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乌诺前列酮与拉坦前列素对眼压升高患者的相加作用。

Additive effect of unoprostone and latanoprost in patients with elevated intraocular pressure.

作者信息

Aung Tin, Chew Paul T K, Oen Francis T S, Chan Yiong-Huak, Thean Lennard H, Yip Leonard, Lim Boon-Ang, Soh Jade, Seah Steve K L

机构信息

Singapore National Eye Centre National University of Singapore Clinical Trials and Epidemiology Research Unit, Singapore.

出版信息

Br J Ophthalmol. 2002 Jan;86(1):75-9. doi: 10.1136/bjo.86.1.75.

Abstract

AIMS

To assess the additive effect of unoprostone and latanoprost in patients with primary open angle glaucoma (POAG) or ocular hypertension (OHT) METHODS: 32 patients with POAG or OHT were randomised to receive either latanoprost once daily or unoprostone twice daily for 4 weeks. After 4 weeks, all patients received both latanoprost and unoprostone for another 4 weeks. The IOP was measured at 9 am and 5 pm on the baseline, day 28, and day 56 visits, and at 9 am on day 14 and day 42 visits. The medications were given to the patients in an open label fashion. The observer was masked to the treatment given. The mean of the measurements was calculated. Safety parameters were also recorded. The additive effect of the medications was assessed by the reduction in intraocular pressure (IOP) when both medications were used, compared with when one medication was used.

RESULTS

28 patients completed both treatment periods and had IOP data available for evaluation. After 1 month of treatment, latanoprost significantly reduced IOP (mean by 6.1 (SEM 0.8) mm Hg (p<0.001) and unoprostone by 4.9 (1.0) mm Hg (p<0.001) from the baseline of 24.4 (0.6) mm Hg and 24.4 (1.1) mm Hg respectively (p = 0.18). When latanoprost once daily was given to patients treated with unoprostone, there was additional IOP lowering of 1.9 (0.6) mm Hg (p = 0.012). However, adding unoprostone to those being treated with latanoprost produced an IOP change of +0.4 (0.5) mm Hg (p = 0.42). Ocular symptoms and findings were mild and equally distributed between treatment groups, and after combined therapy. Hyperaemia and ocular irritation were the most frequently reported events. Over a third of patients experienced ocular irritation with the combination of medications.

CONCLUSIONS

Latanoprost once daily causes additional IOP lowering in eyes which were being treated with unoprostone twice a day. However, there was no additional IOP lowering when unoprostone was added to eyes which were being treated with latanoprost. Both drugs were well tolerated together with few ocular adverse events.

摘要

目的

评估乌诺前列酮和拉坦前列素对原发性开角型青光眼(POAG)或高眼压症(OHT)患者的叠加效应。

方法

32例POAG或OHT患者被随机分为两组,一组每天一次接受拉坦前列素治疗,另一组每天两次接受乌诺前列酮治疗,为期4周。4周后,所有患者再同时接受拉坦前列素和乌诺前列酮治疗4周。在基线、第28天和第56天上午9点和下午5点测量眼压,在第14天和第42天上午9点测量眼压。药物以开放标签的方式给予患者。观察者对所给予的治疗不知情。计算测量值的平均值。还记录了安全参数。通过比较两种药物联合使用时与单独使用一种药物时眼压的降低情况来评估药物的叠加效应。

结果

28例患者完成了两个治疗期并拥有可供评估的眼压数据。治疗1个月后,拉坦前列素使眼压显著降低(平均从基线的24.4(0.6)mmHg降至6.1(0.8)mmHg(p<0.001)),乌诺前列酮使眼压从基线的24.4(1.1)mmHg降至4.9(1.0)mmHg(p<0.001)(p = 0.18)。当在接受乌诺前列酮治疗的患者中每天一次给予拉坦前列素时,眼压进一步降低了1.9(0.6)mmHg(p = 0.012)。然而,在接受拉坦前列素治疗的患者中添加乌诺前列素时,眼压变化为+0.4(0.5)mmHg(p = 0.42)。眼部症状和体征较轻,在治疗组之间以及联合治疗后分布均匀。充血和眼部刺激是最常报告的事件。超过三分之一的患者在联合用药时出现眼部刺激。

结论

每天一次的拉坦前列素在每天两次接受乌诺前列素治疗的眼中可进一步降低眼压。然而,在接受拉坦前列素治疗的眼中添加乌诺前列素时,眼压没有进一步降低。两种药物耐受性良好,眼部不良事件较少。

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