Dankerl Peter, Hammon Matthias, Seuss Hannes, Tröbs Monique, Schuhbaeck Annika, Hell Michaela M, Cavallaro Alexander, Achenbach Stephan, Uder Michael, Marwan Mohamed
Department of Radiology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Maximiliansplatz 1, 91054, Erlangen, Germany.
Department of Cardiology, Universitätsklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Ulmenweg 18, 91054, Erlangen, Germany.
Int J Comput Assist Radiol Surg. 2017 May;12(5):795-802. doi: 10.1007/s11548-016-1470-8. Epub 2016 Sep 7.
To evaluate the performance of computer-aided evaluation software for a comprehensive workup of patients prior to transcatheter aortic valve implantation (TAVI) using low-contrast agent and low radiation dose third-generation dual-source CT angiography.
We evaluated 30 consecutive patients scheduled for TAVI. All patients underwent ECG-triggered high-pitch dual-source CT angiography of the aortic root and aorta with a standardized contrast agent volume (30 ml Imeron350, flow rate 4 ml/s) and low-dose (100 kv/350 mAs) protocol. An expert (10 years of experience) manually evaluated aortic root and iliac access dimensions (distance between coronary ostia and aortic annulus, minimal/maximal diameters and area-derived diameter of the aortic annulus) and best CT-predicted fluoroscopic projection angle as the reference standard. Utilizing computer-aided software (syngo.via), the same pre-TAVI workup was performed and compared to the reference standard.
Mean CTDI[Formula: see text] was 3.46 mGy and mean DLP 217.6 ± 12.1 mGy cm, corresponding to a mean effective dose of 3.7 ± 0.2 mSv. Computer-aided evaluation was successful in all but one patient. Compared to the reference standard, Bland-Altman analysis indicated very good agreement for the distances between aortic annulus and coronary ostia (RCA: mean difference 0.8 mm; 95 % CI 0.4-1.2 mm; LM: mean difference 0.9 mm; 95 % CI 0.5-1.3 mm); however, we demonstrated a systematic overestimation of annulus- derived diameter using the software (mean difference 44.4 mm[Formula: see text]; 95 % CI 30.4-58.3 mm[Formula: see text]). Based on respective annulus dimensions, the recommended prosthesis size (Edwards SAPIEN 3) matched in 26 out of the 29 patients (90 %). CT-derived fluoroscopic projection angles showed an excellent agreement for both methods. Out of 58 iliac arteries, 15 (25 %) arteries could not be segmented by the software. Preprocessing time of the software was 71 ± 11 s (range 51-96 s), and reading time with the software was 118 ± 31 s (range 68-201 s).
In the workup of pre-TAVI CT angiography, computer-aided evaluation of low-contrast, low-dose examinations is feasible with good agreement and quick reading time. However, a systematic overestimation of the aortic annulus area is observed.
使用低对比剂和低辐射剂量的第三代双源CT血管造影术,评估计算机辅助评估软件在经导管主动脉瓣植入术(TAVI)前对患者进行全面检查的性能。
我们评估了30例计划进行TAVI的连续患者。所有患者均接受了心电图触发的主动脉根部和主动脉高螺距双源CT血管造影,使用标准化的对比剂用量(30 ml碘美普尔350,流速4 ml/s)和低剂量(100 kv/350 mAs)方案。一名专家(有10年经验)手动评估主动脉根部和髂动脉入路尺寸(冠状动脉开口与主动脉瓣环之间的距离、主动脉瓣环的最小/最大直径和面积衍生直径)以及最佳CT预测的透视投影角度作为参考标准。使用计算机辅助软件(syngo.via)进行相同的TAVI术前检查,并与参考标准进行比较。
平均CTDI[公式:见原文]为3.46 mGy,平均DLP为217.6±12.1 mGy·cm,对应平均有效剂量为3.7±0.2 mSv。除一名患者外,计算机辅助评估均成功。与参考标准相比,Bland-Altman分析表明主动脉瓣环与冠状动脉开口之间的距离一致性非常好(右冠状动脉:平均差异0.8 mm;95%CI 0.4-1.2 mm;左主干:平均差异0.9 mm;95%CI 0.5-1.3 mm);然而,我们证明使用该软件会系统性高估瓣环衍生直径(平均差异44.4 mm[公式:见原文];95%CI 30.4-58.3 mm[公式:见原文])。根据各自的瓣环尺寸,推荐的假体尺寸(爱德华SAPIEN 3)在29例患者中的26例(90%)中匹配。CT衍生的透视投影角度在两种方法中显示出极好的一致性。在58条髂动脉中,15条(25%)动脉无法被软件分割。软件的预处理时间为71±11 s(范围51-96 s),使用软件的读取时间为118±31 s(范围68-201 s)。
在TAVI术前CT血管造影检查中,计算机辅助评估低对比剂、低剂量检查是可行的,一致性良好且读取时间快。然而,观察到主动脉瓣环面积存在系统性高估。