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尿路感染中的碱化剂:理论上的禁忌证、相互作用和协同作用。

Alkalising agents in urinary tract infections: theoretical contraindications, interactions and synergy.

作者信息

Kavanagh Oisín N

机构信息

School of Pharmacy, Newcastle University, Newcastle upon Tyne, UK.

出版信息

Ther Adv Drug Saf. 2022 Mar 16;13:20420986221080794. doi: 10.1177/20420986221080794. eCollection 2022.

Abstract

INTRODUCTION

Alkalising agents have the potential to enhance the efficacy of many antimicrobial agents used in the treatment of Urinary Tract Infections; they also have the potential to cause significant patient harm if used incorrectly. This work seeks to illustrate and quantify these risks and synergies by modelling drug solubility and supersaturation against pharmacokinetic data for commonly used antibiotic agents.

METHODS

Solubility-pH relationships are employed to quantify the crystalluria risk for compounds which may be reasonably expected to be co-prescribed-or co-administered-with urinary alkalisers (amoxicillin, nitrofurantoin, trimethoprim, sulfamethoxazole and ciprofloxacin). These results are correlated against reports of crystalluria in the literature and in the EU Adverse Drug Reaction database.

RESULTS AND DISCUSSION

We find a correlation between the maximum theoretical supersaturation attainable and crystalluria reports for sulfamethoxazole, amoxicillin and ciprofloxacin. Shifts in urine pH which can be induced by alkalising agents may produce supersaturated states (and thus induce crystalluria) and may also affect antimicrobial efficacy. The importance of employing biorelevant media to improve predictive capacity of this analysis is also discussed.

CONCLUSION

Despite their widespread use, alkalising agents have significant effects on the pharmacokinetics of the most common drugs used to treat UTIs. With self-care set to increase, all OTC products should be critically re-evaluated to ensure patient safety, particularly within contexts where healthcare professionals are not involved in treatment selection. This analysis suggests a need for consistency across patient and healthcare professional documents to improve clarity. Alkalising agents (e.g., sodium and potassium citrate) can be purchased in many locations without the supervision of a healthcare professional.Although they are thought as innocuous agents, alkalisers can greatly influence the way some antibiotics behave in the body and this can potentially cause patient harm.This work illustrates these risks and synergies by modelling drug solubility and supersaturation against pharmacokinetic data for commonly used antibiotic agents.Manufacturers and patients should be aware that the use of alkalising agents with these drugs (and potentially many others) may cause unintended consequences.

摘要

引言

碱化剂有增强许多用于治疗尿路感染的抗菌药物疗效的潜力;但如果使用不当,它们也有可能对患者造成严重伤害。这项研究旨在通过针对常用抗生素药物的药代动力学数据对药物溶解度和过饱和度进行建模,来说明并量化这些风险与协同作用。

方法

利用溶解度与pH值的关系,对合理预期会与尿液碱化剂(阿莫西林、呋喃妥因、甲氧苄啶、磺胺甲恶唑和环丙沙星)联合处方或联合给药的化合物的结晶尿风险进行量化。将这些结果与文献及欧盟药物不良反应数据库中有关结晶尿的报告进行关联分析。

结果与讨论

我们发现磺胺甲恶唑、阿莫西林和环丙沙星可达到的最大理论过饱和度与结晶尿报告之间存在相关性。碱化剂引起的尿液pH值变化可能产生过饱和状态(从而诱发结晶尿),也可能影响抗菌效果。还讨论了使用生物相关介质提高该分析预测能力的重要性。

结论

尽管碱化剂被广泛使用,但它们对用于治疗尿路感染的最常用药物的药代动力学有显著影响。随着自我护理的增加,所有非处方产品都应进行严格重新评估,以确保患者安全,尤其是在医疗保健专业人员不参与治疗选择的情况下。该分析表明,患者和医疗保健专业人员的文件需要保持一致,以提高清晰度。碱化剂(如柠檬酸钠和柠檬酸钾)在许多地方无需医疗保健专业人员监督即可购买。尽管它们被认为是无害的药物,但碱化剂会极大地影响某些抗生素在体内的行为方式,这可能会对患者造成潜在伤害。这项研究通过针对常用抗生素药物的药代动力学数据对药物溶解度和过饱和度进行建模,来说明这些风险与协同作用。制造商和患者应意识到,将碱化剂与这些药物(可能还有许多其他药物)一起使用可能会产生意想不到的后果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf4a/8935415/0e2d69c36932/10.1177_20420986221080794-fig1.jpg

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