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M. Riccabona
• For assessment of intestinal structures, perineal US, detailed analysis of liver surface or renal parenchyma, as well as for appendicitis, mesenteric nodes or pylorus, linear transducers are advisable (frequency range 3–15MHz, depending on age/targeted area); high-resolution curved linear arrays may offer larger eld of view at only slightly reduced resolution—helpful supplement.
2.7.5 Course ofInvestigation andMeasurements
2.7.5.1 General Remarks
Entire targeted area is evaluated in serial longitudinal and axial sections, comple­mented by oblique sections if necessary; always includes surrounding structures and other relevant areas that might cause similar complaints:
• Always assess and document size, contour, shape, position, echostructure and internal anatomy as well as motility/correlation to adjacent structures.
• Documentation is usually standardised for various queries and body areas; even normal ndings are documented in longitudinal and axial section. Pathology needs to be documented in two planes and measured.
• Various documentation standards/recommendations are available (e.g. DEGUM/ OEGUM—see: www.oegum.at/content/view/506/210/).
Standardised images and sections help to improve comparability and reduce
interobserver variation—usually predened by documentation recommenda­tions (more details listed in organ-specic chapters). Three-dimensional US (3DUS) offers possibility to store entire volume of targeted organ thus improving documentation.
2.7.5.2 Transducer Handling
Transducers should be moved slowly, carefully, without pressure, no sudden move­ments and with continuous smooth contact with skin. Specic techniques such as graded compression or positioning manoeuvres helpful, sometimes mandatory (e.g. appendix US), for some applications irreplaceable (for DDx), but try to inform or alert child prior to these measures in order to gain cooperation and avoid sudden unexpected frightening experience. Remember to effectively, but gently clean the transducers after each investigation.
2.7.5.3 Measurements
Basically every organ should be measured, particularly important in paediatric US as sizes vary with age, depending on patient weight/size (see Chap. 7—Measurements).
Measurements are always performed in longitudinal and axial sections and docu-
mented—either as 2-D distance or planimetric denition of (manually) dened plane. In some organs (e.g. kidney) volume calculations based on mathematic equa­tions using a corresponding geometric shape are more reliable and useful than just length measurements.
2 US Methods, Artefacts, Biologic Eects, Practice
All measurements are performed in standardised, representative and reproduc-
ible sections that grant optimal depiction of maximal length and diameters.
Particularly for irregularly shaped organs 3DUS volumetry is better enabling
reliable values,
Organ sizes are assessed according to age-matched normal value graphs. For further details see respective chapter.
Note Measurements are for orientation and not always reliable, may vary signi-
cantly even within one investigator during same examination. Always consider/ check the internal correction factors of the device if you are using the device’s cal­culation program.
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2.8 Documentation andInterpretation
2.8.1 Image Documentation
Every imaging investigation needs to be documented in sufcient diagnostic quality and detail; minimal documentation requirements are usually standardised by indi­vidual hospitals/medical societies in form of guidelines or recommendations (see above).
Documentation is essential not only for medicolegal issues and reimbursement
but also for retrospective reassessment and comparison during follow-up.
Documentation can be performed by various methods: printout from frozen
monitor images using various printing media (video printers, hardcopies, etc.), stor­age to hard disc and export into some storage memory; many hospitals store cap­tured digital images to their PACS.Increasingly not only single images but also short video clips or 3D volumes are stored for improved documentation. Images/ clips can be retrieved from PACS for reading, printout or digital distribution.
2.8.1.1 Media forDocumentation
• Polaroid pictures: rather expensive, suboptimal quality, danger of fading, not used frequently any longer.
• Video paper or colour printers: particularly black and white less expensive, very practical, still used.
Note Durability restricted—prone to fading and damage.
• Multi-format camera: excellent quality, excellent durability, inexpensive in maintenance and for individual copies but requires signicant initial investment. Was the major documentation in the past but increasingly outdated by digital documentation.
• Laser imager: good image quality and durability, comparable to multi-format camera—but even more expensive, and due to large size, difcult to transport; still commonly used in places without PACS.
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M. Riccabona
• Photo camera: acceptable image quality—but cumbersome handling and devel­opment; only rarely used, mainly for teaching or publication purposes.
• Video tape: best documentation of entire investigation, particularly useful/valu­able for echocardiography where it is still commonly used. Setbacks: unpractical handling of all the tapes with signicant space requirements for archiving, dif­cult to retrieve single specic investigation; adequate video players must be available for review. Increasingly being replaced by digital cine-loop clip storage.
