Postoperative cystoid macular edema after pars plana vitrectomy for epiretinal membrane: incidence, anatomical and functional outcomes, and response to intravitreal dexamethasone implant.

IF 3.8 Q2 OPHTHALMOLOGY
Leonardo Provetti Cunha, Manuela Ferreira Guimarães, Leandro Cabral Zacharias, Rony Carlos Preti, Luciana Virgínia Ferreira Costa-Cunha, Mário Luiz Ribeiro Monteiro
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引用次数: 0

Abstract

Background: To determine the incidence of postoperative cystoid macular edema (CME) following pars plana vitrectomy (PPV) with epiretinal membrane (ERM) peeling, and to evaluate the anatomical and functional response to intravitreal dexamethasone implant (Ozurdex; AbbVie) in affected eyes.

Methods: This retrospective, single-center cohort study included 92 consecutive eyes with idiopathic ERM that underwent PPV with ERM peeling by a single surgeon. Eyes were allocated to a control group (n = 84), comprising eyes without postoperative CME, or to a CME group (n = 8), comprising eyes that developed postoperative CME confirmed on swept-source optical coherence tomography (SS-OCT) and subsequently received intravitreal dexamethasone implant (DEX). Best-corrected visual acuity (BCVA, logMAR), central macular thickness (CMT, µm), and intraocular pressure (IOP, mmHg) were assessed preoperatively and postoperatively in both groups, and before and after DEX implantation in the CME group.

Results: The incidence of postoperative CME requiring treatment was 8.7%. Most baseline characteristics were comparable between groups, although preoperative IOP was significantly lower in the CME group. CMT decreased significantly after surgery in both the control group (335.1 ± 37.3 to 289.5 ± 22.9 μm; p < 0.001) and the CME group (382.9 ± 74.6 to 310.9 ± 22.9 μm; p = 0.033); however, postoperative CMT remained significantly higher in the CME group than in controls (p = 0.034). DEX implantation produced an additional significant CMT reduction (379.9 ± 67.1 to 302.7 ± 35.3 μm; p = 0.003), reducing the between-group difference to a non-significant level (p = 0.332). BCVA improved significantly after surgery in the control group (0.32 ± 0.26 to 0.04 ± 0.10 logMAR; p < 0.001) but not in the CME group (p = 0.582). Following DEX implantation, BCVA improved significantly in the CME group (0.47 ± 0.35 to 0.22 ± 0.25 logMAR; p = 0.002), approaching values observed in the control group (p = 0.078). IOP remained stable in controls (p = 0.576). A transient but significant IOP increase was observed in the CME group after surgery (11.5 ± 2.7 to 15.3 ± 3.7 mmHg; p = 0.019), with no further change after DEX implantation (p = 0.747).

Conclusions: Postoperative CME requiring treatment occurred in approximately 1 in 11 eyes following PPV with ERM peeling and was associated with significant anatomical and functional impairment. The present findings suggest that intravitreal dexamethasone implant was associated with improvement in selected cases of postoperative CME without additional impact on IOP; however, larger prospective studies are required to confirm these results.

视网膜前膜玻璃体切除术后膀胱样黄斑水肿:发生率、解剖和功能结局以及对玻璃体内地塞米松植入的反应
背景:探讨玻璃体切割(PPV)伴视网膜前膜(ERM)剥离术后膀胱样黄斑水肿(CME)的发生率,并评价玻璃体内地塞米松植入物(Ozurdex; AbbVie)对病变眼的解剖和功能反应。方法:这项回顾性、单中心队列研究纳入了92只连续的特发性ERM患者,由一名外科医生进行了PPV和ERM剥离。将眼睛分为对照组(n = 84)和CME组(n = 8),对照组由术后无CME的眼睛组成,CME组由经扫源光学相干断层扫描(SS-OCT)证实的术后发生CME的眼睛组成,随后接受玻璃体内地塞米松植入(DEX)。评估两组患者术前、术后最佳矫正视力(BCVA, logMAR)、中央黄斑厚度(CMT,µm)、眼压(IOP, mmHg), CME组患者植入DEX前后。结果:术后需要治疗的CME发生率为8.7%。尽管CME组术前IOP明显较低,但两组间的大多数基线特征具有可比性。两组患者术后CMT均显著下降(335.1±37.3 μm至289.5±22.9 μm); p结论:PPV伴ERM脱皮术后需要治疗的CME发生在11只眼中约1只眼,并伴有明显的解剖和功能损伤。目前的研究结果表明,玻璃体内地塞米松植入与术后CME的改善有关,但对IOP没有额外的影响;然而,需要更大规模的前瞻性研究来证实这些结果。
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来源期刊
CiteScore
3.50
自引率
4.30%
发文量
81
审稿时长
19 weeks
期刊介绍: International Journal of Retina and Vitreous focuses on the ophthalmic subspecialty of vitreoretinal disorders. The journal presents original articles on new approaches to diagnosis, outcomes of clinical trials, innovations in pharmacological therapy and surgical techniques, as well as basic science advances that impact clinical practice. Topical areas include, but are not limited to: -Imaging of the retina, choroid and vitreous -Innovations in optical coherence tomography (OCT) -Small-gauge vitrectomy, retinal detachment, chromovitrectomy -Electroretinography (ERG), microperimetry, other functional tests -Intraocular tumors -Retinal pharmacotherapy & drug delivery -Diabetic retinopathy & other vascular diseases -Age-related macular degeneration (AMD) & other macular entities
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