The present disclosure relates generally to orthopaedic surgical instruments and, more particularly, to surgical instruments used to resect a patient's bone.
Joint arthroplasty is a well-known surgical procedure by which a diseased and/or damaged natural joint is replaced by a prosthetic joint. Typical artificial joints include knee prostheses, hip prostheses, shoulder prostheses, ankle prostheses, and wrist prostheses, among others. To facilitate the replacement of the natural joint with the prosthesis, orthopaedic surgeons use a variety of orthopaedic surgical instruments such as, for example, saws, drills, reamers, rasps, broaches, cutting blocks, drill guides, milling guides, and other surgical instruments.
According to one aspect of the disclosure, an orthopaedic surgical instrument includes a cutting block having a bone-engaging surface and an outer surface positioned opposite the bone-engaging surface, a first cutting guide slot defined in the cutting block, and a second cutting guide slot defined in the cutting block. The first cutting guide slot defines a first imaginary plane, the second cutting guide slot defines a second imaginary plane that extends oblique to the first imaginary plane. The orthopaedic surgical instrument includes a first mounting system configured to secure the cutting block to a bone of a patient. The first mounting system includes a plate removably coupled to the cutting block, and a pair of spikes attached to the plate, each spike having a bone-engaging tip. The orthopaedic surgical instrument also includes a second mounting system configured to secure the cutting block to the bone of the patient. The second mounting system includes a plurality of guide bores extending through the bone-engaging surface and the outer surface of the cutting block, and a plurality of fixation pins configured to be received in the plurality of guide bores, each fixation pin having a bone-engaging tip.
In some embodiments, the second mounting system may be configured to secure the cutting block to the bone of the patient in place of the first mounting system when the plate is detached from the cutting block. In some embodiments, the orthopaedic surgical instrument may include a third cutting guide slot defined in the cutting block. The second cutting guide slot is positioned between the first cutting guide slot and the third cutting guide slot.
In some embodiments, the plurality of guide bores may be positioned between the first cutting guide slot and the second cutting guide slot. Additionally, in some embodiments, the plurality of guide bores may be a first plurality of guide bores, and the second mounting system may include a second plurality of guide bores that are defined in the cutting block between the second cutting guide slot and the third cutting guide slot.
In some embodiments, the orthopaedic surgical instrument may further include a first guide bore positioned on a first side of the second cutting guide slot and a second guide bore positioned on a second side of the second cutting guide slot. Each of the first guide bore and the second guide bore may be sized to receive a fixation pin.
In some embodiments, the bone-engaging surface of the cutting block may have an aperture defined therein, and the plate of the first mounting system may be positioned in the aperture. In some embodiments, the orthopaedic surgical instrument may further include a second plate configured to be positioned in the aperture defined in the bone-engaging surface. The second plate may be devoid of spikes. In some embodiments, the pair of spikes and the plate may be formed as a single monolithic component.
According to another aspect, an orthopaedic surgical instrument includes a cutting block having a bone-engaging surface including an aperture defined therein, a first bracket positioned in the aperture defined in the cutting block, and a second bracket configured to be positioned in the aperture of the cutting block in place of the first bracket. The second bracket has a pair of spikes extending outwardly therefrom, and each spike having a bone-engaging tip. The first bracket and the cutting block cooperate to define a cutting guide slot, and the second bracket and the cutting block cooperate to define the cutting guide slot when the second bracket is positioned in the aperture of the cutting block.
In some embodiments, the cutting guide slot may be a first cutting guide slot that defines a first imaginary plane, and the cutting block may have a second cutting guide slot defined therein. The second cutting guide slot may define a second imaginary plane that extends oblique to the first imaginary plane.
Additionally, in some embodiments, the first cutting guide slot may be a femoral chamfer cutting guide slot and the second cutting guide slot may be an anterior cutting guide slot. In some embodiments, the orthopaedic surgical instrument may include a first mounting system including the second bracket, and a second mounting system configured to secure the cutting block to a bone of a patient in place of the first mounting system. The second mounting system may include a plurality of guide bores defined in the cutting block, and a plurality of fixation pins configured to be received in the plurality of guide bores. Each fixation pin may have a bone-engaging tip.
