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Clinical impact of patient adherence to a fixed-dose combination of olmesartan, amlodipine and hydrochlorothiazide

机译:患者坚持奥美沙坦,氨氯地平和氢氯噻嗪固定剂量联合用药的临床影响

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Background and objectives: Recent findings from randomized clinical trials indicate an improved patient adherence and blood pressure (BP) control by using fixed-dose combinations (FDCs) in the treatment of hypertension. The aim of the present study was to verify those data in a large real-world sample of hypertensive patients and to cross-check adherence evaluation performed by physicians and patients self-assessment. Methods: A European multi-center, prospective, 24-week, non-interventional study was conducted including 14,979 patients with essential hypertension and new treatment with olmesartan, amlodipine and hydrochlorothiazide as an FDC. Patients' adherence was measured using the Morisky Medication Adherence Scale (MMAS-8) and a non-standardized questionnaire was used by physicians and patients for self-assessment. Results: The mean age of the patients was 63.9 ± 11.78 years and 46.5 % were women. One or more cardiovascular risk factors were present in 71.9 % of patients and 94.7 % had been treated for hypertension before study entry. Mean adherence to medication by MMAS-8 improved from 6.0 to 6.9 at study end. Corresponding improvements of adherence were seen on physicians' and patients' self-assessments throughout the study. Mean decrease of systolic/diastolic BP was 26.4/12.8 mmHg without a relevant difference between the MMAS-8 adherence levels. BP target achievement improved from 55.3 to 67.7 % in patients with low versus high adherence. The overall rate of patients with adverse drug reactions was very low (1.76 %) but more frequent in patients with low adherence. Conclusions: Our data confirm previous clinical trial data on the improvement of medication adherence by switching antihypertensive combination therapy to an FDC and a subsequent improvement in BP target achievement. An observed trend toward a reduction in adverse drug reactions needs to be further investigated in clinical trials.
机译:背景与目的:随机临床试验的最新发现表明,通过使用固定剂量组合(FDC)治疗高血压,可以改善患者的依从性和血压(BP)控制。本研究的目的是验证现实世界中大量高血压患者样本中的那些数据,并交叉检查医师和患者自我评估所进行的依从性评估。方法:进行了一项欧洲多中心,前瞻性,为期24周的非干预性研究,纳入了14979名原发性高血压患者,并接受了奥美沙坦,氨氯地平和氢氯噻嗪作为FDC的新治疗。使用Morisky药物依从性量表(MMAS-8)评估患者的依从性,医师和患者使用非标准化问卷进行自我评估。结果:患者的平均年龄为63.9±11.78岁,女性为46.5%。在进入研究之前,有71.9%的患者存在一种或多种心血管危险因素,并且94.7%的患者已经接受过高血压治疗。在研究结束时,MMAS-8对药物的平均依从性从6.0提高到6.9。在整个研究过程中,医师和患者的自我评估均显示出依从性的相应改善。收缩压/舒张压的平均下降为26.4 / 12.8 mmHg,而MMAS-8依从性水平之间无相关差异。低与高依从性患者的BP目标达成率从55.3%提高到67.7%。药物不良反应患者的总体发生率非常低(1.76%),但依从性低的患者则更为常见。结论:我们的数据证实了以前的临床试验数据,即通过将降压联合疗法改为FDC以及随后的BP目标实现改善,药物依从性得到改善。在临床试验中需要进一步研究观察到的药物不良反应减少的趋势。

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