US20130018476A1 - Shoulder prosthesis - Google Patents

Shoulder prosthesis Download PDF

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Publication number
US20130018476A1
US20130018476A1 US13/343,039 US201213343039A US2013018476A1 US 20130018476 A1 US20130018476 A1 US 20130018476A1 US 201213343039 A US201213343039 A US 201213343039A US 2013018476 A1 US2013018476 A1 US 2013018476A1
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United States
Prior art keywords
prosthesis
central body
end
arms
portion
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US13/343,039
Inventor
Nicholas J. Katrana
Nathan A. Winslow
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Biomet Manufacturing LLC
Original Assignee
Biomet Manufacturing LLC
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to US13/182,026 priority Critical patent/US8506638B2/en
Application filed by Biomet Manufacturing LLC filed Critical Biomet Manufacturing LLC
Priority to US13/343,039 priority patent/US20130018476A1/en
Assigned to BIOMET MANUFACTURING CORP. reassignment BIOMET MANUFACTURING CORP. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: KATRANA, NICHOLAS J., WINSLOW, NATHAN A.
Priority claimed from PCT/US2012/069720 external-priority patent/WO2013103499A1/en
Publication of US20130018476A1 publication Critical patent/US20130018476A1/en
Assigned to BIOMET MANUFACTURING, LLC reassignment BIOMET MANUFACTURING, LLC CHANGE OF NAME (SEE DOCUMENT FOR DETAILS). Assignors: BIOMET MANUFACTURING CORPORATION
Application status is Abandoned legal-status Critical

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/40Joints for shoulders
    • A61F2/4014Humeral heads or necks; Connections of endoprosthetic heads or necks to endoprosthetic humeral shafts
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/40Joints for shoulders
    • A61F2/4003Replacing only the epiphyseal or metaphyseal parts of the humerus, i.e. endoprosthesis not comprising an entire humeral shaft
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/46Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
    • A61F2/4603Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof
    • A61F2/4612Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof of shoulders
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    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
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    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30108Shapes
    • A61F2002/3011Cross-sections or two-dimensional shapes
    • A61F2002/30159Concave polygonal shapes
    • A61F2002/30163Concave polygonal shapes cruciform, different from X-shaped
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30108Shapes
    • A61F2002/3011Cross-sections or two-dimensional shapes
    • A61F2002/30159Concave polygonal shapes
    • A61F2002/30171Concave polygonal shapes rosette- or star-shaped
    • AHUMAN NECESSITIES
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    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30331Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by longitudinally pushing a protrusion into a complementarily-shaped recess, e.g. held by friction fit
    • A61F2002/30332Conically- or frustoconically-shaped protrusion and recess
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2002/30001Additional features of subject-matter classified in A61F2/28, A61F2/30 and subgroups thereof
    • A61F2002/30316The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
    • A61F2002/30329Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements
    • A61F2002/30405Connections or couplings between prosthetic parts, e.g. between modular parts; Connecting elements made by screwing complementary threads machined on the parts themselves
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surfaces, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surfaces, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30878Special external or bone-contacting surfaces, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts
    • A61F2002/30891Plurality of protrusions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surfaces, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surfaces, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30878Special external or bone-contacting surfaces, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves with non-sharp protrusions, for instance contacting the bone for anchoring, e.g. keels, pegs, pins, posts, shanks, stems, struts
    • A61F2002/30897Stepped protrusions, i.e. having discrete diameter changes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/30767Special external or bone-contacting surfaces, e.g. coating for improving bone ingrowth
    • A61F2/30771Special external or bone-contacting surfaces, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves
    • A61F2002/30904Special external or bone-contacting surfaces, e.g. coating for improving bone ingrowth applied in original prostheses, e.g. holes or grooves serrated profile, i.e. saw-toothed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/40Joints for shoulders
    • A61F2/4003Replacing only the epiphyseal or metaphyseal parts of the humerus, i.e. endoprosthesis not comprising an entire humeral shaft
    • A61F2002/4007Replacing only the epiphyseal or metaphyseal parts of the humerus, i.e. endoprosthesis not comprising an entire humeral shaft implanted without ablation of the whole natural humeral head
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/40Joints for shoulders
    • A61F2/4014Humeral heads or necks; Connections of endoprosthetic heads or necks to endoprosthetic humeral shafts
    • A61F2002/4018Heads or epiphyseal parts of humerus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/40Joints for shoulders
    • A61F2/4014Humeral heads or necks; Connections of endoprosthetic heads or necks to endoprosthetic humeral shafts
    • A61F2002/4037Connections of heads to necks
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F2/00Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
    • A61F2/02Prostheses implantable into the body
    • A61F2/30Joints
    • A61F2/46Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor
    • A61F2/4603Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof
    • A61F2002/4629Special tools or methods for implanting or extracting artificial joints, accessories, bone grafts or substitutes, or particular adaptations therefor for insertion or extraction of endoprosthetic joints or of accessories thereof connected to the endoprosthesis or implant via a threaded connection

Abstract

A prosthesis is provided and may include a central body having a longitudinal axis and an opening that receives an installation tool. The prosthesis may further include a plurality of arms each having a first end proximate to the central body and a second end extending from the central body in a first direction substantially perpendicular to the longitudinal axis. The second end may include a greater width than the first end measured in a second direction substantially perpendicular to the first direction.

Description

    CROSS-REFERENCE TO RELATED APPLICATIONS
  • This application is a continuation-in-part of U.S. patent application Ser. No. 13/182,026 filed on Jul. 13, 2011. The entire disclosure of the above application is incorporated herein by reference.
  • FIELD
  • The present disclosure relates to a shoulder prosthesis and more particularly to a shoulder prosthesis having a stemless humeral component.
  • BACKGROUND
  • This section provides background information related to the present disclosure which is not necessarily prior art.
  • The shoulder joint includes the humerus, the clavicle, and the scapula, which cooperate to afford a range of motion of the humerus relative to the scapula and clavicle during arm movement. Specifically, a proximal end of the humerus is disposed adjacent to the glenoid fossa of the scapula and is permitted to move relative to the glenoid fossa to provide a range of motion to the humerus relative to the scapula.
  • Joint replacement surgery such as a partial or total shoulder arthroplasty may be required when the shoulder joint causes pain during use or is otherwise damaged. For example, the shoulder joint may be damaged due to osteoarthritis, whereby progressive wearing away of cartilage results in bare bone being exposed within the shoulder joint. Under such circumstances, it is often necessary to undergo a partial or total shoulder arthroplasty in order to relieve pain and increase the range of motion of the humerus by rebuilding portions of the shoulder joint.
