Meta-Analysis of Usefulness of Percutaneous Left Ventricular Assist Devices for High-Risk Percutaneous Coronary

Alexandros Briasoulis1, Tesfaye Telila1, Mohan Palla1

  • 1Division of Cardiology, Detroit Medical Center, Wayne State University, Detroit, Michigan.

Insights

Percutaneous left ventricular assist devices (PVADs) support high-risk PCI patients. Impella and TandemHeart devices show comparable short-term mortality and bleeding rates in this population.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Medical Devices

Background:

  • High-risk percutaneous coronary intervention (PCI) is complex, involving patients with extensive coronary artery disease, reduced left ventricular function, and high surgical risk.
  • Percutaneous left ventricular assist devices (PVADs) offer crucial hemodynamic support in these challenging PCI cases.

Purpose of the Study:

  • To systematically evaluate the impact of PVADs on mortality, myocardial infarction, and complication rates in patients undergoing high-risk PCI.
  • To compare the periprocedural outcomes of Impella and TandemHeart devices in high-risk PCI.

Main Methods:

  • A systematic literature search was conducted across MEDLINE, PUBMED, EMBASE, and Cochrane for prospective controlled trials and cohort studies.
  • Studies focused on patients receiving hemodynamic support with PVADs during high-risk PCI.
  • Primary outcomes included 30-day mortality, 30-day myocardial infarction, major bleeding, and vascular complications.

Main Results:

  • The analysis included 12 studies with 1,346 participants using Impella 2.5 L and 8 cohort studies with 205 participants using TandemHeart.
  • Short-term mortality rates were 3.5% for Impella and 8% for TandemHeart.
  • Major bleeding rates were 7.1% for Impella and 3.6% for TandemHeart.

Conclusions:

  • Both Impella and TandemHeart PVADs demonstrate comparable periprocedural outcomes in patients undergoing high-risk PCI.
  • PVADs provide essential hemodynamic support for high-risk PCI, with similar safety and efficacy profiles between the two devices studied.

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