Connors J E, DiPiro J T, Hayter R G, Hooker K D, Stanfield J A, Young T R
University of Georgia College of Pharmacy, Augusta.
Antimicrob Agents Chemother. 1990 Jun;34(6):1128-31. doi: 10.1128/AAC.34.6.1128.
A continuous intravenous infusion was used to assess the tissue penetration of cefazolin (14 subjects) and cefuroxime (15 subjects) in orthopedic surgery patients. Subjects were randomly assigned to receive a continuous intravenous infusion of cefazolin (mean, 178.6 mg/h) or cefuroxime (mean, 330.0 mg/h) at a rate estimated to achieve a target steady-state total concentration of 50 micrograms/ml in serum. The infusion was initiated 12 to 14 h before surgery, and blood and muscle tissue samples were collected intraoperatively at the times of incision and wound closure. Although there was a significant difference between the free concentrations of cefazolin (at incision, 9.3 micrograms/ml; at closure, 9.2 micrograms/ml) and cefuroxime in serum (at incision, 26.9 micrograms/ml; at closure, 31.8 micrograms/ml), there was no difference in the total concentrations in muscle at either surgical incision (cefazolin, 6.1 micrograms/g; cefuroxime, 5.6 micrograms/g) or wound closure (cefazolin, 7.7 micrograms/g; cefuroxime, 7.4 micrograms/g). There was a significant correlation between the pooled free serum and total muscle concentrations for cefazolin (P = 0.001); however, there was no correlation between these variables with the pooled cefuroxime data (P = 0.403). These findings indicate that the free drug concentration in serum alone is not consistently predictive of the total concentration of cephalosporin in muscle.
采用持续静脉输注法评估头孢唑林(14例受试者)和头孢呋辛(15例受试者)在骨科手术患者中的组织穿透性。受试者被随机分配,以估计能使血清中目标稳态总浓度达到50微克/毫升的速率,持续静脉输注头孢唑林(平均178.6毫克/小时)或头孢呋辛(平均330.0毫克/小时)。在手术前12至14小时开始输注,术中在切开和伤口闭合时采集血液和肌肉组织样本。尽管血清中头孢唑林的游离浓度(切开时为9.3微克/毫升;闭合时为9.2微克/毫升)与头孢呋辛(切开时为26.9微克/毫升;闭合时为31.8微克/毫升)之间存在显著差异,但在手术切开(头孢唑林为6.1微克/克;头孢呋辛为5.6微克/克)或伤口闭合(头孢唑林为7.7微克/克;头孢呋辛为7.4微克/克)时,肌肉中的总浓度并无差异。头孢唑林的合并游离血清浓度与总肌肉浓度之间存在显著相关性(P = 0.001);然而,这些变量与头孢呋辛的合并数据之间无相关性(P = 0.403)。这些发现表明,仅血清中的游离药物浓度并不能始终如一地预测肌肉中头孢菌素的总浓度。