U.S. patent application number 13/969922 was filed with the patent office on 2013-12-12 for stabilization system and method.
This patent application is currently assigned to Zimmer Spine, Inc.. The applicant listed for this patent is Zimmer Spine, Inc.. Invention is credited to Brian J. Bergeron, K. Scott Ely, Charles R. Forton, Jeremy J. Lemoine, Peter T. Miller.
Application Number | 20130331891 13/969922 |
Document ID | / |
Family ID | 40670400 |
Filed Date | 2013-12-12 |
United States Patent
Application |
20130331891 |
Kind Code |
A1 |
Bergeron; Brian J. ; et
al. |
December 12, 2013 |
STABILIZATION SYSTEM AND METHOD
Abstract
The disclosure relates to systems and methods of spinal
stabilization. Embodiments include minimally invasive methods of
delivering a rod having a non-circular cross-sectional profile
using a wire having an accommodating non-circular cross-sectional
profile to inhibit movement of the rod relative to the wire. A rod
or a segment of the rod having a non-circular cross-sectional
profile may be aligned with the wire and advanced and coupled to
bone fastener assemblies which are anchored in vertebrae. The rod
is then securely seated in collars of the bone fastener assemblies
to stabilize the spine.
Inventors: |
Bergeron; Brian J.; (Austin,
TX) ; Ely; K. Scott; (Cedar Park, TX) ;
Forton; Charles R.; (Leander, TX) ; Lemoine; Jeremy
J.; (Austin, TX) ; Miller; Peter T.; (Austin,
TX) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Zimmer Spine, Inc. |
Minneapolis |
MN |
US |
|
|
Assignee: |
Zimmer Spine, Inc.
Minneapolis
MN
|
Family ID: |
40670400 |
Appl. No.: |
13/969922 |
Filed: |
August 19, 2013 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
13086149 |
Apr 13, 2011 |
8512381 |
|
|
13969922 |
|
|
|
|
11946644 |
Nov 28, 2007 |
7947064 |
|
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13086149 |
|
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Current U.S.
Class: |
606/272 |
Current CPC
Class: |
A61B 17/7038 20130101;
A61B 17/7005 20130101; A61B 17/7032 20130101; A61B 17/1671
20130101; A61B 17/1757 20130101; A61B 17/1655 20130101; A61B
17/7091 20130101; A61B 17/701 20130101; A61B 17/7011 20130101; A61B
17/7083 20130101 |
Class at
Publication: |
606/272 |
International
Class: |
A61B 17/70 20060101
A61B017/70 |
Claims
1. A system for stabilizing a portion of a spine, comprising: a
connection member having a head, a base, and a neck connecting the
head and base, the neck being narrower than the head and base; and
at least two bone fastener assemblies, each bone fastener assembly
comprising a pedicle screw with a collar for coupling the
connection member to adjacent vertebrae.
2. The system of claim 1, wherein the base of the connection member
includes a curved portion.
3. The system of claim 1, wherein the head of the connection member
has a non-circular cross-section.
4. The system of claim 1, wherein the head of the connection member
has a flat upper surface.
5. The system of claim 1, wherein the collar includes: two upwardly
extending walls forming a passage having a profile for receiving a
portion of the connection member; and a threaded portion.
6. The system of claim 5, further comprising a threaded closure
member for engaging the threaded portion of the collar to couple
the connection member in the passage.
7. The system of claim 1, wherein the connection member includes
more than one segment.
8. The system of claim 1, wherein the bone fastener assemblies are
polyaxial.
9. The system of claim 1, wherein the bone fastener assemblies are
fixed angle.
10. A system for stabilizing a portion of a spine, comprising: a
connection member having a flat top, a curved base, and a neck
connecting the flat top and curved base; at least two bone fastener
assemblies, each bone fastener assembly comprising: a pedicle screw
with a collar for coupling the connection member to a vertebra, the
collar comprising: two upwardly extending walls forming a passage
having a profile for receiving a portion of the connection member;
and a threaded portion; and a threaded closure member for engaging
the threaded portion of the collar to couple the connection member
in the passage.
11. The system of claim 10, wherein the neck of the connection
member is narrower than the flat top and curved base.
12. The system of claim 10, wherein the connection member includes
more than one segment.
13. The system of claim 10, wherein the bone fastener assemblies
are polyaxial.
14. The system of claim 10, wherein the bone fastener assemblies
are fixed angle.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 13/086,149, filed Apr. 13, 2011, which is a
continuation of U.S. patent application Ser. No. 11/946,644, filed
Nov. 28, 2007, now U.S. Pat. No. 7,947,064, the complete
disclosures of which are incorporated herein by reference.
TECHNICAL FIELD OF THE DISCLOSURE
[0002] The disclosure describes various spine stabilization systems
and methods, including systems and methods for inserting spinal
stabilization rods in a minimally invasive surgery.
BACKGROUND OF THE DISCLOSURE
[0003] Bone may be subject to degeneration caused by trauma,
disease, and/or aging.
[0004] Degeneration may destabilize bone and affect surrounding
structures. For example, destabilization of a spine may result in
alteration of a natural spacing between adjacent vertebrae.
Alteration of a natural spacing between adjacent vertebrae may
subject nerves that pass between vertebral bodies to pressure.
Pressure applied to the nerves may cause pain and/or nerve damage.
Maintaining the natural spacing between vertebrae may reduce
pressure applied to nerves that pass between vertebral bodies. A
spine stabilization procedure may be performed to maintain the
natural spacing between vertebrae and promote spinal stability.
Spinal stabilization may involve accessing a portion of the spine
through soft tissue. Conventional stabilization systems may require
a large incision and/or multiple incisions in the soft tissue to
provide access to a portion of the spine to be stabilized.
Conventional procedures may result in trauma to the soft tissue,
for example, due to muscle stripping. Spine stabilization systems
for a lumbar region of the spine may be inserted during a spine
stabilization procedure using a posterior spinal approach.
Conventional systems and methods for posterolateral spinal fusion
may involve dissecting and retracting soft tissue proximate the
surgical site. Dissection and retraction of soft tissue may cause
trauma to the soft tissue, and extend recovery time.
SUMMARY OF THE DISCLOSURE
[0005] Minimally invasive procedures and systems may reduce
recovery time as well as trauma to the soft tissue surrounding a
stabilization site. The disclosure describes embodiments of systems
and methods for spinal stabilization, particularly systems and
methods that utilize a wire having a non-circular cross-sectional
profile to deliver, preferably percutaneously, an elongated member
(e.g., a rod). According to one embodiment, a system for
stabilizing a portion of a spine comprises a rod having a
non-circular cross-sectional profile and a length to span between
two vertebrae, two bone fastener assemblies, and a wire for
percutaneous advancement of the rod to the passage in a bone
fastener assembly anchored to a vertebra. In some embodiments, the
wire comprises a non-circular cross-sectional profile complementary
to the non-circular cross-sectional profile of the rod for engaging
the rod to inhibit rotational movement of the rod relative to the
wire. In some embodiments, each bone fastener assembly includes a
pedicle screw for advancement into a vertebra, a collar for
coupling the rod to the pedicle screw, and a threaded closure
member for engaging the threaded portion of the collar to couple
the rod in a passage in the collar. A collar may have two upwardly
extending walls forming a passage having a profile for receiving
and accommodating a portion of the non-circular cross-sectional
profile of the rod. A collar may have an opening forming a passage
having a profile for receiving and accommodating a portion of the
non-circular cross-sectional profile of the rod. In some
embodiments, the non-circular cross-sectional profile of the rod
may include an array of surfaces, a flange, a slot, a cannulated
passage along a length of the rod, or a recessed portion along a
length of the rod. In some embodiments, the rod comprises two
segments, wherein each segment has a complementary non-circular
cross-sectional profile for engaging the non-circular
cross-sectional profile of the wire to inhibit rotational movement
of the segment relative to the wire, a surface for engagement with
a collar, a leading end for displacing tissue during advancement of
a segment along the wire, and a trailing end comprising an
engagement feature for connecting with an adjacent segment, wherein
connecting the two segments forms a rod to span a vertebral level.
In some embodiments, each segment comprises a cannulated passage
through a portion thereof. In some embodiments, the cannulated
passage extends along a central axis, is offset from a central
axis, or is oriented askew to a longitudinal axis. In some
embodiments, the rod comprises a curvature, bend, or angle along a
length thereof. In some embodiments, the rod comprises a recessed
portion located along the length and oriented transverse to the
longitudinal axis. In some embodiments, the wire has a
cross-sectional profile and a curvature for engaging the recessed
portion. In some embodiments, the recessed portion is oriented at a
selected angle relative to the longitudinal axis or a groove
extending around at least a portion of the outer surface. In some
embodiments, coupling a rod having a non-circular profile to a bone
screw comprises positioning a portion of a wire having a
non-circular cross-sectional profile complementary to the rod in a
first passage through the collar and positioning a portion of the
rod in the second passage and engaging a closure member in the
collar. In some embodiments, engaging the closure member provides
sufficient clearance for the wire to be withdrawn. In some
embodiments, engaging the closure member securely couples the wire
and rod to the bone screw.
[0006] According to another embodiment, a method for stabilizing a
portion of a spine comprises the steps of making a first incision
for anchoring a first bone fastener assembly in a first vertebra,
making a second incision for anchoring a second bone fastener
assembly in a second vertebra, making a third incision for entry of
a wire having a non-circular cross sectional profile, making a
fourth incision for exiting of the wire, advancing the wire through
the third incision for positioning near the first and second bone
fastener assemblies, engaging a rod with the wire, rotating the
wire to rotate the rod, and securing the rod to the first and
second bone screws, wherein the rod spans at least one vertebral
level. In some embodiments, a bone fastener assembly comprises
includes a bone screw having a threaded shank for engaging a
portion of a vertebra and a head portion connected to the threaded
shank, a collar with a bottom portion having an opening for
receiving a portion of a bone screw and two upwardly extending
walls forming a first passage for receiving the rod and forming a
second passage for receiving a portion of a wire, a threaded
portion, and a threaded closure member threaded for engaging the
threaded portion of the collar. In some embodiments, the rod has a
non-circular cross-sectional profile, wherein the rod's
non-circular cross-sectional profile is complementary to the wire's
non-circular cross-sectional profile for engaging the wire to
inhibit rotational movement of the rod relative to the wire. In
some embodiments, the rod comprises two or more segments. In some
embodiments, the method comprises engaging a first segment of a rod
to the wire, advancing the first segment along the wire to a second
passage in the first collar, engaging a second segment of the rod
to the wire, advancing the second segment to a second passage in
the second collar, and connecting a leading end of the second
segment with the trailing end of the first segment to span a
vertebral level with a rod having first and second curvatures. In
some embodiments, each segment of a rod comprises a complementary
non-circular cross-sectional profile for engaging the non-circular
cross-sectional profile of the wire to inhibit rotational movement
of the segment relative to the wire, a surface for engagement with
a collar, a leading end for displacing tissue during advancement of
a segment along the wire, and a trailing end comprising an
engagement feature for connecting with the leading end of an
adjacent segment, wherein one or more segments form a rod that can
connect to two or more collars to span one or more vertebral
levels.
[0007] According to another embodiment, the present disclosure
includes a method for advancing a rod into a body. The method may
include advancing a first bone fastener assembly via a first
incision in the body, anchoring the first bone fastener assembly to
a first vertebra, advancing a second bone fastener assembly via a
second incision in the body, anchoring the second bone fastener
assembly to a second vertebra, advancing a wire into the body via a
third incision, advancing the wire through transverse openings in
the first and second bone fastener assemblies to define a path,
advancing the wire out of the body via a fourth incision, engaging
a rod with the wire, and advancing the rod through the transverse
openings in the first and second bone fastener assemblies along the
path. In some embodiments, a bone fastener assembly includes a bone
screw having a threaded portion and a head portion coupled to a
collar. The collar may have an opening for receiving the head
portion of the bone screw and a passage oriented transverse to the
opening for receiving the wire or rod or both. In some embodiments,
the wire comprises a non-circular cross-sectional profile and the
rod comprises a non-circular cross-sectional profile complementary
to the wire cross-sectional profile. In some embodiments, the wire
maintains the radial orientation of the rod during advancement
along the wire. In some embodiments, the rod comprises a passage
along a portion thereof. In some embodiments, the step of advancing
the rod comprises moving the rod along the wire. In some
embodiments, the rod comprises an attachment feature for attaching
the rod to the wire. In some embodiments, the step of advancing the
rod comprises moving the wire. In some embodiments, the step of
advancing the rod comprises advancing the rod from the third
incision to the fourth incision. In some embodiments, the step of
advancing the rod comprises advancing the rod from the fourth
incision to the third incision. In some embodiments, the rod
comprises two segments, wherein each segment comprises a surface
for engagement with a collar, a leading end for displacing tissue
during advancement through the body, and a trailing end comprising
a connection feature for connecting with an adjacent segment,
wherein connecting the two segments forms a rod, wherein engaging
the two connected segments to the two bone fastener assemblies
spans a vertebral level.
[0008] Embodiments disclosed herein provide many advantages. For
example, in embodiments of the spine stabilization system and
method disclosed herein, a spinal rod is not confined to a fixed
arc during insertion.
