Clinical validation and efficacy of a temperature-controlled ventilation system (TcAF) in the OR to reduce surgical site infections

Microbiological burden of room-air in operating theatres is a known risk factor for surgical site infections. However, it is unclear how to best evaluate efficacy and efficiency under routine clinical conditions. Moreover, there still is a lack of data to assess the impact on infection rates. The ai...

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Autores principales: Bulitta Clemens, Vasiuk Sergeii, Vasylchyshyn Yaroslav, Vasyuk Volodymyr, Guttenberger Regina, Buhl Sebastian
Formato: article
Lenguaje:EN
Publicado: De Gruyter 2020
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Acceso en línea:https://doaj.org/article/48e72057b83d4a839a51d317ec984095
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spelling oai:doaj.org-article:48e72057b83d4a839a51d317ec9840952021-12-05T14:10:42ZClinical validation and efficacy of a temperature-controlled ventilation system (TcAF) in the OR to reduce surgical site infections2364-550410.1515/cdbme-2020-3077https://doaj.org/article/48e72057b83d4a839a51d317ec9840952020-09-01T00:00:00Zhttps://doi.org/10.1515/cdbme-2020-3077https://doaj.org/toc/2364-5504Microbiological burden of room-air in operating theatres is a known risk factor for surgical site infections. However, it is unclear how to best evaluate efficacy and efficiency under routine clinical conditions. Moreover, there still is a lack of data to assess the impact on infection rates. The aim of this study was to evaluate a temperature-controlled ventilation system (TcAF) under routine clinical conditions and assess its impact on infection rates. 10 clinical installations of the TcAF system Opragon (Avidicare AB, Sweden) were assessed during live surgeries according to the Swedish SIS TS 39: 2015 standard. Furthermore, a retrospective analysis of 1,000 consecutive cases of primary total joint arthroplasty (hip, knee) before and 1000 after installation of the TcAF system was performed. Endpoints for clinical outcome were length of stay and infection rates. Our results show that requirements of the Swedish standard were met or significantly exceeded by the TcAF system reliably and robustly ensuring "ultra-clean" air in the entire operating theatre and demonstrating the capability to reduce the risk of airborne microbial transmission under routine clinical conditions. The study shows positive impact on key clinical outcome parameters in line with previous research by Charnley and Lidwell.Bulitta ClemensVasiuk SergeiiVasylchyshyn YaroslavVasyuk VolodymyrGuttenberger ReginaBuhl SebastianDe Gruyterarticletemperature controlled airflowsurgical site infection (ssi)ultraclean airoperating roomMedicineRENCurrent Directions in Biomedical Engineering, Vol 6, Iss 3, Pp 301-303 (2020)
institution DOAJ
collection DOAJ
language EN
topic temperature controlled airflow
surgical site infection (ssi)
ultraclean air
operating room
Medicine
R
spellingShingle temperature controlled airflow
surgical site infection (ssi)
ultraclean air
operating room
Medicine
R
Bulitta Clemens
Vasiuk Sergeii
Vasylchyshyn Yaroslav
Vasyuk Volodymyr
Guttenberger Regina
Buhl Sebastian
Clinical validation and efficacy of a temperature-controlled ventilation system (TcAF) in the OR to reduce surgical site infections
description Microbiological burden of room-air in operating theatres is a known risk factor for surgical site infections. However, it is unclear how to best evaluate efficacy and efficiency under routine clinical conditions. Moreover, there still is a lack of data to assess the impact on infection rates. The aim of this study was to evaluate a temperature-controlled ventilation system (TcAF) under routine clinical conditions and assess its impact on infection rates. 10 clinical installations of the TcAF system Opragon (Avidicare AB, Sweden) were assessed during live surgeries according to the Swedish SIS TS 39: 2015 standard. Furthermore, a retrospective analysis of 1,000 consecutive cases of primary total joint arthroplasty (hip, knee) before and 1000 after installation of the TcAF system was performed. Endpoints for clinical outcome were length of stay and infection rates. Our results show that requirements of the Swedish standard were met or significantly exceeded by the TcAF system reliably and robustly ensuring "ultra-clean" air in the entire operating theatre and demonstrating the capability to reduce the risk of airborne microbial transmission under routine clinical conditions. The study shows positive impact on key clinical outcome parameters in line with previous research by Charnley and Lidwell.
format article
author Bulitta Clemens
Vasiuk Sergeii
Vasylchyshyn Yaroslav
Vasyuk Volodymyr
Guttenberger Regina
Buhl Sebastian
author_facet Bulitta Clemens
Vasiuk Sergeii
Vasylchyshyn Yaroslav
Vasyuk Volodymyr
Guttenberger Regina
Buhl Sebastian
author_sort Bulitta Clemens
title Clinical validation and efficacy of a temperature-controlled ventilation system (TcAF) in the OR to reduce surgical site infections
title_short Clinical validation and efficacy of a temperature-controlled ventilation system (TcAF) in the OR to reduce surgical site infections
title_full Clinical validation and efficacy of a temperature-controlled ventilation system (TcAF) in the OR to reduce surgical site infections
title_fullStr Clinical validation and efficacy of a temperature-controlled ventilation system (TcAF) in the OR to reduce surgical site infections
title_full_unstemmed Clinical validation and efficacy of a temperature-controlled ventilation system (TcAF) in the OR to reduce surgical site infections
title_sort clinical validation and efficacy of a temperature-controlled ventilation system (tcaf) in the or to reduce surgical site infections
publisher De Gruyter
publishDate 2020
url https://doaj.org/article/48e72057b83d4a839a51d317ec984095
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