Effects of Catheter-Based Renal Denervation in Hypertension: A Systematic Review and Meta-Analysis.

IF 35.5 1区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS Circulation Pub Date : 2024-11-12 Epub Date: 2024-10-02 DOI:10.1161/CIRCULATIONAHA.124.069709
Davor Vukadinović, Lucas Lauder, David E Kandzari, Deepak L Bhatt, Ajay J Kirtane, Elazer R Edelman, Roland E Schmieder, Michel Azizi, Michael Böhm, Felix Mahfoud
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Abstract

Background: Several sham-controlled trials have investigated the efficacy and safety of catheter-based renal denervation (RDN) with mixed outcomes. We aimed to perform a comprehensive meta-analysis of all randomized, sham-controlled trials investigating RDN with first- and second-generation devices in hypertension.

Methods: We searched MEDLINE and the Cochrane Library for eligible trials. Outcomes included both efficacy (24-hour and office systolic [SBP] and diastolic blood pressure [DBP]) and safety (all-cause death, vascular complication, renal artery stenosis >70%, hypertensive crisis) of RDN. We performed a study-level, pairwise, random-effects meta-analysis of the summary data.

Results: Ten trials comprising 2478 patients with hypertension while being either off or on treatment were included. Compared with sham, RDN reduced 24-hour and office systolic blood pressure by 4.4 mm Hg (95% CI, 2.7 to 6.1; P<0.00001) and 6.6 mm Hg (95% CI, 3.6 to 9.7; P<0.0001), respectively. The 24-hour and office diastolic blood pressure paralleled these findings (-2.6 mm Hg [95% CI, -3.6 to -1.5]; P<0.00001; -3.5 mm Hg [95% CI, -5.4 to -1.6]; P=0.0003). There was no difference in 24-hour and office systolic blood pressure reduction between trials with and without concomitant antihypertensive medication (P for interaction, 0.62 and 0.73, respectively). There was no relevant difference in vascular complications (odds ratio, 1.69 [95% CI, 0.57 to 5.0]; P=0.34), renal artery stenosis (odds ratio, 1.50 [95% CI, 0.06 to 36.97]; P=0.80), hypertensive crisis (odds ratio, 0.65 [95% CI, 0.30 to 1.38]; P=0.26), and all-cause death (odds ratio, 1.76 [95% CI, 0.34 to 9.20]; P=0.50) between RDN and sham groups. Change of renal function based on estimated glomerular filtration rate was comparable between groups (P for interaction, 0.84). There was significant heterogeneity between trials.

Conclusions: RDN safely reduces ambulatory and office systolic blood pressure/diastolic blood pressure versus a sham procedure in the presence and absence of antihypertensive medications.

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导管式肾脏去神经治疗高血压的效果:系统综述与元分析》。
背景:多项假对照试验研究了导管肾脏去神经支配(RDN)的有效性和安全性,结果不一。我们旨在对所有使用第一代和第二代设备对高血压进行肾脏去神经支配的随机假对照试验进行全面的荟萃分析:我们检索了 MEDLINE 和 Cochrane 图书馆中符合条件的试验。结果包括 RDN 的疗效(24 小时和诊室收缩压 [SBP] 和舒张压 [DBP])和安全性(全因死亡、血管并发症、肾动脉狭窄 > 70%、高血压危象)。我们对汇总数据进行了研究层面的配对随机效应荟萃分析:结果:共纳入了 10 项试验,包括 2478 名停药或正在接受治疗的高血压患者。与假治疗相比,RDN 可使 24 小时和办公室收缩压降低 4.4 mm Hg(95% CI,2.7 至 6.1;PPPP=0.0003)。在同时服用和未服用降压药的试验中,24 小时和办公室收缩压的降低幅度没有差异(交互作用的 P 分别为 0.62 和 0.73)。血管并发症(几率比,1.69 [95% CI,0.57 至 5.0];P=0.34)、肾动脉狭窄(几率比,1.50 [95% CI,0.06 至 36.97];P=0.80)、高血压危象(几率比,0.65 [95% CI,0.30 至 1.38];P=0.26)和全因死亡(几率比,1.76 [95% CI,0.34 至 9.20];P=0.50)在 RDN 组和假肾组之间存在差异。根据估计肾小球滤过率计算的肾功能变化在各组之间不相上下(交互作用的 P 为 0.84)。试验之间存在明显的异质性:结论:在服用或未服用降压药的情况下,与假手术相比,RDN能安全地降低流动和办公室收缩压/舒张压。
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来源期刊
Circulation
Circulation 医学-外周血管病
CiteScore
45.70
自引率
2.10%
发文量
1473
审稿时长
2 months
期刊介绍: Circulation is a platform that publishes a diverse range of content related to cardiovascular health and disease. This includes original research manuscripts, review articles, and other contributions spanning observational studies, clinical trials, epidemiology, health services, outcomes studies, and advancements in basic and translational research. The journal serves as a vital resource for professionals and researchers in the field of cardiovascular health, providing a comprehensive platform for disseminating knowledge and fostering advancements in the understanding and management of cardiovascular issues.
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