Faculty of Medical Sciences, University of Kragujevac, Svetozara Markovića 69, Kragujevac, 34000, Serbia.
Department of Pharmacology and Toxicology, Faculty of Medical Sciences, University of Kragujevac, Svetozara Markovića 69, Kragujevac, 34000, Serbia.
Intern Emerg Med. 2019 Apr;14(3):411-422. doi: 10.1007/s11739-018-1994-8. Epub 2018 Nov 27.
The objective of this study is to evaluate potential drug-drug interactions (pDDIs) and risk factors for pDDIs in three phases of an acute coronary syndrome (ACS) treatment: from the point of first medical contact to the coronary angiography (first phase), after coronary angiography to the last day of hospitalization (second phase), and at discharge from hospital (third phase). This retrospective observational cohort clinical study was conducted at the Clinic for Cardiology of the Clinical Centre Kragujevac, a public tertiary care hospital in Kragujevac, Serbia. Micromedex interaction checker was used to detect pDDIs. This study included 245 ACS patients. All patients were exposed to at least one pDDI in all the phases of treatment. Mean total number of pDDIs was 9.47 ± 6.07, 10.11 ± 6.92, and 6.29 ± 3.66 in first, second, and third phases, respectively. Age, > 6 h from the beginning of the symptoms to admission, primary PCI, STE-ACS, COPD, delirium, hyperlipidemia, hypertension, obesity, systolic blood pressure at admission, TIMI risk score at admission, ALT, LDL, number of physicians who prescribed drugs to a single patient, number of prescribed drugs, and various pharmacological classes increased risk of pDDIs. Mechanical ventilation, dementia, and drug allergy noted in the medical documentation protected against them. Effects of heart failure, diabetes, and aPTT depended on phase of treatment and severity of pDDI. In conclusion, physicians should be vigilant to the possibility of pDDIs in patients harbouring factors that may increase their rate.
本研究旨在评估急性冠状动脉综合征(ACS)治疗三个阶段中潜在的药物-药物相互作用(pDDI)和 pDDI 的风险因素:从首次医疗接触到冠状动脉造影(第一阶段)、冠状动脉造影后至住院最后一天(第二阶段)和出院时(第三阶段)。这是一项在塞尔维亚克拉古耶瓦茨临床中心心脏病学诊所进行的回顾性观察队列临床研究。使用 Micromedex 相互作用检查器来检测 pDDI。这项研究纳入了 245 名 ACS 患者。所有患者在治疗的所有阶段均至少发生了一种 pDDI。第一、二、三阶段的平均 pDDI 总数分别为 9.47±6.07、10.11±6.92 和 6.29±3.66。年龄、症状开始至入院的时间>6 小时、直接经皮冠状动脉介入治疗、ST 段抬高型心肌梗死、慢性阻塞性肺病、谵妄、高脂血症、高血压、肥胖、入院时收缩压、入院时 TIMI 风险评分、丙氨酸氨基转移酶、低密度脂蛋白、为单一患者开处方的医生人数、处方药物数量和各种药理类别均增加了 pDDI 的风险。在医疗记录中注意到的机械通气、痴呆和药物过敏可预防 pDDI。心力衰竭、糖尿病和 aPTT 的影响取决于治疗阶段和 pDDI 的严重程度。总之,医生应警惕可能发生 pDDI 的患者存在增加 pDDI 发生率的因素。