TY - JOUR
T1 - Safety, usability, and performance of a wireless left atrial pressure monitoring system in patients with heart failure
T2 - the VECTOR-HF trial
AU - the VECTOR-HF Trial Investigators
AU - D'Amario, Domenico
AU - Meerkin, David
AU - Restivo, Attilio
AU - Ince, Hüseyin
AU - Sievert, Horst
AU - Wiese, Andrea
AU - Schaefer, Ulrich
AU - Trani, Carlo
AU - Bayes-Genis, Antoni
AU - Leyva, Francisco
AU - Whinnett, Zachary I.
AU - Di Mario, Carlo
AU - Jonas, Michael
AU - Manhal, Habib
AU - Amat-Santos, Ignacio J.
AU - Del Trigo, Maria
AU - Gal, Tuvia Ben
AU - Avraham, Binyamin Ben
AU - Hasin, Tal
AU - Feickert, Sebastian
AU - D'Ancona, Giuseppe
AU - Altisent, Omar Abdul Jawad
AU - Koren, Oran
AU - Caspi, Oren
AU - Abraham, William T.
AU - Crea, Filippo
AU - Anker, Stefan D.
AU - Kornowski, Ran
AU - Perl, Leor
N1 - Publisher Copyright:
© 2023 The Authors. European Journal of Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.
PY - 2023/6
Y1 - 2023/6
N2 - 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.
AB - 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.
KW - Device
KW - Digital health
KW - Haemodynamic remote monitoring
KW - Heart failure
KW - Remote care
UR - http://www.scopus.com/inward/record.url?scp=85159123292&partnerID=8YFLogxK
U2 - 10.1002/ejhf.2869
DO - 10.1002/ejhf.2869
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C2 - 37092287
AN - SCOPUS:85159123292
SN - 1388-9842
VL - 25
SP - 902
EP - 911
JO - European Journal of Heart Failure
JF - European Journal of Heart Failure
IS - 6
ER -