Treatment of orthopedic infections caused by resistant staphylococci
Language English Country United States Media print
Document type Clinical Trial, Journal Article, Research Support, Non-U.S. Gov't
PubMed
17702467
DOI
10.1007/bf02931310
Knihovny.cz E-resources
- MeSH
- Acetamides therapeutic use MeSH
- Anti-Infective Agents therapeutic use MeSH
- Adult MeSH
- Prosthesis-Related Infections drug therapy microbiology MeSH
- Middle Aged MeSH
- Humans MeSH
- Linezolid MeSH
- Microbial Sensitivity Tests MeSH
- Osteomyelitis drug therapy microbiology MeSH
- Oxazolidinones therapeutic use MeSH
- Methicillin Resistance drug effects MeSH
- Aged MeSH
- Staphylococcal Infections drug therapy MeSH
- Staphylococcus aureus drug effects MeSH
- Treatment Outcome MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Clinical Trial MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Acetamides MeSH
- Anti-Infective Agents MeSH
- Linezolid MeSH
- Oxazolidinones MeSH
During 1999-2005 we treated 15 patients with linezolid for relevant infections of locomotion apparatus (7 cases with endoprosthesis infection, 5x osteomyelitis and 3x another infection). With the exception of one case the antibiotic therapy was always combined with appropriate surgical intervention. Average period of linezolid administration was 26 d; linezolid was applied from the beginning intravenously on average for 10 d, and then orally for 16 d (average). There were no undesirable effects in the file. Success rate reached 86.6%. MRSA strains were proved by standard methods: growth on Mueller-Hinton agar with increased concentration of NaCl and 2 mg/L of oxacilline, and measuring inhibitory zones around cephoxitine disk. The sensitivity to other antibiotics was specified by disk-diffusion test; that to linezolid was verified by E-test. Linezolid represents a medical reserve for the treatment of multiresistant Gram-positive infections or for emergencies, when allergy onset, high toxicity risk, intolerance, etc. do not allow to use other, in vitro effective, antibiotics.
See more in PubMed
Antimicrob Agents Chemother. 2003 Dec;47(12):3964-6 PubMed
Lancet. 2001 Jul 21;358(9277):207-8 PubMed
Clin Microbiol Infect. 2005 Jul;11 Suppl 4:33-42 PubMed
Lancet. 2001 Apr 14;357(9263):1179 PubMed
Antimicrob Agents Chemother. 2005 Jun;49(6):2260-6 PubMed
Curr Opin Investig Drugs. 2005 Feb;6(2):185-90 PubMed
Mayo Clin Proc. 2004 Sep;79(9):1137-44 PubMed
J Antimicrob Chemother. 2002 Jul;50(1):73-7 PubMed
Am J Surg. 2004 Dec;188(6):760-6 PubMed
Antimicrob Agents Chemother. 2000 Dec;44(12):3408-13 PubMed
BMJ. 2000 Jan 22;320(7229):213-6 PubMed
Folia Microbiol (Praha). 2006;51(5):381-6 PubMed
Expert Opin Drug Saf. 2004 Sep;3(5):405-14 PubMed
Folia Microbiol (Praha). 2005;50(3):187-94 PubMed
Folia Microbiol (Praha). 2006;51(3):236-8 PubMed
Curr Opin Infect Dis. 2003 Dec;16(6):515-9 PubMed
Antimicrob Agents Chemother. 1998 Dec;42(12):3251-5 PubMed
J Mol Biol. 1999 Nov 19;294(1):93-101 PubMed
Ann Pharmacother. 2004 Jun;38(6):986-8 PubMed
Clin Orthop Relat Res. 2004 Oct;(427):67-71 PubMed
Infection. 2004 Feb;32(1):8-14 PubMed
J Antimicrob Chemother. 2005 Mar;55(3):387-90 PubMed
Clin Infect Dis. 1997 Apr;24(4):584-602 PubMed