Panagiotis Dervenis, Nikolaos Dervenis, David Steel, Teresa Sandinha, Paris Tranos, Panagiotis Vasilakis, Ioannis Liampas, Chrysoula Doxani, Elias Zintzaras
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引用次数: 4
Abstract
Background: Diabetic retinopathy is a leading cause of visual loss in the working population. Pars plana vitrectomy has become the mainstream treatment option for severe proliferative diabetic retinopathy (PDR) associated with significant vitreous haemorrhage and/or tractional retinal detachment. Despite the advances in surgical equipment, diabetic vitrectomy remains a challenging operation, requiring advanced microsurgical skills, especially in the presence of tractional retinal detachment. Preoperative intravitreal bevacizumab has been widely employed as an adjuvant to ease surgical difficulty and improve postoperative prognosis.Aims: This study aims to assess the effectiveness of preoperative intravitreal bevacizumab in reducing intraoperative complications and improving postoperative outcomes in patients undergoing vitrectomy for the complications of PDR.
Methods: A literature search was conducted using the PubMed, Cochrane, and ClinicalTrials.gov databases to identify all related studies published before 31/10/2020. Prespecified outcome measures were operation time, intraoperative iatrogenic retinal breaks, best-corrected visual acuity in the last follow-up visit, the presence of any postoperative vitreous haemorrhage and the need to re-operate. Evidence synthesis was performed using Fixed or Random Effects models, depending on the heterogeneity of the included studies. Heterogeneity was assessed using Q-statistic and I2. Additional meta-regression models, subgroup analyses and sensitivity analyses were performed as appropriate.
Results: Thirteen randomized control trials, with a total of 688 eyes were included in this review. Comparison of the intraoperative data showed that bevacizumab reduced operation time (p < 0.001), minimized iatrogenic retinal breaks (p < 0.001), provided better long-term visual acuity outcomes (p = 0.005), and prevented vitreous haemorrhage (p < 0.001) and the need for reoperation (p = 0.001 < 0.05). Findings were strongly corroborated by additional sensitivity and subgroup analyses.
Conclusion: Preoperative administration of bevacizumab is effective in reducing intraoperative complications and improving the postoperative prognosis of diabetic vitrectomy.PROSPERO registration number: CRD42021219280.
背景:糖尿病视网膜病变是工作人群视力丧失的主要原因。玻璃体切除已成为严重增殖性糖尿病视网膜病变(PDR)伴严重玻璃体出血和/或牵引性视网膜脱离的主流治疗选择。尽管手术设备的进步,糖尿病玻璃体切除术仍然是一个具有挑战性的手术,需要先进的显微外科技术,特别是在牵引性视网膜脱离的存在。术前玻璃体内贝伐单抗作为辅助治疗被广泛应用,以缓解手术难度,改善术后预后。目的:本研究旨在评估术前玻璃体内贝伐单抗在减少PDR并发症玻璃体切除术患者术中并发症和改善术后预后方面的有效性。方法:使用PubMed、Cochrane和ClinicalTrials.gov数据库进行文献检索,确定2020年10月31日之前发表的所有相关研究。预先规定的结果测量是手术时间,术中医源性视网膜断裂,最后一次随访的最佳矫正视力,术后玻璃体出血的存在和再次手术的需要。根据纳入研究的异质性,采用固定效应或随机效应模型进行证据综合。采用q统计量和I2评价异质性。适当时进行meta回归模型、亚组分析和敏感性分析。结果:本综述纳入13项随机对照试验,共688只眼。术中资料对比显示,贝伐单抗可缩短手术时间(p p = 0.005),预防玻璃体出血(p p = 0.001)。结论:术前给予贝伐单抗可有效减少糖尿病玻璃体切除术术中并发症,改善术后预后。普洛斯彼罗注册号:CRD42021219280。