Cargando…

An in vitro comparison of standard cleaning to a continuous passive disinfection cap for the decontamination of needle-free connectors

BACKGROUND: The optimal decontamination method for needle-free connectors is still unresolved. The objective of this study was to determine if a continuous passive disinfection cap is as effective as standard cleaning for the microbial decontamination of injection ports of two types of needle-free c...

Descripción completa

Detalles Bibliográficos
Autores principales: Casey, Anna L., Karpanen, Tarja J., Nightingale, Peter, Elliott, Tom S. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5887218/
https://www.ncbi.nlm.nih.gov/pubmed/29632665
http://dx.doi.org/10.1186/s13756-018-0342-0
Descripción
Sumario:BACKGROUND: The optimal decontamination method for needle-free connectors is still unresolved. The objective of this study was to determine if a continuous passive disinfection cap is as effective as standard cleaning for the microbial decontamination of injection ports of two types of needle-free connectors. METHODS: The injection ports of needle-free connectors were inoculated with Staphylococcus aureus and allowed to dry. Disinfection caps containing 70% (v/v) isopropyl alcohol (IPA) were attached to the connectors for one, three or 7 days and were compared with needle-free connectors cleaned with 2% (w/v) chlorhexidine gluconate (CHG) in 70% (v/v) IPA. The number of S. aureus remaining on the injection ports was evaluated. Median log(10) reductions and 95% confidence interval (CI) were calculated and data analyzed using the Mann-Whitney test. RESULTS: The application of the disinfection cap resulted in a significantly higher reduction in S. aureus than the 2% (w/v) CHG in 70% (v/v) IPA wipe, achieving a > 5 Log(10) reduction in CFU at each time point. CONCLUSIONS: The disinfection caps resulted in a significantly higher reduction in S.aureus on the injection ports when compared to the use of a 2% (w/v) CHG in 70% (v/v) IPA wipe. This offers an explanation for the lower rates of central-line associated bloodstream infection (CLABSI) associated with the use of disinfection caps reported in clinical studies.