Pathophysiology of visual disorders induced by phosphodiesterase inhibitors in the treatment of erectile dysfunction

被引:25
作者
Moschos, Marilita M. [1 ]
Nitoda, Eirini [1 ]
机构
[1] Univ Athens, Sch Med, Dept Ophthalmol 1, 6 Ikarias St, Athens 14578, Greece
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2016年 / 10卷
关键词
erectile dysfunction; pathophysiological mechanisms; phosphodiesterase inhibitors; PDE5; visual disorders; ISCHEMIC OPTIC NEUROPATHY; SILDENAFIL CITRATE; INTRAOCULAR-PRESSURE; ORAL SILDENAFIL; VIAGRA; TADALAFIL; HEMODYNAMICS; EXPRESSION; THICKNESS; PERFUSION;
D O I
10.2147/DDDT.S118015
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Aim: The aim of this review was to summarize the ocular action of the most common phosphodiesterase (PDE) inhibitors used for the treatment of erectile dysfunction and the subsequent visual disorders. Method: This is a literature review of several important articles focusing on the pathophysiology of visual disorders induced by PDE inhibitors. Results: PDE inhibitors have been associated with ocular side effects, including changes in color vision and light perception, blurred vision, transient alterations in electroretinogram ( ERG), conjunctival hyperemia, ocular pain, and photophobia. Sildenafil and tadalafil may induce reversible increase in intraocular pressure and be involved in the development of nonarteritic ischemic optic neuropathy. Reversible idiopathic serous macular detachment, central serous chorioretinopathy, and ERG disturbances have been related to the significant impact of sildenafil and tadalafil on retinal perfusion. Discussion: So far, PDE inhibitors do not seem to cause permanent toxic effects on chorioretinal tissue and photoreceptors. However, physicians should write down any visual symptom observed during PDE treatment and refer the patients to ophthalmologists.
引用
收藏
页码:3407 / 3412
页数:6
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