Abstract
Ultrasonic guided waves have recently been used in fracture evaluation and fracture healing monitoring. An axial transmission technique has been used to quantify the impact of the gap breakage width and fracture angle on the amplitudes of low order guided wave modes S0 and A0 under a 100 kHz narrowband excitation. In our two dimensional finite-difference time-domain (2D-FDTD) simulation, the long bones are modeled as three layers with a soft tissue overlay and marrow underlay. The simulations of the transversely and obliquely fractured long bones show that the amplitudes of both S0 and A0 decrease as the gap breakage widens. Fixing the crack width, the increase of the fracture angle relative to the cross section perpendicular to the long axis enhances the amplitude of A0, while the amplitude of S0 shows a nonmonotonic trend with the decrease of the fracture angle. The amplitude ratio between the S0 and A0 modes is used to quantitatively evaluate the fracture width and angles. The study suggests that the low order guided wave modes S0 and A0 have potentials for transverse and oblique bone fracture evaluation and fracture healing monitoring.
1. Introduction
Long bone fractures are typically classified by their shape complexity, locations, such as transverse, oblique, spiral, comminuted, compression, and greenstick fractures, and so forth [1]. Approximately 7.9 million patients sustain fractures in the United States annually, and up to 10% go on to have impaired bone healing, resulting in a delayed union or a nonunion [2]. More than 3 million incident fractures at a cost of $35 billion are predicted for 2025 [3]. Long bone fractures represent one of the most commonly sustained injuries following trauma and account for nearly 4% of emergency department visits in the United States each year [4]. Therefore, fracture diagnosis and subsequent healing monitoring are vital [5–7]. Although conventional X-ray radiographies are still the most common methods to evaluate fractures and monitor the subsequent healing process, ultrasonic measurement is emerging as an alternative owing to its advantages of being quick, portable, noninvasive, and inexpensive [4, 8–14]. Especially for pediatric long bone fractures, ultrasound does not necessitate exposing children to ionizing radiation, which has been linked with cancer [4, 15].
Pulse echo ultrasonic imaging showed its advantage in pediatric fracture assessment owing to children's relative thinner soft tissue compared with that of adults [10]. Li et al. proposed a split-step Fourier echo imaging method to process the signals measured by axial scanning and image the oblique cracks in the cervine long bone plate, which illustrates the potential of better resolution for ultrasound imaging [16]. However, ultrasonography still cannot detect fractures with a width less than 1 mm [9].
Axial transmission ultrasound has drawn more and more attention recently [17–20]. Two techniques have already been proposed, first arriving signal (FAS) [17, 20–23] and guided wave [19, 24–27]. 2D-FDTD simulations and in vitro experiments on the bovine tibia have been performed, and the results illustrated that both transverse and oblique cracks resulted in the amplitude loss and velocity decrease of FAS [20]. The increase of the fracture angle would impair the sensitivity of the crack width assessment. Further simulation and experimental measurements of bovine femur samples in vitro were performed [21, 28], and the influence of bone mineralization was analyzed. The results showed that the speed of the FAS could reflect the long bone fracture healing stages. An in vitro experiment on the sheep tibia confirmed that the speed of FAS had the capability to detect the long bone fracture healing stages [29]. FAS is found to be relatively low magnitude compared with the subsequently arriving guided waves and is only sensitive to changes in the periosteal regions along the propagating path of the long cortical bone [21].
Ultrasonic guided waves propagate throughout the whole waveguide with great sensitivity to the boundary conditions, such as the endosteal and periosteal regions of the long cortical bone. Previous numerical and experimental studies mainly focus on relatively high frequency [19, 26, 32]. The propagation of guided waves in long bones with different healing stages was analyzed using finite element simulation, and it was found that the cortical fracture significantly affected the propagation of guided waves [19, 26]. However, the serious mode overlap and conversion prevent accurate quantification. Many mode recognition and separation algorithms have been proposed, such as the Radon transform [33, 34], wideband dispersion reversal method [35], sparse SVD based mode extraction [36], time-frequency ridge extraction [25], and joint spectrum separation ridge extraction [37]. However, limited by the complexity of clinical measurement, the severe multimode overlap still highly complicates the ultrasonic guided wave based long cortical bone fracture evaluation.
