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Percutaneous large-bore axillary access is a safe alternative to surgical approach: A systematic review
Geoffrey Southmayd1, Azizul Hoque1, Amir Kaki2
1Division of Cardiology, Emory University School of Medicine, Atlanta, Georgia.
Insights
Large-bore axillary arterial access via percutaneous transaxillary (pTAX) and surgical transaxillary (sTAX) approaches show similar cardiovascular outcomes. The pTAX approach demonstrated significantly less major bleeding compared to the sTAX method.
Area of Science:
- Cardiovascular Interventions
- Vascular Access Techniques
- Interventional Cardiology
Background:
- Severe peripheral arterial disease (PAD) can preclude traditional femoral artery access for cardiac interventions.
- The axillary artery serves as an alternative access route for procedures like transcatheter aortic valve replacement (TAVR) and mechanical circulatory support.
- Limited comparative data exists between percutaneous transaxillary (pTAX) and surgical transaxillary (sTAX) approaches.
Purpose of the Study:
- To systematically review and compare cardiovascular outcomes of large-bore axillary arterial access using percutaneous and surgical methods.
- To evaluate the safety and efficacy of pTAX versus sTAX approaches in patients undergoing cardiac interventions.
Main Methods:
- A systematic literature search of Pubmed and Medline databases was conducted up to January 2019.
- Studies involving pTAX or sTAX approaches for TAVR or Impella insertion were included.
- Primary outcomes assessed included access-related mortality, 30-day mortality, stroke, major vascular complications, and major bleeding.
Main Results:
- Twenty-two studies met inclusion criteria, with heterogeneous patient data (69% TAVR/31% Impella for pTAX; 96% TAVR/4% Impella for sTAX).
- The pTAX group experienced more cardiogenic shock.
- Compared to sTAX, pTAX showed similar 30-day mortality, stroke rates, and major vascular complications, but significantly less major bleeding (2.7% vs. 17.9%).
Conclusions:
- Large-bore percutaneous transaxillary access demonstrates comparable 30-day mortality, stroke rates, and major vascular complications to the surgical transaxillary approach.
- The percutaneous approach offers a significant advantage by reducing major bleeding events.
- Further studies are warranted to validate these findings.
Objectives:
To systematically review relevant literature regarding cardiovascular outcomes of large-bore axillary arterial access via percutaneous and surgical approaches.
Background:
In patients with severe peripheral arterial disease (PAD) undergoing cardiac interventions, large-bore femoral access may be prohibitive. The axillary artery provides an alternative vascular access for transcatheter aortic valve replacement (TAVR) or mechanical circulatory support. There have been limited comparisons of percutaneous transaxillary (pTAX) approach with the more traditional surgical transaxillary (sTAX) approach.
Methods:
Pubmed and Medline databases were queried through January 2019 for studies describing pTAX or sTAX approaches with TAVR or Impella insertion. Primary outcomes were access-related mortality, 30-day mortality, stroke, major vascular complications, and major bleeding.
Results:
One hundred and fifty five studies were reviewed, with additional unpublished data from 1 institution. Twenty-two studies met the inclusion criteria. Patient data was heterogeneous, with 69% TAVR and 31% Impella use in the pTAX group, and 96% TAVR and 4% Impella use in the sTAX group. There was more cardiogenic shock in the pTAX group. When compared to surgical approach, the percutaneous approach had similar 30-day mortality for TAVR (5.6% vs 4.6%, OR non-significant) and Impella (43.4% vs 38.6%, OR non-significant), similar stroke rates (4.3% vs 4.2%, OR non-significant), similar major vascular complications (2.8% vs 2.3%, OR non-significant) and less major bleeding (2.7% vs 17.9%, OR significant).
Conclusions:
Data suggests large-bore pTAX access has similar 30-day mortality, stroke rates, and major vascular complications as sTAX access, with less major bleeding. Additional studies are needed to validate results.
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