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螺旋CT中造影剂注射优化用于肺栓塞的诊断

Contrast medium injection optimisation in spiral CT for the diagnosis of pulmonary embolism.

作者信息

Gattoni Filippo, Tagliaferri Beatrice, Scali Paolo, Brioschi Sonia, Boioli Faustino

机构信息

Servizio di Radiologia, Ospedale Fatebenefratelli e Oftalmico, Milan, Italy.

出版信息

Radiol Med. 2003 May-Jun;105(5-6):416-24.

Abstract

PURPOSE

Spiral CT, normally a highly accurate diagnostic method to diagnose pulmonary embolism, has its weak point in the synchronisation of contrast medium (CM) injection and the start of the acquisition, essential to obtain optimal vascular enhancement. The aim of this paper is to introduce a method to control the CM injection based on the enhancement of blood vessels in the diagnosis of pulmonary embolism.

MATERIALS AND METHODS

The CARE bolus software pilots an electronic trigger that first monitors the CM passage, then starts the acquisition procedure when the intensity of enhancement reaches a pre-set value. Our spiral CT has a 6-second scan delay between the trigger's "go-ahead" and the start of the acquisition. During this interval, the CM reaches the pulmonary venous system, enhancing it and making the diagnosis of pulmonary embolism more difficult. This problem was overcome by injecting a slow bolus (30 ml; 1.5 ml/s flow rate) before the CM that triggers the start of the scan when the CM is only present in the pulmonary arteries. We examined 80 patients (36 men, 44 women, mean age 66.9, age range 18 to 89 years). All patients were examined for clinically, radiographically or scintigraphically suspected pulmonary embolism. We evaluated the enhancement of pulmonary arteries on a scale from 0 (poor) to 10 (excellent), image quality (excellent, fair, poor), the examination time and patient tolerance. The results were compared with those obtained in a group of 80 patients studied with CARE bolus without a timing bolus.

RESULTS

Monitor scans were performed with the ROI that triggers the sequence centred on the right heart (trigger value set at 30/35 HU). There were no diagnostic artefacts caused by the enhancement of pulmonary veins due the timing bolus. The average time per procedure was less than 30 min and the time needed to reach the trigger value was 15 sec (range: 10-24 sec). The average volume of CM injected was 130 ml (timing bolus: 30 ml, scan bolus: 100 ml). There were no adverse events to CM injection. The arterial enhancement scored 7 to 10 for 45 patients (56%), 4 to 6 for 23 (28.5%) and 1 to 3 for 12 (15.0%). Image quality was excellent in 52 patients (65.0%), fair in 18 (22.5%) and poor in 10 (12.5%). Comparing arterial enhancement and image quality, we observed that in the cases where enhancement had scored 7 to 10, image quality was excellent, and in the 7 cases where image quality was poor, so was enhancement (1 to 3). We also made a comparison between procedures carried out with and without the timing bolus. We observed that the use of the timing bolus increases the number of exams with high scores for arterial enhancement, and therefore increases the overall number of examinations with optimal enhancement.

DISCUSSION AND CONCLUSIONS

In order to be diagnostically useful, spiral CT requires good vascular enhancement and synchronisation of the start of acquisitions with the highest concentration of CM, as an incorrect scan delay will lead to artefacts and interpretation errors. The proposed method allows correct timing of the CM injection. The diagnostic bolus is preceded by a slow-flow timing bolus that is intercepted by the electronic trigger, which starts the scan when the CM passes into the right heart and pulmonary arteries. The slow-flow bolus volume was 30 ml injected at 1.5 ml/s, whereas the volume of the real bolus was 100 ml, injected at 4.5 ml/s. Monitor scans were performed with the trigger ROI centred on the right heart (trigger value set at 30/35 HU). The time needed for the complete spiral CT exam did not exceed 30 min. The first low-flow bolus injection takes approximately 10 min, but this time becomes shorter as the operator's experience grows. The correct positioning of the ROI on the right heart is the most time-consuming step in the procedure. The procedure was well accepted by all patients with no complaints due to the CM or to the duration of the procedure. There is a high level of concordance between arterial enhancement and image quality. In conclusion, the proposed method is simple, easy to reproduce, and does not give rise to interpretation problems. It is well accepted by patients and suffers few limitations, mainly represented by patients with severe cardiac arrhythmia.

摘要

目的

螺旋CT通常是诊断肺栓塞的一种高度准确的诊断方法,但在造影剂(CM)注射与采集开始的同步方面存在弱点,而这对于获得最佳血管强化至关重要。本文的目的是介绍一种在肺栓塞诊断中基于血管强化来控制CM注射的方法。

材料与方法

CARE bolus软件驱动一个电子触发器,该触发器首先监测CM通过情况,然后在强化强度达到预设值时启动采集程序。我们的螺旋CT在触发器“开始”与采集开始之间有6秒的扫描延迟。在此间隔期间,CM到达肺静脉系统,对其进行强化,从而使肺栓塞的诊断更加困难。通过在触发扫描开始的CM之前注射一个慢速团注(30ml;流速1.5ml/s)来克服这个问题,此时CM仅存在于肺动脉中。我们检查了80例患者(36名男性,44名女性,平均年龄66.9岁,年龄范围18至89岁)。所有患者均因临床、影像学或闪烁扫描怀疑患有肺栓塞而接受检查。我们从0(差)到10(优)对肺动脉强化进行评分,评估图像质量(优、良、差)、检查时间和患者耐受性。将结果与一组80例使用CARE bolus且未进行定时团注的患者的结果进行比较。

结果

使用以右心为中心触发序列的感兴趣区(ROI)进行监测扫描(触发值设定为30/35HU)。定时团注未因肺静脉强化导致诊断伪影。每个程序的平均时间少于30分钟,达到触发值所需时间为15秒(范围:10 - 24秒)。注射的CM平均体积为130ml(定时团注:30ml,扫描团注:100ml)。CM注射未出现不良事件。45例患者(56%)的动脉强化评分为7至10分,23例(28.5%)为4至6分,12例(15.0%)为1至三分。52例患者(65.0%)的图像质量为优,18例(22.5%)为良,10例(12.5%)为差。比较动脉强化和图像质量,我们观察到在强化评分为7至10分的病例中,图像质量为优,在图像质量差的7例病例中,强化也差(1至3分)。我们还对使用和未使用定时团注的程序进行了比较。我们观察到使用定时团注增加了动脉强化高分的检查数量,因此增加了总体最佳强化检查的数量。

讨论与结论

为了在诊断上有用,螺旋CT需要良好的血管强化以及采集开始与CM最高浓度的同步,因为不正确的扫描延迟会导致伪影和解读错误。所提出的方法允许正确的CM注射定时。诊断团注之前有一个慢速流动的定时团注,该定时团注被电子触发器拦截,当CM进入右心和肺动脉时,电子触发器启动扫描。慢速流动团注体积为30ml,以1.5ml/s的流速注射,而实际团注体积为100ml,以4.5ml/s的流速注射。使用以右心为中心的触发ROI进行监测扫描(触发值设定为30/35HU)。完整螺旋CT检查所需时间不超过30分钟。第一次低流速团注注射大约需要10分钟,但随着操作员经验的增加,这个时间会缩短。在右心正确定位ROI是该程序中最耗时的步骤。该程序为所有患者所接受,没有患者因CM或程序持续时间而抱怨。动脉强化与图像质量之间有高度的一致性。总之,所提出的方法简单、易于重复,不会引起解读问题。它为患者所接受,且限制较少,主要是严重心律失常患者。

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