• Digital documentation—today the most used method. All modern systems store digital images and short clips to hard drive, can be exported either to workstation and PACS or transferred to other storage media such as optical discs and external hard drive.
2.8.2 Report
Documentation not only includes representative images but also the nal writ­ten report.
Reports vary with institution and country—usually referring physician gets nal
report but no or only some selected representative images, unless images can be retrieved from PACS or another digital environment.
Note Archiving demands vary with country, include both images and report. When
setting up an US service, adequate precautions to comply with local documentation, archiving and regulatory demands are mandatory.
2.8.2.1 How toIssue aReport
US is an ongoing real-time investigation that (except for video tape documentation or 3DUS) cannot be entirely documented. Description of investigation is essential; should be included—not only all areas assessed but also listing all areas and aspects which could not be properly visualised (e.g. due to overlapping gas) as far as rele­vant for investigation or actual query, to allow referring physician to perceive restrictions of investigation.
After descriptive part (usually includes description of organs, measurements/
sizes, with relation to age, weight/size) responsible reader should state a conclusive diagnosis rating importance of individual ndings with respect to clinical symptoms and query.
2.8.2.2 Diagnosis
Diagnosis—interpretation of ndings retrieved from US investigation, should com­prehensively and conspicuously draw conclusion from ndings detailed in descrip­tion stating diagnosis and listing important DDx. One should always include limitations of investigation and—if applicable—list supplementing imaging steps.
Note Purpose of structured report—to enable referring physicians to reassess inter-
pretation of ndings. Additional ndings received in the meantime or changed/dete-
2 US Methods, Artefacts, Biologic Eects, Practice
37
riorated patient symptoms may indicate re-evaluation. By dividing report into descriptive part and diagnostic assumption, referring physicians are enabled to draw different conclusions in the light of recent changes. Not as important in patients with normal or unequivocal clear-cut ndings/screening conditions—here short report versions can be used.
2.8.2.3 Predefined Reports
Predened report forms are increasingly in use trying to standardise reports and to integrate them into electronic systems; however, often tend to become very exten­sive or may not provide sufcient exibility to properly communicate all aspects of individual investigations, particularly in rare ndings.
2.8.2.4 Nomenclature
Use of proper terms and consistent nomenclature is extremely important; stan­dardised image orientation is recommended.
Topographic denitions on US image:
• In general (abdominal and small part US): cranial/proximal, left; caudal/distal, right; right image side usually left image (supine position).
• Neurosonography: frontal—left in sagittal views; for coronal sections right image side—left patient side. See respective Chapters.
• Echocardiography: see Chap. 11.
• Hip US: see Chap. 15.
• Use of pictograms and markers as well as image inscriptions helpful.
Note One has to dene whether axial descriptions refer to body or organ axis.
• A number of typical sonomorphologic descriptions used referring to denition and contour, echotexture (inhomogeneous or not, etc.), its relative mobility (good, poor, missing, etc.) and echogenicity (echoic or echogenic, hyperechoic, anechoic, etc.). Use them consistently.
(Color) Doppler US: Theory, Artefacts,
fc
o
×
α
Typical Applications inChildhood
MichaelRiccabona

3.1 Doppler Sonography

3.1.1 The Doppler Phenomenon
Frequency of reected wave is changed if the ultrasound beam is reected by mov­ing particles (Doppler effect).
Application
• Doppler effect mostly used to assess ow direction and velocity—mostly of blood. Basically other types of movement also depictable, usually causing arte­facts, but may be diagnostically valuable (e.g. twinkling sign, uereteric jet, “swirls”, uid colour sign).
• Based on known sound velocity, sound beam direction, its emitted frequency and the direction of imaged motion (e.g. course of vessel on screen—thus dening angle α between sound beam and motion direction), ow velocity can be calcu­lated using the Doppler equation based on the measured frequency shift of received echoes.
• Velocity can only be calculated if Doppler angle is known—only with low angles (<10–15°) this can be neglected without signicant measurement errors.
• Doppler equation:
3
d
=
M. Riccabona (*) Department of Radiology, Division of Pediatric Radiology, Medical University Graz and University Hospital Graz, Graz, Austria e-mail: michael.riccabona@medunigraz.at
© Springer Nature Switzerland AG 2020 M. Riccabona (ed.), Pediatric Ultrasound,
https://doi.org/10.1007/978-3-030-47910-7_3
f
×2cos
39
40
M. Riccabona
V=velocity (m/sec), fo=emitted frequency (MHz), fd=frequency shift (kHz), c=speed of sound in tissue (m/sec), α=angle between sound beam and move-
ment direction (Doppler angle).