  • In performing a total shoulder arthroplasty, a surgeon resects a portion of the proximal end of the humerus that is received by the glenoid fossa. Once the distal end of the humerus is resected, the surgeon may then ream the humerus to access the humeral canal. Providing access to the humeral canal allows the surgeon to insert a humeral component into the humeral canal. A prosthetic hemispherical humeral head may then be attached to a proximal end of the humeral component such that the resected portion of the humerus is replaced by the prosthetic hemispherical humeral head. If necessary, the surgeon will likewise replace a portion of the glenoid fossa to provide a bearing surface against which the humeral head may articulate. Upon completion of the shoulder arthroplasty, pain is typically alleviated and the patient is provided with an increased range of motion at the shoulder joint.
  • While conventional shoulder prosthetics used during shoulder arthroplasty adequately provide the patient with an increased range of motion, conventional shoulder prosthetics require insertion of a stem into the humeral canal of the humerus, thereby increasing the overall weight, size, and cost of the humeral component. Furthermore, because the surgeon is required to insert the stem of the humeral component into the humeral canal, the surgical procedure is somewhat complex, as the surgeon is first required to resect the proximal end of the humerus and subsequently ream the humeral canal prior to inserting the stem of the humeral component into the humeral canal. Increasing the complexity of the joint-replacement surgery increases the time in which the surgeon must spend in performing the procedure and therefore increases the overall cost of the procedure. Finally, requiring insertion of the stem into the humeral component results in additional bone removal, thereby increasing trauma and post-operative pain.
  • SUMMARY
  • This section provides a general summary of the disclosure, and is not a comprehensive disclosure of its full scope or all of its features.
  • A prosthesis is provided and may include a central body having a longitudinal axis and an opening that receives an installation tool. The prosthesis may further include a plurality of arms each having a first end proximate to the central body and a second end extending from the central body in a first direction substantially perpendicular to the longitudinal axis. The second end may include a greater width than the first end measured in a second direction substantially perpendicular to the first direction.
  • In another configuration, a prosthesis is provided and may include a central body having a longitudinal axis and a plurality of arms each having a first end proximate to the central body and a second end extending from the central body in a first direction substantially perpendicular to the longitudinal axis. The plurality of arms may each include at least one tapered surface that provides the plurality of arms with an increasing thickness extending in a direction from the first end to the second end.
  • Further areas of applicability will become apparent from the description provided herein. The description and specific examples in this summary are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.
  • DRAWINGS
  • The drawings described herein are for illustrative purposes only of selected embodiments and not all possible implementations, and are not intended to limit the scope of the present disclosure.
  • FIG. 1 is a side view of a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure;
  • FIG. 2 is a top view of the humeral component of FIG. 1;
  • FIG. 3 is a perspective view of the humeral component of FIG. 1;
  • FIG. 4 is a side view of a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure;
  • FIG. 5 is a top view of the humeral component of FIG. 4;
  • FIG. 6 is a perspective view of the humeral component of FIG. 4;
  • FIG. 7 is a side view of a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure;
  • FIG. 8 is a top view of the humeral component of FIG. 7;
  • FIG. 9 is a perspective view of the humeral component of FIG. 7;
  • FIG. 10 is a cross-sectional view of the humeral component of FIG. 7 taken along line 10-10 of FIG. 8;
  • FIG. 11 is a side view of a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure;
  • FIG. 12 is a top view of the humeral component of FIG. 11;
  • FIG. 13 is a perspective view of the humeral component of FIG. 11;
  • FIG. 14 is a side view of a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure;
  • FIG. 15 is a top view of the humeral component of FIG. 14;
  • FIG. 16 is a perspective view of the humeral component of FIG. 14;
  • FIG. 17 is a cross-sectional view of the humeral component of FIG. 14 taken along line 17-17 of FIG. 15;
  • FIG. 18 is a cross-sectional view of the shoulder prosthesis of FIG. 14 taken along line 17-17 of FIG. 15 and including an alternate arm construction;
  • FIG. 19 is a cross-sectional view of the humeral component of FIG. 14 taken along line 17-17 of FIG. 15 and including an alternate arm construction;
  • FIG. 20 is a cross-sectional view of the humeral component of FIG. 14 taken along line 17-17 of FIG. 15 and including an alternate arm construction;
  • FIG. 21 is a cross-sectional view of the humeral component of FIG. 14 taken along line 17-17 of FIG. 15 and including an alternate arm construction;
  • FIG. 22 is a cross-sectional view of the humeral component of FIG. 14 taken along line 17-17 of FIG. 15 and including an alternate arm construction;
  • FIG. 23 is a perspective view of a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure;
  • FIG. 24 is a side view of the humeral component of FIG. 23;
  • FIG. 25 is a cross-sectional view of the humeral component of FIG. 24 taken along line 25-25;
  • FIG. 26 is a partial cross-sectional view of the humeral component of FIG. 24 taken along line 26-26;
  • FIG. 27 is a perspective view of a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure;
  • FIG. 28 is a side view of the humeral component of FIG. 27;
  • FIG. 29 is a partial cross-sectional view of the humeral component of FIG. 28 taken along line 29-29;
  • FIG. 30 is a cross-sectional view of the humeral component of FIG. 28 taken along line 30-30;
  • FIG. 31 is a perspective view of a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure receiving a humeral head;
  • FIG. 32 is an exploded view of the humeral component and humeral head of FIG. 31;
  • FIG. 33 is a partial perspective view of a proximal end of the humerus showing a line of resection;
  • FIG. 34 is a partial side view of the humerus with a portion of the bone removed to show a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure received within a resected portion of the humerus; and
  • FIG. 35 is a partial side view of the humerus with a portion of the bone removed to show a humeral component of a shoulder prosthesis in accordance with the principles of the present disclosure being inserted therein.
  • Corresponding reference numerals indicate corresponding parts throughout the several views of the drawings.
  • DETAILED DESCRIPTION
  • Example embodiments will now be described more fully with reference to the accompanying drawings.
  • Example embodiments are provided so that this disclosure will be thorough, and will fully convey the scope to those who are skilled in the art. Numerous specific details are set forth such as examples of specific components, devices, and methods, to provide a thorough understanding of embodiments of the present disclosure. It will be apparent to those skilled in the art that specific details need not be employed, that example embodiments may be embodied in many different forms and that neither should be construed to limit the scope of the disclosure. In some example embodiments, well-known processes, well-known device structures, and well-known technologies are not described in detail.