Recently, a narrowband frequency excitation of the low order guided modes was applied to evaluate the fracture of the long cortical bone, which significantly simplifies the mode identification and signal processing [27, 38, 39]. Simulation studies and in vitro experiments demonstrated that only two fundamental modes, S0 and A0, can be excited, and the mode conversion between S0 and A0 is capable of indicating the depth of the diaphyseal cracks [27]. However, in the previous study, only transverse cracks are analyzed in the results. Actually bone fractures are often in irregular shapes and with oblique angles to the axial direction of the long bone. Aiming to investigating the impact of irregularities of cortical fractures, a 2D-FDTD simulation was carried out in this paper. We attempt to quantitatively illustrate the possibilities of using low order guided waves to evaluate the oblique fractures in long bones.
2. Methods
2.1. Guided Mode Excitation
Ultrasound propagation through a waveguide is always accompanied with the mode conversion between shear and longitudinal waves. After multiple refractions and reflections, wave packets with a similar phase will propagate together as a stable guided mode. Guided waves in the plates, also named Lamb waves, can be general grouped as symmetric and antisymmetric modes according to their different vibration features. In a plate, the vibration is constrained to the Rayleigh-Lamb equations [40]:
(1) |
where h is the plate thickness and the angular wave number k is the ratio between the phase velocity Vp and angular frequency ω. VL and VT are the bulk longitudinal and shear wave velocities, respectively. The numerical solutions of (1) constitute the dispersion curves which can be expressed as functions of the frequency thickness product f · h.
Group velocity dispersion curves of a free cortical bone plate are shown in Figure 1, where the red and black lines are the symmetric and antisymmetric Lamb modes, respectively. The material parameters of cortical bone are given in Table 1.
Figure 1.
Group velocity dispersion curves of a free bovine tibia cortical bone plate. The red and black lines are the symmetric and asymmetric Lamb modes, respectively.
Table 1.
Parameters of cortical bone and soft tissue.
As shown in Figure 1, only two Lamb modes exist at the low frequency thickness (f · h) range (<1 MHz·mm). On the contrary, at the high f · h range (>1 MHz·mm), there exist many high order modes which brings the challenges of mode separation. Thus, simulations are performed on the low f · h range. Narrowband low frequency sinusoids (5-cycle Gaussian-modulated pulse with a 100 kHz central frequency) are employed in our simulation to merely excite two fundamental guided waves, symmetric mode S0 and asymmetric mode A0.
2.2. Numerical Simulation and Models
The numerical simulation of the axial transmission ultrasound in the long bone is performed using a self-developed two-dimension (2D) finite-difference time-domain (FDTD) software that can numerically solve the wave field in the time and space domains [20, 23]. As shown in Figure 2, a model with dimension of 300 mm × 16 mm is used to model the obliquely fractured long bone.
Figure 2.
Simulation model of obliquely fractured long bone (h = 4 mm) with overlying 2 mm thick soft tissue and underlying 10 mm thick marrow.
The long bones are built as three layers, 2 mm thick overlaying soft tissue, 4 mm thick cortical bone, and 10 mm thick marrow. The perfectly matched layers (PML) were arranged at the two ends of the model and the beneath the marrow layer to avoid the reflection. A free boundary condition is applied on upper layer of soft tissue. In the middle of the cortical bone layer, a crack is set with a width w and fracture angle θ relative to the y-axis. The crack width w changes from 0 mm (intact) to 1 mm with an interval of 0.125 mm. The fracture angle θ changes from 0° (vertical) to 83°. Constrained by the model's resolution of 0.025 mm, the fracture angle cannot be set continuously. Consequently, the fracture angles are modeled with 0°, 14°, 18°, 26°, 37°, 45°, 53°, 63°, 76°, and 83°. A pair of transducers are kept in contact with the soft tissue with the incident angle of 0°. The radius of the transducer is 5 mm. The distance from the transmitter to the central y-axis z1 is 60 mm, and the distance from the receiver to the central y-axis z2 is changeable from 30 mm to 90 mm with an interval of 2.5 mm. The material properties used in the simulation are given in Table 1, and the simulation temporal discretization is 0.015 μs.
2.3. Data Processing
In this study, a low frequency narrowband Gaussian-modulated pulse is used to avoid multimode overlapping. Thus, only two fundamental guided modes, S0 and A0, are excited in the received guide waves, so that the mode packets can be identified and separated by simple temporal windows [38, 41].
The peak amplitude of the A0 and S0 wave packets is obtained to calculate the amplitude ratio between the two modes. The energy characteristics of the A0 mode and S0 mode are investigated with fracture angles and widths variation.