[0009] Yet another advantage provided by embodiments of the spine
stabilization system and method disclosed herein is that the
additional components used for percutaneous delivery of a spinal
rod can be easy to place and use.
BRIEF DESCRIPTION OF THE FIGURES
[0010] Additional features and advantages of the embodiments will
become apparent to those skilled in the art with the benefit of the
following detailed description and upon reference to the
accompanying drawings in which:
[0011] FIGS. 1 and 2 depict perspective views of embodiments of a
portion of a spine stabilization system.
[0012] FIG. 3 depicts a perspective view of one embodiment of a
portion of a bone fastener assembly.
[0013] FIG. 4 depicts a side view of one embodiment of a portion of
a bone fastener assembly.
[0014] FIG. 5 depicts a front view of one embodiment of a bone
fastener assembly with a collar that allows for angulation of a
bone fastener relative to the collar in a conical range of motion
that is symmetrical relative to an axis that passes through a
central axis of the collar and a central axis of a bone
fastener.
[0015] FIG. 6A depicts a front view of one embodiment of a bone
fastener assembly with a collar that allows for angulation of a
bone fastener relative to the collar in a conical range of motion
that is not symmetrical relative to an axis that passes through a
central axis of the collar and a central axis of a bone fastener.
The collar allows additional lateral bias relative to a non-biased
collar.
[0016] FIG. 6B depicts a side view of one embodiment of a bone
fastener assembly with a collar that allows for angulation of a
bone fastener relative to the collar in a conical range of motion
that is not symmetrical relative to an axis that passes through a
central axis of the collar and a central axis of a bone fastener.
The collar allows additional caudal or cephalid bias relative to a
non-biased collar.
[0017] FIG. 7A depicts a schematic side view representation of
embodiments of bone fastener assemblies positioned in
vertebrae.
[0018] FIG. 7B depicts a schematic top view representation of one
embodiment of a single-level spine stabilization system.
[0019] FIG. 8 depicts a perspective view of one embodiment of a
targeting needle.
[0020] FIG. 9 depicts a perspective view of an outer housing of a
targeting needle.
[0021] FIG. 10 depicts a perspective view of one embodiment of a
member of a targeting needle.
[0022] FIG. 11 depicts a perspective view of one embodiment of a
guide wire.
[0023] FIG. 12 depicts a perspective view of one embodiment of a
guide wire.
[0024] FIG. 13 depicts a perspective view of one embodiment of a
multi-channel sleeve.
[0025] FIG. 14 depicts a cross-sectional representation of a
portion of the sleeve with the bone fastener assembly taken
substantially along line 14-14 of FIG. 13.
[0026] FIG. 15 depicts a perspective view of one embodiment of a
single-channel sleeve.
[0027] FIG. 16 depicts a partial cross-sectional representation of
one embodiment of a sleeve coupled to a collar of a bone fastener
assembly.
[0028] FIG. 17 depicts top view representation of one embodiment of
a collar.
[0029] FIG. 18 depicts a partial cross-sectional representation of
one embodiment of a sleeve coupled to one embodiment of a collar of
a bone fastener assembly, such as the collar depicted in FIG.
17.
[0030] FIG. 19 depicts a top view representation of one embodiment
of a collar.
[0031] FIG. 20 depicts a partial cross-sectional representation of
one embodiment of a sleeve coupled to one embodiment of a collar of
a bone fastener assembly, such as the collar depicted in FIG.
19.
[0032] FIG. 21 depicts a partial cross-sectional view of one
embodiment of a sleeve with an inner sleeve.
[0033] FIG. 22 depicts a partial cross-sectional representation of
one embodiment of a sleeve coupled to a collar of a bone fastener
assembly.
[0034] FIG. 23 depicts a partial cross-sectional representation of
one embodiment of a sleeve coupled to a collar of a bone fastener
assembly.
[0035] FIG. 24 depicts a partial cross-sectional representation of
one embodiment of a sleeve coupled to a collar of a bone fastener
assembly.
[0036] FIG. 25 depicts a cross-sectional representation of one
embodiment of a hinged sleeve coupled to a collar of a bone
fastener assembly.
[0037] FIG. 26 depicts a cross-sectional representation of one
embodiment of a hinged sleeve coupled to a collar of a bone
fastener assembly.
[0038] FIG. 27 depicts a schematic representation of sleeve
embodiments coupled to collars of a spine stabilization system.
[0039] FIG. 28 depicts a schematic representation of sleeve
embodiments with connections that allow relative movement of
portions of a sleeve.
[0040] FIG. 29 depicts a perspective view of one embodiment of
sleeves that are coupled to bone fastener assemblies.
[0041] FIG. 30 depicts a schematic view of sleeve embodiments that
are coupled to one embodiment of a frame.
[0042] FIG. 31 depicts a perspective view of one embodiment of a
driver coupled to a bone fastener and a sleeve.
[0043] FIG. 32 depicts a partial cross-sectional view of one
embodiment of a bone fastener and collar coupled to a driver
positioned in a dilator.
[0044] FIG. 33 depicts a side view of one embodiment of a rod
having multiple segments.
[0045] FIG. 34 depicts a side view of one embodiment of a segment
of one embodiment of a rod.
[0046] FIG. 35 depicts a side view of one embodiment of a segment
of one embodiment of a rod.
[0047] FIG. 36 depicts a side view of one embodiment of a segment
of one embodiment of a rod.
[0048] FIG. 37 depicts a side view of one embodiment of a spine
stabilization system illustrating a method for advancing a rod into
one embodiment of a bone fastener assembly.
[0049] FIG. 38 depicts a perspective view of one embodiment of a
spine stabilization system illustrating a method for advancing a
rod into one embodiment of a bone fastener assembly.
[0050] FIGS. 39A and 39B depict perspective views of a tool
designed to position a closure member in a collar coupled to a bone
fastener.
[0051] FIGS. 40A and 40B depict perspective views of a tool
designed to position a closure member in a collar coupled to a bone
fastener.
[0052] FIG. 41 depicts one embodiment of a counter torque wrench
coupled to a sleeve.
[0053] FIG. 42 depicts one embodiment of a counter torque
wrench.
[0054] FIG. 43 depicts a schematic view of the counter torque
wrench shown in FIG. 42 coupled to a rod.
[0055] FIGS. 44A-44E depict schematic views of guide wire placement
during a minimally invasive spine stabilization procedure.
[0056] FIGS. 45A-45D depict schematic views of tissue dilation
during a minimally invasive spine stabilization procedure.
[0057] FIGS. 46A-46F depict schematic views of vertebra preparation
for receiving a bone fastener assembly during a minimally invasive
spine stabilization procedure.
[0058] FIGS. 47A-47D depict schematic views of insertion of a
sleeve and bone fastener assembly during a minimally invasive spine
stabilization procedure.
[0059] FIG. 48 depicts a side view of one embodiment of a rod.
[0060] FIG. 49 depicts a side view of one embodiment of a rod.
[0061] FIG. 50 depicts a side view of one embodiment of a rod.
[0062] FIG. 51 depicts a side view of one embodiment of a rod.
[0063] FIGS. 52A-52D depict schematic views of a sleeve removal
during a minimally invasive spine stabilization procedure.
[0064] Specific embodiments are shown by way of example in the
drawings and will herein be described in detail. The drawings may
not be to scale. It should be understood that the drawings and
detailed description thereto are not intended to limit the
embodiments to the particular form disclosed.
DETAILED DESCRIPTION OF THE DISCLOSURE
[0065] A spine stabilization system may be installed in a patient
to stabilize a portion of a spine. Spinal stabilization may be
used, but is not limited to use, in patients having degenerative
disc disease, spinal stenosis, spondylolisthesis, pseudoarthrosis,
and/or spinal deformities; in patients having fracture or other
vertebral trauma; and in patients after tumor resection. A spine
stabilization system may be installed using a minimally invasive
procedure. An instrumentation set may include instruments and spine
stabilization system components for forming a spine stabilization
system in a patient.
[0066] A minimally invasive procedure may be used to limit an
amount of trauma to soft tissue surrounding vertebrae that are to
be stabilized. Particularly, a procedure may be used to
percutaneously deliver a spinal rod. In some embodiments, the
natural flexibility of skin and soft tissue may be used to limit
the length and/or depth of an incision or incisions needed during
the stabilization procedure. Minimally invasive procedures may
provide limited direct visibility in vivo. Forming a spine
stabilization system using a minimally invasive procedure may
include using tools to position system components in the body. A
minimally invasive procedure may be performed after installation of
one or more spinal implants in a patient. The spinal implant or
spinal implants may be inserted using an anterior procedure and/or
a lateral procedure. The patient may be turned and a minimally
invasive procedure may be used to install a posterior spine
stabilization system. A minimally invasive procedure for
stabilizing the spine may be performed without prior insertion of
one or more spinal implants in some patients. In some patients, a
minimally invasive procedure may be used to install a spine
stabilization system after one or more spinal implants are inserted
using a posterior spinal approach. A spine stabilization system may
be used to achieve rigid pedicle fixation while minimizing the
amount of damage to surrounding tissue. In some embodiments, a
spine stabilization system may be used to provide stability to two
adjacent vertebrae (i.e., one vertebral level). A spine
stabilization system may include two bone fastener assemblies. One
bone fastener assembly may be positioned in each of the vertebrae
to be stabilized. A wire may be advanced to the bone fastener
assemblies. A rod may be advanced along the wire and coupled and
secured to the bone fastener assemblies. As used herein, "coupled"
components may directly contact each other or may be separated by
one or more intervening members. In some embodiments, a single
spine stabilization system may be installed in a patient. Such a
system may be referred to as a unilateral, single-level
stabilization system or a single-level, two-point stabilization
system. In some embodiments, two spine stabilization systems may be
installed in a patient on opposite sides of a spine. Such a system
may be referred to as a bilateral, single-level stabilization
system or a single-level, four-point stabilization system.
[0067] In some embodiments, a spine stabilization system may
provide stability to three or more vertebrae (i.e., two or more
vertebral levels). In a two vertebral level spine stabilization
system, the spine stabilization system may include three bone
fastener assemblies. One bone fastener assembly may be positioned
in each of the vertebrae to be stabilized. A wire may be advanced
through an incision and passed through the bone fastener
assemblies. A rod may be advanced along the wire and coupled and
secured to the three bone fastener assemblies. In some embodiments,
a single two-level spine stabilization system may be installed in a
patient. Such a system may be referred to as a unilateral,
two-level stabilization system or a two-level, three-point
stabilization system. In some embodiments, two three-point spine
stabilization systems may be installed in a patient on opposite
sides of a spine. Such a system may be referred to as a bilateral,
two-level stabilization system or a two-level, six-point
stabilization system. In some embodiments, combination systems may
be installed. For example, a two-point stabilization system may be
installed on one side of a spine, and a three-point stabilization
system may be installed on the opposite side of the spine. The
composite system may be referred to a five-point stabilization
system. Minimally invasive procedures may reduce trauma to soft
tissue surrounding vertebrae that are to be stabilized. Only small
openings may need to be made in a patient. For example, for a
single-level stabilization procedure on one side of the spine, the
surgical procedure may be performed through four small incisions
formed in the skin of the patient.
[0068] Components of spine stabilization systems may be made of
materials including, but not limited to, titanium, titanium alloys,
stainless steel, ceramics, and/or polymers. Some components of a
spine stabilization system may be autoclaved and/or chemically
sterilized. Components that may not be autoclaved and/or chemically
sterilized may be made of sterile materials. Components made of
sterile materials may be placed in working relation to other
sterile components during assembly of a spine stabilization system.
Spine stabilization systems may be used to correct problems in
lumbar, thoracic, and/or cervical portions of a spine. Various
embodiments of a spine stabilization system may be used from the C1
vertebra to the sacrum. For example, a spine stabilization system
may be implanted posterior to the spine to maintain distraction
between adjacent vertebral bodies in a lumbar portion of the
spine.
[0069] Recently, it has become increasingly popular to insert
spinal fixation rods percutaneously. One existing system is a
sextant or tripod that delivers a fixation rod via a fixed
trajectory along a fixed arc (i.e., such systems have a fixed pivot
point). One problem is that such systems do not easily accommodate
procedures in which the spinal curvature does not easily align
along an arc achievable by the sextant.
[0070] Embodiments of the present disclosure may be used in a wide
variety of medical applications where the minimally invasive
implantation of a rod may be desirable. The systems and methods
described herein may find utility in medical procedures where it is
desirable to construct a spine fixation system having selected
curvature.
