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Efficacy and Safety of Catheter-Based Radiofrequency Renal Denervation in Chinese Patients With Uncontrolled Hypertension: The Randomized, Sham-Controlled, Multi-Center Iberis-HTN Trial

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机构: [1]Fuwai Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences [2]Department of Cardiology and Cardiovascular Research Institute Basel, University Heart Center, University Hospital Basel, Switzerland [3]Medical Research & Biometrics Center, National Center for Cardiovascular Diseases, The Chinese Academy of Medical Sciences [4]Lanzhou University Second Hospital, China [5]Zhengzhou Central Hospital Affiliated to Zhengzhou University, China [6]West China Hospital, Sichuan University, China [7]The First Affiliated Hospital of Chengdu Medical Collage, China [8]Affiliated Hospital of Hebei University [9]Xinxiang Central Hospital, China [10]Tangshan Workers' Hospital [11]The Second Affiliated Hospital of Nanchang University [12]Xuzhou Central Hospital [13]Daping Hospital, The Third Military Medical University [14]The Affiliated Hospital of Hangzhou Normal University [15]Ruijin Hospital, Shanghai Jiaotong University School of Medicine [16]Inner Mongolia Autonomous Region People's Hospital [17]Henan Provincial Chest Hospital [18]Hospital of Chengdu University of Traditional Chinese Medicine [19]EastPoint Innovation Center, Hangzhou, China [20]Shanghai Angiocare Medical Technology, China [21]Division of Cardiovascular Medicine, Department of Medicine, Jichi Medical University School of Medicine, Tochigi Japan
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关键词: antihypertensive agents blood pressure denervation hypertension

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Renal denervation (RDN) can lower blood pressure (BP) in patients with hypertension in both the presence and absence of medication. This is the first sham-controlled trial investigating the safety and efficacy of RDN in China.This prospective, multicenter, randomized, patient- and outcome-assessor-blinded, sham-controlled trial investigated radiofrequency RDN in patients with hypertension on standardized triple antihypertensive therapy. Eligible patients were randomized 1:1 to undergo RDN using a multi-electrode radiofrequency catheter (Iberis; AngioCare, Shanghai, China) or a sham procedure. The primary efficacy outcome was the between-group difference in baseline-adjusted change in mean 24-hour ambulatory systolic BP from randomization to 6 months.Of 217 randomized patients (mean age, 45.3±10.2 years; 21% female), 107 were randomized to RDN and 110 were randomized to sham control. At 6 months, there was a greater reduction in 24-hour systolic BP in the RDN (-13.0±12.1 mm Hg) compared with the sham control group (-3.0±13.0 mm Hg; baseline-adjusted between-group difference, -9.4 mm Hg [95% CI, -12.8 to -5.9]; P<0.001). Compared with sham, 24-hour diastolic BP was lowered by -5.0 mm Hg ([95% CI, -7.5 to -2.4]; P<0.001) 6 months after RDN, and office systolic and diastolic BP was lowered by -6.4 mm Hg ([95% CI, -10.5 to -2.3]; P=0.003) and -5.1 mm Hg ([95% CI, -8.2 to -2.0]; P=0.001), respectively. One patient in the RDN group experienced an access site complication (hematoma), which resolved without sequelae. No other major device- or procedure-related safety events occurred through follow-up.In this trial of Chinese patients with uncontrolled hypertension on a standardized triple pharmacotherapy, RDN was safe and reduced ambulatory and office BP at 6 months compared with sham.URL: https://clinicaltrials.gov; Unique identifier: NCT02901704.

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大类 | 1 区 医学
小类 | 1 区 心脏和心血管系统 1 区 外周血管病
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Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Q1 PERIPHERAL VASCULAR DISEASE

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第一作者机构: [1]Fuwai Hospital, Peking Union Medical College & Chinese Academy of Medical Sciences
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