Department of Ophthalmology, Federal University of São Paulo, São Paulo, São Paulo, Brazil.
Glaucoma Department, Hospital de Olhos de Sergipe, Aracaju, Sergipe, Brazil.
PLoS One. 2022 May 26;17(5):e0268623. doi: 10.1371/journal.pone.0268623. eCollection 2022.
This unicentric randomized clinical trial was designed to compare the surgical outcomes of mitomycin C-enhanced trabeculectomy (MMC-TRAB) with and without subtenon triamcinolone acetonide (TAAC) injection in patients with non-inflammatory glaucomas. This trial is registered at the Brazilian Registry of Clinical Trials (ReBEC) under the register number RBR-53f8nh. Consecutive non-inflammatory glaucoma patients requiring surgical intervention were randomized into two groups. In the control group, eyes underwent standard MMC-TRAB, while in the intervention group, besides the standard MMC-TRAB, these eyes also received a subtenon TAAC injection (4mg) close to the bleb site at the end of the surgery. The main outcomes of the study were surgical success rates, intraocular pressure (IOP) and number of medications at all timepoints. Success was defined as IOP ≤ 15 mmHg and subdivided in complete or qualified according to the need of medication. A total of 75 eyes of 63 different patients were included (intervention group = 39 eyes; control group = 36 eyes). There was no difference between groups at baseline (p>0.11). Multivariable regression analysis indicated that IOP levels were significantly lower in the intervention group at 18 and 24 months of follow-up when number of medications was considered as a covariate (P<0.001). Complete success rates were higher in the intervention group at 06 (90.9% vs 68.7%; p = 0.03), 12 (87.2% vs 66.7%; p = 0.02) and 18 months (87.2% vs 66.7%; p = 0.02). Additionally, although success rates at 24 months were higher in the intervention group (82.0% vs 66.7%; p = 0.09), this difference did not reach statistical significance. Qualified success rates did not significantly differ between groups at all timepoints. In conclusion, this study found significantly lower IOPs levels at 18 and 24 months of follow-up and higher complete success rates until 18 months of follow-up, with the use of subtenon TAAC as an adjuvant to standard MMC-TRABs in non-inflammatory glaucoma patients.
这项单中心随机临床试验旨在比较丝裂霉素 C 增强小梁切除术(MMC-TRAB)联合和不联合曲安奈德(TAAC)眼周注射在非炎症性青光眼患者中的手术效果。本试验已在巴西临床试验注册中心(ReBEC)注册,注册号为 RBR-53f8nh。连续需要手术干预的非炎症性青光眼患者被随机分为两组。在对照组中,眼接受标准 MMC-TRAB,而在干预组中,除了标准 MMC-TRAB 外,这些眼在手术结束时还在滤过泡部位附近接受了眼周 TAAC 注射(4mg)。研究的主要结局是手术成功率、眼压(IOP)和所有时间点的药物数量。成功定义为 IOP≤15mmHg,并根据药物需求分为完全成功或合格成功。共有 63 名患者的 75 只眼(干预组=39 只眼;对照组=36 只眼)纳入研究。两组患者在基线时无差异(p>0.11)。多变量回归分析表明,当考虑药物数量作为协变量时,干预组在随访 18 和 24 个月时 IOP 水平显著较低(P<0.001)。干预组在 06 个月(90.9% vs. 68.7%;p=0.03)、12 个月(87.2% vs. 66.7%;p=0.02)和 18 个月(87.2% vs. 66.7%;p=0.02)时完全成功率更高。此外,尽管干预组在 24 个月时的成功率更高(82.0% vs. 66.7%;p=0.09),但这一差异没有统计学意义。在所有时间点,合格成功率在两组之间没有显著差异。总之,本研究发现,在随访 18 和 24 个月时,眼周注射曲安奈德作为非炎症性青光眼患者标准 MMC-TRAB 的辅助治疗,可显著降低眼压,在 18 个月时的完全成功率更高。