An evaluation of the use of chlorine dioxide (Tristel One-Shot) in an automated washer/disinfector (Medivator) fitted with a chlorine dioxide generator for decontamination of flexible endoscopes
D. Coates, An evaluation of the use of chlorine dioxide (Tristel One-Shot) in an automated washer/disinfector (Medivator) fitted with a chlorine dioxide generator for decontamination of flexible endoscopes, J HOSP INF, 48(1), 2001, pp. 55-65
Microbiological tests were carried out to evaluate a new chlorine dioxide s
terilant: Tristel One-Shot. Preliminary in vitro suspension tests showed th
at solutions containing around 140 ppm chlorine dioxide achieved a reductio
n factor exceeding 10(6) of Staphylococcus aureus in 1 min and of Bacillus
subtilis spores in 2.5 min in the presence of 3 g/L bovine albumin. Subsequ
ent tests evaluated the effectiveness of Tristel One-Shot in a Medivator wa
sher/ disinfector fitted with a Tristel Generator for processing flexible e
ndoscopes. Each test run involved three stages. In the first, the instrumen
t and air-water channels of a gastroscope were inoculated with a suspension
of Pseudomonas aeruginosa (10(8) cfu/ml) in 10% sodium glutamate and serum
(0, 5 or 10%) and then drained, partially dried, and saline flushed throug
h for total viable counts (TVCs). In the second stage, the channels were re
-inoculated with test organisms; detergent was flushed through the channels
which were then brushed; and saline was flushed through for TVCs. In the t
hird stage, the channels were re-inoculated; detergent was flushed through
the channels which were then brushed; the endoscope was processed in the Me
divator; and saline was flushed through for TVCs. Carrying out all three st
ages enabled determination of (1) the contribution played by manual cleanin
g of channels prior to processing in the Medivator, and (2) the combined ef
fect of manual cleaning followed by processing. Two series of test runs wer
e done. In the first, the Tristel Generator was set to generate 230 ppm chl
orine dioxide, and in the second 150 ppm. In the first, cleaning followed b
y processing in the Medivator consistently achieved a >10(6)-fold reduction
of test organisms, and in the second a >10(5)-fold reduction. Pre-cleaning
of channels was very important-when done the initial concentration of seru
m in the inoculum (0-10%) had no affect on the results obtained after proce
ssing. (C) 200 1 The Hospital Infection Society.