Objective: to explore the centralized disinfection management measures and implementation effect of CDC. Methods: in this survey, two time periods were selected. Firstly, from January to December 2019, CDC carried out...Objective: to explore the centralized disinfection management measures and implementation effect of CDC. Methods: in this survey, two time periods were selected. Firstly, from January to December 2019, CDC carried out routine disinfection measures, and selected 180 materials as the reference group. Secondly, from January to December 2020, CDC carried out centralized disinfection management, and selected 180 materials as the experimental group, and compared the implementation effects of the two groups. Results: from the data study, it can be seen that the scores of each index of the experimental group have obvious advantages, which are more referential than those of the reference group, and the differences between groups are obvious (P < 0.05), with statistical significance. The specific values are as follows: according to the comparison between the two groups, the qualified rate of instrument disinfection in the reference group is 90.0%, and the probability of infection is 7.50%, and the qualified rate of instrument disinfection in the experimental group is 99.5%, and the probability of infection is 1.00%. From the comparison of occupational protection consciousness between the two groups, it can be seen that the scores of each index of the experimental group are better than those of the reference group, and there is a significant difference between the two groups (P < 0.05), which is statistically significant. Conclusion: the centralized management of disinfection in CDC is more effective, which can improve the qualified rate of disinfection and reduce the probability of infection, and has significant clinical application value.展开更多
Objective: to analyze the quality control methods of disinfection supply room in CDC. Methods: 100 subjects examined in CDC from February 2020 to February 2021 were selected as the control group, and 100 subjects exam...Objective: to analyze the quality control methods of disinfection supply room in CDC. Methods: 100 subjects examined in CDC from February 2020 to February 2021 were selected as the control group, and 100 subjects examined in CDC from February 2021 to February 2022 as the observation group. The control group was given routine management, while the observation group was given quality control. Results: the management quality of the observation group was better than that of the control group (P<0.05). Conclusion: in the process of disinfection of the disinfection supply room of CDC, effective theoretical control should be adhered to ensure that the examinee receives effective quality management in CDC, and the quality of disinfection and sterilization in CDC should be controlled, so as to avoid cross-infection in the hospital, and at the same time, improve the safety of the examinees inspection, which has a high clinical mechanism. In the process of operation, the effective inspection mechanism should be continuously operated, so as to improve the working ability of the disinfection supply room in an all-round way, which has a high clinical value and ensures disease control.展开更多
文摘Objective: to explore the centralized disinfection management measures and implementation effect of CDC. Methods: in this survey, two time periods were selected. Firstly, from January to December 2019, CDC carried out routine disinfection measures, and selected 180 materials as the reference group. Secondly, from January to December 2020, CDC carried out centralized disinfection management, and selected 180 materials as the experimental group, and compared the implementation effects of the two groups. Results: from the data study, it can be seen that the scores of each index of the experimental group have obvious advantages, which are more referential than those of the reference group, and the differences between groups are obvious (P < 0.05), with statistical significance. The specific values are as follows: according to the comparison between the two groups, the qualified rate of instrument disinfection in the reference group is 90.0%, and the probability of infection is 7.50%, and the qualified rate of instrument disinfection in the experimental group is 99.5%, and the probability of infection is 1.00%. From the comparison of occupational protection consciousness between the two groups, it can be seen that the scores of each index of the experimental group are better than those of the reference group, and there is a significant difference between the two groups (P < 0.05), which is statistically significant. Conclusion: the centralized management of disinfection in CDC is more effective, which can improve the qualified rate of disinfection and reduce the probability of infection, and has significant clinical application value.
文摘Objective: to analyze the quality control methods of disinfection supply room in CDC. Methods: 100 subjects examined in CDC from February 2020 to February 2021 were selected as the control group, and 100 subjects examined in CDC from February 2021 to February 2022 as the observation group. The control group was given routine management, while the observation group was given quality control. Results: the management quality of the observation group was better than that of the control group (P<0.05). Conclusion: in the process of disinfection of the disinfection supply room of CDC, effective theoretical control should be adhered to ensure that the examinee receives effective quality management in CDC, and the quality of disinfection and sterilization in CDC should be controlled, so as to avoid cross-infection in the hospital, and at the same time, improve the safety of the examinees inspection, which has a high clinical mechanism. In the process of operation, the effective inspection mechanism should be continuously operated, so as to improve the working ability of the disinfection supply room in an all-round way, which has a high clinical value and ensures disease control.