Vancomycin therapeutic drug monitoring: is it necessary?
- PMID: 8347913
- DOI: 10.1177/106002809302700514
Vancomycin therapeutic drug monitoring: is it necessary?
Abstract
Objective: To review the literature and assess the validity of obtaining vancomycin serum drug concentrations in patients.
Data sources: A MEDLINE search of the English literature and a bibliographic review of articles pertaining to vancomycin serum concentrations, their use, and the rationale of cited therapeutic ranges.
Study selection and data extraction: Studies pertaining to the use of vancomycin concentrations in the clinical setting, methods for predicting these concentrations, and studies that reported efficacy or toxicity associated with vancomycin use and possible correlation of serum concentrations.
Data synthesis: The usefulness of vancomycin serum concentrations, the determination of a therapeutic range of values, and their correlation to antibacterial efficacy and drug toxicity in the clinical setting are controversial. Old reports of toxicities need to be critically examined due to lack of information and the actual frequency of toxic reactions. The efficacy of vancomycin's antibacterial effect and its correlation with reported therapeutic ranges may advocate obtaining a vancomycin trough concentration in certain groups of patients.
Conclusions: Determination of serum vancomycin concentrations in the clinical setting and their usefulness in patient care is questionable and unnecessary in the majority of patients.
Similar articles
-
[Measurements of vancomycin concentrations in the blood - a method of personalization the antibiotic therapy in patients with chronic kidney disease].Pol Merkur Lekarski. 2017 Apr 21;42(250):145-150. Pol Merkur Lekarski. 2017. PMID: 28530212 Polish.
-
Trough concentration over 12.1 mg/L is a major risk factor of vancomycin-related nephrotoxicity in patients with therapeutic drug monitoring.Ther Drug Monit. 2014 Oct;36(5):606-11. doi: 10.1097/FTD.0000000000000061. Ther Drug Monit. 2014. PMID: 24577126
-
Why monitor peak vancomycin concentrations?Lancet. 1995 Mar 11;345(8950):646; author reply 646-7. Lancet. 1995. PMID: 7898193 No abstract available.
-
Serum vancomycin concentrations: reappraisal of their clinical value.Clin Infect Dis. 1994 Apr;18(4):533-43. Clin Infect Dis. 1994. PMID: 8038306 Review.
-
Neonatal vancomycin continuous infusion: still a confusion?Pediatr Infect Dis J. 2014 Jun;33(6):600-5. doi: 10.1097/INF.0000000000000243. Pediatr Infect Dis J. 2014. PMID: 24378952 Review.
Cited by
-
Vancomycin Serum Concentration Monitoring : The Middle Ground is Best.Clin Drug Investig. 1996 Aug;12(2):105-18. doi: 10.2165/00044011-199612020-00006. Clin Drug Investig. 1996. PMID: 24610671
-
Pharmacokinetic and pharmacodynamic issues in the treatment of bacterial infectious diseases.Eur J Clin Microbiol Infect Dis. 2004 Apr;23(4):271-88. doi: 10.1007/s10096-004-1107-7. Epub 2004 Mar 10. Eur J Clin Microbiol Infect Dis. 2004. PMID: 15015030 Review.
-
Minimisation of aminoglycoside toxicity in patients with cystic fibrosis.Thorax. 1996 Apr;51(4):369-73. doi: 10.1136/thx.51.4.369. Thorax. 1996. PMID: 8733487 Free PMC article. Clinical Trial.
-
The importance of pharmacokinetic/pharmacodynamic surrogate markers to outcome. Focus on antibacterial agents.Clin Pharmacokinet. 1995 Feb;28(2):143-60. doi: 10.2165/00003088-199528020-00005. Clin Pharmacokinet. 1995. PMID: 7736689 Review.
-
Comparison of conventional dosing versus continuous-infusion vancomycin therapy for patients with suspected or documented gram-positive infections.Antimicrob Agents Chemother. 1996 Mar;40(3):696-700. doi: 10.1128/AAC.40.3.696. Antimicrob Agents Chemother. 1996. PMID: 8851595 Free PMC article. Clinical Trial.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical