, Hsinchu Department of Optometry, Central Taiwan University of Science and Technology, Taichung, Taiwan.

出版信息

Medicine (Baltimore). 2017 Nov;96(47):e8868. doi: 10.1097/MD.0000000000008868.

Abstract

To evaluate the safety and efficiency in macular edema patients who concurrently received a single injection of a dexamethasone intravitreal implant (DEX, 0.7 mg) and ranibizumab (2.3 mg).A retrospective cohort study was conducted, and medical records from 2012 to 2016 were reviewed. Patients who received concurrent DEX and ranibizumab injections with a follow-up period of at least 3 months were enrolled in the study group. An age and gender-matched group received ranibizumab injections and was designated the control group. The best-corrected visual acuity (BCVA), central macular thickness (CMT) and intraocular pressure (IOP) were included in the analysis. Steroid-induced ocular hypertension (SIOH) is defined as either an elevation of more than 10 mmHg from baseline or a single IOP measurement of more than 30 mmHg.A total of 26 patients were enrolled in the current study with 13 patients in each group. Both the BCVA (P = .04) and CMT (P < .01) achieved significant improvement after the follow-up period in the study group. The IOP increased after the injection but no significant elevation was observed throughout the follow-up period in the study group (P = .15). For SIOH, 1 patient in the study group had an elevated IOP of 10 mmHg (7.7%) at 2 postoperative months, and no single IOP measurement of more than 30 mmHg was obtained. Five patients (38.5%) in the study group received medical treatment that successfully retarded their IOP elevation, and no individuals required surgical management. In the control group, there were no significant fluctuations concerning BCVA, CMT, and IOP, and no ocular hypertension was observed. According to the inter-group analysis, the CMT and BCVA recovered more significantly in the study group than in the control group.Concurrent injection of DEX and ranibizumab is a preliminary method that shows effectiveness in treating ME. Furthermore, safety is also guaranteed, with moderate levels of severity and transient IOP elevation being observed. A future large-scale study is necessary to evaluate the long-term effects and safety of this combined treatment.

摘要

评估同时接受单次玻璃体内注射地塞米松植入剂(DEX,0.7毫克)和雷珠单抗(2.3毫克)的黄斑水肿患者的安全性和有效性。进行了一项回顾性队列研究,并回顾了2012年至2016年的医疗记录。接受DEX和雷珠单抗联合注射且随访期至少3个月的患者纳入研究组。一个年龄和性别匹配的组接受雷珠单抗注射,被指定为对照组。分析包括最佳矫正视力(BCVA)、中心黄斑厚度(CMT)和眼压(IOP)。类固醇诱导的高眼压(SIOH)定义为眼压较基线升高超过10 mmHg或单次眼压测量值超过30 mmHg。本研究共纳入26例患者,每组13例。随访期后,研究组的BCVA(P = 0.04)和CMT(P < 0.01)均有显著改善。研究组注射后眼压升高,但在整个随访期未观察到显著升高(P = 0.15)。对于SIOH,研究组1例患者术后2个月眼压升高10 mmHg(7.7%),未获得单次眼压测量值超过30 mmHg的情况。研究组5例患者(38.5%)接受药物治疗成功延缓了眼压升高,无人需要手术治疗。对照组的BCVA、CMT和IOP无显著波动,未观察到高眼压。根据组间分析,研究组的CMT和BCVA恢复情况比对照组更显著。同时注射DEX和雷珠单抗是一种初步方法,在治疗黄斑水肿方面显示出有效性。此外,安全性也得到保证,观察到的严重程度为中度,眼压短暂升高。未来有必要进行大规模研究来评估这种联合治疗的长期效果和安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75f4/5709006/d8dc86e9501b/medi-96-e8868-g003.jpg

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