Fish D N, North D S
Department of Pharmacy Practice, School of Pharmacy, University of Colorado Health Sciences Center, Denver 80262, USA.
Pharmacotherapy. 2001 Jan;21(1):35-59. doi: 10.1592/phco.21.1.35.34440.
Gatifloxacin is a new 8-methoxy-fluoroquinolone antibiotic approved for use in the United States in December 1999. It has a broad spectrum of activity with potent activity against gram-positive bacteria, including penicillin-resistant Streptococcus pneumoniae, as well as excellent activity against gram-negative and atypical organisms. Gatifloxacin is available in both oral and injectable forms and is administered once/day. Bioavailability is 96%, with a plasma half-life of approximately 8 hours in individuals with normal renal function. Elimination is primarily renal excretion of unchanged drug with no cytochrome P450-mediated metabolism. The drug is distributed extensively into tissues and fluids and has a favorable pharmacodynamic profile against important pathogens. It had excellent efficacy in clinical studies of acute sinusitis, acute bacterial exacerbations of chronic bronchitis, community-acquired pneumonia, complicated and uncomplicated urinary tract infections and pyelonephritis, skin and skin structure infections, and uncomplicated gonococcal infections. The agent is well tolerated, with no evidence of hepatic, cardiac, or phototoxicity noted thus far. Drug interactions are uncommon; however, like other fluoroquinolones, coadministration with multivalent cations should be avoided due to significantly decreased absorption. Gatifloxacin should prove to be a safe and effective agent for a wide variety of infections.
加替沙星是一种新型的8-甲氧基氟喹诺酮类抗生素,于1999年12月在美国获批使用。它具有广泛的抗菌活性,对革兰氏阳性菌,包括耐青霉素的肺炎链球菌有强效活性,对革兰氏阴性菌和非典型病原体也有出色活性。加替沙星有口服和注射两种剂型,每日给药一次。生物利用度为96%,肾功能正常者的血浆半衰期约为8小时。消除主要通过肾脏排泄原形药物,无细胞色素P450介导的代谢。该药物广泛分布于组织和体液中,对重要病原体具有良好的药效学特征。在急性鼻窦炎、慢性支气管炎急性细菌感染、社区获得性肺炎、复杂性和非复杂性尿路感染及肾盂肾炎、皮肤及皮肤结构感染和非复杂性淋球菌感染的临床研究中,它有出色疗效。该药物耐受性良好,目前尚无肝毒性、心脏毒性或光毒性的证据。药物相互作用不常见;然而,与其他氟喹诺酮类药物一样,由于吸收显著减少,应避免与多价阳离子合用。加替沙星应被证明是一种对多种感染安全有效的药物。