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Related Experiment Video

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Core/shell Printing Scaffolds For Tissue Engineering Of Tubular Structures
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Extracorporeal Support Vascular Access: 3D Printing Custom Cannulas.

Andrew Zhang1,2, Megha M Jacob1,2, Auldynn J Chambers2

  • 1From the Extracorporeal Life Support Laboratory, Department of Surgery, University of Michigan, Ann Arbor, Michigan.

ASAIO Journal (American Society for Artificial Internal Organs : 1992)
|July 17, 2025
PubMed
Summary
This summary is machine-generated.

This study developed novel 3D-printed 6 Fr cannulas for extracorporeal life support (ECLS) in premature infants. These 3D-printed cannulas demonstrate suitable flow rates for neonatal ECLS applications.

Keywords:
3D printingECMOcannulasextracorporeal life supportextracorporeal membrane oxygenationpremature infantspressure drop

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Area of Science:

  • Biomedical Engineering
  • Medical Device Development
  • Pediatric Critical Care

Background:

  • Extracorporeal life support (ECLS) requires patient-specific vascular access cannulas.
  • Existing drainage cannulas are unsuitable for neonates weighing less than 1.5 kg.

Purpose of the Study:

  • To develop and evaluate a novel 6 Fr drainage cannula for ECLS in small patients using 3D printing.
  • To assess the performance of 3D-printed cannulas in vitro and in vivo.

Main Methods:

  • Cannulas were manufactured using stereolithography 3D printing (Form 3 and Form 3B printers).
  • In vitro testing involved 3% glycerol to measure drainage pressure and flow rates.
  • In vivo testing was conducted using an ECLS piglet model.

Main Results:

  • 3D-printed cannulas demonstrated appropriate flow rates (~100 ml/kg/min) for neonatal ECLS.
  • In vitro tests showed favorable drainage pressures and maximum flow rates for both printer types.
  • In vivo testing in piglets confirmed functional blood flow rates at acceptable drainage pressures.

Conclusions:

  • 3D-printed 6 Fr cannulas are a viable option for ECLS in premature infants.
  • The fabrication process is minimally complex, offering a promising solution for neonatal vascular access.
  • Further preclinical optimization using translational models is recommended.