In some embodiments, the plurality of guide bores may be positioned between the femoral chamfer cutting guide slot and the anterior cutting guide slot. In some embodiments, the orthopaedic surgical instrument may further include a posterior cutting guide slot defined in the cutting block.
In some embodiments, the plurality of guide bores may be a first plurality of guide bores. The second mounting system may include a second plurality of guide bores that are defined in the cutting block between the posterior cutting guide slot and the femoral chamfer cutting guide slot.
In some embodiments, the first bracket and the cutting block may cooperate to define a third cutting guide slot, and the second bracket and the cutting block may cooperate to define the third cutting guide slot when the second bracket is positioned in the aperture of the cutting block.
According to another aspect, an orthopaedic surgical instrument includes a cutting block, an anterior cutting guide slot defined in the cutting block, an anterior chamfer cutting guide slot defined in the cutting block, and a first mounting system configured to secure the cutting block to a bone of a patient. The first mounting system includes a plate removably coupled to the cutting block and a pair of spikes attached to the plate, each spike having a bone-engaging tip. The orthopaedic surgical instrument also includes a second mounting system configured to secure the cutting block to the bone of the patient when the plate is detached from the cutting block. The second mounting system includes a plurality of guide bores extending through the cutting block, and a plurality of fixation pins configured to be received in the plurality of guide bores. Each fixation pin has a bone-engaging tip.
In some embodiments, the cutting block may include a body having an aperture defined therein. The plate may be received in the aperture.
In some embodiments, the plate and the body may cooperate to define the anterior chamfer cutting guide slot.
Additionally, in some embodiments, the orthopaedic surgical instrument may include a posterior chamfer cutting guide slot defined by the plate and the body of the cutting block.
In some embodiments, the orthopaedic surgical instrument may include a second plate configured to be positioned in the aperture in place of the plate. The second plate may cooperate to define the anterior chamfer cutting guide slot and the posterior chamfer cutting guide slot when the second plate is positioned in the aperture.
The detailed description particularly refers to the following figures, in which:
While the concepts of the present disclosure are susceptible to various modifications and alternative forms, specific exemplary embodiments thereof have been shown by way of example in the drawings and will herein be described in detail. It should be understood, however, that there is no intent to limit the concepts of the present disclosure to the particular forms disclosed, but on the contrary, the intention is to cover all modifications, equivalents, and alternatives falling within the spirit and scope of the invention as defined by the appended claims.
Terms representing anatomical references, such as anterior, posterior, medial, lateral, superior, inferior, etcetera, may be used throughout the specification in reference to the orthopaedic implants and surgical instruments described herein as well as in reference to the patient's natural anatomy. Such terms have well-understood meanings in both the study of anatomy and the field of orthopaedics. Use of such anatomical reference terms in the written description and claims is intended to be consistent with their well-understood meanings unless noted otherwise.
Referring to
The modular mounting system 14 includes a plate or bracket 32 that is sized and shaped to be positioned in the aperture 30 of the cutting block 12. The other modular mounting system 16 includes a plate or bracket 34 that is sized and shaped to be positioned in the aperture 30 in place of the bracket 32 of the system 14. The surgical instrument 10 also includes a plurality of cutting slots or guides 40, and each cutting guide 40 is defined by opposing guide surfaces 42, as described in greater detail below. Each cutting guide 40 is sized and shaped to receive the blade (not shown) of a surgical saw or other cutting instrument and orient the blade to resect the patient's bone during an orthopaedic surgical procedure.
