Abstract
Tissue elasticity remains an essential biomarker of health and is indicative of irregularities such as tumors or infection. The timely detection of such abnormalities is crucial for the prevention of disease progression and complications that arise from late-stage illnesses. However, at both the bedside and the operating table, there is a distinct lack of tactile feedback for deep-seated tissue. As surgical techniques advance toward remote or minimally invasive options to reduce infection risk and hasten healing time, surgeons lose the ability to manually palpate tissue. Furthermore, palpation of deep structures results in decreased accuracy, with the additional barrier of needing years of experience for adequate confidence of diagnoses. This review delves into the current modalities used to fulfill the clinical need of quantifying physical touch. It covers research efforts involving tactile sensing for remote or minimally invasive surgeries, as well as the potential of ultrasound elastography to further this field with non-invasive real-time imaging of the organ’s biomechanical properties. Elastography monitors tissue response to acoustic or mechanical energy and reconstructs an image representative of the elastic profile in the region of interest. This intuitive visualization of tissue elasticity surpasses the tactile information provided by sensors currently used to augment or supplement manual palpation. Focusing on common ultrasound elastography modalities, we evaluate various sensing mechanisms used for measuring tactile information and describe their emerging use in clinical settings where palpation is insufficient or restricted. With the ongoing advancements in ultrasound technology, particularly the emergence of micromachined ultrasound transducers, these devices hold great potential in facilitating early detection of tissue abnormalities and providing an objective measure of patient health.
1. Introduction
Many diseases and health concerns have a shorter treatment time and a higher rate of survival if detected at an early stage. During annual checkups, physicians traditionally use manual palpation to assess the progression of illnesses, either by taking arterial (e.g., carotid, radial) pulse measurements or by detecting tumor nodules in soft tissue (e.g., lymph nodes, breast masses) (). Because the tissue’s elasticity is variable depending on its health, this practice involves applying pressure to tissue or organs (1–5 cm depression) and using tactile feedback to localize stiff nodules or irregularities that need to be examined further (). However, the physician’s reading of patient health is limited by tissue depth, practitioner experience, and thick layers of fat or ascites covering the region of interest, raising the need for noninvasive and quantitative appraisals of tissue elasticity.
Furthermore, while physicians can rely on their sense of touch to qualitatively assess the biomechanical properties of the tissue at the bedside, there is a clear lack of tactile feedback in minimally invasive and remote surgeries. Although these procedures have become increasingly popular due to expedited healing times and mitigated risks for infection, pain, blood loss, and trauma, surgeons lose their ability to palpate tissue (). Tactile feedback is crucial for interoperative decisions, like determining locations for incisions, and patient safety from surgical instruments. There have been various efforts to develop sensors to assess tissue stiffness in these settings to recoup physical touch (). These systems must enable a reliable and quantifiable method to “palpate” tissue by not only capturing the response to pressure but also by measuring the applied force to accurately interpret the feedback. There are 4 main types of sensors for tactile feedback: resistive, capacitive, piezoelectric, and optical (). These sensors have made tremendous strides in the field of minimally invasive surgeries, allowing clinicians to assess tissue characteristics in cases where manual palpation is impractical due to small incisions. However, they solely provide sensory information and do not offer noninvasive imaging of the tissue’s elastic profile.
Ultrasound can fulfill this visual shortcoming by enabling real-time, noninvasive imaging. It is a widely accepted clinical tool that emits sound waves at high frequencies (20 kHz) to treat and image tissues without ionizing radiation. Therapeutic ultrasound focuses high-intensity acoustic waves to a precise location to remotely treat the tissue, either by modifying it (e.g., muscle therapy, neuromodulation) with intensities at 1–4 W/cm, or damaging it (e.g., tumor ablation, dissolving blood clots) using intensities greater than 1 kW/ (, ). Diagnostic ultrasound, on the other hand, provides imaging capabilities at much lower intensities so that the tissue can be assessed for any abnormalities. These transducers emit ultrasound waves and receive the echoed signal that reflects off any structures it encounters (, ). Studies have shown that diagnostic ultrasound yields more consistent and accurate diagnoses compared to traditional palpation methods, with a 10-fold increase in accuracy when using ultrasound in some applications (, ). This can largely be attributed to the visual capabilities of ultrasound, where stiffness signals are quantitatively processed and displayed to the practitioner, unlike with traditional palpation where the clinician can only rely on qualitative metrics like physical touch. Diagnostic ultrasound is safer, less expensive, and more portable than radiography, computed tomography (CT), and magnetic resonance imaging (MRI); these benefits allow for easier integration of ultrasound into robotic and teleoperative systems for remote diagnosis (). In this review, we focus on diagnostic ultrasound—specifically, elastography—for its ability to augment tactile feedback. Ultrasound elastography can mimic manual palpation in both superficial and deep structures in a quantifiable manner, providing clinically valuable insights.
The next section of this review describes the sensors used for visualizing tactile feedback in clinical settings. Subsequently, we delve into ultrasound elastography and the 2 main modalities used to measure tissue elasticity: (1) strain and (2) shear wave imaging. We focus on the fundamentals of these imaging techniques and explore the potential growth of this practice using advancements in ultrasound probe fabrication (i.e., micro-electromechanical systems). Finally, the integration of elasticity imaging into clinical ultrasound devices for visualizing tactile feedback is discussed. The paper concludes with a consideration of the limitations of these systems as well a discussion on the increased accessibility and scope of elastography due to breakthroughs in artificial intelligence and wearable technology.
2. Sensors for tactile feedback
Since tissue responses vary based on the input force and tissue health, tactile sensors that quantify the applied pressure and feedback can serve as an alternative to manual palpation. Moreover, compared to open surgeries, where physicians can rely on their sense of touch and vision to localize tumors, blood vessels, and tissue swelling, it is significantly more challenging for physicians to receive tactile feedback in minimally invasive surgeries. While MRI or CT scans can provide stiffness information of the anatomy before surgery, there are several causes of mismatch between preoperative and interoperative patient status, including organ shift, swelling, and deformations.
There are several factors to consider when designing sensors for surgical and diagnostic applications, including resolution, size, weight, sensitivity, biocompatibility, sterilizability, and modularity (). The 4 main types of tactile sensors used for supplementing tissue palpation are resistive, capacitive, piezoelectric, and optical sensors (Figure 1) (). These sensors obtain information through physical touch and can characterize tumor properties such as size, depth, and elasticity through hardness or pressure measurements. The primary differences between these sensors are their transduction methods. While there are several reviews that focus on the fabrication methods, physical theories, and biomedical applications of these sensors (, , ), this section aims to highlight the sensing devices that are specifically important for visualizing tactile feedback in clinical settings. Table 1 provides an overview of these technologies and their applications.
Figure 1
Table 1
| Sensor | Operating principle | Application | Reference |
|---|---|---|---|
| Resistive | Resistance changes in metal strain gauges result from changes in geometry (e.g., length, cross-section) | Stiffness mapping | ( |
| Hard nodule detection | |||
| Robotic tissue palpation | |||
| Capacitive | Two conductive objects with a space between them respond to applied voltage differences | Probe that mimics human fingertip tactile sensing | ( |
| Surgical forceps for tactile feedback | |||
| Piezoelectric | Applied mechanical stress can generate an electric response | Robotic-based tissue palpation system | ( |
| Portable pen-like devices for oral cancer screening | |||
| Measuring elasticity of tissue | |||
| Optical | Acts as a wavelength-selective mirror in which light within a narrow spectral width will be reflected and remaining light will be transmitted | Fiber Bragg Grating-based force sensors used in robotic palpation for haptic perception in surgeries | ( |
Sensors for tactile feedback.