  • The terminology used herein is for the purpose of describing particular example embodiments only and is not intended to be limiting. As used herein, the singular forms “a,” “an,” and “the” may be intended to include the plural forms as well, unless the context clearly indicates otherwise. The terms “comprises,” “comprising,” “including,” and “having,” are inclusive and therefore specify the presence of stated features, integers, steps, operations, elements, and/or components, but do not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components, and/or groups thereof. The method steps, processes, and operations described herein are not to be construed as necessarily requiring their performance in the particular order discussed or illustrated, unless specifically identified as an order of performance. It is also to be understood that additional or alternative steps may be employed.
  • When an element or layer is referred to as being “on,” “engaged to,” “connected to,” or “coupled to” another element or layer, it may be directly on, engaged, connected or coupled to the other element or layer, or intervening elements or layers may be present. In contrast, when an element is referred to as being “directly on,” “directly engaged to,” “directly connected to,” or “directly coupled to” another element or layer, there may be no intervening elements or layers present. Other words used to describe the relationship between elements should be interpreted in a like fashion (e.g., “between” versus “directly between,” “adjacent” versus “directly adjacent,” etc.). As used herein, the term “and/or” includes any and all combinations of one or more of the associated listed items.
  • Although the terms first, second, third, etc. may be used herein to describe various elements, components, regions, layers and/or sections, these elements, components, regions, layers and/or sections should not be limited by these terms. These terms may be only used to distinguish one element, component, region, layer or section from another region, layer or section. Terms such as “first,” “second,” and other numerical terms when used herein do not imply a sequence or order unless clearly indicated by the context. Thus, a first element, component, region, layer or section discussed below could be termed a second element, component, region, layer or section without departing from the teachings of the example embodiments.
  • Spatially relative terms, such as “inner,” “outer,” “beneath,” “below,” “lower,” “above,” “upper,” and the like, may be used herein for ease of description to describe one element or feature's relationship to another element(s) or feature(s) as illustrated in the figures. Spatially relative terms may be intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the figures. For example, if the device in the figures is turned over, elements described as “below” or “beneath” other elements or features would then be oriented “above” the other elements or features. Thus, the example term “below” can encompass both an orientation of above and below. The device may be otherwise oriented (rotated 90 degrees or at other orientations) and the spatially relative descriptors used herein interpreted accordingly.
  • With particular reference to FIGS. 1-3, a prosthesis 10 is provided and may include a central body 12 and a plurality of wings or arms 14 extending generally from the central body 12. The prosthesis 10 may be received within a resected humeral head (FIGS. 34, 35) and may provide the resected humerus with a structure to support a prosthetic humeral head 16 (FIGS. 31, 34). The prosthetic humeral head 16 may be received by the prosthesis 10 once the prosthesis 10 is installed in the resected humerus during a partial or total shoulder arthroplasty or, alternatively, may be received by the prosthesis 10 prior to insertion of the prosthesis 10 into the proximal humerus.
  • The central body 12 may include a substantially cylindrical shape having a longitudinal axis 18 and a bore 20 at least partially formed therein. The bore 20 may be substantially circular and may include a central axis that is aligned with the longitudinal axis 18 and may include a first portion 22 and a second portion 24. The first portion 22 is disposed proximate to an opening 26 of the central body 12 and may include a Morse taper. The second portion 24 is disposed generally adjacent to the first portion 22 and may include a smaller diameter than the first portion 22. The second portion 24 may include a series of threads 28 (FIG. 2) for use during installation or removal of the prosthesis 10 from the humerus. The bore 20 may extend completely through the central body 12 and along the longitudinal axis 18 or, alternatively, may be a blind bore. Regardless of the particular construction of the bore 20, the first portion 22 is in fluid communication with the second portion 24 such that access to the second portion 24 is obtained via the first portion 22 at the opening 26 of the central body 12.
  • The central body 12 may include a substantially uniform outer surface 30 and a distal end 32 having a radiused, beveled, or chamfered outer edge 34. The radiused or beveled outer edge 34 may be positioned at the distal end 32 to facilitate insertion of the distal end 32 into a resected end of the humerus during installation (FIGS. 34, 35).
  • The arms 14 extend generally away from the central body 12 in a direction substantially perpendicular to the longitudinal axis 18. The arms 14 may be positioned relative to the central body 12 such that an imaginary line 36 bisecting the central body 12 in a direction substantially perpendicular to the longitudinal axis 18 of the central body 12 extends through a pair of the arms 14 (FIG. 2). In one configuration, the plurality of arms 14 may include six arms such that three such lines 36 may intersect the longitudinal axis 18 while concurrently passing through respective pairs of the six arms 14.
  • Each arm 14 may be integrally formed with the central body 12 and may include a first end 38 disposed at a junction of each arm 14 and the central body 12 and a second end 40 formed at an opposite end of each arm 14 from the first end 38. The first end 38 may be tapered to increase the overall width of each arm 14 at the junction of each arm 14 and the central body 12. Increasing the width of each arm 14 at a junction of the central body 12 and each arm 14 increases the strength of the arms at the junction between the arms 14 and the central body 12, thereby increasing the overall strength of each arm 14 and the connection of each arm 14 to the central body 12.
  • The second end 40 of each arm 14 may include a series of alternating peaks 42 and valleys 44, as shown in FIG. 1. The peaks 42 may be truncated such that each peak 42 terminates at a substantially planar surface 46. The valleys 44 may be positioned such that each valley 44 is defined by a first surface 48 that is substantially perpendicular to the longitudinal axis 18 of the central body 12 and a second surface 50 that is substantially parallel to the longitudinal axis 18 of the central body 12.
  • With particular reference to FIGS. 4-6, a prosthesis 10 a is shown to include a central body 12 a and a plurality of wings or arms 14 a. In view of the substantial similarity in structure and function of the components associated with the prosthesis 10 with respect to the prosthesis 10 a, like reference numerals are used hereinafter and in the drawings to identify like components while like reference numerals containing letter extensions are used to identify those components that have been modified.
  • The central body 12 a may include a bore 20 a extending at least partially therethrough and along a longitudinal axis 18 of the central body 12 a. The bore 20 a may include a first portion 22 and a second portion 24 a. The bore 20 may extend completely through the central body 12 a or, alternatively, may be a blind bore that extends only partially through the central body 12 a. Regardless of the particular construction of the bore 20 a, the first portion 22 is in fluid communication with the second portion 24 a such that the second portion 24 a is accessed via the first portion 22 and opening 26 of the central body 12 a.
  • The second portion 24 a is disposed generally adjacent to the first portion 22 and may include a substantially square shape. The shape of the second portion 24 a may be designed to matingly receive a tool (FIG. 35) during installation of the prosthesis 10 a to prevent relative rotational movement between the prosthesis 10 a and the tool at the second portion 24 a. While the second portion 24 a is shown as including a substantially square shape, the second portion 24 a could include virtually any shape that permits the second portion 24 a of the bore 20 to matingly receive a tool therein.
