首页> 外文会议>Engineering in Medicine and Biology Society, 2000. Proceedings of the 22nd Annual International Conference of the IEEE >The dose distribution around the edges of an improved32P source for endovascular brachytherapy: a Monte Carlostudy
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The dose distribution around the edges of an improved32P source for endovascular brachytherapy: a Monte Carlostudy

机译:剂量分布在边缘周围改善了 32 P用于血管内近距离放射治疗的来源:蒙特卡洛研究

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Endovascular brachytherapy has proven to be an effective tool inthe reduction of restenosis following balloon angioplasty for coronaryheart disease, while the range of optimal doses and precise targettissue are still unknown. However, over-dosing has been associated withincreased thrombogenicity and permanent damage to vessel walls.Under-dosing has been found to stimulate neointima formation, causingrestenosis. It has been suggested that restenosis near the edges (edgeeffect) of the intervention may be caused by the dose falloff towardsnear the source ends. Monte Carlo code EGS4 was used to calculate thedose distribution around the ends of a Guidant 32P source. Atthe ends of the source the 100% isodose curve was found to bend backtoward the source starting at about 3 mm from the end of the activesource (prescription to 2 mm radius). The 80% isodose line crossed theprescription line 1 mm from the source ends. Further calculationspredicted improvement can be achieved by changing the specific activitywithin 1 mm of the ends of the source. A four-fold increase in specificactivity in 0.5 mm segments at the ends of the source, followed by a 0.5mm gap between the ends and the middle part of the source, kept the 100%isodose line at the prescription distance to within 0.5 mm of the activelength of the source without any over-dosing. With five times theactivity in the terminal segments, a “full length source” isachieved, involving a small over-dosing
机译:血管内近距离放疗已被证明是一种有效的工具 减少冠状动脉球囊成形术后的再狭窄 心脏病,而最佳剂量和精确目标范围 组织仍是未知的。但是,过量使用与 血栓形成增加,对血管壁造成永久性损害。 已发现剂量不足会刺激新内膜形成,从而引起 再狭窄。有人建议边缘附近再狭窄(边缘 的干预效果可能是由于剂量下降导致的 在源头附近。蒙特卡罗代码EGS4用于计算 Guidant 32 P来源末端周围的剂量分布。在 在源的末端发现了100%等剂量曲线向后弯曲 朝向源头,距有源端约3 mm 光源(半径2毫米的处方)。 80%的等剂量线越过 处方线距源头1毫米。进一步的计算 可以通过更改特定活动来实现预期的改进 距光源末端1毫米以内。比重提高了四倍 放射源末端的0.5毫米片段中的活度,随后是0.5 源的两端和中间部分之间的距离为mm,保持100% 处方距离处的等剂量线距有效成分0.5毫米以内 源的长度而没有任何过量。与五倍 终端段中的活动,“全长源”是 实现,涉及少量的过量

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