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在一家三级青光眼中心,固定剂量复方奈他洛尔0.02%/拉坦前列素0.005%的有效性和耐受性。

The effectiveness and tolerability of fixed-dose combination netarsudil 0.02%/latanoprost 0.005% at a tertiary glaucoma center.

作者信息

Wong Jae-Chiang, Shiuey Eric J, Razeghinejad Reza, Shukla Aakriti G, Kolomeyer Natasha N, Myers Jonathan S, Pro Michael J, Lee Daniel

机构信息

Glaucoma Research Center, Wills Eye Hospital, 840 Walnut Street, Suite 1100, Philadelphia, PA, 19107, USA.

Rowan University School of Osteopathic Medicine, Stratford, NJ, USA.

出版信息

Graefes Arch Clin Exp Ophthalmol. 2023 Jan;261(1):193-200. doi: 10.1007/s00417-022-05780-w. Epub 2022 Jul 29.

Abstract

PURPOSE

To assess real-world effectiveness and tolerability of fixed-dose combination netarsudil 0.02%/latanoprost 0.005% (FCNL) in management of glaucoma patients in a tertiary eye care center.

METHODS

This retrospective cohort study included glaucoma patients initiated on FCNL from January 2018 to July 2021 with at least 1-month follow-up. Demographic and clinical data were collected at baseline and at follow-up visits through 12 months. Patient-solicited side effects were recorded at each visit. Maximum glaucoma pharmacotherapy was defined as surgery/laser being the next treatment option following an intensive pharmacotherapy regimen, or when pharmacotherapy could not be increased due to allergy/intolerance or all pharmacologic mechanisms already being in use.

RESULTS

Seventy-nine eyes of 47 patients were included. Mean age was 67.7 ± 14.7 years. Baseline IOP was 18.7 ± 4.9 mmHg; mean change in IOP (∆IOP) each study visit compared to baseline ranged from - 1.6 ± 3.5 to - 4.4 ± 4.1 mmHg (all p < 0.05). The eyes on maximum glaucoma pharmacotherapy (73.4%) had similar ∆IOP compared to those on non-maximal therapy at each visit (p > 0.2 for all). Forty-three (54.4%) eyes were switched from a prostaglandin analog alone, producing a 1-month IOP reduction of - 4.7 ± 3.9 mmHg at 1 month which remained significant at each visit for the 12-month study period (all p < 0.05). Across all study visits, conjunctival hyperemia was documented in 26 (32.9%) eyes. Subjective blurry vision was reported in 22 (27.8%) eyes without significant worsening of visual acuity at any visit (all p > 0.05). Six (7.6%) and 7 (8.9%) eyes required further medical or surgical/laser intervention, respectively. Kaplan-Meier analysis revealed no significant difference in the need for subsequent medical or surgical intervention between those on maximum and non-maximal pharmacotherapy (p > 0.4).

CONCLUSION

FCNL was well-tolerated and demonstrated a significant and sustained reduction in IOP, even as last-line therapy before incisional or laser surgery in those on maximum glaucoma pharmacotherapy. FCNL is a viable treatment option for glaucomatous eyes before consideration of surgical intervention.

摘要

目的

评估固定剂量复方奈他前列素0.02%/拉坦前列素0.005%(FCNL)在三级眼科护理中心青光眼患者管理中的实际有效性和耐受性。

方法

这项回顾性队列研究纳入了2018年1月至2021年7月开始使用FCNL且至少随访1个月的青光眼患者。在基线和随访至12个月期间收集人口统计学和临床数据。每次就诊时记录患者自述的副作用。最大青光眼药物治疗定义为在强化药物治疗方案后手术/激光作为下一个治疗选择,或者由于过敏/不耐受或所有药物机制均已使用而无法增加药物治疗时。

结果

纳入了47例患者的79只眼。平均年龄为67.7±14.7岁。基线眼压为18.7±4.9 mmHg;与基线相比,每次研究就诊时眼压的平均变化(∆IOP)范围为-1.6±3.5至-4.4±4.1 mmHg(所有p<0.05)。接受最大青光眼药物治疗的眼(73.4%)在每次就诊时与未接受最大治疗的眼相比,∆IOP相似(所有p>0.2)。43只眼(54.4%)从单独使用前列腺素类似物转换而来,在1个月时眼压降低-4.7±3.9 mmHg,在12个月研究期间的每次就诊时仍具有显著性(所有p<0.05)。在所有研究就诊中,26只眼(32.9%)记录有结膜充血。22只眼(27.8%)报告有主观视物模糊,在任何就诊时视力均无明显恶化(所有p>0.05)。分别有6只眼(7.6%)和7只眼(8.9%)需要进一步的药物或手术/激光干预。Kaplan-Meier分析显示,接受最大和非最大药物治疗的患者在后续药物或手术干预需求方面无显著差异(p>0.4)。

结论

FCNL耐受性良好,即使作为接受最大青光眼药物治疗的患者在切开或激光手术前的最后一线治疗,也能显著且持续降低眼压。在考虑手术干预之前,FCNL是青光眼患者的一种可行治疗选择。

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