  • The arms 14 a extend generally from the central body 12 in a direction substantially perpendicular to the longitudinal axis 18 of the central body 12 a. As with the prosthesis 10, the plurality of arms 14 a may include six arms 14 a, whereby a line 36 bisecting the central body 12 a and passing through the longitudinal axis 18 likewise passes through a pair of the arms 14 a. Because the plurality of arms 14 a are shown to include six arms, three such lines 36 could be constructed. Each arm 14 a may include a first end 38 disposed at a junction of the central body 12 a and each arm 14 a as well as a second end 40. Further, each arm 14 may include a series of alternating peaks 42 and valleys 44 at the second end 40, as shown in FIGS. 4 and 6.
  • The arms 14 a may additionally include a recess 52 that extends generally between the outer surface 30 and the second end 40 of each arm 14 a. The recess 52 may be defined by a first planar surface 54 and a second planar surface 56 that are each substantially perpendicular to the longitudinal axis 18, are substantially parallel to one another, and extend in different planes. A substantially vertical surface 58 may extend generally between and connect the first planar surface 54 and the second planar surface 56 and may be substantially parallel to the longitudinal axis 18 of the central body 12 a. The recess 52 allows for bone to grow over the top of each arm 14 a and for placement of bone graft to help facilitate bone growth, which may allow for enhanced stability.
  • With particular reference to FIGS. 7-10, a prosthesis 60 is provided and may include a central body 62 and a plurality of wings or arms 64. As with the prosthetics 10, 10 a, the prosthesis 60 may be received within a resected portion of a humerus during a partial or total shoulder arthroplasty. The prosthesis 60 provides a structure for receiving and supporting a prosthetic humeral head 16 once the prosthesis 60 is installed in the resected portion of the humerus.
  • The central body 62 may include a bore 66 having a first portion 68 and a second portion 70. The first portion 68 may include a Morse taper and may extend generally between a first end 72 of the central body 62 and the second portion 70. The second portion 70 may be disposed adjacent to the first portion 68 and may extend generally between the first portion 68 and a second end 74 of the central body 62. The second portion 70 may include a substantially square shape, as shown in FIG. 8, to matingly receive a tool (not shown) during installation of the prosthesis 60 into a resected portion of a humerus. Interaction between the tool and the second portion 70 restricts relative rotation between the prosthesis 60 and the tool at the second portion 70 during installation of the prosthesis 60 into the humerus. While the second portion 70 is described and shown as including a substantially square shape, the second portion 70 could include any shape that permits mating engagement with a tool during installation of the prosthesis 60 to restrict relative rotation between the prosthesis 60 and the tool. Further, while the second portion 70 is described as matingly receiving the tool to restrict relative rotation therebetween, some rotation between the second portion 70 and the tool may be permitted.
  • The bore 66 may extend completely through the central body 62 along a longitudinal axis 76 of the central body 62. While the bore 66 is described and shown as extending completely through the central body 62 along the longitudinal axis 76, the bore 66 could alternatively be a blind bore that only partially extends through the central body 62.
  • The central body 62 may additionally include a substantially uniform outer surface 78 as well as a chamfer 80 that facilitates insertion of the central body 62 into a resected portion of a humerus during installation of the prosthesis 60. The outer surface 78 of the central body 62 may provide the central body 62 with a substantially constant, cylindrical shape extending along a length of the central body 62, as shown in FIG. 9.
  • The arms 64 extend generally from the central body 62 in a direction substantially perpendicular to the longitudinal axis 76. The plurality of arms 64 may include six arms 64, whereby an imaginary line 82 bisecting the central body 62 passes through a pair of arms 64 (FIG. 8). Because the plurality of arms 64 is shown as including six arms 64, three such lines 82 could be constructed.
  • Each arm 64 may include a proximal end 84 and a distal end 86. The proximal end 84 may be located at a junction of each arm 64 and the central body 62 and may provide each arm 64 with an increased width at the junction. Providing each arm 64 with an area of increased width at the junction of the central body 62 and each arm 64 strengthens the connection of the arms 64 to the central body 62 by increasing the material located at the junction of the central body 62 and the arms 64.
  • The distal end 86 of each arm 64 may include a first surface 88, a second surface 90, and a third surface 92. The first surface 88 may be formed at an acute angle (β) relative to the longitudinal axis 76 of the central body 62 (FIG. 10). The second surface 90 may extend from the central body 62 in a direction substantially perpendicular to the longitudinal axis 76 and may be located proximate to the second end 74 of the central body 62. The third surface 92 may extend generally between the first surface 88 and the second surface 90 and may include a series of peaks 94 and valleys 96. An imaginary line connecting the peaks 94 may be formed at an obtuse angle (Ω) relative to the first surface (88) and may be formed at an acute angle (Σ) relative to the longitudinal axis (76).
  • The arms 64 may additionally include a recess 98 disposed generally between the distal end 86 of each arm 64 and the outer surface 78 of the central body 62. The recess 98 may be defined generally by a first planar surface 100, a second planar surface 102, and a surface 104. The first planar surface 100 and the second planar surface 102 extend generally from the central body 62 in a direction substantially perpendicular to the longitudinal axis 76. The first planar surface 100 and the second planar surface 102 may be substantially parallel to one another and may be located in different planes such that the first planar surface 100 is located closer to the first end 72 of the central body 62 and the second planar surface 102 is located closer to the second end 74 of the central body 62, as shown in FIG. 10. The surface 104 extends between the first planar surface 100 and the second planar surface 102 to connect the first planar surface 100 and the second planar surface 102. The surface 104 may be planar and may be connected to surfaces 100 and 102 by radii. The first planar surface 100, second planar surface 102, and surface 104 cooperate with the outer surface 78 of the central body 62 to define the recess 98 of each arm 64.
  • With particular reference to FIGS. 11-13, a prosthesis 106 is shown to include a central body 108 and a plurality of wings or arms 110. As with the prosthetics 10, 10 a, 60, the prosthesis 106 may be used during a partial or total shoulder arthroplasty and may be received within a resected portion of a humerus. The prosthesis 106 may provide a structure on which a prosthetic humeral head 16 may be supported relative to the resected portion of the humerus.
