109 Biofilm Removal Efficacy after Manual and Automated Cleaning of Cardiac Catheters

Saturday, April 2, 2011
Trinity Ballroom (Hilton Anatole)
Silma M. Cunha Pinheiro Ribeiro, PHD , Nursing School - Federal University of Minas Gerais - Brazil, Belo Horizonte, Brazil
Jose Antonio Guimaraes Ferreira , Nursing School - Federal University of Minas Gerais - Brazil, Belo Horizonte, Brazil
Vania Regina Goveia , Nursing School - Federal University of Minas Gerais - Brazil, Belo Horizonte, Brazil
Maria Aparecida Resende , Nursing School - Federal University of Minas Gerais - Brazil, Belo Horizonte, Brazil
Background: The removal of biofilm is a challenge when reprocessing cardiac catheters.

Objective: To compare the efficacy of manual and automated cleaning methods using two enzymatic detergents.

Methods: Experimental study involving 36 cardiac catheters that were inoculated with Artifical Soil Test contaminated with 106CFU/ml of P. aeruginosa, E. faecalis e C. albicans during two hours. Each catheter was connected in a line with trypticase soy broth (560ml) during 22h inside and incubator at 35oC.   The enzymatic detergents were diluted with sterile water at 45oC for the detergent 1 and room temperature for the detergent 2.In the manual cleaning catheter was immersed in the detergent for 5 minutes when the solution was flush with a 10ml syringe. Sterile gauze was used to dry external surface. The rinsing was performed with sterile water by immersion for 5 minutes using the same technique. They were dried using three air flushes of a syringe. The automated cleaning was performed using a pump with lines connected to the catheters by luer-lock under 2Kgf pressure during 5 minutes. The rinsing was performed with sterile water during 5 minutes and dried with compressed air during 5 minutes and wipped off the external surface with gauze. One cut (1cm) of the medial and distal part of the catheter were collected to perform a microbial load counts in trypticase soy agar plate and incubated at 35oC for 48 hours. Others cuts of the same region were collected to perform scanning electron microscopy. The fragments was fixed by placing them into 5% glutaraldehyde in cacodylate buffer (0.067M, pH 6.2). Then dehydrated in a graded series of ethanol (30, 50, 70, 90 and 100%) for 10 min each at room temperature and immersed in hexamethyldisilazane overnight at room temperature. The specimens were  mounted on aluminum stubs with silver paint, sputter coated with 25-nm gold particles, and examined with a Zeiss-DSM 950. Positive and negative controls were performed.

Results: After manual cleaning with detergent 1, was detected 5,8 UFC log10/cm2 and after automated process 0,8 UFC log10/cm2 of P.aeruginosa. Related the same bacteria with the detergent 2, was detected 6,8 UFC log10/cm2  and 1,8 UFC log10/cm2 , respectively. After manual cleaning with detergent 1, was detected 2,6 UFC log10/cm2 and after automated process 0,4 UFC log10/cm2 of S.faecalis. Related the same bacteria with the detergent 2, was detected 6,5 UFC log10/cm2  and 1,4 UFC log10/cm2 , respectively. It was not recovered C. albicans in both processes. The electron microscopy showed similar results.

Conclusions: The detergent 1 seems better and the automated process too.