2.1. Resistive sensors
A resistive sensor is a sensor that converts an application of an external force to a change in electrical resistance, allowing for force, temperature, pressure, or displacement measurements with high resolution. Strain gauges, which are a type of resistive sensor, are leveraged in robotic designs for minimally invasive surgeries for measuring tissue stiffness. With the working principle that resistance is directly proportional to the length and inversely proportional to the area of the conductor, deformation to the conductor’s geometry from an applied force can be measured. Low-cost triaxial force sensors have been developed for hard nodule detection using an electronic system of force-sensitive resistors (
Beccani et al. (
It is important to note that resistive sensors come with several challenges that need to be addressed for reliable clinical use. These challenges include lower sensitivity compared to other modalities and high power consumption. Moreover, the hysteresis characteristic of resistive sensors, which results in a difference in output of any measurement value upon a change in direction (e.g., approaching the measurement value with increasing pressure first and then with decreasing pressure), may result in lack of reliability and repeatability unless compensated with nonlinear calibrations or sensor design (
2.2. Capacitive sensors
Capacitive sensing is often favored in medical device design due to its high electrical sensitivity, low power consumption, and repeatability (
One particular advancement in robotic probes for soft tissue palpation includes a variable lever mechanism that allows for stiffness control to enhance tumor detection accuracy and improve localization and depth estimation of abdominal organs (
Despite the many advantages of capacitive sensors, it is important to note their limitations. These sensors are prone to exhibit high non-linearity, causing discrepancies between the output signal and the measured applied force especially at high sensitivities. This requires additional signal processing to ensure the output signal is representative of the measured force. Additionally, these sensors are highly sensitive to changes in humidity and temperature, susceptible to noise and limited in sensing range, which restrict their applications (
2.3. Piezoelectric sensors
Piezoelectric sensors, typically made with ceramic or crystal materials, generate electrical charge proportional to the applied physical force (e.g., pressure, temperature, vibration) (
Similarly, portable pen-like devices with miniaturized tactile sensors were made to quantitatively measure tissue elasticity for oral cancer screening (
To optimize the performance of tactile sensors in real-time, variable-impedance piezoelectric-based sensors can measure tissue hardness with a 6.2 times increase in measurement range. The sensing range is evaluated against a set threshold signal-to-noise ratio for effective measurement. This sensing mechanism varies the mechanical impedance of the tactile element to improve sensitivities at various stiffness levels by using a unique double-cantilever structure (
Similar to capacitive sensors, piezoelectric sensors are also temperature sensitive—a challenging limitation in a surgical set up where temperature varies up to 20C between the operating room and core-body (
2.4. Optical sensors
Optical sensors convert changes in the properties of light (e.g., polarization, intensity, wavelength) into electronic signals. These sensors exhibit high accuracy, resolution, bandwidth, and immunity to electromagnetic interference, which is ideal for system integration (
Furthermore, FBG-based 3-axis tactile sensors have been proposed for a more comprehensive haptic perception tool in surgeries (Figure 1D) (
Despite many research efforts to integrate tactile sensing in minimally invasive surgeries, to our knowledge there are no established mainstream commercialized products. Regardless, it is evident that these sensors provide a quantitative alternative to manual palpation, especially when clinicians have limited sense of touch in robotic-assisted surgeries (
3. Ultrasound for elasticity imaging
Ultrasound makes up approximately a third of the global medical imaging market (
The two main techniques for elastography are strain imaging and shear wave imaging (
Figure 2

Three common ultrasound elastography modalities. (A) Strain elastography applies a physical compression force from the transducer, computing stiffness based on the resulting tissue displacements. This technique provides qualitative information on the relative stiffness between tissues, where tissues exhibiting greater resistance to the applied manual compression indicate higher stiffness. The hard nodule, indicated in dark brown, is compressed from the physical pressing of the transducer, which is represented by the arrow. The shadow of the dark mass indicates the original form of the nodule, and the fully colored form is the present form of the mass due to physical pressure being applied to it. (B) Shear wave elastography (SWE) emits a pulse wave into the tissue and tracks the perpendicularly-induced propagating shear waves. The tracked speed is computed into an elasticity value as waves travel faster through stiffer tissues including the brown lump in the figure. (C) Acoustic radiation force impulse (ARFI) imaging tracks the impulse response of the tissue after generating displacement at the region of interest with an ultrasound pulse, shown with the arrow. The change in shape of the hard nodule, indicated by the brown mass, is due to the application of ultrasound pressure. Detection of a breast mass is captured by (D) strain elastography, (E) shear wave elastography (SWE), and (F) acoustic radiation force impulse (ARFI). In each image, the breast mass was hard (HD), while the surrounding tissue was soft (SF). Images were adapted from (
3.1. Strain imaging
Strain imaging can be broadly classified into 2 main categories by the measured physical quantity: strain elastography and acoustic radiation force impulse (ARFI) strain imaging (
Although strain elastography enables tissue elasticity visualization, it can be challenging to reproduce. Since the measurements from this method use external stimuli, the resulting assessment is subjective to the manual pressure administered by the operator and the contact angle of the transducer. Additionally, this modality does not inherently correct for internal sources of stress introduced by respiratory and cardiac processes. In order to completely quantify this process, an applied force sensor or automatic indentation system must be implemented. Finally, commercial ultrasound elastography systems rely on assumptions of the tissue, such as linearity, elasticity, incompressibility, and symmetry (
ARFI strain imaging, on the contrary, induces microscale displacement in tissues by using ARF (i.e., pushing pulse caused by sound energy) as an excitation method and tracks changes in mechanical properties as the tissue returns to baseline (Figure 2C) (
A notable advantage of this technique is its ability to image beyond slip boundaries and stiff backgrounds (
Unlike strain elastography or SWE, ARFI has higher depth penetration and can image deeper tissue which is not reachable by manual compression. However, ARFI has limited spatial resolution and must be calibrated very carefully for adequate examination. Under ideal conditions, where tissue density and generation of shear waves are constant, the elasticity can be confidently calculated based on the shear wave velocity measurements. In clinical settings, however, the operator must take into account the environmental (i.e., physical, geometrical, and anatomical) factors that may modify the speed of shear wave propagation in the tissue of interest and lead to unreliable results (
3.2. Shear wave imaging
Shear wave imaging uses an applied stress (ARFI or mechanical vibration) to generate shear waves that propagate either parallel or perpendicular to the plane of excitation. This modality consists of 3 main approaches: 1D transient elastography (1D-TE), point shear wave elastography (pSWE), and 2D shear wave elastography (2D-SWE) (
1D-TE is primarily used to assess the elasticity of deep tissue or organs, such as the liver. A mechanical device exerts a vibrating pressure on the surface to generate shear waves at a single point that propagate through the tissue (
pSWE uses ARFI as an excitation method to generate displacement in a localized region of the tissue. By measuring the velocity of shear waves induced by ARFI at a single focal location, Young’s modulus of the medium can be determined to indicate material elasticity (
In 2D-SWE, shear waves, which are generated by a force or a stress applied to a solid material, can be induced either mechanically by pressing down on the tissue or with an ultrasound transducer that generates ARF (
Table 2 provides a comparison of the ultrasound elastography imaging technologies discussed: strain elastography, ARFI imaging, 2D-SWE, 1D-TE, and pSWE. Both strain and shear wave imaging are leveraged in the medical devices discussed in section 5, which focuses ultrasound systems that quantify tactile feedback and reviews their clinical applications.
