Department of Vascular Medicine, University Medical Center Utrecht, Utrecht University, the Netherlands.
Division of Cardiology, Emory University School of Medicine, Atlanta, Georgia, USA.
JACC Cardiovasc Interv. 2022 Feb 14;15(3):321-332. doi: 10.1016/j.jcin.2021.12.015.
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.
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.
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.
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.
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).
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。
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。
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。
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)。
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)。