INTRACORTICAL BONE STRESS FIELDS CALCULATED FROM IN VIVO STRAIN MEASUREMENTS

1980 ◽  
pp. 426-429
Author(s):  
R. Vasu ◽  
D.R. Carter ◽  
D.M. Spengler ◽  
R.T. Dueland
1981 ◽  
Vol 14 (1) ◽  
pp. 63-70 ◽  
Author(s):  
Dennis R. Carter ◽  
R. Vasu ◽  
Dan M. Spengler ◽  
R.T. Dueland

2008 ◽  
Vol 41 ◽  
pp. S40
Author(s):  
Ingrid Masson ◽  
Pierre Boutouyrie ◽  
Stéphane Laurent ◽  
Jay D Humphrey ◽  
Mustapha Zidi

1981 ◽  
pp. 19-24
Author(s):  
E.S. Bessman ◽  
D.R. Carter ◽  
W.H. Harris

2000 ◽  
Vol 82-B (4) ◽  
pp. 591-594 ◽  
Author(s):  
C. Milgrom ◽  
A. Finestone ◽  
A. Simkin ◽  
I. Ekenman ◽  
S. Mendelson ◽  
...  

2012 ◽  
Vol 45 (1) ◽  
pp. 27-40 ◽  
Author(s):  
R. Al Nazer ◽  
J. Lanovaz ◽  
C. Kawalilak ◽  
J.D. Johnston ◽  
S. Kontulainen

1982 ◽  
Vol 104 (3) ◽  
pp. 226-231 ◽  
Author(s):  
E. S. Bessman ◽  
D. R. Carter ◽  
J. C. McCarthy ◽  
W. H. Harris

A numerical technique is presented to evaluate and correct the zero-strain reference points determined experimentally for certain in-vivo strain rosette applications on long bones. The method is used to determine whether significant transverse stresses are present at the gage site during in-vivo activities. If transverse stresses are shown to be negligible, the experimentally determined zeroes can be appropriately adjusted to provide an increased accuracy of the strain measurements. In addition, the transverse Poisson’s ratio is calculated and can be incorporated in subsequent in-vivo stress calculations.


2015 ◽  
Vol 31 (12) ◽  
pp. e289-e305 ◽  
Author(s):  
Apicella Davide ◽  
Aversa Raffaella ◽  
Tatullo Marco ◽  
Simeone Michele ◽  
Jamaluddin Syed ◽  
...  

2016 ◽  
Vol 39 (2) ◽  
pp. 108-125 ◽  
Author(s):  
David Rosen ◽  
Yu Wang ◽  
Jingfeng Jiang

Viscoelasticity Imaging (VEI) has been proposed to measure relaxation time constants for characterization of in vivo breast lesions. In this technique, an external compression force on the tissue being imaged is maintained for a fixed period of time to induce strain creep. A sequence of ultrasound echo signals is then utilized to generate time-resolved strain measurements. Relaxation time constants can be obtained by fitting local time-resolved strain measurements to a viscoelastic tissue model (e.g., a modified Kevin-Voigt model). In this study, our primary objective is to quantitatively evaluate the contrast transfer efficiency (CTE) of VEI, which contains useful information regarding image interpretations. Using an open-source simulator for virtual breast quasi-static elastography (VBQE), we conducted a case study of contrast transfer efficiency of VEI. In multiple three-dimensional (3D) numerical breast phantoms containing various degrees of heterogeneity, finite element (FE) simulations in conjunction with quasi-linear viscoelastic constitutive tissue models were performed to mimic data acquisition of VEI under freehand scanning. Our results suggested that there were losses in CTE, and the losses could be as high as −18 dB. FE results also qualitatively corroborated clinical observations, for example, artifacts around tissue interfaces.


2004 ◽  
Vol 126 (6) ◽  
pp. 699-708 ◽  
Author(s):  
Blayne A. Roeder ◽  
Klod Kokini ◽  
J. Paul Robinson ◽  
Sherry L. Voytik-Harbin

The ability to create extracellular matrix (ECM) constructs that are mechanically and biochemically similar to those found in vivo and to understand how their properties affect cellular responses will drive the next generation of tissue engineering strategies. To date, many mechanisms by which cells biochemically communicate with the ECM are known. However, the mechanisms by which mechanical information is transmitted between cells and their ECM remain to be elucidated. “Self-assembled” collagen matrices provide an in vitro-model system to study the mechanical behavior of ECM. To begin to understand how the ECM and the cells interact mechanically, the three-dimensional (3D) mechanical properties of the ECM must be quantified at the micro-(local) level in addition to information measured at the macro-(global) level. Here we describe an incremental digital volume correlation (IDVC) algorithm to quantify large (>0.05) 3D mechanical strains in the microstructure of 3D collagen matrices in response to applied mechanical loads. Strain measurements from the IDVC algorithm rely on 3D confocal images acquired from collagen matrices under applied mechanical loads. The accuracy and the precision of the IDVC algorithm was verified by comparing both image volumes collected in succession when no deformation was applied to the ECM (zero strain) and image volumes to which simulated deformations were applied in both 1D and 3D (simulated strains). Results indicate that the IDVC algorithm can accurately and precisely determine the 3D strain state inside largely deformed collagen ECMs. Finally, the usefulness of the algorithm was demonstrated by measuring the microlevel 3D strain response of a collagen ECM loaded in tension.


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