Table 2
| Modality | Excitation | Advantages | Limitations |
|---|---|---|---|
| Strain elastography | Applied manual compression ( | No additional specialized equipment required ( | Qualitative measurements ( |
| Internal physiological mechanism ( | Simple low-cost design ( | Applied compression is operator-dependent ( | |
| More commonly used ( | High inter-observer variability ( | ||
| coustic radiation force impulse (ARFI) imaging | Acoustic radiation force ( | Image beyond slip boundaries ( | Limited spatial resolution ( |
| Quantitative results ( | |||
| Excitation is operator independent ( | Requires careful calibration ( | ||
| Higher depth penetration ( | |||
| 1D transient elastography (1D-TE) | Mechanical vibration generates shear waves ( | Fast acquisition ( | Ascites or increased thickness of adipose tissue ( |
| Widespread availability ( | Fixed sampling area (single location) ( | ||
| Deep tissue elasticity assessment ( | |||
| Point shear wave elastography (pSWE) | ARFI generates shear waves in single focal zone ( | Precise localization of tissue stiffness ( | Fixed sampling area (small) ( |
| Can be performed in patients with ascites ( | |||
| Visualization avoids vessels ( | Increased thickness of adipose tissue ( | ||
| 2D shear wave elastography (2D-SWE) | ARFI generates shear waves in multiple focal zones ( | Real-time monitoring of shear waves ( | Signal artifacts at tissue-tumor interface ( |
| Greater field of view ( | Increased thickness of adipose tissue ( | ||
| High reproducibility ( | |||
| Not affected by ascites ( |
Modalities of ultrasound elastography.
4. Improvements with micromachined ultrasound transducers
Fundamental principles of ultrasound elasticity imaging can be applied to emerging technologies and algorithms to expand its uses in the medical field. Conventional piezoelectric transducers convert mechanical energy into electrical energy, with an active piezoelectric layer between 2 electrodes. The most common type of transducer for medical ultrasound imaging is developed with piezoceramics, which have high sensitivity but low efficiency for transmitting sound energy into tissue (
4.1. Piezoelectric micromachined ultrasonic transducers
As opposed to bulk piezoelectric transducers, which require matching layers, PMUTs are devised on the principle of bending and vibrating a thin piezoelectric film (
Figure 3

A sample schematic of (A) piezoelectric micromachined ultrasound transducer (PMUT) technology in a standard ultrasound probe. PMUTs have piezoelectric elements sandwiched between 2 electrodes and lie on top of a thin silicone dioxide membrane suspended over a silicon-based substrate. (B) Capacitive micromachined ultrasound transducer (CMUT) technology in transmit (red wiring) and in receive (cyan wiring). The bottom layer consists of a silicon substrate (bottom electrode) and the top layer is a membrane with a thin metal layer over it (top electrode) suspended over a narrow gap to prevent contact between the 2 electrodes for electrostatic actuation.
PMUT have been developed to achieve both superficial, high-resolution imaging and deep, low-resolution imaging (
The high-density capabilities of PMUTs, such as real-time volumetric imaging, provide insight into tissue stiffness and occlusions in a reliable and refined manner. These functionalities, along with miniaturization, pave the future for advancements in tactile feedback system design.
4.2. Capacitive micromachined ultrasonic transducer
CMUTs have a similar design to PMUTs but without the piezoelectric film. While PMUTs operate using the piezoelectric effect, CMUTs operate by leveraging the electrostatic force between the top and bottom electrodes on the cell (
CMUTs exhibit high sensitivity, increased resolution, and wide bandwidth (
4.3. Applications in elastography and considerations
MUTs not only have increased density of cells, but lower power consumption and acoustic impedance, allowing higher-quality ultrasound images (
It is important to note, however, that the fabrication process for MUTs is complex and requires careful design and precise manufacturing. Because transducer development requires for the gap between elements to be less than half the wavelength in the medium to minimize side lobes from constructive interference of the ultrasonic wave, it is very difficult to dice a transducer that operates at high frequencies (
5. Clinical tools using ultrasound to visualize and quantify tactile information
This section delves into the current research in clinical systems that use ultrasound to visualize and quantify tactile information and its emerging use in medicine. We discuss the use of ultrasound elastography both in surgical contexts, where physical touch is limited, as well as for objective and quantitative assessments of tissue health for diagnostic purposes. Elastography demonstrates greater accuracy in tumor detection compared with manual palpation, as it can characterize deep tissue or nodules under layers of fat with increased reliability (71, 1). Here, we will highlight examples of robotic and hand-held systems that use ultrasound for clinical evaluations and their respective applications (Figure 4).
Figure 4

Examples of ultrasound systems for tactile information: (A) Hand-held ultrasound indentation system using acoustic radiation force in a pen-sized probe to assess neck tissue fibrosis (72). (B) Linear-array ultrasound transducers to image and differentiate breast lesions (73). (C) Automatic robotic-assisted palpation on the abdomen to generate a stiffness map to produce haptic feedback for remote or minimally invasive surgeries (74). (D) Ultrasound sensor to assess the transverse carpal ligament in carpal tunnel syndrome (75). (E) Differentiating diabetic and non-diabetic patients by studying the biomechanical properties of plantar soft tissues using an air-jet indentation system and ultrasound system (76).
5.1. Neck tissue
With ARF, the user can employ a pen-size ultrasound probe to measure tissue displacement after applying stress to the tissue. By loading and unloading the probe onto the tissue, the difference in tissue elasticity can be computed using the continuously emitted ultrasound pulses. According to Zheng et al. (72), this technique provides sufficient accuracy and consistency for adequate assessment of neck tissue fibrosis (72). The hand-held ultrasound indentation system consists of a load cell (10 N strain gauge) to record the force response of the tissue and an ultrasound transducer (9 mm diameter, 5 MHz frequency) for imaging (Figure 4A). After applying pressure to palpate neck tissue, the Young’s modulus of the region of interest is calculated from the load-indentation response of the tissue. Unhealthy tissues (e.g., fibrosis) exhibited increased stiffness under loading, indicating that viscoelasticity parameters could discriminate soft tissue with varying degrees of fibrosis. Further research in identifying viscoelastic properties of soft materials (e.g., tissues) uses a low-cost dynamic indentation system to measure the shear modulus of a medium in response to applied pressure (77). A better understanding of tissue characteristics with quantitative measurements of viscoelasticity mitigates the inter-observer variations that often accompany manual palpation and operator-dependent imaging. The ability to identify variations in tissue elasticity with ARF is a result of greater independence from boundary conditions, decreased susceptibility to artifacts, and a reduced rate of decay of strain signal-to-noise ratio compared with conventional elastography (78). The effectiveness of ARF is highly dependent on the skill and experience of the operator and is limited by the penetration depth of the ultrasound waves.
5.2. Breast lesions
Additionally, some ultrasound systems use linear array transducers to image and differentiate breast lesions, using real-time visual feedback of tissue elastic properties to guide positioning and compression (Figure 4B) (73). This system provides high contrast-to-noise ratios in the resulting freehand elasticity maps which are displayed with the corresponding B-mode image (
5.3. Abdomen
An advantageous application of elastography to obtain tactile information is in robotic surgeries, where surgeons have limited or no physical access to the region of interest. Several research efforts are underway to integrate elastography in robotic systems in an effort to gain the same information from manual palpation in these settings. B-mode supplemented with laparoscopic elastography allows clinicians to differentiate between lesions with various elasticity and identify the lesion boundary with increased confidence compared to using a single modality alone (82,
To increase the ease and accuracy of this method, automatic robot-assisted elastography was developed to allow for teleoperative control of the ultrasound probe and provide haptic feedback to the clinician to complement the resulting strain elastography image (Figure 4C) (74). The continuous palpation motion with an ultrasound probe in this robotic system enables real-time estimations of the elastic parameters of tissue, allowing for increased accuracy in tumor detection and localization. These elasticity parameters are rendered with haptic force feedback during real-time tissue examinations to artificially restore manual palpation. The robot-assisted system generates force from the estimated elastograms produced by the automatic palpation movement of the robotic ultrasound probe and renders it through the haptic device (74). The force is calculated based on the general principles of elastic Hooke’s law (Equation 2),where is the reactive force generated by an elastic material, is the cross-sectional area of the region of interest (i.e., where the stress is applied), is the Young’s modulus of the material, and is the observed strain. This system has been evaluated with an abdominal phantom, exhibiting promising results for clinical use; however, additional developmental work is needed to validate its functionality in various types of tissue (74).
