Literature DB >> 12918578

Flow vectorial analysis in an artificial implantable lung.

Akio Funakubo1, Ichiro Taga, John W McGillicuddy, Yasuhiro Fukui, Ronald B Hirschl, Robert H Bartlett.   

Abstract

An artificial implantable lung would be a useful device to support patients awaiting lung transplantation. A suitable device must offer low resistance and adequate gas exchange, be impermeable to plasma, and nonthrombogenic. Although plasma permeability is an intrinsic quality of the materials, the other requirements are largely a function of device geometry, particularly as it relates to fluid dynamics. Using a CAD system and the requirements of a membrane surface area of 1.5 m2 and an inlet outlet port distance of 12 cm, we designed 10 models that varied in their other dimensions. Computational fluid dynamic (CFD) software was applied to the models to determine which minimized regions of low flow velocity. A prototype built to these specifications was used in an in vivo ovine experiment to verify the CFD predictions. The prototype was placed in parallel to the native pulmonary circulation (pulmonary artery to left atrium) for 120 minutes while the activated coagulation times were kept between 110 and 120 seconds and device flow was maintained between 1.5 and 2.5 L/min. Examination of the prototype confirmed a correlation between predicted areas of low flow and thrombus formation. Although nearly identical low flow velocity conditions exist at both the inlet and outlet ports, thrombus formation occurs only near the outlet port. This finding agrees with detailed vectorial analysis, which predicts a more complex flow pattern near the outlet port. Although near the inlet port flow vectors are nearly parallel, near the outlet port flow vectors collide. This area of flow collision corresponds to the area of thrombus formation in vivo. The addition of microflow vectorial analysis to flow velocity predictions allows for improved accuracy in predicting regions at risk of thrombosis in an artificial implantable lung.

Entities:  

Mesh:

Year:  2003        PMID: 12918578

Source DB:  PubMed          Journal:  ASAIO J        ISSN: 1058-2916            Impact factor:   2.872


  13 in total

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4.  A mock circulation loop to test extracorporeal CO2 elimination setups.

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5.  THE ROLE OF POROUS MEDIA IN MODELING FLUID FLOW WITHIN HOLLOW FIBER MEMBRANES OF THE TOTAL ARTIFICIAL LUNG.

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6.  Effect of blood flow on platelets, leukocytes, and extracellular vesicles in thrombosis of simulated neonatal extracorporeal circulation.

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Journal:  J Thromb Haemost       Date:  2019-11-14       Impact factor: 5.824

7.  Life span of different extracorporeal membrane systems for severe respiratory failure in the clinical practice.

Authors:  Alois Philipp; Filip De Somer; Maik Foltan; Andre Bredthauer; Lars Krenkel; Florian Zeman; Karla Lehle
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Review 8.  Physiological and Technical Considerations of Extracorporeal CO2 Removal.

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9.  Impact of membrane lung surface area and blood flow on extracorporeal CO2 removal during severe respiratory acidosis.

Authors:  Christian Karagiannidis; Stephan Strassmann; Daniel Brodie; Philine Ritter; Anders Larsson; Ralf Borchardt; Wolfram Windisch
Journal:  Intensive Care Med Exp       Date:  2017-08-01

10.  Bench Validation of a Compact Low-Flow CO2 Removal Device.

Authors:  Alexandra G May; R Garrett Jeffries; Brian J Frankowski; Greg W Burgreen; William J Federspiel
Journal:  Intensive Care Med Exp       Date:  2018-09-24
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