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This guideline is meant to be a general outline for adult patients in the general ward setting
with relatively stable renal function. Patient populations not applicable for this guideline
include pediatrics, neonates, burns patients, ICU patients and dialysis patients.
Vancomycin Overview
1. Vancomycin is a glycopeptide antibiotic which exhibits time-dependent killing.
2. The AUC (area under serum drug concentration-versus-time curve) to MIC ratio of 400
correlates best with efficacy. For practicality reasons, trough blood levels are used as a
surrogate marker of efficacy.
3. If MIC 1, AUC/MIC 400 can be achieved for most patients.
4. If MIC 2, consult ID and choose alternative agent.
5. Monitoring peak blood levels is NOT recommended as they do not correlate with efficacy
or toxicity.
1
Therapeutic Drug Monitoring
1. Trough levels should be obtained within 30minutes before next scheduled dose
2. Obtain troughs prior to 3rd or 4th dose of new regimen or when estimated to be at steady state
based on estimated drug clearance and half- life.
3. Consider checking trough prior to 2nd dose for q48h regimens
4. Consider checking trough prior to 3rd dose for q24h regimens
5. In general, administer scheduled dose only after an expected vancomycin level returns. When in
doubt, to clarify with ward pharmacist
6. Once target trough attained, repeat trough weekly, or earlier if renal function changes
significantly or if nephrotoxic drugs are concomitantly used (i.e., amphotericin, aminoglycosides,
etc.)
7. Serum vancomycin trough level monitoring is recommended for:
a. Patients receiving therapy > 3 days
b. Morbidly obese patients
c. Patients with renal dysfunction
d. Patients with a fluctuating volume of distribution (e.g., oncology patients, ICU patients,
dialysis patients, post-surgery patients)
e. High risk of nephrotoxicity (e.g., Concurrent nephrotoxic drugs like aminoglycosides)
8. Trough monitoring is NOT needed for:
a. Surgical prophylaxis (expected duration < 3 days)
b. Mild skin and soft tissue infections (SSTIs)in patients with normal renal function and who
are NOT morbidly obese with dose of 1g q12h (eg. Using vancomycin for patients with
SSTIs who are allergic/intolerant to beta-lactams)
c. Patients on oral vancomycin regimens for Clostridium difficile
Dosing Adjustments based on true trough levels (i.e., levels within 30min before next dose)
Trough Level Adjustments
< 10 Increase dose by 500mg or 50% of dose (whichever is greater) at same interval.
If renal function improves, can consider shortening interval
10-15 Within goal : no change
If below goal : increase dose by 250mg -500mg + keep same interval OR if at
20mg/kg/dose can consider reduced dose with more frequent dosing
15 20 Within goal : no change
If above goal : decrease dose by 250mg 500mg and keep interval , if renal
function worsens, consider extending interval
> 20 Hold dose and recheck in 12-24 hours, when in goal range, resume at extended
interval/lower dose.
2
Administration Guidelines
Prepared by: Ms Hooi Pik Yee (Pharmacy), Mr. Yeoh Siang Fei (Pharmacy), Dr. Caroline Tee
(Pharmacy), Dr. Grant Sklar (Pharmacy) and Dr. Dale Fisher (Medicine) Date: February 2014
References
1. Cockcroft D, Gault MD. Prediction of creatinine clearance from serum creatinine. Nephron,
16:31-41, 1976
3. Liu C, Bayer A, Cosgrove SE, et al. Clinical practice guidelines by the infectious diseases society
of america for the treatment of methicillin-resistant Staphylococcus aureus infections in
adults and children. Clin Infect Dis 2011; 52:e18
4. Moellering Jr. RC. Editorial: Monitoring serum vancomycin levels: climbing the
mountain because it is there? Clin Infect Dis 1994;18:544-6.