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Use of the Cardiovascular Polypill in Secondary Prevention of Cerebrovascular Disease: A Real-Life Tertiary Hospital Cohort Study of 104 Patients
Cerebrovascular Diseases Extra Pub Date : 2020-11-11 , DOI: 10.1159/000511064
Victoria Ros-Castelló , Elena Natera-Villalba , Ana Gómez-López , Arantxa Sánchez-Sánchez , Juan Luis Chico-García , Sebastian García-Madrona , Rocio Vera-Lechuga , Consuelo Matute-Lozano , Alicia de Felipe Mimbrera , Antonio Cruz-Culebras , Araceli Alonso-Canovas , Jaime Masjuan

Background: The use of the cardiovascular polypill, a fixed-dose combination treatment, is conceived to improve adherence. However, randomized controlled trials (RCTs) may overestimate it. Studies focusing on cerebrovascular disease and real-life efficacy compared with conventional treatment are lacking. Methods: This is a retrospective, hospital-based cohort study of acute ischaemic stroke patients who were prescribed a polypill (aspirin 100 mg, atorvastatin 20/40 mg, ramipril 2.5/5/10 mg) versus conventional treatment (aspirin 100 mg and other blood pressure/lipid-lowering agents) in secondary prevention (2017–2018). Clinical records were reviewed 90 days after discharge for stroke recurrence, vascular risk factor control, and safety. Adherence was assessed using the adapted Morisky-Green scale. Results: A total of 104 patients were included (61% male; mean age 69.7 ± 13.9 years); 54 were treated with the polypill and 50 with conventional treatment. No baseline differences in clinical or demographic variables were detected. No recurrences were registered in the polypill group, compared to 1 recurrence in the conventional treatment group. A significant reduction of systolic blood pressure (SBP) was achieved in the polypill group (12.1 mm Hg) compared to the conventional treatment group (6.8 mm Hg) (p = 0.002). No significant differences were detected regarding the goal of LDL cholesterol ≤70 mg/dL (41 vs. 44%). The adverse events were mild and their frequency was similar in the two groups (9 vs. 2%, ns). Adherence was similarly good in the two groups (93 vs. 88%, ns). Polypill group adherence was similar to that reported in a previous meta-analysis of RCTs (93 vs. 84%, ns). Conclusion: In our experience, the cardiovascular polypill achieved a higher reduction in SBP levels and was well tolerated. Adherence was similar to that found in the previous literature, which is remarkable given the real-life setting of our study.
Cerebrovasc Dis Extra 2020;10:166–173


中文翻译:

心血管息肉在二级预防脑血管疾病中的应用:现实生活中的三级医院队列研究,共104例患者

背景:心血管多药是一种固定剂量的联合治疗,旨在改善依从性。但是,随机对照试验(RCT)可能会高估它。与常规治疗相比,缺乏针对脑血管疾病和实际疗效的研究。方法:这是一项针对急性缺血性中风患者的回顾性,基于医院的队列研究,这些患者接受了多药治疗(阿司匹林100 mg,阿托伐他汀20/40 mg,雷米普利2.5 / 5/10 mg)与常规治疗(阿司匹林100 mg和其他血压) /降脂药)在二级预防中(2017-2018)。出院后90天回顾临床记录,以中风复发,控制血管危险因素和安全性。使用改良的Morisky-Green量表评估粘附性。结果:共纳入104例患者(男性61%;平均年龄69.7±13.9岁);息肉治疗54例,常规治疗50例。未检测到临床或人口统计学变量的基线差异。在多药丸组中未发现复发,而常规治疗组中只有1次复发。与传统治疗组(6.8 mm Hg)相比,多药丸组(12.1 mm Hg)的收缩压(SBP)显着降低(p= 0.002)。对于LDL胆固醇≤70 mg / dL的目标,未发现明显差异(41%对44%)。两组的不良事件轻微,发生频率相似(9%vs. 2%,ns)。两组的依从性也相似(93比88%,ns)。Polypill组的依从性与先前对RCT的荟萃分析中报道的相似(93比84%,ns)。结论:根据我们的经验,心血管息肉药可降低SBP水平并具有良好的耐受性。坚持与以前的文献中发现的相似,考虑到我们研究的真实情况,这一点非常显着。
Cerebrovasc Dis Extra 2020; 10:166–173
更新日期:2020-11-12
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