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玻璃体内地塞米松植入物在白内障合并黄斑水肿患者行超声乳化术中的应用。

Use of intravitreal dexamethasone implant in patients with cataract and macular edema undergoing phacoemulsification.

作者信息

Sze Amy M, Luk Fiona O, Yip Terri P, Lee Gary K, Chan Carmen K

机构信息

Hong Kong Eye Hospital & Department of Ophthalmology and Visual Sciences, The Chinese University of Hong Kong, Kowloon - Hong Kong.

出版信息

Eur J Ophthalmol. 2015 Mar-Apr;25(2):168-72. doi: 10.5301/ejo.5000523. Epub 2014 Oct 21.

Abstract

PURPOSE

To study the safety and efficacy of intravitreal dexamethasone implant in patients with cataract and macular edema undergoing phacoemulsification and intraocular lens (IOL) implantation.

METHODS

Twenty-four eyes with macular edema secondary to diabetic retinopathy (diabetic macular edema [DME]) and retinal vein occlusion (RVO) were retrospectively reviewed. These eyes underwent phacoemulsification with IOL implantation and intravitreal dexamethasone implant 0.7 mg at the same setting between September 2012 and September 2013. Demographic data, best-corrected visual acuity (BCVA), central macular thickness (CMT), intraocular pressure (IOP), surgical time, and complications were recorded.

RESULTS

Twelve eyes had DME and 12 eyes had RVO (10 central RVO and 2 branch RVO). Median baseline logMAR BCVA was 1.0 (Snellen 20/200) and mean baseline CMT was 530.2 ± 218.9 µm. Median follow-up duration was 13 months. At last follow-up, median visual acuity improved significantly to 0.523 (Snellen 20/66) (p = 0.003) and CMT decreased to 300.7 ± 78.1 µm (p = 0.000). Median surgical time was 23 minutes. There were no intraoperative complications. In 12 eyes, macular edema recurred, requiring further treatment, and median time to recurrences was 21 weeks. One eye had raised IOP after second dexamethasone implant for recurrent macular edema. No major complication such as vitreous hemorrhage, retinal detachment, or endophthalmitis occurred.

CONCLUSIONS

Combined cataract surgery with intravitreal dexamethasone implant seems to be safe and effective in treating patients with cataract and macular edema in this small case series. A larger prospective study with longer follow-up is necessary to demonstrate the long-term benefit of this combined procedure.

摘要

目的

研究玻璃体内注射地塞米松植入物在患有白内障和黄斑水肿且接受超声乳化白内障吸除术和人工晶状体(IOL)植入术患者中的安全性和有效性。

方法

回顾性分析24只因糖尿病性视网膜病变(糖尿病性黄斑水肿[DME])和视网膜静脉阻塞(RVO)继发黄斑水肿的眼睛。这些眼睛在2012年9月至2013年9月期间于同一时间接受了超声乳化白内障吸除联合IOL植入术及玻璃体内注射0.7 mg地塞米松植入物。记录人口统计学数据、最佳矫正视力(BCVA)、中心黄斑厚度(CMT)、眼压(IOP)、手术时间和并发症情况。

结果

12只眼睛患有DME,12只眼睛患有RVO(10只中央RVO和2只分支RVO)。基线logMAR BCVA中位数为1.0(Snellen 20/200),平均基线CMT为530.2±218.9 µm。中位随访时间为13个月。在最后一次随访时,中位视力显著提高至0.523(Snellen 20/66)(p = 0.003),CMT降至300.7±78.1 µm(p = 0.000)。中位手术时间为23分钟。术中无并发症发生。12只眼睛黄斑水肿复发,需要进一步治疗,复发的中位时间为21周。1只眼睛在因复发性黄斑水肿第二次注射地塞米松植入物后眼压升高。未发生玻璃体出血、视网膜脱离或眼内炎等严重并发症。

结论

在此小病例系列中,白内障手术联合玻璃体内注射地塞米松植入物治疗患有白内障和黄斑水肿的患者似乎是安全有效的。需要进行一项更大规模、随访时间更长的前瞻性研究来证明这种联合手术的长期益处。

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