  • The central body 108 may include a substantially circular shape and may include a bore 112 at least partially formed therethrough and extending along a longitudinal axis 114 of the central body 108. The bore 112 may include a first portion 116 and a second portion 118. The bore 112 may extend completely through the central body 108 or, alternatively, the bore 112 may be a blind bore extending only partially through the central body 108. Regardless of the particular construction of the bore 112, the first portion 116 may include a Morse taper for receiving a portion of the prosthetic humeral head 16.
  • The second portion 118 may include a series of threads (not shown) or, alternatively, a shape for mating engagement with a tool (FIG. 35). The tool may matingly engage the second portion 118 to facilitate attachment between the tool and the central body 108 of the prosthesis 106 during installation of the prosthesis 106 into the resected portion of the humerus during a partial or total shoulder arthroplasty. Engagement between the tool and the second portion 118 of the central body 108 inhibits relative rotation between the tool and the central body 108 during installation of the prosthesis 106 and, as a result, enhances the ability of the tool to engage and position the prosthesis 106 within the resected portion of the humerus.
  • The central body 108 may additionally include an outer surface 120 that defines the substantially cylindrical shape of the central body 108. The outer surface 120 may extend between a first end 122 and a second end 124 (FIG. 11). The second end 124 may include a chamfer 126 to facilitate insertion of the central body 108 into the resected portion of the humerus.
  • With continued reference to FIGS. 11-13, the arms 110 are shown as including a first end 128 and a second end 130. The first end 128 may include an increased thickness at a junction of the central body 108 and each arm 110 to increase the overall contact area between the central body 108 and each arm 110. Increasing the thickness of each arm 110 at the first end 128 increases the strength of the arms 110 at the central body 108 and, as a result, improves the overall strength of the prosthesis 106.
  • The second end 130 is formed on an opposite end of each arm 110 from the first end 128 and may include a first planar surface 132, a second planar surface 134, and a third planar surface 136. The first planar surface 132, second planar surface 134, and third planar surface 136 may all be formed at an acute angle relative to the longitudinal axis 114 of the central body 108. For example, the first planar surface 132 may be formed at an acute angle (θ) relative to the longitudinal axis 114, the second planar surface 134 may be formed at an acute angle (ψ), and the third planar surface 136 may be formed at an acute angle (φ) relative to the longitudinal axis 114. In addition, the first planar surface 132, second planar surface 134, and third planar surface 136 may be formed at an obtuse angle relative to one another. For example, the third planar surface 136 may be formed at an obtuse angle (δ) relative to the second planar surface 134. Likewise, the second planar surface 134 may be formed at an obtuse angle (α) relative to the first planar surface 132.
  • The arms 110 may extend from the central body 108 in a direction substantially perpendicular to the longitudinal axis 114 of the central body 108. As such, an imaginary line 138 passing through the longitudinal axis 114 and bisecting the central body 108 likewise passes through a pair of the arms 110, as shown in FIG. 12. Because the plurality of arms 110 is shown to include six arms, three such lines 138 could be constructed.
  • The arms 110 may include a recess 140 extending generally between the outer surface 120 of the central body 108 and the second end 130 of each arm 110. The recess 140 may be defined generally by a first planar surface 142, a second planar surface 144, and a third planar surface 146. The first planar surface 142 and the second planar surface 144 may extend generally from the central body 108 in a direction substantially perpendicular to the longitudinal axis 114. The first planar surface 142 may be substantially parallel to the second planar surface 144, whereby the first planar surface 142 and the second planar surface 144 extend in different planes.
  • As described, the first planar surface 142 is disposed closer to the first end 122 of the central body 108 and the second planar surface 144 is disposed closer to the second end 124 of the central body 108. The third planar surface 146 is disposed generally between the first planar surface 142 and the second planar surface 144 and may be formed substantially parallel to the longitudinal axis 114 of the central body 108. As such, the third planar surface 146 may be substantially parallel to the outer surface 120 of the central body 108 to define the recesses 140 of the arms 110.
  • With particular reference to FIGS. 23-26, a prosthesis 200 is shown to include a central body 202 and a plurality of wings or arms 204. As with the prosthetics 10, 10 a, 60, 106, the prosthesis 200 may be used during a partial, total, or reverse shoulder arthroplasty and may be received within a resected portion of a humerus. The prosthesis 200 may provide a structure on which a prosthetic humeral head 16 may be supported relative to the resected portion of the humerus.
  • The central body 202 may include a substantially circular shape and may include a bore 206 at least partially formed therethrough and extending along a longitudinal axis 208 (FIG. 25) of the central body 202. The bore 206 may include a first portion 210 and a second portion 212. The bore 206 may extend completely through the central body 202 or, alternatively, the bore 206 may be a blind bore extending only partially through the central body 202. Regardless of the particular construction of the bore 206, the first portion 210 may include a Morse taper for receiving a portion of a reverse humeral tray (not shown) or a portion of the prosthetic humeral head 16. Further, the first portion 210 may include a substantially uniform inner surface (FIG. 25) or, alternatively, may include a series of threads or steps, as shown in conjunction with the device shown in FIG. 30.
  • The second portion 212 may include a series of threads 214 or, alternatively, a shape for mating engagement with a tool (FIG. 35). The tool may matingly engage the second portion 212 to facilitate attachment between the tool and the central body 202 of the prosthesis 200 during installation of the prosthesis 200 into the resected portion of the humerus during a partial or total shoulder arthroplasty. Engagement between the tool and the second portion 212 of the central body 202 inhibits relative rotation between the tool and the central body 202 during installation of the prosthesis 200 and, as a result, enhances the ability of the tool to engage and position the prosthesis 200 within the resected portion of the humerus.
  • The central body 202 may additionally include an outer surface 216 that defines the substantially cylindrical shape of the central body 202. The outer surface 216 may extend between a first end 218 and a second end 220 (FIG. 24). The second end 220 may include a chamfer (not shown) to facilitate insertion of the central body 202 into the resected portion of the humerus.
  • With continued reference to FIGS. 23-26, the arms 204 are shown as including a first end 222 and a second end 224. The first end 222 may be attached to the central body 202 such that the arms 204 extend from the central body 202 in a first direction (D1) substantially perpendicular to the longitudinal axis 208. The arms 204 may be located relative to the central body 202 such that an imaginary line passing through the longitudinal axis 208 and bisecting the central body 202 likewise passes through a pair of the arms 204. Because the plurality of arms 204 is shown to include six arms, three such lines could be constructed.
  • The second end 224 is formed on an opposite end of each arm 204 from the first end 222 and may include a greater width than the first end 222 measured in a second direction (D2) substantially perpendicular to the first direction (D1). Providing the second end 224 with a greater width than the first end 222 may also provide each arm 204 with a tapered surface 226 extending generally between the first end 222 and the second end 224. The tapered surface 226 may additionally include a series of steps 228 that cooperate to define a series of recesses 230.