The propagation delays of these two converted modes can be calculated by (2a) and (2b) [27]. If z1 equals z2, the wave packets of the two converted modes merge into a mixed wave packet propagating between the original S0 and A0 modes
(2a) |
(2b) |
At 100 kHz, the duration of the 5 cycle excitation Gaussian-modulated pulse is 50 μs, and the group velocities of S0 and A0 are 3.95 km/s and 1.51 km/s, respectively. We measure the peaks of the two wave packets in time domain, which are the maximum amplitudes of the two original modes S0 and A0 and calculate the amplitude ratio between them for use in evaluating the long bone crack width with different fracture angles.
3. Results
Figure 3 shows the envelope curves extracted from fractured long bones with different fracture degrees and fracture oblique angles. The envelope amplitude is depicted in different colors with maxima in red and 0 in gray. The propagation distance z varies from 90 mm to 150 mm with an interval of 2.5 mm.
Figure 3.
The envelope diagrams of the received signals (90 mm < z < 150 mm) with different fracture degree and oblique angles, (a) intact model, (b) transverse fracture model with 0.5 mm wide crack, (c) transverse fracture model with 1.0 mm wide crack, (d) 45° oblique fracture model with 0.5 mm wide crack, (e) 45° oblique fracture model with 1.0 mm wide crack, (f) 83° oblique fractured model with 0.5 mm wide crack, and (g) 83° oblique fracture model with 1.0 mm wide crack.
Figure 3(a) shows the envelopes of the received waveforms with two Lamb modes S0 and A0 in the intact bone. The amplitude of antisymmetric mode A0 is much higher than that of S0, because of the perpendicular incidence and reception angles. No converted modes are observed in this model. However, in Figures 3(b) and 3(c) for transverse fracture with 0.5 mm and 1 mm wide cracks, both the S0 and A0 amplitudes attenuate significantly. As shown in Figures 3(d) and 3(e), the converted modes can be observed from the results of the 45° oblique fracture. According to the velocity analysis, the converted modes usually exist between the two original modes S0 and A0. Furthermore, the peak amplitudes of the conversion modes and original mode are difficult to be extracted due to mode overlapping. For larger fracture angle models in Figures 3(f) and 3(g), it seems that the original mode energy still can transmit through the cracks without obvious appearance of the converted modes. With a fixed fracture angle, the increasing of the crack width may lead to the amplitude reduction of both S0 and A0, such as in Figures 3(a), 3(b), and 3(c). In Figures 3(b), 3(d), and 3(f), with a fixed crack width, the increasing fracture angle may lead to the amplitude increasing of transmitted energy of the A0 mode, but the change of the S0 amplitude is nonmonotonic. To quantitatively illustrate the mode conversion, we further investigate different models with crack and fracture angle variation.
3.1. A0 Mode Amplitude Analysis
Figure 4(a) presents the A0 amplitude changes as functions of the crack width and fracture angles. The propagation distance z is fixed at 120 mm. With the crack width increasing, a decrease trend of the A0 amplitude can be observed, which is sensitive to the small crack (w < 0.25 mm).
Figure 4.
Amplitudes of A0 change as functions of the crack width w and the fracture angle θ; (a) with a fixed θ, the A0 amplitude curves with w variation; (b) with a fixed w, the A0 amplitude curves with θ variation; and (c) the B-spline fitting results of A0 amplitude to θ and w.
The A0 amplitudes decrease more than 95% in the 0° and 18° fractures, but they are almost constant as w increases to large angles (θ > 53°). Figure 4(b) shows the variation of the A0 amplitude with the fracture angle. The A0 amplitude obtained from the intact model is set as a benchmark. The A0 amplitude shows three stages in the increase of the fracture angle: a slow increase for small angles (θ < 20°), a rapid increase for the range of 20°~50°, and a final slow increase for large angles (θ > 50°). Figure 4(c) shows the A0 amplitude changes with the crack width and fracture angle in three dimensions. A B-spline fitting is performed to obtain the smooth amplitude functions. It shows that, comparing with the wide cracks and transverse fractures, the narrow cracks or the large angle oblique cracks can enhance the A0 mode transmission with larger A0 amplitude. The sensitivity of the A0 amplitude to the crack width and fracture angle shows potentials for fracture evaluation.
