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Validity Periods of Sterilization Products: Focus on Packing Materials and Storage Environments

±Ù°üÀý°Ç°­ÇÐȸÁö 2023³â 30±Ç 3È£ p.263 ~ 272
KMID : 0123520230300030263
¹ÚÇöÈñ ( Park Hyun-Hee ) - 

À̱¤¿Á ( Lee Kwang-Ok ) - 

Abstract

Purpose: The aim of this study was to provide a scientific basis for shelf life and re-establish the shelf life in a hospitalenvironment by investigating the validity periods of various packaging materials.

Methods: We selected six departmentsto store sterilized items, prepared 482 sterilized items, and stored them for 12 months. Each sample was tested usinga microbiological culture in the laboratory every two weeks. When the result was positive, the sample was consideredcontaminated. The temperature and relative humidity were measured using an automatic control system to investigatethe storage environment during the study period.

Results: Except for two samples, which were positive in the 22nd and28th weeks, 480 samples were negative. The temperature and relative humidity of the sample storage area weremeasured every week. The annual average temperature was 23.6¡¾1.6¡É, and the mean relative humidity was 35.1¡¾15.2%. The cabinets used in this study were the two-open and four-closed types.

Conclusion: This study confirmed thevalidity of the expiration date in a hospital environment. Based on the results, the nonwoven fabric remained sterile formore than nine months. No case of contamination of the paper-plastic pouch packaging was observed, owing to themicrobial culture for two months.
KeyWords
Æ÷ÀåÀç, ¸ê±Õ, ±â±¸¿À¿°
Ackaging materials, Sterilization, Equipment contamination
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