TY - JOUR
T1 - A fully dynamic multi-compartmental poroelastic system
T2 - application to aqueductal stenosis
AU - Chou, Dean
AU - Vardakis, John C.
AU - Guo, Liwei
AU - Tully, Brett J.
AU - Ventikos, Yiannis
N1 - Funding Information:
We acknowledge support, contributions and insight from VPH-DARE@IT ( FP7-ICT-2011-9-601055 ), a collaborative Research Project funded under the Co-operation specific programme of the Seventh Framework Programme of the European Union for research, technological development and demonstration activities.
Publisher Copyright:
© 2015 The Authors
PY - 2016/7/26
Y1 - 2016/7/26
N2 - This study proposes the implementation of a fully dynamic four-network poroelastic model which is underpinned by multiple-network poroelastic theory (MPET), in order to account for the effects of varying stages of aqueductal stenosis and atresia during acute hydrocephalus. The innovation of the fully dynamic MPET implementation is that it avoids the commonplace assumption of quasi-steady behaviour; instead, it incorporates all transient terms in the casting of the equations and in the numerical solution of the resulting discrete system. It was observed that the application of mild stenosis allows for a constant value of amalgamated ventricular displacement in under 2.4 h, whereas the application of a severe stenosis delays this settlement to approximately 10 h. A completely blocked aqueduct does not show a clear sign of reaching a steady ventricular displacement after 24 h. The increasing ventricular pressure (complemented with ventriculomegaly) during severe stenosis is causing the trans-parenchymal tissue region to respond, and this coping mechanism is most attenuated at the regions closest to the skull and the ventricles. After 9 h, the parenchymal tissue shows to be coping well with the additional pressure burden, since both ventriculomegaly and ventricular CSF (cerebrospinal fluid) pressure show small increases between 9 and 24 h. Localised swelling in the periventricular region could also be observed through CSF fluid content, whilst dilation results showed stretch and compression of cortical tissue adjacent to the ventricles and skull.
AB - This study proposes the implementation of a fully dynamic four-network poroelastic model which is underpinned by multiple-network poroelastic theory (MPET), in order to account for the effects of varying stages of aqueductal stenosis and atresia during acute hydrocephalus. The innovation of the fully dynamic MPET implementation is that it avoids the commonplace assumption of quasi-steady behaviour; instead, it incorporates all transient terms in the casting of the equations and in the numerical solution of the resulting discrete system. It was observed that the application of mild stenosis allows for a constant value of amalgamated ventricular displacement in under 2.4 h, whereas the application of a severe stenosis delays this settlement to approximately 10 h. A completely blocked aqueduct does not show a clear sign of reaching a steady ventricular displacement after 24 h. The increasing ventricular pressure (complemented with ventriculomegaly) during severe stenosis is causing the trans-parenchymal tissue region to respond, and this coping mechanism is most attenuated at the regions closest to the skull and the ventricles. After 9 h, the parenchymal tissue shows to be coping well with the additional pressure burden, since both ventriculomegaly and ventricular CSF (cerebrospinal fluid) pressure show small increases between 9 and 24 h. Localised swelling in the periventricular region could also be observed through CSF fluid content, whilst dilation results showed stretch and compression of cortical tissue adjacent to the ventricles and skull.
KW - Aqueduct
KW - Cerebrospinal fluid
KW - Hydrocephalus
KW - Multiple-network poroelastic theory
KW - Stenosis
UR - http://www.scopus.com/inward/record.url?scp=84949655384&partnerID=8YFLogxK
U2 - 10.1016/j.jbiomech.2015.11.025
DO - 10.1016/j.jbiomech.2015.11.025
M3 - Article
C2 - 26671218
AN - SCOPUS:84949655384
SN - 0021-9290
VL - 49
SP - 2306
EP - 2312
JO - Journal of Biomechanics
JF - Journal of Biomechanics
IS - 11
ER -