3.2. S0 Mode Amplitude Analysis
Figure 5(a) presents the S0 amplitude changes as functions of the crack width with different fracture angles. The propagation distance z is fixed at 120 mm. The S0 amplitude obtained in an intact model is used as a benchmark. With a fixed fracture angle, the S0 amplitude decreases with the crack widening. As shown in Figure 5(b), with a fixed crack width, the S0 amplitude shows a nonmonotonic trend with the fracture angle variation, and the minimal S0 amplitude is obtained at the range of 30° to 60°, which is smaller than the amplitude obtained in the model with a transverse fracture. The S0 amplitude decreases as the fracture angle increases, and then it increases as the fracture angle further increases, ultimately coming close to the value of the intact model at 83°. Figure 5(c) shows the B-spline fitting results of the S0 amplitude variation with the crack width and fracture angle in three-dimensional form. It can be found that the S0 amplitude generally decreases as the crack width increases, but it also shows a nonmonotonic trend to the fracture angle.
Figure 5.
Amplitudes of S0 change as functions of crack width w and fracture angle θ; (a) with a fixed θ, the S0 amplitude curves with w variation; (b) with a fixed w, the S0 amplitudes curves with θ variation; and (c) the B-spline fitting results of S0 amplitude to θ and w.
3.3. Impact of Crack Width and Fracture Angle on S0/A0
The above results indicate that the S0 and A0 amplitudes can reflect the w change of fractured long bones with different angles. However, in actual clinical use, the magnitudes of the guided modes are easily affected by many factors such as the coupling conditions and excitation energy. Thus, the amplitude ratio between S0 and A0 can be adopted as a more robust parameter.
To investigate the impact of the propagation distance, the average amplitude ratios are computed from the multichannel signals (90 < z < 150 mm with an interval of 2.5 mm). Figures 6(a) and 6(b) present the amplitude ratio changes with the variance of w and θ, respectively, where the error bar denotes the root mean square errors (RMSE) of the ratios obtained at different propagation distances for each fractured model.
Figure 6.
Amplitude ratios (dB) between S0 and A0 varying as functions of crack width w and fracture angle θ; (a) with a fixed θ, the amplitude ratio (dB) changes with w, where the error bars denote the standard errors for results obtained at different propagation distances z (90 < z < 150 mm); (b) with a fixed crack width w, the amplitude ratio (dB) changes with θ, where the error bars denote the standard errors for results obtained at different propagation distances z (90 < z < 150 mm); and (c) distance z = 120 mm, the B-spline fitting results of the amplitude ratios (dB) varying with fracture angle θ and crack width w.
As shown in Figure 6(a), for small angles (θ < 26°), the amplitude ratio increases with w. Comparing with the intact model, the amplitude ratios between the S0 and A0 modes in the fracture bone increase by values of 27.4 dB and 7.8 dB for 0° and 26°, respectively. However, for large angles (θ > 26°), the amplitude ratio decreases with the crack width by an average of 12.4 dB. Comparing to the intact model, with the oblique fracture angles of 53° and 63°, amplitude ratios between the S0 and A0 modes decrease by 19.8 dB and 22.9 dB, respectively.
Figure 6(b) presents the amplitude ratio of S0 and A0 varying with the fracture angle. It can be seen that the amplitude ratio curves first decrease as the fracture angle increases and then increase with angle increases. For 0.25 mm and 1 mm wide cracks, the turning points are approximately 35° and 60°. It can be found that, with a wide crack, the turn points of the amplitude ratio curves appear out with large angle.
The results reveal that the propagation distance has a small impact on the amplitude ratio with an average RSME of 0.78 dB. Furthermore, it is notable in Figures 6(a) and 6(b) that the largest RMSE of the amplitude ratio between the S0 and A0 modes can be obtained in the fractured bones with a small oblique angles (0°, 26°, and 37°) and large crack widths (w > 0.5 mm). For other fracture angles (θ > 26°), the average RSME of the amplitude ratio between the S0 and A0 modes is 0.46 dB. The small RSME reveals that the propagation distance variation between 60 mm and 150 mm has a small impact on the amplitude ratio parameter.
Figure 6(c) is the B-spline fitting result of the amplitude ratio parameter varying with the fracture angle θ and crack width w at a 120 mm distance. As shown in Figure 5(a), the line cross actually indicates that, in the oblique fractured bone model, with the crack widening the decline slopes of the S0 amplitude curves are different. The decline slope corresponding to the 63° fracture is more negative than those of other angles. Such a phenomenon also can be learned from the amplitude ratios curves between the S0 and A0 modes in Figure 6(c). It can be seen that the amplitude ratio may be able to indicate the oblique angle and the crack width of the bone fractures.
