U.S. patent application number 15/443262 was filed with the patent office on 2018-01-18 for shoulder arthroplasty instrumentation.
The applicant listed for this patent is Joseph LIPMAN, Darrick LO, Andrew D. PEARLE. Invention is credited to Joseph LIPMAN, Darrick LO, Andrew D. PEARLE.
Application Number | 20180014834 15/443262 |
Document ID | / |
Family ID | 45871377 |
Filed Date | 2018-01-18 |
United States Patent
Application |
20180014834 |
Kind Code |
A1 |
LO; Darrick ; et
al. |
January 18, 2018 |
SHOULDER ARTHROPLASTY INSTRUMENTATION
Abstract
Patient specific shoulder component implant instruments are
described for hemi and total, normal and reverse shoulder
arthroplasty.
Inventors: |
LO; Darrick; (Green Brook,
NJ) ; LIPMAN; Joseph; (New York, NY) ; PEARLE;
Andrew D.; (Rye, NY) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
LO; Darrick
LIPMAN; Joseph
PEARLE; Andrew D. |
Green Brook
New York
Rye |
NJ
NY
NY |
US
US
US |
|
|
Family ID: |
45871377 |
Appl. No.: |
15/443262 |
Filed: |
February 27, 2017 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
13075378 |
Mar 30, 2011 |
9579106 |
|
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15443262 |
|
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|
61319484 |
Mar 31, 2010 |
|
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61325435 |
Apr 19, 2010 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61B 2034/108 20160201;
A61B 17/15 20130101; A61B 17/1778 20161101; A61B 2017/568
20130101 |
International
Class: |
A61B 17/15 20060101
A61B017/15; A61B 17/17 20060101 A61B017/17 |
Claims
1. A patient specific instrument for facilitating the implant of a
humeral component comprising: an instrument body having a cap like
shape with an inner surface and an outer surface; said inner
surface matching the humeral joint articular surface of said
patient; a hook surface feature located proximate said inner
surface matching the humeral joint non-articular joint surface;
said instrument body having one or more holes passing from said
inner surface to said outer surface; a cutting block formed
integrally with said instrument body; said cutting block having one
or more pin guides for directing pins into the humeral head; said
cutting block having a saw slot located above said pin guides for
directing a surgical saw.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. application Ser.
No. 13/075,378, filed Mar. 30, 2011, entitled "Shoulder
Arthroplasty Instrumentation" which claims the benefit of and
incorporates herein by reference both U.S. Provisional Patent
Application No. 61/319,484, filed Mar. 31, 2010 entitled "Patient
Specific Instruments" and U.S. Provisional Patent Application No.
61/325,435, filed Apr. 19, 2010 entitled "Reverse Total Shoulder
Arthroplasty Instrumentation".
INCORPORATION BY REFERENCE
[0002] All publications and patent applications mentioned in this
specification are incorporated herein by reference in their
entirety to the same extent as if each individual publication or
patent application was specifically and individually indicated to
be incorporated by reference.
FIELD
[0003] The present invention relates to patient specific
instrumentation to facilitate implantation of a total shoulder
joint and to the process and technique for creating the
instruments.
BACKGROUND
[0004] Shoulder hemiarthroplasty is commonly used to treat patients
with glenohumeral joint arthrosis. Total shoulder arthroplasty may
be indicated for patients without a good articular surface on the
glenoid at the time of surgery. For patients with glenohumeral
joint arthrosis and an additional deficient rotator cuff, reverse
total shoulder arthroplasty may be indicated. The 12%, 15%, and 22%
revision rates, respectively, remains high compared to hip and knee
arthroplasty. Glenoid component loosening and instability are
important complications and may be caused by poor positioning of
the component. An accurate placement of the complementary humeral
cut is also important to achieve a stable joint.
[0005] There is a continuing need to improve the instruments used
to facilitate the implantation of total shoulder joint
components.
SUMMARY OF THE DISCLOSURE
[0006] Patient specific instruments according to the invention
carry surfaces and features that facilitate implantation of
shoulder implant components. These surfaces are patient specific
and they conform to the actual diseased joint surfaces presented by
the patient. In use the physician uses the instruments to align and
direct surgical cuts, to prepare the patient to receive an
otherwise standard and conventional joint components of either
"normal" or "reverse" configurations.