In the illustrative embodiment, the cutting block 12 and the brackets 32, 34 of the instrument 10 are formed from metallic materials such as, for example, steel, titanium alloy, or cobalt chromium alloy. It should be appreciated that in other embodiments the cutting block 12 and the brackets 32, 34 may be formed from polymeric materials such as, for example, polyamide, polyphenylsulfone, or polyketone. In such embodiments, the guide surfaces 42 of the instrument 10 may be formed from a metallic material such as those described above. It should be understood that any number of combinations of polymeric and metallic materials may be used to form the cutting block 12 and the brackets 32, 34.
As shown in
The cutting guides 40 of the instrument 10 also include an anterior cutting guide 54, which is defined at the upper end 28 of the cutting block 12. The cutting guide 54 is defined between opposing guide surfaces 42, which extend between an opening 56 (see
The orthopaedic surgical instrument 10 also includes a pair of chamfer cutting guides 70, 72 positioned between the posterior cutting guide 44 and the anterior cutting guide 54. In the illustrative embodiment, the cutting block 12 and the brackets 32, 34 cooperate to define the chamfer cutting guides 70, 72. As shown in
As shown in
Similarly, when the bracket 34 is positioned in the aperture 30 in place of the bracket 32, the upper guide surface 100 of the bracket 34 faces the guide surface 80 of the cutting block 12 such the upper guide surface 100 cooperates with the guide surfaces 76, 80 to define the chamfer cutting guide 70. The lower guide surface 102 of the bracket 34 faces the guide surface 82 of the cutting block 12 such that the lower guide surface 102 cooperates with the guide surfaces 78, 82 to define the other chamfer cutting guide 72.
An imaginary resection plane 110 is defined by the chamfer cutting guide 70. The resection plane 110 extends through the distal end 18 of the patient's femur 20 when the cutting block 12 is secured thereto. The other chamfer cutting guide 72 defines another imaginary resection plane 112, which also extends through the distal end 18 of the patient's femur 20 when the cutting block 12 is secured thereto. In that way, the chamfer cutting guides 70, 72 may be used by the orthopaedic surgeon during the resection of the patient's femur 20. The resection planes 110, 112 of the chamfer cutting guides 70, 72 extend obliquely relative to the resection planes 50, 60 defined by the posterior cutting guide 44 and the anterior cutting guide 54, respectively.
As shown in
When the bracket 32 is secured to the cutting block 12, the bone-engaging surface 122 is co-planar with the bone-engaging surface 24 of the cutting block 12. Additionally, as shown in
The orthopaedic surgical instrument 10 includes a locking mechanism configured to secure the bracket 32 to the cutting block 12. In the illustrative embodiment, the locking mechanism includes the plugs 118 of the brackets 32 and the surfaces defining the notches 124 of the cutting block 12. The plugs 118 are sized to engage the surfaces defining the notches 124, thereby creating a frictional interlock therebetween and securing the bracket 32 to the cutting block 12. In other embodiments, the instrument 10 may include other locking mechanisms such as, for example, fasteners, latches, tabs, and so forth to secure the bracket 32 to the cutting block 12.
As shown in
The bracket 34 of the modular mounting system 16 also includes a pair of spikes 154 that extend outwardly from the bone-engaging surface 152. As shown in
When the bracket 34 is secured to the cutting block 12, the bone-engaging surface 152 is co-planar with the bone-engaging surface 24 of the cutting block 12, and the spikes 154 extend outwardly therefrom. Additionally, each plug 138 of the bracket 34 is received in a corresponding notch 124 of the cutting block 12 when the bracket 34 is secured to the cutting block 12. Similar to the bracket 34, the plugs 138 of the bracket 34 and the surfaces of the notches 124 of the cutting block 12 form a locking mechanism configured to secure the bracket 34 to the cutting block 12. The plugs 138 are sized to engage the surfaces defining the notches 124, thereby creating a frictional interlock therebetween and securing the bracket 34 to the cutting block 12.
