Vancomycin: Difference between revisions

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== Background ==
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==Background==
   
* A [[:Category:Glycopeptides|glycopeptide]] antibiotic
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*A [[:Category:Glycopeptides|glycopeptide]] antibiotic
   
=== Mechanism of action ===
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===Mechanism of action===
   
* Inhibits cross-linking of peptidoglycans in the cell wall
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*Inhibits cross-linking of peptidoglycans in the cell wall
   
=== Pharmacodynamics ===
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===Pharmacodynamics===
   
* Efficacy predicted by AUC to MIC ratio
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*Efficacy predicted by AUC to MIC ratio
   
 
==Indications==
 
==Indications==
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*Common dose
 
*Common dose
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**Loading dose of 20 mg/kg given once for serious infections
**15mg/kg/dose with timing based on renal function (q12h if normal)
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**15 mg/kg/dose with timing based on renal function (q12h if normal)
**Titrate based on serum trough drawn within hour before fourth dose
 
  +
**Titrate based on monitoring parameters (below)
*Target trough
 
  +
**Adjustments assume linear pharmacokinetics,so a doubling of the daily dose, for example, should double the trough or AUC:MIC
**10-15 for low-risk infections
 
**15-20 for high-risk [[Staphylococcus aureus]] infections such as osteomyelitis, meningitis, and bacteremia
 
*Current guidelines recommend more involved PK/PD monitoring[[CiteRef::rybak2020th]]
 
**Target AUC/MIC<sub>BMD</sub> ratio of 400 to 600
 
   
 
===Obesity===
 
===Obesity===
   
 
*Dosing should use actual body weight, with a maximum loading dose of 3 g
 
*Dosing should use actual body weight, with a maximum loading dose of 3 g
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  +
=== Monitoring ===
  +
  +
* Based on PK/PD modelling, the '''trough level''' was previously used to dose vancomycin
 
** Serum trough drawn within hour before fourth dose
 
** 10-15 for low-risk infections
 
**15-20 for high-risk [[Staphylococcus aureus]] infections such as osteomyelitis, meningitis, and bacteremia
 
* Current guidelines recommend '''AUC:MIC''' monitoring using Bayesian calculators[[CiteRef::rybak2020th]]
 
** Target AUC/MIC<sub>BMD</sub> ratio of 400 to 600 for serious [[Staphylococcus aureus]] infections
   
 
==Adverse Reactions==
 
==Adverse Reactions==

Revision as of 10:07, 16 July 2020

Background

Mechanism of action

  • Inhibits cross-linking of peptidoglycans in the cell wall

Pharmacodynamics

  • Efficacy predicted by AUC to MIC ratio

Indications

  • Suspected or confirmed MRSA

Dosing

  • Common dose
    • Loading dose of 20 mg/kg given once for serious infections
    • 15 mg/kg/dose with timing based on renal function (q12h if normal)
    • Titrate based on monitoring parameters (below)
    • Adjustments assume linear pharmacokinetics,so a doubling of the daily dose, for example, should double the trough or AUC:MIC

Obesity

  • Dosing should use actual body weight, with a maximum loading dose of 3 g

Monitoring

  • Based on PK/PD modelling, the trough level was previously used to dose vancomycin
    • Serum trough drawn within hour before fourth dose
    • 10-15 for low-risk infections
    • 15-20 for high-risk Staphylococcus aureus infections such as osteomyelitis, meningitis, and bacteremia
  • Current guidelines recommend AUC:MIC monitoring using Bayesian calculators1

Adverse Reactions

Renal Failures

  • Risk factors
    • Prolonged courses >21 days
    • Higher trough
    • Concomitant nephrotoxic medication
    • Older age
    • CKD/AKI
    • Liver disease
    • Peritonitis
    • Neutropenia
    • Male sex
  • Mechanism of injury: oxidative stress in the proximal tubular cells

Red Person Syndrome

  • Rash, pruritis, and hypotension, with onset of vancomycin, resolves on stopping
  • Very high incidence previously
  • Histamine-mediated
  • Can decrease dose or prolong infusion, prophylactic antihistamines

References

  1. ^  Michael J Rybak, Jennifer Le, Thomas P Lodise, Donald P Levine, John S Bradley, Catherine Liu, Bruce A Mueller, Manjunath P Pai, Annie Wong-Beringer, John C Rotschafer, Keith A Rodvold, Holly D Maples, Benjamin M Lomaestro. Therapeutic monitoring of vancomycin for serious methicillin-resistant Staphylococcus aureus infections: A revised consensus guideline and review by the American Society of Health-System Pharmacists, the Infectious Diseases Society of America, the Pediatric Infectious Diseases Society, and the Society of Infectious Diseases Pharmacists. American Journal of Health-System Pharmacy. 2020. doi:10.1093/ajhp/zxaa036.