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血管内压力反射增强治疗耐药性高血压:CALM-FIM 研究 3 年结果。

Treatment of Resistant Hypertension With Endovascular Baroreflex Amplification: 3-Year Results From the CALM-FIM Study.

机构信息

Department of Vascular Medicine, University Medical Center Utrecht, Utrecht University, the Netherlands.

Division of Cardiology, Emory University School of Medicine, Atlanta, Georgia, USA.

出版信息

JACC Cardiovasc Interv. 2022 Feb 14;15(3):321-332. doi: 10.1016/j.jcin.2021.12.015.

Abstract

OBJECTIVES

The aim of this study was to evaluate the long-term (3-year) safety and effectiveness of endovascular baroreflex amplification (EVBA) from both the European and American CALM-FIM cohorts.

BACKGROUND

The CALM-FIM study demonstrated that EVBA in patients with resistant hypertension significantly lowered blood pressure (BP) with an acceptable safety profile during 6-month follow-up.

METHODS

The CALM-FIM studies were prospective, nonrandomized, first-in-human studies that enrolled patients with resistant hypertension (office systolic BP ≥160 mm Hg and mean 24-hour ambulatory BP ≥130/80 mm Hg despite a stable regimen of ≥3 antihypertensive medications, including a diuretic agent). The incidence of (serious) adverse events and changes in BP, heart rate, and prescribed antihypertensive medication up to 3 years after implantation were determined.

RESULTS

The Mobius device was implanted in 47 patients (30 in Europe, 17 in the United States; mean age 54 years, 23 women). Five serious adverse events (hypotension, n = 2; hypertension, n = 1; vascular access complications, n = 2) and 2 transient ischemic attacks occurred within 30 days postprocedure. Two strokes and 1 transient ischemic attack occurred more than 2 years postimplantation. Mean office BP at baseline was 181 ± 17/107 ± 16 mm Hg and decreased by 25/12 mm Hg (95% CI: 17-33/8-17 mm Hg) at 6 months and 30/12 mm Hg (95% CI: 21-38/8-17 mm Hg) at 3 years. Mean 24-hour ambulatory BP at baseline was 166 ± 16/98 ± 15 mm Hg and decreased by 20/11 mm Hg (95% CI: 14-25/8-15 mm Hg) at 6 months.

CONCLUSIONS

EVBA with the MobiusHD was effective in reducing BP at 3-year follow-up and appears to have an acceptable safety profile in patients with uncomplicated implantation, although data from randomized sham-controlled trials are needed to further evaluate the risk-benefit profile. (Controlling and Lowering Blood Pressure With the MobiusHD™ [CALM-FIM_EUR], NCT01911897; Controlling and Lowering Blood Pressure With the MobiusHD™ [CALM-FIM_US], NCT01831895).

摘要

目的

本研究旨在评估欧洲和美国 CALM-FIM 队列中血管紧张素受体反射增强(EVBA)的长期(3 年)安全性和有效性。

背景

CALM-FIM 研究表明,在接受难治性高血压治疗的患者中,EVBA 可显著降低血压(BP),在 6 个月的随访中具有可接受的安全性。

方法

CALM-FIM 研究为前瞻性、非随机、首次人体研究,纳入难治性高血压患者(诊室收缩压≥160mmHg,平均 24 小时动态血压≥130/80mmHg,尽管使用了稳定的降压药物方案,包括≥3 种降压药物,包括利尿剂)。在植入后 3 年内,确定(严重)不良事件的发生率和 BP、心率以及规定的降压药物的变化。

结果

在 47 名患者(欧洲 30 名,美国 17 名;平均年龄 54 岁,23 名女性)中植入了 Mobius 装置。术后 30 天内发生 5 例严重不良事件(低血压 2 例;高血压 1 例;血管通路并发症 2 例)和 2 例短暂性脑缺血发作。2 例卒中和 1 例短暂性脑缺血发作发生在植入后 2 年以上。基线时诊室 BP 平均为 181±17/107±16mmHg,6 个月时降低 25/12mmHg(95%CI:17-33/8-17mmHg),3 年时降低 30/12mmHg(95%CI:21-38/8-17mmHg)。基线时平均 24 小时动态血压为 166±16/98±15mmHg,6 个月时降低 20/11mmHg(95%CI:14-25/8-15mmHg)。

结论

在 3 年随访时,MobiusHD 介导的 EVBA 可有效降低血压,在无并发症植入的患者中似乎具有可接受的安全性,但需要随机假手术对照试验的数据来进一步评估风险效益比。(用 MobiusHD™ 控制和降低血压[CALM-FIM_EUR],NCT01911897;用 MobiusHD™ 控制和降低血压[CALM-FIM_US],NCT01831895)。

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