Soliman Wael, Vinten Martin, Sander Birgit, Soliman Kamell Abd El-Naser, Yehya Sameer, Rahman Mohamed Saad Abdel, Larsen Michael
Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Glostrup, Denmark.
Acta Ophthalmol. 2008 Jun;86(4):365-71. doi: 10.1111/j.1600-0420.2007.01057.x. Epub 2007 Nov 17.
To assess the effect of intravitreal bevacizumab on diabetic macular oedema (DMO) and retinal vessel calibres.
We performed a consecutive case series study in which 10 consecutive eyes with diffuse DMO, two of which had not previously been treated, received an intravitreal injection of bevacizumab 1 mg, which was followed by two more injections at 6-week intervals. Fundus photography and optical coherence tomography (OCT) were carried out at baseline immediately before injection and at 1, 2.5 and 4 months after the first injection. Outcome measures were best corrected visual acuity (BCVA) in Early Treatment Diabetic Retinopathy Study letters, macular volume, foveal subfield thickness and vessel diameter measurement.
Intravitreal administration of bevacizumab was followed by a mean increase in BCVA of 7.3 +/- 17 (mean +/- standard deviation) letters between baseline and month 4, which was 1 month after the last injection (p < 0.0001). This was accompanied by a reduction in mean macular volume from 9.90 +/- 1.9 mm(3) to 8.96 +/- 2.4 mm(3) (p = 0.002) and in foveal subfield thickness from 447 +/- 117 microm to 388 +/- 117 microm (p = 0.03). Two eyes with early proliferative diabetic retinopathy lost all signs of proliferation without any evidence of fibrosis. Although there was a trend towards vasoconstriction, the changes in vessel diameters (arteries and veins) after 4 months of intravitreal Avastin injection were not statistically significant (p = 0.9 and p = 0.17, respectively). Foveal thickness in non-injected fellow eyes with DMO changed from 428 +/- 153 microm at baseline to 383 +/- 151 microm at 4 months (p = 0.1), which did not reach statistical significance.
Intravitreal bevacizumab 1 mg every 6 weeks was followed by a moderate reduction in DMO without normalization of foveal and macular thickness. Our observations suggest that a larger study where patients are examined sooner after injection is needed to elucidate the potential relationship between changes in retinal vessel diameters and thickness changes in DMO.
评估玻璃体内注射贝伐单抗对糖尿病性黄斑水肿(DMO)和视网膜血管管径的影响。
我们进行了一项连续病例系列研究,10例连续的弥漫性DMO患者的眼睛,其中2例此前未接受过治疗,接受了1毫克玻璃体内注射贝伐单抗,随后每隔6周再注射两次。在注射前即刻的基线以及首次注射后1、2.5和4个月进行眼底摄影和光学相干断层扫描(OCT)。观察指标为早期糖尿病性视网膜病变研究字母表中的最佳矫正视力(BCVA)、黄斑体积、黄斑中心凹子区域厚度和血管直径测量。
玻璃体内注射贝伐单抗后,在基线至第4个月(即最后一次注射后1个月)期间,BCVA平均增加7.3±17(平均值±标准差)个字母(p<0.0001)。同时,平均黄斑体积从9.90±1.9立方毫米降至8.96±2.4立方毫米(p = 0.002),黄斑中心凹子区域厚度从447±117微米降至388±117微米(p = 0.03)。2例早期增殖性糖尿病视网膜病变患者的所有增殖迹象消失,且无纤维化迹象。尽管有血管收缩趋势,但玻璃体内注射阿瓦斯汀4个月后血管直径(动脉和静脉)的变化无统计学意义(分别为p = 0.9和p = 0.17)。未注射的患有DMO的对侧眼的黄斑中心凹厚度从基线时的428±153微米变为4个月时的383±151微米(p = 0.1),未达到统计学意义。
每6周玻璃体内注射1毫克贝伐单抗后,DMO有适度减轻,但黄斑中心凹和黄斑厚度未恢复正常。我们的观察结果表明,需要进行一项更大规模的研究,在注射后更早对患者进行检查,以阐明视网膜血管直径变化与DMO厚度变化之间的潜在关系。