[0007] The process of the invention that results in the creation of
a set of patient specific instruments takes a computed tomographic
(CT) or magnetic resonance imaging (MRI) file of the patient's
shoulder and presents it to a user on a computer screen. The user
using a mouse or other pointing device defines reference points on
the image to define geometric axes, planes and offsets. Next the
user imports and aligns a computer automated design (CAD) file of
the implant component with the native anatomy. The image of the
implant component is merged and displayed with the anatomy image.
Using a rule based system the user finds an optimum location for
the glenoid component of the implant. Once the optimum location for
the glenoid component is defined a custom instrument CAD file is
created and a glenoid placement instrument or tool is generated
from the file using conventional techniques. The tool is formed
from plastic and/or metal that can be sterilized and used directly
in the surgery.
[0008] In general the glenoid instrument consists of an oval or egg
shaped "disk" with a protruding stalk like "handle". The disk has
an upper surface and a lower surface, and a side wall separating
the two.
[0009] In general the humeral instrument consists of a "cap" like
structure connected to an offset "block" feature. There is a
clearance volume between the "cap" and "block". The cap has an
inner surface and an outer surface.
[0010] With the glenoid instrument defined and created a companion
humeral cutting instrument is generated to guide the resection of
bone in preparation for the implantation of the humeral component
of the total shoulder implant system. The humeral instrument is
likewise defined and manufactured from sterilizable plastic and/or
metal in a process similar to the glenoid component. The
instruments are used together and they share several
characteristics.
[0011] The glenoid instrument has a complementary surface to a
surface of the diseased joint formed in the lower surface.
[0012] The glenoid instrument has one or more index surfaces
adjacent to its articular lower surface that facilitate placement
of the tool during surgery.
[0013] The glenoid instrument has windows to permit visual
confirmation of placement.
[0014] The glenoid instrument has a handle to assist in proper
positioning of the instrument.
[0015] The glenoid instrument has holes that aid in defining the
direction of screws should screw placement be pre-operatively
determined.
[0016] The humeral resection guide instrument or humeral instrument
has a complementary surface matching the humeral head contour on
its inner surface.
[0017] The humeral resection guide instrument has one or more index
surfaces adjacent to its articular inner surface of the cap portion
that facilitates the placement of the tool during surgery.
[0018] The humeral resection guide instrument has a block offset
from the cap that includes a saw slot that directs the use of a
surgical saw to remove the humeral head.
[0019] The humeral resection guide instrument has holes that accept
pins or other fasteners which connect the block portion of the
humeral instrument to the proximal humerus bone.
BRIEF DESCRIPTION OF THE DRAWINGS
[0020] In the figures of the drawings like reference numerals
indicate identical structure, wherein:
[0021] FIG. 1 is a view of the glenoid component instrument;
[0022] FIG. 2 is a view of the glenoid component instrument;
[0023] FIG. 3 is a view of the glenoid component instrument;
[0024] FIG. 4 is a view of the glenoid component instrument;
[0025] FIG. 5 is a view of the glenoid component instrument;
[0026] FIG. 6 shows the humeral component cutting block
instrument;
[0027] FIG. 7 shows the humeral component cutting block
instrument;
[0028] FIG. 8 shows the humeral component cutting block
instrument;
[0029] FIG. 9 shows the humeral component cutting block
instrument;
[0030] FIG. 10 shows the humeral component cutting block
instrument;
[0031] FIG. 11 shows the glenoid instrument in use placed against
the glenoid;
[0032] FIG. 12 shows the glenoid instrument in use placed against
the glenoid;
[0033] FIG. 13 shows the glenoid instrument in use placed against
the glenoid;
[0034] FIG. 14 shows the glenoid instrument in use placed against
the glenoid;
[0035] FIG. 15 shows the glenoid instrument in use placed against
the glenoid;
[0036] FIG. 16 shows the humeral cutting guide block in use against
the humeral head;
[0037] FIG. 17 shows the humeral cutting guide block in use against
the humeral head;
[0038] FIG. 18 shows the humeral cutting guide block in use against
the humeral head;
[0039] FIG. 19 shows the humeral cutting guide block in use against
the humeral head;
[0040] FIG. 20 shows the humeral cutting guide block in use against
the humeral head;
[0041] FIG. 21 shows glenoid components in place;
[0042] FIG. 22 shows glenoid components in place;
[0043] FIG. 23 shows glenoid components in place;
[0044] FIG. 24 shows humeral components in place;
[0045] FIG. 25 shows humeral components in place;
[0046] FIG. 26 shows humeral components in place;
[0047] FIG. 27 shows a human shoulder joint;
[0048] FIG. 28 is a flowchart of the process for making the
instruments;
[0049] FIG. 29 shows anatomic geometry;
[0050] FIG. 30 shows part of a step in the process;
[0051] FIG. 31 shows part of a step in the process;
[0052] FIG. 32 shows anatomic geometry;
[0053] FIG. 33 shows part of a step in the process; and,
[0054] FIG. 34 shows part of a step in the process.
