Khoshnevis Sepideh, Matthew Brothers R, Diller Kenneth R
Department of Biomedical Engineering, The University of Texas at Austin, 107 W. Dean Keeton Street, Stop C0800, Austin, TX 78712 e-mail:
Department of Kinesiology, University of Texas at Arlington, MAC 114, Arlington, TX 78229 e-mail:
J Eng Sci Med Diagn Ther. 2018 Nov;1(4):0410071-410079. doi: 10.1115/1.4041463. Epub 2018 Oct 1.
Cryotherapy is commonly used for the management of soft tissue injury. The dose effect of the applied cooling temperature has not been quantified previously. Six subjects were exposed during five different experiments to local skin temperatures of 16.6 °C, 19.8 °C, 24.7 °C, 27.3 °C, and 37.2 °C for 1 h of active heat transfer followed by 2 h of passive environmental interaction. Skin blood perfusion and temperature were measured continuously at treatment and control sites. All treatments resulted in significant changes in cutaneous vascular conductance (CVC, skin perfusion/mean arterial pressure) compared to baseline values. The drop in CVC for cooling to both 19.8 °C and 16.6 °C was significantly larger than for 27.3 °C (P < 0.05 and P < 0.0005, respectively). The depression of CVC for cooling to 16.6 °C was significantly larger than at 24.7 °C (P < 0.05). Active warming at 37.2 °C produced more than a twofold increase in CVC (P < 0.05). A simulation model was developed to describe the coupled effects of exposure time and temperature on skin perfusion. The model was applied to define an equivalent cooling dose defined by exposure time and temperature that produced equivalent changes in skin perfusion. The model was verified with data from 22 independent cryotherapy experiments. The equivalent doses were applied to develop a nomogram to identify therapeutic time and temperature combinations that would produce a targeted vascular response. The nomogram may be applied to design cryotherapy protocols that will yield a desired vascular response history that may combine the benefits of tissue temperature reduction while diminishing the risk of collateral ischemic injury.
冷冻疗法常用于软组织损伤的治疗。以往尚未对所施加的冷却温度的剂量效应进行量化。在五个不同的实验中,六名受试者暴露于16.6°C、19.8°C、24.7°C、27.3°C和37.2°C的局部皮肤温度下,进行1小时的主动热传递,随后进行2小时的被动环境相互作用。在治疗部位和对照部位连续测量皮肤血流灌注和温度。与基线值相比,所有治疗均导致皮肤血管传导性(CVC,皮肤灌注/平均动脉压)发生显著变化。冷却至19.8°C和16.6°C时CVC的下降显著大于冷却至27.3°C时(分别为P < 0.05和P < 0.0005)。冷却至16.6°C时CVC的降低显著大于冷却至24.7°C时(P < 0.05)。在37.2°C下主动升温使CVC增加了两倍多(P < 0.05)。开发了一个模拟模型来描述暴露时间和温度对皮肤灌注的联合效应。该模型用于定义由暴露时间和温度定义的等效冷却剂量,该剂量会使皮肤灌注产生等效变化。该模型用来自22个独立冷冻疗法实验的数据进行了验证。应用等效剂量来制定列线图,以确定能产生靶向血管反应的治疗时间和温度组合。该列线图可用于设计冷冻疗法方案,该方案将产生所需的血管反应过程,既能结合组织温度降低的益处,又能降低继发性缺血性损伤的风险。