玻璃体腔内注射康柏西普联合玻璃体切除术治疗增殖性糖尿病视网膜病变疗效观察
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  • 英文篇名:Effect of intravitreal injection of Conbercept combined with pars plana vitreomy on patients with proliferative diabetic retinopathy
  • 作者:姚永屿 ; 夏鸿慧 ; 范卫 ; 甄铭伟
  • 英文作者:YAO Yong-yu;XIA Hong-hui;FAN Wei;ZHEN Ming-wei;Department of Ophthalmology, Zhaoqing Gaoyao People's Hospital;
  • 关键词:康柏西普 ; 玻璃体腔内注射 ; 玻璃体切除术 ; 增殖性糖尿病视网膜病变 ; 疗效
  • 英文关键词:Conbercept;;Intravitreal injection;;Pars plana vitreomy;;Proliferative diabetic retinopathy;;Curative effect
  • 中文刊名:HAIN
  • 英文刊名:Hainan Medical Journal
  • 机构:肇庆市高要区人民医院眼科;
  • 出版日期:2019-04-10
  • 出版单位:海南医学
  • 年:2019
  • 期:v.30
  • 基金:广东省肇庆市科技创新计划项目(编号:201804031205)
  • 语种:中文;
  • 页:HAIN201907016
  • 页数:4
  • CN:07
  • ISSN:46-1025/R
  • 分类号:58-61
摘要
目的探讨玻璃体腔内注射康柏西普联合玻璃体切除术(PPV)治疗增殖性糖尿病视网膜病变(PDR的临床效果。方法选择2016年6月至2018年9月肇庆市高要区人民医院收治的PDR患者56例(56只眼)为研究对象,以随机数表法将患者分为观察组与对照组各28例(28只眼),对照组给予常规PPV术,观察组给予玻璃体腔内注射康柏西普联合PPV手术治疗,比较两组患者术中出血发生率、手术时间、术中电凝止血率、术中医源性视网膜裂孔率、视力改变情况、再次手术率、激光补充治疗率及并发症情况。结果观察组患者的手术时间为(72.11±9.81) min,明显少于对照组的(99.21±8.11) min,术中出血发生率为10.7%,明显低于对照组的50.0%、电凝止血发生率为7.1%,明显低于对照组的57.1%,医源性视网膜裂孔发生率为10.7%,明显低于对照组的46.4%,以上各项指标比较差异均有统计学意义(P<0.05);观察组与对照组患者术后最佳矫正视力(BCVA)分别为(3.99±0.56) D、(4.01±0.32) D,均明显高于术前的(2.56±0.32) D、(2.59±0.21) D,差异均有统计学意义(P<0.05),但术后两组患者的BCVA比较差异无统计学意义(P>0.05);观察组患者术后激光补充治疗(1.51±0.90)次,明显少于对照组的(2.54±0.82)次,并发症发生率为10.7%,明显低于对照组46.4%,差异均有统计学意义(P<0.05)。结论玻璃体腔内注射康柏西普联合PPV能够有效降低PDR手术治疗难度,同时能够减少术中出血,缩短手术时间,更好的改善患者术后视力,降低术后激光补充治疗率,且并发症少,手术安全性高。
        Objective To discuss the effect of intravitreal injection of Conbercept combined with pars plana vitreomy on patients with proliferative diabetic retinopathy. Methods A total of 56 patients with proliferative diabetic retinopathy(56 eyes) at Zhaoqing Gaoyao People's Hospital from Jun. 2016 to Sep. 2018 were divided into the observation group(n=28) and the control group(n=28) according to the random number table method. The observation group was treated with intravitreal injection of Conbercept combined with pars plana vitreomy, and the control group was treated with pars plana vitreomy. Then the operative time, intraoperative bleeding rate, intraoperative electrocoagulation hemostasis rate, intraoperative iatrogenic retinal hole rate, visual acuity changes, reoperation rate, laser supplementary therapy rate, and complications were compared between the two groups. Results The operative time, the incidences of bleeding, electrocoagulation hemostasis, and iatrogenic retinal hole of the observation group were(72.11±9.81) min, 10.7%,7.1%, 10.7%, significantly lower than the corresponding(99.21±8.11) min, 50.0%, 57.1%, 46.4% in the control group(P<0.05). The best-corrected visual acuity(BCVA) after the operation were(3.99±0.56) D in the observation group versus(4.01±0.32) D in the control group(P>0.05), significantly higher than(2.56±0.32) D and(2.59±0.21) D before the operation(P<0.05). The frequency of laser supplementary therapy was 1.51±0.90 in the observation group versus 2.54±0.82 in the control group(P<0.05), and the incidence of complications was 10.7% versus 46.4%(P<0.05). Conclusion Intravitreal injection of Compacil combined with pars plana vitreomy in the treatment of proliferative diabetic retinopathy can effectively reduce the difficulty of operation, shorten the operation time, reduce the incidence of intraoperative bleeding, improve the visual acuity of patients, and reduce the incidence of postoperative laser supplementation, with fewer complications and high safety.
引文
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