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Related Concept Videos

Scanning Electron Microscopy01:07

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A scanning electron microscope (SEM) is used to study the surface features of a sample by using an electron beam that scans the sample surface in a two-dimensional manner. Typically, areas between ~1 centimeter to 5 micrometers in width can be imaged. SEM can be used to image bacteria, viruses, tissues as well as larger samples like insects. Conventional SEM gives a magnification ranging from 20X to 30,000X and spatial resolution of 50 to 100 nanometers.
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Related Experiment Video

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Measuring and Modeling Contractile Drying in Human Stratum Corneum
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The subepidermal moisture scanner: the technology explained.

Amit Gefen1, Graham Ross2

  • 1Professor of Biomedical Engineering, The Herbert J. Berman Chair in Vascular Bioengineering; Department of Biomedical Engineering, Faculty of Engineering, Tel Aviv University, Tel Aviv 6997801 Israel.

Journal of Wound Care
|February 15, 2020
PubMed
Summary
This summary is machine-generated.

The subepidermal moisture (SEM) scanner detects early signs of tissue fluid changes, specifically micro-oedema, to identify pressure ulcers (PUs) before skin breakdown occurs. This technology aids in proactive patient care and prevention of pressure injuries.

Keywords:
SEM scannerlaboratory testing and modellinglocalised oedemapressure injurypressure ulcerpressure ulcer prevention

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Area of Science:

  • Biophysics
  • Biomedical Engineering
  • Medical Device Technology

Background:

  • Pressure ulcers (PUs) are a significant clinical concern, often developing under intact skin.
  • Early detection of tissue changes is crucial for preventing PU formation.
  • Existing methods may not detect the earliest physiological alterations preceding visible skin damage.

Purpose of the Study:

  • To explain the biophysical principles and design of the subepidermal moisture (SEM) scanner.
  • To describe the operational mode of the SEM scanner for monitoring tissue health.
  • To detail its application in detecting early signs of pressure ulcers (PUs) or pressure injuries.

Main Methods:

  • Measuring tissue capacitance (biocapacitance) to assess fluid content at a depth of several millimeters.
  • Utilizing the 'SEM-delta' value to compare measurements between healthy and at-risk tissue sites.
  • Employing computer simulations (in silico) and laboratory testing prior to clinical application.

Main Results:

  • The SEM scanner effectively detects micro-oedema, an early indicator of PU development.
  • The SEM-delta calculation normalizes for systemic fluid changes, providing a reliable quantitative measure.
  • Clinical trials demonstrate the SEM scanner's success in early PU detection under intact skin.

Conclusions:

  • The SEM scanner's technology, based on measuring biocapacitance and detecting micro-oedema, enables early identification of pressure ulcers.
  • Targeting the physical biomarker of oedema contributes to the device's documented clinical efficacy.
  • The SEM scanner represents a significant advancement in non-invasive tissue monitoring for PU prevention.