Mitchell D P, Rowan M, Loughman E, Ridge C A, MacMahon P J
Department of Radiology, Whitty Building, North Circular Road, Mater Misericordiae University Hospital, Dublin 7, Ireland.
Eur J Radiol. 2017 Jan;86:184-189. doi: 10.1016/j.ejrad.2016.11.011. Epub 2016 Nov 8.
The aims of our study were to evaluate the contribution of contrast-monitoring techniques to breast dose in pregnant and non-pregnant women, and to investigate the effect of a reduced peak kilovoltage (kV) monitoring scan protocol on breast dose and Computed Tomography Pulmonary Angiography (CTPA) diagnostic quality.
Single center retrospective study of 221 female patients undergoing a reduced kV 80kV contrast-monitoring CTPA protocol compared to 281 patients using the conventional 120kV contrast-monitoring protocol (Siemens Somatom Definition AS+). 99 pregnant patients analyzed separately. ImPACT dosimetry software was used to calculate dose. Group subsets were evaluated to assess CTPA diagnostic quality.
The contrast-monitoring component of a CTPA study constituted 27% of the overall breast dose when using a standard 120kV protocol compared to only 7% of the overall breast dose in the 80kV study group. The dose to the breast from the contrast-monitoring component alone was reduced by 79% in the non-pregnant patients (0.36mGy±0.37 versus 1.7mGy±1.02; p<0.001), and by 88% in the pregnant population (0.25mGy±0.67 versus 2.24mGy±1.61; p<0.001). There was no statistical difference in CTPA diagnostic quality or timing.
Despite a short scan length and relatively small DLP, contrast-monitoring techniques (test-bolus or bolus-tracked) set at 120kV can account for 27% of the overall breast dose accrued from a CTPA study. By decreasing the kilovoltage of the contrast-monitoring component, a significant reduction in breast dose for pregnant and non-pregnant female patients can be achieved without affecting CTPA quality or timing.
我们研究的目的是评估对比剂监测技术对孕妇和非孕妇乳房剂量的影响,并研究降低峰值千伏(kV)监测扫描方案对乳房剂量和计算机断层扫描肺血管造影(CTPA)诊断质量的影响。
对221例接受80kV降低千伏对比剂监测CTPA方案的女性患者进行单中心回顾性研究,并与281例使用传统120kV对比剂监测方案(西门子Somatom Definition AS+)的患者进行比较。对99例孕妇进行单独分析。使用ImPACT剂量测定软件计算剂量。对分组子集进行评估以评估CTPA诊断质量。
使用标准120kV方案时,CTPA研究的对比剂监测部分占乳房总剂量的27%,而在80kV研究组中仅占乳房总剂量的7%。仅对比剂监测部分对非孕妇乳房的剂量降低了79%(0.36mGy±0.37对1.7mGy±1.02;p<0.001),对孕妇群体降低了88%(0.25mGy±0.67对2.24mGy±1.61;p<0.001)。CTPA诊断质量或检查时间无统计学差异。
尽管扫描长度较短且剂量长度乘积(DLP)相对较小,但设置为120kV的对比剂监测技术(试验团注或团注追踪)可占CTPA研究累积乳房总剂量的27%。通过降低对比剂监测部分的千伏,可以在不影响CTPA质量或检查时间的情况下,显著降低孕妇和非孕妇女性患者的乳房剂量。