Vancomycin: Difference between revisions
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== |
==Background== |
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*A [[:Category:Glycopeptides|glycopeptide]] antibiotic |
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* Suspected or confirmed MRSA |
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== |
===Mechanism of Action=== |
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*Inhibits cross-linking of peptidoglycans in the cell wall |
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* Common dose |
|||
** 15mg/kg/dose with timing based on renal function (q12h if normal) |
|||
** Titrate based on serum trough drawn within hour before fourth dose |
|||
* Target trough |
|||
** 10-15 for low-risk infections |
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** 15-20 for high-risk infections such as osteomyelitis, meningitis, and bacteremia |
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===Mechanisms of Resistance=== |
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== Adverse Reactions == |
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*Alterations in peptidoglycans conferred by chromosomal or plasmid-mediated ''vanA'', ''vanB'', or ''vanC'' |
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=== Renal Failures === |
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===Spectrum of Activity=== |
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* Risk factors |
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** Prolonged courses >21 days |
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** Higher trough |
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** Concomitant nephrotoxic medication |
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** Older age |
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** CKD/AKI |
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** Liver disease |
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** Peritonitis |
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** Neutropenia |
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** Male sex |
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* Mechanism of injury: oxidative stress in the proximal tubular cells |
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*Broadly active against Gram-positive bacteria, including anaerobes |
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=== Red Man Syndrome === |
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*Not active against Gram-negative bacteria |
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*Notable resistance occurs in: |
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**[[Clostridium innocuum]] |
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**[[Enterococcus gallinarum]], [[Enterococcus casseliflavus]], and [[Enterococcus flavus]] (chromosomal ''vanC'') |
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**[[Erysipelothrix rhusiopathiae]] |
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**[[Lactobacillus]], except [[Lactobacillus acidophilus]] and [[Lacobacillus delbrueckii]] |
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**[[Leuconostoc]] |
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**[[Pediococcus]] |
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**[[Weissella]] |
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===Pharmacokinetics and Pharmacodynamics=== |
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* Rash, pruritis, and hypotension, with onset of vancomycin, resolves on stopping |
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* Very high incidence previously |
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* Histamine-mediated |
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* Can decrease dose or prolong infusion, prophylactic antihistamines |
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*Bactericidal |
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[[Category:Antibiotics]] |
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*Concentration-independent with post-antibiotic effect |
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*Efficacy predicted by AUC<sub>24</sub>:MIC |
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===Clinical Breakpoints=== |
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{| class="wikitable" |
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! rowspan="2" |Species |
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! colspan="3" |Breakpoints (μg/mL) |
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|- |
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!S |
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!I |
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!R |
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|- |
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|[[Staphylococcus aureus]] |
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|≤2 |
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|4-8 |
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|≥16 |
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|- |
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|[[Staphylococcus]] species other than [[Staphylococcus aureus]] |
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|≤4 |
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|8-16 |
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|≥32 |
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|- |
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|[[Enterococcus]] |
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|≤4 |
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|8-16 |
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|≥32 |
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|- |
