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在冲绳儿童高血压干预与防治研究(OKIDS)中进行的奥美沙坦临床试验(OCTOPUS):设计与方法

Olmesartan clinical trial in Okinawan patients under OKIDS (OCTOPUS) study: design and methods.

作者信息

Iseki Kunitoshi, Tokuyama Kiyoyuki, Shiohira Yoshiki, Higa Akira, Hirano Hiroshi, Toma Shigeki, Kohagura Kentaro, Ueda Shinichiro

机构信息

Dialysis Unit, University Hospital of The Ryukyus, 207 Uehara, Nishihara, Okinawa, 903-0215, Japan.

Tokuyama Clinic, Urasoe, Okinawa, Japan.

出版信息

Clin Exp Nephrol. 2009 Apr;13(2):145-151. doi: 10.1007/s10157-008-0116-8. Epub 2008 Dec 20.

Abstract

BACKGROUND

Guidelines for treatment of hypertension are not available for chronic hemodialysis (HD) population, despite the high mortality rate due to cardiovascular disease (CVD). Survival is much better among hypertensive patients than normal to hypotensive patients. Target levels of blood pressure and the class of antihypertensive drugs have not been examined in prospective studies.

METHODS

We designed a prospective randomized controlled study among hypertensive HD patients in Okinawa (Okinawa Dialysis Study, OKIDS). The outcomes will be compared between two treatment regimens, such as (1) renin-angiotensin system (RAS) inhibitor Olmesartan and others, and (2) antihypertensive drugs without RAS inhibitors, in a parallel fashion. The title of the study is Olmesartan Clinical Trial in Okinawan Patients under OKIDS (OCTOPUS). Outcomes are any cause of death and CVD in 3 years in a total of 462 patients. Subjects are age 20-79 years and ambulatory on thrice weekly HD treatment. Eligible patients have resistant hypertension: pre-HD session blood pressure 140/90 mmHg and over for more than 1 month regardless with the use of antihypertensive drugs. Patients treated with RAS drugs are eligible if they continue to be hypertensive for more than 1 month after switching to non-RAS antihypertensive drugs.

CONCLUSION

This study provides evidence for the target levels of blood pressure at a pre-HD session and the impact of RAS inhibitors. We also evaluate the usefulness of home blood pressure monitoring in HD patients.

摘要

背景

尽管心血管疾病(CVD)导致慢性血液透析(HD)人群死亡率很高,但目前尚无针对该人群的高血压治疗指南。高血压患者的生存率远高于血压正常或偏低的患者。前瞻性研究尚未对血压目标水平和抗高血压药物类别进行检验。

方法

我们在冲绳设计了一项针对高血压HD患者的前瞻性随机对照研究(冲绳透析研究,OKIDS)。将以平行方式比较两种治疗方案的结果,例如(1)肾素-血管紧张素系统(RAS)抑制剂奥美沙坦及其他药物,以及(2)不含RAS抑制剂的抗高血压药物。该研究的标题是OKIDS下冲绳患者的奥美沙坦临床试验(OCTOPUS)。结局是总共462例患者在3年内的任何原因死亡和CVD。受试者年龄在20 - 79岁之间,每周进行三次HD门诊治疗。符合条件的患者患有顽固性高血压:HD治疗前血压≥140/90 mmHg且持续超过1个月,无论是否使用抗高血压药物。使用RAS药物治疗的患者,如果在改用非RAS抗高血压药物后仍持续高血压超过1个月,则符合条件。

结论

本研究为HD治疗前的血压目标水平以及RAS抑制剂的影响提供了证据。我们还评估了家庭血压监测在HD患者中的有用性。

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