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PhXA41对高眼压症或原发性开角型青光眼患者的降眼压作用。

Ocular hypotensive effect of PhXA41 in patients with ocular hypertension or primary open-angle glaucoma.

作者信息

Hotehama Y, Mishima H K, Kitazawa Y, Masuda K

机构信息

Department of Ophthalmology, Hiroshima University School of Medicine, Japan.

出版信息

Jpn J Ophthalmol. 1993;37(3):270-4.

PMID:8295364
Abstract

A study was carried out to assess the clinical efficacy of PhXA41, a new phenyl-substituted prostaglandin F2 alpha-isopropyl ester analogue, using a single administration in 35 subjects with ocular hypertension or primary open-angle glaucoma. PhXA41 caused a dose-dependent intraocular pressure (IOP) reduction which continued 24 hours or more after administration. The mean IOP reduction 8 hours after treatment compared with the baseline IOP was 3.4, 4.9 and 5.9 mmHg for the doses of 25, 50 and 100 micrograms/ml, respectively. Although slight conjunctival hyperemia occurred in some patients, it disappeared by the next day with no treatment. No aqueous flare or cells were detected, no significant change in pupillary diameter was found, and no systemic symptom was reported. Thus, PhXA41 was well tolerated in subjects with ocular hypertension or primary open-angle glaucoma. Furthermore, its IOP-reducing effect was so long-lasting that a once daily application may suffice for clinical use.

摘要

开展了一项研究,以评估新型苯基取代的前列腺素F2α异丙酯类似物PhXA41在35例高眼压症或原发性开角型青光眼患者单次给药后的临床疗效。PhXA41可引起眼压(IOP)呈剂量依赖性降低,给药后持续24小时或更长时间。治疗8小时后,与基线眼压相比,25、50和100微克/毫升剂量的平均眼压降低分别为3.4、4.9和5.9毫米汞柱。虽然一些患者出现了轻微的结膜充血,但未经治疗第二天就消失了。未检测到房水闪光或细胞,瞳孔直径未发现明显变化,也未报告全身症状。因此,PhXA41在高眼压症或原发性开角型青光眼患者中耐受性良好。此外,其降低眼压的作用持续时间很长,每天应用一次可能足以满足临床使用。

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