The modular mounting system 14 of the instrument 10 also includes a plurality of fixation pins 160. As shown in
The modular mounting system 14 also includes another plurality of guide bores 168 positioned between the opening 74 of the chamfer cutting guides 70, 72 and the posterior cutting guide 44. Each guide bore 168 is sized to receive one of the fixation pins 160. As shown in
The modular mounting system 14 of the orthopaedic surgical instrument 10 further includes a guide bore 178 positioned on each side of the opening 74 of the chamfer cutting guides 70, 72. Each guide bore 178 is sized to receive one of the fixation pins 160. As shown in
In operation, the surgeon may utilize the orthopaedic surgical instrument 10 to prepare the distal end 18 of the patient's femur 20 to receive a prosthetic femoral component. To do so, the surgeon may secure the cutting block 12 to the patient's femur 20 using the modular mounting system 14 or the modular mounting system 16. The surgeon may then use the cutting guides 40 of the cutting block 12 to guide a cutting saw blade in making a series of resections of the distal end 18 of the patient's femur 20.
During an orthopaedic surgical procedure, the surgeon may first resect the distal end 18 of the patient's femur 20 to create a surgically-prepared distal surface 190. If the surgeon selects the modular mounting system 14, the instrument 10 may be assembled by aligning the bracket 32 with the aperture 30 defined in the cutting block 12. The surgeon or other user may advance the bracket 32 into the aperture 30 such that the plugs 118 of the bracket 32 are received in the notches 124 of the cutting block 12. As described above, the plugs 118 frictionally engage the cutting block 12 to secure the bracket 32 to the cutting block 12.
The surgeon may secure a pair of fixation pins 160 of the modular mounting system 14 to the surgically-prepared distal surface 190 of the patient's femur 20, as shown in
After attaching the fixation pins 160, the surgeon may position the cutting block 12 and the bracket 32 on the surgically-prepared distal surface 190. To do so, the surgeon may align the shafts 162 of the fixation pins 160 with a pair of guide bores 166 of the cutting block 12. The surgeon may then advance the cutting block 12 over the shafts 162 in the direction indicated by arrow 192 in
The surgeon may use the cutting block 12 to make a number of resections of the distal end 18 of the patient's femur 20. For example, as shown in
The surgeon may also use the chamfer cutting guides 70, 72 of the instrument 10 to make chamfer cuts on the patient's femur 20. To do so, the surgeon may insert fixation pins 160 through the bores 178 positioned on each side of the opening 74 of the chamfer cutting guides 70, 72. The surgeon may remove any fixation pins 160 from the bores 166, 168 before advancing the surgical cutting saw 194 through each chamfer cutting guides 70, 72 to resect the distal end 18 of the patients' femur 20.
Instead of the modular mounting system 14, the surgeon may select the modular mounting system 16 to secure the cutting block 12 to the patient's femur 20. In that case, the instrument 10 may be assembled by aligning the bracket 34 with the aperture 30 defined in the cutting block 12. The surgeon or other user may advance the bracket 34 into the aperture 30 such that the plugs 138 of the bracket 34 are received in the notches 124 of the cutting block 12. As described above, the plugs 138 frictionally engage the cutting block 12 to secure the bracket 34 to the cutting block 12.
The surgeon may form a pair of holes 200 in the surgically-prepared distal surface 190 of the patient's femur 20. As shown in
After forming the holes 200, the surgeon may position the cutting block 12 and the bracket 34 on the surgically-prepared distal surface 190. To do so, the surgeon may align the spikes 154 of the modular mounting system 16 with the holes 200 and advance the tips 158 of the spikes 154 into the holes 200. The bone-engaging surface 152 of the bracket 34 and the bone-engaging surface 24 of the cutting block 12 contact the surgically-prepared distal surface 190 when the instrument 10 is positioned on the distal end 18 of the patient's femur 20.
