Additional reduction in Intraocular pressure achieved with latanoprost in normal-tension glaucoma patients previously treated with unoprostone

被引:8
作者
Enoki, Miho
Saito, Jun
Hara, Makiko
Uchida, Tetsuya
Sagara, Takeshi
Nishida, Teruo
机构
[1] Ogori Daiichi Gen Hosp, Dept Ophthalmol, Yamaguchi 7540002, Japan
[2] Yamaguchi Univ, Sch Med, Dept Biomol Recognit & Ophthalmol, Ube, Yamaguchi 755, Japan
关键词
intraocular pressure; latanoprost; normal-tension glaucoma; prostaglandin F-2 alpha; unoprostone;
D O I
10.1007/s10384-005-0334-5
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: To determine whether treatment with latanoprost eye drops is able to further reduce intraocular pressure (IOP) in normal-tension glaucoma (NTG) patients whose IOP has been well controlled with unoprostone. Patients and Methods: A total of 34 eyes (34 individuals) with NTG that had been treated with 0.12% unoprostone eye drops twice daily for >= 3 months were switched to treatment once daily with eye drops containing 0.005% latanoprost. IOP was measured before and 1, 2, and 3 months after the switch to latanoprost. Results: The mean IOP of all eyes was decreased significantly by 1.8, 2.9, and 2.3 mmHg at 1, 2, and 3 months after the switch from unoprostone to latanoprost treatment. The IOP of patients with an initial IOP of <= 12 or > 12mmHg was reduced by 11.0 or 19.9%, respectively, after 3 months on latanoprost. The IOP of 30 (88.2%) of the 34 eyes was further reduced by the switch from unoprostone to latanoprost. Conclusions: Latanoprost reduced the IOP of NTG patients who had already been treated with unoprostone, even though both drugs are prostaglandin-related. Switching to latanoprost might thus achieve a maximal decrease in IOP and thereby better prevent damage to the optic nerve and loss of visual field in NTG patients.
引用
收藏
页码:334 / 337
页数:4
相关论文
共 26 条
[1]  
Alward WL, 1998, AM J OPHTHALMOL, V126, P498
[2]   Comparison of latanoprost and timolol in patients with ocular hypertension and glaucoma - A six-month, masked, multicenter trial in the United States [J].
Camras, CB ;
Cioffi, GA ;
VanBuskirk, EM ;
Fraser, J ;
Stewart, WC ;
Stewart, JA ;
Lustgarten, J ;
Schumer, RA ;
Podos, SM ;
Arroyo, M ;
Nitzberg, S ;
Ritch, R ;
Abundo, G ;
Caronia, R ;
Liebmann, J ;
Steinberger, D ;
Krupin, T ;
Rosenberg, LF ;
Ruderman, JM ;
Clarkson, K ;
Weinreb, RN ;
Ochabsi, R ;
Sherwood, M ;
Smith, MF ;
Stokes, DW ;
Zam, ZS ;
Wilensky, J ;
Hillman, D ;
Kaplan, B ;
Gates, V ;
Nail, C ;
Zimmerman, T ;
Fechtner, R ;
Fenton, R ;
Fenton, J ;
Higginbotham, EJ ;
Johnson, AT ;
PollackRundle, CJ ;
Weiss, E ;
Yablonski, ME ;
Tannenbaum, MH ;
Ibrahim, F ;
Ohia, E ;
Neely, D ;
Minckler, D ;
Heuer, D ;
Lee, P ;
Padea, M ;
Kaufman, PL ;
Heatley, GA .
OPHTHALMOLOGY, 1996, 103 (01) :138-147
[3]  
Grunwald JE, 1998, INVEST OPHTH VIS SCI, V39, P2329
[4]   The prevalence of primary open-angle glaucoma in Japanese - The Tajimi study [J].
Iwase, A ;
Suzuki, Y ;
Araie, M ;
Yamamoto, T ;
Abe, H ;
Shirato, S ;
Kuwayama, Y ;
Mishima, HK ;
Shimizu, H ;
Tomita, G ;
Inoue, Y ;
Kitazawa, Y .
OPHTHALMOLOGY, 2004, 111 (09) :1641-1648
[5]  
Iwata Kazuo, 1992, Acta Societatis Ophthalmologicae Japonicae, V96, P1501
[6]  
JONAS JB, 1989, INVEST OPHTH VIS SCI, V30, P1604
[7]   Isopropyl unoprostone increases the activities of matrix metalloproteinases in cultured monkey ciliary muscle cells [J].
Kashiwagi, K ;
Jin, M ;
Suzuki, M ;
Tanaka, Y ;
Iizuka, Y ;
Tsukahara, S .
JOURNAL OF GLAUCOMA, 2001, 10 (04) :271-276
[8]   TUNEL-positive ganglion cells in human primary open-angle glaucoma [J].
Kerrigan, LA ;
Zack, DJ ;
Quigley, HA ;
Smith, SD ;
Pease, ME .
ARCHIVES OF OPHTHALMOLOGY, 1997, 115 (08) :1031-1035
[9]  
KITAZAWA Y, 1986, OPHTHALMOLOGY, V93, P853
[10]   Visual field defect and perfusion of the juxtapapillary retina and the neuroretinal rim area in primary open-angle glaucoma [J].
Michelson, G ;
Langhans, MJ ;
Harazny, J ;
Dichtl, A .
GRAEFES ARCHIVE FOR CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 1998, 236 (02) :80-85