  • The steps 228 and recesses 230 may be used to retain the prosthesis 200 once installed by allowing cement, bone-growth material, and/or other material to collect within each recess 230. Further, each recess 230 may terminate at an edge 232 of an adjacent step 228, whereby the edge 232 is positioned to engage the surrounding bone and/or tissue to restrict removal of the prosthesis 200 once installed. The edge 232 may include a somewhat sharp corner that allows the edge 232 to facilitate engagement with the surrounding bone.
  • During installation, the prosthesis 200 is driven into a resected humerus and applies a force on the surrounding bone due to the tapered surfaces 226 of the arms 204. Specifically, the resected humerus is typically prepared such that the humerus includes a size and shape that accommodates the prosthesis 200. For example, the resected humerus could be undersized relative to the prosthesis 200 such that the prosthesis 200 is in a press-fit relationship with the humerus upon installation. Alternatively, the resected humerus could be oversized to allow the prosthesis 200 to be cemented within the humerus.
  • Assuming the resected humerus is undersized relative to the prosthesis 200, when the prosthesis 200 is driven into the humerus, the tapered surfaces 226 of the arms 204 apply a compressive force on the surrounding bone, thereby ensuring a tight fit between the prosthesis 200 and the bone. This tight fit may be maintained due to engagement between the edges 232 of the steps 228 and the surrounding bone when the prosthesis 200 is forcibly inserted into a resected humerus and may retain a position of the prosthesis 200 relative to the humerus once the force applied to the prosthesis 200 is released.
  • The arms 204 may also include a series of steps 234 and recesses 236 formed in a surface 238 of the arms 204 that extends generally between the first end 222 and the second end 224. As with the steps 228 and recesses 230, the steps 234 and recesses 236 may facilitate retention of the prosthesis 200 within a humerus by allowing cement, bone-growth material, and/or other material to collect within each recess 236.
  • The arms 204 may include a recess 240 extending generally between the outer surface 120 of the central body 202 and the second end 224 of each arm 204. The recess 240 may receive cement, bone-growth material, and/or other material to help retain the prosthesis 200 within the resected humerus.
  • With particular reference to FIGS. 27-30, a prosthesis 300 is shown to include a central body 302 and a plurality of wings or arms 304. As with the prosthetics 10, 10 a, 60, 200 the prosthesis 300 may be used during a partial or total shoulder arthroplasty and may be received within a resected portion of a humerus. The prosthesis 300 may provide a structure on which a prosthetic humeral head 16 may be supported relative to the resected portion of the humerus.
  • The central body 302 may include a substantially circular shape and may include a bore 306 at least partially formed therethrough and extending along a longitudinal axis 308 (FIG. 25) of the central body 302. The bore 306 may include a first portion 310 and a second portion 312. The bore 306 may extend completely through the central body 302 or, alternatively, the bore 306 may be a blind bore extending only partially through the central body 302. Regardless of the particular construction of the bore 306, the first portion 310 may include a Morse taper for receiving a portion of the prosthetic humeral head 16. Further, the first portion 310 may include a substantially uniform inner surface (as is shown in FIG. 25 with respect to prosthesis 200) or, alternatively, may include a series of threads or steps 311 (FIG. 30).
  • The second portion 312 may include a series of threads 314 or, alternatively, a shape for mating engagement with a tool (FIG. 35). The tool may matingly engage the second portion 312 to facilitate attachment between the tool and the central body 302 of the prosthesis 300 during installation of the prosthesis 300 into the resected portion of the humerus during a partial or total shoulder arthroplasty. Engagement between the tool and the second portion 312 of the central body 302 inhibits relative rotation between the tool and the central body 302 during installation of the prosthesis 300 and, as a result, enhances the ability of the tool to engage and position the prosthesis 300 within the resected portion of the humerus.
  • The central body 302 may additionally include an outer surface 316 that defines the substantially cylindrical shape of the central body 302. The outer surface 316 may extend between a first end 318 and a second end 320 (FIG. 28). The second end 320 may include a chamfer (not shown) to facilitate insertion of the central body 302 into the resected portion of the humerus.
  • With continued reference to FIGS. 27-30, the arms 304 are shown as including a first end 322 and a second end 324. The first end 322 may be attached to the central body 302 such that the arms 304 extend from the central body 302 in a first direction (D1) substantially perpendicular to the longitudinal axis 308. The arms 304 may be located relative to the central body 302 such that an imaginary line passing through the longitudinal axis 308 and bisecting the central body 302 likewise passes through a pair of the arms 304. Because the plurality of arms 304 is shown to include six arms, three such lines could be constructed.
  • The second end 324 is formed on an opposite end of each arm 304 from the first end 322 and may include a greater width than the first end 22 measured in a second direction (D2) substantially perpendicular to the first direction (D1). Providing the second end 324 with a greater width than the first end 322 may also provide each arm 304 with a tapered surface 326 extending generally between the first end 322 and the second end 324. The tapered surface 326 may be substantially planar, thereby providing each arm 304 with a substantially smooth surface extending between the first end 322 and the second end 324.
  • During installation, the prosthesis 300 is driven into a resected humerus and may apply a force on the surrounding bone due to the tapered surfaces 326 of the arms 304. Specifically, the resected humerus is typically prepared such that the humerus includes a size and shape that is either undersized or oversized relative to the prosthesis 300. Namely, the resected humerus may be undersized to provide a press-fit between the resected humerus and the prosthesis 300 upon installation or, alternatively, could be oversized to allow the prosthesis 300 to be cemented within the humerus. Assuming that the resected humerus is undersized, when the prosthesis 300 is driven into the humerus, the tapered surfaces 326 of the arms 304 apply a compressive force on the surrounding bone, thereby ensuring a tight fit between the prosthesis 300 and the bone.
  • The arms 304 may also include a series of steps 334 and recesses 336 formed in a surface 338 of the arms 304 that extends generally between the first end 322 and the second end 324. The steps 334 and recesses 336 may facilitate retention of the prosthesis 300 within a humerus by allowing cement, bone-growth material, and/or other material to collect within each recess 336.
  • The arms 304 may include a recess 340 extending generally between the outer surface 120 of the central body 302 and the second end 324 of each arm 304. The recess 340 may receive cement, bone-growth material, and/or other material to help retain the prosthesis 300 within the resected humerus.
  • While the prosthetics 200, 300 are described as including tapered surfaces, any of the prosthetics 10, 10 a, 60, 106 could similarly include tapered surfaces to facilitate retention of the prosthetics 10, 10 a, 60, 106 in the resected humerus. Namely, each of the prosthetics 10, 10 a, 60, 106, 200, 300 could include arms having tapered surfaces in a similar fashion as shown and described with respect to tapered surfaces 226, 326 of prosthetics 200, 300.
