Auckland Bioengineering Institute
Musculo-skeletal System Group current projects
This research aims to analyse body shape differences within the population using 3D body surface scanning and relate these findings to underlying musculoskeletal structure and function. 3D body scanning is a non-invasive procedure that takes only a few seconds. The result is a detailed virtual representation of the body surface. Anthropometric analysis provide useful information to health care providers, fashion industry and manufacturing sectors.
We are currently conducting pilot work in setting up measurement system and imaging protocols.
Contact
Katja Oberhofer
Email: k.oberhofer@auckland.ac.nz
This project is aimed at creating a detailed model of skeletal muscle function, incorporating a full set of anatomical and physiological data. Individual skeletal muscle fibres are represented within a 3-dimensional muscle geometry. The muscle geometry is created from CT sections of the body and includes important anatomical information such as fibre angles and intramuscular tendons. The muscle is activated using a detailed control system, which can represent normal muscle activation, or altered activation. The mechanical deformation of the muscle as a result of muscle activation is calculated using a novel constitutive law. The project has been done in collaboration with AgResearch.
In addition, work involving the simulation of electrical stimulation of skeletal muscle and nerve tissue has been undertaken. Finite element models have been created of the strength of electrical fields passing through skin, and other body tissue, and the resulting action of skeletal muscle and nerve tissue as a result of the electric field.
Contact
John Davidson
Email: jdav108@aucklanduni.ac.nz
Oliver Roehrle
Email: roehrle@mechbau.uni-stuttgart.de
Juliana Kim
Email: juliana.kim@auckland.ac.nz
Deep vein thrombosis (DVT) is a common problem in hospitalised patients. A commonly used prophylaxis against DVT is application of external pressure (e.g. compression stocking). The aim of this computational model is to simulate the action of external compression on the lower leg, investigate the flow in deep as well as superficial veins and estimate the vessel wall shear stress changes. The wall stress influences the tissue plasminogen activator (t-PA) and its gene expressions. t-Pa then converts plasmingen to active plasmin, which dissolves fibrin and prevents thrombus formation. We intend to simulate dorsi and plantar flexion of the foot to determine the effect of these manoeuvres on blood flow. The coupled model has other applications such as comfort analysis in sitting.
Contact
Kumar Mithraratne
Email: p.mithraratne@auckland.ac.nz
Fractures of the pelvis and acetabulum are among the most serious injuries treated by orthopaedic surgeons, requiring rapid and precise treatment and, in some cases, one or more surgical procedures. Biomechanically based computer models of the hip joint will be a great aid in understanding mechanisms of the fracture and hence in developing better fixation techniques. Moreover subject-specific finite element models of patients with pelvic/acetabular fractures will be a powerful tool for surgical planning and patient management. We are developing a computer model of the hip joint that includes all the major bones and soft tissues in the joint. The model will be used to investigate how fracture occurs under various impact conditions. Moreover the fracture pelvis model will be used to optimize techniques for fracture reduction by performing extensive biomechanical testing in silico.
Contact
Vickie Shim
Email: v.shim@auckland.ac.nz