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|[[Streptococcus pneumoniae]] |
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|≤1 |
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|— |
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|— |
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|- |
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|[[β-hemolytic streptococci]] |
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|≤1 |
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|— |
|||
|— |
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|} |
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==Dosing== |
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=== Intermittent Infusion === |
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*Common dose |
|||
**Loading dose of 25-30 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 |
|||
==== Renal Dosing ==== |
|||
* CrCl >100 mL/min: 15-20 mg/kg q8-12h |
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* CrCCl 50 to 100: 15-20 mg/kg q12h |
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* CrCl 20-49: 15-20 mg/kg q24h |
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* CrCl <20: 15-20 mg/kg q48h |
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* '''Hemodialysis:''' target pre-dialysis levels of 15 to 20 |
|||
** If next HD in 1 day, give 15 mg/kg |
|||
** If next HD in 2 days, give 25 mg/kg |
|||
** If next HD in 3 days, give 35 mg/kg |
|||
** Give at rate of 15 mg/min over the last 120 minutes of HD to coincide with the end of dialysis |
|||
**Alternatively: |
|||
***< 70 kg: 1000mg IV x 1, then 500mg post-dialysis |
|||
***70 –100kg: 1250mg IV x 1, then 750mg post-dialysis |
|||
***>100 kg: 1500mg IV x 1, then 1000mg post-dialysis |
|||
* CAPD: 7.5 mg/kg q48-96h |
|||
* CRRT: 10-15 mg/kg q24-48h |
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====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 calculators[[CiteRef::rybak2020th]] |
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**Use peak 60 min after infusion and trough 1 to 60 minutes before next dose, and record times accurately |
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**Target AUC/MIC<sub>BMD</sub> ratio of 400 to 600 for serious [[Staphylococcus aureus]] infections |
|||
=== Continuous Infusion === |
|||
* Particularly useful in the following patients: |
|||
** Total daily doses of 4 g or higher, since it will lower the total dose and therefore associated toxicitynephro |
|||
** Home antibiotic therapy, to simplify drug monitoring |
|||
* At least as safe and effective as intermittent infusion |
|||
* Limited by pump availability and IV access |
|||
* Consider '''loading dose''' in patients who are not already on intermittent infusion and who are hemodynamically unstable |
|||
* Initial dose based on creatinine clearance and weight |
|||
{| class="wikitable" |
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!TBW (kg) |
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!CrCl (mL/min) |
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!Load (mg) |
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!Maintenance (mg/24h) |
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|- |
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|<100 |
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| rowspan="3" |≥90 |
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|1000 |
|||
|2000 |
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|- |
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|100-119 |
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|1500 |
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|2500 |
|||
|- |
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|≥120 |
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|2000 |
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|3000 |
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|- |
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! colspan="4" |Obesity and Renal Failure |
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|- |
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| rowspan="5" |100-115 |
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|70-89 |
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|1000 |
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|1750 |
|||
|- |
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|50-69 |
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|1000 |
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|1250 |
|||
|- |
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|40-49 |
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|1000 |
|||
|1000 |
|||
|- |
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|30-39 |
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|1000 |
|||
|750 |
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|- |
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|20-29 |
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|1000 |
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|500 |
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|- |
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| rowspan="5" |116-139 |
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|70-89 |
|||
|1250 |
|||
|2000 |
|||
|- |
|||
|50-69 |
|||
|1250 |
|||
|1500 |
|||
|- |
|||
|40-49 |
|||
|1250 |
|||
|1250 |
|||
|- |
|||
|30-39 |
|||
|1250 |
|||
|1000 |
|||
|- |
|||
|20-29 |
|||
|1250 |
|||
|750 |
|||
|- |
|||
| rowspan="5" |140-159 |
|||
|70-89 |
|||
|1500 |
|||
|2500 |
|||
|- |
|||
|50-69 |
|||
|1500 |
|||
|1750 |
|||
|- |
|||
|40-49 |
|||
|1500 |
|||
|1500 |
|||
|- |
|||
|30-39 |
|||
|1500 |
|||
|1250 |
|||
|- |
|||
|20-29 |
|||
|1500 |
|||
|750 |
|||
|- |
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| rowspan="5" |160-179 |
|||
|70-89 |
|||
|1500 |
|||
|2750 |
|||
|- |
|||
|50-69 |