How Doppler Information Is Displayed
• Received signals exhibit frequency shift—used for calculation. Result displayed acoustically (ow noise) or graphically; the latter achieved by complex signal analysis (based on fast Fourier analysis) creating ow graph on monitor—ow velocity and direction on y-axis, with time encoded on x-axis (see Fig. 2.2).
• Averaged ow velocity information can be superimposed on conventional grey scale US image by colour displays called colour Doppler sonography (CDS, Fig.3.1).
3.1.2 Different Techniques andApplications
ofDoppler Sonography
3.1.2.1 Continuous Wave Doppler (CW)
Principle
• Simultaneous emission and receiving of US beam with two different crystals allows assessment of all movements that occur throughout entire beam range.
• Reected signals undergo spectral analysis to decode different ow velocities and directions.
• Information then displayed by modulating graph intensity depending on distribu­tion of individual ow velocity (Fig.3.2).
Application
• CW Doppler used for quantitative assessment and analysis of high ow veloci­ties—particularly in echocardiography or in severe stenosis.
• Also used for acoustic depiction and assessment of ow in angiology or phlebol­ogy as well as for vessel puncture (“Doppler stick”, Fig.3.2).
Fig. 3.1 CDS—general display. Colours superimposed on grey scale image display ow direction and mean ow direction; the colour bar in the left of the image indicates the respective scale (red towards transducer, blue away from transducer, 0.29m/s—depictable mean peak velocity—without aliasing)
3 (Color) Doppler US: Theory, Artefacts, Typical Applications inChildhood
Fig. 3.2 CW Doppler Scheme. CW Doppler is a single constant US beam without dening any pulse repetition. Usually applied by a small stick-like apparatus that is easily portable; can also be integrated in normal US devices. All ow velocities within range of beam are depicted and dis­played no matter whether they come from different locations. No aliasing—excellent for analysing very high ow velocities. Method used in echocardiography and for orienting information, e.g. patency of vessel, signs of signicant ow alteration (e.g. screening for leg vein thrombosis) or nding a vessel for puncture, as well as for transcranial Doppler in adults/adolescents (e.g. sickle cell anaemia)
41
Restrictions
• All information throughout entire beam is displayed—no identication of spe­cic ow information of individual area.
3.1.2.2 Pulsed Wave Doppler (PW)
Principle Offers the benet to individually target and analyse ow in a sin­gle vessel.
• PW Doppler uses a crystal that alternatingly is used to send and then to receive. After transmitting a short well-dened US signal—longer receive period is acti­vated to register reected echoes.
• Time interval between sending and receiving can be dened—signal can be exactly located at a specic denable depth.
• Volume of sampled area can be dened by variation of receive time (sample volume).
• Thus, one can choose individually adaptable partitions at variable sizes through­out imaged eld; all other areas within are neglected.
• Flow velocity measurements can be performed after applying angle correction (Fig.3.3, Table3.1).
Intrinsic Restrictions
• By using predened send/receive time and sample volume, a maximum value is dened above which ow velocities cannot be measured (Nyquist border). This correlates with the pulse repetition frequency (PRF).
42
Fig. 3.3 PW Doppler/angle correction and graphic display. (a) PW Doppler: vessel seen by B-Mode or CDS; the Doppler angle is corrected by manually moving line into vessel/ow long axis. Doppler gate is placed at vessel; gate size should be adapted to vessel diameter. (b) Respective graphic ow display after Fourier analysis. Relatively turbulent arterial ow—has a more homog­enous white appearance with little dark areas under the Doppler trace. Laminar ow usually has a clear “Doppler window” and only exhibits a narrow line of maximum velocities. Y-axis encodes ow velocity, x-axis encodes time
M. Riccabona
Table 3.1 Angle dependency of Doppler US measurements
Degree 20° 0.94 6 60° 0.5 50 80° 0.17 83
Cosine-induced error for Doppler measurements depending on insonation angle: lower angles have less error than higher angles; reliable measure­ments can only be achieved up to 50°–60°
cos
Error (%)
• Aliasing—velocities higher than Nyquist border cannot be displayed and may occur on bottom of Doppler trace, creating partially confusing images and inter­fering particularly with automated measurements. Aliasing takes place as soon as PRF is at least twice the maximum Doppler frequency (Nyquist frequency) caused by the frequency shift from reection at moving particle.