When designing medical robotics for ultrasound imaging and tissue elasticity assessment, there are several considerations to address before commercialization and clinical practice. The system must be rigorously and robustly tested for patient safety as there are potential dangers of clamping, squeezing, and applying uncomfortable pressure. Additionally, integration of remote control and raw ultrasound data access requires development of open platforms and collaboration, as these processes in commercial systems are proprietary (83). For these reasons, there are currently only commercially available teleoperated ultrasound systems: MGIUS-R3 (MGI Tech Co.) system (San Jose, California, USA) and MELODY (AdEchoTech) system (Mississauga, Ontario, CA) (84, 85). While patients and examiners accept telesonography for improving access to care, advanced solutions to image quality, autonomy of image acquisition, and robotic navigation are necessary to facilitate commercialization and to eventually reach a fully independent platform (86). Even though autonomous operation has not yet been achieved, there are several research efforts working to accomplish this goal, discussed in (83). Artificial intelligence is at the forefront of these efforts, playing a significant role in robotic path planning. It has several uses, ranging from creating a patient-specific body atlas by segmenting organs based on MRI data to compensating for motion and deformation noise commonly associated with ultrasound for image analysis.
These ultrasound-based robotic systems can also be improved with the use of tactile sensing (i.e., resistive, capacitive, piezoelectric, optical), which has been demonstrated in the context of minimally invasive surgeries (87). The integration of these sensor arrays with ultrasound introduces a multi-modal clinical tool to remotely detect pressure and to measure the underlying stiffness of an object to achieve more reliable tissue assessments. The low-cost disposable sensors ( mm, 90 sensing elements, 30 Hz update rate) combined with the linear-array transducer (128 elements, 4–9 MHz operating frequency range) have been shown to achieve higher tumor localization accuracy compared to evaluations with ultrasound alone (87).
Developing research in liver elastography using CMUTs is an interesting alternative to overcoming the limitations of traditional approaches like 1D-TE. Due to signal degradation from subcutaneous fat or large exploration depth, a transducer with a broader frequency range would be beneficial. This would allow for precise adjustment of the operating frequency to minimize tissue attenuation. CMUTs are particularly beneficial in this regard, as they typically have a frequency bandwidth of 110%. Certon et al. (88) reported that a fabricated single-cell CMUT connected to a FibroScan device (Echosens, Paris, France) produced comparable shear wave maps to one from a counterpart piezoelectric (PZT) probe (88). In this study, a CMUT cell () was designed with a surface micromachining process to have similar acoustic characteristics to the PZT-single element (8 mm diameter) used for 1D-TE. Both of these probes were used on an acoustic phantom (8.5 kPa stiffness) at a frequency of 2.5 and 5 MHz and the measured shear wave speed for the CMUT and PZT probes were 1.65 and 1.68 m/s, respectively. While many improvements need to be made to the CMUT design, such as increasing the element surface ratio, mechanical focusing, and developing an electronic front-end, there is promise for CMUT-based elastography applications. Moreover, in (89), a 2D CMUT array (center frequency 7.5 mm) was developed for high intensity focused ultrasound (HIFU) and imaging. In HIFU mode, the transducer emits a short high intensity ultrasound wave (shear wave) to the target region in the liver to induce a deformation in the tissue. This applied strain is then measured in elastography mode, which captures an image and calculates shear wave speed of the deformed tissue. While this device still needs to be rigorously tested and evaluated for performance and safety, it is working towards establishing a non-invasive, accurate, and less expensive alternative to other diagnostic methods (e.g., liver biopsy, blood test, MRI, CT) (89).
5.4. Hand tendons
A tissue ultrasound palpation sensor can assess the transverse carpal ligament by examining the thickness and stiffness of the transverse ligament in carpal tunnel syndrome (Figure 4D) (75, 90). This sensor is connected to a personal computer via a universal serial bus (USB) to provide real-time signal and indentation force information and an improved user interface. The finger-sized probe, consisting of an ultrasound transducer (5 MHz operating frequency) and load cell, pushes against soft tissue to measure both the thickness and elastic profile of the region of interest. The compression force (20 N) is applied with a cylindrical ultrasound indenter (9 mm diameter), and the deformation within the wrist during indentation is calculated based on the speed of sound and time-of-flight of the ultrasound signal. With motion-mode (M-mode) ultrasound, his system distinguishes between the different layers of tissue (e.g., soft tissue, carpal tunnel) within the wrist, rather than solely providing an overall measurement of tissue thickness and elasticity. Chen et al. (91) demonstrated that 2D shear wave velocity images of hand tendons could be mapped for healthy and injured tendons using high-frequency ultrasound elastography (40 MHz) and a handheld vibration system to continuously vibrate and measure shear wave speed synchronously (91). This system overcame the previous barrier of high-resolution shear wave imaging, with a spatial resolution of 147 m for a more accurate assessment of small tendon stiffness in hands.
Since tendons change in rigidity depending on their health, elastography is a promising tool to monitor the severity of hand injuries and assess their healing during rehabilitation. Due to the small size of tendons in the hand (on the scale of a few millimeters), high-resolution imaging with high-frequency ultrasound SWE and a continuous vibration method is used to measure the shear wave velocity (92). This technique employed a 40-MHz ultrasound array transducer in a hand-held probe to characterize hand tissue and was successfully able to differentiate between healthy and injured tendons.
5.5. Plantar soft tissue
The handheld capabilities of tissue ultrasound palpation sensors have also been applied to the study of biomechanical properties of plantar soft tissues to determine characteristic differences between diabetic and non-diabetic subjects (Figure 4E) (76). This study used an ultrasound transducer (10 MHz, 3 mm diameter) and a 10 N load cell to record the force during indentation to complete an offline analysis of the stiffness of tissues. The strain and applied stress were determined based on ultrasound time of flight, using a pen-style probe and a single-channel pulser–receiver with an analog-to-digital converter. The transducer was covered with a deformable elastomer tip, and the axial deformation during palpation was then used to calculate the applied force. The corresponding stress and strain were calculated in real-time in pulse-echo mode, where the transducer emits short pulses and measures the time to receive the reflection (93).
6. Discussion and conclusion
Palpation has been long used by clinicians for diagnostic purposes. However, it presents many limitations and requires supplemental technology for quantitative information. Although many studies have discussed tactile sensors for numerically identifying the tissue’s feedback response, this review focuses on the potential of ultrasound to detect and image the stiffness of both superficial and deep tissue.
Recent advancements that allow ultrasound to be integrated into convenient, cost-effective, pen-sized probes have facilitated the convergence of ultrasound elasticity imaging with palpation. Furthermore, ultrasound can be used in situations where palpation is not possible, such as remote or minimally invasive surgeries. The small size of the incision, while necessary for shorter healing times, prevents surgeons from palpating organs and eliminates tactile feedback. This physical assessment can be restored visually and quantitatively via ultrasound. Along with presurgical diagnosis and surgical navigation, ultrasound is an excellent candidate for applications in needle and catheter guidance, with increased success rate of cannulation particularly in patients with difficult intravenous access (94–96). Current state-of-the-art hand-held ultrasound probes use computational approaches to produce high-resolution and easily interpretable images, but lack the elasticity imaging that is necessary for real-time quantitative assessment of tissue health (97).
