Division of Applied Mechanics, Center for Devices and Radiological Health, Food and Drug Administration, Silver Spring, Maryland (all authors), and Office of Product Evaluation and Quality, Center for Devices and Radiological Health, Food and Drug Administration (Ms. Price, Drs. Gibeily and Nandy).
Division of Applied Mechanics, Center for Devices and Radiological Health, Food and Drug Administration, Silver Spring, Maryland (all authors), and Office of Product Evaluation and Quality, Center for Devices and Radiological Health, Food and Drug Administration (Ms. Price, Drs. Gibeily and Nandy)..
J Minim Invasive Gynecol. 2020 Mar-Apr;27(3):655-664. doi: 10.1016/j.jmig.2019.05.006. Epub 2019 May 21.
To determine the ability of tissue containment systems to prevent leakage of cancer cell surrogates when subjected to forces encountered during power morcellation procedures.
In vitro study.
Medical device research laboratory.
Samples from 7 different legally marketed tissue containment bags (1 of which is indicated for power morcellation) were subjected to dye and bacteriophage penetration tests at pressures ranging from 0.5 to 50 times the insufflation pressure. The minimum pressure required to cause bag leakage was measured. Subsequently, the morcellation leakage safety factor for each bag was determined as the ratio of the minimum leakage pressure of the bag to the total pressure contributed from insufflation pressure and mechanical forces acting during the power morcellation procedure.
The leakage performance of the bags varied markedly from brand to brand. No correlation was found between leakage pressure and the bag material or the total bag thickness. The leakage pressures ranged from 26 mmHg to >1293 mmHg for the 7 bags, and safety factors ranged from 1 to 50 when only the insufflation pressure was considered. However, if the morcellation forces were included in the calculation, the safety factor dropped by 6-fold for all brands and dropped below 1, indicating likelihood of leakage, for 2 of the 7 brands.
This study provides a mechanism for more realistically simulating the conditions experienced by containment bags during morcellation and quantifying the level of safety provided by the bags.
确定组织容纳系统在经受粉碎过程中遇到的力时防止癌细胞替代物泄漏的能力。
体外研究。
医疗器械研究实验室。
将来自 7 种不同的市售组织容纳袋(其中 1 种被指示用于动力粉碎)的样本在压力范围为 0.5 至 50 倍充气压力下进行染料和噬菌体渗透试验。测量导致袋泄漏的最小压力。随后,通过将袋的最小泄漏压力除以充气压力和动力粉碎过程中施加的机械力的总压力来确定每个袋的粉碎泄漏安全系数。
袋的泄漏性能因品牌而异。袋的泄漏压力与袋材料或总袋厚度之间没有相关性。7 个袋子的泄漏压力范围为 26mmHg 至>1293mmHg,仅考虑充气压力时,安全系数范围为 1 至 50。然而,如果将粉碎力纳入计算,所有品牌的安全系数下降了 6 倍,对于 7 个品牌中的 2 个,安全系数降至 1 以下,表明有泄漏的可能性。
本研究提供了一种更真实地模拟容纳袋在粉碎过程中所经历的条件并量化袋提供的安全水平的机制。