Department of Ophthalmology, Rigshospitalet, Copenhagen, Denmark.
Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Acta Ophthalmol. 2018 May;96(3):267-278. doi: 10.1111/aos.13638. Epub 2017 Dec 14.
To investigate long-term functional and anatomical outcomes, discontinuation patterns, drug switching and rates of nonimprovement in patients treated with ranibizumab pro re nata (PRN) regimen for diabetic macular oedema (DME) according to the Danish national guidelines.
Retrospective cohort study of 566 eyes in 566 patients with centre-involved DME who started intravitreal treatment with ranibizumab between January 2011 and December 2013 in the Greater Copenhagen region. Data were retrieved from a database and patient records between January 2011 and March 2016 and analysed using mixed-model statistics.
At the conclusion of follow-up, 24.6% were in active ranibizumab follow-up, 25.4% had switched to other intravitreal pharmacotherapy, 31.6% had been discontinued because of disease stability, 13.8% had been lost to follow-up, 1.4% had been discontinued because of low visual acuity (VA), and 3.2% had died. At baseline, mean best-corrected visual acuity (BCVA) and mean central subfield thickness (CST) were 64.9 (±15.0) letters and 400.2 (±120.3) μm. Mean change in BCVA and mean change in CST from baseline to 3, 12, 24, 36 and 48 months of follow-up were +3.9, +3.5, +2.7, +1.8, +2.3 letters and -97.4, -102.6, -106.9, -105.9, -131.6 μm, respectively. Mean number of injections was 6.1 in year 1 and 1.8 in year 4. In 93 patients, drug switching to aflibercept showed no difference between the two drugs on BCVA or CST. In 79 patients, CST decreased <10% compared to baseline during the first year.
In a single-centre clinical setting, 566 patients treated for DME with ranibizumab according to the Danish national guidelines were followed for up to 4 years. Best-corrected visual acuity (BCVA) outcomes are in the low end of clinical studies, but studied on a wider population and achieved with fewer injections.
根据丹麦国家指南,调查接受雷珠单抗按需治疗(PRN)方案治疗糖尿病黄斑水肿(DME)的患者的长期功能和解剖结果、停药模式、药物转换以及无改善率。
对 2011 年 1 月至 2013 年 12 月在哥本哈根地区中心接受雷珠单抗玻璃体内治疗的 566 例累及中心的 DME 患者的 566 只眼进行回顾性队列研究。数据于 2011 年 1 月至 2016 年 3 月从数据库和患者记录中检索,采用混合模型统计进行分析。
在随访结束时,24.6%的患者处于雷珠单抗的活跃随访中,25.4%的患者已转为其他玻璃体内药物治疗,31.6%的患者因疾病稳定而停药,13.8%的患者失访,1.4%的患者因视力不佳而停药,3.2%的患者死亡。基线时,最佳矫正视力(BCVA)和中央视网膜厚度(CST)的平均值分别为 64.9(±15.0)个字母和 400.2(±120.3)μm。从基线到 3、12、24、36 和 48 个月随访时,BCVA 的平均变化和 CST 的平均变化分别为+3.9、+3.5、+2.7、+1.8 和+2.3 个字母和-97.4、-102.6、-106.9、-105.9、-131.6μm。第一年的注射次数为 6.1,第四年的注射次数为 1.8。在 93 例患者中,药物转换为阿柏西普治疗后,两种药物在 BCVA 或 CST 方面无差异。在 79 例患者中,第一年 CST 较基线下降<10%。
在单一中心临床环境中,566 例根据丹麦国家指南接受雷珠单抗治疗的 DME 患者接受了长达 4 年的随访。最佳矫正视力(BCVA)结果处于临床研究的较低水平,但研究人群更广,注射次数更少。