SUMMARY A standardized test procedure is described in which finger-tips are inoculated with broth cultures of organisms (Staphylococcus aureus, Staphyloccocus saprophyticus, Escherichia coli, and Pseudomonas aeruginosa): counts are made from washings of hands after disinfection with various antiseptic-detergents, alcoholic solutions, or unmedicated soap. 70% alcohol, with or without chlorhexidine, was the most effective preparation. The two antiseptic detergents showed variable results, but against Gram-negative bacilli neither was significantly more effective than plain soap. Some tests were also made on the death rate of organisms dried on the skin without disinfection.Disinfection of the skin may be assessed either by measuring the reduction in numbers of natural (including resident) bacteria or of bacteria artificially applied to the skin, that is, transients (Price, 1938;Lowbury et al., 1964a;Manner et al., 1975
Glutaraldehyde is used to disinfect flexible and other heat‐sensitive endoscopes often with the aid of automated systems. Mycobacterium chelonae is being isolated with increasing frequency from these washer disinfectors and processed endoscopes. This has, on occasions, led to misdiagnosis and iatrogenic infections. Recent reports suggest that disinfecting machines, on a sessional or regular basis, with 2% glutaraldehyde may have selected and therefore encouraged the growth of strains of Myco. chelonae, possibly in biofilm, with decreasing susceptibility to glutaraldehyde. In view of this, the resistance of three strains of Myco. chelonae var. chelonae (the type strain NCTC 946 and two machine isolates) was tested against 2% glutaraldehyde and a wide range of alternative disinfectants. Disinfectants tested were a chlorine releasing agent, sodium dichloroisocyanurate at 1000 ppm and 10 000 ppm av Cl, 0·35% peracetic acid (NuCidex, Johnson & Johnson), 70% industrial methylated spirit (IMS), 1% peroxygen compound (‘Virkon’, Antec International) and 10% succine dialdehyde (‘Gigasept’, Sanofi Winthrop). Suspension and carrier tests were carried out in the presence and absence of an organic load. Results showed the type strain, which had not been exposed to the selective pressure of disinfectant usage, to be very sensitive to most disinfectants with the exception of 1% Virkon. The washer disinfector isolates, on the other hand, were extremely resistant to 2% glutaraldehyde and showed greater resistance to 1% Virkon and 1000 ppm NaDCC. Purchasing machines in which the entire fluid pathways, including those for delivering rinse water, are disinfected with an appropriate agent during each cycle are preferred. If this is not possible then sessional cleaning and disinfection at the start of each day and regular maintenance should prevent biofilm formation and contamination with disinfectant‐resistant strains of mycobacteria. In addition to machine disinfection, the use of sterile or bacteria‐free (filtered <0·45μm) water is essential for bronchoscopes and all invasive endoscopes. If there is doubt over the effectiveness of the machine disinfection procedure or water quality, the channels and surfaces of endoscopes may be rinsed with 70% IMS after automated processing.
Impression plates from initially clean horizontal surfaces and floor areas in surgical wards showed a rapid accumulation of bacteria, mainly micrococci, which reached a fluctuating equilibrium after about 24 h. A later increase in bacterial contamination (mainly with aerobic sporing bacilli) to a higher equilibrium level after about 14 days occurred on uncleaned areas. Walls, even if left unwashed, acquired very few bacteria, but many were deposited locally when the wall was touched by a subject whose skin carried large numbers of staphylococci; moist exposed plaster was also heavily contaminated.Regular use of a disinfectant (‘Sudol’ 1 in 100) in cleaning a ward floor did not reduce the equilibrium level of bacteria on the floor.The transfer of staphylococci from contaminated to clean areas on the soles of shoes was demonstrated; the use of tacky and disinfectant mats did not appreciably reduce the transfer of bacteria by this route.Staphylococci deposited on a wall by a disperser were shown to be transferred from the contaminated area of wall to the hands of another subject who did not previously carry the organism; this subject was shown to transfer the staphylo-coccus to a wall which he touched.Attempts to redisperse by air movementStaph. aureuswhich had been shed by a disperser or by a contaminated blanket on to the floor surfaces had little effect; neither blowing with a hair dryer nor brisk exercise appeared to lift any of the staphylococci from a vinyl surface, and only small numbers were lifted by these measures from a terrazzo surface.The hazards of infection from the inanimate environment are discussed.
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