|||
|1500 |
|||
|2000 |
|||
|- |
|||
|40-49 |
|||
|1500 |
|||
|1500 |
|||
|- |
|||
|30-39 |
|||
|1500 |
|||
|1250 |
|||
|- |
|||
|20-29 |
|||
|1500 |
|||
|1000 |
|||
|- |
|||
| rowspan="5" |180-199 |
|||
|70-89 |
|||
|1750 |
|||
|3000 |
|||
|- |
|||
|50-69 |
|||
|1750 |
|||
|2500 |
|||
|- |
|||
|40-49 |
|||
|1750 |
|||
|2000 |
|||
|- |
|||
|30-39 |
|||
|1750 |
|||
|1500 |
|||
|- |
|||
|20-29 |
|||
|1750 |
|||
|1000 |
|||
|} |
|||
==== Monitoring ==== |
|||
* Random vancomycin levels |
|||
** First level is 24 hours after starting |
|||
** Monitor weekly, any time the patient is unstable, and 24 hours after any dose adjustments |
|||
** Target levels are typically 15 to 20 |
|||
* Serum creatinine should be measured twice weekly |
|||
* CBC monitored weekly |
|||
==Adverse Reactions== |
|||
*Primarily include [[Adverse drug reaction::renal failure]] and [[Adverse drug reaction::red person syndrome]] |
|||
===Renal Failures=== |
|||
*Dose-dependent risk, with significant increase with trough over 15 |
|||
*Lower risk with AUC-based dosing, which promotes lower dosing, and with continuous infusion |
|||
*Risk factors: prolonged courses >21 days, higher troughs, concomitant nephrotoxic medication, older age, [[CKD]]/[[AKI]], [[liver disease]], [[peritonitis]], [[neutropenia]], and male sex |
|||
*Mechanism of injury: either AIN or ATN from oxidative stress in the proximal tubular cells |
|||
**May be able to detect it early with serum Kim-1 elevation, or NGAL elevation (though less specific) |
|||
===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 |
|||
[[Category:Glycopeptides]] |
Latest revision as of 02:09, 10 October 2022
Background
- A glycopeptide antibiotic
Mechanism of Action
- Inhibits cross-linking of peptidoglycans in the cell wall
Mechanisms of Resistance
- Alterations in peptidoglycans conferred by chromosomal or plasmid-mediated vanA, vanB, or vanC
Spectrum of Activity
- Broadly active against Gram-positive bacteria, including anaerobes
- Not active against Gram-negative bacteria
- Notable resistance occurs in:
Pharmacokinetics and Pharmacodynamics
- Bactericidal
- Concentration-independent with post-antibiotic effect
- Efficacy predicted by AUC24:MIC
Clinical Breakpoints
Species | Breakpoints (μg/mL) | ||
---|---|---|---|
S | I | R | |
Staphylococcus aureus | ≤2 | 4-8 | ≥16 |
Staphylococcus species other than Staphylococcus aureus | ≤4 | 8-16 | ≥32 |
Enterococcus | ≤4 | 8-16 | ≥32 |
Streptococcus pneumoniae | ≤1 | — | — |
β-hemolytic streptococci | ≤1 | — | — |
Dosing
Intermittent Infusion
- Common dose
- Loading dose of 25-30 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
Renal Dosing
- CrCl >100 mL/min: 15-20 mg/kg q8-12h
- CrCCl 50 to 100: 15-20 mg/kg q12h
- CrCl 20-49: 15-20 mg/kg q24h
- CrCl <20: 15-20 mg/kg q48h
- Hemodialysis: target pre-dialysis levels of 15 to 20
- If next HD in 1 day, give 15 mg/kg
- If next HD in 2 days, give 25 mg/kg
- If next HD in 3 days, give 35 mg/kg
- Give at rate of 15 mg/min over the last 120 minutes of HD to coincide with the end of dialysis
- Alternatively:
- < 70 kg: 1000mg IV x 1, then 500mg post-dialysis
- 70 –100kg: 1250mg IV x 1, then 750mg post-dialysis
- >100 kg: 1500mg IV x 1, then 1000mg post-dialysis
- CAPD: 7.5 mg/kg q48-96h
- CRRT: 10-15 mg/kg q24-48h
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
- Use peak 60 min after infusion and trough 1 to 60 minutes before next dose, and record times accurately
- Target AUC/MICBMD ratio of 400 to 600 for serious Staphylococcus aureus infections
Continuous Infusion
- Particularly useful in the following patients:
- Total daily doses of 4 g or higher, since it will lower the total dose and therefore associated toxicitynephro
- Home antibiotic therapy, to simplify drug monitoring
- At least as safe and effective as intermittent infusion
- Limited by pump availability and IV access
- Consider loading dose in patients who are not already on intermittent infusion and who are hemodynamically unstable
- Initial dose based on creatinine clearance and weight
TBW (kg) | CrCl (mL/min) | Load (mg) | Maintenance (mg/24h) |
---|---|---|---|
<100 | ≥90 | 1000 | 2000 |
100-119 | 1500 | 2500 | |
≥120 | 2000 | 3000 | |
Obesity and Renal Failure | |||
100-115 | 70-89 | 1000 | 1750 |
50-69 | 1000 | 1250 | |
40-49 | 1000 | 1000 | |
30-39 | 1000 | 750 | |
20-29 | 1000 | 500 | |
116-139 | 70-89 | 1250 | 2000 |
50-69 | 1250 | 1500 | |
40-49 | 1250 | 1250 | |
30-39 | 1250 | 1000 | |
20-29 | 1250 | 750 | |
140-159 | 70-89 | 1500 | 2500 |
50-69 | 1500 | 1750 | |
40-49 | 1500 | 1500 | |
30-39 | 1500 | 1250 | |
20-29 | 1500 | 750 | |
160-179 | 70-89 | 1500 | 2750 |
50-69 | 1500 | 2000 | |
40-49 | 1500 | 1500 | |
30-39 | 1500 | 1250 | |
20-29 | 1500 | 1000 | |
180-199 | 70-89 | 1750 | 3000 |
50-69 | 1750 | 2500 | |
40-49 | 1750 | 2000 | |
30-39 | 1750 | 1500 | |
20-29 | 1750 | 1000 |
Monitoring
- Random vancomycin levels
- First level is 24 hours after starting
- Monitor weekly, any time the patient is unstable, and 24 hours after any dose adjustments
- Target levels are typically 15 to 20
- Serum creatinine should be measured twice weekly
- CBC monitored weekly
Adverse Reactions
- Primarily include renal failure and red person syndrome
Renal Failures
- Dose-dependent risk, with significant increase with trough over 15
- Lower risk with AUC-based dosing, which promotes lower dosing, and with continuous infusion
- Risk factors: prolonged courses >21 days, higher troughs, concomitant nephrotoxic medication, older age, CKD/AKI, liver disease, peritonitis, neutropenia, and male sex
- Mechanism of injury: either AIN or ATN from oxidative stress in the proximal tubular cells
- May be able to detect it early with serum Kim-1 elevation, or NGAL elevation (though less specific)
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
- ^ 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.