Short-term Efficacy and Safety of Omidenepag Isopropyl 0.002% w/v Therapy for Patients with Primary Open-angle Glaucoma and Ocular Hypertension

IF 0.1 Q4 OPHTHALMOLOGY
Jung Soo Kim, Jung Lim Kim
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引用次数: 0

Abstract

Purpose: To analyze the short-term efficacy and safety of omidenepag isopropyl 0.002% (w/v) in patients with primary open-angle glaucoma and ocular hypertension.Methods: Data on 36 patients with primary open-angle glaucoma and ocular hypertension treated with omidenepag isopropyl 0.002% (w/v) from January 2021 to May 2022 were retrospectively analyzed. We investigated whether the drug lowered the intraocular pressure (IOP) at 1 and 3 months compared to baseline. Possible side effects were sought at each visit.Results: The mean patient age was 59.2 years at the time of treatment. Of the 36 patients, 33 had primary open-angle glaucoma and 3 had ocular hypertension. The baseline IOP was 15.9 ± 3.6 mmHg, which significantly decreased to 13.7 ± 2.8 and 13.4 ± 2.9 mmHg at 1 and 3 months, respectively, following instillation of omidenepag isopropyl 0.002% (w/v) (both p < 0.01). Twelve patients (29.2%) experienced side effects including hyperemia, ocular pain, and itching but only two (5.5%) stopped using the medication.Conclusions: In the short-term, ominedepag isopropyl 0.002% (w/v) is effective and safe in patients with primary open-angle glaucoma and ocular hypertension.
0.002%异丙基奥米尼帕格w/v治疗原发性开角型青光眼和高眼压的近期疗效和安全性
目的:分析0.002%异丙基奥米尼帕格(w/v)治疗原发性开角型青光眼合并高眼压的近期疗效和安全性。方法:回顾性分析2021年1月至2022年5月用0.002%异丙基奥米尼帕治疗的36例原发性开角型青光眼伴高眼压患者的资料。我们调查了与基线相比,该药是否降低了1个月和3个月的眼压(IOP)。每次就诊时都要寻找可能的副作用。结果:患者治疗时平均年龄为59.2岁。36例患者中33例为原发性开角型青光眼,3例为高眼压。基线IOP为15.9±3.6 mmHg,在滴注0.002%异丙基(w/v) omidenepag后1个月和3个月分别显著降至13.7±2.8和13.4±2.9 mmHg(均为<i>p</i>& lt;0.01)。12名患者(29.2%)出现充血、眼痛和瘙痒等副作用,但只有2名患者(5.5%)停止使用该药。结论:0.002%奥米地帕格异丙基(w/v)在短期内对原发性开角型青光眼合并高眼压患者是安全有效的。
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来源期刊
CiteScore
0.20
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0.00%
发文量
126
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