Literature DB >> 20021290

Clinical outcomes and nephrotoxicity associated with vancomycin trough concentrations during treatment of deep-seated infections.

Elizabeth D Hermsen1, Monica Hanson, Jayashri Sankaranarayanan, Julie A Stoner, Marius C Florescu, Mark E Rupp.   

Abstract

OBJECTIVE: Higher vancomycin concentrations are thought necessary for treatment of deep-seated methicillin-resistant Staphylococcus aureus (MRSA) infection, yet this may result in greater risk of nephrotoxicity. We evaluated the relationship of serum vancomycin trough concentration with clinical outcomes and nephrotoxicity for patients with deep-seated MRSA infection.
METHODS: A retrospective cohort study evaluated adults with MRSA pneumonia, endocarditis or osteomyelitis who received vancomycin for > or = 5 days from June 2005 to June 2007. Patients were stratified by mean vancomycin trough level [low (< 15 mg/l), high (> or = 15 mg/l)]. Outcomes were clinical response, mortality, length of stay (LOS) and nephrotoxicity. Three definitions of nephrotoxicity were used: i) rise in serum creatinine (SCr) > or = 0.5 mg/dl; ii) 50% increase in SCr; and iii) 25% decrease in estimated creatinine clearance.
RESULTS: Fifty-five patients experiencing MRSA pneumonia (n = 28), endocarditis (n = 9), osteomyelitis (n = 20) and multiple infections (n = 2) were stratified into low (n = 39) and high (n = 16) groups. High group patients were more likely to be septic (p = 0.01) and have a higher APACHE II score (p = 0.01). After adjustment for APACHE II score, clinical response rates among survivors did not differ significantly. Risk of death was not significantly different between the high (19%) and low (5%) group patients (p = 0.1). LOS did not differ significantly between groups (p = 0.7). Nephrotoxicity occurred in the low and high groups, respectively, for 10 and 31% (p = 0.04) with definition 1, 10 and 31% (p = 0.04) with definition 2, and 13 and 25% (p = 0.1) with definition 3. After adjustment for APACHE II score, odds of nephrotoxicity based on definitions 1 or 2 were increased among the high versus low groups (OR = 3.27, 95% CI: 0.7 - 15.25, p = 0.1), although not statistically significant.
CONCLUSIONS: Clinical outcomes did not differ significantly between high and low trough groups for deep-seated MRSA infections. Nephrotoxicity was consistently higher in the high trough group, regardless of the definition used.

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Year:  2010        PMID: 20021290     DOI: 10.1517/14740330903413514

Source DB:  PubMed          Journal:  Expert Opin Drug Saf        ISSN: 1474-0338            Impact factor:   4.250


  27 in total

Review 1.  Vancomycin-induced nephrotoxicity: mechanism, incidence, risk factors and special populations. A literature review.

Authors:  Sepideh Elyasi; Hossein Khalili; Simin Dashti-Khavidaki; Amirhooshang Mohammadpour
Journal:  Eur J Clin Pharmacol       Date:  2012-03-13       Impact factor: 2.953

Review 2.  Systematic review and meta-analysis of vancomycin-induced nephrotoxicity associated with dosing schedules that maintain troughs between 15 and 20 milligrams per liter.

Authors:  S J van Hal; D L Paterson; T P Lodise
Journal:  Antimicrob Agents Chemother       Date:  2012-11-19       Impact factor: 5.191

Review 3.  Prevention of vancomycin induced nephrotoxicity: a review of preclinical data.

Authors:  Sepideh Elyasi; Hossein Khalili; Shima Hatamkhani; Simin Dashti-Khavidaki
Journal:  Eur J Clin Pharmacol       Date:  2012-09-21       Impact factor: 2.953

4.  Identification of risk factors for nephrotoxicity in patients receiving extended-duration, high-trough vancomycin therapy.

Authors:  Claire Contreiras; Michael Legal; Tim T Y Lau; Rosanne Thalakada; Stephen Shalansky; Mary H H Ensom
Journal:  Can J Hosp Pharm       Date:  2014-03

5.  Comparison of the Predictive Performance Between Cystatin C and Serum Creatinine by Vancomycin via a Population Pharmacokinetic Models: A Prospective Study in a Chinese Population.

Authors:  Ren Zhang; Ming Chen; Tao-Tao Liu; Jie-Jiu Lu; Chun-le Lv
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2020-02       Impact factor: 2.441

6.  Development of acute kidney injury during continuous infusion of vancomycin in septic patients.

Authors:  S Cianferoni; A Devigili; E Ocampos-Martinez; L Penaccini; S Scolletta; A Abdelhadii; D De Backer; M Beumier; F Jacobs; J-L Vincent; F S Taccone
Journal:  Infection       Date:  2013-04-10       Impact factor: 3.553

7.  Evaluation of risk factors for vancomycin-induced nephrotoxicity.

Authors:  So Jin Park; Na Ri Lim; Hyo Jung Park; Jae Wook Yang; Min-Ji Kim; Kyunga Kim; Yong Won In; Young Mee Lee
Journal:  Int J Clin Pharm       Date:  2018-05-09

8.  Outcomes and Nephrotoxicity Associated with Vancomycin Treatment in Patients 80 Years and Older.

Authors:  Yunchao Wang; Ning Dai; Wei Wei; Chunyan Jiang
Journal:  Clin Interv Aging       Date:  2021-06-01       Impact factor: 4.458

9.  Therapeutic monitoring of vancomycin according to initial dosing regimen in pediatric patients.

Authors:  Dae Il Kim; Mi Sun Im; Jin Hyoung Choi; Jina Lee; Eun Hwa Choi; Hoan Jong Lee
Journal:  Korean J Pediatr       Date:  2010-12-31

Review 10.  Treatment of complicated skin and soft-tissue infections caused by resistant bacteria: value of linezolid, tigecycline, daptomycin and vancomycin.

Authors:  Christian Eckmann; M Dryden
Journal:  Eur J Med Res       Date:  2010-11-30       Impact factor: 2.175

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