Principles of Three-Dimensional Ultrasound


Introduction

Since 1974, when the first three-dimensional echocardiography (3DE) images of the heart were obtained by Dekker and colleagues, 3DE technology has greatly evolved. The development of the real-time volumetric acquisition technique, along with significant technological advances in computer and transducer technologies, have significantly improved the image quality and the practical feasibility of 3DE, allowing its implementation in clinical practice. 3DE data sets can be acquired from either transthoracic (TTE) or transesophageal (TEE) approach, allowing real-time visualization of the cardiac structures from any spatial point of view. 3DE has been demonstrated to be superior to two-dimensional echocardiography (2DE) in various clinical scenarios, such as (1) quantification of cardiac chamber volumes and function,(2) assessment of the mechanisms and severity of heart valve diseases, (3) evaluation of cardiac complex anatomy and defects in congenital valve diseases, and (4) patient selection and monitoring during cardiac interventional procedures ( Boxes 5.1 and 5.2 ). However, to take the best use of this technique, a full understanding of its technical principles, as well as of its strengths and limitations, is essential.

BOX 5.1
Main Indications to 3D Transthoracic Echocardiography

  • 1.

    Patients with distorted left ventricular anatomy (aneurysm, extensive wall motion abnormalities, etc.) in whom accurate measurement of volumes will be clinically relevant

  • 2.

    Patients with left ventricular dysfunction who may be candidates for device implantation or complex surgical procedures

  • 3.

    Patients with heart failure, or right heart diseases that may affect right ventricular size and function

  • 4.

    Mitral valve assessment in patients referred to mitral valve surgery

  • 5.

    Evaluation of mitral stenosis

  • 6.

    Patients with tricuspid stenosis and/or more than mild tricuspid regurgitation in whom assessment of tricuspid valve morphology and severity of regurgitation will be clinically relevant

  • 7.

    Congenital heart diseases

  • 8.

    Patients with acceptable acoustic window quality with unclear anatomy by two-dimensional imaging

BOX 5.2
Main Indications to 3D Transoesophageal Echocardiography

  • 1.

    Assessment of mitral valve anatomy in patients in whom the data will be clinically relevant for management: mitral stenosis, functional or degenerative mitral regurgitation, congenital abnormality, endocarditis

  • 2.

    Left ventricular outflow tract sizing in patients referred for transcatheter aortic valve replacement (TAVR) who cannot undergo cardiac tomography

  • 3.

    Assessment of aortic valve anatomy in patients with aortic regurgitation, candidates to aortic valve repair

  • 4.

    Left atrial appendage orifice sizing in candidates for device closure

  • 5.

    Assessment of atrial septal defect anatomy and size in candidates for device closure

  • 6.

    Suspected or known mitral valve prosthesis structural or nonstructural dysfunction or endocarditis

  • 7.

    Guiding/monitoring interventional procedures in the cath lab

  • 8.

    Pre- and postoperative assessment of mitral valve and congenital heart disease cardiac surgery

  • 9.

    Cases with uncertain 2D anatomy in transthoracic and transesophageal studies

Fully Sampled Matrix Array Transducers

Considerable advancements in hardware and software, involving microelectronic techniques, image formation algorithms, and digital processing, have led to the development of fully sampled matrix array transducers, which enabled the volumetric 3DE acquisition with good imaging quality within a short acquisition time ( Fig. 5.1 ). At present, matrix array transducers are composed of nearly 3000 piezoelectric elements (as opposed to only 128 elements in a conventional 2DE phased-array transducer), with operating frequencies ranging from 2 to 4 MHz for TTE and from 5 to 7 MHz and TEE imaging. The piezoelectric elements are arranged in rows and columns to form of a rectangular grid (i.e., matrix configuration), individually connected and simultaneously active (fully sampled). The electronically controlled phased firing of the piezoelectric elements enable to generate a scan line that propagates radially (y, axial direction) and can be steered both laterally (x, azimuthal direction) and in elevation (z, vertical direction) to acquire a pyramidal volumetric data set (see Fig. 5.1 A and B ).

FIG. 5.1, The electronically controlled phased firing of the piezoelectric elements enable to generate a scan line that propagates radially ( y , axial direction) and can be steered both laterally ( x , azimuthal direction) and in elevation ( z , vertical direction) to acquire a pyramidal volumetric data set (A), by fully sampled matrix array transducers (B). Volume pyramids can be acquired over a series of consecutive cardiac cycles, using a number of electrocardiogram-gated subvolumes (C). (Courtesy of Bernard E. Bulwer, MD, FASE.)

