Laminar flow operating room air purification system requirements:
1. The clean operating room of Class I~III and other clean rooms of Class I~II shall be subjected to dynamic control of air cleaning system return and return air;
2. Class IV clean operating room and other clean rooms of Class III and IV can be dynamically controlled by local air purification equipment with high efficiency or sub-efficient filter at the end, and set up engineering full-time personnel to be responsible for computer dynamic monitoring during operation;
3. Non-clean areas can be cleaned by local purification equipment (air purifier);
4. It is strictly forbidden to use local air purification equipment with chemical stimulation and carcinogenic factors;
5. The air supply end device of the air purification system should be sealed and not leaked;
6. The negative pressure operating room and the room producing the pathogenic aerosol should be equipped with a separate air purification system, and the high efficiency filter should be installed at the air outlet;
7. Air outlets with pathogenic aerosols should be sealed.
Quality evaluation and monitoring of laminar flow operating rooms:
1. Before the clean operation department is put into operation, it should be comprehensively evaluated by the qualified engineering quality inspection department and archived as the basic material of the surgery department;
2. The clean operation department conducts daily dynamic monitoring. The mandatory test items are the bacterial concentration and the static pressure difference of the air. The monitoring standard should meet the requirements of Table 3; the static dust concentration and the sedimentation bacteria concentration are measured by comprehensive performance or the annual inspection data. Prevail. The density of bacteria after disinfection shall be based on the test data after each disinfection;
3. The unit can be monitored and recorded by the purification automatic control system every day, and the problems can be solved in time;
4. Check the cleaning status of the local clean-up and return air outlet equipment in the non-clean area every month, and find out the problems in time;
5. Monitor and record at least one static air purification effect on each level of clean operating room every month;
6. Conduct a comprehensive assessment of the comprehensive performance of the clean surgical department including the use of dust particles, high-efficiency filters, leak detection, and working conditions of parts, monitoring and recording;
7. Monitor and record the positive and negative pressure of the clean surgery department every six months.
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