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Felodipine-Metoprolol Combination Tablet: Maintained Health-Related Quality of Life in the Presence of Substantial Blood Pressure Reduction

机译:非洛地平-美托洛尔联合片剂:在大幅降低血压的情况下维持与健康有关的生活质量

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Background: Most treated hypertensive patients do not achieve adequate blood pressure (BP) control. Initiating therapy with two drugs has been suggested when BP is >20/10 mm Hg above goal. To ensure patients' compliance, such treatment needs to be well tolerated and must not compromise health-related quality of life (HRQL). The primary objective of this study was to compare the effects on HRQL of initiating treatment with felodipine + metoprolol (F+M) fixed combination tablets, or enalapril (E), or placebo (P). Methods: A total of 947 patients of both sexes with primary hypertension (diastolic BP 95 to 110 mm Hg), aged 20 to 70 years, participated in this randomized, double-blind, parallel group, 12-week, multicenter trial. Treatment was initiated with F+M 5 + 50 mg, or E 10 mg, or P. Doses were doubled after 4 or 8 weeks if diastolic BP was >90 mm Hg. The HRQL was measured at baseline and at the last visit using two validated questionnaires: the Psychological General Well-being Index (PGWB) and the Subjective Symptom Assessment Profile (SSA-P). Office BP was measured at trough, that is, 24 h after the previous dose. Results: The HRQL was high at baseline and generally well maintained during the study. For example, the mean (SD) PGWB total score was 104 (16) at baseline and 105 (16) at 12 weeks in all three treatment groups. The BP reductions after F+M (18/14 mm Hg) and E (12/9 mm Hg) were significantly greater than after P (7/7 mm Hg), and the reduction after F+M was significantly greater than after E. Conclusions: The HRQL is maintained in the presence of substantial BP reduction during antihypertensive treatment with F+M fixed combination tablets. Am J Hypertens 2005;18:1313-1319 © 2005 American Journal of Hypertension, Ltd
机译:背景:大多数接受治疗的高血压患者均未达到适当的血压(BP)控制。当血压高于目标值> 20/10 mm Hg时,建议使用两种药物开始治疗。为确保患者依从性,此类治疗需要良好的耐受性,并且不得损害与健康相关的生活质量(HRQL)。这项研究的主要目的是比较开始使用非洛地平+的治疗对HRQL的影响。美托洛尔(F&M;)固定组合片剂,依那普利(E)或安慰剂(P)。方法:这项年龄为20至70岁的原发性高血压(舒张压BP 95至110 mm Hg)男女共947例,参加了这项随机,双盲,平行组,为期12周的多中心试验。用F+ M 5+开始治疗。 50 mg或E 10 mg或P。如果舒张压BP> 90 mm Hg,则在4或8周后加倍剂量。使用两个经过验证的问卷在基线和最后一次就诊时测量HRQL:心理总体健康指数(PGWB)和主观症状评估资料(SSA-P)。在低谷(即前一剂后24小时)测量Office BP。结果:HRQL在基线时很高,并且在研究过程中总体保持良好。例如,在所有三个治疗组中,平均(SD)PGWB总得分在基线时为104(16),在12周时为105(16)。 F+ M(18/14 mm Hg)和E(12/9 mm Hg)后的BP降低显着大于P(7/7 mm Hg)后的BP,F+ M之后的BP显着大于E之后的BP降低结论:在用F+ M固定组合降压药进行降压治疗期间,HRQL维持在血压明显降低的情况下。 Am J Hypertens 2005; 18:1313-1319©2005 American Journal of Hypertension,Ltd

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