透過您的圖書館登入
IP:18.222.179.186
  • 期刊
  • OpenAccess

Intravitreal Bevacizumab for Macular Edema Secondary to Branch Retinal Vein Occlusion-A Short-Term Result

眼內注射BEVACIZUMAB治療分枝視網膜靜脈阻塞引起黃斑部水腫之療效-短期結果報告

摘要


目的:評估眼內注射bevacizumab治療分枝視網膜靜脈阻塞所造成之黃斑部水腫的安全性與療效。 方法:本篇為回溯性的研究,總共收集了24位因分枝視網膜靜脈阻塞引起黃斑水腫的病人。這些病人皆接受玻璃體內注射2.5毫克bevacizumab的治療,並且根據臨床檢查變化決定是否重覆注射。所有的病人皆追蹤至少3個月以上,主要研究結果則包括最佳矯正視力與中央視網膜厚度的變化。 結果:24位病人的平均年齡為59.8歲(40到75歲)。從產生症狀到接受治療的平均時間為14周(2到56周),平均追蹤時間為10.1個月(3到30個月)。平均視力從治療前的6/50,在最後一次迫蹤時進步到6/16(P值<0.01)。平均中央視網膜厚度從治療前的439(標準差112)微米,到最後一次追蹤時下降到246(標準差106)微米(P值<0.01)。在追蹤期間,沒有任何眼壓升高(眼壓>21毫米汞柱)、視網膜裂孔、玻璃體出血或者眼內炎的併發症發生。 結論:以玻璃體內注射2.5毫克bevacizumab來治療分枝視網膜靜脈引起的黃斑部水腫是有效且安全的選擇。然而,長期的療效及安全性需要進一步的研究。

關鍵字

無資料

並列摘要


Purpose: To evaluate the short-term safety and efficacy of intravitreal bevacizumab for the management of macular edema secondary to branch retinal vein occlusion (BRVO). Methods: A retrospective, non-comparative, consecutive, interventional case series of twenty-four eyes from 24 patients. Patients received repeated intravitreal injections of 2.5 mg bevacizumab. Main outcome measures were best-corrected visual acuity (BCVA) and central retinal thickness (CRT) in a minimum follow-up of 3 months. Results: Patients presented at a mean age of 59.8 years (range 40-75). Mean duration of symptoms was 14 weeks (range 2-56), and mean follow-up period was 10.1 months (range 3-30). Mean (SD) BCVA at baseline was 1.17 (±0.51) logMAR, improving to 0.62 (±0.53) logMAR at the last follow-up (p<0.01). Mean (SD) CRT at baseline was 439 (±112)μm, declining to 246 (±106)μm at the last follow-up (p<0.01). No increased intraocular pressure, retinal tear, vitreous hemorrhage or endophthalmitis was noted during the follow-up period. Conclusions: Intravitreal injection of 2.5 mg bevacizumb appears to be an effective and safe treatment option for BRVO related macular edema. However, further studies are necessary to evaluate the long-term effect.

延伸閱讀