Fischell Tim A, Fischell David R, Ghazarossian Vartan E, Vega Félix, Ebner Adrian
Borgess Heart Institute, 1521 Gull Road, Kalamazoo, MI, 49008, USA; Ablative Solutions, 801 Hermosa Way, Menlo Park, CA, 94025, USA.
Ablative Solutions, 801 Hermosa Way, Menlo Park, CA, 94025, USA.
Cardiovasc Revasc Med. 2015 Jun;16(4):221-7. doi: 10.1016/j.carrev.2015.04.008. Epub 2015 May 6.
BACKGROUND/PURPOSE: We update the pre-clinical and early clinical results using a novel endovascular approach, to perform chemical renal denervation, via peri-adventitial injection of micro-doses of dehydrated alcohol (ethanol-EtOH).
METHODS/MATERIALS: A novel, three-needle delivery device (Peregrine™) was used to denervate the renal arteries of adult swine (n = 17) and in a first-in-man feasibility study (n = 18). In the pre-clinical testing EtOH was infused bilaterally with one infusion per renal artery into to the perivascular space, using EtOH doses of 0.3 ml/artery (n = 8), and 0.6 ml/artery (n = 9), and with saline sham control (0.4 ml/artery n = 3). Renal parenchymal norepinephrine (NE) concentration (performed blindly), and safety were the primary endpoints. Data from the first-in-man study (n = 18) to evaluate device performance, safety and peri-procedural pain are reported.
In the pre-clinical testing renal function was unchanged at 3-month follow-up. Angiography at 90 days (n = 34 arteries) demonstrated normal appearing renal arteries, unchanged from baseline, and without stenosis or other abnormalities. The reductions in mean renal parenchymal NE reductions at 3 months were 68% and 88% at doses of 0.3 and 0.6 ml, respectively (p < 0.001 vs. controls). In the first-in-man study, there was 100% device success, no complications, a mean treatment time of 4.3 ± 3 minutes/artery, and minimal or no patient discomfort during treatment. Angiography at 6-months showed no evidence of renal artery stenosis, and evidence of a reduction of blood pressure from baseline.
Perivascular RDN using micro-doses of alcohol is a promising alternative to energy-based systems to achieve dose-dependent, predictable, safe and essentially painless renal denervation. Further clinical evaluation is warranted.
(For annotated table of contents) This paper describes the preclinical results, in a porcine model, and the early first-in-man results, using the Peregrine™ chemical renal denervation catheter to perform renal sympathetic denervation using micro-doses of alcohol.
背景/目的:我们采用一种新型血管内方法,通过在肾外膜周围注射微量脱水酒精(乙醇-EtOH)来进行化学性肾去神经支配,更新临床前和早期临床结果。
方法/材料:一种新型的三针输送装置(Peregrine™)用于对成年猪(n = 17)的肾动脉进行去神经支配,并开展了一项首例人体可行性研究(n = 18)。在临床前测试中,双侧注入EtOH,每条肾动脉向血管周围间隙注入一次,EtOH剂量分别为0.3 ml/动脉(n = 8)和0.6 ml/动脉(n = 9),并设置生理盐水假手术对照组(0.4 ml/动脉,n = 3)。肾实质去甲肾上腺素(NE)浓度(盲法进行)和安全性为主要终点。报告了首例人体研究(n = 18)中评估装置性能、安全性和围手术期疼痛的数据。
在临床前测试中,3个月随访时肾功能未改变。90天时的血管造影(n = 34条动脉)显示肾动脉外观正常,与基线相比无变化,无狭窄或其他异常。3个月时,剂量为0.3 ml和0.6 ml时,平均肾实质NE降低分别为68%和88%(与对照组相比,p < 0.001)。在首例人体研究中,装置成功率为100%,无并发症,平均治疗时间为4.3±3分钟/动脉,治疗期间患者不适轻微或无不适。6个月时的血管造影显示无肾动脉狭窄证据,且有血压较基线降低的证据。
使用微量酒精进行血管周围肾去神经支配是一种有前景的替代基于能量系统的方法,可实现剂量依赖性、可预测、安全且基本无痛的肾去神经支配。有必要进行进一步的临床评估。
(用于带注释的目录)本文描述了在猪模型中的临床前结果,以及使用Peregrine™化学性肾去神经支配导管通过微量酒精进行肾交感神经去神经支配的首例人体早期结果。