Heart failure & cardiomyopathies

Left Atrial to Coronary Sinus Shunting for Treatment of Symptomatic Heart Failure

JACC Cardiovasc IntervPublished Early feasibility study

Authors' conclusion

In this single-arm experience, the APTURE Transcatheter Shunt System in patients with symptomatic HF was observed to be safe and resulted in reduction in pulmonary capillary wedge pressure and clinically meaningful improvements in HF symptoms and quality of life indices.

Study context

Population
Patients with symptomatic heart failure (HF) with pulmonary capillary wedge pressure >15 mm Hg at rest or 25 mm Hg during exerciseattempted implantation
Participants
87 patients
Outcome
Primary safety outcome
Follow-up
30 days
Methodological detailssingle-arm, multicentre (18 centres), Enrolment May 2018 to September 2022
  • Single-arm
  • Multicentre (18 centres)
  • Enrolment May 2018 to September 2022

Main finding

As reported in the abstract

Primary safety outcome occurred in 2 patients

2.3%

Further findings

Device success

Device success achieved in 78 patients
90%

NYHA class I to II · 6 months

Participants achieving NYHA class I to II
67%

KCCQ overall summary score improvement · 6 months

23-point improvement (95% CI: 17-29 points)
P < 0.0001

20-W exercise PCWP · 6 months

7 mm Hg lower (95% CI: −11 to −4 mm Hg)
P < 0.0001
No change in right atrial pressure or other right heart function indices

Safety

Device occlusions or associated adverse events after implantation

No device occlusions or associated adverse events

Original publication

Left Atrial to Coronary Sinus Shunting for Treatment of Symptomatic Heart Failure. JACC Cardiovasc Interv. Published 21 March 2023. doi:10.1016/j.jcin.2023.03.012

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