Czarnecka D, Koch E M W, Gottwald-Hostalek U
Cardiologist , Krakow , Poland.
Curr Med Res Opin. 2015 May;31(5):875-81. doi: 10.1185/03007995.2015.1027676. Epub 2015 Apr 8.
The study objective was assessing patient adherence to a fixed-dose combination (FDC) of bisoprolol and amlodipine in daily practice in patients who had been switched from the free to the fixed-dose combination prior to recruitment.
The non-investigational study was carried out in Poland. Patients over 18 years of age with essential hypertension were recruited if they had already been switched from a free combination to the FDC at least 4 weeks prior to recruitment. Exclusion criteria included pregnancy, lactation, any contraindication to the FDC, and other antihypertensive treatment. Adherence was measured by tablet count (tablets taken divided by tablets prescribed, times 100) and defined as follows: excellent >90%, good 76-90%, moderate 51-75%, bad ≤50%. Other patient data, clinical findings and laboratory values were recorded upon availability at study start, after 3 months (voluntary) and after 6 months.
Data of 4288 patients (mean age: 59 years; gender: 50% each) were documented. The average daily doses of the FDC were 5.8 mg bisoprolol and 6.4 mg amlodipine. These doses differ only slightly from those of the free combination. After 3 months' treatment with the FDC, a dose increase was carried out in 113 patients for bisoprolol and in 126 for amlodipine. After 6 months of FDC treatment, 82% of the participants of the study showed excellent adherence and for a further 15% the adherence could be considered good. This strong adherence may have led to the observed reduction in systolic and diastolic blood pressure of 11% (Cohen's D efficient size 1.23). In addition, pulse pressure decreased from 58.8 mm to 52.2 mm. Also in diabetic patients (21% of the cohort), further reduction of systolic blood pressure values could be achieved (mean before 150 mm, after 133), wherein the initial differences compared to patients without diabetes had disappeared. The pulse rate also changed from 75 b/min to 68 b/min under the FDC.
These study results clearly show that the FDC leads to excellent patient adherence and therefore may result in better blood pressure control. Blood pressure control is crucial in the risk reduction of cardiovascular events. The key limitation of this study is that the study design does not allow a direct comparison of patient adherence under the free and the fixed-dose combination.
本研究的目的是评估在日常实践中,招募前已从自由联合用药转换为固定剂量联合用药的患者对比索洛尔和氨氯地平固定剂量联合制剂(FDC)的依从性。
这项非研究性研究在波兰开展。招募年龄超过18岁的原发性高血压患者,前提是他们在招募前至少4周已从自由联合用药转换为FDC。排除标准包括妊娠、哺乳期、FDC的任何禁忌症以及其他抗高血压治疗。通过药片计数法(服用的药片数除以开的药片数,再乘以100)测量依从性,定义如下:优秀>90%,良好76 - 90%,中等51 - 75%,差≤50%。在研究开始时、3个月后(自愿)和6个月后,如有可用数据,记录其他患者数据、临床发现和实验室值。
记录了4288例患者的数据(平均年龄:59岁;性别:各占50%)。FDC的平均日剂量为比索洛尔5.8mg和氨氯地平6.4mg。这些剂量与自由联合用药的剂量仅略有不同。FDC治疗3个月后,113例患者增加了比索洛尔剂量,126例患者增加了氨氯地平剂量。FDC治疗6个月后,82%的研究参与者表现出优秀的依从性,另有15%的依从性可被认为良好。这种高度依从性可能导致观察到收缩压和舒张压降低了11%(科恩效应量为1.23)。此外,脉压从58.8mmHg降至52.2mmHg。在糖尿病患者(占队列的21%)中,收缩压值也进一步降低(之前平均为150mmHg,之后为133mmHg),其中与非糖尿病患者相比的初始差异已消失。在FDC治疗下,心率也从75次/分钟变为68次/分钟。
这些研究结果清楚地表明,FDC导致患者高度依从,因此可能带来更好的血压控制。血压控制对于降低心血管事件风险至关重要。本研究的关键局限性在于研究设计不允许直接比较自由联合用药和固定剂量联合用药下患者的依从性。