The study was conducted during an eight-year period, from January 2012 to January 2020, at Emergency Department of our University Hospital. Patients enrolled in the study included all children up to 14 years old who were admitted for referred BAT and had positive clinical, laboratory and/or US findings. Research was performed in accordance with the Declaration of Helsinki. The research was approved by ethical and deontology committee (Protocol number: 21234) of General University Hospital of Alexandroupolis and science committee of our hospital. Informed consent was obtained from all participants and/or their legal guardians.
All the imaging methods were performed by two radiologists (one pediatric radiologist and one general) and the CEUS scans were followed by CECT within 30 minutes. All parents were informed about the imaging method (CEUS) and signed a consent form (deemed “off-label” method). Moreover, parents/guardians were informed that their children will be monitored for possible side effects after CEUS for about a year period. All CEUS scans were compared with CECT results as CECT is the gold standard in the evaluation of the injured patient [4].
During the eight-year study period, 59 children with age ranged from 4 to 14 years old (38 boys and 21 girls) were referred to the Emergency Department of our University Hospital with reported abdominal injury. These patients initially underwent conventional US that followed FAST. Thirty-two of them (21 boys and 11 girls) with minor injuries, normal physical examination, negative US and laboratory results within normal limits were discharged after 24 hours observation without undergoing further investigation. The rest twenty-seven patients, which form our study population, suffered from more severe injuries with positive clinical, laboratory and/or US findings (Table 1).
Table 1
demographics and outcomes
|
age
|
sex
|
US/FAST
|
CEUS
|
CECT
|
1
|
14
|
male
|
+ (fluid)
|
Liver laceration
|
Liver laceration
|
2
|
9
|
female
|
+ (fluid)
|
L lacer + R Kidney
|
L lacer + R Kidney
|
3
|
13
|
male
|
+ (fluid)
|
spleen contusion
|
spleen contusion
|
4
|
11
|
female
|
-
|
spleen rapture
|
spleen rapture
|
5
|
8
|
female
|
+ (fluid) / spleen suspicion
|
-
|
-
|
6
|
11
|
male
|
+ (fluid)
|
-
|
-
|
7
|
14
|
female
|
+ (focal liver hypoattenuation)
|
spleen rapture
|
spleen rapture
|
8
|
14
|
male
|
-
|
spleen contusion
|
spleen contusion
|
9
|
14
|
male
|
+ (fluid)
|
spleen contusion
|
spleen contusion
|
10
|
14
|
female
|
+ (fluid) / liver suspicion
|
-
|
-
|
11
|
9
|
male
|
+ (focal liver hypoattenuation)
|
Liver laceration
|
Liver laceration
|
12
|
8
|
female
|
-
|
-
|
-
|
13
|
4
|
male
|
-
|
-
|
-
|
14
|
12
|
male
|
-
|
-
|
-
|
15
|
11
|
male
|
-
|
-
|
-
|
16
|
13
|
male
|
-
|
-
|
-
|
17
|
8
|
female
|
-
|
-
|
-
|
18
|
13
|
female
|
-
|
-
|
-
|
19
|
12
|
male
|
-
|
-
|
-
|
20
|
14
|
male
|
-
|
-
|
-
|
21
|
13
|
female
|
-
|
-
|
-
|
22
|
8
|
male
|
-
|
-
|
-
|
23
|
4
|
female
|
-
|
-
|
-
|
24
|
12
|
male
|
-
|
-
|
-
|
25
|
11
|
female
|
-
|
-
|
-
|
26
|
13
|
male
|
-
|
-
|
-
|
27
|
8
|
male
|
-
|
-
|
-
|
FAST = Focused Assessment with Sonography for Trauma, CEUS = Contrast Enhanced Ultrasound,
CECT = contrast-enhanced CT, - = negative results
|
Ultrasonography and Contrast-Enhanced Ultrasonography
Patients initially underwent FAST examination, and in suspicious and stable patients CEUS and CECT was performed. The CEUS-exam started typically from the kidneys, continued with the liver and ended in the spleen (Fig. 1). In cases, with not an appropriate imaging effect a resumption of the method with second intravenous injection was followed. The overall time needed was up to 5 min for each contrast agent injection.
The CEUS procedure requires contrast medium injection and US machine suitable to CEUS software. All CEUS studies were performed with a 5 − 1 MHz convex array transducer in a Philips iU22 ultrasound machine. The contrast media which was used in our study was SonoVueTM (Bracco, Milano, Italy). SonoVueTM is an agent made of microbubbles stabilized by phospholipids and containing Sulphur hexafluoride (SF6), an innocuous gas. The microbubbles have a diameter ranged from 1 micron to 7 microns (1 micron is equal to 0,0001 cm). This contrast medium is blood-pool agent with a non-linear reverberation on US. The microbubbles remain intravascular and produce a non-linear harmonic response that can be separated from the tissue signal using contrast harmonic US (equipment’s software). Our dosage schemes for SonoVueTM were adjusted to 0.03mL per kg (0.03mL/kg) per every intravenous injection. In generally SonoVueTM suspension was administered by syringe bolus using an existing peripheral vein in a maximum amount of 0.3 ml for children weighing < 20 kg and 0.5 ml for children weighing ≥ 20 kg. This was followed by a 5 or 10 ml normal saline flush respectively. Vital signs were monitored at 2 min intervals during the CEUS-study and also 30 mins and 1 hour after completion of contrast injection for possible adverse reaction symptoms. This monitoring was completed with the recording of other side effects such as nausea, vomiting, dizziness etc.
On baseline US if lesions were visible, they were recognized as a hypoechoic or hyperechoic alteration(s) within the organ. On CEUS, when lesions were present in solid organ were clearly visible in all patients. The lesions were depicted as a perfusion defect (demarcated hypoechoic area compared to the adjacent parenchyma) with ill-defined or well-defined margins with or without interruption of the organ profile and margins. If lack of perfusion of a part(s) of the organ was present an arterial lesion was suspected while the presence of microbubbles (reflections) outside of the lacerated organ was defined as an active bleeding.
The arterial phase (first 30 sec) of CEUS were captured as video movie while selective spots from other phases also were recorded. CECT was performed within 30 minutes with intravenous injection of a nonionic contrast agent (1,5 ml/kg) and during the arterial phase, the venous phase and a late-phase study (5–15 min), with the latter performed if fluid collections were revealed to identify more accurately any active bleeding and/or urinoma.
Data were analyzed using Microsoft Excel. The sensitivity, specificity, positive and negative predictive value of conventional US and CEUS were determined compared to CECT.