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本文引用的文献

1
Bimatoprost Sustained-Release Implants for Glaucoma Therapy: 6-Month Results From a Phase I/II Clinical Trial.用于青光眼治疗的比马前列素缓释植入剂:一项I/II期临床试验的6个月结果
Am J Ophthalmol. 2017 Mar;175:137-147. doi: 10.1016/j.ajo.2016.11.020. Epub 2016 Dec 22.
2
Bimatoprost 0.03% Solution for the Treatment of Nonfacial Vitiligo.0.03%比马前列素溶液用于治疗非面部白癜风。
J Drugs Dermatol. 2016 Jun 1;15(6):703-10.
3
Six-Month Intraocular Pressure Reduction with a Topical Bimatoprost Ocular Insert: Results of a Phase II Randomized Controlled Study.局部用比马前列素眼用插入剂降低眼压 6 个月:Ⅱ期随机对照研究结果。
Ophthalmology. 2016 Aug;123(8):1685-1694. doi: 10.1016/j.ophtha.2016.04.026. Epub 2016 May 5.
4
Primary Open-Angle Glaucoma Preferred Practice Pattern(®) Guidelines.原发性开角型青光眼临床实践指南(®)。
Ophthalmology. 2016 Jan;123(1):P41-P111. doi: 10.1016/j.ophtha.2015.10.053. Epub 2015 Nov 12.
5
Bimatoprost-induced chemical blepharoplasty.比马前列素诱导的化学性睑成形术。
J Drugs Dermatol. 2015 May;14(5):472-7.
6
Bimatoprost versus Mometasone Furoate in the Treatment of Scalp Alopecia Areata: A Pilot Study.比马前列素与糠酸莫米松治疗头皮斑秃的初步研究
Dermatology. 2015;230(4):308-13. doi: 10.1159/000371416. Epub 2015 Mar 4.
7
Global prevalence of glaucoma and projections of glaucoma burden through 2040: a systematic review and meta-analysis.全球青光眼患病率及 2040 年青光眼负担预测:系统评价和荟萃分析。
Ophthalmology. 2014 Nov;121(11):2081-90. doi: 10.1016/j.ophtha.2014.05.013. Epub 2014 Jun 26.
8
The pathophysiology and treatment of glaucoma: a review.青光眼的病理生理学和治疗:综述。
JAMA. 2014 May 14;311(18):1901-11. doi: 10.1001/jama.2014.3192.
9
Bimatoprost 0.01% or 0.03% in patients with glaucoma or ocular hypertension previously treated with latanoprost: two randomized 12-week trials.对于先前使用拉坦前列素治疗过的青光眼或高眼压症患者,使用0.01%或0.03%的比马前列素:两项为期12周的随机试验。
Clin Ophthalmol. 2014 Mar 27;8:643-52. doi: 10.2147/OPTH.S59197. eCollection 2014.
10
Bimatoprost 0.03%/timolol 0.5% preservative-free ophthalmic solution versus bimatoprost 0.03%/timolol 0.5% ophthalmic solution (Ganfort) for glaucoma or ocular hypertension: a 12-week randomised controlled trial.0.03%比马前列素/0.5%噻吗洛尔无防腐剂滴眼液与 0.03%比马前列素/0.5%噻吗洛尔滴眼液(甘氟特)治疗青光眼或高眼压症:一项为期 12 周的随机对照试验。
Br J Ophthalmol. 2014 Jul;98(7):926-31. doi: 10.1136/bjophthalmol-2013-304064. Epub 2014 Mar 25.

高眼压症患者的考量因素:比马前列素滴眼液的作用

Patient considerations in ocular hypertension: role of bimatoprost ophthalmic solution.

作者信息

Lee Daniel, Mantravadi Anand V, Myers Jonathan S

机构信息

Glaucoma Service, Wills Eye Hospital, Philadelphia, PA, USA.

出版信息

Clin Ophthalmol. 2017 Jul 10;11:1273-1280. doi: 10.2147/OPTH.S118689. eCollection 2017.

DOI:10.2147/OPTH.S118689
PMID:28744094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5513827/
Abstract

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.

摘要

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。