Objective: Compare the use of the VTM previously to the implementation of a controlled protocol (1st period), with 2 other distinct periods. At the 2nd period we used a VTM protocol with a 5-15 ug/dL vancomycin serum level target, and at the 3rd period a 10-20 ug/dL vancomycin serum level target.
Methods: We compared among the three analyzed periods: Days of vancomycin used, grams of vancomycin used, number of blood collection for vancomycins per patient, number of collected blood failures per patient, adequated blood collections (i.e. performed until 2 hours before the next dose) and adequated therapeutic targets, according to the analyzed period. We also studied patients with toxic levels (> 30 ug/dL) and with under dosing (< 5 ug/dL). Cases of osteomyelitis and endocarditis were not included in this study and the 3rd period adjustment was conducted through a serum level greater than 10 ug/dL by some evidence to avoid bacterial resistance with these vancomycin levels.
Results: The results can be viewed in table 1.
Table 1: Comparison of the three study periods.
Indicators |
1st period (n=47) Previously to VTM protocol (5-15ug/dL) |
2nd period (n=55) VTM protocol (5-15ug/dL) |
3rd period (n=55) VTM protocol (10-20ug/dL) |
Consumption of vancomycin |
|
|
|
Days used per patient |
10.3 |
7.8 |
8.1 |
Grams used per patient |
11.2 |
6.8 |
9.2 |
Serum levels of vancomycin |
|
|
|
Nº of blood collections per patient |
5.0 |
7.0 |
7.1 |
Nº of collected blood failures per patient |
4.7 |
0.6 |
0.05 |
Adequated blood collections (performed until 2 hours before the next dose) |
22% |
84% |
87% |
Adequated therapeutic targets |
67.4% |
72.5% |
68.5% |
Adverse events |
|
|
|
Patients with toxic levels (>30 ug/dL) |
14.9% |
3.6% |
12.7% |
Patients with under dosing (<5 ug/dL) |
21.3% |
7.3% |
9.1% |
Conclusions: The elaboration of a VTM protocol, training staff and engagement of laboratory to speed up the liberation of results may decrease the number of collection´s failure, increase the number of adequated blood collections and reduce the number of patients receiving suboptimal dose. Toxic doses of vancomycin were higher in the 3rd period compared to the 2nd, it could be related to a desired high target level.