Nawar Amin E
Ophthalmology Department, Faculty of Medicine, Tanta University, Tanta, 31516, Egypt.
BMC Ophthalmol. 2025 Jul 3;25(1):350. doi: 10.1186/s12886-025-03972-6.
The present study evaluated the efficacy of combined use of suprachoroidal injection of triamcinolone acetonide (SCTA) using a modified custom needle with topical nepafenac 0.3% in the treatment of pseudophakic cystoid macular edema (PCME).
A prospective randomized study that included sixty eyes of 60 patients with PCME. Patients were divided in two groups, group (1) included 30 patients who received topical nepafenac 0.3% eye drops alone and group (2) that included 30 patients who received a single SCTA (4 mg/0.1 ml) combined with topical nepafenac 0.3% eye drops.
In group 1, the central macular thickness (CMT) decreased from 457.4 ± 81.4 um to 252.9 ± 54.6 um after 12 months. In respect to group 2, CMT declined from 455.1 ± 79.6 um to 213.7 ± 14.2 um after 12 months. The CMT was more significantly reduced in group 2 after 1,3,6,9 and 12 months (p value < 0.001). Group 1 showed improvement of best corrected visual acuity (BCVA) by log MAR from 0.9(0.8-1) to 0.2(0.1-0.4) after 12 months, while group 2 showed improvement from 0.9(0.8-1) to 0.1(0-0.1) after 12 months. More significant improvement of BCVA was detected in group 2 after 1,3,6 and 9 months with p value < 0.001 and after 12 months with p value 0.001.
Combined SCTA using this modified custom needle with topical nepafenac 0.3% resulted in better anatomical and functional results in PCME patients compared to topical nepafenac 0.3% alone. The study was prospectively registered with clinical trial.gov ID (NCT04690608) in 27-12-2020.
本研究评估了使用改良定制针头脉络膜上腔注射曲安奈德(SCTA)联合0.3%奈帕芬酸局部用药治疗人工晶状体眼黄斑囊样水肿(PCME)的疗效。
一项前瞻性随机研究,纳入60例PCME患者的60只眼。患者分为两组,第(1)组包括30例仅接受0.3%奈帕芬酸滴眼液局部用药的患者,第(2)组包括30例接受单次SCTA(4mg/0.1ml)联合0.3%奈帕芬酸滴眼液局部用药的患者。
第1组,12个月后中心黄斑厚度(CMT)从457.4±81.4μm降至252.9±54.6μm。第2组,12个月后CMT从455.1±79.6μm降至213.7±14.2μm。第2组在1、3、6、9和12个月后CMT降低更显著(p值<0.001)。第1组12个月后最佳矫正视力(BCVA)以log MAR表示从0.9(0.8 - 1)提高到0.2(0.1 - 0.4),而第2组12个月后从0.9(0.8 - 1)提高到0.1(0 - 0.1)。第2组在1、3、6和9个月后BCVA改善更显著,p值<0.001,12个月后p值为0.001。
与单独使用0.3%奈帕芬酸局部用药相比, 使用这种改良定制针头联合0.3%奈帕芬酸局部用药的SCTA在PCME患者中产生了更好的解剖学和功能学结果。该研究于2020年12月27日在clinicaltrial.gov上进行了前瞻性注册,注册号为NCT04690608。