DETAILED DESCRIPTION
Glenoid Component Instrument
[0055] FIG. 1 through FIG. 5 should be considered together as they
show the same glenoid component instrument 10 from several
different perspectives. The glenoid component instrument 10 has a
handle 12 attached to a generally oval or egg shaped disk shaped
instrument body 14. The disk shaped body 14 has a patient specific
conformal lower surface 16 that matches the surface of the
articular portion of the glenoid joint. Adjacent the patient
specific bottom surface 16 is a hook like feature that matches an
off articular bony portion of the glenoid. This hook 18 is also
patient specific and one or more such hooks may be formed depending
on the patient anatomy. These features are placed on the sidewall
17 of the disk shaped instrument body. Also present are holes
passing through the disk element of the instrument body from the
lower surface to the upper surface. Holes useful for directing
screws or the like are seen at reference numeral 20 and 22. A hole
or slot for cutting a keel slot or peg hole is seen at reference
numeral 24. Additional holes acting as windows to allow
visualization of the native surface are shown at reference numeral
23. Holes for bone pins can also be used to hold the glenoid
instrument in place.
Humeral Component Cutting Block Instrument
[0056] FIG. 6 through FIG. 10 should be considered together as they
show the same humeral component instrument from several different
perspectives. The humeral component instrument 30 has a generally
cap shaped element 31 with a patient specific conformal inner
surface 32 that can wrap around the humeral head. There is also at
least one guide surface 34 feature that is patient specific and off
the articulating surface of the joint. Apertures labeled 36 and 38
in the form of windows are cut through the cap from the inner
surface to the outer surface to permit visualization of the joint
surface. Adjacent to cap 31 is a block feature 39 having a saw
guiding slot 40 that overlies several pin holes typified by hole
42. These holes may be used to place Steinman pins or other
fixation devices. There will usually be three holes at differing
inclinations to rigidly attach the cutting block 30 to the bone.
The block element 39 is offset from the cap 31 element by a
clearance space. The fixation devices traverse this clearance space
when they are pushed in to position.
Use of the Glenoid Instrument
[0057] FIG. 11 through FIG. 15 should be considered together as
they show the same glenoid instrument in contact with the glenoid
portion of the glenohumeral joint. Typically the physician holds
the handle with his hand 50 and presses the instrument body against
the joint surface 51. Tactile and visual clues that result from the
patient conformal surfaces allow and facilitate registration of the
instrument body with the native anatomy.
Use of the Humeral Head Cutting Block Guide
[0058] FIG. 16 through FIG. 20 should be considered together as
they show the same cutting block in contact with the humeral head.
In use the cap feature overlays the humeral head 52 and the
conformal inner surface and index surface 34 align the instrument
with the bone. Once the instrument is fastened to the bone via
fixation holes 42, the saw may enter slot 40 and resect the bone.
As seen best in FIG. 20 the clearance space allows the humeral
instrument to accommodate muscle 37 and other tissue with minimal
injury.
Glenoid Component in Position
[0059] FIG. 21 through FIG. 23 should be considered together as
they show the glenoid implant component 62 in place on the glenoid.
Both a "normal" glenoid component 62 is shown as well as a
"reverse" glenoid component 64 in dotted outline.
Humeral Component in Position
[0060] FIG. 24 through FIG. 26 should be considered together as the
show the "normal" humeral implant component 66 in place on the
humerus. FIG. 26 and FIG. 25 depict a "reverse" humeral component
68 in place on the bone.
Overview of Instrument Creation and Use
[0061] FIG. 27 shows a human shoulder joint.
[0062] FIG. 28 shows a flowchart of the process beginning with the
collection of patient data in process step 100. This data is used
by process 120 to convert and display the native anatomy to a user.
In process step 130 the image data is used with implant specific
data to design the two instruments. In process step 140
instrumentation data is used to manufacture physical instruments.
In process step 150 the surgeon use the physical instruments to
carry out the surgery.
