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持续静脉输注期间头孢他啶的稳定性及吡啶毒性

Ceftazidime stability and pyridine toxicity during continuous i.v. infusion.

作者信息

Jones Terry E, Selby P R, Mellor Coby S, Cheam Dat Boon

机构信息

Pharmacy Department, The Queen Elizabeth Hospital, Woodville, South Australia.

Hospital Pharmacy Services, Ashford, South Australia.

出版信息

Am J Health Syst Pharm. 2019 Feb 1;76(4):200-205. doi: 10.1093/ajhp/zxy035.

Abstract

PURPOSE

This article reviews the literature concerning ceftazidime stability and potential for toxicity from pyridine (a degradation product) in the light of decades of apparent safe use of this antibiotic when given by continuous i.v. infusion but recent changes in regulatory body/manufacturer advise a need to change infusion devices more frequently.

SUMMARY

In the outpatient setting, ceftazidime is ideally administered by continuous i.v. infusion because of its short half-life and lack of post-antibiotic effect. While continuous i.v. infusion provides the optimal pharmacokinetic/pharmacodynamic profile, the frequency with which infusion devices need to be changed is critical to the practicality in the outpatient setting, especially where trained staff are required to visit the patient in their home to change the device. The rate of ceftazidime degradation (and pyridine formation) is temperature, concentration, and solvent dependent. By using the lowest effective dose (guided by pathogen minimum inhibitory concentration [MIC] so as to achieve a blood concentration ≥ 4 × MIC over the whole dosage interval), keeping ceftazidime concentration ≤ 3%, using 0.9% sodium chloride injection as diluent and maintaining temperature between 15-25°C when connected to the patient, the amount of pyridine formed over a 24-hour period can be minimized and toxicity prevented. When pathogen MIC dictates that > 6 g ceftazidime/day is required, alternative antibiotics should be considered and/or greater attention paid to temperature and concentration of the infusion solution.

CONCLUSION

Ceftazidime can be used safely and effectively via continuous i.v. infusion in the outpatient setting with once-daily changes of infusion device provided the concentration and temperature of the infusion solution is controlled. In this way, more frequent changes of infusion device (that increase the risk of blood-borne infection and reduce the practicality of continuous i.v. infusion in the home) can be avoided.

摘要

目的

本文回顾了有关头孢他啶稳定性以及吡啶(一种降解产物)潜在毒性的文献,鉴于这种抗生素通过持续静脉输注给药数十年以来表面上安全使用,但近期监管机构/制造商的建议发生了变化,需要更频繁地更换输液装置。

总结

在门诊环境中,由于头孢他啶半衰期短且缺乏抗生素后效应,理想的给药方式是持续静脉输注。虽然持续静脉输注可提供最佳的药代动力学/药效学特征,但更换输液装置的频率对于门诊环境中的实用性至关重要,尤其是在需要训练有素的工作人员到患者家中更换装置的情况下。头孢他啶的降解速率(以及吡啶的形成)取决于温度、浓度和溶剂。通过使用最低有效剂量(以病原体最低抑菌浓度[MIC]为指导,以便在整个给药间隔内实现血药浓度≥4×MIC),使头孢他啶浓度≤3%,使用0.9%氯化钠注射液作为稀释剂,并在与患者连接时将温度保持在15-25°C,可以将24小时内形成的吡啶量降至最低并预防毒性。当病原体MIC表明每天需要>6g头孢他啶时,应考虑使用替代抗生素和/或更加关注输液溶液的温度和浓度。

结论

在门诊环境中,通过持续静脉输注安全有效地使用头孢他啶,只要控制输液溶液的浓度和温度,每天更换一次输液装置即可。通过这种方式,可以避免更频繁地更换输液装置(这会增加血行感染的风险并降低家庭持续静脉输注的实用性)。

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