Gastrointestinal endoscopes cleaned without detergent substance following an automated endoscope washer/disinfector dysfunction.
Détails
ID Serval
serval:BIB_6E089774EED7
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Gastrointestinal endoscopes cleaned without detergent substance following an automated endoscope washer/disinfector dysfunction.
Périodique
Gastroenterologie clinique et biologique
ISSN
0399-8320 (Print)
ISSN-L
0399-8320
Statut éditorial
Publié
Date de publication
05/2006
Volume
30
Numéro
5
Pages
665-668
Langue
anglais
Notes
Publication types: Journal Article
Publication Status: ppublish
Publication Status: ppublish
Résumé
To report cases of gastrointestinal endoscopies performed with endoscopes that were reprocessed without detergent substance during a period of dysfunction of the automated endoscope reprocessor (AER).
A dysfunction of the AER for the cycles requiring detergent substance was reported at the Grenoble University Hospital on March 2005. During this period, 72 patients had potentially been exposed to a contaminated endoscope. A recall procedure was organized and serologic tests (HIV, HCV, HBV) were performed 3 and 6 months after the AER incident.
Within the 72 patients convened, 56 (77.8%) were seen in consultation and accepted the serologic screening. Finally, serologic screening was done for 59 patients (81.9%) and no seroconversion for HIV, HCV, or HBV was observed. The final attrition rate was 13 patients (18.1%).
No viral infection was transmitted during the AER dysfunction. After this AER incident, the monitoring of the endoscopic procedures and the traceability of the cleaning process were both improved to prevent further incidents.
A dysfunction of the AER for the cycles requiring detergent substance was reported at the Grenoble University Hospital on March 2005. During this period, 72 patients had potentially been exposed to a contaminated endoscope. A recall procedure was organized and serologic tests (HIV, HCV, HBV) were performed 3 and 6 months after the AER incident.
Within the 72 patients convened, 56 (77.8%) were seen in consultation and accepted the serologic screening. Finally, serologic screening was done for 59 patients (81.9%) and no seroconversion for HIV, HCV, or HBV was observed. The final attrition rate was 13 patients (18.1%).
No viral infection was transmitted during the AER dysfunction. After this AER incident, the monitoring of the endoscopic procedures and the traceability of the cleaning process were both improved to prevent further incidents.
Mots-clé
Cross Infection/prevention & control, Detergents, Disinfection/instrumentation, Endoscopes, Gastrointestinal, Equipment Contamination/prevention & control, Equipment Failure, Equipment Reuse, Humans
Pubmed
Création de la notice
06/01/2017 9:43
Dernière modification de la notice
21/08/2019 6:35
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