TY - JOUR
T1 - Evaluation of microbial occurrence in reusable robotic instruments for minimally invasive surgery
T2 - A pilot study
AU - Pelzer, Roy J.
AU - Van Der Zwet, Wil C.
AU - Eggen, Mike M.E.G.
AU - Beard, Ashley
AU - Savelkoul, Paul H.M.
AU - Dirks, Jeanne A.M.C.
N1 - Publisher Copyright:
© 2024 Public Library of Science. All rights reserved.
PY - 2024/4/1
Y1 - 2024/4/1
N2 - In recent decades, minimally invasive surgery has become the favoured surgical technique, with increasing utilisation of robotic surgery to enhance patient outcomes. However, the design complexity of surgical robotic instruments can pose challenges in maintaining adequate cleaning, disinfection and sterilisation particularly of the device s interior. In our hospital, robotic instruments are reused for a maximum of ten successive patients, following the manufacturer s guidelines. To the best of our knowledge, neither the manufacturer nor ISO standards have specified any methods to determine the sterility of robotic instruments after cleaning, disinfection and sterilisation procedures. In a small pilot study, we used a locally developed protocol to evaluate the sterility of 20 da Vinci SI robotic instruments, with the aim of determining whether the recommended cleaning, disinfection and sterilisation process is adequate to achieve safe usage in subsequent patients. None of the 20 instruments showed viable micro-organisms, therefore the robotic instruments were considered sterile, and suitable for re-use. We recommend our protocol to other hospitals, to be used as an essential control element in the assessment of their unique reprocessing technique for robotic instruments.
AB - In recent decades, minimally invasive surgery has become the favoured surgical technique, with increasing utilisation of robotic surgery to enhance patient outcomes. However, the design complexity of surgical robotic instruments can pose challenges in maintaining adequate cleaning, disinfection and sterilisation particularly of the device s interior. In our hospital, robotic instruments are reused for a maximum of ten successive patients, following the manufacturer s guidelines. To the best of our knowledge, neither the manufacturer nor ISO standards have specified any methods to determine the sterility of robotic instruments after cleaning, disinfection and sterilisation procedures. In a small pilot study, we used a locally developed protocol to evaluate the sterility of 20 da Vinci SI robotic instruments, with the aim of determining whether the recommended cleaning, disinfection and sterilisation process is adequate to achieve safe usage in subsequent patients. None of the 20 instruments showed viable micro-organisms, therefore the robotic instruments were considered sterile, and suitable for re-use. We recommend our protocol to other hospitals, to be used as an essential control element in the assessment of their unique reprocessing technique for robotic instruments.
U2 - 10.1371/journal.pone.0300355
DO - 10.1371/journal.pone.0300355
M3 - Article
SN - 1932-6203
VL - 19
JO - PLOS ONE
JF - PLOS ONE
IS - 4 April
M1 - e0300355
ER -