Bendtsen Mathias A F, Bue Mats, Hanberg Pelle, Slater Josefine, Thomassen Maja B, Hansen Jakob, Søballe Kjeld, Öbrink-Hansen Kristina, Stilling Maiken
Department of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.
Aarhus Microdialysis Research Group, Aarhus University Hospital, Aarhus, Denmark.
Bone Joint Res. 2021 Jan;10(1):60-67. doi: 10.1302/2046-3758.101.BJR-2020-0250.R1.
Flucloxacillin is commonly administered intravenously for perioperative antimicrobial prophylaxis, while oral administration is typical for prophylaxis following smaller traumatic wounds. We assessed the time, for which the free flucloxacillin concentration was maintained above the minimum inhibitory concentration (T > MIC) for methicillin-susceptible in soft and bone tissue, after intravenous and oral administration, using microdialysis in a porcine model.
A total of 16 pigs were randomly allocated to either intravenous (Group IV) or oral (Group PO) flucloxacillin 1 g every six hours during a 24-hour period. Microdialysis was used for sampling in cancellous and cortical bone, subcutaneous tissue, and the knee joint. In addition, plasma was sampled. The flucloxacillin T > MIC was evaluated using a low MIC target (0.5 μg/ml) and a high MIC target (2.0 μg/ml).
Intravenous administration resulted in longer T > MIC (0.5 μg/ml) compared to oral administration, except for cortical bone. In Group IV, all pigs reached a concentration of 0.5 μg/ml in all compartments. The mean T > MIC (0.5 μg/ml) was 149 minutes (95% confidence interval (CI) 119 to 179; range 68 to 323) in subcutaneous tissue and 61 minutes (95% CI 29 to 94; range 0 to 121) to 106 minutes (95% CI 76 to 136; range 71 to 154) in bone tissue. In Group PO, 0/8 pigs reached a concentration of 0.5 μg/ml in all compartments. For the high MIC target (2.0 μg/ml), T > MIC was close to zero minutes in both groups across compartments.
Although intravenous administration of flucloxacillin 1 g provided higher fT > MIC for the low MIC target compared to oral administration, concentrations were surprisingly low, particularly for bone tissue. Achievement of sufficient bone and soft tissue flucloxacillin concentrations may require a dose increase or continuous administration. Cite this article: 2021;10(1):60-67.
氟氯西林通常通过静脉注射用于围手术期抗菌预防,而对于较小创伤伤口后的预防则通常采用口服给药。我们在猪模型中使用微透析技术,评估静脉注射和口服给药后,氟氯西林在软组织和骨组织中游离浓度维持在对甲氧西林敏感菌的最低抑菌浓度以上的时间(T>MIC)。
在24小时内,将16头猪随机分为两组,分别静脉注射(IV组)或口服(PO组)氟氯西林,每6小时1g。采用微透析技术在松质骨、皮质骨、皮下组织和膝关节进行采样。此外,还采集了血浆样本。使用低MIC靶点(0.5μg/ml)和高MIC靶点(2.0μg/ml)评估氟氯西林的T>MIC。
与口服给药相比,静脉注射导致T>MIC(0.5μg/ml)更长,但皮质骨除外。在IV组中,所有猪的所有组织中均达到了0.5μg/ml的浓度。皮下组织中T>MIC(0.5μg/ml)的平均时间为149分钟(95%置信区间(CI)119至179;范围68至323),骨组织中为61分钟(95%CI 29至94;范围0至121)至106分钟(95%CI 76至136;范围71至154)。在PO组中,8头猪中无一头在所有组织中达到0.5μg/ml的浓度。对于高MIC靶点(2.0μg/ml),两组所有组织中的T>MIC均接近零分钟。
尽管与口服给药相比,静脉注射1g氟氯西林在低MIC靶点下提供了更高的fT>MIC,但浓度出奇地低,尤其是在骨组织中。要达到足够的骨组织和软组织氟氯西林浓度,可能需要增加剂量或持续给药。引用本文:2021;10(1):60-67。