Krizova Deli, Vokrojova Magdalena, Liehneova Katerina, Studeny Pavel
Ophthalmology Department, 3rd Medical Faculty of Charles University and University Hospital Kralovske Vinohrady, Srobarova 50, 10034 Prague, Czech Republic.
J Ophthalmol. 2014;2014:178132. doi: 10.1155/2014/178132. Epub 2014 Mar 23.
Purpose. To evaluate antiangiogenic effect of local use of bevacizumab (anti-VEGF antibody) in patients with corneal neovascularization. Methods. Patients were divided into two groups. All patients suffered from some form of corneal neovascularization (NV). Patients in group A received 0.2-0.5 mL of bevacizumab solution subconjunctivally (concentration 25 mg/mL) in a single dose. Group A included 28 eyes from 27. Patients in group B applied bevacizumab eye drops twice daily (concentration 2.5 mg/mL) for two weeks. Group B included 38 eyes from 35 patients. We evaluated the number of corneal segments affected by NV, CDVA, and the incidence of complications and subjective complaints related to the treatment. The minimum follow-up period was six months. Results. By the 6-month follow-up, in group A the percentage reduction of the affected peripheral segments was 21.6% and of the central segments was 9.6%; in group B the percentage reduction of the central segments was 22.7% and of the central segments was 38.04%. In both groups we noticed a statistically significant reduction in the extent of NV. Conclusion. The use of bevacizumab seems to be an effective and safe method in the treatment of corneal neovascularization, either in the subconjunctival or topical application form.
目的。评估局部使用贝伐单抗(抗血管内皮生长因子抗体)对角膜新生血管患者的抗血管生成作用。方法。将患者分为两组。所有患者均患有某种形式的角膜新生血管(NV)。A组患者结膜下注射0.2 - 0.5毫升贝伐单抗溶液(浓度25毫克/毫升),单次给药。A组包括来自27例患者的28只眼。B组患者每天两次使用贝伐单抗滴眼液(浓度2.5毫克/毫升),持续两周。B组包括来自35例患者的38只眼。我们评估了受NV影响的角膜节段数量、最佳矫正视力(CDVA)以及与治疗相关的并发症发生率和主观不适。最短随访期为6个月。结果。到6个月随访时,A组受影响的周边节段减少百分比为21.6%,中央节段为9.6%;B组中央节段减少百分比为22.7%,中央节段为38.04%。两组中我们均观察到NV范围有统计学意义的减少。结论。贝伐单抗无论是结膜下注射还是局部应用,似乎都是治疗角膜新生血管的一种有效且安全的方法。