Compared to other imaging modalities, such as radiography, MRI and CT, ultrasound is safer, more affordable, and portable (
Although ultrasound introduces numerous advantages, certain limitations need to be addressed, including probe size, requirements for an acoustic coupling interface (e.g., gel), and user proficiency needed to adeptly obtain and interpret the ultrasound images. Furthermore, because ultrasound cannot image bone due to high attenuation and distortion of the acoustic wave, noninvasive imaging of organs fully encompassed in bone, such as the brain or spinal cord, poses a challenge. Presently, surgical procedures that remove a portion of the skull (i.e., craniotomy) or the lamina surrounding the spinal cord (i.e., laminectomy) are required to gain access to real-time imaging. Techniques described by Lu et al. (98) investigate the use of an anisotropic, acoustic complementary metamaterial to restore acoustic fields that are distorted by bone and similar impenetrable materials (98). This material has been demonstrated to acoustically cancel out the effects of aberrating layers and noninvasively enhance sound transmission.
Future works can be centered on machine learning approaches to provide automatic localization and classification of tumors in ultrasound images based on tissue elasticity. This direction can further lead to automated clinical tools for accurate computer-aided diagnosis and improved patient outcomes. There are several research efforts on advanced beamforming (99, 100) and deep learning (101, 102) to address some of the current drawbacks of ultrasound imaging and elastography. Shadowing, which is an artifact at interfaces with high acoustic impedance mismatch (e.g., soft tissue and air), can inhibit the operator’s ability to identify abnormalities because of overwhelming ultrasound wave absorption or reflection. This results in signal loss and dark shadows that obscure the region of interest. Another limitation is reverberation, in which ultrasound beams are trapped in between 2 strong reflectors, which significantly degrades image quality and accuracy. We commonly observe this in lung scans, where the ultrasound beam can be reflected multiple times between the pleural surface and the skin-transducer interface (103). Finally, acoustic cluttering, as the name suggests, results in noise and speckling in the image, which detracts from focusing on a region of interest (104). These current imaging impediments need to be addressed with image and signal processing techniques to assist clinicians and further improve the benefits of using ultrasound with palpation.
Integration with tactile sensors for a multi-modal approach can also help mitigate the current drawbacks of these ultrasound-based systems while retaining the added benefit of visualization and high sensing depth (87). The clinical accessibility of ultrasound elastography will only continue to improve as breakthroughs in wearable technology are made, allowing for serial assessment of tissues to aid with early detection and continuous supervision of pathophysiological conditions (105). Hu et al. (106) has demonstrated a stretchable ultrasonic array for measuring tissue elasticity up to 4 cm beneath the skin (106). This flexible array conforms to skin and maps 3D distributions of the Young’s modulus to track the evolution of lesions at a spatial resolution of 0.5 mm. The accelerating field of flexible ultrasonics combined with artificial intelligence for automatic classification of lesions and prediction of the trajectory of diseases is facilitating a future for accessible and preventative medicine. Increased reliability and sensitivity in state-of-the-art ultrasound systems compared with traditional methods of localizing unhealthy tissue can lead to the treatment of diseases before they progress to a more insidious state.
Funding
AM acknowledges funding support from the National Science Foundation (NSF) STTR Phase 1 Award (#: 1938939), Defense Advanced Research Projects Agency (DARPA) Award (#: N660012024075), and Johns Hopkins Institute for Clinical and Translational Research (ICTR)’s Clinical Research Scholars Program (KL2), administered by the National Institutes of Health (NIH) National Center for Advancing Translational Sciences (NCATS).
Statements
Author contributions
AK, AM, and NVT devised the review topic and scope, and AM and NVT provided their expertise in ultrasound and tactile feedback sensors to revise manuscript drafts. AK conducted the literature search and wrote the manuscript. KMKL designed Figures 2D–F, helped with review organization, and provided feedback on the manuscript drafts. MJK designed Figures 2A–C and 3 and provided feedback on the manuscript drafts. SS designed Figures 1 and 4 and provided feedback on the manuscript drafts.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
References
1.
NoletPSYuHCôtéPMeyerALKristmanVLSuttonD, et al. Reliability, validity of manual palpation for the assessment of patients with low back pain: a systematic, critical review. Chiropr Man Ther. (2021) 29:33. 10.1186/s12998-021-00384-3
2.
SogunroOA. How to palpate the abdomen during an abdominal exam Abdominal Examination Clinical Guide. MedMastery (2021). Retrieved fromhttps://www.medmastery.com/guides/abdominal-examination-clinical-guide/how-palpate-abdomen-during-abdominal-exam
3.
BandariNDargahiJPackirisamyM. Tactile sensors for minimally invasive surgery: a review of the state-of-the-art, applications, and perspectives. IEEE Access. (2019) 8:7682–708. 10.1109/ACCESS.2019.2962636
4.
OthmanWLaiZHAAbrilCBarajas-GamboaJSCorcellesRKrohM, et al. Tactile sensing for minimally invasive surgery: conventional methods and potential emerging tactile technologies. Front Robot AI. (2022) 8-2021:376. 10.3389/frobt.2021.705662
5.
CheungVY. High-intensity focused ultrasound therapy. Best Pract Res Clin Obstet Gynaecol. (2018) 46:74–83. 10.1016/j.bpobgyn.2017.09.002
6.
BestTMWilkKEMoormanCTDraperDO. Low intensity ultrasound for promoting soft tissue healing: a systematic review of the literature, medical technology. Int Med Rev (Washington, DC: Online). (2016) 2(11):271. 10.18103/imr.v2i11.271
7.
ZhaoTSuLXiaW. Optical ultrasound generation, detection for intravascular imaging: a review. J Healthc Eng. (2018) 2018. 10.1155/2018/3182483
8.
IzadifarZIzadifarZChapmanDBabynP. An introduction to high intensity focused ultrasound: systematic review on principles, devices,, clinical applications. J Clin Med. (2020) 9:460. 10.3390/jcm9020460
9.
SiddiquiNYuEBoulisSYou-TenKE. Ultrasound is superior to palpation in identifying the cricothyroid membrane in subjects with poorly defined neck landmarks: a randomized clinical trial. Anesthesiology. (2018) 129:1132–9. 10.1097/ALN.0000000000002454
10.
BoursierJFFournetABassaninoJManasseroMBeduASLeperlierD. Ultrasonography is more accurate than percutaneous palpation for identifying targeted thoracolumbar intervertebral disc spaces in dogs. Vet Radiol Ultrasound. (2018) 59:749–57. 10.1111/vru.12672
11.
DuanBXiongLGuanXFuYZhangY. Tele-operated robotic ultrasound system for medical diagnosis. Biomed Signal Process Control. (2021) 70:102900. 10.1016/j.bspc.2021.102900
12.
ChiCSunXXueNLiTLiuC. Recent progress in technologies for tactile sensors. Sensors. (2018) 18:948. 10.3390/s18040948
13.
LiLYuBYangCVagdargiPSrivatsanRAChosetH. Development of an inexpensive tri-axial force sensor for minimally invasive surgery. 2017 IEEE/RSJ International Conference on Intelligent Robots and Systems (IROS). IEEE (2017). p. 906–913.
14.
HerzigNMaiolinoPIidaFNanayakkaraT. A variable stiffness robotic probe for soft tissue palpation. IEEE Robot Autom Lett. (2018) 3:1168–75. 10.1109/LRA.2018.2793961
15.
JuFWangYZhangZWangYYunYGuoH, et al. A miniature piezoelectric spiral tactile sensor for tissue hardness palpation with catheter robot in minimally invasive surgery. Smart Mater Struct. (2019) 28:025033. 10.1088/1361-665X/aafc8d
16.
LiTPanARenH. Reaction force mapping by 3-axis tactile sensing with arbitrary angles for tissue hard-inclusion localization. IEEE Trans Biomed Eng. (2020) 68:26–35. 10.1109/TBME.2020.2991209
17.
