According to the national soft endoscope cleaning standard and the difference between the previous and latest version, the origin decontamination equipment is upgraded. Sensory control monitoring results in the last year shows that the average cleaning time for a single endoscope has been reduced from 20 min 55 s to 17 min 16 s. The number of bacterial colony has been reduced from 6.8 to 3.1. The pass rate of sensory control monitoring keeps steady. The upgraded decontamination equipment not only meets the requirements of the latest version of the standard,but also improves the efficiency and effectiveness of electronic endoscope disinfection.
Disinfection ; Endoscopes ; Equipment Contamination

The measuring methods of the linearity errors and the cross contamination are very hard to grasp in testing the clinical analyzer's specifications. In this paper, the measuring steps and the data processing methods are introduced in detail in combination with the living examples and taking the form of the lists so as to help the technical personnels to understand the verification regulation of clinical analyzers correctly and to carry out the technical supervision effectively.
Chemistry Techniques, Analytical ; instrumentation ; methods ; Equipment Contamination

PURPOSE: This was a study on the expiration date of Ethylene Oxide (EO) gas sterilization and effects of the environmental factors of temperature, humidity and type of cabinet in sterile goods storage area on the expiration date. METHODS: Sterile goods storage areas from 13 departments in one hospital were selected and 455 EO gas sterilization samples were prepared and kept in those areas over the 14 months of the study. Each sample was tested with a microbiological culture in the laboratory every week. If the result was positive, the sample was regarded as contaminated. The researcher visited once a month to check the temperature, humidity and type of cabinet. RESULTS: With the exception of 1 sample which was positive at 56th week. 454 samples were confirmed as negative. The environment of the samples storage area was measured monthly. The annual average temperature was 24.2+/-1.6degrees C, and the mean relative humidity 34.7+/-15.2%. The types of cabinet were 7 open and 6 closed. CONCLUSION: The results of the microbiological culture at 13 months showed that none of the samples were contaminated. Therefore the hospital's existing Expiration Date can be extended from 6 months to 13~14 months.
Equipment Contamination ; Ethylene Oxide* ; Humidity ; Sterilization*

This paper selects the bag-type infusion sets for single use as samples, which are produced by different manufacturers and based on the ethylene oxide sterilization. The ethylene oxide sterilization residues in different parts of samples are detected by colorimetric analysis. Combined the comparison of the ethylene oxide residues testing results in the different parts of the same sample with the actual situation in clinical use, more reasonable sampling positions are found to detect the ethylene oxide sterilization residues. The result of this experiment will play a guiding role in the detection of the actual samples.
Disposable Equipment ; Equipment Contamination ; prevention & control ; Ethylene Oxide ; analysis

OBJECTIVEIt has been demonstrated that when a high-speed handpiece stops rotating, negative pressure will form. Thus, contaminating fluid in which there are many kinds of bacteria and viruses from the external environment will retract into various compartments of the handpiece and the dental unit. The purpose of the study is to compare the preventing effect of antisuction designed handpiece and conventional handpiece on viral contamination at different rotating times.

METHODSTwenty handpieces with or without antisuction device (10 of each) were used in the study. Each handpiece was submerged into 10(-6) microg/microl HBV particle solution rotating 5 and 10 times respectively (every time rotating for 10 seconds). Samples were obtained from the water line and chip air line of the handpieces and examined by RT-PCR.

RESULTSAt the same rotating times, there was statistical significance of the viral concentration between the two kinds of handpieces (P < 0.05) . However, there was no statistical significance of the viral concentration between different rotating times in each group (P > 0.05).

CONCLUSIONContamination taking place in both water and air lines of dental handpiece was not enhanced by increasing the number of rotating times of the handpiece. The antisuction devices installed into the water line and chip air line were demonstrated to prevent viral contamination effectively.

OBJECTIVETo investigate the effects on performances of high-speed dental handpieces subjected to autoclaving.

METHODSThe method of trial used to evaluate the effect of autoclaving included that ten chemical and ten biological indicators were arranged in each trial group being set by one sort of temperature and sterilization time. The range of temperature was from 100 degrees C to 134 degrees C and the sterilization time was from 1 to 45 minutes. The reliability of autoclaving was evaluated by the result of chemical indicator and the endospores of Bacillus stearothermophilus subjected to autoclaving. Ten newly imported and ten new domestic dental handpieces in two different brands were used to carry out this trial. The effects produced by autoclaving on performances of dental handpieces subjected to different type autoclaves were evaluated by some parameters.

RESULTSThe eligible outcome in killing test of the 221 sterilized dental handpieces proved that the sterilization effect of autoclaving on dental handpieces was reliable. The chemical indicators showed that under the condition of 121 degrees C it needed 20 minutes to reach sterilization standard in the inner package and only 15 minutes on the outer package, and under the condition of 134 degrees C it took 4 minutes to reach sterilization standard in the inner package while only 2 minutes on the outer package. This outcome proved that material with package was more time-consuming than that without package during autoclaving. Autoclaving has positive effects on the performance of dental handpieces, while the autoclave with less-time full sterilization cycle has less effect on it. The performance of dental handpieces sterilized by the autoclave with 6-minute full sterilization cycle might be restorable within certain times of sterilization cycle.

CONCLUSIONThe sterilization effect of autoclaving is reliable. In order to reduce the influence on the performance of dental handpieces subjected to autoclaving, it should be reasonable to use the autoclave by which a full sterilization cycle might take less time and no use of package.

Despite the worldwide application of sperm-freezing technology as a means of preserving male fertility functions, few reports are seen about the transmission of microorganisms to cryopreserved sperm via contaminated liquid nitrogen (LN). Although the risk of cross-contamination between samples stored in liquid nitrogen is "vanishingly small", it must be accepted as a finite risk and all reasonable measures taken to reduce the likelihood of its occurrence. Moreover, all methods employed, including collection, cryopreservation, storage and thawing of human sperm as well as the clinical use of cryobanked human sperm, must reduce the risk of contamination from any source throughout the entire process.
Cryopreservation ; methods ; Equipment Contamination ; Humans ; Male ; Semen Preservation ; methods

OBJECTIVEDiscuss sterilization effect of B-class pulsation table top vacuum pressure steam sterilizer for dental handpiece.

METHODSAnalysis selection of sterilizer for dental handpiece and sterilization management processes and sterilization effect monitoring, evaluation of monitoring result and effective sterilization method.

RESULTSThe B-class pulsation table top vacuum pressure steam sterilizer to dental handpiece in West China Stomatological Hospital of Sichuan University met the requirement of the chemical and biological monitoring. Its efficiency of sterilization was 100%. The results of aerobic culture, anaerobic culture, B-type hepatitis mark monitoring to sterilized dental handpiece were negative.

CONCLUSIONIt is effective method for dental handpiece sterilization to use B-class pulsation table top vacuum pressure steam sterilizer.

Firstly, the essay introduces the definition of bio-burden, the significance of determination of bio-burden and the specific performance requirements. Then, the essay introduces the method selection and validation on the bio-burden determination of surgical drapes, gowns and clean air suits.
Equipment Contamination ; Surgical Attire ; microbiology ; standards ; Surgical Drapes ; microbiology ; standards

OBJECTIVEAnalyzing the performance of microbial barrier of needleless positive pressure closed connectors.

METHODSThree kinds of brand needleless positive pressure closed connectors were chosen to do the access of microorganisms test.

RESULTSPositive results were detected in the three experimental groups.

CONCLUSIONSSo far, lots of the connectors are not qualified strictly on the market, some improvement is required in the structure design and process.