Auburn University Harrison School of Pharmacy, Huntsville, AL, USA.
Ann Pharmacother. 2011 May;45(5):582-9. doi: 10.1345/aph.1P588. Epub 2011 Apr 26.
Because of concerns regarding increasing microbial resistance to vancomycin, adult treatment guidelines recommend higher trough concentrations based on the type of infectious process. Although these recommendations are not specific to pediatrics, the principles can be extrapolated. Desired higher trough serum concentrations will require escalated dosages of vancomycin in children.
To evaluate current dosing regimens and subsequent trough serum concentrations of vancomycin in children, compare these to reference recommended dosages and guidelines, and predict a dosing equation to achieve desired serum concentrations.
Pharmacokinetic parameters of children in a community teaching hospital who were prescribed vancomycin from January 2005 to May 2010 were evaluated in this retrospective chart review. Vancomycin dosing and subsequent serum concentrations were analyzed. Therapeutic serum concentrations were evaluated and compared to vancomycin prescribing and monitoring guidelines by year.
Four hundred thirty-five trough serum concentrations determined in 295 patients were analyzed. The average dosages, when evaluated by year, were 48 mg/kg/day (2005-2008) and 59 mg/kg/day (2009-2010). Using trough concentration recommendations of 5-15 mg/L, vancomycin regimens provided therapeutic trough concentrations 78% of the time from 2005 to 2008. Using 10-20 mg/L as the trough recommendations in 2009-2010, only 49% of serum concentrations reached a therapeutic level. Based on our predictive equation for children aged 1 month-18 years with normal renal function, a vancomycin dosage of 70 mg/kg/day is required to provide trough serum concentrations of 10 mg/L; a dosage of 85 mg/kg/day is required to provide trough serum concentrations of 15 mg/L.
Our institution was primarily using vancomycin dosing regimens that were recommended in pediatric references (40-60 mg/kg/day), which resulted in subtherapeutic serum concentrations in our population based on new monitoring recommendations. Considering that the currently desired therapeutic trough concentrations of vancomycin are 10-20 mg/L, the total daily dosage should be increased.
由于担心万古霉素对微生物的耐药性不断增加,成人治疗指南建议根据感染类型调整更高的谷浓度。虽然这些建议并非专门针对儿科,但这些原则可以推断出来。想要达到更高的谷浓度,就需要在儿童中增加万古霉素的剂量。
评估儿童目前的万古霉素剂量方案和随后的谷浓度,将其与参考推荐剂量和指南进行比较,并预测达到所需血清浓度的剂量方程。
本回顾性图表审查评估了 2005 年 1 月至 2010 年 5 月期间在一家社区教学医院接受万古霉素治疗的儿童的药代动力学参数。分析了万古霉素的剂量和随后的血清浓度。根据年份评估了治疗性血清浓度,并将其与万古霉素的处方和监测指南进行了比较。
分析了 295 名患者的 435 个谷浓度。当按年份评估时,平均剂量分别为 2005-2008 年的 48mg/kg/天和 2009-2010 年的 59mg/kg/天。使用 5-15mg/L 的谷浓度建议,2005-2008 年万古霉素方案提供治疗性谷浓度的时间为 78%。在 2009-2010 年将 10-20mg/L 作为谷浓度建议时,只有 49%的血清浓度达到治疗水平。根据我们为肾功能正常的 1 个月至 18 岁儿童的预测方程,需要 70mg/kg/天的万古霉素剂量才能提供 10mg/L 的谷血清浓度;需要 85mg/kg/天的剂量才能提供 15mg/L 的谷血清浓度。
我们的机构主要使用儿科参考中推荐的万古霉素剂量方案(40-60mg/kg/天),根据新的监测建议,这导致我们人群中的血清浓度低于治疗水平。考虑到目前万古霉素所需的治疗性谷浓度为 10-20mg/L,总日剂量应增加。