WonCHLeeJHSaleheenF. Tactile sensing systems for tumor characterization: a review. IEEE Sens J. (2021) 21:12578–88. 10.1109/JSEN.2021.3078369
18.
PengYYangNXuQDaiYWangZ. Recent advances in flexible tactile sensors for intelligent systems. Sensors. (2021) 21:5392. 10.3390/s21165392
19.
BeccaniMDi NataliCSlikerLJSchoenJARentschlerMEValdastriP. Wireless tissue palpation for intraoperative detection of lumps in the soft tissue. IEEE Trans Biomed Eng. (2014) 61:353–61. 10.1109/TBME.2013.2279337
20.
KimUKimYBSoJSeokDYChoiHR. Sensorized surgical forceps for robotic-assisted minimally invasive surgery. IEEE Trans Ind Electron. (2018) 65:9604–13. 10.1109/TIE.2018.2821626
21.
ShaikhMOLinCMLeeDHChiangWFChenIHChuangCH. Portable pen-like device with miniaturized tactile sensor for quantitative tissue palpation in oral cancer screening. IEEE Sens J. (2020) 20:9610–7. 10.1109/JSEN.2020.2992767
22.
JuFYunYZhangZWangYWangYZhangL, et al. A variable-impedance piezoelectric tactile sensor with tunable sensing performance for tissue hardness sensing in robotic tumor palpation. Smart Mater Struct. (2018) 27:115039. 10.1088/1361-665X/aae54f
23.
CampisanoFOzelSRamakrishnanADwivediAGkotsisNOnalCD, et al. Towards a soft robotic skin for autonomous tissue palpation. 2017 IEEE International Conference on Robotics and Automation (ICRA). IEEE (2017). p. 6150–6155.
24.
YaoHYangWChengWTanYJSeeHHLiS, et al. Near–hysteresis-free soft tactile electronic skins for wearables and reliable machine learning. Proc Natl Acad Sci. (2020) 117:25352–9. 10.1073/pnas.2010989117
25.
PandeyMMishraG. Types of sensor, their applications, advantages and disadvantages. Emerging Technologies in Data Mining and Information Security: Proceedings of IEMIS 2018. Vol. 3. Springer (2019). p. 791–804.
26.
MatikaRIbrahimMPatwardhanA. The importance of body temperature: an anesthesiologist’s perspective. Temperature (Austin). (2016) 4(1):9–12. 10.1080/23328940.2016.1243509
27.
PendãoCSilvaI. Optical fiber sensors and sensing networks: Overview of the main principles and applications. Sensors. (2022) 22:7554–76. 10.3390/s22197554
28.
RohanRVenkadeshwaranKRanjanP. Recent advancements of fiber Bragg grating sensors in biomedical application: a review. J Opt. (2023) 1–12. 10.1007/s12596-023-01134-9
29.
LvCWangSShiC. A high-precision and miniature fiber Bragg grating-based force sensor for tissue palpation during minimally invasive surgery. Ann Biomed Eng. (2020) 48:669–81. 10.1007/s10439-019-02388-w
30.
Fortune Business Insights. Medical Imaging Equipment Market. Fortune Business Insights(2023). Retrieved fromhttps://www.fortunebusinessinsights.com/industry-reports/medical-imaging-equipment-market-100382
31.
FangCSidhuPS. Ultrasound-based liver elastography: current results and future perspectives. Abdom Radiol. (2020) 45:3463–72. 10.1007/s00261-020-02717-x
32.
MaoYJLimHJNiMYanWHWongDWCCheungJCW. Breast tumour classification using ultrasound elastography with machine learning: a systematic scoping review. Cancers. (2022) 14:367. 10.3390/cancers14020367
33.
SnojŽWuCTaljanovicMDumić-ČuleIDrakonakiEKlauserAS. Ultrasound elastography in musculoskeletal radiology: past, present, future. Seminars in Musculoskeletal Radiology. Vol. 24. Thieme Medical Publishers (2020). p. 156–166.
34.
ZhaoCKXuHX. Ultrasound elastography of the thyroid: principles and current status. Ultrasonography. (2019) 38:106. 10.14366/usg.18037
35.
AnticoMSasazawaFWuLJaiprakashARobertsJCrawfordR, et al. Ultrasound guidance in minimally invasive robotic procedures. Med Image Anal. (2019) 54:149–67. 10.1016/j.media.2019.01.002
36.
ZhouBYangXZhangXCurranWJLiuT. Ultrasound elastography for lung disease assessment. IEEE Trans Ultrason Ferroelectr Freq Control. (2020) 67:2249–57. 10.1109/TUFFC.2020.3026536
37.
MizukoshiKKuribayashiMHirayamaKYabuzakiJKurosumiMHamanakaY. Examination of age-related changes of viscoelasticity in the dermis and subcutaneous fat layer using ultrasound elastography. Skin Res Technol. (2021) 27:618–26. 10.1111/srt.12994.
38.
SigristRMLiauJEl KaffasAChammasMCWillmannJK. Ultrasound elastography: review of techniques, clinical applications. Theranostics. (2017) 7:1303. 10.7150/thno.18650
39.
DietrichCFBarrRGFarrokhADigheMHockeMJenssenC, et al. Strain elastography-how to do it?Ultrasound Int Open. (2017) 3:E137–49. 10.1055/s-0043-119412
40.
GürüfAÖztürkMBayrakIKPolatAV. Shear wave versus strain elastography in the differentiation of benign, malignant breast lesions. Turk J Med Sci. (2019) 49:1509–17. 10.3906/sag-1905-15
41.
WangSDWangLLiZXWeiKLLiaoXHChenYY, et al. Differential diagnostic performance of acoustic radiation force impulse imaging in small breast cancers: is it valuable?Sci Rep. (2017) 7:1–9. 10.1038/s41598-017-08004-y
42.
OzturkAGrajoJRDhyaniMAnthonyBWSamirAE. Principles of ultrasound elastography. Abdom Radiol. (2018) 43:773–85. 10.1007/s00261-018-1475-6
43.
MagalhãesMBelo-OliveiraPCasalta-LopesJCostaYGonçaloMGomesP, et al. Diagnostic value of ARFI (acoustic radiation force impulse) in differentiating benign from malignant breast lesions. Acad Radiol. (2017) 24:45–52. 10.1016/j.acra.2016.09.001
44.
GuoRLuGQinBFeiB. Ultrasound imaging technologies for breast cancer detection, management: a review. Ultrasound Med Biol. (2018) 44:37–70. 10.1016/j.ultrasmedbio.2017.09.012
45.
BrunoCMinnitiSBucciAPozzi MucelliR. ARFI: from basic principles to clinical applications in diffuse chronic disease—a review. Insights Imaging. (2016) 7:735–46. 10.1007/s13244-016-0514-5
46.
FonceaCGPopescuALupusoruRFofiuRSirliRDanilaM, et al. Comparative study between pSWE and 2D-SWE techniques integrated in the same ultrasound machine, with Transient Elastography as the reference method. Med Ultrason. (2020) 22:13–9. 10.11152/mu-2179
47.
TaljanovicMSGimberLHBeckerGWLattLDKlauserASMelvilleDM, et al. Shear-wave elastography: basic physics and musculoskeletal applications. Radiographics. (2017) 37:855–70. 10.1148/rg.2017160116
48.
ZvietcovichFBaddourNRollandJPParkerKJ. Shear wave propagation in viscoelastic media: validation of an approximate forward model. Phys Med Biol. (2019) 64:025008. 10.1088/1361-6560/aaf59a
49.
KennedyPWagnerMCastéraLHongCWJohnsonCLSirlinCB, et al. Quantitative elastography methods in liver disease: current evidence and future directions. Radiology. (2018) 286:738. 10.1148/radiol.2018170601
50.
