Vancomycin, metronidazole, and tetracyclines
- PMID: 1586910
Vancomycin, metronidazole, and tetracyclines
Abstract
Over the last 30 years, the impurities in the vancomycin product have been reduced, perhaps resulting in a lower rate of adverse reactions. Vancomycin is bactericidal against most susceptible organisms, but is bacteriostatic against the enterococcus. Vancomycin is the drug of choice for methicillin-resistant Staphylococcus aureus. Vancomycin attains good tissue and bone penetration and must be administered intravenously for systemic infections. It is eliminated renally with a half-life of about 6 hours; this half-life is prolonged with advanced age and reduced renal function. Significant adverse reactions can be minimized with careful attention to administration technique. Metronidazole has excellent tissue penetration; its antibacterial site of action is within anaerobic bacterial cells. Metronidazole is cleared by hepatic metabolism with a half-life of about 7 to 8 hours. The half-life is unchanged with renal dysfunction but is prolonged in patients with hepatic function impairment. Although adverse effects are relatively minor, there is an important interaction with warfarin. For podiatric infections, metronidazole can be used in skin- and soft-tissue infections; anaerobes in bone and joint infections are rare. Topical metronidazole has been used successfully in the treatment of decubitus ulcers, and this needs further evaluation. The most commonly used tetracyclines are tetracycline, doxycycline, and minocycline. The tetracyclines are broad spectrum antimicrobial agents, but their usefulness is limited by resistant strains. Tetracycline's absorption is significantly impaired by food, and it is cleared renally and fecally. Doxycycline has the highest protein binding and the longest half-life; it is cleared both renally and fecally without hepatic metabolism. Minocycline has the best absorption and tissue penetration; the unchanged drug is cleared renally and fecally, and it also undergoes hepatic metabolism. All tetracyclines have important adverse reactions with respect to teeth and bones, and they are contraindicated during pregnancy and for children under age eight.
Similar articles
-
Tigecycline: first of a new class of antimicrobial agents.Pharmacotherapy. 2006 Aug;26(8):1099-110. doi: 10.1592/phco.26.8.1099. Pharmacotherapy. 2006. PMID: 16863487 Review.
-
Antimicrobial spectrum, pharmacology and therapeutic use of antibiotics. Part 1: tetracyclines.Am J Hosp Pharm. 1977 Jan;34(1):49-57. Am J Hosp Pharm. 1977. PMID: 318799 Review.
-
Linezolid tissue penetration and serum activity against strains of methicillin-resistant Staphylococcus aureus with reduced vancomycin susceptibility in diabetic patients with foot infections.J Antimicrob Chemother. 2007 Oct;60(4):819-23. doi: 10.1093/jac/dkm271. Epub 2007 Aug 1. J Antimicrob Chemother. 2007. PMID: 17673476
-
[Tetracyclines, sulfonamides and metronidazole].Enferm Infecc Microbiol Clin. 2003 Nov;21(9):520-8; quiz 529, 533. doi: 10.1016/s0213-005x(03)72999-1. Enferm Infecc Microbiol Clin. 2003. PMID: 14572387 Review. Spanish.
-
Metronidazole.Obstet Gynecol Clin North Am. 1992 Sep;19(3):497-510. Obstet Gynecol Clin North Am. 1992. PMID: 1436927 Review.
Cited by
-
Antimicrobial Activity of Divaricatic Acid Isolated from the Lichen Evernia mesomorpha against Methicillin-Resistant Staphylococcus aureus.Molecules. 2018 Nov 23;23(12):3068. doi: 10.3390/molecules23123068. Molecules. 2018. PMID: 30477128 Free PMC article.
-
Characteristics of hospitalized children infected with macrolide-resistant Mycoplasma pneumoniae.Braz J Infect Dis. 2014 May-Jun;18(3):294-9. doi: 10.1016/j.bjid.2013.09.004. Epub 2014 Jan 3. Braz J Infect Dis. 2014. PMID: 24389284 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Medical