Glenoid Component Instrument Creation Process
[0063] A software program Mimics.RTM. is used to take MRI or CT
data and to create a 3-dimensional image of the glenoid and
scapular spine that can be manipulated on the computer screen. The
user defines three points, including a glenoid center point in the
center of the glenoid articular surface, a junction point along the
ridge of the scapular spine where the medial border and scapular
spine meet, and an inferior point at the most distal end of the
scapular spine. These three reference points depicted in FIG. 30
are used to define a coronal plane, which may be displayed on the
image. A transverse plane orthogonal to the coronal plane is
created through the glenoid center point and scapular spine
junction point. Next a sagittal plane is created orthogonal to said
two planes and centered on the center point of the glenoid as seen
in FIG. 30. A reference anatomic axis may then be defined as the
intersection of the transverse and sagittal planes. These steps may
also be performed in a conventional software package such as
"Pro/E" from PTC software company in Needham Mass. which is widely
used to define parts in the CAD industry.
[0064] In order to reproduce the normal anatomic orientation of the
glenoid after TSA, the ideal orientation of the glenoid component
should have 4 degrees of superior inclination and 1 degree of
retroversion. Therefore, the central peg or keel should achieve
this orientation given adequate bone stock. In reverse total
shoulder arthroplasty, the glenoid component should have 5 degrees
of inferior inclination seen at reference numeral 200 in FIG. 29,
close to neutral version, and slight inferior translation to
minimize notching. This is seen in FIG. 29 and FIG. 32. Therefore,
the inclination and version of the glenoid component will be
referenced from the sagittal plane as defined. For example, the
inclination plane can pass through an axis created by the
intersection of the sagittal and transverse planes at 4 degrees of
superior inclination as seen at reference numeral 210 in FIG. 29. A
second axis can then pass through the coronal and inclination
plane. The version plane can pass through said second axis at 1
degree of retroversion as seen at reference numeral 220 in FIG. 32.
At this point, the version plane will represent the proper
orientation of the glenoid component; the glenoid component
plane.
[0065] The alignment of the implant with the native bones is
depicted in FIG. 31. At this point the operator and likely
physician will review the position and size of the implant
customized for this patient. With the implant location and size
determined, Pro/E is used to create a template instrument that will
be used to help align the glenoid component during the surgery. A
portion of the glenoid component instrument is designed to conform
to the native bone. The first surface of said portion of the
glenoid component instrument has a surface that is 3D inverse of
the native surface of the glenoid created via a Boolean subtraction
operation where the native surface of the glenoid is subtracted
from the template instrument. An approximately 1 mm gap between the
bony surface of the glenoid and the inverse surface of the glenoid
component instrument is added when using CT data to accommodate
cartilage and/or slight errors in the reconstruction. This surface
is created in Geomagic.RTM.. A second surface of said portion of
the glenoid component instrument captures a bony surface close to
but outside of the glenoid articular surface. Said second surface
is an extending feature that is similarly created using a Boolean
subtraction operation, and is used to help in the proper
positioning of the instrument with respect to the bone. Said second
surface wraps around the anterior aspect of the glenoid surface
because it is easy to reference with a traditional delto-pectoral
surgical approach, and can be used to lever the instrument over the
glenoid. At least one and perhaps as many as three such features
around the perimeter of the glenoid will be defined for the
instrument depending largely upon the condition of the bone
structure, its geometry, and surgical exposure.
[0066] The glenoid component instrument has a set of apertures that
can function as windows to observe tissue and or as guide to direct
cutting tools into the glenoid. For example, the instrument may
carry a center hole for a drill bit to pass for a central peg
designed glenoid component, or a slot to facilitate cutting a keel
slot designed for a glenoid component. The orientation of the
center aperture will be normal to glenoid component plane and be
centered based on pre-operative plan. Peripheral holes in the
instrument can be added to match any peripheral pegs/keels/screws
or the like that the glenoid component may require. The peripheral
holes will control the orientation of the glenoid component in
rotation about the central axis for the glenoid component. The
location of the holes or windows or slots will determine the
rotation of the glenoid component. Next, the location of viewing
slot(s) is defined for the instrument. These slots will be
positioned so that they can be observed by the physician during the
surgery and will communicate with the bony surface so that the
presence or absence of a bony surface in the window helps verify
the seating of the instrument. The remainder of the glenoid
component instrument includes an extending handle that is directed
away (usually anteriorly) from the axis of the peg/keel, as
depicted in FIG. 15, in order to allow the drill to access the
instrument.
[0067] For reverse total shoulder arthroplasty, a second glenoid
component instrument can be used to target peripheral fixation
screws for the glenoid component. After pre-operatively determining
the depth of the reaming operation used to seat the glenoid
component, the surgeon or engineer can pre-operatively determine
the number, length, and alignment of said peripheral fixation
screws.
