Shaikh Fahad Feroz, Jatoi Shafi Muhammad
Dr. Rebecca, MBBS. Department of Ophthalmology, Isra University Hospital, Hyderabad, Pakistan.
Dr. Fahad Feroz Shaikh, FCPS, FVR, FRCS. Department of Ophthalmology, Isra University Hospital, Hyderabad, Pakistan.
Pak J Med Sci. 2021 Jan-Feb;37(1):157-161. doi: 10.12669/pjms.37.1.3141.
To compare efficacy of intravitreal bevacizumab augmented with Panretinal photocoagulation versus Panretinal photocoagulation alone in high risk proliferative diabetic retinopathy.
This is Randomized clinical control trial study conducted at ISRA University Hospital, Hyderabad from July 2018 to December 2018. A total of 76 eyes were randomized into two groups, 38 eyes undergone PRP plus intravitreal bevacizumab, while 38 eyes had PRP alone. Status of neovessels was assessed before and after treatment with the help of fundus fluorescein angiography. Neovessels at disc (NVD's) and neovessels elsewhere (NVE's) were assessed with the disc surface diameter.
Seventy-six eyes were enrolled in this randomized clinical trial into two groups consecutively, that all completed the six months follow-up. In the PRP group mean BCVA (logMAR) worsened significantly from mean 0.30±0.07 to mean 0.40±0.04 at a 30 day and mean 0.40±0.04 at day 90. While BCVA become improved from 0.30±0.05 to 0.1±0.03 at week four and 0.1±0.02 at week 12 in PRP-Plus group. There was significant change in regression of NVES in PRP only group at week 4 is 2.25±0.75 (=0.00004) and at 12 weeks 2.00±0.50 (=0.00002), while in PRP + intravitreal bevacizumab group at 4 week was 1±0.5 ( =0.0001) and at 12 week was 0.75±0.25 (0.0001).
Intravitreal Bevacizumab augmented with PRP is more effective in early regression of neovessels in high risk PDR patients.
比较玻璃体内注射贝伐单抗联合全视网膜光凝与单纯全视网膜光凝治疗高危增殖性糖尿病视网膜病变的疗效。
这是一项于2018年7月至2018年12月在海得拉巴的ISRA大学医院进行的随机临床对照试验研究。总共76只眼被随机分为两组,38只眼接受全视网膜光凝联合玻璃体内注射贝伐单抗治疗,而38只眼仅接受全视网膜光凝治疗。在眼底荧光血管造影的帮助下评估治疗前后新生血管的状况。用视盘表面直径评估视盘新生血管(NVD)和其他部位新生血管(NVE)。
76只眼连续纳入该随机临床试验并分为两组,所有患者均完成了六个月的随访。在全视网膜光凝组,平均最佳矫正视力(logMAR)在30天时从平均0.30±0.07显著恶化至平均0.40±0.04,在90天时为平均0.40±0.04。而在全视网膜光凝联合组,最佳矫正视力在四周时从0.30±0.05改善至0.1±0.03,在12周时为0.1±0.02。仅接受全视网膜光凝组在第4周时新生血管消退有显著变化,为2.25±0.75(P = 0.00004),在12周时为2.00±0.50(P = 0.00002),而在全视网膜光凝联合玻璃体内注射贝伐单抗组,第4周时为1±0.5(P = 0.0001),在12周时为0.75±0.25(P = 0.0001)。
全视网膜光凝联合玻璃体内注射贝伐单抗在高危增殖性糖尿病视网膜病变患者新生血管的早期消退方面更有效。