[0071] FIG. 1 illustrates one embodiment of a portion of a spine
stabilization system, which comprises bone fastener assembly 102
and rod 104 (shown in a cross-sectional view). As will be described
below in more detail, wire 400 (shown in a cross-sectional view in
conjunction with rod 104) is useful for the percutaneous
advancement of rod 104 into the body and through collar 112 of bone
fastener assembly 102 for constructing a spine stabilization system
without requiring a sextant. Wire 400 can be formed of titanium,
titanium alloys, stainless steel, ceramics, polyethersulfone, PEEK,
polymers or other biocompatible material and can be formed as a
single piece of material or as multiple pieces that are coupled
together. As shown in FIG. 1, wire 400 may have a non-circular
cross-sectional profile. Wire 400 may include two or more surfaces
400a-400n. For example, FIG. 1 depicts one embodiment in which wire
400 may have a cross-sectional profile defined by surfaces 400a,
400b, 400c, 400d, 400e, 400f, 400g and 400h. While wire 400 is
shown in FIG. 1 as having curved sides with different radiuses of
curvature and straight sides of different lengths, wire 400 can
have a variety of shapes including, but not limited to, a
rectangular profile, a trapezoidal opening, a square profile, an
ovoid profile, an egg-shaped profile, a tapered profile, and
combinations and/or portions thereof.
[0072] Rod 104 may have a cross-sectional profile that is
complementary to the cross-sectional profile of wire 400. As shown
in FIG. 1, rod 104 may have a cross-sectional profile defined by
surfaces 104a, 104b and 104c to enable rod 104 to engage wire 400.
Advantageously, the cross-sectional profile of wire 400 may inhibit
rotational movement of rod 104 relative to wire 400 so the
orientation of rod 104 is maintained during the advancement of rod
104 into the body.
[0073] As shown in FIG. 1, collar 112 may have transverse opening
116 for receiving wire 400 and rod 104. In FIG. 1, transverse
opening 116 may have a profile that allows wire 400 and/or rod 104
to pass through collar 112 in only one orientation. Advantageously,
components of spinal system 100 may be advanced along wire 400 such
that they reach collar 112 in a selected orientation.
[0074] As shown in FIGS. 1 and 2, opening 116 of collar 112 may
have two different sections. A first section, 116A, may be small
enough to allow passage of wire 400 only. A second section, 116B
may allow passage of wire 400 and rod 104.
[0075] In some procedures, it may be desirable to index rod 104 or
tools on wire 400. FIG. 2 depicts a perspective view of one
embodiment of a portion of spine stabilization system 100 in which
rod 104 may be indexed on wire 400. To index rod 104 on wire 400 in
FIG. 2, rod 104 may be rotated such that surface 104a contacts any
of surfaces 400a-400f. An advantage of this embodiment is the
capability to percutaneously construct rod 104 having a desired
curvature. Indexing rod 104 on wire 400 may be particularly useful
for embodiments in which rod 104 is formed by two or more segments,
discussed below.
[0076] FIG. 3 depicts one embodiment of bone fastener assembly
components. Components of bone fastener assembly 102 depicted in
FIG. 3 may include, but are not limited to, bone fastener 108 and
collar 112. Bone fastener 108 may be used to anchor bone fastener
assembly 102 to a vertebra.
[0077] A bone fastener may be, but is not limited to, a bone screw,
a ring shank fastener, a barb, a nail, a brad, or a trocar. Bone
fasteners and/or bone fastener assemblies may be provided in
various lengths in an instrumentation set to accommodate
variability in vertebral bodies. For example, an instrumentation
set for stabilizing vertebrae in a lumbar region of the spine may
include bone fastener assemblies with lengths ranging from about 30
mm to about 75 mm in 5 mm increments. A bone fastener assembly may
be stamped with indicia (i.e., printing on a side of the collar).
In some embodiments, a bone fastener assembly or a bone fastener
may be color-coded to indicate a length of the bone fastener. In
certain embodiments, a bone fastener with a 30 mm thread length may
have a magenta color, a bone fastener with a 35 mm thread length
may have an orange color, and a bone fastener with a 55 mm thread
length may have a blue color. Other colors may be used as desired.
Each bone fastener provided in an instrumentation set may have
substantially the same thread profile and thread pitch. In one
embodiment, the thread may have about a 4 mm major diameter and
about a 2.5 mm minor diameter with a cancellous thread profile. In
certain embodiments, the minor diameter of the thread may be in a
range from about 1.5 mm to about 4 mm or larger. In certain
embodiments, the major diameter of the thread may be in a range
from about 3.5 mm to about 6.5 mm or larger. Bone fasteners with
other thread dimensions and/or thread profiles may also be used. A
thread profile of the bone fasteners may allow bone purchase to be
maximized when the bone fastener is positioned in vertebral
bone.
[0078] Bone fastener 108 may include a shank, a head, and a neck.
The shank may include threading. In some embodiments, threading may
include a self-tapping start. A self-tapping start may facilitate
insertion of bone fastener 108 into vertebral bone. The head of
bone fastener 108 may include various configurations to engage a
driver that inserts the bone fastener into a vertebra. In some
embodiments, the driver may also be used to remove an installed
bone fastener from a vertebra. In some embodiments, the head may
include one or more tool portions. Tool portions may be recesses
and/or protrusions designed to engage a portion of the driver. In
some embodiments, bone fastener 108 may be cannulated for use in a
minimally invasive procedure. The neck of bone fastener 108 may
have a smaller diameter than adjacent portions of the head and the
shank. The diameter of the neck may fix the maximum angle that the
collar of the bone fastener assembly can be rotated relative to
bone fastener 108.
[0079] In some embodiments, the neck may be sized to allow up to
about 40.degree. or more of angulation of the collar relative to
the bone fastener. In some embodiments, the neck may be sized to
allow up to about 30.degree. of angulation of the collar relative
to the bone fastener. In some embodiments, the neck may be sized to
allow up to about 20.degree. of angulation of the collar relative
to the bone fastener.
[0080] As used herein, the term "collar" includes any element that
wholly or partially encloses or receives one or more other
elements. A collar may enclose or receive elements including, but
not limited to, a bone fastener, a closure member, a ring, and/or a
rod. In some embodiments, a collar may couple two or more other
elements together (e.g., a rod and a bone fastener). A collar may
have any of various physical forms. In some embodiments, a collar
may have a "U" shape, however it is to be understood that a collar
may also have other shapes. A collar may be open or closed. A
collar having a slot and an open top, such as collar 112 shown in
FIG. 3, may be referred to as an "open collar." A bone fastener
assembly that includes an open collar may be referred to as an
"open fastener." In some embodiments, a rod may be top loaded into
the open fastener. A closure member may be coupled to the collar to
secure the rod to the open fastener.
[0081] A collar that does not include a slot and an open top, such
as depicted in FIGS. 1 and 2, may be referred to as a "closed
collar." A spinal implant that includes a closed collar may be
referred to as a "closed implant." A closed collar may include an
aperture, bore, or other feature in side surfaces for accommodating
other components of a stabilization system (e.g., a rod or wire,
discussed below). A setscrew may be used to securely couple a rod
to a closed implant.
[0082] Collar 112 may include a body and arms. The arms may extend
from the body. The body of collar 112 may be greater in width than
a width across the arms of collar 112 (i.e., the body may have a
maximum effective outer diameter greater than a maximum effective
outer diameter of the arms). A reduced width across the arms may
allow a detachable member to be coupled to the arms without
substantially increasing a maximum effective outer diameter along a
length of collar 112. Thus, a reduced width across the arms may
reduce bulk at a surgical site. A height of collar body may range
from about 3 millimeters (mm) to about 7 mm. In one embodiment, a
height of the collar body is about 5 mm. The collar body may
include an opening in a lower surface. Inner surfaces and/or outer
surfaces of collar 112 may be surface treated or include coatings
and/or coverings to modify frictional properties or other
properties of the collar. Inner surfaces of the arms may include a
modified thread. The modified thread may engage a complementary
modified thread of a closure member to secure a rod to a bone
fastener assembly. The modified thread may have a constant pitch or
a variable pitch. A height and a width of the arms may vary. The
arms may range in height from about 8 mm to about 15 mm. In one
embodiment, a height of the arms is about 11 mm. A width (i.e.,
effective diameter) of the arms may range from about 5 mm to 14 mm.
The arms and the collar body may form a slot. The slot may be sized
to receive a rod. A slot may include, but is not limited to, an
elongated opening of constant width, an elongated opening of
variable width, a rectangular opening, a trapezoidal opening, a
circular opening, a square opening, an ovoid opening, an egg-shaped
opening, a tapered opening, and combinations and/or portions
thereof. In some embodiments, a first portion of the slot may have
different dimensions than a second portion of the slot. In certain
embodiments, a portion of a slot in the first arm may have
different dimensions than a portion of a slot in the second
arm.
[0083] When rod 104 is positioned in a slot, a portion of rod 104
may contact a head of bone fastener 108 positioned in collar 112.
The arms may include ridges or flanges. Flanges may allow collar
112 to be coupled to a detachable member so that translational
motion of collar 112 relative to the detachable member is
inhibited. Flanges may also include notches. A movable member of a
detachable member may extend into a notch. When the movable member
is positioned in a notch, a channel in the detachable member may
align with a slot in collar 112. With the movable member positioned
in a notch, rotational movement of collar 112 relative to the
detachable member may be inhibited.
[0084] In some embodiments, a bone fastener assembly may be a fixed
angle fastener. FIG. 4 depicts one embodiment of a fixed angle bone
fastener. Collar 112 and bone fastener 108 may be formed as a
unitary bone fastener assembly 102. A fixed angle fastener may be
positioned as the first bone fastener assembly inserted into a
vertebra.
[0085] FIG. 5 depicts bone fastener assembly 102 with central axis
158 of collar 112 aligned with central axis 160 of bone fastener
108. Bone fastener 108 may be angulated in a symmetrical conical
range of motion characterized by angle a about the aligned axes.
Bone fastener 108 may be constrained from motion outside of limit
axis 162 by contact between neck 120 of bone fastener 108 and
collar 112. Alignment of axis 160 of bone fastener 108 with central
axis 158 of collar 112 may be considered a neutral position
relative to the range of motion. The alignment is a neutral
position because bone fastener 108 may be angulated an equal amount
in any direction from central axis 158. When a driver is inserted
into bone fastener 108, axis 160 of bone fastener 108 may be
substantially aligned with axis 158 of collar 112 to facilitate
insertion of the bone fastener into a vertebral body. In certain
embodiments, a range of motion of a collar may be skewed from a
full conical range of motion relative to aligned central axes of
the collar and a bone fastener coupled to the collar. In some
embodiments, a distal end of a collar may be shaped to skew, or
bias, the range of motion from the range of motion depicted in FIG.
8.
[0086] FIGS. 6A and 6B depict bone fastener assemblies 102 with
biased collars 112. Body 140 of biased collar 112 may be shaped to
restrict relative movement of bone fastener 108 (and/or the collar)
to a skewed conical range of motion defined by limit axes 162. As
depicted by limit axes 162 in FIG. 6A, a first arm 142 of collar
112 may approach bone fastener 108 more closely than a second arm
of the collar. Similarly, as suggested by limit axes 162 in FIG.
6B, collar 112 may be oriented such that the slot formed by arms
142 may not be parallel (e.g., an opening on one side of collar 112
may be higher than a second opening on the other side). Other
biased collars may be designed to selectively restrict relative
movement of collars and/or bone fasteners. In some embodiments, a
biased collar may be attached to a detachable member such that a
surgeon performing a minimally invasive procedure may selectively
align the portion of the collar with the greater range of motion as
needed. For example, the collar depicted in FIGS. 6A-6B may be
coupled to a single-level (e.g., C-shaped) sleeve so that the side
of the collar (i.e., the side of the slot) with a larger range of
motion is positioned next to a channel opening of the sleeve.
[0087] When a biased collar of a bone fastener assembly is coupled
to a detachable member and a drive mechanism is coupled to a bone
fastener of the bone fastener assembly, central axis 158 of collar
112 may align with central axis 160 of bone fastener 108 to
facilitate insertion of the bone fastener into bone. In some
embodiments, the bias of the collar may be so large that a flexible
drive member is needed to drive the bone fastener into bone. In
some embodiments, one or more biased collars may be used in a spine
stabilization system. The spine stabilization systems may be
single-level systems or multi-level systems. Biased collars may be
used to accommodate the increasing angle of the pedicle corridor
for each lumbar vertebra. The angle may increase by about five
degrees for each successive lumbar vertebra.
[0088] FIGS. 7A and 7B depict inferior and posterior views of a
single-level spine stabilization system including bone fastener
assembly 102A coupled to pedicle 164A and vertebra 166A and bone
fastener assembly 102B coupled to pedicle 164B and vertebra 166B. A
bone fastener of bone fastener assembly 102A may engage pedicle
164A at pedicle angle .PHI.A relative to sagittal plane 168.
Pedicle angle .PHI.A may range between about 13.degree. and about
17.degree.. Collar 112A of bone fastener assembly 102A may be
unbiased. Pedicle angle .PHI.B may range between about 18.degree.
and about 22.degree.. Collar 112B may have a bias angle .beta. of
about 5.degree.. Bone fastener assembly 102B may engage pedicle
164B at pedicle angle .PHI.B. Because the bias of collar 112B is
approximately equal to the difference between the pedicle angles of
the two vertebrae, slots 150A and 150B in bone fastener assemblies
102A and 102B, respectively, may be generally aligned when both
bone fasteners are in neutral positions. Angulation of either or
both collars of the bone fastener assemblies may allow fine
adjustment of engagement angles of the bone fasteners. In addition,
collar angulation may allow adjustment in the orientation of bone
fasteners in a sagittal plane (i.e., to conform to lordosis of a
spine) while still allowing the collars to be easily coupled with
rod 104. Rod 104 may be disposed in slots 150A and 150B and secured
by closure members.
