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玻璃体内注射康柏西普联合全视网膜光凝治疗无黄斑水肿的重度非增殖性糖尿病视网膜病变的疗效

Efficacy of intravitreal conbercept combined with panretinal photocoagulation for severe nonproliferative diabetic retinopathy without macular edema.

作者信息

Zhao Ning, Guan Jian, Cai Na, Liu Ning-Ning

机构信息

Department of Ophthalmology, the First Affiliated Hospital of China Medical University, Shenyang 110001, Liaoning Province, China.

出版信息

Int J Ophthalmol. 2022 Apr 18;15(4):615-619. doi: 10.18240/ijo.2022.04.15. eCollection 2022.

Abstract

AIM

To assess efficacy of intravitreal conbercept (IVC) injection in combination with panretinal photocoagulation (PRP) PRP alone in patients with severe nonproliferative diabetic retinopathy (SNPDR) without macular edema (ME).

METHODS

Forty-eight patients with SNPDR without ME (56 eyes) were divided into the PRP group and IVC+PRP group (the pulse group) in this retrospective clinical study. Conbercept was intravitreally administered to patients in the pulse group 1wk before treatment with PRP and followed up for 1, 3, and 6mo. The best-corrected visual acuity (BCVA, logMAR), center foveal thickness (CFT), visual acuity (VA) improvement, and adverse reactions were compared between groups.

RESULTS

In the PRP group, the BCVA reduced at 1 and 3mo before improving at 6mo. In the pulse group, baseline BCVA decreased continuously at 1mo, increased at 3 and 6mo. BCVA in the pulse group was better than that in the PRP group at 1, 3, and 6mo. There was an increase in CFT in the PRP group during follow-up compared with baseline. In the pulse group, CFT was increased at 1mo relative to baseline, steadily decreased to the baseline level at 3 and 6mo. There was a more significant reduction in CFT in the pulse group during follow-up compared with the PRP group. The effective rates of VA in the PRP and the pulse groups were 81.48% and 100%, respectively.

CONCLUSION

As PRP pretreatment, a single dose of IVC administration has beneficial effects for preventing PRP-induced foveal thickening and increasing VA in patients with SNPDR without ME.

摘要

目的

评估玻璃体内注射康柏西普(IVC)联合全视网膜光凝(PRP)与单纯PRP治疗无黄斑水肿(ME)的重度非增殖性糖尿病视网膜病变(SNPDR)患者的疗效。

方法

在这项回顾性临床研究中,48例无ME的SNPDR患者(56只眼)被分为PRP组和IVC+PRP组(联合组)。联合组患者在PRP治疗前1周接受玻璃体内注射康柏西普,并随访1、3和6个月。比较两组之间的最佳矫正视力(BCVA,logMAR)、中心凹厚度(CFT)、视力(VA)改善情况及不良反应。

结果

PRP组中,BCVA在1个月和3个月时下降,6个月时改善。联合组中,基线BCVA在1个月时持续下降,3个月和6个月时升高。联合组在1个月、3个月和6个月时的BCVA均优于PRP组。与基线相比,PRP组随访期间CFT增加。联合组中,CFT在1个月时相对于基线增加,在3个月和6个月时稳定下降至基线水平。联合组随访期间CFT的下降幅度比PRP组更显著。PRP组和联合组的VA有效率分别为81.48%和100%。

结论

作为PRP预处理,单次玻璃体内注射IVC对预防PRP引起的黄斑增厚和提高无ME的SNPDR患者的视力有有益作用。

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The Evolving Treatment of Diabetic Retinopathy.糖尿病视网膜病变的治疗进展
Clin Ophthalmol. 2020 Mar 4;14:653-678. doi: 10.2147/OPTH.S236637. eCollection 2020.

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