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Use of a new pneumatic system to support capillary microperfusion in surgical wound healing: an animal model

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60162694%3AG44__%2F19%3A00541689" target="_blank" >RIV/60162694:G44__/19:00541689 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/00216208:11150/19:10398637 RIV/00179906:_____/19:10398637

  • Výsledek na webu

    <a href="https://www.magonlinelibrary.com/toc/jowc/28/4" target="_blank" >https://www.magonlinelibrary.com/toc/jowc/28/4</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.12968/jowc.2019.28.4.229" target="_blank" >10.12968/jowc.2019.28.4.229</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Use of a new pneumatic system to support capillary microperfusion in surgical wound healing: an animal model

  • Popis výsledku v původním jazyce

    Objective: To test the efficacy of the a developed medical device, based on the principle of mechanical support of capillary microperfusion. Method: In this pilot study involving experimental animals, each pig had two standardised surgical wounds. A cuff that delivered pneumatic three-second micropulses was applied to the wound designated as the 'experimental wound'. The pressure inside the cuff was kept at a level <10mmHg so that during the pulse, the pressure would decrease by one third of the established value. The second wound, designated as the 'control wound', was covered with a standard dressing. Over the course of five days, the pressure inside the cuff was monitored. After the five days, the experimental animal was euthanised and two specimens were collected for histological analysis (one sample from each wound site). Wound healing parameters for the experimental and control wounds were examined by a pathologist. The level of statistical significance was set at 0.05. Results: In this study, 10 experimental animals were used. The average pressure in the cuffs was 8.46mmHg (standard deviation: 3.86). No disparities in wound healing were observed in cases of different average pressures in the experimental wound. With respect to wound healing parameters, a statistically significant difference (p<0.05) was found in favour of the experimental wound. The occurrence of histological signs of poor healing was identical in both study wounds. Conclusion: The study shows that a device for the support of capillary microperfusion of the surgical wound had a positive effect. It was confirmed that the mechanical support system of capillary microperfusion was safe and reliable. Declaration of interest: The study received financial support from the institutional grant agency of the University Hospital Hradec Kralove. The authors have no conflicts of interest to declare.

  • Název v anglickém jazyce

    Use of a new pneumatic system to support capillary microperfusion in surgical wound healing: an animal model

  • Popis výsledku anglicky

    Objective: To test the efficacy of the a developed medical device, based on the principle of mechanical support of capillary microperfusion. Method: In this pilot study involving experimental animals, each pig had two standardised surgical wounds. A cuff that delivered pneumatic three-second micropulses was applied to the wound designated as the 'experimental wound'. The pressure inside the cuff was kept at a level <10mmHg so that during the pulse, the pressure would decrease by one third of the established value. The second wound, designated as the 'control wound', was covered with a standard dressing. Over the course of five days, the pressure inside the cuff was monitored. After the five days, the experimental animal was euthanised and two specimens were collected for histological analysis (one sample from each wound site). Wound healing parameters for the experimental and control wounds were examined by a pathologist. The level of statistical significance was set at 0.05. Results: In this study, 10 experimental animals were used. The average pressure in the cuffs was 8.46mmHg (standard deviation: 3.86). No disparities in wound healing were observed in cases of different average pressures in the experimental wound. With respect to wound healing parameters, a statistically significant difference (p<0.05) was found in favour of the experimental wound. The occurrence of histological signs of poor healing was identical in both study wounds. Conclusion: The study shows that a device for the support of capillary microperfusion of the surgical wound had a positive effect. It was confirmed that the mechanical support system of capillary microperfusion was safe and reliable. Declaration of interest: The study received financial support from the institutional grant agency of the University Hospital Hradec Kralove. The authors have no conflicts of interest to declare.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30216 - Dermatology and venereal diseases

Návaznosti výsledku

  • Projekt

  • Návaznosti

    S - Specificky vyzkum na vysokych skolach<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2019

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Journal of Wound Care

  • ISSN

    0969-0700

  • e-ISSN

    2052-2916

  • Svazek periodika

    28

  • Číslo periodika v rámci svazku

    4

  • Stát vydavatele periodika

    GB - Spojené království Velké Británie a Severního Irska

  • Počet stran výsledku

    9

  • Strana od-do

    229-237

  • Kód UT WoS článku

    000463574700007

  • EID výsledku v databázi Scopus

    2-s2.0-85064282122