Hospital Pharmacy Services, Mayo Clinic, Rochester, MN, USA.
Antimicrob Agents Chemother. 2012 Dec;56(12):6181-5. doi: 10.1128/AAC.00459-12. Epub 2012 Sep 17.
The vancomycin dose necessary for the achievement of target serum trough concentrations during continuous venovenous hemofiltration (CVVH) remains to be elucidated. This was a retrospective cohort study of critically ill adults at a tertiary medical center on concurrent CVVH and vancomycin between 2006 and 2010 with a steady-state vancomycin trough concentration. The 87 included patients were grouped according to low (≤30 ml/kg/h; n = 10) or high (>30 ml/kg/h; n = 77) CVVH hemofiltration rate (HFR) for analysis. Vancomycin goal trough achievement occurred in only 32 (37%) patients. The primary endpoint of trough attainment significantly differed between HFR subgroups: 90% versus 30% in low- and high-HFR individuals, respectively (P < 0.001). Patients with subtherapeutic trough concentrations had a median (interquartile range) HFR of 40 ml/kg/h (range, 37 to 47 ml/kg/h) compared to 36 ml/kg/h (range, 30 to 39 ml/kg/h) in those who achieved the trough goal. Irrespective of goal trough, an inverse correlation existed between HFR and serum vancomycin concentration (r = -0.423; P < 0.001). In the subgroup of 14 methicillin-resistant Staphylococcus aureus (MRSA) patients, trough achievement was similar to the aggregate cohort (36%). Mortality at 28 days was unrelated to trough achievement in both the overall sample (P = 0.516) and in culture-positive MRSA patients (P = 0.396). Critically ill patients undergoing CVVH therapy may experience clinically significant reductions in goal vancomycin troughs. The results of the present study justify prospective evaluations in this population to determine the optimal vancomycin dosing strategy for attainment of goal trough concentrations.
在连续静脉-静脉血液滤过 (CVVH) 期间,实现目标血清谷浓度所需的万古霉素剂量仍需阐明。这是一项回顾性队列研究,纳入了 2006 年至 2010 年期间在三级医疗中心接受同时进行的 CVVH 和万古霉素治疗的重症成人患者,这些患者的稳态万古霉素谷浓度稳定。87 例患者根据低(≤30 ml/kg/h;n = 10)或高(>30 ml/kg/h;n = 77)CVVH 血液滤过率(HFR)进行分组分析。仅 32 例(37%)患者达到目标谷浓度。谷浓度达标率在 HFR 亚组之间存在显著差异:低 HFR 组和高 HFR 组分别为 90%和 30%(P < 0.001)。谷浓度低于治疗范围的患者的中位(四分位间距)HFR 为 40 ml/kg/h(范围 37 至 47 ml/kg/h),而达到谷浓度目标的患者的 HFR 为 36 ml/kg/h(范围 30 至 39 ml/kg/h)。无论目标谷浓度如何,HFR 与血清万古霉素浓度呈负相关(r = -0.423;P < 0.001)。在 14 例耐甲氧西林金黄色葡萄球菌(MRSA)患者亚组中,谷浓度达标率与总队列相似(36%)。在整个样本(P = 0.516)和培养阳性 MRSA 患者(P = 0.396)中,28 天死亡率与谷浓度达标无关。接受 CVVH 治疗的重症患者可能会经历目标万古霉素谷浓度的临床显著降低。本研究结果证明,在该人群中进行前瞻性评估以确定实现目标谷浓度的最佳万古霉素给药策略是合理的。