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基于导管的超声肾去神经术治疗耐药性高血压患者:随机、对照的 REQUIRE 试验。

Catheter-based ultrasound renal denervation in patients with resistant hypertension: the randomized, controlled REQUIRE trial.

机构信息

Division of Cardiovascular Medicine, Department of Medicine, Jichi Medical University School of Medicine, Tochigi, Japan.

Department of Cardiology, Kishiwada Tokushukai Hospital, Osaka, Japan.

出版信息

Hypertens Res. 2022 Feb;45(2):221-231. doi: 10.1038/s41440-021-00754-7. Epub 2021 Oct 15.

Abstract

Renal denervation is a promising new non-pharmacological treatment for resistant hypertension. However, there is a lack of data from Asian patients. The REQUIRE trial investigated the blood pressure-lowering efficacy of renal denervation in treated patients with resistant hypertension from Japan and South Korea. Adults with resistant hypertension (seated office blood pressure ≥150/90 mmHg and 24-hour ambulatory systolic blood pressure ≥140 mmHg) with suitable renal artery anatomy were randomized to ultrasound renal denervation or a sham procedure. The primary endpoint was change from baseline in 24-hour ambulatory systolic blood pressure at 3 months. A total of 143 patients were included (72 renal denervation, 71 sham control). Reduction from baseline in 24-hour ambulatory systolic blood pressure at 3 months was not significantly different between the renal denervation (-6.6 mmHg) and sham control (-6.5 mmHg) groups (difference: -0.1, 95% confidence interval -5.5, 5.3; p = 0.971). Reductions from baseline in home and office systolic blood pressure (differences: -1.8 mmHg [p = 0.488] and -2.0 mmHg [p = 0.511], respectively), and medication load, did not differ significantly between the two groups. The procedure-/device-related major adverse events was not seen. This study did not show a significant difference in ambulatory blood pressure reductions between renal denervation and a sham procedure in treated patients with resistant hypertension. Although blood pressure reduction after renal denervation was similar to other sham-controlled studies, the sham group in this study showed much greater reduction. This unexpected blood pressure reduction in the sham control group highlights study design issues that will be addressed in a new trial. CLINICAL TRIAL REGISTRATION: NCT02918305 ( http://www.clinicaltrials.gov ).

摘要

肾动脉去神经术是一种有前途的治疗耐药性高血压的非药物治疗方法。然而,亚洲患者的数据缺乏。REQUIRE 试验研究了肾动脉去神经术在来自日本和韩国的耐药性高血压治疗患者中的降压疗效。适合肾动脉解剖结构的成年耐药性高血压患者(坐位诊室血压≥150/90mmHg,24 小时动态收缩压≥140mmHg)被随机分为超声肾动脉去神经术或假手术组。主要终点是 3 个月时 24 小时动态收缩压自基线的变化。共纳入 143 例患者(肾动脉去神经术组 72 例,假手术对照组 71 例)。3 个月时 24 小时动态收缩压自基线的降低在肾动脉去神经术组(-6.6mmHg)和假手术对照组(-6.5mmHg)之间无显著差异(差值:-0.1mmHg,95%置信区间-5.5mmHg,5.3mmHg;p=0.971)。家庭和诊室收缩压自基线的降低(差值:-1.8mmHg [p=0.488]和-2.0mmHg [p=0.511])和药物负荷在两组之间无显著差异。未观察到与操作/设备相关的主要不良事件。本研究未显示肾动脉去神经术与耐药性高血压治疗患者的假手术相比,在动态血压降低方面有显著差异。尽管肾动脉去神经术后的血压降低与其他假对照研究相似,但本研究的假手术组显示出更大的降低。假手术对照组中这种意外的血压降低突出了研究设计问题,这些问题将在一项新的试验中得到解决。临床试验注册:NCT02918305(http://www.clinicaltrials.gov)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a857/8766280/64402993a557/41440_2021_754_Fig1_HTML.jpg

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