Zhu Wei, Hao Yanlei, Yuan Zhongfang, Huang Chunmei
Department of Ophthalmology, Central Hospital Affiliated to Shandong First Medical University, Jinan, Shandong 250013, P.R. China.
Exp Ther Med. 2023 May 9;25(6):301. doi: 10.3892/etm.2023.12000. eCollection 2023 Jun.
The aim of the present study was to evaluate the 1-year outcomes of a high-dose aflibercept injection [4 mg 2+ pro re nata (PRN) scheme] for individuals with myopic choroidal neovascularization (mCNV) through optical coherence tomography (OCT) follow-ups. A total of 16 consecutive patients (7 males and 9 females; sixteen eyes) with mCNV were enrolled in this retrospective study. The mean age was 30.5±3.35 years and mean spherical equivalent was -7.31±0.90 D. Subjects received 4 mg aflibercept intravitreal injection on the day of diagnosis and 35 days later. Further injections of aflibercept were required when the following were detected by OCT and fluorescein angiography: i) Decrease in best corrected visual acuity (BCVA); ii) aggravation of metamorphopsia; iii) macular oedema; iv) macular haemorrhage; v) increase in retinal thickness; and vi) leakage. Ophthalmic examination and OCT were performed at the baseline, as well as at 1, 2, 4, 6, 8, 10 and 12 months after the initial aflibercept injection. BCVA and central retinal thickness (CRT) were evaluated at each follow-up. The results showed that the vision of all subjects improved following the aflibercept intravitreal injection. The mean BCVA improved from 0.35±0.15 logarithm of the minimal angle of resolution (logMAR) at the baseline to 0.12±0.05 logMAR at final follow-up (P<0.05). A reduction in metamorphopsia was observed and the mean CRT was reduced from 345.38±34.69 µm of pre-treatment levels to 222.75±8.98 µm at the last postoperative visit (P<0.05). The mean number of injections in the present study was 2.13±0.5. Out of all patients, 13 received two injections and 3 subjects received three injections. The mean follow-up was 13.41±1.17 months. Based on the outcomes, it was found that an intravitreal injection of high-dose aflibercept (4 mg 2+PRN scheme) is effective for vision improvement and stabilization. In addition, it also significantly alleviated metamorphopsia and reduced the CRT in patients treated with mCNV. During the follow-up, the eyesight of the patients was stable.
本研究旨在通过光学相干断层扫描(OCT)随访评估高剂量阿柏西普注射[4毫克,2次及按需(PRN)方案]治疗近视性脉络膜新生血管(mCNV)患者的1年疗效。本回顾性研究共纳入16例连续的mCNV患者(7例男性和9例女性;16只眼)。平均年龄为30.5±3.35岁,平均等效球镜度数为-7.31±0.90 D。受试者在诊断当天及35天后接受4毫克阿柏西普玻璃体腔内注射。当通过OCT和荧光素血管造影检测到以下情况时,需要进一步注射阿柏西普:i)最佳矫正视力(BCVA)下降;ii)视物变形加重;iii)黄斑水肿;iv)黄斑出血;v)视网膜厚度增加;vi)渗漏。在基线以及首次阿柏西普注射后的1、2、4、6、8、10和12个月进行眼科检查和OCT检查。每次随访时评估BCVA和中心视网膜厚度(CRT)。结果显示,所有受试者在接受阿柏西普玻璃体腔内注射后视力均有改善。平均BCVA从基线时的0.35±0.15最小分辨角对数(logMAR)提高到最终随访时的0.12±0.05 logMAR(P<0.05)。观察到视物变形减轻,平均CRT从治疗前水平的345.38±34.69 µm降至术后最后一次随访时的222.75±8.98 µm(P<0.05)。本研究中的平均注射次数为2.13±0.5次。所有患者中,13例接受了两次注射,3例接受了三次注射。平均随访时间为13.41±1.17个月。基于这些结果,发现玻璃体腔内注射高剂量阿柏西普(4毫克,2次+PRN方案)对改善和稳定视力有效。此外,它还显著减轻了视物变形,并降低了mCNV治疗患者的CRT。在随访期间,患者的视力稳定。