O'Connell A M, Lyon S M, O'Sullivan P, Given M F, Morrin M, Lee M J
Department of Radiology, Beaumont Hospital, Dublin, Ireland.
Clin Radiol. 2008 Apr;63(4):401-6. doi: 10.1016/j.crad.2007.10.002. Epub 2008 Jan 31.
The primary aim of this prospective pilot study was to determine if the administration of intravenous secretin prior to contrast-enhanced computed tomography (CT) improves pancreatic enhancement and pancreatic tumor conspicuity. The second aim was to determine the optimal timing for secretin administration prior to contrast-enhanced CT.
Local ethics committee approval was obtained. 35 patients (18 men, 17 women; mean age, 67.6 years; age range; 25 to 86 years) with known or suspected pancreatic malignancy or an abdominal malignancy underwent a helical CT of the pancreas. The pancreas was first localised on an unenhanced scan using 10mm sections. Following 120 ml of intravenous 300 mg/ml of non ionic contrast medium (CM), injected at a rate of 5 ml/s, images of the pancreas (3mm slice thickness) and liver (8mm slice thickness) were obtained at 40 and 70 seconds respectively. A second CT was obtained 1-5 days after the first one using the same CT and intravenous contrast medium injection parameters. However 100 IU of secretin was given as an intravenous bolus between 0 and 5 min prior to intravenous contrast medium administration. Each patient acted as their own control. The attenuation in Hounsfield Units (HU) was recorded on non-contrast, pancreatic phase and portal venous phases for both secretin and non-secretin CTs, in the pancreas and pancreatic tumors (where present). Tumor conspicuity was calculated (in the 19 patients with pancreatic adenocarcinomas) by subtracting pancreatic tumor attenuation from pancreatic attenuation. Statistical evaluation comparing pre and post secretin enhancement was performed using matched paired t-tests.
A significant increase in pancreatic enhancement was observed when secretin was injected at 2 to 3 min before contrast material injection (the increase in pancreatic density following secretin at 2 min was 31.5+/-10 HU (29.2%) (p=.035); and at 3 min was 23.2+/-7.8 HU (22.7%) (p=.041). Pancreatic tumor conspicuity in the pancreatic phase was most marked when secretin was injected between 2 to 4 min before contrast medium, with 4 min showing a statistically significant increase in tumor conspicuity, 48.2+/-14.2 HU (p=.04).
Imaging in the pancreatic phase 2 to 4 min after administration of intravenous secretin leads to greater enhancement of the pancreas with greater tumor conspicuity, than imaging without secretin.
这项前瞻性试点研究的主要目的是确定在增强计算机断层扫描(CT)前静脉注射胰泌素是否能改善胰腺强化及胰腺肿瘤的显影。第二个目的是确定在增强CT前注射胰泌素的最佳时机。
获得了当地伦理委员会的批准。35例已知或疑似胰腺恶性肿瘤或腹部恶性肿瘤的患者(18例男性,17例女性;平均年龄67.6岁;年龄范围25至86岁)接受了胰腺螺旋CT检查。首先在未增强扫描中使用10mm层厚对胰腺进行定位。在静脉注射120ml 300mg/ml的非离子型造影剂(CM),注射速率为5ml/s后,分别在40秒和70秒时获取胰腺(层厚3mm)和肝脏(层厚8mm)的图像。在第一次CT检查后的1 - 5天,使用相同的CT和静脉造影剂注射参数进行第二次CT检查。然而,在静脉注射造影剂前0至5分钟内静脉推注100IU胰泌素。每位患者作为自身对照。记录胰泌素CT和非胰泌素CT在非增强、胰腺期和门静脉期胰腺及胰腺肿瘤(如有)的亨氏单位(HU)衰减值。通过从胰腺衰减值中减去胰腺肿瘤衰减值来计算肿瘤显影度(在19例胰腺腺癌患者中)。使用配对t检验对注射胰泌素前后的强化情况进行统计学评估。
在注射造影剂前2至3分钟注射胰泌素时,观察到胰腺强化显著增加(在2分钟时注射胰泌素后胰腺密度增加31.5±10 HU(29.2%)(p = 0.035);在3分钟时为23.2±7.8 HU(22.7%)(p = 0.041))。在胰腺期,当在注射造影剂前2至4分钟注射胰泌素时,胰腺肿瘤显影最为明显,4分钟时肿瘤显影度有统计学显著增加,为48.2±14.2 HU(p = 0.04)。
与未使用胰泌素成像相比,静脉注射胰泌素后2至4分钟的胰腺期成像可使胰腺强化更明显,肿瘤显影度更高。