Liver |
Targeted evaluation of the enhancement pattern of a focal lesion in real time |
Timing of vascular phases different from adults and varies based on age |
Arterial phase may start as quickly as 5 s following the administration of microbubbles |
May need to do a “sweep scan” to search for focal lesions or trauma |
Transplantation |
Knowledge of the surgical technique and the exact type of vascular anastomosis is essential for accurate diagnosis |
Colour and spectral Doppler imaging is still required to assess clinically significant vascular stenosis |
Kidney |
Rapid cortical enhancement followed by medullary phase lasting up to 2 min post-injection |
No evaluation of pelvicalyceal system as microbubbles are not excreted |
Spleen |
Targeted evaluation of the perfusion pattern of a focal lesion |
Keep in mind the peculiar enhancement pattern of spleen including inhomogeneous (“zebra-like”) initial phase and long-lasting homogeneous delayed enhancement |
May need to do a “sweep scan” to detect focal lesions particularly in trauma |
Trauma |
Two separate doses of microbubbles administered for liver and right kidney and then spleen and left kidney ± pancreas |
Examination starting from side of clinical concern |
Kidneys should be evaluated first owing to earlier enhancement, in the arterial phase, whereas liver and spleen can be assessed during the portal venous phases |
Traumatic lesions appear as well-demarcated hypoechoic (non-enhancing) areas |
Careful evaluation of the vasculature will detect any pseudoaneurysms |
Bowel |
4 h of fasting required |
Conventional ultrasonography precedes to detect thickened loops |
Lower dose of microbubbles are administered when low-frequency transducers are used |
Higher dose of microbubbles are administered when high-frequency transducers are used |
Quantification of mural enhancement is valuable |
Lung/pleura |
Targeted evaluation can be performed using coronal plane, similarly to conventional ultrasonography |