Towards force-correlated ultrasound volume elastography

This thesis proposes three ultrasound-based methods that enable quantification of tissue and organ properties with potential applications as non-invasive, image-based biomarkers: force-controlled elasticity quantification for the identification of strain hardening; registration and segmentation of B-mode images to measure organ volumes; and force-correlated three-dimensional elasticity maps. In order to allow for the simultaneous collection of tissue elasticity and compressive force, a shear wave elasticity enabled ultrasound probe was integrated with a load cell which measured the sonographer-applied preload. The device was used to demonstrate the strong preload dependence of elasticity in ex-vivo bovine liver, illustrating the importance of accounting for preload when using elastography to assess tissue health. Finally, this device enables the quantification of strain hardening as an additional metric for tissue health. The capability organ volume measurements through freehand ultrasound imaging was demonstrated in a clinical study in which kidney volumes were obtained from ultrasound sweeps and compared to ground truth data from CT scans. While the technology needs to be refined to achieve better agreement between the measured volumes, the initial results of this ongoing study allowed for the identification of an ideal acquisition strategy. These findings will inform future data collection to achieve an improved accuracy. The acquisition of three-dimensional force-correlated elasticity maps was demonstrated on a phantom with the successful detection of a high-stiffness lesion embedded in bulk material. The presented technology has the potential to be a quantitative replacement for manual palpation. Given further refinement, this technology could be used to replace needle biopsy in various diseases in which progression correlates with tissue stiffness, such as thyroid nodules or liver fibrosis and cirrhosis. Our method, unlike the inherently localized needle biopsy, allows for the assessment of tissue over a broad volume, potentially improving reliability and repeatability in diagnosing and staging diffuse diseases.

Department dc:contributor.department

Massachusetts Institute of Technology. Department of Mechanical Engineering.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2017

Author dc:creator

• Graule, Moritz Alexander

Advisor dc:contributor.advisor

• Brian W. Anthony.

• Mechanical Engineering.

Statement dc:rights

• MIT theses are protected by copyright. They may be viewed, downloaded, or printed from this source but further reproduction or distribution in any format is prohibited without written permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/113757

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/113757