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Immediate ambulation following diagnostic coronary angiography procedures utilizing a vascular closure device (The

Christopher H Crocker1, Kevin T Cragun, Farris K Timimi

  • 1Division of Cardiovascular Diseases and Internal Medicine, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.

Insights

The Closer device safely and effectively enables immediate ambulation after diagnostic coronary angiography for most patients, achieving 96% hemostasis and allowing 89% to walk immediately.

Area of Science:

  • Cardiology
  • Vascular Surgery
  • Medical Devices

Background:

  • Diagnostic coronary angiography requires vascular access closure.
  • Traditional methods may involve prolonged bed rest, delaying patient ambulation.
  • Suture-mediated closure devices offer a potential alternative for faster recovery.

Purpose of the Study:

  • To evaluate the safety and efficacy of The Closer, a suture-mediated vascular closure device.
  • To assess the feasibility of immediate patient ambulation following its use.
  • To determine the rate of complications associated with The Closer in this setting.

Main Methods:

  • Retrospective analysis of 487 patients undergoing diagnostic coronary angiography.
  • Utilized The Closer device for vascular closure.
  • Implemented an immediate ambulation protocol, with some patients assigned intermediate bed rest.
  • Monitored for hemostasis, bleeding, and access site complications.

Main Results:

  • 89% of patients achieved immediate ambulation (mean 6.3 minutes).
  • 7% experienced intermediate bed rest (mean 105.2 minutes) due to minor bleeding or physician preference.
  • Overall hemostasis was achieved in 96% of patients.
  • A low rate of complications was observed, with 0.8% experiencing recurrent bleeding and no major adverse events like hematoma, fistula, or infection.

Conclusions:

  • The Closer is a safe and effective device for vascular closure after diagnostic coronary angiography.
  • It facilitates rapid patient ambulation, improving patient experience and potentially reducing healthcare costs.
  • The device demonstrates a favorable safety profile with minimal complications.
Abstract

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