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心力衰竭患者中无线左心房压力监测系统的安全性、可用性和性能:VECTOR-HF试验

Safety, usability, and performance of a wireless left atrial pressure monitoring system in patients with heart failure: the VECTOR-HF trial.

作者信息

D'Amario Domenico, Meerkin David, Restivo Attilio, Ince Hüseyin, Sievert Horst, Wiese Andrea, Schaefer Ulrich, Trani Carlo, Bayes-Genis Antoni, Leyva Francisco, Whinnett Zachary I, Di Mario Carlo, Jonas Michael, Manhal Habib, Amat-Santos Ignacio J, Del Trigo Maria, Gal Tuvia Ben, Avraham Binyamin Ben, Hasin Tal, Feickert Sebastian, D'Ancona Giuseppe, Altisent Omar Abdul-Jawad, Koren Oran, Caspi Oren, Abraham William T, Crea Filippo, Anker Stefan D, Kornowski Ran, Perl Leor

机构信息

Department of Cardiovascular Sciences, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Department of Cardiovascular and Thoracic Sciences, Catholic University of the Sacred Heart, Rome, Italy.

出版信息

Eur J Heart Fail. 2023 Jun;25(6):902-911. doi: 10.1002/ejhf.2869. Epub 2023 May 10.

Abstract

AIMS

In heart failure (HF), implantable haemodynamic monitoring devices have been shown to optimize therapy, anticipating clinical decompensation and preventing hospitalization. Direct left-sided haemodynamic sensors offer theoretical benefits beyond pulmonary artery pressure monitoring systems. We evaluated the safety, usability, and performance of a novel left atrial pressure (LAP) monitoring system in HF patients.

METHODS AND RESULTS

The VECTOR-HF study (NCT03775161) was a first-in-human, prospective, multicentre, single-arm, clinical trial enrolling 30 patients with HF. The device consisted of an interatrial positioned leadless sensor, able to transmit LAP data wirelessly. After 3 months, a right heart catheterization was performed to correlate mean pulmonary capillary wedge pressure (PCWP) with simultaneous mean LAP obtained from the device. Remote LAP measurements were then used to guide patient management. The miniaturized device was successfully implanted in all 30 patients, without acute major adverse cardiac and neurological events (MACNE). At 3 months, freedom from short-term MACNE was 97%. Agreement between sensor-calculated LAP and PCWP was consistent, with a mean difference of -0.22 ± 4.92 mmHg, the correlation coefficient and the Lin's concordance correlation coefficient values were equal to 0.79 (p < 0.0001) and 0.776 (95% confidence interval 0.582-0.886), respectively. Preliminary experience with V-LAP-based HF management was associated with significant improvements in New York Heart Association (NYHA) functional class (32% of patients reached NYHA class II at 6 months, p < 0.005; 60% of patients at 12 months, p < 0.005) and 6-min walk test distance (from 244.59 ± 119.59 m at baseline to 311.78 ± 129.88 m after 6 months, p < 0.05, and 343.95 ± 146.15 m after 12 months, p < 0.05).

CONCLUSION

The V-LAP™ monitoring system proved to be generally safe and provided a good correlation with invasive PCWP. Initial evidence also suggests possible improvement in HF clinical symptoms.

摘要

目的

在心力衰竭(HF)患者中,植入式血流动力学监测设备已被证明可优化治疗,预测临床失代偿并预防住院。直接左侧血流动力学传感器具有超越肺动脉压力监测系统的理论优势。我们评估了一种新型左心房压力(LAP)监测系统在HF患者中的安全性、可用性和性能。

方法与结果

VECTOR-HF研究(NCT03775161)是一项首次人体、前瞻性、多中心、单臂临床试验,纳入30例HF患者。该设备由一个位于心房内的无导线传感器组成,能够无线传输LAP数据。3个月后,进行右心导管检查,以将平均肺毛细血管楔压(PCWP)与从该设备获得的同步平均LAP进行关联。然后使用远程LAP测量来指导患者管理。该小型化设备成功植入所有30例患者,无急性重大心脏和神经不良事件(MACNE)。3个月时,短期无MACNE的比例为97%。传感器计算的LAP与PCWP之间的一致性良好,平均差值为-0.22±4.92 mmHg,相关系数和林氏一致性相关系数值分别为0.79(p<0.0001)和0.776(95%置信区间0.582-0.886)。基于V-LAP的HF管理的初步经验与纽约心脏协会(NYHA)功能分级的显著改善相关(6个月时32%的患者达到NYHA II级,p<0.005;12个月时60%的患者达到NYHA II级,p<0.005)以及6分钟步行试验距离的改善(从基线时的244.59±119.59米增加到6个月后的311.78±129.88米,p<0.05,12个月后为343.95±146.15米,p<0.05)。

结论

V-LAP™监测系统被证明总体安全,与有创PCWP具有良好的相关性。初步证据还表明HF临床症状可能得到改善。

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