He Chang-Zhu, Lu Song-Jie, Zeng Zhao-Jun, Liu Jun-Qiao, Qiu Qin, Xue Fu-Li, He Yu
Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan, China.
Department of Ophthalmology, Chengdu First People's Hospital/Chengdu Integrated TCM and Western Medicine Hospital, Chengdu, Sichuan, China.
Front Med (Lausanne). 2024 Jul 31;11:1405261. doi: 10.3389/fmed.2024.1405261. eCollection 2024.
The intraocular injections of anti-vascular endothelial growth factor (anti-VEGF) demonstrates significant efficacy in inhibiting the formation of ocular neovascularization in neovascular glaucoma (NVG). Ahmed glaucoma valve implantation (AGVI) is extensively employed for the management of diverse glaucoma types.
To further evaluate the efficacy and safety of anti-VEGF combined with AGVI in the treatment of neovascular glaucoma.
A thorough search for randomized controlled trials (RCTs) was conducted across eight databases: PubMed, EMBASE, the Cochrane Library, Web of Science, China National Knowledge Infrastructure, Wanfang, SinoMed, and VIP. The search period was set from the inception of each database until March 2, 2024, to identify RCTs investigating the effectiveness and safety of combining AGVI with anti-VEGF therapy for NVG. We used the Cochrane Risk of Bias Assessment Tool to evaluate the quality of the literature and performed statistical analysis using Stata 15.0 software.
Fourteen RCTs were included in this study. Compared with AGVI alone, the combination of anti-VEGF drugs and AGVI can reduce postoperative intraocular pressure (IOP) at 1 week [WMD = -4.03, 95% CI (-5.73, -2.34), < 0.001], 1 month [WMD = -5.39, 95% CI (-7.05, -3.74), < 0.001], 3 months [WMD = -6.59, 95% CI (-7.85, -5.32), < 0.001], 6 months [WMD = -4.99, 95% CI (-9.56, -0.43), = 0.032], and more than 12 months [WMD = -3.86, 95% CI (-6.82, -0.90), = 0.011], with a higher Effective rate [RR = 1.27, 95% CI (1.18, 1.37), < 0.001], decreased incidence of postoperative hyphema [RR = 0.24, 95% CI (0.15, 0.39), < 0.001], reduced use of postoperative antiglaucoma medications [WMD = -0.48, 95% CI (-0.61, -0.35), < 0.001], and decreased aqueous humor VEGF levels [SMD = -2.84, 95% CI (-4.37, -1.31), < 0.001].
In comparison to AGVI alone, the combination of AGVI with anti-VEGF therapy has better effects in reducing IOP at various time intervals, diminishing postoperative antiglaucoma medication requirements and reducing aqueous humor VEGF levels. Furthermore, it effectively minimizes the incidence of postoperative hyphema. Nevertheless, due to the variability in the quality of the trials included, further high-quality experiments will be required in the future to substantiate this conclusion.
PROSPERO, identifier CRD42024519862, https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024519862.
眼内注射抗血管内皮生长因子(anti-VEGF)在抑制新生血管性青光眼(NVG)眼内新生血管形成方面显示出显著疗效。艾哈迈德青光眼阀植入术(AGVI)被广泛用于治疗各种类型的青光眼。
进一步评估抗VEGF联合AGVI治疗新生血管性青光眼的疗效和安全性。
全面检索了八个数据库中的随机对照试验(RCT):PubMed、EMBASE、Cochrane图书馆、科学网、中国知网、万方、中国生物医学文献数据库和维普资讯。检索期设定为从每个数据库建立到2024年3月2日,以确定研究AGVI联合抗VEGF治疗NVG有效性和安全性的RCT。我们使用Cochrane偏倚风险评估工具评估文献质量,并使用Stata 15.0软件进行统计分析。
本研究纳入了14项RCT。与单纯AGVI相比,抗VEGF药物与AGVI联合使用可在术后1周[加权均数差(WMD)=-4.03,95%置信区间(CI)(-5.73,-2.34),P<0.001]、1个月[WMD=-5.39,95%CI(-7.05,-3.74),P<0.001]、3个月[WMD=-6.59,95%CI(-7.85,-5.32),P<0.001]、6个月[WMD=-4.99,95%CI(-9.56,-0.43),P=0.032]和超过12个月[WMD=-3.86,95%CI(-6.82,-0.90),P=0.011]降低术后眼压(IOP),有效率更高[相对危险度(RR)=1.27,95%CI(1.18,1.37),P<0.001],术后前房积血发生率降低[RR=0.24,95%CI(0.15,0.39),P<0.001],术后抗青光眼药物使用减少[WMD=-0.48,95%CI(-0.61,-0.35),P<0.001],房水VEGF水平降低[标准化均数差(SMD)=-2.84,95%CI(-4.37,-1.31),P<0.001]。
与单纯AGVI相比,AGVI联合抗VEGF治疗在不同时间间隔降低眼压、减少术后抗青光眼药物需求和降低房水VEGF水平方面效果更好。此外,它能有效降低术后前房积血的发生率。然而,由于纳入试验质量存在差异,未来需要进一步的高质量实验来证实这一结论。
PROSPERO,标识符CRD42024519862,https://www.crd.york.ac.uk/prospero/display_record.php?ID=CRD42024519862 。