Acute renal failure associated with vancomycin and β‐lactams for the treatment of osteomyelitis in diabetics: piperacillin–tazobactam as compared with cefepime. (21st November 2013)
- Record Type:
- Journal Article
- Title:
- Acute renal failure associated with vancomycin and β‐lactams for the treatment of osteomyelitis in diabetics: piperacillin–tazobactam as compared with cefepime. (21st November 2013)
- Main Title:
- Acute renal failure associated with vancomycin and β‐lactams for the treatment of osteomyelitis in diabetics: piperacillin–tazobactam as compared with cefepime
- Authors:
- Moenster, R. P.
Linneman, T. W.
Finnegan, P. M.
Hand, S.
Thomas, Z.
McDonald, J. R.
Grobusch, M. - Abstract:
- <abstract abstract-type="main" id="clm12410-abs-0001"> <title>Abstract</title> <p>Few data are available on the nephrotoxic potential of vancomycin when combined with certain β‐lactam antibiotics for the treatment of osteomyelitis (OM). A retrospective cohort study was conducted of all diabetic patients with OM treated with vancomycin plus piperacillin–tazobactam (VPT) or vancomycin plus cefepime (VC) for at least 72 h at a VA Medical Center between 1 January 2006 and 31 December 2011. All patients with a creatinine clearance (CrCl) of ≤40 mL/min, a blood urea nitrogen/serum creatinine (SCr) ratio of ≥20 : 1 or an absolute neutrophil count of &lt;500 cells/mm<sup>3</sup> were excluded. The primary outcome was development of acute renal failure (ARF), defined as an increase in SCr of 0.5 mg/dL or 50% of baseline. One hundred and thirty‐nine patients met the inclusion criteria; 109 in the piperacillin–tazobactam group and 30 in the cefepime group. Among patients receiving VPT, 29.3% (32/109) developed ARF, as compared with 13.3% (4/30) receiving VC (p 0.099). Among patients receiving high‐dose therapy (≥18 g of piperacillin–tazobactam daily or ≥3 g of cefepime daily), 37.5% (9/24) receiving VPT and 17.6% (3/17) receiving VC developed ARF (p 0.29). A multiple logistic regression analysis identified weight and average vancomycin trough as the only significant predictors of ARF; the choice of VPT as therapy yielded an OR of 3.45 (95% CI 0.96–12.40; p 0.057). The authors were<abstract abstract-type="main" id="clm12410-abs-0001"> <title>Abstract</title> <p>Few data are available on the nephrotoxic potential of vancomycin when combined with certain β‐lactam antibiotics for the treatment of osteomyelitis (OM). A retrospective cohort study was conducted of all diabetic patients with OM treated with vancomycin plus piperacillin–tazobactam (VPT) or vancomycin plus cefepime (VC) for at least 72 h at a VA Medical Center between 1 January 2006 and 31 December 2011. All patients with a creatinine clearance (CrCl) of ≤40 mL/min, a blood urea nitrogen/serum creatinine (SCr) ratio of ≥20 : 1 or an absolute neutrophil count of &lt;500 cells/mm<sup>3</sup> were excluded. The primary outcome was development of acute renal failure (ARF), defined as an increase in SCr of 0.5 mg/dL or 50% of baseline. One hundred and thirty‐nine patients met the inclusion criteria; 109 in the piperacillin–tazobactam group and 30 in the cefepime group. Among patients receiving VPT, 29.3% (32/109) developed ARF, as compared with 13.3% (4/30) receiving VC (p 0.099). Among patients receiving high‐dose therapy (≥18 g of piperacillin–tazobactam daily or ≥3 g of cefepime daily), 37.5% (9/24) receiving VPT and 17.6% (3/17) receiving VC developed ARF (p 0.29). A multiple logistic regression analysis identified weight and average vancomycin trough as the only significant predictors of ARF; the choice of VPT as therapy yielded an OR of 3.45 (95% CI 0.96–12.40; p 0.057). The authors were unable to detect a statistically significant difference in ARF between groups; however, the power requirement was not met. Further study with a larger patient population seems warranted.</p> </abstract> … (more)
- Is Part Of:
- Clinical microbiology and infection. Volume 20:Number 6(2014:Jun.)
- Journal:
- Clinical microbiology and infection
- Issue:
- Volume 20:Number 6(2014:Jun.)
- Issue Display:
- Volume 20, Issue 6 (2014)
- Year:
- 2014
- Volume:
- 20
- Issue:
- 6
- Issue Sort Value:
- 2014-0020-0006-0000
- Page Start:
- O384
- Page End:
- O389
- Publication Date:
- 2013-11-21
- Subjects:
- Medical microbiology -- Periodicals
Diagnostic microbiology -- Periodicals
Communicable diseases -- Periodicals
Infection -- Periodicals
616.01 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1469-0691 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1469-0691.12410 ↗
- Languages:
- English
- ISSNs:
- 1198-743X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3286.305520
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3443.xml