Ak. Deva et al., ESTABLISHMENT OF AN IN-USE TESTING METHOD FOR EVALUATING DISINFECTIONOF SURGICAL-INSTRUMENTS USING THE DUCK HEPATITIS-B MODEL, The Journal of hospital infection, 33(2), 1996, pp. 119-130
Nosocomial transmission of hepatitis B virus (HBV), associated with in
terventional procedures, has been attributed to its survival on improp
erly decontaminated instruments. To date, guidelines for chemical dis
infection of potentially contaminated heat-sensitive instruments have
been based largely on extrapolation of data from in-vitro disinfectant
testing. Direct infectivity testing has not been possible for HBV bec
ause of the lack of a practical culture assay or susceptible experimen
tal animal model. In this study the related duck hepadnavirus was used
to simulate in-vivo transmission of a HBV during surgery, and to eval
uate the effectiveness of 2% glutaraldehyde disinfection of surgical l
aparoscopes. Multiple laparoscopic liver biopsies were performed on 'b
iohazardous' duck hepatitis B (DHBV) positive ducks. Laparoscopes were
then subjected to different disinfection regimes using 2% glutaraldeh
yde, and residual infectivity tested by placing their tips into the pe
ritoneal cavities of uninfected four-day-old ducklings. Direct transmi
ssion of DHBV occurred in all ducks when laparoscopes were not washed.
Rinsing with water lowered the transmission rate to 64% and no infect
ion transmission occurred after 5 min of contact time with the disinfe
ctant. In contrast, previous in-vitro studies had shown complete viral
inactivation after a shorter period of disinfection. It is postulated
that the longer inactivation time observed in our study may be a resu
lt of surface interactions of virus and instrument, interfering with d
isinfectant access or activity. Tests of instrument surface samples fo
r viral DNA by the polymerase chain reaction (PCR) did not correlate w
ith transmission of virus infection in vivo. PCR is an inappropriate t
est for evaluating the efficacy of disinfectant action despite its sen
sitivity. This in use method will allow testing of other decontaminati
on procedures and their effectiveness on more complex surgical instrum
ents.