2013
DOI: 10.1007/s10156-013-0599-4
|View full text |Cite
|
Sign up to set email alerts
|

Practice guidelines for therapeutic drug monitoring of vancomycin: a consensus review of the Japanese Society of Chemotherapy and the Japanese Society of Therapeutic Drug Monitoring

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

4
176
0
5

Year Published

2016
2016
2023
2023

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 160 publications
(191 citation statements)
references
References 103 publications
4
176
0
5
Order By: Relevance
“…The use of an LD in critically ill patients is a widely recommended strategy and has been supported by several guides and studies (8)(9)(10)(11)(20)(21)(22)(23). Although there is no strong evidence to support the real clinical impact of this method, it has been suggested that its use is associated with better clinical cure rates in critically ill patients (24).…”
Section: Discussionmentioning
confidence: 99%
See 3 more Smart Citations
“…The use of an LD in critically ill patients is a widely recommended strategy and has been supported by several guides and studies (8)(9)(10)(11)(20)(21)(22)(23). Although there is no strong evidence to support the real clinical impact of this method, it has been suggested that its use is associated with better clinical cure rates in critically ill patients (24).…”
Section: Discussionmentioning
confidence: 99%
“…AUC 0 -24 /MIC values of Ն400 have demonstrated clinical and microbiological efficacy against lower respiratory tract infections by methicillinresistant Staphylococcus aureus (7), which have been later validated by international recommendations and guidelines (8)(9)(10)(11). On the other hand, lower values have shown not only poor infection eradication but also require longer treatments and a higher mortality rate (12)(13)(14).…”
mentioning
confidence: 95%
See 2 more Smart Citations
“…10) No patients in this survey were diagnosed with severe infection and the optimal concentrations were defined as: VCM and TEIC, trough concentration of 10-20 µg/mL; ABK, trough concentration of <2.0 µg/ mL and peak concentration of 9-20 µg/mL. [11][12][13] Achievement was recorded if the optimal drug concentration was reached once during treatment. We checked the incidence of acute renal injury, defined as an increase in serum creatinine to ≥1.5 times baseline after drug administration.…”
Section: )mentioning
confidence: 99%