Currently matrix-array probes are available for both TTE and TEE imaging and, in addition to the conventional 2D-Doppler imaging, they enable three different acquisition modalities: multiplane 2DE imaging, real-time (or live) 3DE imaging, and multibeat ECG-gated 3DE imaging, all three with/without color flow information ( Chapter 10 , “3D Image Acquisition”).

Previous 3DE equipment could only acquire and display in real-time volumetric data sets of a relatively small size (about 30° × 50°). These pyramids were sufficiently large to allow a partial display of the ventricles or of the valvular structures; the larger volumes needed to encompass the whole structure required at least four smaller component volumes acquired over a series of consecutive cardiac cycles to yield a 90° × 90° image (see Fig. 5.1C ). However, the technology evolved and the current 3DE systems have the capability of acquiring and displaying single-beat volumes as 90° × 90° pyramids in real time (see Fig 5.1A ), with improved temporal and spatial resolution (even though significantly lower than by multi-beat acquisition).

A major technological breakthrough that allowed manufacturers to develop fully sampled matrix array transducers was the electronics miniaturization and microbeamforming. Several miniaturized circuit boards have been incorporated into the matrix-array transducer, allowing partial beamforming to be performed in the transducer itself, reducing both power consumption and the size of the connecting cable. In addition, more advanced crystal manufacturing processes (such as the PureWave crystal technology), by increasing the efficiency of transduction and of conversion process between electrical power and ultrasound energy, helped reduce heat production.

Physics of Three-Dimensional Ultrasound

3DE is an ultrasound technique; consequently it is limited by the speed of ultrasound in human body tissues (∼1540 m/s in myocardial tissue and blood). The image depth determines the distance a single pulse has to travel backward and forward, resulting in the maximum number of pulses per second. The acquisition is performed by a pyramidal volume with the desired beam spacing in each dimension (spatial resolution), which is related to the volumes per second that can be imaged (temporal resolution). As a consequence, similarly to 2DE, there is an inverse relationship between temporal resolution, acquisition volume size, and spatial resolution, as represented in the equation:


Volume rate ( temporal resolution ) = 1,540 × Number of parallel received beams ( volume size ) 2 × volume width / lateral resolution 2 × Volume depth ( spatial resolution )

According to the structure of interest and specific requirements, the volume rate can be augmented by decreasing the volume width or depth, or by increasing the number of parallel receiving beams (line density). However, decreasing the volume width or depth can limit the capability to acquire the whole structure of interest, and increasing the number of parallel receiving beams may adversely affect the signal-to-noise ratio and the image quality. Manufacturers have developed several approaches to overcome this issue, such as the development of multibeat ECG-gated acquisition, real-time zoom acquisition, and parallel receive beamforming.

Multibeat ECG-Gated Acquisition

This technique uses a number of ECG-gated subvolumes acquired from consecutive cardiac cycles (see Fig. 5.1C ), stitched together in position and size, to increase the size of the pyramidal volume maintaining the volume rate (>30 Hz). Nevertheless, the pyramidal volume should be optimized to the smaller volume capable to encompass the cardiac structure of interest, for the highest spatial resolution. The main limitation of gated imaging is the occurrence of stitching artifacts, shown as subvolume malalignments in the pyramidal imaging, which may impede proper image interpretation or quantification. Those can occur by transducer movement, cardiac translation motion due to respiration, or change in cardiac cycle length (arrhythmias; Fig. 5.2 and ).

FIG. 5.2, Multibeat acquisition of the mitral valve by 3D TEE in a patient with P1 flail while breathing normally. Several stitching artifacts (B, yellow arrows ) between the subvolumes (delimited by the white dashed lines in A) are shown.

Real-Time Zoom Acquisition

Real-time zoom mode is ideal for the study of a restricted structure of interest, with high spatial and temporal resolution. The operator can adjust the area of acquisition with the minimum lateral and elevation width, and the ultrasound system automatically crops the adjacent structures to provide a real-time display of the structure of interest. If the structure of interest is large, the temporal resolution can be further increased by using a multibeat zoom acquisition. The main disadvantage of real-time zoom is the limited ability to show the anatomic relationships between the structure of interest and surrounding structures. However, it is of great use to study the mitral valve, particularly by TEE, and whenever a large ECG-gated acquisition is not feasible (arrhythmias, patient unable to breath hold, etc.; Fig. 5.3 and , ).