4. Discussion
This study presents a quantitative investigation of using low order guided wave modes to evaluate long bone fractures with oblique fracture angles. A 2D-FDTD simulation is performed in a three-layer model. Using a 100 kHz narrowband excitation, only two guided wave modes, S0 and A0, are excited. The impact of the crack width and fracture angle on the S0 and A0 amplitudes is thoroughly studied. The crack width increase leads to amplitude decreases for both the A0 and S0 modes (Figures 4(a) and 5(a)). The A0 amplitude shows a monotonic relationship with the fracture angle (Figure 4(b)), while the S0 amplitude shows a nonmonotonic relationship (Figure 5(b)). Although only simulation is performed in this study, the simulation results yielded interesting findings, including the use of the amplitude ratio to evaluate the crack width and fracture angle (Figures 6(a) and 6(b)). These findings illustrate the potential of guided mode conversion for the quantitative prediction of the cortical bone fracture degree and healing status.
To reduce the influence of the coupling and excitation, the amplitude ratio between S0 and A0 is adopted to evaluate the long bone fracture degree. The amplitude ratio shows a two-stage change with the fracture angle (Figure 6(b)). In the first stage, the amplitude ratio decreases as the angle increases, and the average decrease at different widths is 6.1 dB/10°. In the second stage, the amplitude ratio increases with the further increase in the angle, and the average increase at different widths is 4.9 dB/10°. The increase of crack width raises the amplitude ratio for small angles (θ < 26°) (Figure 6(a)), while it decreases the amplitude ratio for large angles (θ > 26°). The amplitude ratio between S0 and A0 shows a great capacity for fracture width detection with different fracture angles, even for very small crack widths (w < 1 mm): 27.4 dB/mm for a transverse fracture, 19.2 dB/mm for a 18° oblique fracture, −19.8 dB/mm for a 53° oblique fracture, and −22.9 dB/mm for a 63° oblique fracture (Figure 6(a)).
It has been demonstrated that when the cortical bone thickness (h) is much larger than the longitudinal wave length (λ), the speed of FAS is larger than that of the S0 mode, but for very thin plate, the speed of the FAS signal approaches the velocity of S0 mode [17]. Numerical and experimental results showed that the detection accuracy of the amplitude of FAS for the transverse and oblique crack widths was approximately 2 dB/mm in a 6 mm thick long bone plate at an excitation of 200 kHz (h ≈ 0.3λ) [20]. In the performed study, as the excitation frequency is 100 kHz and the cortical bone plate thickness is 4 mm (λ ≈ 40 mm, h ≈ 0.1λ), the FAS can be regarded as the ultrasonic Lamb mode S0. Compared with high frequency excitation, these simulation results show that the amplitude ratio between S0 and A0 may also be used to detect the crack width. In addition, for the oblique fracture model with a 37~63° fracture, the S0 amplitude significantly decreases as the crack width increases, so it is relatively hard to measure mode S0. Therefore, the incident angle should be optimized to increase the excitation of S0. The different distance signal results reveal that the propagation distance has a small impact on the amplitude ratio, with an average RSME of 0.78 dB. These results indicate the theoretical feasibility for the clinical application.
In the performed simulation, we consider that the crack surface is uniform, but it is actually irregular, which will affect the propagations of S0 and A0. Moreover, the crack region is filled with soft tissue in our simulation, while actually the tissue in the crack site will gradually recover, with a callus appearing and changing during the healing [26, 42–44]. Further experiments are needed to validate our hypothesis that the amplitude ratio between the S0 and A0 modes can indeed facilitate long bone fracture and healing process evaluation.
5. Conclusions
The impacts of the crack width and fracture angle on the low order guided wave S0 and A0 amplitudes were studied in a three-layer model (soft tissue, cortical bone, and marrow) using the 2D-FDTD simulation. The results show that the S0 and A0 amplitudes decrease as the crack width increases. The A0 amplitude increases as the fracture angle increases, while the S0 amplitude firstly decreases and then increases. To avoid the influence of coupling conditions and excitation signals, the use of the amplitude ratio between S0 and A0 is proposed to evaluate crack width changes at different fracture angles. The results indicate that the amplitude ratio between S0 and A0 is sensitive to the crack width in fractures with different oblique angles. The amplitude ratio shows good capability for crack width evaluation, with sensitivities of 25.1 dB/mm for a transverse fracture, 18.7dB/mm for an 18° oblique fracture, and −23.3 dB/mm for 53° oblique fracture. The average RSME of 0.78 dB for different propagation distances indicates the small distance impact on the amplitude ratio. Thus, the amplitude ratio between S0 and A0 has the capability of reflecting the long bone fracture status, including the crack width and angle. The variation of the amplitude ratio with the crack width and fracture angle was further discussed, which shows its good potential for monitoring the fracture angle and crack width in fractured long cortical bone.
