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局部眼部 TRPV1 拮抗剂 SAF312(利伐曲普坦)治疗屈光性角膜切削术后疼痛。

Topical Ocular TRPV1 Antagonist SAF312 (Libvatrep) for Postoperative Pain After Photorefractive Keratectomy.

机构信息

Vance Thompson Vision, Sioux Falls, SD, USA.

University of South Dakota, Sanford School of Medicine, Sioux Falls, SD, USA.

出版信息

Transl Vis Sci Technol. 2023 Mar 1;12(3):7. doi: 10.1167/tvst.12.3.7.

Abstract

PURPOSE

Evaluation of safety and efficacy of topical ocular SAF312 (Libvatrep) in post-photorefractive keratectomy (PRK) pain.

METHODS

In this placebo (vehicle)-controlled, participant- and investigator-masked study, 40 participants were randomized (1:1) to two treatment sequences in a bilateral PRK crossover design (SAF312 2.5% followed by vehicle [or vice versa], one eye drop, four times daily for 72 hours after PRK). Primary endpoints were visual analog scale (VAS) pain scores at 6 hours after first drop of study drug and average VAS scores over 0 to 12 hours postoperatively. Secondary endpoints included postoperative oral rescue medication (ORM) use and adverse events (AEs).

RESULTS

All 40 participants completed the study. Both primary endpoints were met; mean difference in VAS pain scores between SAF312- and vehicle-treated eyes was -11.13 (P = 0.005, -25%) at 6 hours postoperatively and -8.56 (P = 0.017, -22%) over 0 to 12 hours. Mean VAS pain scores with SAF312 were consistently lower than with vehicle from 1 hour postoperatively up to 30 hours (P ≤ 0.10 observed in 8/11 time points). Less ORM was taken with SAF312 up to 0 to 72 hours postoperatively, with a trend of fewer participants taking ORM at 0 to 24 hours postoperatively with SAF312 versus vehicle. No serious AEs were reported. All ocular AEs were mild and transient, and none were drug related. SAF312-treated eyes showed no delay in wound healing and had a lower grade 4 conjunctival hyperemia 24 hours postoperatively versus vehicle-treated eyes.

CONCLUSIONS

SAF312 was well tolerated and effective in reducing ocular pain post-PRK.

TRANSLATIONAL RELEVANCE

Topical SAF312 presents a new therapeutic option for patients undergoing PRK.

摘要

目的

评估局部眼部 SAF312(利伐曲普)在光折射性角膜切削术(PRK)后疼痛中的安全性和疗效。

方法

在这项安慰剂(载体)对照、参与者和研究者盲法研究中,40 名参与者按照双侧 PRK 交叉设计(SAF312 2.5% 后接载体[或反之],单次滴眼,每日 4 次,共 72 小时)随机(1:1)分为两组。主要终点为首次滴药后 6 小时的视觉模拟评分(VAS)疼痛评分和术后 0 至 12 小时的平均 VAS 评分。次要终点包括术后口服解救药物(ORM)使用和不良事件(AE)。

结果

所有 40 名参与者均完成了研究。两个主要终点均达到;SAF312 治疗眼与载体治疗眼的 VAS 疼痛评分差异在术后 6 小时为-11.13(P = 0.005,-25%),在术后 0 至 12 小时为-8.56(P = 0.017,-22%)。SAF312 治疗后的平均 VAS 疼痛评分从术后 1 小时至 30 小时持续低于载体治疗(8/11 个时间点观察到 P ≤ 0.10)。SAF312 治疗至术后 0 至 72 小时的 ORM 用量较少,与载体治疗相比,SAF312 治疗至术后 0 至 24 小时的参与者中,使用 ORM 的人数呈减少趋势。未报告严重 AE。所有眼部 AE 均为轻度和一过性,且均与药物无关。SAF312 治疗的眼睛在术后 24 小时未见伤口愈合延迟,且 4 级结膜充血程度低于载体治疗的眼睛。

结论

SAF312 耐受性良好,能有效减轻 PRK 术后眼部疼痛。

翻译

这是一篇医学论文的摘要,主要内容是评估一种名为 SAF312 的局部眼部药物在光折射性角膜切削术后疼痛中的安全性和疗效。研究采用了安慰剂对照、参与者和研究者盲法的设计,结果表明 SAF312 能有效减轻术后疼痛,且耐受性良好。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0989/10020951/52eb261fc1e6/tvst-12-3-7-f001.jpg

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