FIG. 5.3, Real-time 3D zoom acquisition of the mitral valve by 3D TEE in a patient with Barlow disease and P2 flail with ruptured chord (arrow) , in atrial fibrillation. LAA, Left atrial appendage.

Parallel Receive Beamforming

Beamforming is a technique used to process signals so that directionally or spatially selected signals can be sent or received from sensor arrays. Parallel receive beamforming uses a high-end imaging engine, wherein the system transmits one wide beam and receives multiple narrow beams in parallel, and requires a platform with higher volume/information rate. The transmit beamformer transmits timed pulses thousands of times per second, and the receive beamformer generates multiple beams through parallel and real-time processing of echo. The number of receive beams generated in parallel by the receive beamformer determines the maximum information rate the imaging system can achieve. In this way, the volume rate/temporal resolution ratio is increased by a factor equal to the number of received beams. Nevertheless, the finite speed of sound through tissue imposes a physical limit on the maximum number of pulses that can be fired per second, as it takes hundreds of microseconds for a round trip pulse to reach the deepest depth, and then to propagate back to the acoustic array. Conversely, the size of the volume, target volume rate, and lateral resolution determines the total number of beams needed per second. For example, to obtain a full volume (90° × 90°), 16-cm depth pyramidal volume at 25 volumes/s, the system needs to receive 100,000–200,000 beams/s, depending on the lateral resolution. Since the emission rate is around 5000 transmitted pulses, the system needs to form 20 to 40 beams in parallel for each transmit pulse, and even higher for real-time imaging of motion. However, there are limits to the increase in the number of parallel beams, since it leads to an increase in size, cost, and power consumption of the beamforming electronics, as well as deterioration of the signal-to-noise ratio and contrast resolution. To overcome this problem, manufactures have been developing innovative technologies for beamforming, image forming, and processing (nSIGHT imaging, Philips Healthcare; XDclear and cSound, GE Healthcare; coherent volume formation, Siemens Healthcare; etc.), which allow us to increase the spatial resolution, clarity, and overall quality of the 3DE images, and to reduce noise.

Similar to what occurs with conventional 2DE imaging, the use of 3D color Doppler further impacts the spatial and temporal resolution of the 3DE images. The use of 3D color Doppler in real time is limited by lower frame rates and by the smaller volume size. Conversely, the multibeat 3D color full-volume can be affected by stitching artifacts. The TEE approach for 3D color acquisition provides higher spatial resolution and superior image quality than TTE. The limited spatial and temporal resolution of 3D color Doppler used to be a major limitation, but it has greatly improved with the advancing technology, and color Doppler volumes can be currently obtained with up to 40 voxels/s ( Fig. 5.4 and ).

FIG. 5.4, 3D TEE imaging of a mitral bioprosthesis after percutaneous periprosthetic leak closure using two vascular plugs (A) and 3DTEE color Doppler imaging showing multiple residual leaks between the devices (B).

Finally, the image quality of the 3DE data sets is also affected by the point spread function. The point spread function describes the imaging system response to a point input, which is represented as a single pixel. The degree of spreading (blurring) of any point object varies according to the dimension employed. In current 3DE systems, the degree of spreading (blurring) is around 0.5 mm in the axial (y) dimension, 2.5 mm in the lateral (x) dimension, and 3 mm in the elevation (z) dimension. As a result, higher resolution images should be expected when acquired using the axial dimension (i.e., parasternal views), rather than the elevation dimension (i.e., apical views), and when acquiring the structure of interest in the center of the pyramidal volume sector, rather than in an eccentric position.

As a consequence, to obtain effective 3DE images, it is pivotal that the appropriate acquisition window and modality are selected, and that acquisition settings are optimized according to the desired structure of interest.

Display of Three-Dimensional Echocardiographic Images

The 3DE graphic reproduction of cardiac structures on flat 2D monitors has been made possible using computer graphics techniques. Since the different structures (blood, pericardial fluid, air) within the heart have distinct physical properties and different abilities to reflect ultrasound, segmentation is performed by setting a threshold of echo intensity. Once segmented, the 3DE data set can be displayed using a series of rendering options: 2D tomographic slices, volume rendering, surface rendering, and wireframe rendering.

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