Department of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Department of Cardiology, Skåne University Hospital, Malmö, Sweden.
J Endovasc Ther. 2020 Jun;27(3):468-472. doi: 10.1177/1526602820912223. Epub 2020 Mar 20.
To validate a new 2D-3D registration method of fusion imaging during aortic repair in a system prepared only for 3D-3D registration and to compare radiation doses and accuracy. The study involved 189 patients, including 94 patients (median age 70 years; 85 men) who underwent abdominal endovascular aneurysm repair (EVAR) with 2D-3D fusion on an Artis zee imaging system and 95 EVAR patients (median age 70 years; 81 men) from a prior study who had 3D-3D registration done using cone beam computed tomography (CBCT). For the 2D-3D registration, an offline CBCT of the empty operating table was imported into the intraoperative dataset and superimposed on the preoperative computed tomography angiogram (CTA). Then 2 intraoperative single-frame 2D images of the skeleton were aligned with the patient's skeleton on the preoperative CTA to complete the registration process. A digital subtraction angiogram was done to correct any misalignment of the aortic CTA volume. Values are given as the median [interquartile range (IQR) Q1, Q3]. The 2D-3D registration had an accuracy of 4.0 mm (IQR 3.0, 5.0) after bone matching compared with the final correction with DSA (78% within 5 mm). By applying the 2D-3D protocol the radiation exposure (dose area product) from the registration of the fusion image was significantly reduced compared with the 3D-3D registration [1.12 Gy∙cm (IQR 0.41, 2.14) vs 43.4 Gy∙cm (IQR 37.1, 49.0), respectively; p<0.001). The new 2D-3D registration protocol based on 2 single-frame images avoids an intraoperative CBCT and can be used for fusion imaging registration in a system originally designed for 3D-3D only. This 2D-3D registration protocol is accurate and leads to a significant reduction in radiation exposure.
为了验证一种新的融合成像 2D-3D 配准方法在仅为 3D-3D 配准设计的系统中进行主动脉修复的有效性,并比较其辐射剂量和准确性。这项研究纳入了 189 例患者,其中 94 例(中位年龄 70 岁;85 例男性)患者在 Artis zee 成像系统上接受了 2D-3D 融合腹主动脉瘤腔内修复术(EVAR),95 例 EVAR 患者(中位年龄 70 岁;81 例男性)来自先前的研究,使用锥形束 CT(CBCT)进行了 3D-3D 配准。对于 2D-3D 配准,将空手术台的离线 CBCT 导入术中数据集并与术前 CT 血管造影(CTA)叠加。然后,将 2 张术中的骨骼单帧 2D 图像与术前 CTA 上的患者骨骼对齐,以完成配准过程。进行数字减影血管造影术以纠正主动脉 CTA 容积的任何配准不良。数值以中位数[四分位距(IQR)Q1、Q3]表示。与最终用 DSA 校正相比(78%在 5mm 以内),骨骼匹配后的 2D-3D 配准精度为 4.0mm(IQR 3.0,5.0)。通过应用 2D-3D 方案,与 3D-3D 配准相比,融合图像配准的辐射暴露(剂量面积产物)显著降低[分别为 1.12Gy·cm(IQR 0.41,2.14)和 43.4Gy·cm(IQR 37.1,49.0);p<0.001]。基于 2 张单帧图像的新 2D-3D 配准方案避免了术中 CBCT,可以在最初仅为 3D-3D 设计的系统中用于融合成像配准。这种 2D-3D 配准方案准确,并导致辐射暴露显著降低。