Different venous approaches for implantation of cardiac electronic devices. A network meta-analysis

Ioannis Anagnostopoulos1, Charalampos Kossyvakis1, Maria Kousta1

  • 1Cardiology Department, Athens General Hospital "G. Gennimatas", Athens, Greece.

Insights

Axillary vein puncture (AVP) and cephalic vein cutdown (CVC) reduce risks of pneumothorax and lead failure compared to subclavian vein puncture (SVP). AVP may decrease the need for additional venous access, warranting further clinical investigation.

Area of Science:

  • Cardiology
  • Medical Devices
  • Interventional Procedures

Background:

  • Venous access for cardiac device implantation is linked to complications.
  • Previous studies suggest cephalic vein cutdown (CVC) is safer but less effective than subclavian vein puncture (SVP).
  • Comparisons involving axillary vein puncture (AVP) are limited.

Purpose of the Study:

  • To compare the safety and efficacy of different venous access techniques for cardiac device lead placement.
  • To evaluate pneumothorax and lead failure rates across subclavian vein puncture (SVP), cephalic vein cutdown (CVC), and axillary vein puncture (AVP).

Main Methods:

  • A systematic literature search was conducted for studies comparing at least two venous access approaches.
  • A frequentist random effects network meta-analysis was employed.
  • Outcomes analyzed included pneumothorax, lead failure (LF), bleeding, infectious complications, and procedural success.

Main Results:

  • Thirty-six studies were analyzed, primarily comparing SVP and CVC.
  • Both AVP and CVC showed reduced odds of pneumothorax and LF compared to SVP.
  • No significant differences in pneumothorax or LF were found between AVP and CVC. CVC more frequently required additional venous access compared to AVP and SVP.

Conclusions:

  • Axillary vein puncture (AVP) and cephalic vein cutdown (CVC) appear safer than subclavian vein puncture (SVP) regarding pneumothorax and lead failure.
  • AVP may reduce the need for repeat venous access compared to CVC.
  • Further clinical evaluation of AVP is recommended.
Abstract