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首页> 外文期刊>American Journal of Ophthalmology: The International Journal of Ophthalmology >Intravitreal Injection of Expansile Perfluoropropane (C for the Treatment of Vitreomacular Traction
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Intravitreal Injection of Expansile Perfluoropropane (C for the Treatment of Vitreomacular Traction

机译:玻璃体腔注射膨胀性全氟丙烷(C)治疗玻璃体牵引

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PURPOSE: To study the efficacy of a single intravitreal injection of expansile gas in releasing vitreomacular traction. DESIGN: Retrospective, interventional case series. METHODS: Fifteen eyes of 14 consecutive patients with symptomatic and persistent vitreomacular traction (> 3 months' duration) on spectral-domain optical coherence tomography (SD OCT) received a single intravitreal injection of 0.3 mL 100% perfluoropropane (C_3F_8) as an alternative to pars plana vitrectomy (PPV). Primary outcome was the number of eyes with complete vitreomacular traction release on OCT 1 month following treatment. Secondary outcomes included changes in visual acuity (VA), foveal contour, central foveal thickness, and maximal foveal thickness 1 month following treatment, and final VA. RESULTS: Mean age (± SD) was 72.1 ± 12.6 years. Mean follow-up was 398.7 ± 174.4 days. Vitreomacular traction was idiopathic in 7 eyes and associated with diabetes in 6. One month following treatment, vitreomacular traction was released in 6 eyes (40%). Three further eyes (20%) had resolution of vitreomacular traction within 6 months, 4 (27%) underwent PPV, and 2 (13%) subsequently declined surgery. Foveal contour was restored in 7 eyes (47%). VA and central foveal thickness were similar 1 month following treatment, but maximal foveal thickness decreased by 65.8 fxm (P = .041). Mean final VA decreased 0.03 logMAR units from baseline (P = .536). Eyes with vitreomacular traction release within 1 month had less extensive vitreomacular traction (P = .037), low vitreous face reflectivity, and maximal foveal thickness <500 mum (P = .004) pretreatment. There were no associated adverse events. CONCLUSIONS: Intravitreal C_3F_8 injection could offer a minimally invasive alternative to PPV in patients with symptomatic and persistent vitreomacular traction. It appears particularly effective in eyes with less extensive vitreomacular traction and low vitreous face reflectivity on SD OCT. Further studies are warranted.
机译:目的:研究玻璃体内单次注射膨胀气体在释放玻璃体牵引方面的功效。设计:回顾性介入病例系列。方法:连续14例有症状和持续玻璃体牵引(持续时间> 3个月)的14眼患者在光谱域光学相干断层扫描(SD OCT)上接受玻璃体腔注射0.3 mL 100%全氟丙烷(C_3F_8)替代平面玻璃体切除术(PPV)。主要结局是治疗后1个月OCT完全释放玻璃体牵引力的眼数。次要结果包括治疗后1个月的视敏度(VA),中央凹轮廓,中央中央凹厚度和最大中央凹厚度的变化,以及最终的VA。结果:平均年龄(±SD)为72.1±12.6岁。平均随访时间为398.7±174.4天。玻璃体牵引是特发性的,有7眼,与糖尿病相关的是6例。治疗后1个月,玻璃体牵引的释放是6眼(40%)。另外三只眼(20%)在6个月内有玻璃体眼牵引力消退,有4例(27%)接受了PPV,随后有2例(13%)拒绝了手术。 7只眼(47%)恢复了中央凹轮廓。治疗后1个月VA和中央凹的厚度相似,但最大中央凹的厚度减少了65.8 fxm(P = .041)。平均最终VA比基线降低了0.03 logMAR单位(P = .536)。在1个月内释放玻璃体牵引力的眼睛进行的玻璃体牵引力降低(P = .037),玻璃体表面反射率低以及最大中央凹厚度<500 mum(P = .004)进行预处理。没有相关的不良事件。结论:玻璃体腔内注射C_3F_8可以为有症状和持续性玻璃体牵引的患者提供PPV的微创替代方法。它在SD OCT上对玻璃体眼牵引力较弱且玻璃体面部反射率较低的眼睛中显得特别有效。值得进一步研究。

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