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An analytic model for the flow induced in syringomyelia cavities

Published online by Cambridge University Press:  05 January 2024

G.L. Nozaleda
Affiliation:
Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, CA 92093-0411, USA
J. Alaminos-Quesada
Affiliation:
Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, CA 92093-0411, USA
W. Coenen
Affiliation:
Grupo de Mecánica de Fluidos, Universidad Carlos III de Madrid, Leganés 28911, Spain
V. Haughton
Affiliation:
School of Medicine and Public Health, University of Wisconsin-Madison, Madison, WI 53706, USA
A.L. Sánchez*
Affiliation:
Department of Mechanical and Aerospace Engineering, University of California San Diego, La Jolla, CA 92093-0411, USA
*
Email address for correspondence: alsp@eng.ucsd.edu

Abstract

A simple two-dimensional fluid–structure interaction problem, involving viscous oscillatory flow in a channel separated by an elastic membrane from a fluid-filled slender cavity, is analysed to shed light on the flow dynamics pertaining to syringomyelia, a neurological disorder characterized by the appearance of a large tubular cavity (syrinx) within the spinal cord. The focus is on configurations in which the velocity induced in the cavity, representing the syrinx, is comparable to that found in the channel, representing the subarachnoid space surrounding the spinal cord, both flows being coupled through a linear elastic equation describing the membrane deformation. An asymptotic analysis for small stroke lengths leads to closed-form expressions for the leading-order oscillatory flow, and also for the stationary flow associated with the first-order corrections, the latter involving a steady distribution of transmembrane pressure. The magnitude of the induced flow is found to depend strongly on the frequency, with the result that for channel flow rates of non-sinusoidal waveform, as those found in the spinal canal, higher harmonics can dominate the sloshing motion in the cavity, in agreement with previous in vivo observations. Under some conditions, the cycle-averaged transmembrane pressure, also showing a marked dependence on the frequency, changes sign on increasing the cavity transverse dimension (i.e. orthogonal to the cord axis), underscoring the importance of cavity size in connection with the underlying hydrodynamics. The analytic results presented here can be instrumental in guiding future numerical investigations, needed to clarify the pathogenesis of syringomyelia cavities.

Information

Type
JFM Papers
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/4.0), which permits unrestricted re-use, distribution and reproduction, provided the original article is properly cited.
Copyright
© The Author(s), 2024. Published by Cambridge University Press.
Figure 0

Figure 1. Schematic representation of the problem, including (a) a general view of the central nervous system for a subject having a syringomyelia syrinx at the cervical level, (b) view of the cross-section of the spinal canal at a syrinx-free location, (c) a close view of the cavity with indication of the induced sloshing motion, (d) illustration of the longitudinal flow along the spinal SAS and (e) close view of a spinal cord periarterial space.

Figure 1

Figure 2. Schematic representations of canalicular (a) and extracanalicular (b) syringomyelia, and of the canonical model investigated here (c). The schematic (a) of the canalicular syrinx depicts a Chiari I malformation, while no specific cause is indicated for the extracanalicular case shown in (b).

Figure 2

Figure 3. Oscillatory flow for a configuration with $\alpha =5$, $H=1$ and $\mathcal {T}=$ (ac) $0.0001$, (df) $0.01$ and (gi) $0.05$. (a,d,h) The variation with time of the channel (blue) and cavity (red) flow rates $Q_0^o=\int _0^1 u_0^o \,{\rm d} y$ and $Q_0^c=\int _{-H}^0 u_0^c \,{\rm d} y$ at $x=0.5$ evaluated using (3.16). (b,e,h,c,f,i) Streamlines and colour contours of vorticity at $t={\rm \pi} /4$ and $t={\rm \pi}$ along with the corresponding membrane displacement $\xi _0$. To facilitate comparisons, a fixed constant streamline spacing of $\delta \psi _0=0.05$ has been used in representing the streamlines, with the stream function $\psi _0$ computed using $\partial \psi _0/\partial y=u_0$ and $\partial \psi _0/\partial x=-v_0$.

