Department of Ophthalmology, Graduate of Medicine, Faculty of Medicine, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Miyata Eye Hospital, Miyazaki, Japan.
Jpn J Ophthalmol. 2022 Sep;66(5):434-439. doi: 10.1007/s10384-022-00934-z. Epub 2022 Jul 30.
To evaluate omidenepag isopropyl (OMDI) for its efficacy in intraocular pressure control (IOP) and adverse reactions following administrations in Japanese patients with open-angle glaucoma (OAG) over a 3-month period.
Retrospective observational study.
Group 1 included untreated OAG patients, Group 2 included OAG patients treated with prostaglandin F (FP) receptor agonists (monotherapy) and Group 3 included OAG patients treated with multidrug therapy, including FP receptor agonists. OMDI was newly administered in Group 1, and FP receptor agonists were switched to OMDI in Group 2. In Group 3, all other ocular hypotensive medications were continued except FP receptor agonists. IOP changes were examined, and adverse reactions were retrieved from the medical records.
Group 1 included 32 eyes, Group 2, 20 eyes and Group 3, 17 eyes. In Group 1, the baseline IOP was 15.7 mmHg (95% confidence interval [CI] 14.7-16.8 mmHg). After eyedrop treatment, the IOP was 14.1 mmHg (P < 0.001) at 1 month and 13.7 mmHg (P < 0.001) at 3 months. By contrast, in Group 2 and Group 3, switching FP receptor agonists to OMDI did not result in significant IOP changes (P ≥ 0.71). Six patients developed adverse reactions (hyperemia, headache, ocular pain, and swollen eyelids).
New administration of OMDI significantly reduced the IOP. Furthermore, the IOP did not change after switching from FP receptor agonists to OMDI, including multidrug therapy. OMDI can be used as a first-line drug and is comparable to FP receptor agonists in Japanese patients with OAG.
评估在 3 个月内,日本开角型青光眼(OAG)患者使用异丙基奥米登前列腺素(OMDI)治疗的降眼压效果及不良反应。
回顾性观察研究。
第 1 组为未治疗的 OAG 患者,第 2 组为 OAG 患者(单药治疗)使用前列腺素 F(FP)受体激动剂治疗,第 3 组为 OAG 患者(多药治疗),包括 FP 受体激动剂。第 1 组新使用 OMDI,第 2 组将 FP 受体激动剂转换为 OMDI。第 3 组,除 FP 受体激动剂外,继续使用其他所有降眼压药物。检查眼压变化,并从病历中检索不良反应。
第 1 组包括 32 只眼,第 2 组包括 20 只眼,第 3 组包括 17 只眼。第 1 组的基线眼压为 15.7mmHg(95%置信区间[CI]为 14.7-16.8mmHg)。滴眼治疗后,第 1 个月时眼压为 14.1mmHg(P<0.001),第 3 个月时眼压为 13.7mmHg(P<0.001)。相比之下,第 2 组和第 3 组将 FP 受体激动剂转换为 OMDI 并不会导致眼压显著变化(P≥0.71)。6 名患者出现不良反应(充血、头痛、眼痛和眼睑肿胀)。
新使用 OMDI 可显著降低眼压。此外,从 FP 受体激动剂转换为 OMDI 后,包括多药治疗,眼压并未改变。OMDI 可作为一线药物,在日本 OAG 患者中与 FP 受体激动剂相当。