Abe Shintaro, Haraga Isao, Kiyomi Fumiaki, Kumano Hitomi, Gohara Akira, Matsumoto Shigehiro, Yamaura Ken
Department of Anesthesiology, Fukuoka University Faculty of Medicine, 7-45-1 Nanakuma, Jonan-ku, Fukuoka-shi, Fukuoka, 814-0180, Japan.
Department of Anesthesia, Fukuoka University Chikushi Hospital, 1-1-1 Zokumyouin, Chikushino-shi, Fukuoka, 818-8502, Japan.
JA Clin Rep. 2018 Aug 29;4(1):61. doi: 10.1186/s40981-018-0197-7.
Two opening methods are used for injection needle products: the "peel-apart method" where the adhesive surface of the packaging mount is peeled off, and the "push-off top method," where the needle hub is pressed against the mount to break it. However, the risks of bacterial contamination as a result of opening method remain unknown. The aim of our study was to evaluate the bacterial contamination of needle hubs upon the opening of injection needles by the peel-apart or push-off top method under various conditions.
Bacterial contamination upon the opening of injection needles was examined in two materials, paper and plastic. Various concentrations of Staphylococcus aureus were applied to the mount and were maintained under wet or dry conditions. Injection needles were opened using the peel-apart or push-off top method. Needle hub contamination was examined using agar medium colony counting. Clinically assumed conditions (the hands and saliva of anesthesiologists) were also evaluated. Data were statistically examined using the Cochran-Mantel-Haenszel, Jonckheere, and Fisher's exact tests.
The lateral surfaces of needle hubs were contaminated using the push-off top method, but not by the peel-apart method, in a manner that was dependent on S. aureus concentrations. No significant differences were observed between mount materials. Needle hub contamination was significantly more severe for the wet than for the dry opening portion. The clinically assumed condition study revealed that the lateral and bottom surfaces of the needle hub were contaminated significantly more in the saliva contamination group than in the dry and wet hand groups.
The bacterial contamination of needle hubs may occur upon the opening of injection needles when the push-off top method is used and may be affected by hands contaminated with saliva under clinical conditions.
注射针产品有两种开启方式:“剥开法”,即剥开包装座的粘性表面;“推顶法”,即将针座压在包装座上使其破裂。然而,开启方式导致细菌污染的风险尚不清楚。我们研究的目的是评估在各种条件下,通过剥开法或推顶法开启注射针时针座的细菌污染情况。
在纸张和塑料两种材料上检测注射针开启时的细菌污染情况。将不同浓度的金黄色葡萄球菌接种到包装座上,并保持在潮湿或干燥条件下。使用剥开法或推顶法开启注射针。采用琼脂培养基菌落计数法检测针座污染情况。还评估了临床假定条件(麻醉医生的手和唾液)。使用 Cochr an-Mantel-Haenszel检验、Jonckheere检验和Fisher精确检验对数据进行统计学分析。
采用推顶法时针座侧面会被污染,而剥开法不会,且污染情况取决于金黄色葡萄球菌的浓度。包装座材料之间未观察到显著差异。开启部分潮湿时针座污染明显比干燥时严重。临床假定条件研究表明,唾液污染组针座侧面和底部的污染明显比干手组和湿手组严重。
使用推顶法开启注射针时,针座可能会发生细菌污染,并且在临床条件下可能会受到被唾液污染的手的影响。