As described above in regard to the modular mounting system 14, the surgeon may use the cutting block 12 to make a number of resections of the distal end 18 of the patient's femur 20. The surgeon may advance the surgical cutting saw 194 through the cutting guide 54 to engage the patient's femur 20 and operate the surgical saw 194 to surgically prepare an anterior surface of the patient's femur 20 to receive the prosthetic femoral component. The surgeon may similarly use the posterior cutting guide 44 to resect the posterior condyles 196 of the patient's femur 20 and surgically prepare the posterior surfaces of the patient's femur 20 to receive the prosthetic femoral component. The surgeon may also use the chamfer cutting guides 70, 72 of the instrument 10 to make chamfer cuts on the patient's femur 20.
Referring now to
The modular mounting system 216 includes a plate or bracket 234 that is sized and shaped to be positioned in the aperture 230. The surgical instrument 10 also includes a plurality of cutting slots or guides 40, and each cutting guide 40 is defined by opposing guide surfaces 42. Each cutting guide 40 is sized and shaped to receive the blade (not shown) of a surgical saw or other cutting instrument and orient the blade to resect the patient's bone during an orthopaedic surgical procedure.
The instrument 210 includes a posterior cutting guide 44, which is defined at the lower end 26 of the cutting block 212, and an anterior cutting guide 54, which is defined at the upper end 28 of the cutting block 212. The instrument 210 also includes a pair of chamfer cutting guides 270, 272 positioned between the posterior cutting guide 44 and the anterior cutting guide 54. Similar to the cutting block 12 described above in regard to
As shown in
When the bracket 234 is secured to the cutting block 212, the bone-engaging surface 286 is co-planar with the bone-engaging surface 224 of the cutting block 212, and the spikes 288 extend outwardly therefrom. The body 284 is sized to engage the surfaces defining the aperture 230, thereby creating a frictional interlock therebetween and securing the bracket 234 to the cutting block 212. In other embodiments, the instrument 210 may include other locking mechanisms such as, for example, fasteners, latches, tabs, and so forth to secure the bracket 234 to the cutting block 212.
The modular mounting system 214, like the modular mounting system 14 described above in regard to
In operation, the surgeon may utilize the orthopaedic surgical instrument 210 to prepare the distal end 18 of the patient's femur 20 to receive a prosthetic femoral component. To do so, the surgeon may secure the cutting block 212 to the patient's femur 20 using the modular mounting system 214 or the modular mounting system 216. The surgeon may then use the cutting guides 40 of the cutting block 212 to guide a cutting saw blade in making a series of resections of the distal end 18 of the patient's femur 20.
If the surgeon selects the modular mounting system 214, the surgeon may secure a pair of fixation pins 160 of the modular mounting system 214 to the surgically-prepared distal surface 190 of the patient's femur 20 in the manner described above in regard to
Instead of the modular mounting system 214, the surgeon may select the modular mounting system 216 to secure the cutting block 212 to the patient's femur 20. In that case, the instrument 210 may be assembled by aligning the bracket 234 with the aperture 230 defined in the cutting block 212. The surgeon or other user may advance the bracket 234 into the aperture 230 such that the body 284 of the bracket 234 is received in the aperture 230 of the cutting block 212. As described above, the body 284 frictionally engages the cutting block 212 to secure the bracket 234 thereto.
The surgeon may form a pair of holes 200 in the surgically-prepared distal surface 190 of the patient's femur 20 in the manner described above in regard to
While the disclosure has been illustrated and described in detail in the drawings and foregoing description, such an illustration and description is to be considered as exemplary and not restrictive in character, it being understood that only illustrative embodiments have been shown and described and that all changes and modifications that come within the spirit of the disclosure are desired to be protected.
There are a plurality of advantages of the present disclosure arising from the various features of the method, apparatus, and system described herein. It will be noted that alternative embodiments of the method, apparatus, and system of the present disclosure may not include all of the features described yet still benefit from at least some of the advantages of such features. Those of ordinary skill in the art may readily devise their own implementations of the method, apparatus, and system that incorporate one or more of the features of the present invention and fall within the spirit and scope of the present disclosure as defined by the appended claims.