Lee Daniel, Mantravadi Anand V, Myers Jonathan S
Glaucoma Service, Wills Eye Hospital, Philadelphia, PA, USA.
Clin Ophthalmol. 2017 Jul 10;11:1273-1280. doi: 10.2147/OPTH.S118689. eCollection 2017.
Glaucoma is a leading cause of irreversible blindness worldwide. The reduction of intraocular pressure has been well established as an effective treatment to prevent both the development and the progression of all forms of glaucoma. Bimatoprost 0.03% ophthalmic solution, introduced in 2001, is a synthetic prostamide with the unique mechanism of improving both uveoscleral and trabecular outflow. Comparative studies with other pharmacotherapies have shown favorable results for bimatoprost as a potent ocular hypotensive agent that is generally well tolerated. Common side effects include conjunctival hyperemia, eyelash growth, iris pigmentation and periorbital changes. Hyperemia rates were reduced following the introduction of bimatoprost 0.01%. Bimatoprost should be used with caution in those with higher risk of developing ocular inflammation and macular edema. However, the perceived risk of bimatoprost in these patient populations is likely greater than the actual risk observed in practice. Bimatoprost is currently in the center of several clinical trials including its use for dermatologic applications and sustained-release therapies for the treatment of ocular hypertension and glaucoma.
青光眼是全球不可逆性失明的主要原因。降低眼压已被确认为预防各种形式青光眼的发生和进展的有效治疗方法。2001年推出的0.03%比马前列素滴眼液是一种合成前列腺酰胺,具有改善葡萄膜巩膜和小梁网房水流出的独特机制。与其他药物疗法的比较研究表明,比马前列素作为一种强效降眼压药物,通常耐受性良好,效果良好。常见副作用包括结膜充血、睫毛生长、虹膜色素沉着和眶周变化。引入0.01%比马前列素后,充血率有所降低。对于有发生眼部炎症和黄斑水肿高风险的患者,应谨慎使用比马前列素。然而,在这些患者群体中对比马前列素的感知风险可能大于实际观察到的风险。比马前列素目前处于多项临床试验的核心,包括其在皮肤科应用以及用于治疗高眼压症和青光眼的缓释疗法。