Department of Internal Medicine, Saarland University Hospital, Geb. 41, Kirrberger Strasse 1, 66421 Homburg/Saar, Germany.
Department of Nephrology and Hypertension, University Hospital Erlangen, Maximilianspl. 2, 91054 Erlangen, Germany.
Eur Heart J. 2019 Nov 1;40(42):3474-3482. doi: 10.1093/eurheartj/ehz118.
Several studies and registries have demonstrated sustained reductions in blood pressure (BP) after renal denervation (RDN). The long-term safety and efficacy after RDN in real-world patients with uncontrolled hypertension, however, remains unknown. The objective of this study was to assess the long-term safety and efficacy of RDN, including its effects on renal function.
The Global SYMPLICITY Registry is a prospective, open-label registry conducted at 196 active sites worldwide in hypertensive patients receiving RDN treatment. Among 2237 patients enrolled and treated with the SYMPLICITY Flex catheter, 1742 were eligible for follow-up at 3 years. Baseline office and 24-h ambulatory systolic BP (SBP) were 166 ± 25 and 154 ± 18 mmHg, respectively. SBP reduction after RDN was sustained over 3 years, including decreases in both office (-16.5 ± 28.6 mmHg, P < 0.001) and 24-h ambulatory SBP (-8.0 ± 20.0 mmHg; P < 0.001). Twenty-one percent of patients had a baseline estimated glomerular filtration rate (eGFR) <60 mL/min/1.73 m2. Between baseline and 3 years, renal function declined by 7.1 mL/min/1.73 m2 in patients without chronic kidney disease (CKD; eGFR ≥60 mL/min/1.73 m2; baseline eGFR 87 ± 17 mL/min/1.73 m2) and by 3.7 mL/min/1.73 m2 in patients with CKD (eGFR <60 mL/min/1.73 m2; baseline eGFR 47 ± 11 mL/min/1.73 m2). No long-term safety concerns were observed following the RDN procedure.
Long-term data from the Global SYMPLICITY Registry representing the largest available cohort of hypertensive patients receiving RDN in a real-world clinical setting demonstrate both the safety and efficacy of the procedure with significant and sustained office and ambulatory BP reductions out to 3 years.
多项研究和注册研究表明,肾去神经术(RDN)可使血压(BP)持续降低。然而,在未得到控制的高血压的真实世界患者中,RDN 后的长期安全性和疗效仍不清楚。本研究旨在评估 RDN 的长期安全性和疗效,包括其对肾功能的影响。
全球 SYMPLICITY 注册研究是一项在全球 196 个活跃地点进行的前瞻性、开放性注册研究,在接受 RDN 治疗的高血压患者中开展。在 2237 名接受 SYMPLICITY Flex 导管治疗的患者中,1742 名患者符合 3 年随访条件。基线时诊室和 24 小时动态收缩压(SBP)分别为 166±25mmHg 和 154±18mmHg。RDN 后 SBP 持续降低超过 3 年,包括诊室 SBP 降低(-16.5±28.6mmHg,P<0.001)和 24 小时动态 SBP 降低(-8.0±20.0mmHg;P<0.001)。21%的患者基线估算肾小球滤过率(eGFR)<60mL/min/1.73m2。在无慢性肾脏病(CKD;eGFR≥60mL/min/1.73m2;基线 eGFR 87±17mL/min/1.73m2)的患者中,从基线到 3 年时肾功能下降 7.1mL/min/1.73m2,在 CKD(eGFR<60mL/min/1.73m2;基线 eGFR 47±11mL/min/1.73m2)患者中肾功能下降 3.7mL/min/1.73m2。RDN 术后未观察到长期安全性问题。
全球 SYMPLICITY 注册研究的长期数据代表了最大的接受 RDN 的高血压患者真实世界队列,证明了该治疗方法的安全性和疗效,可显著且持续降低诊室和动态血压,长达 3 年。