Figure 3

Figure 4. The variation with time of (a) the membrane displacement $\xi _0$, (b) cavity flow rate $Q_o^c=\int _{-H}^0 u_o^c \,{\rm d} y$ and (c) oscillatory transmembrane pressure difference $p_0^c-p_0^o$ for a cavity with $\alpha =5$, $H=1$ and $\mathcal {T}=0.01$.

Figure 4

Figure 5. The streamwise variation of (ac) the membrane displacement $\xi _0$ and (df) cavity flow rate $Q_0^c=\int _{-H}^0 u_0^c \,{\rm d} y$ at (a,d) $t=0$, (b,e) $t = {\rm \pi}/4$ and (c,f) $t = {\rm \pi}/2$ for $\alpha =3$, $H=2$ and $\mathcal {T}=(10^{-3},10^{-5},10^{-8}$).

Figure 5

Figure 6. The variation with $\mathcal {T}$ of the amplitude of the oscillating flow rate $|\!\int _0^{1/2}\chi \,\text {d}\kern 0.06em x|$ across the central section $x=1/2$ of the cavity for $\alpha =3$ (a) and $\alpha =6$ (b) and four different values of $H=(0.5,1,2,\infty )$. The inset in (a) represents an expanded view of the curves as they merge for increasing $\mathcal {T}$ while that in (b) gives the variation with $\alpha$ of the peak value of $|\!\int _0^{1/2}\chi \,\text {d}\kern 0.06em x|$ for three different values of $H$.

Figure 6

Figure 7. (a) Comparison of the dimensionless flow rate at the entrance of the spinal canal measured by cardiac-gated PC MRI (adapted from Vinje et al.2018) (solid curve) with the sinusoidal signal $Q'/\langle |Q'|\rangle =({\rm \pi} /2) \sin (t)$ (dashed curve). The two waveforms are used to determine the response of the cavity flow for a configuration with $\alpha =5$, $\mathcal {T}=0.02$ and two different cavity widths $H=1$ (red curves) and $H=4$ (blue curves), including (b) the variation with time of the cavity flow rate $Q_0^c=\int _{-H}^0 u_0^c \,{\rm d} y$ at $x=1/2$ determined from (3.25) and (c) the streamwise variation of the transmural steady pressure difference $\langle\, p_{1}^{c}\rangle -\langle\, p_{1}^{o}\rangle$ computed from (4.28). For consistency with (a), the solid/dashed curves in (b,c) are computed with the complex/sinusoidal channel-flow waveforms.

Figure 7

Figure 8. Secondary flow for $H=1.5$ and $\alpha =6$ with $\mathcal {T}=0.01$ (a,c,e,g) and $\mathcal {T}=0.001$ (b,d,f,h) including (a,b) streamlines, colour contours of vorticity and channel and cavity flow rates corresponding to the steady-streaming velocity $\langle \boldsymbol {v_1}\rangle =(\langle u_1\rangle,\langle v_1 \rangle )$, (c,d) streamlines and colour contours of vorticity corresponding to the Stokes drift velocity $\boldsymbol {v}_{SD}=(u_{SD},v_{SD})$, (e,f) streamlines and colour contours of vorticity corresponding to the mean Lagrangian velocity $\boldsymbol {v}_L=\langle \boldsymbol {v_1}\rangle +\boldsymbol {v}_{SD}$ and (g,h) membrane deformation $\langle \xi _1 \rangle$ and stationary transmembrane pressure difference $\langle\, p_{1}^{c}\rangle -\langle\, p_{1}^{o}\rangle$.

Figure 8

Figure 9. The variation with $\mathcal {T}$ of the spatially averaged transmembrane pressure difference $\int _{0}^{1} (\langle\, p_{1}^{c}\rangle -\langle\, p_{1}^{o}\rangle ) \,\text {d}\kern 0.06em x$ for $\alpha =3$ (a) and $\alpha =6$ (b) with $H=(0.5,1,2,\infty )$. The inset on the right depicts the evolution with $\alpha$ of the peak values of $\int _{0}^{1}(\langle\, p_{1}^{c}\rangle -\langle\, p_{1}^{o}\rangle )\, \text {d}\kern 0.06em x$ for $H=2$ (red) and $H=\infty$ (black).