Changes in thromboinflammatory profiles across the generations of transcatheter aortic heart valves

J Thromb Thrombolysis. 2019 Feb;47(2):174-178. doi: 10.1007/s11239-018-1782-3.

Abstract

The transcatheter aortic valve replacement (TAVR) procedure was developed to provide patients with severe aortic stenosis an alternative to the surgical aortic valve replacement. Since the approval of the original SAPIEN the technology has rapidly evolved. While several approaches can be used for valve deployment, as delivery systems have become smaller and more flexible, the transfemoral approach has become the dominant technique for valve deployment. One hundred and forty five patients undergoing TAVR receiving one of four valve types (Sapien, Sapien XT, Sapien3 or CoreValve) via the femoral artery were included in this study. Platelet count, white blood cells count (WBC), Interleukin-6 (IL-6), and Serum Amyloid A (SAA) were determined before and after TAVR. Platelet counts declined after the procedure regardless of the valve type and were dependent upon the baseline platelet count. Use of conscious sedation blunted the decline in platelet count. With the newer generation valves, the rise in WBC post-TAVR was lower than observed with the Sapien, in keeping with less systemic inflammation. Consistent with WBC, IL-6 levels were lower following deployment of the newer generation valves. Elevations in plasma SAA, which occur following myocardial injury, were not reduced with the newer valves. Evolution of the TAVR technology has occurred rapidly over the last 5 years. The newer devices and smaller delivery systems are associated with less systemic inflammation, as reflected in WBC and plasma IL-6 levels. However, the acute phase reactant SAA remains unchanged, possibly reflecting different triggers for SAA following TAVR.

Keywords: Inflammation; Platelet; Transcatheter aortic valve replacement.

Publication types

  • Comparative Study

MeSH terms

  • Aortic Valve / diagnostic imaging
  • Aortic Valve / physiopathology
  • Aortic Valve / surgery*
  • Aortic Valve Stenosis / diagnostic imaging
  • Aortic Valve Stenosis / physiopathology
  • Aortic Valve Stenosis / surgery*
  • Biomarkers / blood
  • Blood Platelets / metabolism
  • Heart Valve Prosthesis*
  • Humans
  • Inflammation / blood*
  • Inflammation / diagnosis
  • Inflammation / etiology
  • Inflammation Mediators / blood*
  • Interleukin-6 / blood
  • Leukocyte Count
  • Leukocytes / metabolism
  • Platelet Count
  • Prospective Studies
  • Prosthesis Design
  • Risk Factors
  • Serum Amyloid A Protein / metabolism
  • Severity of Illness Index
  • Time Factors
  • Transcatheter Aortic Valve Replacement / adverse effects*
  • Transcatheter Aortic Valve Replacement / instrumentation*
  • Treatment Outcome

Substances

  • Biomarkers
  • IL6 protein, human
  • Inflammation Mediators
  • Interleukin-6
  • Serum Amyloid A Protein