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血管内肾交感神经去神经术改善射血分数降低的心力衰竭:IMPROVE-HF-I研究

Endovascular renal sympathetic denervation to improve heart failure with reduced ejection fraction: the IMPROVE-HF-I study.

作者信息

Feyz L, Nannan Panday R, Henneman M, Verzijlbergen F, Constantinescu A A, van Dalen B M, Brugts J J, Caliskan K, Geleijnse M L, Kardys I, Van Mieghem N M, Manintveld O, Daemen J

机构信息

University Medical Center, Department of Cardiology, Erasmus MC, Rotterdam, The Netherlands.

Department of Radiology and Nuclear Medicine, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.

出版信息

Neth Heart J. 2022 Mar;30(3):149-159. doi: 10.1007/s12471-021-01633-z. Epub 2021 Oct 5.

Abstract

INTRODUCTION

The aim of the present study was to assess the safety and efficacy of renal sympathetic denervation (RDN) in patients with heart failure with reduced ejection fraction (HFrEF).

METHODS

We randomly assigned 50 patients with a left ventricular ejection fraction (LVEF) ≤ 35% and NYHA class ≥ II, in a 1:1 ratio, to either RDN and optimal medical therapy (OMT) or OMT alone. The primary safety endpoint was the occurrence of a combined endpoint of cardiovascular death, rehospitalisation for heart failure, and acute kidney injury at 6 months. The primary efficacy endpoint was the change in iodine-123 meta-iodobenzylguanidine (I‑MIBG) heart-to-mediastinum ratio (HMR) at 6 months.

RESULTS

Mean age was 60 ± 9 years, 86% was male and mean LVEF was 33 ± 8%. At 6 months, the primary safety endpoint occurred in 8.3% vs 8.0% in the RDN and OMT groups, respectively (p = 0.97). At 6 months, the mean change in late HMR was -0.02 (95% CI: -0.08 to 0.12) in the RDN group, versus -0.02 (95% CI: -0.09 to 0.12) in the OMT group (p = 0.95) whereas the mean change in washout rate was 2.34 (95% CI: -6.35 to 1.67) in the RDN group versus -2.59 (95% CI: -1.61 to 6.79) in the OMT group (p-value 0.09).

CONCLUSION

RDN with the Vessix system in patients with HFrEF was safe, but did not result in significant changes in cardiac sympathetic nerve activity at 6 months as measured using I‑MIBG.

摘要

引言

本研究旨在评估肾交感神经消融术(RDN)在射血分数降低的心力衰竭(HFrEF)患者中的安全性和有效性。

方法

我们将50例左心室射血分数(LVEF)≤35%且纽约心脏协会(NYHA)心功能分级≥II级的患者按1:1的比例随机分为RDN联合最佳药物治疗(OMT)组或单纯OMT组。主要安全终点是6个月时心血管死亡、因心力衰竭再次住院和急性肾损伤的复合终点事件的发生情况。主要疗效终点是6个月时碘-123间碘苄胍(I-MIBG)心/纵隔比值(HMR)的变化。

结果

平均年龄为60±9岁,男性占86%,平均LVEF为33±8%。6个月时,RDN组和OMT组主要安全终点事件的发生率分别为8.3%和8.0%(p = 0.97)。6个月时,RDN组晚期HMR的平均变化为-0.02(95%可信区间:-0.08至0.12),OMT组为-0.02(95%可信区间:-0.09至0.12)(p = 0.95);而RDN组清除率的平均变化为2.34(95%可信区间:-6.35至1.67),OMT组为-2.59(95%可信区间:-1.61至6.79)(p值为0.09)。

结论

在HFrEF患者中使用Vessix系统进行RDN是安全的,但在6个月时,使用I-MIBG测量未发现心脏交感神经活动有显著变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2eed/8881518/4681c955e72a/12471_2021_1633_Fig1_HTML.jpg

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