Acknowledgments
This work was supported by the National Natural Science Foundation of China (11327405, 11304043, and 11525416) and the Ph.D. Programs Foundation of the Ministry of Education of China (20130071110020).
Competing Interests
The authors state that they have no conflict of interests.
References
- 1.Iyer K. M. Anatomy of Bone, Fracture, and Fracture Healing. pp. 1–11, 2013.
- 2.Wu N., Lee Y.-C., Segina D., et al. Economic burden of illness among US patients experiencing fracture nonunion. Orthopedic Research and Reviews. 2013;5:21–33. [Google Scholar]
- 3.Burge R., Dawson-Hughes B., Solomon D. H., Wong J. B., King A., Tosteson A. Incidence and economic burden of osteoporosis-related fractures in the United States, 2005–2025. Journal of Bone and Mineral Research. 2007;22(3):465–475. doi: 10.1359/jbmr.061113. [DOI] [PubMed] [Google Scholar]
- 4.Barata I., Spencer R., Raio C., Ward M., Sama A. 15 ultrasound detection of long bone fractures in pediatric emergency department patients. Annals of Emergency Medicine. 2011;58(4):S182–S183. [Google Scholar]
- 5.Burge R., Dawson-Hughes B., Solomon D. H., Wong J. B., King A., Tosteson A. Incidence and economic burden of osteoporosis-related fractures in the United States, 2005-2025. Journal of Bone and Mineral Research. 2007;22(3):465–475. doi: 10.1359/jbmr.061113. [DOI] [PubMed] [Google Scholar]
- 6.Dempster D. W. Osteoporosis and the burden of osteoporosis-related fractures. The American Journal of Managed Care. 2011;17(supplement 6):S164–S169. [PubMed] [Google Scholar]
- 7.Corso P., Finkelstein E., Miller T., Fiebelkorn I., Zaloshnja E. Incidence and lifetime costs of injuries in the United States. Injury Prevention. 2006;12(4):212–218. doi: 10.1136/ip.2005.010983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Wong L. C. Y., Chiu W. K., Russ M., Liew S. Review of techniques for monitoring the healing fracture of bones for implementation in an internally fixated pelvis. Medical Engineering & Physics. 2012;34(2):140–152. doi: 10.1016/j.medengphy.2011.08.011. [DOI] [PubMed] [Google Scholar]
- 9.Rabiner J. E., Khine H., Avner J. R., Friedman L. M., Tsung J. W. Accuracy of point-of-care ultrasonography for diagnosis of elbow fractures in children. Annals of Emergency Medicine. 2013;61(1):9–17. doi: 10.1016/j.annemergmed.2012.07.112. [DOI] [PubMed] [Google Scholar]
- 10.Cross K. P. Bedside ultrasound for pediatric long bone fractures. Clinical Pediatric Emergency Medicine. 2011;12(1):27–36. doi: 10.1016/j.cpem.2010.12.002. [DOI] [Google Scholar]
- 11.Huang Q., Xie B., Ye P., Chen Z. 3-D ultrasonic strain imaging based on a linear scanning system. IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control. 2015;62(2):392–400. doi: 10.1109/tuffc.2014.006665. [DOI] [PubMed] [Google Scholar]
- 12.Huang Q., Huang Y., Hu W., Li X. Bezier interpolation for 3-D freehand ultrasound. IEEE Transactions on Human-Machine Systems. 2015;45(3):385–392. doi: 10.1109/THMS.2014.2374551. [DOI] [Google Scholar]
- 13.Liu C., Xu F., Ta D., et al. Measurement of the human calcaneus in vivo using ultrasonic backscatter spectral centroid shift. Journal of Ultrasound in Medicine. 2016;35(10):2197–2208. doi: 10.7863/ultra.15.03030. [DOI] [PubMed] [Google Scholar]
- 14.Chen Z., Chen Y., Huang Q. Development of a wireless and near real-time 3D ultrasound strain imaging system. IEEE Transactions on Biomedical Circuits and Systems. 2016;10(2):394–403. doi: 10.1109/tbcas.2015.2420117. [DOI] [PubMed] [Google Scholar]
- 15.Eckert K., Ackermann O., Schweiger B., Radeloff E., Liedgens P. Ultrasound evaluation of elbow fractures in children. Journal of Medical Ultrasonics. 2013;40(4):443–451. doi: 10.1007/s10396-013-0446-3. [DOI] [PubMed] [Google Scholar]
