Özokcu Kübra, Diesveld Maaike M E, Gipmans Suzan G H, Peeters Laura E J, van den Born Bert-Jan, Borgsteede Sander D
Department of Hospital Pharmacy, Meander Medisch Centrum, Amersfoort, Netherlands.
Department of Hospital Pharmacy, Ziekenhuis Rivierenland, Tiel, Netherlands.
Front Pharmacol. 2024 Apr 17;15:1360146. doi: 10.3389/fphar.2024.1360146. eCollection 2024.
Hypertension, a significant risk factor for cardiovascular diseases, demands proactive management as cardiovascular diseases remain the leading cause of death worldwide. Reducing systolic and diastolic blood pressure levels below recommended reference values of <140/90 mmHg can lead to a significant reduction of the risk of CVD and all-cause mortality. However, treatment of hypertension can be difficult and the presence of comorbidities could further complicate this treatment. Drugs used to manage these comorbidities may inadvertently have an impact on blood pressure, resulting in a phenomenon known as drug-disease interaction. This study aims to assess the safety of medication that can affect blood pressure in patients with hypertension and provide practical recommendations for healthcare professionals.
For the development of recommendations for the drug-disease interaction (DDSI) hypertension, a six-step plan that combined literature selection and multidisciplinary expert opinion was used. The process involved (1) defining the scope of the DDSI and selecting relevant drugs, (2) collecting evidence, (3) data-extraction, (4) reaching of expert consensus, (5) publication and implementation of the recommendations in healthcare systems and (6) updating the information.
An increase of 10 mmHg in systolic blood pressure and 5 mmHg in diastolic blood pressure was defined as clinically relevant. Corticosteroids, danazol, and yohimbine caused a clinically relevant DDSI with hypertension. Several other drugs with warnings for hypertension in the official product information were assessed to have no clinically relevant DDSI due to minor influence or lack of data on blood pressure. Drugs with evidence for a relevant change in blood pressure which are prescribed under close monitoring of blood pressure according to clinical guidelines, were deemed to be not clinically relevant for signalling.
This study provides specific recommendations that can be implemented directly in clinical practice, for example, in clinical decision support systems, potentially resulting in safer drug use in patients with hypertension and better healthcare by reducing alert fatigue. Future research should focus on evaluating the effectiveness of implementation strategies and their impact on reducing unsafe use of medication in patients with hypertension.
高血压是心血管疾病的重要危险因素,鉴于心血管疾病仍是全球主要死因,因此需要积极管理。将收缩压和舒张压水平降至低于推荐参考值<140/90 mmHg可显著降低心血管疾病风险和全因死亡率。然而,高血压治疗可能困难,合并症的存在会使这种治疗更加复杂。用于治疗这些合并症的药物可能会无意中影响血压,导致药物-疾病相互作用现象。本研究旨在评估可影响高血压患者血压的药物安全性,并为医疗保健专业人员提供实用建议。
为制定药物-疾病相互作用(DDSI)高血压的建议,采用了结合文献筛选和多学科专家意见的六步计划。该过程包括:(1)界定DDSI范围并选择相关药物;(2)收集证据;(3)数据提取;(4)达成专家共识;(5)在医疗系统中发布并实施建议;(6)更新信息。
收缩压升高10 mmHg和舒张压升高5 mmHg被定义为具有临床相关性。皮质类固醇、达那唑和育亨宾与高血压存在临床相关的DDSI。官方产品信息中对高血压有警示的其他几种药物,因对血压影响较小或缺乏血压数据,被评估为无临床相关的DDSI。根据临床指南在密切监测血压情况下开具的、有证据表明血压有相关变化的药物,被认为对信号传递无临床相关性。
本研究提供了可直接在临床实践中实施的具体建议,例如在临床决策支持系统中,通过减少警报疲劳,可能使高血压患者用药更安全,医疗保健更好。未来研究应侧重于评估实施策略的有效性及其对减少高血压患者不安全用药的影响。