期刊文献+

比索洛尔/氢氯噻嗪复方片治疗中国轻中度原发性高血压的临床疗效和安全性研究 被引量:34

The clinical efficiency and safety of bisorpolol hydrochlorothiazide in patients with mild to moderate essential hypertension
原文传递
导出
摘要 目的采用24小时动态血压监测观察比索洛尔/氢氯噻嗪复方片(Lodoz)治疗90例中国轻、中度高血压患者的降压效果和安全性。方法选择90例收缩压<180 mm Hg(1 mm Hg= 0.133 kPa),舒张压95-109 mm Hg的轻、中度高血压患者,口服Lodoz(2.5 mg/6.25 mg)共4周或Lodoz(5 mg/6.25 mg)8周,用24小时动态血压监测评价治疗4周、8周后动态血压变化及安全性。结果(1)4周和8周末诊室收缩压/舒张压分别降低(14.89±10.99)/(10.37±7.35)mm Hg和(19.40±10.55)/(13.31±7.77)mm Hg,全天、日间、夜间的24小时动态平均血压均明显降低,差异有统计学意义(P均<0.05)。4周和8周末的总有效率分别为59.3%和69.8%。(2)Lodoz(2.5 mg/6.25 mg)对收缩压和舒张压的谷/峰比值(T/P比值)分别为91.5%和94.4%,降压平滑指数(SI)为9.07/6.48;Lodoz(5 mg/6.25 mg)对收缩压和舒张压的T/P比值为79.9%和80.5%,SI为4.17/4.47。(3)Lodoz可能有使“非勺型”血压转变为“勺型”血压的趋势。(4)不良反应主要有血尿酸升高、头晕、头痛、腹泻、口干、肢端发凉、蚁行感,均为轻度。结论Lodoz能够持续、平稳、有效地降低24小时血压,且安全性良好。 Objective To investigate the efficacy and safety of bisorpolol/hydrochlorothiazide (Lodoz) in patients with mild and moderate essential hypertension. Methods After 2 weeks of placebo run-in period, 90 hypertensive patients with sitting diastolic blood pressure ( DBP ) between 95 and 109 mm Hg( 1 mm Hg =0. 133 kPa) and systolic blood pressure (SBP) below 180 mm Hg were treated by Lodoz (2.5mg/6. 25mg/day) for4 weeks. If DBP 〉90 mm Hg at4 weeks, Lodoz (5mg/6. 25 mg/day) was given for another 8 weeks. Clinic systolic and diastolic blood pressure measurements and ambulatory blood pressure monitoring (ABPM) were performed at the end of placebo run-in period and at 4 and 8 weeks. Results After 4 or 8 weeks treatment with Lodoz, clinic systolic and diastolic blood pressure, the 24-hour mean, daytime and nocturnal blood pressures reduced significantly compared to placebo run-in period [SBP and DBP reduced (14.89 ± 10.99)/(10.37 ±7.35) mm Hg (4 weeks) and (19.40 ± 10. 55 ) / ( 13. 31 ± 7.77) mm Hg ( 8 weeks ) ] respectively ( P 〈 0. 05 ). The total efficacy rate is 59. 3 % for Lodoz 2. 5mg/6. 25 mg and 69. 8% for Lodoz 5 mg/6. 25 mg. The trough:peak ratio for SBP and DBP were 91.5% and 94.4% with Lodoz 2.5mg/6.25 rag, and 79.9% and 80.5% with Lodoz 5mag/6.25 rag. The smoothness index (SI) for SBP and DBP were 9. 07 and 6.48 with Lodoz 2. 5mg/6. 25mg, and 4. 17 and 4. 47 with Lodoz 5 mg/6.25 mg, respectively. Few side effects were observed during treatment including mild headache and dizziness and slightly increased serum urea acid. Conclusion Lodoz (2. 5 mg/6. 25 mg and 5 mg/6. 25 mg) can effectively reduce the 24 hours blood pressure in patients with mild to moderate essential hypertension.
出处 《中华心血管病杂志》 CAS CSCD 北大核心 2006年第7期605-608,共4页 Chinese Journal of Cardiology
关键词 高血压 比索洛尔 氢氯噻嗪 治疗结果 Hypertension Bisorpolol Hydrochlorothiazide Treatment outcome
  • 相关文献

参考文献5

  • 1European Society of Hypertension-European Society of Cardiology Guidelines Committee. 2003 European Society of Hypertension-European Society of Cardiology guidelines for the management of arterial hypertension. J Hypertens, 2003,21:1011-1053. 被引量:1
  • 2Chobanian AV, Bakris GL, Black HR ,et al. The Seventh Report of the Joint National Committee on Prevention, Detection, Evaluation, and Treatment of High Blood Pressure: the JNC 7 report. JAMA, 2003,289 : 2560 -2572. 被引量:1
  • 3Fenichel RR, Lipicky RJ. Combination products as first-line pharmacotherapy. Arch Intern Med, 1994,154 : 1429-1430. 被引量:1
  • 4Meredith PA. How to evaluate the duration of blood pressure control :the trough: peak ratio and 24-hour monitoring. J Cardiovasc Pharmacol,1998,31 (Suppl 2) :S17-21. 被引量:1
  • 5Rizzoni D, Parati G, Omboni S, et al. Smoothness index but not T/P ratio estimates balanced 24 - hour blood pressure control and predicts regression of organ damage by antihypertensive treatment. J Hypertens, 1997,15 :S7-11. 被引量:1

同被引文献218

引证文献34

二级引证文献164

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部