The second progress report on the Hypertension Objective treatment based on Measurement by Electrical Devices of Blood Pressure (HOMED-BP) study

被引:13
作者
Saito, S
Asayama, K
Ohkubo, T
Kikuya, M
Metoki, H
Obara, T
Hashimoto, J
Totsune, K
Yukio, M
Imai, Y
机构
[1] Tohoku Univ, Grad Sch Pharmaceut Sci & Med, Dept Clin Pharmacol & Therapeut, Sendai, Miyagi 980, Japan
[2] Tohoku Univ, Grad Sch Pharmaceut Sci & Med, Dept Planning Drug Dev & Clin Evaluat, Sendai, Miyagi 980, Japan
[3] Tohoku Univ, 21st Century COE Program, Comprehens Res & Educ Ctr Planning Drug Dev & Clin, Sendai, Miyagi 980, Japan
[4] Miyagi Shakaihoken Hosp, Sendai, Miyagi, Japan
关键词
randomized controlled trial (RCT); prospective randomized open-label blinded-endpoint (PROBE); hypertension; blood pressure measurement at home; Internet;
D O I
10.1097/00126097-200410000-00003
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Background The Hypertension Objective treatment based on Measurement by Electrical Devices of Blood Pressure (HOMED-BP) study is a large-scale intervention trial to determine both optimal target blood pressure (BP) on the basis of self-measured BP at home, and optimal initial anti hypertensive medication. Objective To investigate the quality of randomization at the end of March 2003, and BP-controlled conditions during initial 6 months. Methods We evaluated the number of patients randomized by the end of March 2003, and BP changes during the initial 6 months based on intention-to-treat analysis. Results By the end of March 2003, a total of 1086 patients (12% of a planned randomization of 9000 patients) had been randomized. Among 653 patients who had been followed for !: 6 months after randomization, mean systolic/diastolic BPs at randomization in the calcium antagonist, angiotensin-converting enzyme and angiotensin 11 receptor blocker groups were 149/89, 150/89 and 149/88 mmHg, respectively. Blood pressures were reduced after 3 months (137/83, 139/82 and 136/82 mmHg, respectively), and further reduced after 6 months (1134/81, 135/80 and 133/80 mmHg, respectively), with no significant differences identified between groups. In more-and less-intensive BP-lowering groups, mean systolic/ diastolic BPs at randomization were 149/88 and 150/89 mmHg, respectively. Although BPs were reduced after treatment for 3 months (137/83 and 137/82 mmHg, respectively) and 6 months (134/80 and 135/80 mmHg, respectively) in each target group, significant differences were still not observed between groups. Conclusions Good quality of randomization was observed at the end of March 2003, but rate of achievement for target BPs was insufficient. (C) 2004 Lippincott Williams Wilkins.
引用
收藏
页码:243 / 247
页数:5
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