[0089] In some embodiments, a flexible driver or a polyaxial driver
(e.g., a driver with a universal joint) may be used to drive the
heads of the bone fasteners from a position that is off axis from
the bone fasteners to reduce the size of an opening of the body
needed to implant the spine stabilization system. A closure member
may be coupled to a collar of a bone fastener assembly to fix a rod
positioned in the collar to the bone fastener assembly. In some
embodiments, a closure member may be cannulated. In certain
embodiments, a closure member may have a solid central core. A
closure member with a solid central core may allow more contact
area between the closure member and a driver used to couple the
closure member to the collar. A closure member with a solid central
core may provide a more secure connection to a rod than a
cannulated closure member by providing contact against the rod at a
central portion of the closure member as well as near an edge of
the closure member.
[0090] In one embodiment, a bone fastener assembly and a closure
member may be coupled with a running fit. A running fit (i.e., a
fit in which parts are free to rotate) may result in predictable
loading characteristics of a coupling of bone the fastener assembly
and the closure member. Predictable loading characteristics may
facilitate use of a closure member with a break-off portion
designed to shear off at a predetermined torque. A running fit may
also facilitate removal and replacement of closure members. In some
embodiments, a closure member may include an interference fit
(e.g., crest-to-root radial interference). In one embodiment, a
position (i.e., axial position and angular orientation) of a
modified thread of a collar may be controlled, or "timed," relative
to selected surfaces of the collar. For example, a modified thread
form may be controlled relative to a top surface of a collar and an
angular orientation of the slots of the collar. In some
embodiments, positions of engaging structural elements of other
coupling systems (e.g., thread forms) may be controlled.
Controlling a position of a modified thread form may affect a
thickness of a top modified thread portion of a collar. In one
embodiment, a position of a modified thread form may be selected
such that the thickness of the leading edge of a top modified
thread portion is substantially equal to the full thickness of the
rest of the modified thread. Controlling a position of a modified
thread form of a collar may increase a combined strength of engaged
modified thread portions for a collar of a given size (e.g., wall
height, modified thread dimensions, and thread pitch). Controlling
a position of the modified thread form may reduce a probability of
failure of modified thread portions, and thus reduce a probability
of coupling failure between a collar and a closure member.
Controlling the position of a modified thread form in a collar of a
bone fastener assembly may increase a combined strength of engaged
collar and closure member modified thread portions such that
failure of the modified thread portions does not occur prior to the
intended shearing off of a tool portion of the closure member. For
example, a tool portion of a closure member may be designed to
shear off at about 90 in-lbs of torque, while the combined modified
thread portions may be designed to withstand a torque on the
closure member of at least 120 in-lbs.
[0091] If a thickness of a modified thread portion of a given size
and profile is reduced below a minimum thickness, the modified
thread portion may not significantly contribute to the holding
strength of the modified thread of a collar. In one embodiment, a
position of a modified thread form of a collar may be controlled
such that a thickness of a top modified thread portion is
sufficient for the portion to increase a holding strength of the
collar. In one embodiment, a top modified thread portion may have a
leading edge thickness of about 0.2 mm. In one embodiment, a
position of a modified thread form of a collar may be selected to
ensure that a closure member engages a selected minimum number of
modified thread portions on each arm of the collar. In one
embodiment, at least two modified thread portions having a full
thickness over width w of a collar arm may be engaged by a closure
member at each arm. Alternatively, a closure member may engage
parts of three or more modified thread portions on each arm, with
the total width of the portions equal to at least two full-width
portions. Allowances may be made for tolerances in the components
(e.g., diameter of the rod) and/or anticipated misalignment between
the components, such as misalignment between a rod and a slot. In
one embodiment, a substantially equal number of modified thread
portions in each arm may engage the closure member when a rod is
coupled to a bone fastener assembly.
[0092] Various instruments may be used in a minimally invasive
procedure to form a spine stabilization system in a patient. The
instruments may include, but are not limited to, positioning
needles, guide wires, dilators, bone awls, bone taps, sleeves,
drivers, and mallets. The instruments may be provided in an
instrumentation set. The instrumentation set may also include
components of the spine stabilization system. The components of the
spine stabilization system may include, but are not limited to,
bone fastener assemblies of various sizes and/or lengths, rods, and
closure members. Instruments used to install a spine stabilization
system may be made of materials including, but not limited to,
stainless steel, titanium, titanium alloys, ceramics, and/or
polymers. Some instruments may be autoclaved and/or chemically
sterilized. Some instruments may include components that cannot be
autoclaved or chemically sterilized. Components of instruments that
cannot be autoclaved or chemically sterilized may be made of
sterile materials. The sterile materials may be placed in working
relation to other parts of the instrument that have been
sterilized.
[0093] A targeting needle may be used to locate an entry point in a
vertebral body for a bone fastener of a bone fastener assembly. In
some embodiments, the targeting needle may be a bone marrow biopsy
needle. FIG. 8 depicts one embodiment of targeting needle 198.
Targeting needle 198 may include outer housing 200 and member
202.
[0094] FIG. 9 depicts one embodiment of outer housing 200. Outer
housing 200 may include hollow shaft 204 and handle 206. Scale
markings 208 may be printed, etched, or otherwise placed on hollow
shaft 204. Scale markings 208 may be used to approximate a length
of a bone fastener needed for a vertebra. Handle 206 may provide a
grip that allows a user to manipulate the targeting needle. Handle
206 may include threaded portion 210. Threaded portion 210 may
couple to threading on a portion of a targeting needle member to
secure the member to outer housing 200.
[0095] FIG. 10 depicts one embodiment of member 202 of a targeting
needle. Member 202 may include point 212 and cap 214. Point 212 may
be placed through a hollow shaft of an outer housing of the
targeting needle. Cap 214 may include threading 216. Member 202 may
be rotated relative to the outer housing to couple threading 216
with threading in a handle of the outer housing. In some
embodiments, the member may be coupled to the outer housing by
another type of connection system (e.g., by placement of a key in a
keyway). With member 202 positioned in an outer housing, point 212
may extend from a distal end of a hollow shaft of the outer
housing. Cap 214 may be used as an impact surface for driving the
targeting needle in bone.
[0096] FIG. 11 and FIG. 12 depict embodiments of guide wire 218.
Guide wire 218 may be an 18-gauge K-wire. Guide wire 218 may pass
down a shaft of a targeting needle outer housing. Guide wire 218
may be from about 15 cm to about 65 cm in length. In some
embodiments, guide wires 218 provided in an instrumentation set are
about 46 cm in length. The length of guide wire 218 may allow a
surgeon and/or assistants to hold at least one portion of guide
wire 218 at all times when guide wire 218 is inserted into
vertebral bone, even during insertion, use, and removal of
instruments along a length of guide wire 218. Guide wire 218 that
can be held continuously during a surgical procedure may inhibit
removal or advancement of guide wire 218 from a desired position
during a minimally invasive surgical procedure.
[0097] As depicted in FIG. 11, a distal end of guide wire 218 may
include point 220. Point 220 may facilitate insertion of the distal
end of guide wire 218 into vertebral bone. As depicted in FIG. 12,
a distal end of guide wire 218 may not be pointed. A position of an
unpointed guide wire 218 in bone may be easier to maintain during a
spine stabilization procedure.
[0098] Dilators may be used during a minimally invasive surgical
procedure to push aside tissue and create space to access vertebral
bone. In some embodiments, four tissue dilators of increasing
diameter may be used to establish sufficient working space to
accommodate instruments and spine stabilization system components.
In some embodiments, especially for a mid-vertebra or for
mid-vertebrae of a multi-level stabilization system, only three
dilators may be needed to form sufficient working space. Dilators
in an instrumentation set may increase in diameter incrementally by
a selected amount. For example, outside diameters of dilators in an
instrumentation set may increase sequentially by increments of
about 0.5 mm.
[0099] A detachable member for a single-level vertebral
stabilization system may include one or more channels in a wall of
the detachable member to allow access to an adjacent vertebra. For
some single-level vertebral stabilization procedures, only
single-channel detachable members (i.e., detachable members with a
single channel in a wall of the detachable member) may be used. For
other single-level vertebral stabilization procedures, one or more
multi-channel detachable members (i.e., detachable members with two
or more channels in a wall of the detachable member) may be used.
Channels may provide flexibility to or enhance flexibility of a
multi-channel detachable member. In some embodiments, a proximal
portion of a multi-channel detachable member may have a solid
circumference. A region of solid circumference in a multi-channel
detachable member may enhance stability of the multi-channel
detachable member. In some embodiments, a multi-channel detachable
member may be longer than a single-channel detachable member.
[0100] A detachable member used at a middle vertebra in a
multi-level stabilization procedure may be a multi-channel
detachable member. Channels in a multi-channel detachable member
may allow access to adjacent vertebrae from a middle vertebra. A
detachable member used at an end vertebra of a multi-level
stabilization system may be a single-channel detachable member or a
multi-channel detachable member. A system for coupling a bone
fastener assembly to a multi-channel detachable member may include
a limiter that inhibits spreading of arms of the detachable member
to inhibit release of the bone fastener assembly from the
detachable member.
[0101] A channel in a wall of a detachable member may allow access
to a vertebra that is to be stabilized with a spine stabilization
system being formed. In some embodiments, a single-channel
detachable member may be coupled to a bone fastener assembly to be
inserted into vertebral bone of a first vertebra. The
single-channel detachable member may allow access to a second
vertebra from the first vertebra. In other embodiments, a
multi-channel detachable member may be coupled to a bone fastener
assembly to be inserted into vertebral bone of a first vertebra.
The multi-channel detachable member may allow access from the first
vertebra to adjacent vertebrae.
[0102] Instruments may access a bone fastener assembly through a
passage in a detachable member. In some embodiments, a channel in a
wall of a detachable member may extend a full length of the
detachable member. In some embodiments, especially in embodiments
of multi-channel detachable members, a channel in a wall of a
detachable member may extend only a portion of the length of the
detachable member. In some embodiments, a channel in a wall of a
detachable member may extend 25%, 50%, 75%, 80%, 90%, 95% or more
of the length of the detachable member.
[0103] A channel in a detachable member may be any of a variety of
shapes. In some embodiments, a channel may be a linear opening
parallel to a longitudinal axis of the detachable member. In some
embodiments, a channel may have a non-linear shape including, but
not limited to, a helical pattern, an arc, an "L" shape, or an "S"
shape.
[0104] Movable members may extend through portions of a detachable
member proximate a channel in the detachable member. Movable
members may engage notches in a collar to establish a radial
orientation of the detachable member on the collar and/or to
inhibit rotation of the collar relative to the detachable member. A
distal end of a movable member may be flat, curved, or angled. In
some embodiments, a distal end of a movable member may be threaded.
In other embodiments, a distal end of a movable member may be a
projection that engages an opening in a collar. In some
embodiments, an upper surface of a collar and/or a surface of a
distal end of a movable member may be textured to inhibit rotation
of the collar relative to the detachable member. In certain
embodiments, a proximal end of a movable member may include a tool
engaging portion. A tool engaging portion may include, but is not
limited to, a hex section, a hexalobular section, a tapered
section, a bead, a knot, a keyed opening, a coating, a threading,
and/or a roughened surface for engaging a drive that rotates or
otherwise displaces the movable member.
[0105] A cross section transverse to a longitudinal axis of a
detachable member may have shapes including, but not limited to,
circular, ovoid, square, pentagonal, hexagonal, and combinations
thereof. In some embodiments, a detachable member may be hollow. In
certain embodiments, a thickness of a hollow detachable member may
be uniform. In certain embodiments, a thickness of a hollow
detachable member may vary along the length of the detachable
member. A detachable member with a passage extending longitudinally
from a first end of the detachable member to a second end of the
detachable member may be referred to as a "sleeve".
[0106] FIG. 13 depicts one embodiment of sleeve 244. Sleeve 244 may
be a multi-channel sleeve. Sleeve 244 may include wall 246,
channels 248, passage 250, movable members 252, and flange 254.
Channels 248 may extend from a distal end of sleeve 244 through a
portion of wall 246. Passage 250 may allow instruments to be
positioned and used to manipulate a bone fastener assembly that is
coupled to a distal end of sleeve 244. Movable members 252 may be
part of a system that couples a bone fastener assembly to sleeve
244. In some embodiments, movable members 252 may include tool
engaging portion 256. A driver may be positioned in tool portion
256. The driver (e.g., a hex wrench) may be used to extend or
retract a distal end of movable member 252. A distal end of sleeve
244 may include flange 254 that mates with a complementary flange
on a collar of a bone fastener assembly. A distal end of sleeve 244
may be tapered to reduce bulk (e.g., reduce spin diameter) at a
surgical site.
[0107] FIG. 14 depicts a cross-sectional representation of a
portion of sleeve 244 with bone fastener assembly 102 and rod 104.
