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Improvement of wound healing by regulated oxygen-enriched negative pressure-assisted wound therapy in a rabbit model

Authors :
X. D. Hu
X. M. Lai
Y. Lei
Y. F. Li
Y. Z. Li
Source :
Clinical and experimental dermatology. 43(1)
Publication Year :
2016

Abstract

SummaryBackground Development of drug therapies and other techniques for wound care have resulted in significant improvement of the cure rate and shortening of the healing time for wounds. A modified technique of regulated oxygen-enriched negative pressure-assisted wound therapy (RO-NPT) has been reported. Aim To evaluate the efficacy and impact of RO-NPT on wound recovery and inflammation. Methods Infected wounds were established on 40 adult female white rabbits, which were then randomized to one of four groups: O2 group, regulated negative pressure-assisted wound therapy (RNPT) group, regulated oxygen-enriched negative pressure-assisted wound therapy (RO-NPT) group and healthy control (HC) group. Each day, the O2 group was treated with a constant oxygen supply (1 L/min) to the wound, while the RNPT group was treated with continuous regulated negative pressure (70 ± 5 mmHg) and the RNPT + O2 group was treated with both. The HC group was treated with gauze dressing alone, which was changed every day. Leucocyte count, colony count and wound-healing rate were calculated. Levels of tumour necrosis factor (TNF)-α, interleukin (IL)-1β and IL-8 were evaluated by ELISA. Results RO-RNPT significantly decreased bacterial count and TNF-α level, and increased the wound-healing rate. IL-1β, IL-8 and leucocyte count had a tendency to increase in the early phase of inflammation and a tendency to decrease in the later phase of inflammation in the RO-RNPT group. Conclusions RO-NPT therapy assisted wound recovery and inflammation control compared with the RNPT and oxygen-enriched therapies. RO-NPT therapy also increased levels of IL-1β and IL-8 and attenuated expression of TNF-α in the early phase of inflammation.

Details

ISSN :
13652230
Volume :
43
Issue :
1
Database :
OpenAIRE
Journal :
Clinical and experimental dermatology
Accession number :
edsair.doi.dedup.....d121cbf611e7d69f9b917bc41522134c