- 16.Li H., Le L. H., Sacchi M. D., Lou E. H. M. Ultrasound imaging of long bone fractures and healing with the split-step fourier imaging method. Ultrasound in Medicine & Biology. 2013;39(8):1482–1490. doi: 10.1016/j.ultrasmedbio.2012.10.023. [DOI] [PubMed] [Google Scholar]
- 17.Bossy E., Talmant M., Laugier P. Effect of bone cortical thickness on velocity measurements using ultrasonic axial transmission: a 2D simulation study. Journal of the Acoustical Society of America. 2002;112(1):297–307. doi: 10.1121/1.1480836. [DOI] [PubMed] [Google Scholar]
- 18.Laugier P. Instrumentation for in vivo ultrasonic characterization of bone strength. IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control. 2008;55(6):1179–1196. doi: 10.1109/TUFFC.2008.782. [DOI] [PubMed] [Google Scholar]
- 19.Protopappas V., Vavva M., Fotiadis D., Malizos K. Ultrasonic monitoring of bone fracture healing. IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control. 2008;55(6):1243–1255. doi: 10.1109/TUFFC.2008.787. [DOI] [PubMed] [Google Scholar]
- 20.Dodd S. P., Cunningham J. L., Miles A. W., Gheduzzi S., Humphrey V. F. Ultrasound transmission loss across transverse and oblique bone fractures: an in vitro study. Ultrasound in Medicine & Biology. 2008;34(3):454–462. doi: 10.1016/j.ultrasmedbio.2007.09.002. [DOI] [PubMed] [Google Scholar]
- 21.Machado C. B., de Albuquerque Pereira W. C., Talmant M., Padilla F., Laugier P. Computational evaluation of the compositional factors in fracture healing affecting ultrasound axial transmission measurements. Ultrasound in Medicine & Biology. 2010;36(8):1314–1326. doi: 10.1016/j.ultrasmedbio.2010.05.008. [DOI] [PubMed] [Google Scholar]
- 22.Siegel I. M., Anast G. T., Fields T. The determination of fracture healing by measurement of sound velocity across the fracture site. Surgery, Gynecology & Obstetrics. 1958;107(3):p. 327. [PubMed] [Google Scholar]
- 23.Gheduzzi S., Dodd S. P., Miles A. W., Humphrey V. F., Cunningham J. L. Numerical and experimental simulation of the effect of long bone fracture healing stages on ultrasound transmission across an idealized fracture. The Journal of the Acoustical Society of America. 2009;126(2):887–894. doi: 10.1121/1.3158938. [DOI] [PubMed] [Google Scholar]
- 24.Moilanen P. Ultrasonic guided waves in bone. IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control. 2008;55(6):1277–1286. doi: 10.1109/TUFFC.2008.790. [DOI] [PubMed] [Google Scholar]
- 25.Xu K., Ta D., Wang W. Multiridge-based analysis for separating individual modes from multimodal guided wave signals in long bones. IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control. 2010;57(11):2480–2490. doi: 10.1109/TUFFC.2010.1714. [DOI] [PubMed] [Google Scholar]
- 26.Potsika V. T., Grivas K. N., Protopappas V. C., et al. Application of an effective medium theory for modeling ultrasound wave propagation in healing long bones. Ultrasonics. 2014;54(5):1219–1230. doi: 10.1016/j.ultras.2013.09.002. [DOI] [PubMed] [Google Scholar]
- 27.Xu K., Ta D., He R., Qin Y.-X., Wang W. Axial transmission method for long bone fracture evaluation by ultrasonic guided waves: simulation, phantom and in vitro experiments. Ultrasound in Medicine & Biology. 2014;40(4):817–827. doi: 10.1016/j.ultrasmedbio.2013.10.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Machado C. B., Pereira W. C. D. A., Granke M., Talmant M., Padilla F., Laugier P. Experimental and simulation results on the effect of cortical bone mineralization in ultrasound axial transmission measurements: a model for fracture healing ultrasound monitoring. Bone. 2011;48(5):1202–1209. doi: 10.1016/j.bone.2011.02.021. [DOI] [PubMed] [Google Scholar]
- 29.Barbieri G., Barbieri C. H., Mazzer N., Pelá C. A. Ultrasound propagation velocity and broadband attenuation can help evaluate the healing process of an experimental fracture. Journal of Orthopaedic Research. 2011;29(3):444–451. doi: 10.1002/jor.21258. [DOI] [PubMed] [Google Scholar]