Distal ends of movable members 252 may extend into notches in
collar 112. Portions of walls 246 of sleeve 244 may include
threading. Portions of movable members 252 may include threading
complementary to threaded portions of walls 246. Threading of
movable members 252 may engage threading in walls 246 such that
rotation of the movable members advances or retracts the movable
members relative to the walls.
[0108] As shown in FIG. 14, collar 112 may be designed such that
rod 104 lies below a distal end of sleeve 244. Coupling sleeve 244
to collar 112 above rod 104 may reduce bulk at a surgical site.
With rod 104 coupled to collar 112 below a distal end of sleeve
244, the sleeve may be removed without interference from the rod of
a spine stabilization system.
[0109] FIG. 15 depicts one embodiment of sleeve 244. Sleeve 244 may
be a single-channel sleeve for use in single-level or multi-level
spine stabilization procedures. Sleeve 244 may be used at the
outermost vertebrae to be stabilized during installation of a
multilevel vertebral stabilization system. Sleeve 244 may be
coupled to a collar of a bone fastener assembly with movable
members 252 and/or flange 254. Instruments may be inserted through
passage 250 of sleeve 244 to access an anchored bone fastener
assembly coupled to the sleeve.
[0110] A sleeve may be coupled to a bone fastener assembly in
various ways to inhibit movement of the sleeve relative to a collar
of the bone fastener assembly. A system used to couple the sleeve
to the bone fastener assembly may inhibit rotation and translation
of the sleeve relative to the collar.
[0111] A detachable member may be coupled to a collar of a bone
fastener assembly in various ways. When a detachable member is
coupled to a collar, rotation and translation of the detachable
member relative to the collar may be inhibited. A system used to
couple a detachable member and collar should be simple, inexpensive
to implement, and should not significantly weaken the mechanical
strength of the collar and/or the detachable member. Detachable
members may be coupled to collars using various coupling systems
including, but not limited to, flanges, threaded connections,
interlocking connections (e.g., ratcheting connection systems),
and/or interference fits.
[0112] In one embodiment of an interlocking connection system, a
detachable member may include an opposing pair of deflectable arms.
Each deflectable arm may include a tooth. The deflectable arms may
be forced outwards during coupling of a collar to the detachable
member. When the collar is coupled to the detachable member, the
deflectable arms may be positioned in channels in the collar, with
the teeth positioned in indentions in the collar. The presence of
the deflectable arms in the channels of the collar may inhibit
rotation and translation of the detachable member relative to the
collar. Separation of the detachable member from the collar may be
achieved by insertion of an expander in the detachable member. The
expander may be used to force the deflectable arms outwards and
expel the teeth from the indentions.
[0113] FIGS. 16-26 depict embodiments of sleeves coupled to bone
fastener assemblies. In each bone fastener assembly/sleeve
embodiment depicted in FIGS. 16-24 and FIG. 26, rod 104 and wire
400 positioned in collar 112 of bone fastener assembly 102 would
lie below distal end 427 of sleeve 244. In some embodiments,
seating rod 104 may be accomplished by advancing rod 104 over a
wire (e.g., See FIG. 37 described below). Having rod 104 and wire
400 below the distal end of sleeve 244 reduces bulk at the surgical
site. With sleeve 244 positioned above rod 104, interference of the
secured rod 104 or wire 400 with sleeve 244 is avoided during
removal of sleeve 244.
[0114] FIG. 16 depicts a cross-sectional representation of sleeve
244 including sleeve flange 254. Sleeve 244 may be rotated onto
collar 112 until slot 150 aligns with channel 248. Sleeve flange
254 may engage flange 154 of collar 112 to inhibit translation of
sleeve 244 relative to collar 112 of bone fastener assembly 102.
Wire 400 and rod 104 may be advanced through slot 150 and
positioned in collar 112 below distal end 427 of sleeve 244.
[0115] In some detachable member and collar coupling embodiments,
the detachable member and the collar may include members that work
together to inhibit radial expansion of walls of the detachable
member. In some detachable member and collar coupling embodiments,
a detachable member may include a protrusion that mates with a
complementary groove in a collar. Alternatively, a detachable
member may include a groove that mates with a complementary
protrusion of a collar.
[0116] In some embodiments, a detachable member and/or a collar may
include a locking system to inhibit rotation of the detachable
member relative to the collar. The locking system may be, but is
not limited to, threading, interference fits, frictional
engagement, or a press-fit connection. In some embodiments, a
locking system may inhibit translation and/or rotation of a
detachable member relative to a collar.
[0117] FIG. 17 depicts a top view representation of one embodiment
of collar 112 of a bone fastener assembly. Collar 112 includes
openings 260. In some embodiments, openings 260 may be threaded. In
some embodiments, openings 260 may not include threading. The body
of collar 112 adjacent to openings 260 may include extra material
to provide strength to the collar.
[0118] FIG. 18 depicts a partial cross-sectional representation of
one embodiment of sleeve 244 coupled to one embodiment of collar
112, such as collar 112 depicted in FIG. 18. Distal end portions of
movable members 252 may extend into openings 260. When distal end
portions of movable members 252 are positioned in openings 260,
rotational movement of sleeve 244 relative to collar 112 may be
inhibited. Sleeve 244 may include flange 254. Flange 254 may engage
flange 154 of collar 112 to inhibit translation of sleeve 244
relative to the collar. In one embodiment in which distal end
portions of movable members in a sleeve are threaded and openings
in the collar are threaded, rotation and translation of the collar
relative to the sleeve may be inhibited when distal end portions of
the movable members are positioned in the openings. Wire 400 and
rod 104 may be advanced through slot 150 in collar 112 and
positioned below distal end of sleeve 244. As depicted in FIG. 18,
portion 270 of movable member 252 may include threading. Threading
of portion 270 may engage threading in wall 246 of sleeve 244.
Engagement of threading of portion 270 with threading in wall 246
may allow distal end portion of movable member 252 to advance
towards, or retract from, a distal end of sleeve 244 when the
movable member is rotated.
[0119] FIG. 19 depicts a top view representation of one embodiment
of collar 112 of a bone fastener assembly. Collar 112 may include
notches 156. FIG. 20 depicts a partial cross-sectional
representation of one embodiment of sleeve 244 coupled to one
embodiment of collar 112, such as the collar depicted in FIG. 19.
Distal end portions of movable members 252 of sleeve 244 may be
extended and positioned in notches 156 of collar 112. An
interference fit between the distal end portions of movable members
252 and the body of collar 112 that defines the notches may inhibit
rotation of sleeve 244 relative to the collar. Wire 400 and rod 104
may be advanced through slot 150 in collar 112 and positioned below
distal end of sleeve 244.
[0120] Portion 270 of movable member 252 may include threading.
Threading of portion 270 may engage threading in wall 246 of sleeve
244. Engagement of threading of portion 270 with threading in wall
246 may allow a distal end portion of movable member 252 to advance
towards, or retract from, a distal end of sleeve 244 when the
movable member is rotated.
[0121] In one embodiment, an inner sleeve may be positioned in a
sleeve to inhibit translation and/or rotation of the sleeve
relative to a collar of a bone fastener assembly. FIG. 21 depicts a
cross-sectional view of sleeve 244 with inner sleeve 272. A distal
end of inner sleeve 272 may contact an upper end of collar 112. A
proximal portion of inner sleeve 272 may engage a proximal portion
of sleeve 244. The engagement may allow inner sleeve 272 to apply a
force against collar 112 that presses flange 154 against flange 254
of sleeve 244 to inhibit translation of the sleeve relative to the
collar. The engagement may be, but is not limited to, a threaded
connection, an interference fit, a frictional fit, or a keyway type
of connection. Wire 400 and rod 104 may be advanced through slot
150 in collar 112 and positioned below distal end of sleeve
244.
[0122] In some embodiments, a distal end of an inner sleeve may be
roughened or textured to frictionally engage a proximal surface of
the collar. The frictional engagement may inhibit rotation of the
sleeve relative to the collar. In some embodiments, inner sleeve
272 may include passage 274. A pin may pass through passage 274
into an opening in collar 112. When a pin is positioned through
passage 274 into the opening, rotation of sleeve 244 relative to
collar 112 may be inhibited.
[0123] In some embodiments, threading may be used to couple a
detachable member to a collar. FIG. 22 and FIG. 23 depict partial
cross-sectional representations of sleeves 244 that couple to
collars 112 by threaded connections. Sleeves 244 may include female
threading that is complementary to male threading of collar 112. In
some embodiments, threading of the sleeve and threading of the
collar may be modified threads. Wire 400 and rod 104 may be
advanced through slot 150 in collar 112 and positioned below distal
end of sleeve 244.
[0124] FIG. 24 depicts a partial cross-sectional representation of
sleeve 244 that couples to collar 112 by a threaded connection.
Sleeve 244 may include male threading, and collar 112 may include
complementary female threading. Wire 400 and rod 104 may be
advanced through slot 150 in collar 112 and positioned below distal
end of sleeve 244. In some embodiments, portion 276 of collar 112
that includes threading which mates with threading of sleeve 244
may be a break-off section. Collar 112 may be held in a fixed
position. Torque may be applied to sleeve 244 to shear off portion
276.
[0125] In some embodiments, a detachable member may include a pair
of hinged arms configured to couple to a collar. FIG. 25 and FIG.
26 depict embodiments of sleeves that include hinged portions.
Sleeve 244 may include arms 278. Arms 278 may be pivotally coupled
together by hinge 280. Hinge 280 may be located near a proximal end
of sleeve 244. In some sleeve embodiments, sleeve 244 may include a
locking element or a biasing element (e.g., a spring) near or at
hinge 280. A locking element or biasing element may cause a
clamping force to be exerted on collar 112 to maintain the collar
in the sleeve and/or to inhibit rotation of collar 112 in sleeve
244. In some embodiments, such as in the embodiment depicted in
FIG. 25, flange 254 of sleeve 244 may contact a bottom portion of
collar 112. Wire 400 and rod 104 may be advanced through slot 150
in collar 112 and positioned above distal end of sleeve 244. In
some embodiments, such as in the embodiment depicted in FIG. 26,
flange 254 of sleeve 244 may contact flange 154 of collar 112.
[0126] In some detachable member embodiments, proximal portions of
detachable members may be chamfered to allow ends of the detachable
members to more closely approach each other than detachable members
with a uniform cross section. FIG. 27 depicts sleeves 244 coupled
to collars 112 engaged in adjacent pedicles 164, and rod 104 having
a non-circular cross-sectional profile spanning between collars
112. Sleeves 244 may include chamfered surfaces 282. Chamfered
surfaces 282 may reduce space between proximal ends of sleeves 244.
During some surgical procedures, only one of the sleeves may be
chamfered. During some surgical procedures, the use of a sleeve
with a chamfered surface may allow for smaller incisions than
required when using non-chamfered sleeves. In some embodiments,
other types of detachable members may be used to reduce space
between proximal ends of detachable members. Other types of
detachable members may include, but are not limited to, detachable
members of different lengths, detachable members of different
diameters, and detachable members with flexible end portions.
[0127] Detachable members may be of various lengths. Detachable
members of different lengths may be used in the same surgical
procedure. A detachable member length used in a spine stabilization
procedure may be determined by a patient's anatomy. Detachable
members may be just short enough to allow manipulation by a medical
practitioner above an incision in a patient. In some embodiments,
detachable members may be about 3.5 to about 11.5 cm long. For
example, a single-channel detachable member may be about 10 cm
long. In some embodiments, detachable members may be about 11.5 cm
to about 14 cm long. For example, a single-channel or a
multi-channel detachable member may be about 12.5 cm long. A
multi-channel detachable member may be longer than a single-channel
detachable member. In some embodiments, a multi-channel detachable
member may be at least about 15 cm long. For example, a
multi-channel detachable member may be about 16 cm long. Detachable
members that are too long may require a longer incision and/or a
larger tissue plane for insertion of a spine stabilization system.
Insertion of a rod may be more difficult with detachable members
that are longer than necessary. Detachable members with excess
length may be bulky and hard to manipulate during a surgical
procedure.
[0128] A detachable member may be flexible over its entire length
or include a flexible portion near a proximal end of the detachable
member. A flexible portion may allow positioning of a proximal
portion of a detachable member in a desired location. A flexible
portion may be produced from any of various materials including,
but not limited to, a surgical grade plastic, rubber, or metal. A
flexible portion may be formed of various elements, including, but
not limited to, a tube, a channel, or a plurality of linked
segments.
[0129] FIG. 28 depicts one embodiment of sleeves 244 with a
connection that allows movement of first portion 284 relative to
second portion 286. First portion 284 may be coupled to collar 112
of bone fastener assembly 102, with rod 104 having a non-circular
cross-sectional profile spanning between collars 112. Second
portion 286 may connect to first portion 284 at linkage 288.
Linkage 288 may include, but is not limited to, a locking element,
a pivot point, a hinge, or a pin. In some embodiments, the linkage
may be a ball and socket type of connection that allows rotational
motion of second portion 286 relative to first portion 284. During
some spine stabilization procedures, a detachable member without a
second portion that is able to move relative to a first portion may
be used at one vertebra, and a detachable member with a second
portion that is able to move relative to a first portion may be
used at one or more vertebrae that are to be stabilized.
