Dalbavancin: A novel once-weekly lipoglycopeptide antibiotic

被引:72
作者
Billeter, Marianne [1 ]
Zervos, Marcus J. [2 ,3 ]
Chen, Anne Y. [2 ,3 ]
Dalovisio, Joseph R. [1 ]
Kurukularatne, Changa [1 ]
机构
[1] Alton Ochsner Med Fdn & Ochsner Clin, Dept Infect Dis, New Orleans, LA 70121 USA
[2] Henry Ford Hosp, Div Infect Dis, Dept Internal Med, Detroit, MI 48202 USA
[3] Wayne State Univ, Sch Med, Detroit, MI USA
关键词
D O I
10.1086/526772
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The increasing prevalence of drug-resistant gram-positive cocci, such as methicillin-resistant Staphylococcus aureus, has underscored the need for new agents for the treatment of this type of infection. Dalbavancin, a new lipoglycopeptide, has the desirable characteristics of increased in vitro activity, compared with vancomycin, for most gram-positive pathogenic bacteria, as well as an extremely long half-life, permitting once-weekly intravenous dosing. Clinical studies comparing linezolid with 2 doses of dalbavancin have shown comparable efficacy for the treatment of skin and soft-tissue infection. Dalbavancin has also proven to be effective for therapy of catheter-related bloodstream infections. It has an excellent safety profile in studies to date. Dalbavancin will likely have a significant role in outpatient intravenous therapy for patients with potentially serious drug-resistant gram-positive coccal infections.
引用
收藏
页码:577 / 583
页数:7
相关论文
共 43 条
[1]   In vivo pharmacodynamic activity of the glycopeptide dalbavancin [J].
Andes, David ;
Craig, William A. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2007, 51 (05) :1633-1642
[2]  
APPELBAUM PC, 2003, 41 ANN M INF DIS SOC
[3]   Population pharmacokinetic analysis of dalbavancin, a novel lipoglycopeptide [J].
Buckwalter, M ;
Dowell, JA .
JOURNAL OF CLINICAL PHARMACOLOGY, 2005, 45 (11) :1279-1287
[4]   In-vitro and in-vivo antibacterial activity of BI 397, a new semi-synthetic glycopeptide antibiotic [J].
Candiani, G ;
Abbondi, M ;
Borgonovi, M ;
Romanò, G ;
Parenti, F .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 1999, 44 (02) :179-192
[5]  
CANDIANI GP, 2001, 41 INT C ANT AG CHEM
[6]   Pharmacokinetics and excretion of dalbavancin in the rat [J].
Cavaleri, M ;
Riva, S ;
Valagussa, A ;
Guanci, M ;
Colombo, L ;
Dowell, J ;
Stogniew, M .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2005, 55 :31-35
[7]   Correlation between reduced daptomycin susceptibility and vancomycin resistance in vancomycin-intermediate Staphylococcus aureus [J].
Cui, LZ ;
Tominaga, E ;
Neoh, HM ;
Hiramatsu, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2006, 50 (03) :1079-1082
[8]   Dalbavancin compared with vancomycin for prevention of Staphylococcus aureus colonization of devices in vivo [J].
Darouiche, RO ;
Mansouri, MD .
JOURNAL OF INFECTION, 2005, 50 (03) :206-209
[9]  
DOWELL J, 2003, 43 INT C ANT AG CHEM
[10]  
DOWELL JA, 2004, 44 INT C ANT AG CHEM