LiuYTanHZhangXZhenYGaoFLuX. Prediction of high-risk esophageal varices in patients with chronic liver disease with point and 2d shear wave elastography: a systematic review and meta-analysis. Eur Radiol. (2022) 32:4616–27. 10.1007/s00330-022-08601-0
51.
TishinAAKuznetsovSN. Basic principles, methods ultrasound elastography. Overview elastography known methods depending on the method of creating strain. 2020 IEEE Conference of Russian Young Researchers in Electrical and Electronic Engineering (EIConRus). IEEE (2020). p. 2438–2441.
52.
AhmedAT. Diagnostic utility of strain and shear wave ultrasound elastography in differentiation of benign and malignant solid breast lesions. Egypt J Radiol Nucl Med. (2020) 51:1–8. 10.1186/s43055-020-00181-7
53.
NaganumaHIshidaHUnoANagaiHKurodaHOgawaM. Diagnostic problems in two-dimensional shear wave elastography of the liver. World J Radiol. (2020) 12:76. 10.4329/wjr.v12.i5.76
54.
JeongJYChoYSSohnJH. Role of two-dimensional shear wave elastography in chronic liver diseases: a narrative review. World J Gastroenterol. (2018) 24:3849. 10.3748/wjg.v24.i34.3849
55.
LeadinghamKMKCurryEJ. The abundant promise of ultrasound in neurosurgery: a broad overview and thoughts on ethical paths to realizing its benefits. Ultrasound. (2022) PM357:154.
56.
SawaneMPrasadM. MEMS piezoelectric sensor for self-powered devices: a review. Mater Sci Semicond Process. (2023) 158:107324. 10.1016/j.mssp.2023.107324
57.
DangiAChengCYAgrawalSTiwariSDattaGRBenoitRR, et al. A photoacoustic imaging device using piezoelectric micromachined ultrasound transducers (PMUTs). IEEE Trans Ultrason Ferroelectr Freq Control. (2019) 67:801–9. 10.1109/TUFFC.2019.2956463
58.
JiangXTangHYLuYNgEJTsaiJMBoserBE, et al. Ultrasonic fingerprint sensor with transmit beamforming based on a PMUT array bonded to CMOS circuitry. IEEE Trans Ultrason Ferroelectr Freq Control. (2017) 64:1401–8. 10.1109/TUFFC.2017.2703606
59.
JosephJMaBKhuri-YakubB. Applications of capacitive micromachined ultrasonic transducers: a comprehensive review. IEEE Trans Ultrason Ferroelectr Freq Control. (2021) 69(2):456–67. 10.1109/TUFFC.2021.3112917
60.
LingJWeiYHJiangGYChenYQTianHYangY, et al. Piezoelectric micromachined ultrasonic transducers for ultrasound imaging. 2018 IEEE International Conference on Electron Devices and Solid State Circuits (EDSSC). IEEE (2018). p. 1–2.
61.
ChenXQuMZhuKXieJ. Dual-frequency piezoelectric micromachined ultrasonic transducers via beam-membrane coupled structure. IEEE Electron Device Lett. (2021) 42:919–22. 10.1109/LED.2021.3075853
62.
WuLChenXWangGZhouQ. Dual-frequency piezoelectric micromachined ultrasonic transducers. Appl Phys Lett. (2019) 115:023501. 10.1063/1.5097624
63.
JungJLeeWKangWShinERyuJChoiH. Review of piezoelectric micromachined ultrasonic transducers and their applications. J Micromech Microeng. (2017) 27:113001. 10.1088/1361-6439/aa851b
64.
LeeWRohY. Ultrasonic transducers for medical diagnostic imaging. Biomed Eng Lett. (2017) 7:91–7. 10.1007/s13534-017-0021-8
65.
NaSZhengZAlbertIChenHWongLLLiZ, et al. Design and fabrication of a high-power air-coupled capacitive micromachined ultrasonic transducer array with concentric annular cells. IEEE Trans Electron Devices. (2017) 64:4636–43. 10.1109/TED.2017.2746006
66.
ChanJZhengZBellKLeMRezaPHYeowJT. Photoacoustic imaging with capacitive micromachined ultrasound transducers: principles and developments. Sensors. (2019) 19:3617. 10.3390/s19163617
67.
YashvanthVChowdhuryS. An investigation of silica aerogel to reduce acoustic crosstalk in CMUT arrays. Sensors. (2021) 21:1459. 10.3390/s21041459
68.
JiaLHeCXueCZhangW. The device characteristics and fabrication method of 72-element CMUT array for long-range underwater imaging applications. Microsyst Technol. (2019) 25:1195–202. 10.1007/s00542-018-4062-4
69.
ShinEYeoHGYeonAJinCParkWLeeSC, et al. Development of a high-density piezoelectric micromachined ultrasonic transducer array based on patterned aluminum nitride thin film. Micromachines. (2020) 11:623. 10.3390/mi11060623
70.
WangTLeeC. Electrically switchable multi-frequency piezoelectric micromachined ultrasonic transducer (PMUT). 2016 IEEE 29th International Conference on Micro Electro Mechanical Systems (MEMS). IEEE (2016). p. 1106–1109.
71.
PehlivanMGurbuzMKCingiCAdapinarBDeğirmenciANAcikalinFM, et al. Diagnostic role of ultrasound elastography on lymph node metastases in patients with head and neck cancer. Braz J Otorhinolaryngol. (2019) 85:297–302. 10.1016/j.bjorl.2018.01.002
72.
ZhengYLeungSMakA. Assessment of neck tissue fibrosis using an ultrasound palpation system: a feasibility study. Med Biol Eng Comput. (2000) 38:497–502. 10.1007/BF02345743
73.
HallTJZhuYSpaldingCS. In vivo real-time freehand palpation imaging. Ultrasound Med Biol. (2003) 29:427–35. 10.1016/S0301-5629(02)00733-0
74.
Patlan-RosalesPAKrupaA. Robotic assistance for ultrasound elastography providing autonomous palpation with teleoperation, haptic feedback capabilities. 2020 8th IEEE RAS/EMBS International Conference for Biomedical Robotics and Biomechatronics (BioRob). IEEE (2020). p. 1018–1023.
75.
ZhengYPLiZChoiALuMHChenXHuangQH. Ultrasound palpation sensor for tissue thickness and elasticity measurement–assessment of transverse carpal ligament. Ultrasonics. (2006) 44:e313–7. 10.1016/j.ultras.2006.06.018
76.
ChaoCYZhengYPHuangYPCheingGL. Biomechanical properties of the forefoot plantar soft tissue as measured by an optical coherence tomography-based air-jet indentation system and tissue ultrasound palpation system. Clin Biomech. (2010) 25:594–600. 10.1016/j.clinbiomech.2010.03.008
77.
KorukHYurdaerSBKocHOBesliA. Identification of the viscoelastic properties of soft materials using a convenient dynamic indentation system and procedure. Mater Today: Proc. (2022) 57:464–8. 10.1016/j.matpr.2022.01.188
78.
WangL. Acoustic radiation force based ultrasound elasticity imaging for biomedical applications. Sensors. (2018) 18:2252. 10.3390/s18072252
79.
ZhuYCAlZoubiAJassimSJiangQZhangYWangYB, et al. A generic deep learning framework to classify thyroid and breast lesions in ultrasound images. Ultrasonics. (2021) 110:106300. 10.1016/j.ultras.2020.106300
80.
CiritsisARossiCEberhardMMarconMBeckerASBossA. Automatic classification of ultrasound breast lesions using a deep convolutional neural network mimicking human decision-making. Eur Radiol. (2019) 29:5458–68. 10.1007/s00330-019-06118-7
81.