[0130] When bone fasteners of polyaxial bone fastener assemblies
are positioned in vertebral bone, detachable members coupled to
collars of the bone fastener assemblies may be moved in desired
positions. During surgery, a detachable member in a patient may be
oriented towards an adjacent vertebra that is to be stabilized to
reduce the required incision size.
[0131] In some embodiments, channels of detachable members may face
a direction other than toward each other. FIG. 29 depicts sleeves
244 coupled to collars 112 oriented at an angle so that channels
248 of sleeves 244 face in different directions. In some
embodiments, channels in the detachable member may not be
longitudinal channels down the length of the detachable member. In
embodiments of detachable members with non-longitudinal channels,
the channels of two adjacent detachable members may not face
towards each other when the openings of collars coupled to the
detachable members are aligned.
[0132] In one embodiment, a frame may couple to two or more
detachable members. FIG. 30 depicts a perspective view of sleeves
244 coupled to frame 290. FIG. 30 further depicts rod 104 with a
non-circular cross-sectional profile spanning between two collars
112. As used herein, a "frame" includes any of a variety of
structural elements including, but not limited, rods, bars, cages,
or machined blocks. In some embodiments, frame 290 may provide a
rigid coupling between sleeves 244. In other embodiments, frame 290
may allow for angular or translational movement between sleeves.
For example, frame 290 may include slidable elements that allow
sleeves to be translated toward each other or away from each other
to facilitate compression or distraction of vertebrae.
Alternatively, frame 290 may enable sleeves 244 to pivot toward
each other or away from each other. In some embodiments, frame 290
may allow for movement of sleeves 244 to facilitate spinal
reduction.
[0133] After a bone fastener assembly is coupled to a detachable
member, a driver may be coupled to a bone fastener of the bone
fastener assembly. The driver may be used to insert the bone
fastener into vertebral bone.
[0134] FIG. 31 depicts one embodiment of driver 292 positioned in
sleeve 244. Sleeve 244 is coupled to bone fastener assembly 102.
Driver 292 may be coupled to collar 112 and to bone fastener 108 of
bone fastener assembly 102. Coupling driver 292 to collar 112 and
to bone fastener 108 may ensure proper alignment of the driver
relative to the bone fastener. Coupling driver 292 to collar 112
and to bone fastener 108 may also inhibit movement of collar 112
relative to bone fastener 108 during insertion of bone fastener
108.
[0135] Driver 292 may include outer shaft 294, inner shaft 296, and
removable handle 236. Outer shaft 294 may include threading 298 and
textured portion 300. A portion of outer shaft 294 may be
positioned in a passage through sleeve 244 (passage 250 shown in
FIG. 13). Threading 298 may couple to a modified thread of collar
112. Textured portion 300 may facilitate rotation of outer shaft
294 so that threading 298 engages the modified thread of collar
112. When threading 298 engages the modified thread of collar 112,
driver 292 may be securely coupled to bone fastener assembly 102,
which is securely fastened to sleeve 244.
[0136] A distal end of inner shaft 296 may be coupled to bone
fastener 108 during use. Inner shaft 296 may be coupled at a
proximal end to removable handle 236 during use. Inner shaft 296
may be rotatable relative to outer shaft 294 so that bone fastener
108 can be inserted into vertebral bone. A proximal portion of
inner shaft 296 may include at least one flat portion that fits in
a mating portion of removable handle 236. Removable handle 236 may
be the same removable handle that is used with bone tap 592 that
forms a threaded opening in vertebral bone for a bone fastener 108.
Removable handle 236 may be removed from driver 292 during
insertion of guide wire 218 through driver 292 so that guide wire
218 may be held in at least one place at all times. In some
embodiments, a removable handle for the driver may be unnecessary
given the length of guide wire 218 and/or the length of the driver
(e.g., a long guide wire 218 and/or a short driver).
[0137] FIG. 32 depicts a cross-sectional representation of a
portion of one embodiment of a driver that is coupled to bone
fastener 108 and collar 112 of a bone fastener assembly. Collar 112
is coupled to sleeve 244. Sleeve 244 is positioned in dilator 302.
In some embodiments, clearance between outer shaft 294 and sleeve
244 may be relatively small. In some embodiments, the clearance
between outer shaft 294 and sleeve 244 may range from about 0.1 mm
to about 0.75 mm. For example, the clearance between outer shaft
294 and sleeve 244 may be about 0.25 mm (i.e., an inner diameter of
the sleeve may be about 0.5 mm greater than an outer diameter of
the outer shaft). Also, clearance between sleeve 244 and dilator
302 may be relatively small. The small clearances may inhibit
undesired movement of the instruments relative to each other and/or
reduce bulkiness at the surgical site.
[0138] Thread 298 of outer shaft 294 of the driver may couple to
modified thread 148 of collar 112. Head 304 of inner shaft 296 of
the driver may couple to tool portion 126 of bone fastener 108.
Head 304 may have a complementary shape to tool portion 126 of bone
fastener 108. Guide wire 218 may be inserted into a distal end of
passage 114 of bone fastener 108 and through passage 306 of the
driver. When guide wire 218 is inserted into passage 114 and
passage 306, a removable handle may not be coupled to inner shaft
296.
[0139] In operation, wire 400 can be used to guide components from
the exterior of the patient via a first incision or a second
incision to bone fastener assembly 102 advanced into the patient
via a third insertion such that rod 104 can be guided under tissue
and muscle to another sleeve/collar assembly advanced into the
patient via a fourth incision. A scalpel may be used to make an
incision in the patient. Wire 400 and/or rod 104 can be radiolucent
or contain markers that allow placement of wire 400 and rod 104 to
be viewed under medical imaging such fluoroscopy.
[0140] FIG. 33 depicts a side view of one embodiment of rod 104
comprising segments 404. Segments 404 may connect to other segments
404 using either end, or may have one end for connecting with other
segments 404 and a second end shaped to ease passage through or
under tissue 460. In some embodiments, rod 104 can include rounded,
beveled, tapered or otherwise shaped ends. First segment 404A may
have a desired characteristic, such as the curvature along its
length as depicted in FIG. 33. In FIG. 33, first segment 404A may
be engaged with wire 400 such that a surface aligns with a surface
of wire 400. Second segment 404B may have a desired characteristic,
such as the curvature along its length depicted in FIG. 33. Second
segment 404B may be engaged with wire 400 such that a surface of
second segment 404B aligns with a surface of wire 400. When first
segment 404A and second segment 404B are connected to form rod 104
and attached to bone fastener assemblies 102, spine stabilization
system 100 may have a desired overall curvature. For example, if
segments 404A and 404B have the same curvature, indexing second
segment 404B 180 degrees enables rod 104 to have a single
curvature. Alternatively, if segments 404A and 404B are indexed 180
degrees from each other, rod 104 may have an S-shaped
configuration. An advantage to this embodiment is that an
instrumentation kit may include relatively few segments, and the
surgeon need only index segments 404A, 404B, etc., onto wire 400 to
construct rod 104 having a selected curvature. While the
characteristic of segments 404A and 404B are described as
curvatures with respect to FIG. 33, other characteristics are
possible, such as torsional stiffness, tensile strength,
compressive strength, hardness, biocompatibility, or the like. As
shown in FIG. 33, rod 104 can have passage 406 along a portion
thereof such that rod 104 can be advanced along wire 400. In such
one embodiment, wire 400 can first be run along insertion path 455
to assemblies 450A and 450B as shown in FIG. 33. Rod 104 can then
be placed by guiding rod 104 using wire 400 in passage 406.
[0141] FIGS. 34, 35, and 36 depict side views of segments 404 of
rod 104, in which an end of segment 404 has a feature such as hole
407, groove 408, or notch 409 for attachment to wire 400 such that
rod 104 can be pulled via wire 400. FIG. 34 depicts a side view of
one embodiment of segment 404 having opening 407. FIG. 34 further
depicts segment 404 having two curves. FIG. 35 depicts a side view
of one embodiment of segment 404 having groove 408 extending about
segment 404. FIG. 35 further depicts segment 404 having an angle.
FIG. 36 depicts a side view of segment 404 having notch 409. FIG.
36 further depicts segment 404 having a bend. Those skilled in the
art will appreciate that there are other methods for using wire 400
to advance rod 104 or segments 404. In some embodiments, a bead or
knot located on wire 400 may be larger than passage 406 in segment
404 such that tensioning wire 400 contacts a bead or knot with
segment 404 and further tensioning pulls segment 404 with wire
400.
[0142] FIGS. 37 and 38 illustrate embodiments for placement of rod
104 using wire 400 and assemblies 450A and 450B. Various surgical
tools can be used to position and move rod 104 along wire 400.
Referring to FIG. 37, sleeve 244A can be advanced through a first
incision I.sub.i in tissue 460 and coupled to collar 112A to form
assembly 450A, and sleeve 244B can be advanced through a second
incision I.sub.2 in tissue 460 and coupled to collar 112B to form
assembly 450B. When sleeve 244A is in place, wire 400 can be
inserted into a third incision I.sub.3 in tissue 460. As wire 400
moves, it can displace tissue and muscle to define path 455. Wire
400 may be advanced through openings 116 (not visible in FIG. 37)
in collar 112A and collar 112B, and advanced until wire 400 exits
the patient via a fourth incision I.sub.4 in tissue 460. First
segment 404 of rod 104 can be engaged to wire 400 so that a first
portion of first segment 404 enters the patient through the third
incision I.sub.3, advances along a path defined by wire 400, passes
through a first side of assembly 450A, out the obverse side of
assembly 450A, passes through a first side of assembly 450B, and
may pass out the obverse side of assembly 450B. As shown in FIGS.
37 and 38, wire 400 may pass through openings 116 in collar 112A
and 112B and rod 104 (or segments 404) can pass through openings
116 in collar 112A (shown in FIG. 37) and pass through openings 116
in collar 112B. Segments 404 may be connected to form rod 104. Rod
104 can be oriented by rotating wire 400. Rod may be secured to
bone fastener assemblies 102, forming spine stabilization system
100 individually suited for the patient. Sleeves 244 may be
uncoupled from collars 112 and removed. Wire 400 may be withdrawn
from the third incision I.sub.3 or advanced through the fourth
incision I.sub.4. Alternatively, wire 400 may be cut or severed by
a tool such that a portion of wire 400 remains in the body. In one
embodiment, leaving a portion of wire 400 inside rod 104 may
provide additional support for the spine.
[0143] After rod 104 has been positioned in collars 112 as desired,
closure members may be used to secure rod 104 to collars 112. FIGS.
39A and 39B depict perspective views of driver 354. Driver 354 may
be used to position a closure member in a collar of a bone fastener
assembly.
[0144] FIG. 40A depicts driver 354 with coupled closure member 106
positioned for insertion in sleeve 244 to couple rod 104 having a
non-circular cross-sectional profile to collars 112. After
insertion of driver 354 in sleeve 244, closure member 106 may be
positioned proximate collar 112. With driver 354 positioned in
sleeve 244, as shown in FIG. 40B, the driver may be rotated to
advance closure member 106 in collar 112 and secure rod 104 to
collar 112. When closure member 106 is snug and rod 104 is secured,
driver 354 may be disengaged from closure member 106 and removed
from sleeve 244. In one embodiment, driver 354 may be used to
secured closure member 106. In certain embodiments, driver 354 may
include a mechanism to dislodge a closure member and/or a tool
portion of a closure member from the distal end of the driver.
[0145] In some embodiments, a detachable member may be held with a
counter torque wrench as the tool portion of a closure member is
secured. In one embodiment, about 120 in-lbs of torque may be
required to secure a closure member. A counter torque wrench may
inhibit transfer of force to the patient when a closure member is
being secured to a collar. FIG. 41 depicts one embodiment of
counter torque wrench 364 used to inhibit application of torque to
a patient's spine during a closure member.
[0146] Sleeve 244 may fit in opening 366 of counter torque wrench
364. Counter torque wrench 364 may be positioned near a proximal
end of sleeve 244 during use. Force may be applied to counter
torque wrench 364 in a direction opposite to rotational force
applied to driver 354 to secure closure member 106. Opening 366 in
torque wrench 364 may be of any shape to accommodate a
cross-sectional shape of sleeve 244 and inhibit rotation of the
sleeve during use.
[0147] FIG. 42 depicts one embodiment of counter torque wrench 368
designed to accommodate sleeves. Counter torque wrench 368 may
include hollow shaft 370 and handle 372. Groove 374 may be located
at a distal end of hollow shaft 370. FIG. 43 depicts counter torque
wrench 368 fitted over multi-channel sleeve 244. In one embodiment,
hollow shaft 370 may be inserted through an opening in the body
over sleeve 244 and advanced toward the spine until rod 104 is
seated in groove 374. Counter torque wrench 368 may engage the
spine stabilization system. Force may be applied to counter torque
wrench 368 in a direction opposite to rotational force applied to a
driver used to secure closure member 106. During a minimally
invasive spine stabilization procedure, counter torque wrench 368
may be used with various types of detachable members, including
single-channel sleeves and multi-channel sleeves.
