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首页> 外文期刊>Vascular Health and Risk Management >Adherence with single-pill amlodipine/atorvastatin vs a two-pill regimen
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Adherence with single-pill amlodipine/atorvastatin vs a two-pill regimen

机译:单药氨氯地平/阿托伐他汀与两药方案的依从性

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While clinical trials demonstrate the benefits of blood pressure and cholesterol reduction, medication adherence in clinical practice is problematic. We hypothesized that a single-pill would be superior to a 2-pill regimen for achieving adherence. In this retrospective, cohort study based on pharmacy claims data, patients newly initiated on a calcium channel blocker (CCB) or statin simultaneously or within 30 days, regardless of sequence, were followed (N = 4703). Adherence was measured over 6 months as proportion of days covered (PDC). At baseline, mean age was 63.0 years, 51.6% were female, and mean number of other medications was 7.8. Overall, 16.9% of patients were on single-pill amlodipine/atorvastatin, 15.6% amlodipine + atorvastatin, 24.7% amlodipine + other statin, 13.9% other CCB + atorvastatin, 28.9% other CCB + other statin. Percentages of patients achieving adherence (PDC ≥ 80%) were: 67.7% amlodipine/atorva statin; 49.9% amlodipine + atorvastatin; 40.4% amlodipine + other statin; 46.9% other CCB + atorvastatin; 37.4% other CCB + other statin. After adjusting for treatment selection and cohort differences, odds ratios for adherence with amlodipine/atorvastatin were 1.95 (95% confidence interval [CI], 1.80–2.13) vs amlodipine + atorvastatin, 3.10 (95% CI, 2.85–3.38) vs amlodipine + other statin, 2.06 (95% CI, 1.89–2.24) vs other CCB + atorvastatin, 2.85 (95% CI, 2.61–3.10) vs other CCB + other statin (all p < 0.0001). Single-pill amlodipine/atorvastatin may provide clinical benefits through improving adherence, offering clinicians a practical solution for cardiovascular risk management.
机译:尽管临床试验证明了降低血压和降低胆固醇的好处,但临床实践中依从性仍然存在问题。我们假设单药可以达到2药方案的依从性。在这项基于药房索赔数据的回顾性队列研究中,追踪了同时或在30天内使用钙通道阻滞剂(CCB)或他汀类药物新开始的患者,无论其顺序如何(N = 4703)。在6个月内测量的坚持率是所覆盖天数(PDC)的比例。基线时,平均年龄为63.0岁,女性为51.6%,其他药物的平均数量为7.8。总体而言,单药氨氯地平/阿托伐他汀的患者为16.9%,氨氯地平+阿托伐他汀为15.6%,氨氯地平+其他他汀类药物为24.7%,其他CCB +阿托伐他汀类药物为13.9%,其他CCB +其他他汀类药物为28.9%。达到依从性(PDC≥80%)的患者百分比为:67.7%氨氯地平/阿托伐他汀; 49.9%氨氯地平+阿托伐他汀; 40.4%氨氯地平+其他他汀类药物;其他CCB +阿托伐他汀46.9%;其他CCB +其他他汀类药物占37.4%。调整治疗选择和队列差异后,氨氯地平/阿托伐他汀与氨氯地平+阿托伐他汀的依从性比为1.95(95%置信区间[CI],1.80–2.13),氨氯地平+阿托伐他汀3.10(95%CI,2.85-3.38)其他他汀类药物为2.06(95%CI,1.89–2.24)与其他CCB +阿托伐他汀,2.85(95%CI,2.61–3.10)与其他CCB +其他他汀类药物(均p <0.0001)。单药氨氯地平/阿托伐他汀可通过改善依从性提供临床益处,为临床医生提供心血管风险管理的实用解决方案。

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