Eljaaly Khalid, Helal Asalah, Almandeel Tamather, Algarni Rawan, Alshehri Samah
Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.
Saudi J Biol Sci. 2021 Dec;28(12):6929-6932. doi: 10.1016/j.sjbs.2021.07.065. Epub 2021 Jul 30.
Oral fluoroquinolones and tetracyclines are known to interact with divalent or trivalent cation-containing compounds (DTCCs) via chelation. The objective of this study is to describe the prevalence of these drug-drug interactions (DDIs) in an inpatient setting.
A cross-sectional study of prospectively collected data were conducted at an academic tertiary care hospital. We included hospitalized adults who were receiving oral fluoroquinolones or tetracyclines with DTCCs in 2019. Our hospital uses electronic health records for medication ordering and handwritten medication administration records (MARs). The primary study outcome was the percentage of simultaneous administration of fluoroquinolones or tetracyclines with DTCCs, and the secondary outcome was the percentage of inappropriate separation time.
Among patients who received oral fluoroquinolones or tetracyclines, 47 patients (26.6%) were co-administered DTCCs and included in this study. Ciprofloxacin (n = 29; 61.7%) was the most commonly interacting antibiotic, followed by moxifloxacin (n = 12; 25.5%) and doxycycline (n = 6; 12.8%). The interacting DTCCs included iron-containing products and calcium-containing products, and half of the patients (n = 24; 51%) received DTCCs once daily. Most patients (n = 35; 74.5%) were found to receive oral fluoroquinolones or tetracyclines at the same time as DTCCs, while one (2.1%) received inappropriately separated DTCCs.
Despite being a very known contraindicated DDI, the prevalence of simultaneous co-administration of oral fluoroquinolones or tetracyclines with polyvalent cations was extremely high in a hospital with handwritten MARs. Antimicrobial stewardship programs should target this DDI, and future studies should evaluate the impact of different practical solutions to this problem in different clinical settings.
已知口服氟喹诺酮类药物和四环素类药物会通过螯合作用与含二价或三价阳离子的化合物(DTCCs)发生相互作用。本研究的目的是描述这些药物相互作用(DDIs)在住院患者中的发生率。
在一家学术性三级护理医院对前瞻性收集的数据进行横断面研究。我们纳入了2019年接受口服氟喹诺酮类药物或四环素类药物并同时使用DTCCs的住院成年人。我们医院使用电子健康记录进行药物订购,并使用手写药物管理记录(MARs)。主要研究结果是氟喹诺酮类药物或四环素类药物与DTCCs同时给药的百分比,次要结果是分离时间不当的百分比。
在接受口服氟喹诺酮类药物或四环素类药物的患者中,有47名患者(26.6%)同时使用了DTCCs并纳入本研究。环丙沙星(n = 29;61.7%)是最常发生相互作用的抗生素,其次是莫西沙星(n = 12;25.5%)和多西环素(n = 6;12.8%)。相互作用的DTCCs包括含铁产品和含钙产品,一半的患者(n = 24;51%)每天接受一次DTCCs。大多数患者(n = 35;74.5%)被发现同时接受口服氟喹诺酮类药物或四环素类药物和DTCCs,而有一名患者(2.1%)接受了分离时间不当的DTCCs。
尽管这是一种广为人知的禁忌药物相互作用,但在一家使用手写MARs的医院中,口服氟喹诺酮类药物或四环素类药物与多价阳离子同时给药的发生率极高。抗菌药物管理计划应针对这种药物相互作用,未来的研究应评估不同临床环境中针对该问题的不同实际解决方案的影响。