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碳青霉烯类药物耐药肠杆菌科细菌感染治疗药物监测下连续输注头孢地尔的可行性。

Feasibility of Continuous Infusion of Cefiderocol in Conjunction with the Establishment of Therapeutic Drug Monitoring in Patients with Extensively Drug-Resistant Gram-Negative Bacteria.

机构信息

Department of Anaesthesiology, University of Göttingen Medical Center, Robert-Koch-Str. 40, 37099, Göttingen, Germany.

Institute for Clinical Chemistry/Interdisciplinary UMG Laboratories, University of Göttingen Medical Center, Robert-Koch-Str.40, 37099, Göttingen, Germany.

出版信息

Clin Drug Investig. 2023 Apr;43(4):307-314. doi: 10.1007/s40261-023-01257-8. Epub 2023 Apr 5.

DOI:10.1007/s40261-023-01257-8
PMID:37017874
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10075148/
Abstract

BACKGROUND AND OBJECTIVE

Resistance to antibacterial substances is a huge and still emerging issue, especially with regard to Gram-negative bacteria and in critically ill patients. We report a study in six patients infected with extensively drug-resistant Gram-negative bacteria in a limited outbreak who were successfully managed with a quasi-continuous infusion of cefiderocol.

METHODS

Patients were initially treated with prolonged infusions of cefiderocol over 3 h every 8 h, and the application mode was then switched to a quasi-continuous infusion of 2 g over 8 h, i.e. 6 g in 24 h. Therapeutic drug monitoring (TDM) was established using an in-house liquid chromatography-tandem mass spectrometry (LC-MS/MS) method.

RESULTS

Determined trough plasma concentrations were a median of 50.00 mg/L [95% confidence interval (CI) 27.20, 74.60] and steady-state plasma concentrations were a median of 90.96 mg/L [95% CI 37.80, 124]. No significant differences were detected with respect to acute kidney injury/continuous renal replacement therapy. Plasma concentrations determined from different modes of storage were almost equal when frozen or cooled, but markedly reduced when stored at room temperature.

CONCLUSIONS

(Quasi) continuous application of cefiderocol 6 g/24 h in conjunction with TDM is a feasible mode of application; the sample for TDM should either be immediately analyzed, cooled, or frozen prior to analysis.

摘要

背景与目的

对抗菌物质的耐药性是一个巨大且仍在不断出现的问题,尤其是在革兰氏阴性菌和重症患者中。我们报告了一项在 6 例局限爆发的广泛耐药革兰氏阴性菌感染患者中进行的研究,这些患者成功地接受了头孢他啶-阿维巴坦准连续输注治疗。

方法

患者最初接受 3 h 延长输注头孢他啶-阿维巴坦,每 8 h 1 次,然后将应用模式转换为 2 g 准连续输注,即 24 h 内输注 6 g。采用内部液相色谱-串联质谱(LC-MS/MS)法建立治疗药物监测(TDM)。

结果

测定的谷浓度中位数为 50.00 mg/L [95%置信区间(CI)27.20,74.60],稳态浓度中位数为 90.96 mg/L [95%CI 37.80,124]。急性肾损伤/连续肾脏替代治疗无显著差异。冷冻或冷藏时,不同储存方式下测定的浓度几乎相等,但室温储存时显著降低。

结论

(准)连续应用头孢他啶-阿维巴坦 6 g/24 h 并结合 TDM 是一种可行的应用方式;TDM 的样本应在分析前立即分析、冷却或冷冻。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ea/10075148/7af960c88cc9/40261_2023_1257_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ea/10075148/ebae727ebd71/40261_2023_1257_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ea/10075148/7af960c88cc9/40261_2023_1257_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ea/10075148/ebae727ebd71/40261_2023_1257_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20ea/10075148/7af960c88cc9/40261_2023_1257_Fig2_HTML.jpg

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