- 30.Laugier P. Quantitative ultrasound instrumentation for bone in vivo characterization. Bone Quantitative Ultrasound. 2010:47–71. doi: 10.1007/978-94-007-0017-8_3. [DOI] [Google Scholar]
- 31.Vavva M. G., Protopappas V. C., Gergidis L. N., Charalambopoulos A., Fotiadis D. I., Polyzos D. The effect of boundary conditions on guided wave propagation in two-dimensional models of healing bone. Ultrasonics. 2008;48(6-7):598–606. doi: 10.1016/j.ultras.2008.04.013. [DOI] [PubMed] [Google Scholar]
- 32.Xu K., Ta D., Moilanen P., Wang W. Mode separation of Lamb waves based on dispersion compensation method. Journal of the Acoustical Society of America. 2012;131(4):2714–2722. doi: 10.1121/1.3685482. [DOI] [PubMed] [Google Scholar]
- 33.Tran T. N. H. T., Nguyen K.-C. T., Sacchi M. D., Le L. H. Imaging ultrasonic dispersive guided wave energy in long bones using linear radon transform. Ultrasound in Medicine and Biology. 2014;40(11):2715–2727. doi: 10.1016/j.ultrasmedbio.2014.05.021. [DOI] [PubMed] [Google Scholar]
- 34.Xu K., Ta D., Cassereau D., et al. Multichannel processing for dispersion curves extraction of ultrasonic axial-transmission signals: comparisons and case studies. The Journal of the Acoustical Society of America. 2016;140(3):1758–1770. doi: 10.1121/1.4962491. [DOI] [PubMed] [Google Scholar]
- 35.Xu K., Ta D., Hu B., Laugier P., Wang W. Wideband dispersion reversal of lamb waves. IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control. 2014;61(6):997–1005. doi: 10.1109/TUFFC.2014.2995. [DOI] [PubMed] [Google Scholar]
- 36.Xu K., Minonzio J., Ta D., Hu B., Wang W., Laugier P. Sparse SVD method for high-resolution extraction of the dispersion curves of ultrasonic guided waves. IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control. 2016;63(10):1514–1524. doi: 10.1109/tuffc.2016.2592688. [DOI] [PubMed] [Google Scholar]
- 37.Zhang Z., Xu K., Ta D., Wang W. Joint spectrogram segmentation and ridge-extraction method for separating multimodal guided waves in long bones. Science China: Physics, Mechanics and Astronomy. 2013;56(7):1317–1323. doi: 10.1007/s11433-013-5110-9. [DOI] [Google Scholar]
- 38.Xu K., Ta D., Su Z., Wang W. Transmission analysis of ultrasonic Lamb mode conversion in a plate with partial-thickness notch. Ultrasonics. 2014;54(1):395–401. doi: 10.1016/j.ultras.2013.07.011. [DOI] [PubMed] [Google Scholar]
- 39.Xu K., Liu D., Ta D., Hu B., Wang W. Quantification of guided mode propagation in fractured long bones. Ultrasonics. 2014;54(5):1210–1218. doi: 10.1016/j.ultras.2013.09.015. [DOI] [PubMed] [Google Scholar]
- 40.Rose J. L. Ultrasonic waves in solid media. 2004.
- 41.Bossy E., Talmant M., Defontaine M., Patat F., Laugier P. Bidirectional axial transmission can improve accuracy and precision of ultrasonic velocity measurement in cortical bone: a validation on test materials. IEEE Transactions on Ultrasonics, Ferroelectrics, and Frequency Control. 2004;51(1):71–79. doi: 10.1109/tuffc.2004.1268469. [DOI] [PubMed] [Google Scholar]
- 42.Dudkiewicz I., Heim M., Salai M., Blankstein A. The biology of fracture healing in long bones. Journal of Musculoskeletal Research. 2009;12(2):105–112. doi: 10.1142/s0218957709002225. [DOI] [Google Scholar]
- 43.Comiskey D., MacDonald B. J., McCartney W. T., Synnott K., O'Byrne J. Predicting the external formation of callus tissues in oblique bone fractures: idealised and clinical case studies. Biomechanics and Modeling in Mechanobiology. 2013;12(6):1277–1282. doi: 10.1007/s10237-012-0468-6. [DOI] [PubMed] [Google Scholar]
- 44.Protopappas V. C., Fotiadis D. I., Malizos K. N. Guided ultrasound wave propagation in intact and healing long bones. Ultrasound in Medicine & Biology. 2006;32(5):693–708. doi: 10.1016/j.ultrasmedbio.2006.02.001. [DOI] [PubMed] [Google Scholar]