FujiokaTKatsutaLKubotaKMoriMKikuchiYKatoA, et al. Classification of breast masses on ultrasound shear wave elastography using convolutional neural networks. Ultrason Imaging. (2020) 42:213–20. 10.1177/0161734620932609
82.
BillingsSDeshmukhNKangHJTaylorRBoctorEM. System for robot-assisted real-time laparoscopic ultrasound elastography. Medical Imaging 2012: Image-Guided Procedures, Robotic Interventions, and Modeling. Vol. 8316. International Society for Optics and Photonics (2012). p. 83161W.
83.
von HaxthausenFBöttgerSWulffDHagenahJGarcía-VázquezVIpsenS. Medical robotics for ultrasound imaging: current systems and future trends. Curr Robot Rep. (2021) 2:55–71. 10.1007/s43154-020-00037-y
84.
MGI Tech. (n.d.). MGIUS-R3 robotic ultrasound system. MGI Tech - Instruments Information (2023). https://en.mgi-tech.com/products/instruments_info/11/
85.
VieyresPNovalesCRivasRVilcahuamanLSandovalJClarkT, et al. The next challenge for world wide robotized tele-echography experiment (WORTEX 2012): from engineering success to healthcare delivery. 2013 Peruvian Biomedical Engineering, Bioengineering, Biotechnology and Medical Physics Congress Lima, Peru: “PUCP” (Pontifical Catholic University of Peru) (2013). p. 205–10.
86.
GiulianiMSzczkeśniak-StańczykDMirnigNStollnbergerGSzyszkoMStańczykB, et al. User-centred design and evaluation of a tele-operated echocardiography robot. Health Technol (Berl). (2020) 10:649–65. 10.1007/s12553-019-00399-0
87.
NaiduASNaishMDPatelRV. A breakthrough in tumor localization: Combining tactile sensing and ultrasound to improve tumor localization in robotics-assisted minimally invasive surgery. IEEE Robot Autom Mag. (2017) 24:54–62. 10.1109/MRA.2017.2680544
88.
CertonDAudiereSColinLSenegondNAlquierDGregoireJM, et al. CMUT-based single element transducer applied to 1D transient ultrasound elastography. 2018 IEEE International Ultrasonics Symposium (IUS). IEEE (2018). p. 1–4.
89.
DebnathS. A 2D CMUT array for liver elastography [PhD thesis]. Canada: University of Windsor (2021).
90.
YoshiiYZhaoCAmadioPC. Recent advances in ultrasound diagnosis of carpal tunnel syndrome. Diagnostics. (2020) 10:596. 10.3390/diagnostics10080596
91.
ChenPYYangTHKuoLCHsuHYSuFCHuangCC. Evaluation of hand tendon elastic properties during rehabilitation through high-frequency ultrasound shear elastography. IEEE Trans Ultrason Ferroelectr Freq Control. (2021) 68:2716–26. 10.1109/TUFFC.2021.3077891
92.
ChenPYYangTHKuoLCShihCCHuangCC. Characterization of hand tendons through high-frequency ultrasound elastography. IEEE Trans Ultrason Ferroelectr Freq Control. (2019) 67:37–48. 10.1109/TUFFC.2019.2938147
93.
SchöneMSchulzRTzschätzschHVargaPRaumK. Ultrasound palpation for fast in-situ quantification of articular cartilage stiffness, thickness and relaxation capacity. Biomech Model Mechanobiol. (2017) 16:1171–85. 10.1007/s10237-017-0880-z
94.
PoulsenEAagaardRBisgaardJSørensenHTJuhl-OlsenP. The effects of ultrasound guidance on first-attempt success for difficult peripheral intravenous catheterization: a systematic review and meta-analysis. Eur J Emerg Med. (2023) 30:70–7. 10.1097/MEJ.0000000000000993
95.
van LoonFBuiseMClaassenJDierick-van DaeleABouwmanA. Comparison of ultrasound guidance with palpation and direct visualisation for peripheral vein cannulation in adult patients: a systematic review and meta-analysis. Br J Anaesth. (2018) 121:358–66. 10.1016/j.bja.2018.04.047
96.
TariganTJEAnwarBSSintoRWisnuW. Diagnostic accuracy of palpation versus ultrasound-guided fine needle aspiration biopsy for diagnosis of malignancy in thyroid nodules: a systematic review and meta-analysis. BMC Endocr Disord. (2022) 22:1–15. 10.1186/s12902-022-01085-5
97.
LiuJYXuJForsbergFLiuJ-B, et al. CMUT/CMOS-based butterfly iQ—a portable personal sonoscope. Adv Ultrasound Diagn Ther. (2019) 3:115–8. 10.37015/AUDT.2019.190819
98.
LuQLiXZhangXLuMChenY. Perspective: acoustic metamaterials in future engineering. Engineering. (2022) 17:22–30. 10.1016/j.eng.2022.04.020
99.
HuangXBellMALDingK. Deep learning for ultrasound beamforming in flexible array transducer. IEEE Trans Med Imaging. (2021) 40:3178–89. 10.1109/TMI.2021.3087450
100.
WangYXieXHeQLiaoHZhangHLuoJ. Hadamard-encoded synthetic transmit aperture imaging for improved lateral motion estimation in ultrasound elastography. IEEE Trans Ultrason Ferroelectr Freq Control. (2022) 69:1204–18. 10.1109/TUFFC.2022.3148332
101.
FengSSheaQTKNgKYTangCNKwongEZhengY. Automatic hyoid bone tracking in real-time ultrasound swallowing videos using deep learning based and correlation filter based trackers. Sensors. (2021) 21:3712. 10.3390/s21113712
102.
CiganovicMÖzdemirFFarshadMGökselO. Deep learning techniques for bone surface delineation in ultrasound. Medical Imaging 2019: Ultrasonic Imaging and Tomography. Vol. 10955. SPIE (2019). p. 224–230.
103.
OstrasOSouliotiDEPintonG. Diagnostic ultrasound imaging of the lung: a simulation approach based on propagation and reverberation in the human body. J Acoust Soc Am. (2021) 150:3904–13. 10.1121/10.0007273
104.
LongJLongWBottenusNTraheyG. Coherence-based quantification of acoustic clutter sources in medical ultrasound. J Acoust Soc Am. (2020) 148:1051–62. 10.1121/10.0001790
105.
LaTGLeLH. Flexible and wearable ultrasound device for medical applications: a review on materials, structural designs, and current challenges. Adv Mater Technol. (2022) 7:2100798. 10.1002/admt.202100798
106.
HuHMaYGaoXSongDLiMHuangH, et al. Stretchable ultrasonic arrays for the three-dimensional mapping of the modulus of deep tissue. Nat Biomed Eng. (2023) 1–14. 10.1038/s41551-023-01038-w
Summary
Keywords
ultrasound imaging, elastography, tactile sensors, tissue palpation, micromachined ultrasound transducers
Citation
Kumar A, Kempski Leadingham KM, Kerensky MJ, Sankar S, Thakor NV and Manbachi A (2023) Visualizing tactile feedback: an overview of current technologies with a focus on ultrasound elastography. Front. Med. Technol. 5:1238129. doi: 10.3389/fmedt.2023.1238129
Received
10 June 2023
Accepted
14 September 2023
Published
03 October 2023
Volume
5 - 2023
Edited by
Fei Deng, University of New South Wales, Australia
Reviewed by
Christopher Reiche, The University of Utah, United States Danting Yang, Ningbo University, China Libing Fu, University of Technology Sydney, Australia
Updates

Check for updates
Copyright
© 2023 Kumar, Kempski Leadingham, Kerensky, Sankar, Thakor and Manbachi.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Avisha Kumar akumar80@jhu.edu
Disclaimer
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.