Chen Chih-Hsin, Liu Ya-Chi, Wu Pei-Chang
Department of Ophthalmology, Chang Gung Memorial Hospital, Kaohsiung Medical Center, Chang Gung University College of Medicine, Kaohsiung, Taiwan, People's Republic of China.
J Ocul Pharmacol Ther. 2009 Feb;25(1):83-9. doi: 10.1089/jop.2008.0068.
The aim of this study was to assess the efficacy of phacoemulsification combined with intravitreal (i.v.t.) bevacizumab injection in diabetics with clinically significant macular edema (CSME) and cataract.
This retrospective study included diabetic patients with cataract and CSME who underwent phacoemulsification and intraocular lens implantation with a 2.5-mg bevacizumab i.v.t injection (ivBe) (15 eyes) or without ivBe (controls, 14 eyes). Best-corrected visual acuity (BCVA), central macular thickness (CMT) measured by optic coherence tomography (OCT), and adverse events were recorded.
In the ivBe group, the OCT images demonstrated that CMT (mean +/- standard deviation [SD]) decreased significantly from 466 +/- 105 at baseline to 333 +/- 107, 313 +/- 138 and 333 +/- 111 microm at 4, 8, and 12 weeks, respectively, after treatment (P < 0.05). The visual acuity in logMAR (mean +/- SD) improved significantly from 1.66 +/- 0.39 at baseline to 1.30 +/- 0.50, 1.15 +/- 0.42, 0.99 +/- 0.48, and 1.03+/- 0.44 at 1, 4, 8, and 12 weeks, respectively, after treatment (P < 0.05). However, in the control group, the CMT changed insignificantly from 443 +/- 109 at baseline to 463 +/- 106, 425 +/- 128, and 421 +/- 119 microm at 4, 8 and 12 weeks, respectively after treatment (P > 0.05). The visual acuity in logMAR improved insignificantly from 1.63 +/- 0.42 at baseline to 1.43 +/- 0.53, and 1.39 +/- 0.43 at 1, and 4 weeks (P > 0.05) and significantly to 1.24 +/- 0.45 and 1.18 +/- 0.44 at 8 and 12 weeks, respectively, after treatment (P < 0.05). None of the patients in both groups experienced injection- or surgery-related complications or any obvious systemic adverse events.
The short-term results suggest that phacoemulsification with i.v.t. bevacizumab safely reduces macular edema and improves visual acuity for cataract and CSME in diabetics.
本研究旨在评估超声乳化白内障吸除术联合玻璃体内注射贝伐单抗对患有临床显著性黄斑水肿(CSME)及白内障的糖尿病患者的疗效。
这项回顾性研究纳入了患有白内障及CSME的糖尿病患者,这些患者接受了超声乳化白内障吸除术及人工晶状体植入术,其中15只眼接受了2.5毫克贝伐单抗玻璃体内注射(ivBe),14只眼作为对照组未接受ivBe。记录最佳矫正视力(BCVA)、光学相干断层扫描(OCT)测量的中心黄斑厚度(CMT)以及不良事件。
在ivBe组中,OCT图像显示,治疗后4周、8周和12周时,CMT(平均值±标准差[SD])分别从基线时的466±105显著降至333±107、313±138和333±111微米(P<0.05)。治疗后1周、4周、8周和12周时,logMAR视力(平均值±SD)分别从基线时的1.66±0.39显著提高至1.30±0.50、1.15±0.42、0.99±0.48和1.03±0.44(P<0.05)。然而,在对照组中,治疗后4周、8周和12周时,CMT分别从基线时的443±109无显著变化至463±106、425±128和421±119微米(P>0.05)。治疗后1周和4周时,logMAR视力从基线时的1.63±0.42无显著提高至1.43±0.53和1.39±0.43(P>0.05),而在治疗后8周和12周时分别显著提高至1.24±0.45和1.18±0.44(P<0.05)。两组患者均未发生与注射或手术相关的并发症或任何明显的全身不良事件。
短期结果表明,超声乳化白内障吸除术联合玻璃体内注射贝伐单抗可安全减轻黄斑水肿,并改善糖尿病患者白内障及CSME的视力。