Prolonged loading on the skin can cause pressure ulcers. The loading leads to tissue deformation, causing local injury to the skin or underlying tissue. Current preventive methods are based on risk assessment and periodic control. However, these methods are subjective and there is a great need for more objective tools. Soetens discovered a set of indicators that enable early detection of pressure ulcer development. The set consists of metabolic and inflammatory biomarkers, of which the latter even have the potential to identify patients at risk.

Early detection

In order to survive prolonged loading, cells in the tissue must switch to anaerobic metabolism. The tissue also becomes inflamed. Soetens wanted to investigate whether these two reactions are measurable on the skin. He subjected a group of healthy volunteers to controlled loading of the sacrum, the largest vertebra, which is prone to pressure ulcer development. He then monitored the release of metabolic and inflammatory biomarkers, obtained from sweat and sebum on the skin surface.

Anaerobic metabolism appears to be visible at the skin tissue via lactate and pyruvate. Inflamed skin tissue is detectable via cytokine IL-1α. These indicators are therefore suitable biomarkers for early detection of tissue damage. Cytokine IL-1α even appears to be able to identify potential patients at risk, because a certain group of patients showed an increased response from this biomarker. These results potentially enable the clinical implementation of these biomarkers as an indicator for pressure ulcers.

In addition to clinical applications, the results can also be used to improve the design of preventive measures against pressure ulcers such as matrasses and wheelchairs. Currently their design is based on load distribution and periodic load relief. However, by focusing on the prevention of large internal deformations these measures will prove more effective.

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