Baseline characteristics and early blood pressure control in the CONVINCE trial

被引:128
作者
Black, HR
Elliott, WJ
Neaton, JD
Grandits, G
Grambsch, P
Grimm, RH
Hansson, L
Lacoucière, Y
Muller, J
Sleight, P
Weber, MA
White, WB
Williams, G
Wittes, J
Zanchetti, A
Fakouhi, TD
Anders, RJ
机构
[1] Rush Presbyterian St Lukes Med Ctr, Dept Prevent Med, Chicago, IL 60612 USA
[2] Univ Minnesota, Div Biostat, Minneapolis, MN USA
[3] Uppsala Univ, Dept Geriatr, Uppsala, Sweden
[4] CHU Quebec, Quebec City, PQ, Canada
[5] Massachusetts Gen Hosp, Dept Med, Boston, MA 02114 USA
[6] Univ Oxford, John Radcliffe Hosp, Oxford OX3 9DU, England
[7] Univ Oxford, Dept Med, Oxford OX3 9DU, England
[8] Brookdale Hosp, Dept Med, Brooklyn, NY USA
[9] SUNY Hlth Sci Ctr, Brooklyn, NY 11203 USA
[10] Univ Connecticut, Sch Med, Dept Med, Sect Hypertens & Clin Pharmacol, Farmington, CT USA
[11] Brigham & Womens Hosp, Boston, MA 02115 USA
[12] Harvard Univ, Sch Med, Boston, MA USA
[13] Stat Collaborat, Washington, DC USA
[14] Univ Milan, Milan, Italy
[15] Osped Maggiore, Milan, Italy
[16] Ctr Auxol Italiano Piancavallo, Milan, Italy
[17] Searle Labs, Clin Res, Skokie, IL USA
关键词
clinical trials; verapamil; atenolol; hydrochlorothiazide;
D O I
10.1161/01.HYP.37.1.12
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Blood pressure (BP) control rates around the world are suboptimal, Part 2 of the National Health and Nutrition Educational Survey (NHANES) III indicates that only 27.4% of hypertensive Americans aged 18 to 74 years have a BP of <140/90 mm Hg, We wanted to assess BP control during the first 2 years and to describe the baseline characteristics of patients enrolled in the Controlled ONset Verapamil INvestigation of Cardiovascular Endpoints (CONVINCE) Study, an international clinical trial that compares outcomes in hypertensive patients randomized to initial treatment with either controlled-onset extended-release verapamil or the investigator's choice of atenolol or hydrochlorothiazide. At randomization, BP was <140/90 mm Hg in only 20.3% of the 16 602 subjects (average+/-SD age 65.6+/-7.4 years; 56% women, 84% white/7% black/7% Hispanic). The average BP at enrollment was 148/85 mm Hg for patients taking BP medications (n=13 879) and 161/94 mm Hg for previously untreated patients (n=2723). After medication titration, with a transtelephonic computer that recommended an increase in the dose or number of antihypertensive agents whenever the BP was 140/90 mm Hg, 84.8% of the subjects attained the goal BP, During 2 years of treatment, BP control was maintained in 67% to 69% of the subjects (69% to 71% for systolic BP of <140 mm Hg and 90% for diastolic BP of <90 mm Hg). These data suggest that the control of systolic BP is more difficult than the control of diastolic BP. The US national goal of having 50% of hypertensives with a BP of <140/90 mm Hg may be achievable if a forced titration strategy is used. Interested investigators, free care and medications, and well-educated subjects may make the attainment of such a goal easier in the CONVINCE study than in the general population.
引用
收藏
页码:12 / 18
页数:7
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