[0148] Minimally invasive procedures may involve locating a
surgical site and positions for four skin incisions to access the
surgical sites. First and second incisions may be located above
vertebrae to be stabilized. Third and fourth incisions may be
located along the spine some distance from the first and second
incisions. An opening in the tissue under the skin may be enlarged
to exceed the size of the skin incisions. Movement and/or
stretching of an incision and angulation of collars of bone
fastener assemblies may allow the length of the incision to be
minimized. In some embodiments, minimally invasive insertion of a
spine stabilization system may not be visualized. In certain
embodiments, insertion of a spine stabilization system may be a
top-loading, mini-opening, muscle-splitting, screw fixation
technique.
[0149] In one embodiment of a spine stabilization system insertion
method, the patient may be placed in a prone position on a
radiolucent table with clearance available for a C-arm of a
fluoroscope. For example, a Jackson table with a radiolucent Wilson
frame attachment may be used. The ability to obtain high quality
images is very important. Bolsters, frames, and pads may be
inspected for radiolucency prior to the operation.
[0150] Placing the patient in a knee-chest position (e.g., using an
Andrews table) should be avoided. Care should be taken to avoid
placing the patient's spine in kyphosis during positioning of the
patient.
[0151] The C-arm of the fluoroscope should be able to freely rotate
between the anteroposterior, lateral, and oblique positions for
optimal visualization of pedicle anatomy during the procedure. The
arm should be rotated through a full range of motion prior to
beginning the procedure to ensure that there is no obstruction or
radio-opaque object in the way. The fluoroscope may be positioned
so that Ferguson views and "bullseye" views are obtainable. Once
the patient is positioned and the ability to obtain fluoroscopic
images of the target levels for instrumentation has been confirmed,
the patient may be prepared and draped sterilely.
[0152] For most of the lumbar region, the vertebral pedicle is an
obliquely oriented cylindrical corridor. The angulation varies by
approximately 5 degrees per level (e.g., L1: 5 degrees; L5: 25
degrees). A pre-operative fine-cut computed tomography image may be
examined to determine any unique anatomy of the patient. Acquiring
the pedicle in the most lateral and superior quadrant of the
pedicle may be desirable to avoid the overriding facet during a
minimally invasive procedure. A lateral entry point may allow for
better screw convergence as well as less interference with the
superior adjacent level facet joint. A targeting needle may be
passed in a medial and inferior trajectory, thus following the
natural pathway of the pedicle. Frequent fluoroscopic inspection in
both an anteroposterior and lateral plane may ensure proper passage
of the needle as the needle is inserted into vertebral bone.
[0153] Various techniques may be used to plan the skin incisions
and entry points. In one embodiment, the planning sequence for
single-level stabilization may include the following four steps.
First, an anteropostenor image may be obtained with the spinous
processes centered at the target vertebral bodies. Vertical lines
passing through midpoints of pedicles that are to receive bone
fasteners may be marked on the patient. The lines do not represent
skin entry points. The lines are markers of pedicle entry points
used to estimate angles at which targeting needles to be inserted
to contact the pedicles. In some embodiments, sets of vertical
lines may be drawn corresponding to the lateral edges of the
pedicles instead of lines corresponding to the midpoints of the
pedicles.
[0154] Second, horizontal lines may be marked approximately through
the centers of the pedicles (mid-pedicle lines) on the patient. In
some embodiments, the lines may be drawn on the superior side of
the center axes (superior to the mid-pedicle).
[0155] Third, an oblique or "bullseye" view (i.e., down a
longitudinal axis of a pedicle) may be obtained on each side of the
patient for each pedicle that is to be stabilized. Vertical oblique
view lines may be marked on the skin at the midpoints of each of
the pedicles that are to receive a bone fastener. The oblique view
lines may be drawn in a different color than the vertical lines
drawn during the first step. In some embodiments, vertical lines
may be drawn corresponding to the lateral edges of the pedicles
instead of lines corresponding to the midpoints of the
pedicles.
[0156] The oblique view lines may be about 2 cm to about 3 cm away
from the lateral pedicle border lines marked in the first step. For
larger patients, the oblique view line may be greater than about 3
cm away from the midline marked in the first step. For smaller
patients, the oblique view line may be closer than about 2 cm away
from the midline marked in the first step. The intersection of the
oblique view lines with the horizontal lines drawn in the second
step may represent skin entry points for a targeting needle as the
targeting needle passes through soft tissue at an angle towards the
bony pedicle entry point. A side fluoroscopic image, the horizontal
lines, and the vertical lines may help the surgeon triangulate
between the skin entry points and bony entry points.
[0157] Fourth, an incision may be made in the skin between
mid-pedicle lines along the vertical oblique view lines. The skin
incision may be from about 2 cm to about 4 cm long. In some
embodiments, the incision may be from about 2.5 cm to about 3 cm
long. Limiting the length of the incision may enhance patient
satisfaction with the procedure. The incisions may be
pre-anesthetized with, for example, 1% lidocaine with 1:200,000
epinephrine. To blunt the pain response, a long spinal needle may
be used to dock on the bone entry point and inject the planned
muscle path in a retrograde fashion as well. Once the incision has
been made, tissue surrounding the incision may be pulled and/or
stretched to allow access to a target location in a vertebra.
[0158] After sterile preparation and draping, the pedicle entry
points may be fluoroscopically rechecked to ensure that the
previously marked lines correspond to the intersection of the
midline of the transverse process and the lateral joint and pars
interarticularis. The intersection of the facet and the transverse
process provides a starting point that may help avoid the canal and
follow the natural inclination of lumbar pedicles. For the spine
stabilization system described, in which sleeves coupled to bone
fastener assemblies are substantially unconstrained by insertion
angles of the bone fasteners, patient anatomy may determine the
most advantageous insertion angles of the bone fasteners.
[0159] A scalpel may be used to make a stab wound at the junction
of an oblique view line and a mid-pedicle line. In one embodiment,
the scalpel may be a #11 scalpel. A targeting needle may be passed
through the incision in an oblique lateral to medial trajectory
towards the bony entry point defined by a lateral pedicle border
line. The C-arm of the fluoroscope may be placed in an
anteroposterior position for this maneuver.
[0160] Insertion of a spine stabilization system may include
gradually increasing the diameter of an opening formed in a pedicle
and/or vertebral body to accept a bone fastener assembly. For
example, a targeting needle may have outer diameter of about D. A
bone awl inserted after the targeting needle may have an outer
diameter incrementally larger than the outer diameter of the
targeting needle. As used herein, an incrementally larger diameter
may be large enough to allow a snug but adjustable fit. For
example, the bone awl may have outer diameter of about (D+x). A tap
portion of a bone tap inserted after the bone awl may have a minor
diameter of about (D+2x). A bone fastener may have a minor diameter
of about (D+3x). In some embodiments, x may be between about 0.1 mm
and about 1.0 mm. For example, x may be about 0.5 mm. Incremental
sizing of the targeting needle, bone awl, tap, and bone fastener
may promote a proper fit of the bone fastener in the vertebra to be
stabilized.
[0161] As the targeting needle encounters the bony anatomy,
anteroposterior fluoroscopic images may be used to place the tip of
the needle at the upper outer quadrant of the pedicle. In some
embodiments, the needle may be walked medially along the transverse
process to the pedicle entry point. In some embodiments, the needle
tip may be docked by lightly tapping the tip into the bone with a
mallet or other impact device to drive the tip into the bone. In
some embodiments, the needle tip may be docked by applying downward
pressure to the targeting needle to force the tip into the
bone.
[0162] The fluoroscope may then be moved to a lateral position. The
surgeon may correct the sagittal trajectory of the needle by moving
the needle in an anterior or posterior direction to match the
vector of the pedicle corridor. In some embodiments, a mallet or
other impact device may be used to gently advance the targeting
needle into the pedicle halfway to the pedicle-vertebral body
junction. In other embodiments, force may be applied to the
targeting needle to drive the targeting needle into the pedicle
halfway to the pedicle-vertebral body junction. An anteroposterior
image may then be obtained to confirm that the needle is
approximately halfway across the pedicle in the anteroposterior
view. If the tip is more than halfway across the pedicle in a
lateral to medial projection, the trajectory may be too medial.
Further advancement of the needle may risk passing the needle
through the spinal canal. The needle may be repositioned. A new
starting point or new trajectory may be obtained. If the
anteroposterior image demonstrates that the needle is significantly
lateral in the pedicle, then the needle may have passed along the
lateral portion of the pedicle. A needle that has passed along the
lateral portion of the pedicle may be withdrawn and
repositioned.
[0163] Once a good trajectory has been obtained, the targeting
needle may be advanced using a mallet. In some embodiments, the
needle may be pushed in without a mallet. The targeting needle may
be advanced to the junction of the pedicle and vertebral body under
lateral fluoroscopic guidance. FIG. 44A depicts targeting needle
198 advanced to the junction of pedicle 164. At this point,
confirmation of position and trajectory should be repeated under
anteroposterior fluoroscopy. Targeting needle 198 may be further
advanced to a desired depth within vertebral body 166 using a
mallet or applied force. FIG. 44B depicts targeting needle 198
advanced to the desired depth.
[0164] A scale on targeting needle 198 may be used to approximate a
length of a bone fastener to be used. A first depth of targeting
needle 198 may be measured relative to body surface 376 when
pedicle 164 is first encountered. A second depth of targeting
needle 198 may be measured relative to body surface 376 after the
targeting needle has been advanced to the desired depth in
vertebral body 166. An approximate length of the pedicle screw to
be used may be determined by taking a difference between the depth
measurements.
[0165] After targeting needle 198 has been advanced into the bone,
member 202 of the targeting needle (shown in FIG. 44B) may be
removed from the targeting needle. FIG. 44C depicts outer housing
200 with the member removed. After removal of the member, guide
wire 218 may be placed through a passage in targeting needle 198
into vertebral body 166. FIG. 44D depicts targeting needle 198 with
guide wire 218 positioned through the passage in the targeting
needle. Lateral fluoroscopic images may be obtained to indicate the
position of guide wire 218. In some embodiments, guide wire 218 may
be pushed into vertebral body 166. In certain embodiments, guide
wire 218 may be advanced about 1 cm beyond an end of outer housing
200 to secure the guide wire in vertebral body 166. In some
embodiments, a small diameter tissue dilator may be placed over
guide wire 218 and positioned on an upper surface of the targeting
needle. The tissue dilator may provide stability to guide wire 218.
Added stability from the dilator may allow guide wire 218 to be
successfully tapped into the vertebral body with a small mallet.
Care should be taken to avoid kinking guide wire 218. After guide
wire 218 is secured in vertebral body 166, outer housing 200 may be
removed from the patient. FIG. 44E depicts guide wire 218 after
removal of the targeting needle.
[0166] Once guide wire 218 has been passed through the targeting
needle and the targeting needle has been removed, guide wire 218
may be used as a guide to position one or more successively sized
dilators around a target location in a pedicle. A dilator may be a
conduit with a regular shape (e.g., cylindrical) or an irregular
shape (e.g., C-shaped). A dilator may form an opening through soft
tissue to the pedicle. For patients with a thick fascia, it may be
advantageous to make a nick in the fascia with a scalpel blade to
facilitate passage of the dilators. The dilators may be passed
sequentially over guide wire 218. The dilators may be rotated
during insertion to facilitate dilation of surrounding tissue. The
dilators may be inserted until the leading edges contact the
pedicle. A distal end of a dilator may be tapered to facilitate
positioning of the dilator proximate the pedicle. An
instrumentation set for a spine stabilization system may include
two, three, four, or more successively sized dilators.
[0167] FIG. 45A depicts first dilator 302A positioned around guide
wire 218. First dilator 302A may have an inner diameter just
slightly larger than an outer diameter of guide wire 218. As used
herein, "an inner diameter just slightly larger than an outer
diameter" may mean that the inner diameter is between about 0.03 mm
and about 1.0 mm greater than the outer diameter. For example, an
inner diameter of first dilator 302A may be about 0.5 mm greater
than the outer diameter of guide wire 218.
[0168] FIG. 45B depicts second dilator 302B positioned around first
dilator 302A. Second dilator 302B may have an inner diameter just
slightly larger than an outer diameter of first dilator 302A.
[0169] FIG. 45C depicts third dilator 302C and fourth dilator 302D
and positioned around second dilator 302B. Third dilator 302C may
have an inner diameter just slightly larger than an outer diameter
of second dilator 302B. Fourth dilator 302D may have an inner
diameter slightly larger than an outer diameter of third dilator
302C. Once fourth dilator 302D is in position, dilators 302A, 302B,
302C may be removed, starting with dilator 302A. Lengths of
dilators in a successively sized set may decrease with increasing
diameter to facilitate removal of the smaller dilators. Care should
be taken to avoid dislodging guide wire 218 during insertion and
removal of the dilators. FIG. 45D depicts fourth dilator 302D
positioned around guide wire 218 following removal of dilators
302A, 302B, 302C.
[0170] After tissue dilation has been achieved, a large diameter
dilator (e.g., third dilator 302C or fourth dilator 302D shown in
FIG. 45C) may be used to guide a bone fastener assembly and/or
insertion instruments toward a target location in a pedicle. FIGS.
46A-46F depict portions of a procedure for preparation of pedicle
164 and vertebral body 166 for receiving a bone fastener assembly.
