| Literature DB >> 29145674 |
Ulrike Beilenhoff1, Holger Biering2, Reinhard Blum3, Jadranka Brljak4, Monica Cimbro5, Jean-Marc Dumonceau6, Cesare Hassan7, Michael Jung8, Christiane Neumann9, Michael Pietsch10, Lionel Pineau11, Thierry Ponchon12, Stanislav Rejchrt13, Jean-François Rey14, Verona Schmidt15, Jayne Tillett16, Jeanin van Hooft17.
Abstract
1 Prerequisites. The clinical service provider should obtain confirmation from the endoscope washer-disinfector (EWD) manufacturer that all endoscopes intended to be used can be reprocessed in the EWD. 2 Installation qualification. This can be performed by different parties but national guidelines should define who has the responsibilities, taking into account legal requirements. 3 Operational qualification. This should include parametric tests to verify that the EWD is working according to its specifications. 4 Performance qualification. Testing of cleaning performance, microbiological testing of routinely used endoscopes, and the quality of the final rinse water should be considered in all local guidelines. The extent of these tests depends on local requirements. According to the results of type testing performed during EWD development, other parameters can be tested if local regulatory authorities accept this. Chemical residues on endoscope surfaces should be searched for, if acceptable test methods are available. 5 Routine inspections. National guidelines should consider both technical and performance criteria. Individual risk analyses performed in the validation and requalification processes are helpful for defining appropriate test frequencies for routine inspections. © Georg Thieme Verlag KG Stuttgart · New York.Entities:
Mesh:
Year: 2017 PMID: 29145674 DOI: 10.1055/s-0043-122073
Source DB: PubMed Journal: Endoscopy ISSN: 0013-726X Impact factor: 10.093