Acute kidney injury after percutaneous coronary intervention: Rationale of the AKI-MATRIX (acute kidney injury-minimizing adverse hemorrhagic events by TRansradial access site and systemic implementation of angioX) sub-study

Catheter Cardiovasc Interv. 2015 Nov;86(5):950-7. doi: 10.1002/ccd.25932. Epub 2015 Apr 9.

Abstract

Acute kidney injury (AKI) is an important complication of both diagnostic cardiac catheterization and percutaneous coronary intervention (PCI). A large body of evidence supports that AKI is related to volume of contrast used. Despite several measures are available to reduce the impact of contrast media on AKI, its incidence remains significant as other mechanisms of renal damage are involved. A new paradigm is established according to which bleeding prevention is at least as important as preventing recurrent ischemic events in the management of patients with acute coronary syndromes (ACS) undergoing an invasive approach. Periprocedural bleeding, which is consistently reduced by radial approach, is emerging as a risk factor for the development of AKI. Therefore, the role of vascular access as a measure to prevent AKI needs to be systematically assessed in randomized studies. To date, no prospective comparison on renal outcomes has been carried out in randomized trials between radial and femoral approach. The Minimizing Adverse hemorrhagic events by TRansradial access site and systemic Implementation of AngioX (MATRIX) trial (ClinicalTrials.gov identifier: NCT01433627) has been designed to test whether to minimize bleeding events by using radial access and bivalirudin, across the whole spectrum of patients with ACS undergoing PCI, will result in improved outcomes with respect to both ischemic and bleeding complications. The AKI-MATRIX sub-study will provide a unique opportunity to assess whether the advantages of radial approach may even contribute to the reduction of the risk of AKI in patients with ACS.

Keywords: acute coronary syndromes; acute kidney injury; contrast-induced nephropathy; percutaneous coronary intervention; transradial intervention.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Coronary Syndrome / diagnostic imaging
  • Acute Coronary Syndrome / mortality
  • Acute Coronary Syndrome / therapy*
  • Acute Kidney Injury / diagnosis
  • Acute Kidney Injury / etiology
  • Acute Kidney Injury / mortality
  • Acute Kidney Injury / prevention & control*
  • Antithrombins / administration & dosage*
  • Antithrombins / adverse effects
  • Catheterization, Peripheral / adverse effects
  • Catheterization, Peripheral / methods*
  • Catheterization, Peripheral / mortality
  • Clinical Protocols
  • Contrast Media / adverse effects
  • Coronary Angiography / adverse effects
  • Hemorrhage / diagnosis
  • Hemorrhage / etiology
  • Hemorrhage / mortality
  • Hemorrhage / prevention & control*
  • Hirudins / administration & dosage*
  • Hirudins / adverse effects
  • Humans
  • Incidence
  • Peptide Fragments / administration & dosage*
  • Peptide Fragments / adverse effects
  • Percutaneous Coronary Intervention / adverse effects
  • Percutaneous Coronary Intervention / methods*
  • Percutaneous Coronary Intervention / mortality
  • Prospective Studies
  • Punctures
  • Radial Artery* / diagnostic imaging
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / adverse effects
  • Research Design
  • Risk Factors
  • Time Factors
  • Treatment Outcome

Substances

  • Antithrombins
  • Contrast Media
  • Hirudins
  • Peptide Fragments
  • Recombinant Proteins
  • bivalirudin

Associated data

  • ClinicalTrials.gov/NCT01433627