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中心血压靶向治疗:晚期慢性肾脏病的一项实用随机试验(CENTRAL-CKD):一项临床研究方案

CENtral blood pressure Targeting: a pragmatic RAndomized triaL in advanced Chronic Kidney Disease (CENTRAL-CKD): A Clinical Research Protocol.

作者信息

Goupil Rémi, Nadeau-Fredette Annie-Claire, Prasad Bhanu, Hundemer Gregory L, Suri Rita S, Beaubien-Souligny William, Agharazii Mohsen

机构信息

Hopital du Sacré-Coeur de Montréal, Université de Montréal, QC, Canada.

Hopital Maisonneuve-Rosemont, Université de Montréal, QC, Canada.

出版信息

Can J Kidney Health Dis. 2023 May 6;10:20543581231172407. doi: 10.1177/20543581231172407. eCollection 2023.

Abstract

BACKGROUND

Emerging data favor central blood pressure (BP) over brachial cuff BP to predict cardiovascular and kidney events, as central BP more closely relates to the true aortic BP. Considering that patients with advanced chronic kidney disease (CKD) are at high cardiovascular risk and can have unreliable brachial cuff BP measurements (due to high arterial stiffness), this population could benefit the most from hypertension management using central BP measurements.

OBJECTIVE

To assess the feasibility and efficacy of targeting central BP as opposed to brachial BP in patients with CKD G4-5.

DESIGN

Pragmatic multicentre double-blinded randomized controlled pilot trial.

SETTING

Seven large academic advanced kidney care clinics across Canada.

PATIENTS

A total of 116 adults with CKD G4-5 (estimated glomerular filtration rate [eGFR] < 30 mL/min) and brachial cuff systolic BP between 120 and 160 mm Hg. The key exclusion criteria are 1) ≥ 5 BP drugs, 2) recent acute kidney injury, myocardial infarction, stroke, heart failure or injurious fall, 3) previous kidney replacement therapy.

METHODS

Double-blind randomization to a central or a brachial cuff systolic BP target (both < 130 mm Hg) as measured by a validated central BP device. The study duration is 12 months with follow-up visits every 2 to 4 months, based on local practice. All other aspects of CKD management are at the discretion of the attending nephrologist.

OUTCOMES

: Feasibility of a large-scale trial based on predefined components. : Carotid-femoral pulse wave velocity at 12 months. : Efficacy (eGFR decline, albuminuria, BP drugs, and quality of life); Events (major adverse cardiovascular events, CKD progression, hospitalization, mortality); Safety (low BP events and acute kidney injury).

LIMITATIONS

May be challenging to distinguish whether central BP is truly different from brachial BP to the point of significantly influencing treatment decisions. Therapeutic inertia may be a barrier to successfully completing a randomized trial in a population of CKD G4-5. These 2 aspects will be evaluated in the feasibility assessment of the trial.

CONCLUSION

This is the first trial to evaluate the feasibility and efficacy of using central BP to manage hypertension in advanced CKD, paving the way to a future large-scale trial.

TRIAL REGISTRATION

clinicaltrials.gov (NCT05163158).

摘要

背景

新出现的数据表明,相比于肱动脉袖带血压,中心血压更有助于预测心血管和肾脏事件,因为中心血压与主动脉真实血压的关系更为密切。考虑到晚期慢性肾脏病(CKD)患者心血管风险高,且肱动脉袖带血压测量可能不可靠(由于动脉僵硬度高),这一人群可能从采用中心血压测量的高血压管理中获益最大。

目的

评估在CKD G4-5期患者中以中心血压而非肱动脉血压为目标的可行性和有效性。

设计

实用多中心双盲随机对照试验。

地点

加拿大的7家大型学术性晚期肾脏护理诊所。

患者

共有116例CKD G4-5期成人患者(估计肾小球滤过率[eGFR]<30 mL/min),肱动脉袖带收缩压在120至160 mmHg之间。主要排除标准为:1)使用≥5种降压药物;2)近期发生急性肾损伤、心肌梗死、中风、心力衰竭或有伤害性跌倒;3)既往接受过肾脏替代治疗。

方法

通过经过验证的中心血压设备进行双盲随机分组,分为中心收缩压目标组或肱动脉袖带收缩压目标组(两者均<130 mmHg)。研究持续时间为12个月,根据当地实际情况每2至4个月进行一次随访。CKD管理的所有其他方面由主治肾病专家自行决定。

结局

基于预定义组成部分的大规模试验的可行性。12个月时的颈股脉搏波速度。有效性(eGFR下降、蛋白尿、降压药物使用情况和生活质量);事件(主要不良心血管事件、CKD进展、住院、死亡率);安全性(低血压事件和急性肾损伤)。

局限性

可能难以区分中心血压与肱动脉血压是否真的存在差异,以至于显著影响治疗决策。治疗惰性可能是在CKD G4-5期人群中成功完成随机试验的一个障碍。这两个方面将在试验的可行性评估中进行评价。

结论

这是第一项评估在晚期CKD中使用中心血压管理高血压的可行性和有效性的试验,为未来的大规模试验铺平了道路。

试验注册

clinicaltrials.gov(NCT05163158)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df81/10164859/8de7ba348eff/10.1177_20543581231172407-fig1.jpg

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