3. Classification of Extra-Osseous
TaloTarsal Stabilization Devices
Extra-Osseous Talotarsal Stabilization Devices:
A New Classification System.
Vol. 51, No. 5, p. 613-622, 2012.
4. Classification of Extra-Osseous
TaloTarsal Stabilization Devices
– Type I – Cylinder and Cone designs
• device is placed into the lateral/sinus portion of the sinus
tarsi
• laterally anchored.
– Type II – device is placed into the central portion of
the sinus-
• medially anchored deep into the canalis portion of the
sinus tarsi.
5. • Device design
• Placement/Position within the sinus tarsi
• Soft tissue anchor mechanism
• Angle of insertion/placement
• Functional/Biomechanical
• Device composition
7. Type I EOTTS devices
are inserted
lateral to medial
They are inserted until
the leading/medial
edge touches the
bisection of the talus.
Placed in the sinus
portion of the sinus
tarsi.
8. Type II
Notice the angle of insertion.
HyProCure is inserted
anterior-lateral-distal
to
posterior-medial-proximal
10. The Problem with Type I
• Since they only fit into the outer
portion of the sinus tarsi
• There is direct impact against
the stent with every step taken
• Eventually the stent becomes
dislodged and has to be
replaced.
• These are not biomechanically
friendly.
11. Think about what is occurring during
the gait cycle.
TTJ Supination
Talus externally rotates – pulling the lateral process posteriorly.
12. Think about what is occurring during
the gait cycle.
TTJ Pronation
Talus internally rotates – forcing the lateral process anteriorly
smashing into the arthroereisis device with every step taken.
13. The most stable area of the sinus tarsi
is in the canalis
The reason why there are thick
stronger ligaments in the lateral
sinus portion of the sinus tarsi is
to “check” any excessive amount
of internal rotary force of the talus
on the tarsal mechanism.
14. Let’s Think About This!
If the canalis portion of the sinus tarsi is the
most stable…
…doesn’t it make
sense that this is the most important area
to anchor our talotarsal stabilization device?
15. What is the direction of the sinus tarsi?
It isn’t lateral to medial!
Anterior-distal-lateral
to
Posterior-proximal-medial
16. Let’s Take a Closer Look at the
undersurface of the Talus and HyProCure
17. What/where is the most important
area to stabilize the talus on the
tarsal mechanism?
This is about the most important question that can be
asked as this is what we are trying to achieve.
18. This is the exact area where the talus MUST be prevented from
slipping off its position on the posterior aspect of the calcaneus.
20. Type I Devices
• The tip of the device can
enter into this area of the
sinus tarsi and therefore
stabilize it.
• However, remember that
the majority of forces are
acting laterally so that
that it is possible for the
type I device to “wiggle”
out of place and partially
detach and lose its
function to stabilize the
axis.
21. Type II HyProCure
• The tapered portion of
HyProCure is the real
work-horse as this the
portion that prevents the
talus from dislocating on
the tarsal mechanism.
• The talus glides over
HyProCure.
24. HyProCure – Threaded Section
• The anchoring portion of
HyProCure is the medial
section.
• Although this is not a “screw”
as HyProCure’s threads do
NOT engage into the walls of
the sinus tarsi.
• Their function is to allow
tissue ON-GROWTH to
medially anchor HyProCure
into the sinus tarsi.
25. HyProCure – Tapered Section
• The stabilizing portion
of HyProCure is the
middle tapered section.
• It is smooth so that
there is equal pressure
action on the talus to
lessen any potential of
bone deformation.
26. HyProCure – Lateral Section
• Primary function is to assist
in lateral stability of the
lateral process
• Grove within the “head” of
HyProCure allows also for
tissue on-growth to also
laterally anchor HyProCure
for additional stability.
27. Tissue Adherence
In-growth On-growth
• Tissue incorporates into the
device.
• Not only does the tissue
completely surround the
device it grows internally.
• Sounds good except if the
device has to be removed
these tissue are removed as
well.
• Tissues grow onto the
device but not deep into the
device.
• Advantage is that if the
device has to be removed
the tissues are not.
28. HyProCure’s unique design allows for
multiple points of peripheral soft tissue
on-growth by not in-growth.
29. Does it make a difference what
material makes up the device?
You bet it does!
30. TaloTarsal Stabilization
• Bone
• Silicone
• High Molecular Weight Polyethene
• Combination Titanium and Polyethene
• Titanium
• Poly-lactate Acid (absorbable)
31. Device Material
• Bone – gets absorbed, not reliable, not strong enough
• Silicone – not strong enough, fragments, silicone shards,
not reliable.
• Polyethene – not strong enough, fragments, not reliable.
• Polylactate – absorbs, temporary, loss of correction.
32. EOTTS Device - Titanium
• Material of choice
• Stronger than bone
• Least reactive material implanted into the body
• Does oxidize and can turn tissues a darker color
however this has never been shown to become a
problem.
• Patients can still have MRI, CT, etc., without fear
• Does not set off a metal detector
33. Titanium and Tissue Adherence
• Titanium has extremely small micropores that
allow partial tissue attachment.
• If a HyProCure device has to be remove, twist
it 360 degrees which frees-up the tissue
attachments.