Percutaneous coronary intervention in patients undergoing transcatheter aortic valve implantation: a systematic

Hugo M Aarts1,2, Nicole D van Hemert1, Timion A Meijs1,2

  • 1Department of Cardiology, University Medical Centre Utrecht, Utrecht, The Netherlands.

Insights

Percutaneous coronary intervention (PCI) before transcatheter aortic valve implantation (TAVI) for significant coronary artery disease (CAD) did not improve survival or reduce cardiac events. However, PCI increased major bleeding risk within 30 days.

Area of Science:

  • Cardiology
  • Interventional Cardiology
  • Cardiovascular Surgery

Background:

  • Revascularization significance in patients undergoing transcatheter aortic valve implantation (TAVI) with coronary artery disease (CAD) remains unclear.
  • Current guidelines recommend percutaneous coronary intervention (PCI) for significant proximal CAD in TAVI patients, despite limited evidence.

Purpose of the Study:

  • To systematically review and meta-analyze clinical outcomes comparing TAVI with and without preceding PCI in patients with significant CAD.
  • To evaluate the impact of PCI on mortality, cardiac death, stroke, myocardial infarction, and major bleeding.

Main Methods:

  • Systematic literature search for studies comparing TAVI with and without PCI in patients with significant CAD.
  • Meta-analysis of 14 studies involving 3838 patients (1806 received PCI).
  • Primary endpoints included all-cause mortality, cardiac death, stroke, myocardial infarction, and major bleeding.

Main Results:

  • No significant differences in all-cause mortality at 30 days, 1 year, or beyond.
  • No significant differences in cardiac death, stroke, or myocardial infarction risk.
  • PCI before TAVI was associated with a higher risk of major bleeding within 30 days (OR: 0.66; 95% CI: 0.46-0.94).

Conclusions:

  • Concomitant PCI in patients with significant CAD undergoing TAVI showed no significant short- or long-term clinical outcome benefits.
  • PCI prior to TAVI increased the risk of major bleeding within 30 days.
  • Further randomized controlled trials are needed due to the risk of bias in included studies.
Abstract