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Table 2 Parameters of CT imaging

From: Assessment of tissue perfusion of pancreatic cancer as potential imaging biomarker by means of Intravoxel incoherent motion MRI and CT perfusion: correlation with histological microvessel density as ground truth

Phase

Breathing position

Anatomical coverage

Tube voltage [kVp]

Reference tube current (eff.) [mAs]

Delay [s]

Rotation time [s]

Number of Acquisitions

Collimation [mm]

Slice thickness (recon.) [mm]

Pixel spacing [mm]

Reconstruction Kernel

1) Standard 3-phasic CT scan (only performed if patient didn’t have an in-house CT scan of the abdomen within previous 4 weeks)

Application of 80 ml of nonionic iodinated contrast agent; chaser bolus: 40 ml saline solution; bolus tracking in suprarenal aorta (threshold: 100 HU).

Native

Inspiratory breath-hold

Upper abdomen

120

210

4

0.5

Helical

2 × 64 × 0.6

3

Variable

I30f

Arterial

Inspiratory breath-hold

Upper abdomen

120

210

10

0.5

Helical

2 × 64 × 0.6

3

Variable

I30f

Portal-venous

Inspiratory breath-hold

Whole abdomen

120

210

50

0.5

Helical

2 × 64 × 0.6

3

Variable

I30f

15 min break for contrast medium clearance (as applied in previous studies [35, 42]). Patient remains on CT table. Patient is instructed to a shallow breathing technique for reducing motion artefacts in the perfusion acquisition.

2) Native scan for verification of the correct position of the examination volume for CT perfusion imaging (performed in every patient)

Native

Shallow breathing

Pancreas

120

210

n.a.

0.5

Helical

2 × 64 × 0.6

3

Variable

I30f

3) CT perfusion imaging (performed in every patient)

Application of 80 ml of nonionic iodinated contrast agent; chaser bolus: 40 ml saline solution; flow rate: 5 ml/s.

CT perfusion imaging *

Shallow breathing

Tumor area

80

270

13

0.5 (full rotation); 1.5 (cycle time)

34

32 × 0.6

3 × 5.0

0.6 / 0.6

B30f

  1. The pancreatic CT imaging protocol consisted of 1) a standard 3-phasic CT acquisition which was only performed if the patient didn’t have an in-house CT examination of the abdomen within previous 4 weeks, 2) a native acquisition for verification of the correct position of the examination volume for CT perfusion imaging (performed in every patient), and 3) CT perfusion imaging (performed in every patient). All CT acquisitions were performed with automated tube-current modulation. CT acquisitions from examination series grouped under point 1) and point 2) were performed with automated selection of tube voltage (reference tube voltage listed). An experienced radiologist directly involved in the study was always present during CT imaging. Abbreviations: n.a.: not applicable