Wolfrum Peter, Böhm Elsa Wilma, König Simon, Lorenz Katrin, Stoffelns Bernhard, Korb Christina A
Department of Ophthalmology, University Medical Center of the Johannes Gutenberg-University Mainz, Langenbeckstr. 1, 55131 Mainz, Germany.
J Clin Med. 2025 May 15;14(10):3449. doi: 10.3390/jcm14103449.
Acute submacular hemorrhage (SMH) is a vision-threatening complication common in patients affected by age-related macular degeneration (AMD). This study evaluates safety, long-term clinical outcomes and associated treatment factors following intravitreal triple injection of recombinant tissue plasminogen activator (rtPA), SF gas, and Bevacizumab due to acute SMH secondary to AMD. A retrospective analysis on patients who received treatment between January 2014 and December 2020 ( = 37) was conducted. Visual acuity (VA), central retinal thickness (CRT), central retinal volume (CRV), and axial pigment epithelial detachment height were analyzed at baseline (B), 4 weeks after triple injection (FU1), after the following anti-VEGF injection series (FU2), after 1 year (FU3), after 2 years (FU4), and at the final follow-up examination after 4.4 ± 1.6 years (FU5). Further, treatment courses and clinical outcomes were compared to a patient cohort treated for exudative AMD without prior SMH. Furthermore, an explorative data analysis on final VA was conducted, and adverse events following triple therapy were investigated. Triple injection was performed on average 5.6 ± 5.7 days after onset of symptoms. Patients received 16 ± 3 additional intravitreal anti-VEGF injections due to persistent macular edema over the subsequent 2 years. Significant improvements were observed at FU1 in VA ( < 0.001), CRT ( = 0.005), and CRV ( = 0.007), as well as at FU2 in axial PED height ( < 0.001), with all improvements being stable until final follow-up examination. In the group comparison, patients with SMH demonstrated significantly worse functional and anatomical outcomes at 24 months except for the 24-month CRT, and patients on average received more intravitreal injections. Five of 37 patients (13.5%) experienced a retinal pigment epithelial tear following triple injection. Final VA correlated positively and significantly with FU1 VA, while no correlation was observed with baseline VA, the size or height of SMH, or the number of additional anti-VEGF injections. Triple injection constitutes a simple and effective therapy with long-term functional and anatomical improvements following treatment due to SMH, although patients have an increased risk for RPE tears. The 4-week postoperative VA following triple injection was predictive for long-term visual function.
急性黄斑下出血(SMH)是年龄相关性黄斑变性(AMD)患者中常见的一种威胁视力的并发症。本研究评估了因AMD继发急性SMH而进行玻璃体内三联注射重组组织型纤溶酶原激活剂(rtPA)、SF气体和贝伐单抗后的安全性、长期临床结局及相关治疗因素。对2014年1月至2020年12月期间接受治疗的患者(n = 37)进行了回顾性分析。在基线(B)、三联注射后4周(FU1)、后续抗VEGF注射系列后(FU2)、1年后(FU3)、2年后(FU4)以及4.4±1.6年的最终随访检查(FU5)时分析视力(VA)、中心视网膜厚度(CRT)、中心视网膜体积(CRV)和轴向色素上皮脱离高度。此外,将治疗过程和临床结局与一组未发生过SMH的渗出性AMD患者进行了比较。此外,对最终视力进行了探索性数据分析,并调查了三联疗法后的不良事件。三联注射平均在症状出现后5.6±5.7天进行。在随后的2年中,由于持续性黄斑水肿,患者平均接受了16± 3次额外的玻璃体内抗VEGF注射。在FU1时,VA(P < 0.001)、CRT(P = 0.005)和CRV(P = 0.007)有显著改善,在FU2时轴向PED高度(P < 0.001)有显著改善,所有改善在最终随访检查前均保持稳定。在组间比较中,除24个月时的CRT外,SMH患者在24个月时的功能和解剖学结局明显更差,且患者平均接受的玻璃体内注射次数更多。37例患者中有5例(13.5%)在三联注射后发生了视网膜色素上皮撕裂。最终视力与FU1时的视力呈显著正相关,而与基线视力、SMH的大小或高度以及额外抗VEGF注射的次数均无相关性。三联注射是一种简单有效的治疗方法,治疗后因SMH导致的长期功能和解剖学有改善,尽管患者发生RPE撕裂的风险增加。三联注射后4周的术后视力可预测长期视觉功能。