  • The foregoing prosthetics 10, 10 a, 60, 106, 200, 300 may be formed from any suitable biocompatible material. For example, the prosthetics 10, 10 a, 60, 106, 200, 300 may be formed from a titanium alloy (e.g., Ti-6Al-4V), CoCrMo, Pyrocarbon, or PEEK. In addition, the central bodies 12, 12 a, 62, 108, 202, 302 and/or arms 14, 14 a, 64, 110, 204, 304 may be coated with a porous plasma spray (PPS), Regenerex, or Hydroxy Apatite (HA), or any other appropriate coating that promotes boney ingrowth or ongrowth. Providing the various prosthetics 10, 10 a, 60, 106, 200, 300 with such a coating to promote boney ingrowth or ongrowth helps ensure that the prosthesis 10, 10 a, 60, 106, 200, 300 is retained at a desired position within the resected humerus by encouraging boney ingrowth and/or ongrowth that helps retain the prosthetics 10, 10 a, 60, 106, 200, 300 at the desired position relative to the humerus.
  • The prosthetics 10, 10 a, 60, 106, 200, 300 may be formed from a traditional manufacturing method such as, for example, machining or forging. Alternatively, the prosthetics 10, 10 a, 60, 106, 200, 300 may be formed from an additive manufacturing process such as Electron Beam Melting (EBM) or Direct Metal Laser Sintering (DMLS). If the prosthetics 10, 10 a, 60, 106, 200, 300 are formed from an additive manufacturing process, the prosthetics 10, 10 a, 60, 106, 200, 300 may be machined thereafter to form the Morse taper and inserter mating features within the bores 20, 20 a, 66, 112, 206, 306 of the respective prosthetics 10, 10 a, 60, 106, 200, 300.
  • Utilizing an additive manufacturing process allows the prosthetics 10, 10 a, 60, 106, 200, 300 to be formed in a substantially net shape and may provide each prosthesis 10, 10 a, 60, 106, 200, 300 with a substantially mesh or porous structure. Furthermore, manufacturing the prosthetics 10, 10 a, 60, 106, 200, 300 via an additive manufacturing process allows the prosthetics 10, 10 a, 60, 106, 200, 300 to include areas of solid material adjacent to or embedded within the porous structure of the prosthesis 10, 10 a, 60, 106, 200, 300.
  • With particular reference to FIGS. 14-22, various configurations of the prosthesis 106 are provided, whereby the prosthesis 106 is formed via an additive manufacturing process. FIGS. 14-21 depict at least a portion of the central body 108 and arms 110 as being formed from a porous material, whereby the central body 108 and/or arms 110 include pores formed in between biomaterial. While the prosthesis 106 is described and shown as being formed from an additive manufacturing process and as including a mesh or porous material at the central body 108 and/or arms 110, any of the prosthetics 10, 10 a, 60, 200, 300 could be formed via an additive manufacturing process to include a mesh or porous material.
  • FIGS. 14-16 generally depict the prosthesis 106 as including a porous material that forms a portion of the central body 108 and at least a portion of the arms 110. For example, the cross-sectional view of FIG. 17 identifies a portion of the central body 108 and arms 110 as being formed from a porous material. Forming a portion of the central body 108 from a porous material allows the central body 108 to be machined. For example, the central portion 108 may be machined to include a taper to allow the central portion 108 to properly receive an installation tool and subsequently a portion of a humeral head 16.
  • The arms 110 are shown as including a solid portion 148 disposed generally within the arms 110 and connected to the central portion 108. The solid portion 148 may be configured such that the solid portion 148 mimics the outer profile of each arm 110, whereby the solid portion 148 similarly includes a first surface 150, a second surface 152, and a third surface 154. Namely, the first surface 150, second surface 152, and third surface 154 are respectively disposed adjacent and parallel to surfaces 132, 134, and 136 of each arm 110. In addition, the solid portion 148 may include a fourth surface 156 that is substantially parallel to the first planar surface 142 and a fifth surface 158 that is substantially parallel to the outer surface 120 of the central body 108.
  • The solid portion 148 may be surrounded by a porous material and may be positioned within the arms 110 at virtually any location and may include virtually any shape to provide each arm 110 with additional strength. During manufacturing of the prosthesis 106, the porous material, as well as the solid portion 148, may be formed by depositing layer upon layer until the shape of the prosthesis 106 shown in FIG. 17 is obtained. For example, the layers may be added to one another in any of the (W), (X), (Y), and (Z) directions during manufacturing (FIG. 17).
  • With particular reference to FIG. 18, the prosthesis 106 is shown to include a solid portion 160 having a similar shape to that of the solid portion 148. While the solid portion 160 includes a substantially similar shape as the solid portion 148, the solid portion 160 of FIG. 18 includes additional solid material when compared to the solid portion 148 of FIG. 17. Providing the prosthesis 106 with additional solid material, as shown in FIG. 18, additionally strengthens the arms 110 and, thus, strengthens the overall prosthesis 106.
  • With particular reference to FIG. 19, the prosthesis 106 is shown as being formed entirely from a porous material, except for a portion of the central body 108 to allow the central portion 108 to be machined. In this configuration, the central body 108 and arms 110 are completely formed from a porous material and do not include a solid portion, as shown in FIGS. 17 and 18.
  • With particular reference to FIG. 20, the prosthesis 106 is shown as including a solid portion 162 having a different configuration than the solid portions 148, 160 of FIGS. 17 and 18, respectively. The solid portion 162 includes a first surface 164 that is substantially parallel to the third planar surface 136, as well as a pair of planar surfaces 166 that are substantially parallel to the longitudinal axis 114 of the central body 108. Additionally, the solid portion 162 may include a pair of planar surfaces 168 that are substantially perpendicular to the longitudinal axis 114 of the central body 108.
  • With particular reference to FIG. 21, the prosthesis 106 is shown as including a solid portion 170 having a pair of planar surfaces 172 that are substantially parallel to the longitudinal axis 114 of the central body 108 and a pair of planar surfaces 174 that are substantially perpendicular to the longitudinal axis 114 of the central body 108. As with the solid portions 148, 160, 162, the solid portion 170 adds to the overall strength of the prosthesis 106 by extending into the arms 110 in an effort to strengthen the arms 110 proximate to a junction of the central body 108 and the arms 110.
