Safety and efficacy of Tobramycin 0.3% + Fluormetholone 0.1% (eye drops) fixed combination as a preoperative preparation and postoperative management of patients with wet AMD after intravitreal injection of ranibizumab. An observational, noncomparative single-center study
{"title":"Safety and efficacy of Tobramycin 0.3% + Fluormetholone 0.1% (eye drops) fixed combination as a preoperative preparation and postoperative management of patients with wet AMD after intravitreal injection of ranibizumab. An observational, noncomparative single-center study","authors":"V. P. Fokin, S. V. Balalin, L. Ushakova","doi":"10.25276/0235-4160-2023-1-62-68","DOIUrl":null,"url":null,"abstract":"Purpose. To evaluate safety and efficacy of Floas-T ® (Tobramycin 0.3% + Fluormetholone 0.1%) as a preoperative preparation and postoperative management of patients with wet form of age-related macular degeneration (AMD) before and after intravitreal injection (IVI) of anti-VEGF drugs. Material and methods. 50 patients (50 eyes) with the wet form of AMD were examined and divided into two groups. The first group included 32 patients (32 eyes) with wet form of AMD. The second group consisted of 18 patients (18 eyes) with primary (11 eyes) and advanced (7 eyes) stages of primary open angle glaucoma with normalized IOP and wet form of AMD. Results. There were no significant changes in ВСVA and tonometric IOP values in the two groups before and within 7 days after IVI of ranibizumab and Floas-T ® instillations. Average value of individually tolerable true IOP in patients of the second group was 16,3±1,1 mm Hg, while average value of initial true IOP (14,7±2,56 mm Hg) pre-op was lower than tolerable pressure, indicating that individual norm of ophthalmotonus in glaucoma patients was reached. The difference between the mean values of ocular hydrodynamics in both groups before and 1 week after surgery was also statistically unsignificant (p>0.05). The difference between the mean values of the Schirmer I test was statistically unsignificant in patients in the two groups (p>0.05) before and after surgery, indicating the absence of Floas-T ® effect on tear production. There were no local and systemic side effects of Floas-T ® in 50 patients (50 eyes) during the observation period. Conclusion. Floas-T ® had an antiinflammatory effect without a decrease in the aqueous humor outflow, did not cause a significant increase in IOP in the early postoperative period, did not decrease tear production, and did not cause adverse local and systemic side effects. Floas-T ® can be used as a preoperative preparation and postoperative management drug in patients with wet type of AMD as well as in combination with primary open angle glaucoma when achieving an individual level of intraocular pressure. Key words: wet AMD, preoperative preparation, postoperative management, Floas-T® drug","PeriodicalId":424200,"journal":{"name":"Fyodorov journal of ophthalmic surgery","volume":"21 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fyodorov journal of ophthalmic surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.25276/0235-4160-2023-1-62-68","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Purpose. To evaluate safety and efficacy of Floas-T ® (Tobramycin 0.3% + Fluormetholone 0.1%) as a preoperative preparation and postoperative management of patients with wet form of age-related macular degeneration (AMD) before and after intravitreal injection (IVI) of anti-VEGF drugs. Material and methods. 50 patients (50 eyes) with the wet form of AMD were examined and divided into two groups. The first group included 32 patients (32 eyes) with wet form of AMD. The second group consisted of 18 patients (18 eyes) with primary (11 eyes) and advanced (7 eyes) stages of primary open angle glaucoma with normalized IOP and wet form of AMD. Results. There were no significant changes in ВСVA and tonometric IOP values in the two groups before and within 7 days after IVI of ranibizumab and Floas-T ® instillations. Average value of individually tolerable true IOP in patients of the second group was 16,3±1,1 mm Hg, while average value of initial true IOP (14,7±2,56 mm Hg) pre-op was lower than tolerable pressure, indicating that individual norm of ophthalmotonus in glaucoma patients was reached. The difference between the mean values of ocular hydrodynamics in both groups before and 1 week after surgery was also statistically unsignificant (p>0.05). The difference between the mean values of the Schirmer I test was statistically unsignificant in patients in the two groups (p>0.05) before and after surgery, indicating the absence of Floas-T ® effect on tear production. There were no local and systemic side effects of Floas-T ® in 50 patients (50 eyes) during the observation period. Conclusion. Floas-T ® had an antiinflammatory effect without a decrease in the aqueous humor outflow, did not cause a significant increase in IOP in the early postoperative period, did not decrease tear production, and did not cause adverse local and systemic side effects. Floas-T ® can be used as a preoperative preparation and postoperative management drug in patients with wet type of AMD as well as in combination with primary open angle glaucoma when achieving an individual level of intraocular pressure. Key words: wet AMD, preoperative preparation, postoperative management, Floas-T® drug
目的。评价Floas-T®(妥布霉素0.3% +氟美洛酮0.1%)作为湿型年龄相关性黄斑变性(AMD)患者玻璃体内注射(IVI)抗vegf药物前后的术前准备和术后管理的安全性和有效性。材料和方法。对湿型黄斑变性患者50例(50只眼)进行检查,分为两组。第一组包括32例湿性黄斑变性患者(32只眼)。第二组包括18例(18眼)原发(11眼)和晚期(7眼)伴有正常IOP和湿型AMD的原发性开角型青光眼患者。结果。注射雷尼单抗和Floas-T®后7天内,两组患者的ВСVA和眼压值均无显著变化。第二组患者个体可耐受的真眼压平均值为16.3±1.1 mm Hg,而术前初始真眼压平均值(14.7±2.56 mm Hg)低于可耐受压,达到青光眼患者眼压的个体标准。两组患者术前与术后1周眼水动力学平均值比较,差异均无统计学意义(p>0.05)。两组患者术前、术后Schirmer I检验平均值差异无统计学意义(p>0.05),说明Floas-T®对泪液生成无影响。在观察期间,50例患者(50只眼)未出现Floas-T®的局部和全身副作用。结论。Floas-T®具有抗炎作用,但不会减少房水流出量,不会导致术后早期IOP显著升高,不会减少泪液产生,不会引起局部和全身不良副作用。Floas-T®可用于湿型AMD患者的术前准备和术后管理药物,也可用于原发性开角型青光眼患者,当达到个人眼压水平时。关键词:湿性AMD,术前准备,术后管理,Floas-T®药物