Ophthalmic infections and their anti-infective challenges

被引:25
作者
Alfonso, E
Crider, J
机构
[1] Univ Miami, Sch Med, Bascom Palmer Eye Inst, Miami, FL USA
[2] Alcon Res Ltd, Ft Worth, TX USA
关键词
antibiotic; anti-infectives; moxifloxacin; penetration; potency; safety; therapy; VIGAMOX (R);
D O I
10.1016/j.survophthal.2005.05.001
中图分类号
R77 [眼科学];
学科分类号
100212 [眼科学];
摘要
This introduction provides an overview of the succeeding articles contained within this supplement on the new fourth-generation fluoroquinolone antibiotic product, moxifloxacin ophthalmic solution 0.5% (VIGAMOX((R)), Alcon Laboratories, Inc., Fort Worth, TX). Moxifloxacin was developed specifically to address the increasing incidence of resistance to earlier-generation antibiotic molecules. Structural modifications to the moxifloxacin molecule have decreased the likelihood of the development of resistant organisms. This antibiotic has been shown to possess greater activity than previous-generation molecules against gram-positive bacteria while maintaining excellent potency against gram-negative organisms and nontuberculous (atypical) mycobacteria. Moxifloxacin ophthalmic solution 0.5% exhibits enhanced bioavailability due to a unique molecular structure that combines high lipophilicity for enhanced corneal penetration with high aqueous solubility at physiological pH. Numerous studies have shown that moxifloxacin ophthalmic solution 0.5% has high potency against a broad range of microbial species and a favorable profile in terms of safety and tolerability. The results presented in this supplement provide additional evidence for the potential benefits of moxifloxacin ophthalmic solution 0.5% in surgical prophylaxis and treatment of sight-threatening infections, such as bacterial conjunctivitis, endophthalmitis and keratitis.
引用
收藏
页码:S1 / S6
页数:6
相关论文
共 35 条
[1]
Topical antibacterial therapy for mycobacterial keratitis: Potential for surgical prophylaxis and treatment [J].
Abshire, R ;
Cockrum, P ;
Crider, J ;
Schlech, B .
CLINICAL THERAPEUTICS, 2004, 26 (02) :191-196
[2]
Shifting trends in bacterial keratitis in South Florida and emerging resistance to fluoroquinolones [J].
Alexandrakis, G ;
Alfonso, EC ;
Miller, D .
OPHTHALMOLOGY, 2000, 107 (08) :1497-1502
[3]
Comparative efficacy of topical moxifloxacin versus ciprofloxacin and vancomycin in the treatment of P-aeruginoso and ciprofloxacin-resistant MRSA keratitis in rabbits [J].
Aliprandis, E ;
Ciralsky, J ;
Lai, H ;
Herling, I ;
Katz, HR .
CORNEA, 2005, 24 (02) :201-205
[4]
Antimicrobial prophylaxis for surgery: An advisory statement from the National Surgical Infection Prevention Project [J].
Bratzler, DW ;
Houck, PM .
CLINICAL INFECTIOUS DISEASES, 2004, 38 (12) :1706-1715
[5]
Emerging ciprofloxacin-resistant Pseudomonas aeruginosa [J].
Chaudhry, NA ;
Flynn, HW ;
Murray, TG ;
Tabandeh, H ;
Mello, MO ;
Miller, D .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1999, 128 (04) :509-510
[6]
Effect of prophylactic antibiotics and incision type on the incidence of endophthalmitis after cataract surgery [J].
Colleaux, KM ;
Hamilton, WK .
CANADIAN JOURNAL OF OPHTHALMOLOGY-JOURNAL CANADIEN D OPHTALMOLOGIE, 2000, 35 (07) :373-378
[7]
DURRIE DS, 2005, J OCUL PHARMACOL TH, V1, P236
[8]
Nontuberculous mycobacterial keratitis in South Florida [J].
Ford, JG ;
Huang, AJW ;
Pflugfelder, SC ;
Alfonso, EC ;
Forster, RK ;
Miller, D .
OPHTHALMOLOGY, 1998, 105 (09) :1652-1658
[9]
Emerging fluoroquinolone resistance in bacterial keratitis - A 5-year review [J].
Goldstein, MH ;
Kowalski, RP ;
Gordon, YJ .
OPHTHALMOLOGY, 1999, 106 (07) :1313-1318
[10]
Han DP, 1996, AM J OPHTHALMOL, V122, P1