What are the indications for AngioVac (percutaneous venous cannula system)?

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Last updated: April 11, 2025View editorial policy

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From the Guidelines

The AngioVac system is primarily indicated for the removal of unwanted intravascular material, such as fresh, soft thrombi or emboli, in the venous system, right heart, and pulmonary arteries, particularly for large-volume clot burden that may be difficult to treat with conventional therapies. The indications for AngioVac include:

  • Right atrial or ventricular thrombi
  • Inferior vena cava thrombi
  • Iliofemoral deep vein thrombosis
  • Pulmonary emboli
  • Vegetation removal from cardiac devices or valves
  • Tumor thrombi As reported by the American Heart Association in 2019 1, AngioVac thrombectomy in the PAs has been associated with hemodynamic collapse and RV free wall perforation, highlighting the need for careful patient selection and specialized training. The procedure involves a veno-venous bypass circuit where blood is removed through a large-bore cannula, filtered to remove unwanted material, and then returned to the patient. AngioVac is typically considered when traditional anticoagulation therapy is contraindicated, has failed, or when there is a high risk of complications from standard therapies, as seen in the largest systematic review of AngioVac use, which described access-site hematomas, fatal retroperitoneal bleed, and ICH in some patients 1. Potential complications include vascular injury, bleeding, hemolysis, and air embolism, so patient selection is crucial, and the procedure requires specialized training and equipment, including cardiac surgery backup, and is generally performed in a hybrid operating room or cardiac catheterization laboratory. Recovery time varies based on the underlying condition, but most patients require 24-48 hours of monitoring post-procedure. It is essential to weigh the benefits and risks of AngioVac use, considering the potential for hemodynamic collapse and other complications, as reported in the MAUDE database search, which revealed 34 cases of hemodynamic collapse related to the AngioVac device 1.

From the Research

Indications for Angiovac

  • Intracardiac mass 2, 3
  • Caval thrombus 2, 4
  • Catheter-associated thrombus 2
  • Pulmonary embolism (PE) 2, 4, 5
  • Endocarditis 4, 3
  • Deep vein thrombosis (DVT) 4, 3, 6
  • Right-sided vegetations and right atrial/caval venous thrombi 4
  • Septic emboli 3
  • Cardiac masses 3

Patient Selection

  • Patients who are poor candidates for surgical embolectomy or thrombolytic therapy 2
  • Patients with large central thrombi or masses in-transit who are at risk of complicated PE 2
  • Patients with right-sided endocarditis requiring vegetation debulking, intravascular thrombi, or cardiac masses 3
  • Patients with iliofemoral DVT and long life expectancy 6
  • Patients with acute limb-threatening venous occlusion or severe symptoms from DVT 6

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Percutaneous Vacuum-Assisted Thrombectomy Using AngioVac Aspiration System.

Cardiovascular revascularization medicine : including molecular interventions, 2020

Research

Effectiveness of the vacuum assisted aspiration AngioVac system in the removal of intravascular masses.

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions, 2023

Research

Deep vein thrombosis and pulmonary embolism.

Lancet (London, England), 2016

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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