Department of Ophthalmology and Visual Sciences, University of Nebraska Medical Center, Omaha, NE, USA.
Department of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Indian J Ophthalmol. 2022 Aug;70(8):2906-2910. doi: 10.4103/ijo.IJO_2947_21.
This retrospective chart review of netarsudil (Rhopressa) characterizes intra-ocular pressure (IOP) reduction, drug tolerance, drug cost, and compliance in a tertiary university Midwest clinic in a variety of glaucoma diagnoses on patients prescribed netarsudil 01/2017 to 5/2020.
Patient demographics, primary diagnosis, indication for medication, prescription date, prescription fill status, duration of use, discontinuation reason, and number of IOP-lowering medications were noted. Confounding medication changes were excluded from IOP analysis. The IOP difference between the first visit after starting netarsudil and the baseline (mean before starting netarsudil on the stable medication regimen) was calculated.
A total of 133 patients were prescribed netarsudil (age 69 ± 20 years, 59% females, 79% white, 86% primary glaucoma) as adjunct glaucoma medication (mean medications 3.2 ± 0.9). Indications were lowering IOP (mean baseline IOP 20.0 ± 6 mmHg) and drug regimen simplification. Prescription was not filled by 22/133 subjects because of the cost (68%) and the need for surgery (23%). No demographic factors were associated with prescription fill status. A total of 101 eyes of 76 patients were used for IOP analysis. The mean change in IOP was -0.8 ± 6.4 mmHg, (IOP decrease in 67%, increase or no change in 33% eyes). Netarsudil was discontinued in 52% (50/96) patients; the reasons include surgery for IOP control (42%), allergies (30%), cost (14%), and paradoxical rise in IOP (12%).
Netarsudil was used as adjunct third or fourth line medication at a glaucoma practice in Midwestern USA. 17% of prescriptions went unfilled; netarsudil was discontinued in 52% of patients. IOP response was variable in this population with severe complex glaucoma.
本研究通过回顾性图表分析,描述了一种新型前列腺素类似物奈立定(Rhopressa)在 2017 年 1 月至 2020 年 5 月期间在中西部地区某大学附属医院各种青光眼诊断中的眼压(IOP)降低、药物耐受性、药物费用和依从性。
记录患者人口统计学特征、主要诊断、药物使用指征、处方日期、处方填写状态、使用持续时间、停药原因以及 IOP 降低药物的数量。IOP 分析排除了混杂的药物变化。计算奈立定治疗后首次就诊时的 IOP 与基线(开始奈立定治疗前稳定药物治疗方案的平均 IOP)之间的差异。
共 133 例患者被处方奈立定(年龄 69 ± 20 岁,59%女性,79%白人,86%原发性青光眼)作为辅助性青光眼药物(平均用药 3.2 ± 0.9 种)。使用指征为降低眼压(平均基线眼压 20.0 ± 6mmHg)和简化药物治疗方案。22/133 名患者因费用(68%)和手术需要(23%)而未开处方。没有人口统计学因素与处方填写状态相关。共有 76 名患者的 101 只眼用于 IOP 分析。IOP 的平均变化为-0.8 ± 6.4mmHg(67%的眼睛眼压下降,33%的眼睛眼压升高或不变)。奈立定在 52%(50/96)的患者中被停用;原因包括手术控制眼压(42%)、过敏(30%)、费用(14%)和眼压反常升高(12%)。
奈立定作为辅助性三线或四线药物在一家美国中西部的青光眼诊所使用。17%的处方未被填写;52%的患者停用了奈立定。在这个患有严重复杂青光眼的人群中,IOP 反应各不相同。