Sharp Andrew S P, Fisher Naomi D L
School of Medicine, University College Dublin, Dublin, Ireland.
Dept of Cardiology, Mater Misericordiae University Hospital, Dublin, Ireland.
Am J Hypertens. 2025 Jul 23. doi: 10.1093/ajh/hpaf134.
Hypertension represents the leading risk factor for death globally, affecting one in two adults. Despite dozens of inexpensive medications and lifestyle changes that effectively lower blood pressure, hypertension control rates remain poor. Renal denervation (RDN) is a procedural therapy indicated as an adjunctive treatment for high blood pressure. FDA approval in late 2023 followed the publication of a series of rigorous, second-generation, randomized clinical trials that demonstrated safety and efficacy of the procedure. Two catheters employing radiofrequency (Spyral) and ultrasound (Paradise) are currently approved to ablate renal sympathetic nerves. In randomized sham-controlled trials, RDN lowered blood pressure in patients with mild-to-moderate and true resistant hypertension, and in patients both on and off anti-hypertensive medication. When evaluating patients for RDN, shared decision-making is a critical element, which should include potential benefits and that a minority may not respond to the therapy. There is only one constant predictor of magnitude of response: magnitude of baseline SBP, which is one reason why guidelines recommend prioritization of patients with resistant hypertension, together with patients whose BP cannot be effectively managed with medication. Before referring patients to a trained interventionalist, it is important to optimize medical therapy and adherence, and confirm uncontrolled hypertension out-of-office. Patients should be screened for primary aldosteronism and for other secondary causes of hypertension if clinically indicated, though sleep apnea is not a contraindication to RDN. A team approach is advised, with hypertension specialists and interventionalists collaborating. Data from global registries will augment our knowledge and guide future implementation.
高血压是全球死亡的主要风险因素,影响着二分之一的成年人。尽管有几十种廉价药物和生活方式改变可有效降低血压,但高血压控制率仍然很低。肾去神经支配术(RDN)是一种作为高血压辅助治疗的程序性疗法。2023年末,美国食品药品监督管理局(FDA)批准了该疗法,此前发表了一系列严格的第二代随机临床试验,证明了该手术的安全性和有效性。目前,两种采用射频(Spyral)和超声(Paradise)的导管被批准用于消融肾交感神经。在随机假手术对照试验中,RDN降低了轻度至中度高血压患者、真正顽固性高血压患者以及正在服用和未服用抗高血压药物患者的血压。在评估RDN患者时,共同决策是一个关键要素,这应包括潜在益处以及少数患者可能对该治疗无反应。唯一能持续预测反应程度的因素是基线收缩压(SBP)的幅度,这就是指南建议优先考虑顽固性高血压患者以及血压无法通过药物有效控制的患者的原因之一。在将患者转诊给训练有素的介入专家之前,优化药物治疗和依从性,并在诊室外确认高血压未得到控制非常重要。如果临床有指征,应筛查患者是否患有原发性醛固酮增多症和其他继发性高血压病因,不过睡眠呼吸暂停并非RDN的禁忌证。建议采用团队方法,由高血压专家和介入专家合作。全球登记处的数据将增加我们的知识并指导未来的实施。