Revisão Revisado por pares

Tigecycline: a novel glycylcycline antibiotic

2006; Taylor & Francis; Volume: 4; Issue: 1 Linguagem: Inglês

10.1586/14787210.4.1.9

ISSN

1744-8336

Autores

George G. Zhanel, James A. Karlowsky, Ethan Rubinstein, Daryl J. Hoban,

Tópico(s)

Antimicrobial Resistance in Staphylococcus

Resumo

Tigecycline, the first-in-class glycylcycline, was developed to recapture the broad spectrum of activity of the tetracycline class and to treat patients with difficult-to-treat bacterial infections. Tigecycline's in vitro spectrum of activity encompasses aerobic, facultative and anaerobic Gram-positive and -negative bacteria, including antimicrobial-resistant bacteria such as methicillin-resistant Staphylococcus aureus, vancomycin-resistant Enterococcus faecalis and Enterococcus faecium, and extended-spectrum beta-lactamase-producing Enterobacteriaceae. Clinical trials involving patients with complicated skin and skin-structure infections and complicated intra-abdominal infections, including patients infected with methicillin-resistant S. aureus, demonstrated that tigecycline was bacteriologically and clinically effective with mild-to-moderate gastrointestinal adverse events (i.e., nausea, vomiting and diarrhea) the most commonly reported. Tigecycline is a promising new broad-spectrum parenteral monotherapy for the treatment of patients with Gram-positive and -negative bacterial infections.

Referência(s)