[0068] Said second glenoid component instrument will have a mating
surface that is the 3D inverse of the reamed surface. The second
instrument has a center hole in line with the central peg hole. In
addition, peripheral holes in the second instrument will be in line
with the pre-operatively planned screw locations. Drill taps will
pass through said peripheral holes. The second instrument can also
have as few as one mark on the visible (lateral) surface (e.g. a
mark pointing superiorly) to aid in the rotational alignment of
second instrument. During surgery, the surgeon can use
electrocautery to mark the surface of the glenoid (e.g. a mark
pointing superiorly). The second instrument's mark can now be
aligned to the glenoid's surface mark. Viewing slots on the
instrument will allow the surgeon to verify the seating of the
instrument on the reamed bone. A handle extends laterally from
second instrument but will not interfere with drill.
[0069] Bone modulus can be characterized from the Hounsfield unit
obtained from CT scans. Bone with higher modulus is stronger, and
would be ideal locations for peg/screw fixation. The surgeon or
engineer can use this information to pre-operatively design the
first and/or second instruments to direct the peg/screw into bone
of higher modulus.
[0070] The process has created an instrument that can be used to
define the location of a glenoid implant based upon an analysis of
the native bone structure in conjunction with a representation of
the glenoid implant.
Humeral Head Cutting Block Creation Process
[0071] Similar to the glenoid component instrument, the humeral
head cutting block utilizes MRI or CT data to determine the
appropriate orientation and size of the orthopaedic component. For
shoulder hemiarthroplasty and total shoulder arthroplasty, the
position of the humeral component will be 20 degrees in
retroversion. For reverse total shoulder arthroplasty, it will be
closer to neutral. In order to properly correct the version of the
humeral head, it is recommended that a MRI or CT scan of the elbow
(same side) be taken as well. The diaphysis of the humerus will be
approximated to be a cylinder with its long axis to be defined as
the long axis of the humerus. Landmark points will be placed on the
medial and lateral epicondyles of the distal humerus. A humeral
coronal plane passes through said landmark points and is parallel
to said long axis. The version of the humeral head will be offset
from the coronal plane. If the elbow is not scanned, the calcar of
the humerus can be used as a reference when determining version
angle as depicted in FIG. 33. A calcar landmark point is
identified. In this case, the version plane of the humeral
component is defined as the plane that passes through said calcar
point and the long axis of the humerus. Pre-operative sizing of the
humeral head and humeral component can be performed. Humeral head
resection and implant sizing performed pre-operatively on a left
humerus.
[0072] The level of resection is built into the humeral head
cutting block. Using MRI or CT data, this block engages with the
humeral head by having a backside face that is a 3D inverse of the
native humeral head created via a Boolean subtraction operation
where the native surface of the humeral head is subtracted from a
template block instrument. An approximately 1 mm gap between the
bony surface of the humeral head and the inverse surface of the
humeral head cutting block is added when using CT data to
accommodate cartilage and/or slight errors in the reconstruction.
Said block engages the superior-medial aspect of the head and has
an additional feature that wraps around the lateral side of the
lesser tubercle (subscapularis attachment sight) to additionally
aid in the alignment of the block. The instrument has openings to
allow the subscapularis and rotator cuff to pass 5 without
impingement as depicted in FIG. 20. The slot for the saw blade 40
is located approximately anterior to the humerus, and its cutting
angle (approximately 45 degrees) is dependent on the implant system
being used. Said slot has enough width to ensure that the blade
remains parallel to the slot.
[0073] Other features include a minimum of two non-parallel pin
holes for 10 additional stability of the block to the proximal
humerus. Said pin holes are located distal to the saw blade slot,
and can accept pins screws or other fasteners. Viewing
slots/portals on the block are used to visually ensure that the
instrument is fully seated onto the humeral head. A targeting sight
in line with the long axis of the humerus on the superior surface
of the humeral head cutting block is used to target 15 the humeral
stem reamer.
[0074] The instruments will be steam sterilizable and biocompatible
(e.g. DuraForm polyamide). Both the glenoid component instrument
and the humeral head cutting block have been prototyped and
manufactured. For the proper execution of these instruments during
surgery, it is necessary to minimize the profile and volume of 20
these instruments as much as possible, as the surgical exposure for
these types of procedures are small. Modifications to these
instruments continue to be made to make the operative procedure
more efficient and accurate.
* * * * *