Woods T O, Brown S A, Merritt K, McNamee S G, Hitchins V M
Division of Mechanics & Materials Science, HFZ-150, US Food and Drug Administration, Center for Devices and Radiological Health, Office of Science and Technology, 9200 Corporate Blvd, Rockville, MD 20850, USA.
Biomed Instrum Technol. 2001 Nov-Dec;35(6):391-4.
The purpose of this study was to determine the effect of repeated ethylene oxide sterilization using a standard clinical protocol on sutures, a type of medical device labeled for single use and reported to be reprocessed for use after being opened but not used. Four types of commonly used synthetic absorbable sutures were subjected to 1 and 2 ethylene oxide resterilization cycles. Knot tensile strength was determined for new sutures and for sutures that had been subjected to 1 and 2 ethylene oxide resterilization cycles. As has been found with other types of single-use devices, no general conclusions can be made for absorbable sutures. The strengths of different types of sutures increased, decreased, or stayed the same after repeated sterilization. In addition, the inner packages of some sutures were not intact after reprocessing, possibly exposing the sutures to increased humidity, which can produce degradation leading to loss of strength both immediately and after additional shelf aging and degraded performance after clinical use.
本研究的目的是确定使用标准临床方案对缝线进行重复环氧乙烷灭菌的效果。缝线是一种标明为一次性使用的医疗器械,据报道在打开但未使用后会进行再处理以供使用。四种常用的合成可吸收缝线经历了1次和2次环氧乙烷再灭菌循环。测定了新缝线以及经历了1次和2次环氧乙烷再灭菌循环的缝线的结抗张强度。正如在其他类型的一次性使用设备中所发现的那样,对于可吸收缝线无法得出一般性结论。不同类型的缝线在重复灭菌后强度增加、降低或保持不变。此外,一些缝线的内包装在再处理后不完整,可能使缝线暴露于湿度增加的环境中,这会导致降解,从而立即导致强度损失,在额外的货架期老化后也会导致强度损失,并且在临床使用后性能下降。