[Epidemiologic and tonometric results of a multicenter study of 5,872 patients with ocular hypertension or open-angle glaucoma treated with betaxolol].

H Bourgeois
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引用次数: 0

Abstract

A large french multicenter study has been conducted by 750 ophthalmologists with 5,872 patients with open angle chronic glaucoma or intraocular hypertension. The patients were treated twice a day for a period of six months with Betaxolol eye drops, a Beta-1 betablocker product, and cardioselective. Concerning the total population of patients, 35% had a cardiovascular systemic context, 12.1% had a pulmonary systemic context, 5.2% were diabetic patients. Efficacy, systemic tolerance, visual comfort have been evaluated during the study, for each group of patient. After six months of treatment, intra-ocular pressure of the 5,872 patients has been lowered from 22.61 mmHg to 18.25 mmHg. Patients have reported a global efficacy in 97% of cases, a good systemic tolerance in 91% of the cases. The investigations have reported a global efficacy in 96% of cases and a good systemic tolerance in 91%. Ocular comfort has been reported as acceptable by 89% patients and by 92% of the Investigators. The analysis of the results of the study allows us to say that the Beta-blocker-Beta-1 selective eye drop, can be used in treatment of intraocular hypertension or open angle chronic glaucoma with a high range of efficacy and safety.

[使用倍他洛尔治疗的5,872例高眼压或开角型青光眼患者的多中心研究的流行病学和眼压测量结果]。
750名眼科医生对5872例开角型慢性青光眼或眼内高压患者进行了一项大型法国多中心研究。这些患者在6个月的时间里每天接受两次倍他洛尔滴眼液(一种β -1 β受体阻滞剂产品)和心脏选择性治疗。在患者总数中,35%有心血管系统疾病,12.1%有肺系统疾病,5.2%为糖尿病患者。在研究期间,对每组患者的疗效、全身耐受性、视觉舒适度进行了评估。治疗6个月后,5872例患者眼压由22.61 mmHg降至18.25 mmHg。患者报告97%的病例有整体疗效,91%的病例有良好的全身耐受性。调查报告96%的病例有全球疗效,91%的病例有良好的全身耐受性。据报道,89%的患者和92%的研究者的眼睛舒适度是可接受的。通过对研究结果的分析,我们可以说β -受体阻滞剂- β -1选择性滴眼液,可用于治疗高眼压或开角型慢性青光眼,具有较高的疗效和安全性范围。
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