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经微透析评估猪松质骨和椎间盘内口服和静脉注射后氟氯西林的稳态浓度。

Steady-state concentrations of flucloxacillin in porcine vertebral cancellous bone and intervertebral disc following oral and intravenous administration assessed by microdialysis.

机构信息

Department of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.

Aarhus Microdialysis Research Group, Aarhus University Hospital, Aarhus, Denmark.

出版信息

Eur Spine J. 2022 Jun;31(6):1508-1514. doi: 10.1007/s00586-022-07208-9. Epub 2022 Apr 29.

Abstract

AIMS

Flucloxacillin is a frequently used antibiotic in the treatment of spondylodiscitis. We assessed steady-state concentrations and time above minimal inhibitory concentration (fT > MIC) of flucloxacillin in the intervertebral disc, vertebral cancellous bone, subcutaneous tissue and plasma, after intravenous and oral administration.

METHODS

Sixteen pigs were randomized into two groups; Group Peroral (Group PO) and Group Intravenous (Group IV) received 1 g flucloxacillin every 6 h for 24 h orally or intravenously. Microdialysis was used for sampling in the compartments of interest. A flucloxacillin target of 50% fT > MIC was applied for three MIC targets: 0.125, 0.5 and 2.0 μg/mL.

RESULTS

Intravenous administration resulted in significantly longer fT > MIC for all targets. Target attainment was only reached for the low target of 0.125 μg/mL in Group IV in vertebral cancellous bone, subcutaneous tissue, and plasma (intervertebral disc 47%). In Group IV, mean fT > MIC values in the investigated compartments were in the range of 47-67% of the dosing interval for 0.125 μg/mL, 20-35% for 0.5 μg/mL, and 0-15% for 2.0 μg/mL. In Group PO, mean fT > MIC values for 0.125 μg/mL were in the range of 1-33%. No pigs reached a concentration of 0.5 μg/mL in any of the investigated compartments in Group PO.

CONCLUSION

Administration of 1 g flucloxacillin every 6 h resulted in surprisingly low steady-state fT > MIC after intravenous and oral administration. However, intravenous administration resulted in significantly higher concentrations across compartments compared to oral administration. Sufficient target tissue concentrations for treatment of spondylodiscitis may require a dose increase or alternative dosing regimens.

摘要

目的

氟氯西林是治疗椎间盘炎的常用抗生素。我们评估了静脉和口服给药后氟氯西林在椎间盘、椎体松质骨、皮下组织和血浆中的稳态浓度和高于最小抑菌浓度的时间(fT> MIC)。

方法

将 16 头猪随机分为两组;口服组(Group PO)和静脉组(Group IV)分别给予 1g 氟氯西林,每 6 小时静脉或口服 1 次,共 24 小时。采用微透析法对感兴趣的部位进行采样。应用 50% fT> MIC 的氟氯西林目标浓度,针对三个 MIC 目标:0.125、0.5 和 2.0μg/mL。

结果

静脉给药使所有目标的 fT> MIC 时间明显延长。仅在静脉组的低目标(0.125μg/mL)下,达到了 0.125μg/mL 的低目标,在椎体松质骨、皮下组织和血浆中(椎间盘 47%)达到了目标。在静脉组中,在研究的各个部位,0.125μg/mL 时的平均 fT> MIC 值为给药间隔的 47-67%,0.5μg/mL 时为 20-35%,2.0μg/mL 时为 0-15%。在口服组中,0.125μg/mL 时的平均 fT> MIC 值为 1-33%。在口服组的任何研究部位,均未达到 0.5μg/mL 的浓度。

结论

每 6 小时给予 1g 氟氯西林,静脉和口服给药后,稳态 fT> MIC 均出乎意料地低。然而,与口服给药相比,静脉给药使各部位的浓度显著升高。为治疗椎间盘炎,可能需要增加剂量或采用替代给药方案,以达到足够的靶组织浓度。

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