FIG. 46A depicts bone awl 591 positioned over guide wire 218 in
dilator 302 such that a tip of the bone awl is on or near a surface
of pedicle 164. Bone awl 591 may be driven downwards into pedicle
164 to breach cortical bone of the pedicle. FIG. 46B depicts a
position of bone awl 591 after pedicle 164 has been breached. After
pedicle 164 is breached, bone awl 591 may be removed from dilator
302. FIG. 46C depicts guide wire 218 and dilator 302 after removal
of bone awl 591. In some embodiments, an initial passage may be
formed in the pedicle and the vertebral body using a drill or a
drill and tap combination.
[0171] FIG. 46D depicts tap 592 positioned in dilator 302. After
pedicle 164 is breached, tap 592 may be inserted over guide wire
218 into dilator 302. In one embodiment, dilator 302 may be third
dilator 302C. Tap 592 may be sized to fit snugly inside third
dilator 302C. In some embodiments, dilator 302 may be fourth
dilator 302D. In certain embodiments, fourth dilator 302D may be
inserted over third dilator 302C after bone has been tapped through
the third dilator. Tapping through third dilator 302C rather than
fourth dilator 302D may introduce less bulk at the target site of a
pedicle during the tapping procedure. In some embodiments, an outer
diameter of a sleeve coupled to a bone fastener assembly to be
inserted in the pedicle may be substantially the same as an outer
diameter of third dilator 302C.
[0172] Tap 592 may include removable handle 236 and indicia 240.
Indicia 240 may be a scale. When tap 592 is positioned such that a
first thread flight contacts pedicle 164, a first measurement of
the position of the tap relative to a top of dilator 302 using
indicia 240 may be noted. Tap 592 may be rotated to form a threaded
passage through pedicle 164 and into vertebral body 166 to a
desired depth. In some embodiments, a length of the threaded
portion of tap 592 may be used to determine a depth of a threaded
passage formed in a bone. For a threaded portion of a known length
(e.g., 30 mm, 45 mm, 60 mm), a scaled image (e.g., X-ray image) of
a depth of the threaded portion in a bone monitored during tapping
may allow a medical practitioner to determine the depth of the
threaded passage. In some embodiments, tap 592 may form threads of
major diameter about 0.5 mm smaller than a major diameter of
threads of a bone fastener to be inserted into the threaded
passage.
[0173] FIG. 46E depicts a position of tap 592 after a threaded
passage of a desired length has been formed in pedicle 164 and
vertebral body 166. Care should be exercised to ensure that guide
wire 218 is not bent or kinked during the tapping process. The
position of tap 592 relative to the end of guide wire 218 may be
monitored to ensure that guide wire 218 is not dislodged or removed
from the vertebra. In some embodiments, a position of tap 592 may
be monitored using fluoroscopic imaging.
[0174] After a threaded passage of a desired length has been formed
in pedicle 164 and vertebral body 166, a second measurement of the
position of tap 592 relative to a top of dilator 302 using indicia
240 may be noted. A length of a threaded member may be determined
by taking a difference between the first and second measurements.
In some embodiments, an estimate of length may be derived based
upon fluoroscopic images and a known length of the tap that is
visibly recognizable in the fluoroscopic images. Tap 592 may be
removed from vertebral body 166 and pedicle 164 by rotating the tap
out of the vertebral body and the pedicle. Handle 236 may be
removed from a blade portion of tap 592. The blade portion of tap
592 may be removed from guide wire 218 with control of guide wire
218 initially maintained from above the tap and then from below the
tap. Care may be taken when tap 592 is removed to maintain guide
wire 218 in position and to avoid damage of guide wire 218. FIG.
46F depicts dilator 302 and guide wire 218 after removal of the
tap.
[0175] A bone fastener assembly with a bone fastener of an
appropriate length may be selected for insertion in a patient. The
size of the bone fastener may be verified with measurement indicia
in an instrumentation set. In some embodiments, measurement indicia
may be etched or printed on a portion of an instrumentation set.
For example, the chosen bone fastener embodiment may be placed over
the outline of a bone fastener embodiment printed on a tray of the
instrumentation set.
[0176] The chosen bone fastener assembly may be attached to a
detachable member. In one embodiment, a bone fastener assembly may
be rotated on a flange of a detachable member. Movable members of
the detachable member may be extended into indentations in a collar
of the bone fastener assembly. A driver may be used to extend the
movable members to couple with the collar. When the bone fastener
assembly is coupled to the detachable member, a drive portion of a
fastener driver may be coupled to a tool portion of the bone
fastener. A shaft of the fastener driver may be positioned in the
passage of the detachable member. A removable handle may be
attached to the shaft of the fastener driver. The detachable
member, collar, and bone fastener may be substantially co-axial
when the fastener driver is positioned in the detachable member. In
some embodiments, the removable handle may be attached to the shaft
of the fastener driver after the bone fastener, collar, detachable
member, and fastener driver combination is positioned down guide
wire 218 through a dilator and against a pedicle.
[0177] FIGS. 47A-47D depict portions of a procedure for inserting a
bone fastener assembly into a patient. Driver 292 (coupled to the
bone fastener), and sleeve 244 (coupled to the collar of the bone
fastener assembly) may be inserted along guide wire 218 into
dilator 302. For spine stabilization procedures using four
successively sized dilators, dilator 302 may be fourth dilator
302D. Guide wire 218 represents the trajectory that a bone fastener
or bone fastener assembly may follow toward pedicle 164 during
insertion of a spine stabilization system. In some embodiments,
tissue surrounding the incision may be pulled and/or stretched to
allow a desired angular orientation of the bone fastener assembly
relative to pedicle 164. FIG. 47A depicts driver 292 and sleeve 244
positioned in dilator 302. After insertion of the bone fastener
assembly, sleeve 244, and driver 292 in dilator 302, the driver may
be rotated to thread the bone fastener into pedicle 164 and
vertebral body 166. The bone fastener may be advanced into the
pedicle under fluoroscopic guidance to inhibit breaching of the
pedicle walls. When the tip of the bone fastener advances beyond
the posterior margin of vertebral body 166, guide wire 218 may be
removed to inhibit inadvertent bending of guide wire 218 or
unwanted advancement of guide wire 218.
[0178] The bone fastener may be advanced to bring the collar down
snug to the facet joint. The bone fastener may then be backed off
about a quarter of a turn. Backing the fastener off about a quarter
of a turn may allow for full motion of the collar relative to the
bone fastener. FIG. 47B depicts driver 292 after the bone fastener
has been advanced to the desired depth. After the bone fastener has
been advanced to the desired depth, driver 292 may be removed from
the head of the bone fastener and from dilator 302. FIG. 47C
depicts dilator 302 and sleeve 244 after removal of the driver.
After removal of the driver, dilator 302 may be removed from the
patient. FIG. 47D depicts collar 112 of bone fastener assembly and
sleeve 244 after removal of the dilator.
[0179] After the bone fastener has been secured to the vertebra and
the driver has been removed from the sleeve, the polyaxial nature
of the collar may allow angulation of the sleeve relative to the
bone fastener. Tissue surrounding the incision may be released such
that the sleeve is angled toward a central location between
vertebrae to be stabilized. The sleeve may be moved to facilitate
positioning of instruments and/or to facilitate access to the
adjacent vertebra that is to be stabilized. For example, the sleeve
may be tilted towards the adjacent pedicle so that additional
length of an opening in the patient is not needed. The channel in
the sleeve may be turned toward the adjacent pedicle that is to be
stabilized with the spine stabilization system being formed.
[0180] A rod may be cut to length and contoured as desired. For
example, a medical practitioner may use experience and judgment to
determine curvature of a rod for a patient. A desired curvature for
the rod may be determined using fluoroscopic imaging. In some
embodiments, a curvature of the rod may be chosen such that, when
the rod is secured to the collars of the bone fastener assemblies,
sleeves coupled to the bone fastener assemblies cross at a surface
of the skin. Crossing of the sleeves at a surface of the skin
allows the medical practitioner to minimize trauma to a patient by
minimizing incision length and tissue plane area. The rod may be
bent or shaped with a tool (e.g., a rod bender) to allow insertion
of the rod through channels of sleeves with various spatial
locations and/or various angular orientations.
[0181] Rods may have shapes including, but not limited to,
straight, bent, curved, s-shaped, and z-shaped. FIG. 48 depicts one
embodiment of S-shaped rod 104. FIG. 49 depicts one embodiment of
rod 104 in which the curvature of rod 104 may be configured with
any radius within a range of radii. In some embodiments, the
curvature of rod 104 may have multiple curves of different radii
(for example, multiple level stabilizations). FIG. 50 depicts one
embodiment of bent rod 104. FIG. 51 depicts one embodiment of
straight rod 104. In some embodiments, rods 104 may have a
substantially circular longitudinal cross section. In certain
embodiments, rods 104 may have other cross-sectional shapes
including, but not limited to, regular shapes (oval, rectangular,
rhomboidal, square) and irregular shapes. An instrumentation kit
for a spine stabilization system may include straight rods and/or
pre-shaped rods. Straight rods and/or pre-shaped rods may be
contoured to accommodate patient anatomy if needed during the
surgical procedure.
[0182] With the rod satisfactorily positioned, the rod may be
secured in place with closure members. To ensure alignment of
thread of closure member with thread of collar, the driver may
initially be rotated in a direction that would result in removal of
the closure member from the collar. When the user of the driver
feels engagement of threading of the closure member with threading
of the collar, the user may reverse the direction of rotation of
the driver to secure the closure member to the driver. The closure
member may secure the rod to the collar. Sleeve 244A may serve as a
coaxial guide to inhibit cross-threading during insertion of
closure members 106. When the closure members are snug and rod 104
is secured, collars 112 are angled such that slots in the collars
are substantially perpendicular to the rod. Driver 354 may be
disengaged from the closure member and removed from sleeve 244.
[0183] In some embodiments, counter torque wrench 368 shown in FIG.
42 may be used to inhibit application of torque to a patient's
spine. Counter torque wrench sleeve 370 may be inserted through the
opening in the body over sleeve 244. Counter torque wrench sleeve
370 may be advanced toward the spine until rod 104 is seated in
groove 374 of the counter torque wrench sleeve. Force may be
applied to counter torque wrench 368 in a direction opposite to
rotational force applied to a driver used to secure a closure
member.
[0184] After a closure member is successfully secured to a collar,
the driver may be removed from the sleeve coupled to the anchored
bone fastener assembly. FIG. 52A depicts an assembled spine
stabilization system following removal of driver 354 and wire 400.
Key 262, shown in FIG. 52B, may be used to rotate movable members
in sleeves 244A, 244B. Rotation of movable members in sleeves 244A,
244B may release the movable members from the collars. Thus,
sleeves 244A, 244B may be uncoupled from the collars above the
incision. FIG. 52C depicts assembled spine stabilization system 100
following removal of sleeve 244A. FIG. 52D depicts assembled spine
stabilization system 100 coupled to adjacent pedicles following
removal of sleeve 244B.
[0185] A spine stabilization system may be used to stabilize two or
more vertebral levels (i.e., at least three adjacent vertebrae). In
one embodiment, an incision may be made in the skin between the
outermost vertebrae to be stabilized. A first bone fastener
assembly may be coupled to a first sleeve. The first bone fastener
may be threaded into a first pedicle at a target location such that
the first sleeve extends above the body surface. The first sleeve
may rotate about the head of the first bone fastener. A second bone
fastener assembly may be coupled to a second sleeve and threaded
into the second pedicle through a second incision. A third bone
fastener assembly may be coupled to a third sleeve and threaded
into the third pedicle through a third incision.
[0186] In one embodiment of a method for a two-level spine
stabilization procedure, three incisions may be made above three
target locations over three pedicles. A first bone fastener may be
anchored to the middle pedicle. After the first bone fastener is
secured, second and third bone fasteners may be coupled to outer
pedicles as desired by advancing the second and third bone fastener
assemblies via second and third incisions to outer pedicles. A wire
may be inserted into the patient via a fourth incision and advanced
through the bone fastener assemblies. A rod or two or more segments
forming a rod may be advanced via the fourth incision and passed
through the collars. After a rod has been positioned and seated in
collars as desired, closure members may be used to secure the rod
to the collars. One or more counter torque wrenches may be used
during shearing of the tool portions of the closure members. In one
embodiment, counter torque wrench 364, depicted in FIG. 42, may be
used with sleeves 244. Counter torque wrench 368, depicted in FIG.
43, may be used with multi-channel sleeves and/or single-channel
sleeves.
[0187] Further modifications and alternative embodiments will be
apparent to those skilled in the art in view of this description.
Accordingly, this description is to be construed as illustrative
only and is for the purpose of teaching those skilled in the art
the general manner of carrying out the teachings of the disclosure.
It is to be understood that the embodiments shown and described
herein are to be taken as the presently preferred embodiments.
Elements and materials may be substituted for those illustrated and
described herein, parts and processes may be reversed, and certain
features may be utilized independently, all as would be apparent to
one skilled in the art after having the benefit of this disclosure.
Changes may be made in the elements described herein without
departing from the spirit and scope of the following claims.
* * * * *