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Titel:The Level of Surface Coverage of Surgical Site Disinfection Depends on the Visibility of the Antiseptic Agent—A Virtual Reality Randomized Controlled Trial
Autor:Burchard, Rene
Weitere Verfasser:Sayn, Lukas; Schmidt, Ricardo; Graw, Jan A.; Scheicher, Thomas; Soost, Christian; Gruenewald, Armin
Veröffentlicht:2023
URI:https://archiv.ub.uni-marburg.de/es/2024/0259
URN: urn:nbn:de:hebis:04-es2024-02596
DOI: https://doi.org/10.3390/jcm12041472
DDC:610 Medizin
Publikationsdatum:2024-01-10
Lizenz:https://creativecommons.org/licenses/by/4.0

Dokument

Schlagwörter:
remanent disinfectants, knee, skin antisepsis, surgical site infection, virtual reality

Summary:
Background: Surgical site infections (SSIs) have a significant impact on outcome associated with surgical treatment. Therefore, skin antisepsis has evolved as a standard preoperative procedure in the operating room to reduce the perioperative risk of an SSI. In their “Global Guidelines for the prevention of surgical site infections”, the World Health Organization (WHO) recommend the use of an agent with remanent additives and considers colored agents as helpful. However, colored and remanent disinfectants are not available in Germany. The aim of the present study was to investigate whether using a colored antiseptic solution increases the quality of preoperative skin antisepsis. Methods: This study was designed as a randomized, double-blinded controlled trial. To examine the level of coverage of skin antisepsis, an appropriate virtual reality (VR) environment was generated. Participants could see a movable surgical clamp with a swab in their hand. When touching the skin, the participants recognized an optical change in the appearance of the skin: Using a colored antiseptic solution resulted in orange-colored skin. Using an uncolored agent, a shiny wet look was visible without a change in natural skin color. Results: Data of 141 participants (female: 61.0% (n = 86); mean age: 28 y (Range 18–58 y, SD = 7.53 y)) were included in the study. The level of disinfection coverage was higher in the group using the colored disinfectant. On average, 86.5% (sd = 10.0) of the leg skin was covered when a colored disinfectant was used, whereas only 73.9% (sd = 12.8) of the leg skin was covered when the participants had to use an uncolored agent (p < 0.001, effect size: f = 0.56, η2 = 0.24). Conclusions: The use of an uncolored disinfectant leads to a lower surface coverage of the perioperative skin disinfection. Thus far, it is unclear whether using uncolored disinfectants is associated with higher risks for perioperative infections compared with the use of non-remanent disinfectants. Therefore, further research is necessary and current German guidelines should be re-evaluated accordingly.


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