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The prevalence and preventability of potentially relevant drug‐drug interactions in patients admitted for cardiovascular diseases: A cross‐sectional study

机译:潜在相关药物 - 药物相互作用的患病率和预防性患者患者患者患者:横截面研究

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Summary Aim The aim was to describe the type and prevalence of potentially relevant drug‐drug interactions ( pDDI s) in a population of patients admitted for cardiovascular diseases ( CVD ), and management strategies for reducing the occurrence of pDDI s. Methods A retrospective cross‐sectional study was performed on Cardiology ward of University Clinical Hospital Center in Belgrade, Serbia. A total of 527 patients, with more than one prescription during hospital stay, were enrolled in this study. Data were obtained from medical records. LexiInteract was used as the screening tool. Results At least one potentially relevant pDDI was identified in 83.9% of patients. Occurrence was significantly more prevalent in patients with higher number of drugs, multimorbidity, longer length of stay, arrhythmia, heart failure, infectious and respiratory disease. About 13% of pDDI s exposures were accompanied with concurrent renal or liver disease, as an additional risk for DDI manifestation. Among CVD , patients with a history of myocardial infarction possessed the highest additional risk. The most common potential clinical outcome was the effect on cardiovascular system 48.5%, renal function and/or potassium 22.3%, bleeding 9.5%, impaired glucose control 6.8% and digoxin toxicity 4.6%. Main management strategies to avoid X or D class included using paracetamol instead of NSAID or alternative NSAID (38%), alternative antibiotic or antifungal (20.4%), H 2 receptor antagonist instead of PPI (8.3%), avoiding therapeutic duplication (7.3%), and alternative HMG ‐CoA reductase inhibitor (7%). Heart rate, blood pressure, electrolytes/potassium and blood glucose could have been employed in monitoring for potential consequence of 72.2% C class pDDI s. Conclusions Use of drug interaction screening tools can be beneficial risk mitigation strategy for potentially relevant pDDI s in CVD patients. DDI screening software could be linked to the patient's laboratory results or clinical data regarding renal or liver function, as an approach to reinforce DDI s alert quality.
机译:总结旨在描述潜在的相关药物 - 药物相互作用(PDDIS)在患有心血管疾病(CVD)的患者群体中的类型和患病率,以及用于减少PDDIS的发生的管理策略。方法对塞尔维亚贝尔格莱德大学临床医院中心的心脏病病房进行了回顾性横截面研究。共有527名患者,在住院住宿期间有多个处方,读入这项研究。数据从医疗记录获得。 LexiinterAct被用作筛选工具。结果在83.9%的患者中鉴定了至少一种可能相关的PDDI。药物数量较多,无能为力,保持长度,心律失常,心力衰竭,传染病和呼吸道疾病的患者患者发生显着普遍。大约13%的PDDI S曝光伴有并发肾病或肝病,作为DDI表现的额外风险。在CVD中,心肌梗死病史的患者具有最高的额外风险。最常见的潜在临床结果是对心血管系统的影响48.5%,肾功能和/或钾22.3%,出血9.5%,葡萄糖对照损伤6.8%,高氧毒性4.6%。避免使用扑热息痛而不是NSAIM或替代NSAID(38%),替代抗生素或抗真菌(20.4%),H 2受体拮抗剂代替PPI(8.3%),避免X或D类的主要管理策略,避免PPI(8.3%),避免治疗重复(7.3% )和替代HMG -COA还原酶抑制剂(7%)。心率,血压,电解质/钾和血糖可用于监测72.2%C类PDDIS的潜在后果。结论使用药物相互作用筛查工具可以是CVD患者中潜在相关PDDIS的有益风险缓解策略。 DDI筛选软件可以与患者的实验室结果或有关肾病或肝功能的临床数据相关联,作为加强DDI S警报质量的方法。

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