Factorial anti hypertensive study of an extended-release metoprolol and hydrochlorothiazide combination

被引:22
作者
Papademetriou, Vasilios [1 ]
Hainer, James W.
Sugg, Jennifer
Munzer, Deborah
机构
[1] VA Med Ctr, Washington, DC USA
[2] Georgetown Univ, Med Ctr, Washington, DC 20007 USA
关键词
antihypertensive therapy; beta-adrenergic receptor blockers; thiazide diuretics combination antihypertensive therapy; factorial study design; hypertension; essential; efficacy; safety;
D O I
10.1016/j.amjhyper.2006.05.007
中图分类号
R6 [外科学];
学科分类号
1002 [临床医学]; 100210 [外科学];
摘要
Background: To attain goal blood pressure (BP), many hypertensive patients require combination antihypertensive therapy. Thiazide diuretic/beta-blocker regimens lower BP, and clinical studies indicate that they reduce the risk for cardiovascular consequences of hypertension. Fixed-dose combination tablets can simplify multidrug treatment regimens. Methods: This multicenter, randomized, double-blind, placebo-controlled, unbalanced factorial study (N = 1571) was designed to determine whether hydrochlorothiazide (HCT) and extended release (ER) metoprolol both contribute to an antihypertensive effect. Hypertensive adults with sitting diastolic BP (SiDBP) 95 to 114 mm Hg and systolic BP (SiSBP) < 180 min Hg received one of three hydrochlorothiazide doses (6.25 mg 12.5 mg, or 25 mg), one of four ER-metoprolol doses (25 mg, 50 mg, 100 mg 200 mg), or one of nine of the combinations or placebo for 8 weeks. Results: Blood pressure decreased with all combinations (P <.001 v placebo) reductions were dose related, ranging from 8.7 to 15.7 min Hg (SiDBP) and 9.7 to 18.9 min Hg (SiSBP) (model-derived values). Reductions with L placebo were 5.3 (SiDBP) and 4.2 mm Hg (SiSBP). Both active agents contributed to the combination effect (P .0015 for SiDBP; P =.0006 for SiSBP). Several low-dose combinations were approximately as effective as high doses of the individual agents (differences within I to 2.5 min Hg). The adverse event discontinuation rate was 2.9%. Serum potassium decreased and Uric acid increased with increasing doses of HCT. Conclusions: Extended-release metoprolol/hydrochlorothiazide is an effective antihypertensive combination that offers additive antihypertensive contributions from both components.
引用
收藏
页码:1217 / 1225
页数:9
相关论文
共 17 条
[1]
A COMPARISON OF A CONTROLLED RELEASE (CR ZOK) FORMULATION OF METOPROLOL, ONCE DAILY, WITH CONVENTIONAL METOPROLOL TABLETS, TWICE DAILY, IN MILD TO MODERATE HYPERTENSION [J].
CARRUTHERS, G ;
SHEARER, R ;
TAYLOR, W ;
MOORE, M .
JOURNAL OF CLINICAL PHARMACOLOGY, 1990, 30 (02) :S61-S65
[2]
Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure [J].
Chobanian, AV ;
Bakris, GL ;
Black, HR ;
Cushman, WC ;
Green, LA ;
Izzo, JL ;
Jones, DW ;
Materson, BJ ;
Oparil, S ;
Wright, JT ;
Roccella, EJ .
HYPERTENSION, 2003, 42 (06) :1206-1252
[3]
MORBIDITY AND MORTALITY IN THE SWEDISH TRIAL IN OLD PATIENTS WITH HYPERTENSION (STOP-HYPERTENSION) [J].
DAHLOF, B ;
LINDHOLM, LH ;
HANSSON, L ;
SCHERSTEN, B ;
EKBOM, T ;
WESTER, PO .
LANCET, 1991, 338 (8778) :1281-1285
[4]
Furberg CD, 2000, JAMA-J AM MED ASSOC, V283, P1967
[5]
Antihypertensive medication use among US adults with hypertension [J].
Gu, QP ;
Paulose-Ram, R ;
Dillon, C ;
Burt, V .
CIRCULATION, 2006, 113 (02) :213-221
[6]
Trends in prevalence, awareness, treatment, and control of hypertension in the United States, 1988-2000 [J].
Hajjar, I ;
Kotchen, TA .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2003, 290 (02) :199-206
[7]
Randomised trial of old and new antihypertensive drugs in elderly patients:: cardiovascular mortality and morbidity the Swedish Trial in Old Patients with Hypertension-2 study [J].
Hansson, L ;
Lindholm, LH ;
Ekbom, T ;
Dahlöf, B ;
Lanke, J ;
Scherstén, B ;
Wester, PO ;
Hedner, T ;
de Faire, U .
LANCET, 1999, 354 (9192) :1751-1756
[8]
Metoprolol succinate SR plus hydrochlorothiazide (Beloc-Zok® comp) in patients with essential hypertension in general practice -: A prospective, observational trial in 14 964 patients [J].
Hildemann, SK ;
Fischer, H ;
Pittrow, D ;
Bohlscheid, V .
CLINICAL DRUG INVESTIGATION, 2002, 22 (11) :719-729
[9]
Hung HMJ, 2000, STAT MED, V19, P2079
[10]
ON IDENTIFYING A POSITIVE DOSE-RESPONSE SURFACE FOR COMBINATION AGENTS [J].
HUNG, HMJ .
STATISTICS IN MEDICINE, 1992, 11 (05) :703-711