  • With particular reference to FIG. 22, the prosthesis is shown without having any regions of porous material. As such, the prosthesis 106 shown in FIG. 22 is entirely solid and therefore may be coated with a coating 176 that promotes boney ingrowth or ongrowth once installed in the humerus.
  • With particular reference to FIGS. 31-35, installation of the prosthesis 10 will be described in detail. While the following installation will be described with respect to the prosthesis 10, the following installation could be performed with any of the prosthetics 10, 10 a, 60, 106, 200, 300.
  • During a partial or total shoulder arthroplasty, a surgeon first makes an incision proximate to the shoulder joint of the patient to expose the humerus and glenoid fossa. Once exposed, the surgeon may use a template (not shown) to make a resection of the humerus 178 along line 180 of FIG. 33. Once the humerus 178 is resected, the surgeon may then use a tool such as a central pin and reamer/broach (none shown) to prepare a proximal end of the humerus 178 to allow the humerus 178 to receive the prosthesis 10. In one configuration, the reamer/broach creates a central pocket for receiving the central body 12 as well as a series of recesses extending from the central body 12 in spaced relation to one another in an effort to matingly receive the arms 14 once the prosthesis 10 is inserted into the humerus 178.
  • Prior to inserting the prosthesis 10 into the humerus 178, a suitable adhesive and/or coating may be applied to both retain the prosthesis 10 within the humerus 178 and to promote boney ingrowth and/or ongrowth. If the prosthesis 10 includes a recess such as recesses 52 of prosthesis 10 a, recess 98 of prosthesis 60, or recess 140 of prosthesis 106, a bone graft material may additionally be applied therein to further retain the prosthesis 10 within the humerus 178 and to promote bone growth over and within the recesses 52, 98, 140.
  • Once the prosthesis 10 is positioned relative to the humerus 178, a tool may be received within the bore 20 and may threadably engage the threads 28 of the second portion 28 of the bore 20 (FIG. 35). A force may be applied to the tool in the direction (Z) shown in FIG. 35 to drive the prosthesis 10 into the humerus 178 until the prosthesis 10 is positioned in a desired position relative to the humerus 178.
  • Once the prosthesis 10 is disposed within the humerus 178, a tool 182 may be used to position the prosthetic humeral head 16 relative to the prosthesis 10 such that a portion of the prosthetic humeral head 16 is received within the bore 20 of the prosthesis 10. Specifically, the prosthetic humeral head 16 may include an extension 184 having a Morse taper. The extension 184 may include a male Morse taper while the first portion 22 of the bore 20 includes a mating female Morse taper such that when the extension 184 is received within the bore 20 of the central body 12, the prosthetic humeral head 16 is retained by the prosthesis 10 and held in a desired position relative to the humerus 178.
  • The foregoing description of the embodiments has been provided for purposes of illustration and description. It is not intended to be exhaustive or to limit the disclosure. Individual elements or features of a particular embodiment are generally not limited to that particular embodiment, but, where applicable, are interchangeable and can be used in a selected embodiment, even if not specifically shown or described. The same may also be varied in many ways. Such variations are not to be regarded as a departure from the disclosure, and all such modifications are intended to be included within the scope of the disclosure.

Claims (22)

1. A prosthesis comprising:
a central body having a longitudinal axis and an opening operable to receive an installation tool; and
a plurality of arms each including a first end proximate to said central body and a second end extending from said central body in a first direction substantially perpendicular to said longitudinal axis, said second end including a greater width than said first end measured in a second direction substantially perpendicular to said first direction.
2. The prosthesis of claim 1, further comprising at least one tapered surface extending between said first end and said second end.
3. The prosthesis of claim 2, wherein said at least one tapered surface is substantially planar.
4. The prosthesis of claim 2, wherein said at least one tapered surface includes a series of stepped portions.
5. The prosthesis of claim 1, wherein said first end is spaced apart and separated from said central body.
6. The prosthesis of claim 1, wherein said central body includes a bore in communication with said opening.
7. The prosthesis of claim 6, wherein said bore is one of a blind bore or a through bore.
8. The prosthesis of claim 6, wherein said bore includes a series of stepped portions.
9. The prosthesis of claim 6, wherein said bore has at least one of a threaded portion and a Morse taper.
10. The prosthesis of claim 1, wherein said plurality of arms each include a series of stepped portions that extend between said first end and said second end.
11. The prosthesis of claim 1, wherein said plurality of arms are formed from a porous material.
12. A prosthesis comprising:
a central body having a longitudinal axis; and
a plurality of arms each including a first end proximate to said central body and a second end extending from said central body in a first direction substantially perpendicular to said longitudinal axis, said plurality of arms each including at least one tapered surface that provides said plurality of arms with an increasing thickness extending in a direction from said first end to said second end.
13. The prosthesis of claim 12, wherein said at least one tapered surface includes two tapered surfaces that cooperate to provide said arms with said increasing thickness.
14. The prosthesis of claim 13, wherein said at least one tapered surface is substantially planar.
15. The prosthesis of claim 13, wherein said at least one tapered surface includes a series of stepped portions.
16. The prosthesis of claim 12, wherein said second end includes a greater width than said first end measured in a second direction substantially perpendicular to said first direction.
17. The prosthesis of claim 12, wherein said central body includes a bore in communication with said opening.
18. The prosthesis of claim 17, wherein said bore is one of a blind bore or a through bore.
19. The prosthesis of claim 17, wherein said bore includes a series of stepped portions.
20. The prosthesis of claim 17, wherein said bore has at least one of a threaded portion and a Morse taper.
21. The prosthesis of claim 12, wherein said plurality of arms each include a series of stepped portions that extend between said first end and said second end.
22. The prosthesis of claim 12, wherein said plurality of arms are formed from a porous material.
US13/343,039 2011-07-13 2012-01-04 Shoulder prosthesis Abandoned US20130018476A1 (en)

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EP12814060.5A EP2800541A1 (en) 2012-01-04 2012-12-14 Shoulder prosthesis
US14/041,084 US8876908B2 (en) 2011-07-13 2013-09-30 Shoulder prosthesis
US14/462,680 US9326865B2 (en) 2011-07-13 2014-08-19 Shoulder prosthesis
US14/462,675 US9364334B2 (en) 2011-07-13 2014-08-19 Shoulder prosthesis

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US14/462,680 Active US9326865B2 (en) 2011-07-13 2014-08-19 Shoulder prosthesis
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US20140358239A1 (en) 2014-12-04
US9326865B2 (en) 2016-05-03
US8876908B2 (en) 2014-11-04
US20140358240A1 (en) 2014-12-04
US20140031946A1 (en) 2014-01-30
US9364334B2 (en) 2016-06-14

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