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OCT 观察特发性黄斑前膜的自然病程

A Study of the Natural History of Vitreomacular Traction Syndrome by OCT.

机构信息

Moorfields Eye Hospital NHS Trust, London, United Kingdom.

Moorfields Eye Hospital NHS Trust, London, United Kingdom.

出版信息

Ophthalmology. 2018 May;125(5):701-707. doi: 10.1016/j.ophtha.2017.10.035. Epub 2017 Dec 6.

Abstract

PURPOSE

To examine the natural history of vitreomacular traction syndrome (VMTS) in the absence of other ocular comorbidities.

DESIGN

Retrospective clinical case series.

PARTICIPANTS

A total of 183 eyes of 159 patients diagnosed with VMTS with no other ocular comorbidity.

METHODS

Patients with VMTS were identified from an OCT database at Moorfields Eye Hospital, London. Sequential OCT scans and patient notes were reviewed over a minimum period of 6 months. Data collected included patient demographics, best-corrected visual acuity, and OCT features of vitreomacular adhesion. Contingency tests and binary logistic modeling were used to identify baseline predictors of stability and progression.

MAIN OUTCOME MEASURES

The rates of spontaneous resolution (defined by release of traction), progression to full-thickness macular hole, and surgical intervention were analyzed.

RESULTS

Presenting visual acuity was 0.3±0.3 logMAR units. The mean length of follow-up was 17.4±12.1 months. During this period, VMTS persisted in 60% and resolved in 20% (occurring on average at 15 months). Of the remainder, 12% developed a macular hole and 8% elected to proceed with surgery for symptoms. Focal adhesion <1500 μm was present in 87%. A premacular membrane with macular pucker (PMM) was present in 20%. With persistent VMTS, vision and central foveal thickness remained unchanged. The relative risk of resolution increased in those cases with better presenting visual acuities, lesser foveal thicknesses, and no associated PMMs; vision significantly improved in those cases with resolution.

CONCLUSIONS

VMTS persists in the majority of patients but despite this, visual acuities did not deteriorate significantly over the study period unless patients developed a full-thickness macular hole or required surgical intervention for symptoms. Resolution spontaneously occurred in 20%, with an improvement in vision.

摘要

目的

研究无其他眼部合并症的玻璃体黄斑牵引综合征(VMTS)的自然病程。

设计

回顾性临床病例系列。

参与者

共纳入 159 例患者的 183 只眼,这些患者均被诊断为无其他眼部合并症的 VMTS。

方法

在伦敦 Moorfields 眼科医院的 OCT 数据库中识别出 VMTS 患者。对至少 6 个月的 OCT 扫描和患者病历进行回顾。收集的数据包括患者的人口统计学特征、最佳矫正视力和 OCT 检查的玻璃体黄斑粘连特征。采用列联表分析和二元逻辑回归模型,以确定稳定性和进展的基线预测因素。

主要观察指标

分析自发缓解(定义为牵引松解)、进展为全层黄斑裂孔和手术干预的发生率。

结果

初始视力为 0.3±0.3 logMAR 单位。平均随访时间为 17.4±12.1 个月。在此期间,VMTS 持续存在的比例为 60%,缓解的比例为 20%(平均在 15 个月时发生)。其余患者中,12%发展为黄斑裂孔,8%因症状而行手术治疗。1500μm 以内的局灶性粘连占 87%。存在黄斑前膜伴黄斑皱襞(PMM)的占 20%。持续性 VMTS 时,视力和中心凹视网膜厚度保持不变。存在更好的初始视力、更小的黄斑中心凹厚度和无相关 PMM 的患者,其缓解的相对风险增加;视力显著改善的患者,其缓解程度更高。

结论

尽管 VMTS 持续存在于大多数患者中,但在研究期间,除非患者发生全层黄斑裂孔或因症状需要手术治疗,否则视力并未显著恶化。20%的患者自发缓解,视力得到改善。

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