中国老年高血压合并心房颤动患者血压和胆固醇强化管理的随机对照试验的基本原理和设计

Wei Zhang, Yi Chen, Qi-Fang Huang, Ji-Guang Wang
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引用次数: 1

摘要

摘要高血压显著增加心房颤动患者发生栓塞性中风和全身栓塞的风险,而他汀类药物治疗可以改善高危高血压患者的长期预后。然而,目前尚不清楚高血压和心房颤动患者是否能从强化血压和胆固醇管理中受益。IMPRESSION是一项为期3年的前瞻性、随机、开放标签、盲法终点调查。来自全国约40个临床中心的1200名高血压心房颤动患者将在确认存在高血压和心房颤动后被纳入研究,并将被随机分配到强化或标准血压和胆固醇管理组。所有组的患者将在第一个月底前和每3个月测量一次办公室和家中的血压 此后数月。高血压和心房颤动患者的血压和胆固醇管理策略对3岁时致命性和非致命性中风、急性心肌梗死和心血管死亡的影响 年将进行评估。印象研究方案已获得上海交通大学医学院瑞金医院伦理委员会的批准。本方案中规定的程序符合《赫尔辛基宣言》的原则和良好临床实践指南。CONSORT发表声明后,研究结果将发表在同行评审的科学期刊上(试验注册号:NCT04111419)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rationale and Design of a Randomized Controlled Trial on Intensive Management of Blood PRESSure and Cholesterol in Elderly Chinese with Hypertension and Atrial FibrillatION (IMPRESSION)
Abstract Hypertension significantly increases the risk of embolic stroke and systemic embolism in patients with atrial fibrillation, while statin therapy can improve long-term outcomes in hypertensive patients at high risk. However, it is still unclear whether patients with both hypertension and atrial fibrillation can benefit from intensive management of blood pressure and cholesterol. IMPRESSION is a 3-year prospective, randomized, open-label, blinded-endpoint investigation. A total of 1200 hypertensive patients with atrial fibrillation from about 40 clinical centers nationwide will be included upon confirming the presence of both hypertension and atrial fibrillation and will be randomly assigned to groups for intensive or standard management of blood pressure and cholesterol. Patients in all groups will have office and home blood pressure measured by the end of the first month and every 3 months thereafter. The effects of blood pressure and cholesterol management strategies in patients with hypertension and atrial fibrillation on fatal and non-fatal stroke, acute myocardial infarction, and cardiovascular death at 3 years will be assessed. The IMPRESSION study protocol has received approval from the Ethics Committee of Ruijin Hospital, Shanghai Jiaotong University School of Medicine. The procedures set out in this protocol are in accordance with the principles of the Declaration of Helsinki and Good Clinical Practice guidelines. The results will be published following the CONSORT statement in a peer-reviewed scientific journal (Trial registration number: NCT04111419).
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