New data, new studies, new hopes for renal denervation in patients with uncontrolled hypertension

Vasilios Papademetriou , Konstantinos Stavropoulos , Kostas Imprialos , Michael Doumas , Roland E. Schmieder , Atul Pathak , Costas Tsioufis
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Abstract

Background

following the publication of SYMPLICITY HTN-3 the field of renal of denervation was put on hold. Although SYMPLICITY HTN-3 was well-designed and sham-controlled trial it failed to show any meaningful reduction in office or 24 h ambulatory blood pressure. The procedure was however safe and allowed research to continue. Although several pitfalls of the study have been pointed out, incomplete renal denervation was also implicated. Since then, a great deal of basic and clinical research took place and will be briefly commented on in this article.

Methods and results

Before and after SYMPLICITY-HTN-3, numerous uncontrolled, single or unblinded studies have shown substantial office BP reduction ranging from −7.7 to −32 mmHg and ambulatory BP ranging from −2.2 to 10.2 mmHg. Average weighted office systolic BP reduction was −20.8 mmHg and weighted average 24 h ambulatory BPM reduction was −7.8 mmHg. National and international registries have shown similar BP reductions, but results remained unconvincing due to lack of reliable sham controls. In recent years, 5 well-designed sham – controlled studies (beyond, SYMPLICITY-HTN-3) have been published. Of those studies two were single center and three were multicenter international studies. Four studies used single tip or multi-electrode, radiofrequency catheters and one used focused ultrasound. The three multicenter studies reported positive-placebo subtracted results and established BP reductions measured both in the office and by ambulatory monitoring. No serious adverse events were reported.

Conclusions

It can therefore be concluded that the latest sham controlled studies established efficacy and safety of renal denervation.

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新数据,新研究,高血压患者肾去神经治疗的新希望
背景:在SYMPLICITY HTN-3发表后,肾脏去神经领域被搁置。尽管SYMPLICITY HTN-3是一项设计良好的假对照试验,但它未能显示出任何有意义的办公室或24小时动态血压降低。然而,这个过程是安全的,并允许研究继续进行。虽然研究的几个缺陷已经指出,不完全肾去神经也牵连。从那时起,进行了大量的基础和临床研究,本文将对这些研究进行简要评述。方法和结果:在SYMPLICITY-HTN-3前后,大量非对照、单盲或非盲研究表明,办公室血压显著降低,范围从- 7.7至- 32 mmHg,动态血压范围从- 2.2至10.2 mmHg。平均加权办公室收缩压降低为- 20.8 mmHg,加权平均24小时动态BPM降低为- 7.8 mmHg。国家和国际登记处也显示出类似的BP减少,但由于缺乏可靠的假控制,结果仍然不令人信服。近年来,已经发表了5个设计良好的假对照研究(除了SYMPLICITY-HTN-3)。在这些研究中,两个是单中心研究,三个是多中心国际研究。四项研究使用单电极或多电极、射频导管,一项研究使用聚焦超声。三个多中心研究报告了阳性安慰剂减去结果,并建立了在办公室和动态监测中测量的血压降低。无严重不良事件报告。结论最新的假对照研究证实了肾去神经的有效性和安全性。
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来源期刊
International Journal of Cardiology: Hypertension
International Journal of Cardiology: Hypertension Medicine-Cardiology and Cardiovascular Medicine
CiteScore
0.40
自引率
0.00%
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0
审稿时长
13 weeks
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