Felodipine-metoprolol combination tablet:: Maintained health-related quality of life in the presence of substantial blood pressure reduction

被引:17
作者
Dahlöf, B
Innocenti, AD [1 ]
Elmfeldt, D
Puig, JG
Gundersen, T
Hosie, J
Januszewicz, W
Lindström, CJ
Magometschnigg, D
Tanser, P
Toutouzas, P
Waeber, B
Wiklund, I
机构
[1] AstraZeneca R&D, Med Sci, SE-43183 Molndal, Sweden
[2] Sahlgrens Univ Hosp, Dept Med, Clin Expt Res Lab, Gothenburg, Sweden
[3] Hosp La Paz, Madrid, Spain
[4] Sorlandet Hosp, Arendal, Norway
[5] Great Western Med, Glasgow, Lanark, Scotland
[6] Med Acad, Dept Hypertens, Warsaw, Poland
[7] Vastra Nylands Kretssjukhus, Ekenas, Finland
[8] Kinderspitalgasse, Inst Hypertoniker, Vienna, Austria
[9] St Josephs Hosp, Dept Med, Hamilton, ON, Canada
[10] Hippokrateion Hosp, Athens, Greece
[11] CHU Vaudois, Div Hypertens, CH-1011 Lausanne, Switzerland
关键词
enalapril; felodipine; health-related quality of life; hypertension; metoprolol;
D O I
10.1016/j.amjhyper.2005.04.017
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
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 min 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 nun 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.
引用
收藏
页码:1313 / 1319
页数:7
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