IDEAS home Printed from https://ideas.repec.org/a/taf/gcmbxx/v14y2011i05p411-424.html
   My bibliography  Save this article

Cellular-scale transport in deformed skeletal muscle following spinal cord injury

Author

Listed:
  • Yael Ruschkewitz
  • Amit Gefen

Abstract

Deep tissue injury (DTI) is a severe pressure ulcer initiating in weight-bearing skeletal muscles. Being common in spinal cord injury (SCI) patients, DTI is associated with mechanical cell damage and ischaemia. Muscle microanatomy in SCI patients is characterised by reduced myofibre sizes and smaller, fewer capillaries. We hypothesise that these changes influence mass transport in SCI muscles, making DTI more probable. Using multiphysics models of microscopic cross-sections through normal and SCI muscles, we studied effects of the following factors on transport of glucose and myoglobin (potential biomarker for early DTI detection): (i) abnormal SCI muscle microanatomy, (ii) large tissue deformations and (iii) ischaemia. We found that the build-up of concentrations of glucose and myoglobin is slower for SCI muscles, which could be explained by the pathological SCI microanatomy. These findings overall suggest that microanatomical changes in muscles post-SCI play an important role in the vulnerability of the SCI patients to DTI.

Suggested Citation

  • Yael Ruschkewitz & Amit Gefen, 2011. "Cellular-scale transport in deformed skeletal muscle following spinal cord injury," Computer Methods in Biomechanics and Biomedical Engineering, Taylor & Francis Journals, vol. 14(05), pages 411-424.
  • Handle: RePEc:taf:gcmbxx:v:14:y:2011:i:05:p:411-424
    DOI: 10.1080/10255842.2010.529804
    as

    Download full text from publisher

    File URL: http://hdl.handle.net/10.1080/10255842.2010.529804
    Download Restriction: Access to full text is restricted to subscribers.

    File URL: https://libkey.io/10.1080/10255842.2010.529804?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:taf:gcmbxx:v:14:y:2011:i:05:p:411-424. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Chris Longhurst (email available below). General contact details of provider: http://www.tandfonline.com/gcmb .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.