首页> 外文期刊>Drugs in R&D >Post Hoc Analysis of the CONFIDENCE II, PROTECT I, SHAKE THE HABIT I and SHAKE THE HABIT II Observational Studies in Mild to Moderate Hypertensive Patients Treated with Perindopril and Atorvastatin Concomitantly
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Post Hoc Analysis of the CONFIDENCE II, PROTECT I, SHAKE THE HABIT I and SHAKE THE HABIT II Observational Studies in Mild to Moderate Hypertensive Patients Treated with Perindopril and Atorvastatin Concomitantly

机译:事后分析信心II,保护I,动摇习惯I和动摇习惯II对接受培哚普利和阿托伐他汀治疗的轻度至中度高血压患者的观察性研究

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h3 class="Heading"Background and Objectives/h3p id="Par1" class="Para"Management of hypertension and dyslipidemia is important when considering cardiovascular disease risk; however, achievement of optimal lipid and blood pressure (BP) targets in clinical practice remains inadequate. This analysis sought to estimate the frequency, effectiveness, and safety of co-administrated atorvastatin and perindopril in routine care. h3 class="Heading"Methods/h3p id="Par2" class="Para"We conducted a post hoc analysis of four Canadian, prospective, multi-center, observational studies assessing real-life effectiveness and safety of perindopril?+?atorvastatin in mild-to-moderate hypertensive patients with concomitant dyslipidemia over 16?weeks. The safety population comprised patients receiving one or more doses of free combination perindopril?+?atorvastatin; the full analysis set (FAS) received perindopril?+?atorvastatin at baseline, with one or more post-baseline systolic BP measurements while on treatment. h3 class="Heading"Results/h3p id="Par3" class="Para"A total of 3541 and 3172 patients were included in the safety population and FAS, respectively. At the last observation carried forward, significant reductions in mean systolic BP (? 18.0?mmHg; p ?0.001) and diastolic BP (? 8.9?mmHg; p ?0.001) were observed; target BP was achieved by 73.1% of patients. Emergent adverse events (AEs) were reported in 8.0% of patients, the most common being cough (4.5% of patients), headache (0.9%), and dizziness (0.8%). Four serious AEs were reported among three (0.1%) patients. No differences were observed in effectiveness or safety between studies. h3 class="Heading"Conclusions/h3p id="Par4" class="Para"Concomitant perindopril?+?atorvastatin therapy demonstrated similar efficacy across all studies, with significant reductions in BP and achievement of target BP levels observed in a real-world setting. Results align with known safety profiles of atorvastatin and perindopril, with no unexpected AEs observed when compared with data from treatment with the individual drugs.
机译:class =“ Heading”>背景和目标 id =“ Par1” class =“ Para”>在考虑心血管疾病风险时,高血压和血脂异常的管理很重要。然而,在临床实践中实现最佳脂质和血压(BP)指标仍然不够。该分析旨在评估常规治疗中共同使用阿托伐他汀和培哚普利的频率,有效性和安全性。 class =“ Heading”>方法 id =“ Par2” class =“ Para”>我们对四项加拿大,前瞻性,多中心,观察性研究进行了事后分析,评估了现实生活中的有效性和培哚普利+阿托伐他汀在轻度至中度伴有血脂异常的高血压患者中的安全性超过16周。安全人群包括接受一剂或多剂自由组合培哚普利+阿托伐他汀的患者。完整分析集(FAS)在基线时接受培哚普利+阿托伐他汀治疗,并在治疗期间进行了一次或多次基线后收缩压测量。 class =“ Heading”>结果 id =“ Par3” class =“ Para”>安全人群和FAS分别包括3541和3172名患者。在进行的最后一项观察中,观察到平均收缩压(?18.0?mmHg; p <?0.001)和舒张压(?8.9?mmHg; p <?0.001)显着降低。目标血压达到了73.1%的患者。 8.0%的患者报告了紧急不良事件(AE),最常见的是咳嗽(4.5%的患者),头痛(0.9%)和头晕(0.8%)。在三名(0.1%)患者中报告了四次严重的不良事件。研究之间没有观察到有效性或安全性差异。 class =“ Heading”>结论 id =“ Par4” class =“ Para”>伴随的培哚普利+阿托伐他汀疗法在所有研究中均显示出相似的疗效,并且血压显着降低且达到了目标BP在实际环境中观察到的水平。结果与阿托伐他汀和培哚普利的已知安全性吻合,与单独药物治疗的数据相比,未观察到意外的不良事件。

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