• PRF depends on frequency, depth and minimally on sample volume size—the deeper a vessel, the lower PRF must be set. Consequently, the maximum velocity measurable in deep vessels is relatively low.
Note If the angle approaches 90°, no ow shown/depictable due to the cosine of
90° (=0) although there may be ow.
3.1.2.3 Duplex-Doppler Sonography/Spectral Flow Analysis
Principle
• Combination of B-Mode US with Doppler sonography. Simultaneous perfor­mance and display of B-Mode image and PW-/CW/colour-Doppler- sonography information:
3 (Color) Doppler US: Theory, Artefacts, Typical Applications inChildhood
43
– If three modes performed simultaneously—“triplex-Doppler sonography”,
improving exact location of sample volume, often at sacrice of (temporal) resolution (= low frame rates, alternatively intermittent CDS-image update ...).
• Immensely important for correct assessment: proper angle correction is essential for quantication of blood ow velocity if angle >10°. Doppler ow measure­ments signicantly depend on angle between US beam and motion direction— this tool is essential for ow quantication and measurements (see Table3.1).
Restrictions
• Due to development of the cosine of angle α, measurements at Doppler angles >50 to maximum 60° become inaccurate and unreliable—should not be used for diagnosis.
• When angle reaches 90°, cosine of angle α becomes 0, therefore no Doppler information can be retrieved (= no ow visible even if there is ow).
3.1.2.4 Colour-Coded Doppler Sonography or Colour Doppler
Sonography (CDS)
Principle
• CDS—simultaneous PW Doppler at many individual points of image (dened by “colour box”).
• Depending on equipment, variably averaged mean value of ow velocities and direction encoded by colours superimposed on conventional black and white grey scale B-mode image.
• Depending on colour preset, the main colour usually displays ow direction (e.g. red—towards transducer, blue—away from transducer); ow velocity variations within the same direction are then encoded by different colour intensities or shades (see Fig.3.1).
Application and Restrictions
• Helpful for quick assessment of ow information.
• Helps to quickly nd vessels and differentiate them from other cystic or tubular structures.
• Helps to optimise quantitative PW duplex-Doppler investigation of specic areas.
• Intrinsically does not allow detailed assessment of ow dynamics except for a general impression of laminar versus pulsating ow, ow direction and average ow velocity—no angle correction possible.
• Size of individual samples can be modied impacting frame rate. Additionally other parameters for image optimisation such as ltering and velocity scales to be applied.
Note Slow frame rates caused by high resolution and low ow velocity imaging
may create motion-induced artefacts, particularly in uncooperative children.
3.1.2.5 Amplitude-Coded Colour Doppler Sonography (aCDS)
Synonyms: Angio-mode, Power Doppler (PD), Colour Doppler Energy (CDE).
44
M. Riccabona
Principle
• Does not use ow velocity but integrated velocity spectrum for calculation and colour display.
• Higher sensitivity, reduced angle dependency.
• Uses amplitude of reected Doppler signals that is signicantly dependent on number of reecting particles (much more than on frequency shift)—displays ow volume rather than ow velocity.
• Furthermore—due to homogeneous low background noise—higher output and receive gains can be used, again increasing potential to depict very low ow velocities at poor Doppler angles down to 0.2mm/s in experimental settings.
• Doppler information displayed by colour overlay on grey scale image as in con­ventional CDS (Fig.3.4).
Restrictions
• High sound pressure in tissue.
• No information on ow velocity and ow direction (exception: “bi-directional Power Doppler”).
• Higher risk of motion artefacts (“ash” artefacts).
Application
Used for vessel depiction at poor insonation angle or with low ow velocities.
• Ideal for assessment of peripheral parenchymal vascularisation—particularly helpful in assessing the kidney.
• Due to its low-angle dependency, often used for demonstrating course of vessels at poor insonation angle such as deep abdominal/cervical vessels and on tran­scranial Doppler sonography.
• Can be combined with duplex-Doppler US.
• Most modern aCDS techniques use special acquisition, ltering and postprocess­ing even further improving depiction of ow such as “superb microvascular imaging/SMI” (Canon), “SieFlow” or “Clarify” (Siemens), “(radiant) SlowFlow HD” (GE), or “MFI/Microow Imaging” (Philips).
Fig. 3.4 aCDS (transplant kidney). Power Doppler with low scale settings demonstrates periph­eral vascularity/perfusion of the parenchyma in this transplant kidney; note the physiologically reduced vascularisation of the medullae, not to be mistaken for pathology