c/o Cincinnati Ortho Research Institute, 500 E Business Way, Sharonville, OH, 45241, USA.
RFA Systems, LLC, 24790 Gypsum Way, Aldie, VA, 20105, USA.
J Orthop Surg Res. 2021 Oct 20;16(1):629. doi: 10.1186/s13018-021-02790-y.
The present means of confirming the cure of intra-operative polymethyl methacrylate (PMMA) cement are to wait for the remainder cement to harden. To our knowledge, there is no available technique to determine the precise moment of cure for in-vivo cement beneath the tibial tray. This study uses a novel means to determine cement curing time in two environments. One environment represents the operating theater, and the other environment attempts to model cement conditions under the tibial tray during surgery.
We determined the temperature-versus-time plot of cement curing using the following two temperature sensors: one in a simulated implanted tibial tray and another in the remainder cement. We performed 55 tests using dental methyl methacrylate cement mixed in the same ratio as the orthopedic cement. To simulate in vivo conditions, a simulated stainless-steel tibial tray was implanted on a cancellous bone substitute (Sawbones, Vashon Island, WA, USA) using standard cement technique and subsequently placed in a 90°F (32.2 °C) circulating water bath. We positioned a temperature sensor in the cement mantel and positioned a second sensor in a portion of the remaining cement. The temperature from both sensors was measured simultaneously, beginning at 5 min after mixing and continuing for 20 min. The first derivative of the temperature provided the precise curing time for each condition. We analyzed the results of 55 repeated experiments with an independent samples t-test.
With the described technique, we were able to accurately determine the moment of cure of the cement beneath the simulated tray. There was a mean difference between cure time of 5 min and 26 s (p value < 0.001) between the two conditions.
We validated that our technique was successful in determining the precise time to cure in two different environments.
This was not a clinical trial and did not involve patients as such the level of evidence was Grade A: Consistent 1 and 2.
目前确认术中聚甲基丙烯酸甲酯(PMMA)水泥治愈的方法是等待剩余的水泥凝固。据我们所知,没有可用的技术来确定胫骨托下体内水泥的确切固化时间。本研究使用一种新方法来确定两种环境下的水泥固化时间。一种环境代表手术室,另一种环境试图模拟手术中胫骨托下的水泥条件。
我们使用以下两个温度传感器确定水泥固化的温度-时间曲线:一个位于模拟植入的胫骨托中,另一个位于剩余的水泥中。我们使用与骨科水泥相同比例混合的牙科甲基丙烯酸甲酯水泥进行了 55 次测试。为了模拟体内条件,使用标准的水泥技术将模拟的不锈钢胫骨托植入松质骨替代物(Sawbones,Vashon Island,WA,USA)中,然后将其放置在 90°F(32.2°C)的循环水浴中。我们在水泥护套中放置一个温度传感器,并在剩余水泥的一部分中放置第二个传感器。同时测量两个传感器的温度,从混合后 5 分钟开始,持续 20 分钟。温度的一阶导数为每种情况提供了精确的固化时间。我们使用独立样本 t 检验分析了 55 次重复实验的结果。
使用所描述的技术,我们能够准确确定模拟托下水泥的固化时刻。两种情况下的固化时间平均相差 5 分钟和 26 秒(p 值<0.001)。
我们验证了我们的技术在两种不同环境下成功确定了精确的固化时间。
这不是临床试验,因此没有涉及患者,因此证据水平为 A 级:一致 1 和 2。