He X, McGee S, Coad J E, Schmidlin F, Iaizzo P A, Swanlund D J, Kluge S, Rudie E, Bischof J C
Department of Mechanical Engineering, University of Minnesota, Minneapolis, MN 55455, USA.
Int J Hyperthermia. 2004 Sep;20(6):567-93. doi: 10.1080/0265673042000209770.
Minimally invasive microwave thermal therapies are being developed for the treatment of small renal cell carcinomas (RCC, d<3 cm). This study assessed the thermal history and corresponding tissue injury patterns resulting from microwave treatment of the porcine renal cortex. Three groups of kidneys were evaluated: (1) in vitro treated, (2) in vivo with 2-h post-treatment perfusion (acute) and (3) in vivo with 7-day post-treatment perfusion (chronic). The kidneys were treated with an interstitial water-cooled microwave probe (Urologix, Plymouth, MN) that created a lesion centered in the renal cortex (50 W for 10 min). The thermal histories were recorded at 0.5 cm radial intervals from the probe axis for correlation with the histologic cellular and vascular injury. The kidneys showed a reproducible 2 cm chronic lesion with distinct histologic injury zones identified. The thermal histories at the edge of these zones were found using Lagrangian interpolation. The threshold thermal histories for microvascular injury and stasis appeared to be lower than that for renal epithelial cell injury. The Arrhenius kinetic injury models were fit to the thermal histories and injury data to determine the kinetic parameters (i.e. activation energy and frequency factor) for the thermal injury processes. The resultant activation energies are consistent in magnitude with those for thermally induced protein denaturation. A 3-D finite element thermal model based on the Pennes bioheat equation was developed and solved using ANSYS (V7.0). The real geometry of the kidneys studied and temperature dependent thermal properties were used in this model. The specific absorption rate (SAR) of the microwave probe required for the thermal modelling was experimentally determined. The results from the thermal modelling suggest that the complicated change of local renal blood perfusion with temperature and time during microwave thermal therapy can be predicted, although a first order kinetic model may be insufficient to capture blood flow changes. The local blood perfusion was found to be a complicated function of temperature and time. A non-linear model based on the degree of vascular stasis was introduced to predict the blood perfusion. In conclusion, interstitial microwave thermal therapy in the normal porcine kidney results in predictable thermal and tissue injury behaviour. Future work in human kidney tissue will be necessary to confirm the clinical significance of these results.
微创微波热疗法正在研发用于治疗小肾癌(RCC,直径<3 cm)。本研究评估了猪肾皮质微波治疗后的热历史及相应的组织损伤模式。评估了三组肾脏:(1)体外治疗组,(2)体内治疗后2小时灌注组(急性)和(3)体内治疗后7天灌注组(慢性)。使用间质水冷微波探头(Urologix,明尼苏达州普利茅斯)对肾脏进行治疗,该探头在肾皮质中心形成一个病灶(50 W,持续10分钟)。从探头轴线以0.5 cm的径向间隔记录热历史,以与组织学细胞和血管损伤相关联。肾脏显示出可重复的2 cm慢性病灶,并确定了不同的组织学损伤区域。使用拉格朗日插值法找到这些区域边缘的热历史。微血管损伤和淤滞的阈值热历史似乎低于肾上皮细胞损伤的阈值热历史。将阿伦尼乌斯动力学损伤模型拟合到热历史和损伤数据中,以确定热损伤过程的动力学参数(即活化能和频率因子)。所得活化能的大小与热诱导蛋白质变性的活化能一致。基于彭尼斯生物热方程开发了一个三维有限元热模型,并使用ANSYS(V7.0)求解。该模型使用了所研究肾脏的真实几何形状和温度依赖性热特性。通过实验确定了热模拟所需的微波探头的比吸收率(SAR)。热模拟结果表明,尽管一阶动力学模型可能不足以捕捉血流变化,但微波热疗法期间局部肾血流灌注随温度和时间的复杂变化是可以预测的。发现局部血流灌注是温度和时间的复杂函数。引入了基于血管淤滞程度的非线性模型来预测血流灌注。总之,正常猪肾的间质微波热疗法会导致可预测的热和组织损伤行为。未来有必要对人体肾组织进行研究以证实这些结果的临床意义。