Evidence map›Paper›PMID 24809724›Full record

ArticleAnnals of biomedical engineering2014

Ex vivo lymphatic perfusion system for independently controlling pressure gradient and transmural pressure in isolated vessels.

Jeffrey A Kornuta, J Brandon Dixon

Open access · greenAbstract read
In one paragraph

Article in Annals of biomedical engineering, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. An adaptable research platform for ex vivo normothermic machine perfusion of the liver.International journal of computer assisted radiology and surgery · 2023
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. The Lymphatic System in Disease Processes and Cancer Progression.Annual review of biomedical engineering · 2016
    Review
  10. Article
  11. Effects of dynamic shear and transmural pressure on wall shear stress sensitivity in collecting lymphatic vessels.American journal of physiology. Regulatory, integrative and comparative physiology · 2015
    Article
  12. Lymph node biophysical remodeling is associated with melanoma lymphatic drainage.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2015
    Article
  13. Mechanobiological oscillators control lymph flow.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  14. Bridging the divide between pathogenesis and detection in lymphedema.Seminars in cell & developmental biology · 2015
    Review
  15. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Jeffrey A KornutaWoodruff School of Mechanical Engineering, Georgia Institute of Technology, Atlanta, GA, 30332, USA.
J Brandon Dixon
Georgia Institute of Technology · US

Funding

Quantifying the role of load-induced remodeling in lymphedema progressionR01HL113061 · NHLBI · GEORGIA INSTITUTE OF TECHNOLOGY · PI DIXON, JAMES BRANDON · 2013 to 2017
$2.2M
Quantifying the role of lymphatics in lipid metabolism and transportR00HL091133 · NHLBI · GEORGIA INSTITUTE OF TECHNOLOGY · PI DIXON, JAMES BRANDON · 2009 to 2011
$716k
NHLBI NIH HHS R00 HL091133NHLBI NIH HHS R00HL091133NHLBI NIH HHS R01 HL113061NHLBI NIH HHS R01HL113061
6 · The paper itself

Abstract

In addition to external forces, collecting lymphatic vessels intrinsically contract to transport lymph from the extremities to the venous circulation. As a result, the lymphatic endothelium is routinely exposed to a wide range of dynamic mechanical forces, primarily fluid shear stress and circumferential stress, which have both been shown to affect lymphatic pumping activity. Although various ex vivo perfusion systems exist to study this innate pumping activity in response to mechanical stimuli, none are capable of independently controlling the two primary mechanical forces affecting lymphatic contractility: transaxial pressure gradient, [Formula: see text], which governs fluid shear stress; and average transmural pressure, [Formula: see text], which governs circumferential stress. Hence, the authors describe a novel ex vivo lymphatic perfusion system (ELPS) capable of independently controlling these two outputs using a linear, explicit model predictive control (MPC) algorithm. The ELPS is capable of reproducing arbitrary waveforms within the frequency range observed in the lymphatics in vivo, including a time-varying [Formula: see text] with a constant [Formula: see text], time-varying [Formula: see text] and [Formula: see text], and a constant [Formula: see text] with a time-varying [Formula: see text]. In addition, due to its implementation of syringes to actuate the working fluid, a post-hoc method of estimating both the flow rate through the vessel and fluid wall shear stress over multiple, long (5 s) time windows is also described.

Indexed as

AlgorithmsAnimalsPerfusionPressureRats, Sprague-DawleyStress, MechanicalThoracic Duct

Identifiers

PMID24809724
PMCPMC4437633
OpenAlexW2068581049

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.