Abstract: A surgical marker/connector can be provided in the form of a ring made of a fluoroscopic material, including a shape memory alloy such as NITINOL. The ring preferably includes a plurality of small suture attachments in the form of loops that are disposed on the periphery of the ring and which lie in a plane that includes the ring itself. The loops are large enough to receive sutures which, in turn, can be used to connect the ring to a portion of a patient's body, or to connect separate portions of a patient's body to each other using the marker/connector as an intermediate connector. If the ring is made of a shape memory alloy, the ring can be wrapped tightly about an elongate member such as a mandrel, which than can be inserted into the patient's body through a trochar or cannula. After insertion, the ring will change temperature and resume its original configuration where it can be sutured in place as desired.

Abstract: A surgical drape includes a first, closed container within which a first sheet is disposed. The first sheet has first and second opposed ends, the first end of the first sheet being removable from the container so as to remove a desired portion of the first sheet from the container, the second end of the first sheet remaining within the container. Preferably, the first container is laid across a desired portion of the table prior to placing the patient on the table. After the patient has been positioned properly and prepped, the first sheet can be pulled from underneath the patient and pulled out of the first container so that the sheet covers the table in the area of surgical interest and then covers the entire side or end of the table down to the floor. After the surgical procedure has been completed, the first sheet and the container can be removed and discarded.

Abstract: A surgical clamp assembly includes a clamp having movable jaws, each of which has a clamping surface for engaging a portion of a patient's body. An electrode forms a portion of the clamping surface of at least one of the jaws, the electrode being capable of heating, severing, or cauterizing the portion of the patient's body that is grasped by the clamp. If desired, the clamp assembly can be provided with a retainer that prevents the jaws from being opened accidently. The clamp assembly also can include an actuator that can be detached from the clamp and removed from the operative site, leaving the locked clamp in place. In this type of assembly, when it is desired to remove the clamp, the actuator can be reattached to the clamp and used to disengage the toothed retainer, and thereafter can be used to spread the jaws in order to permit the clamp to be removed.

Abstract: An orthopedic implant having a metal substrate with an articulating surface includes a coating for the articulating surface made of pyrolytic carbon. Typically, the substrate is made of a metal such as titanium or stainless steel, or alloys thereof. The pyrolytic carbon coating preferably is applied by vapor deposition.

Abstract: A surgical retractor includes a pair of small grips that are disposed at the ends of arms that can be moved toward or away from each other. The grips engage and separate the sides of an incision that has been made in a patient. A lifting mechanism that can be attached to one of the arms enables one side of the incision to be raised relative to the other side of the incision. The lifting mechanism includes a clamp that can be connected to the retractor and a foot that is connected to the clamp and which is movable relative thereto. The foot is engageable with the patient such that extension of the foot causes a selected grip to be raised. Retraction of the foot permits the selected grip to be lowered. In the preferred embodiment, the foot is disposed at one end of a notched rack; a rotatable pinion is in contact with the notches to extend and contract the rack; and a pivotally movable pawl permits movement of the rack in one direction and prevents movement of the rack in the other direction.

Abstract: A surgical marker/connector in the form of a ring made of a shape memory alloy such as NITINOL is suitable for laparoscopic installation in a patient's body. The ring preferably includes a plurality of small suture attachments in the form of loops that are disposed on the periphery of the ring and which lie in a plane that includes the ring itself. The loops are large enough to receive sutures which, in turn, can be used to connect the ring to a portion of a patient's body, or to connect separate portions of a patient's body to each other using the marker/connector as an intermediate connector. Prior to installation, the ring can be wrapped tightly about an elongate member such as a mandrel, which than can be inserted into the patient's body through a trochar or cannula. After insertion, the ring will change temperature and resume its original configuration where it can be sutured in place as desired.

Abstract: An orthopedic implant having a metal substrate with an articulating surface includes a coating for the articulating surface made of pyrolytic carbon. Typically, the substrate is made of a metal such as titanium or stainless steel, or alloys thereof. The pyrolytic carbon coating preferably is applied by vapor deposition.

Abstract: A device for occluding a conduit includes first and second members, each with first and second ends. The second ends are connected by a hinge. The first ends interlock to close the device about the conduit. The members are shaped such that they can occlude the conduit without causing the development of damaged or necrotic tissue. If desired, a flexible cover can be provided and the first and second members can be disposed within the cover. If such a cover is used, it will contact the conduit in order to cushion the contact between the members and the conduit, minimize the tendency of the conduit to bleed, and increase traction relative to the conduit. The invention also includes methods for using the device to occlude a conduit.

Abstract: A device for excluding the left atrial appendage (LAA) includes first and second members, each with first and second ends. The second ends are connected by a hinge. The first ends interlock to close the device about the LAA. The members are shaped such that they can exclude the LAA without causing the development of necrotic tissue. If desired, a flexible cover can be provided and the first and second members can be disposed within the cover. If such a cover is used, it will contact the LAA in order to cushion the contact between the members and the LAA and minimize the tendency of the LAA to bleed. The invention also includes methods for using the device to exclude the LAA.

Abstract: A technique for manufacturing a prosthetic tissue heart component involves performing a non-invasive scanning operation on a patient's heart, preferably by CT angiography. Images of the specific dimensions of the heart component to be replaced are generated. The images generated by the scanning operation are used to manufacture the replacement heart component. The invention permits a custom-fit replacement heart component to be installed in a patient. Use of the invention also avoids the need to manufacture or fit the replacement heart component during the course of a surgical procedure.

Abstract: A surgical marker/connector in the form of a circular ring includes a plurality of small suture attachments that are disposed about the periphery of the ring. The suture attachments preferably are in the form of loops that lie in a plane that includes the ring itself. The loops are large enough to receive sutures which, in turn, can be used to connect the ring to a portion of a patient's body, or to connect separate portions of a patient's body to each other using the marker/connector as an intermediate connector. At least a portion of the marker/connector is made of a material that can be observed by fluoroscopic examination.

Abstract: A technique to manufacture small joint orthopedic implants includes the steps of taking standard radiographs of a pathologic joint and the corresponding non-pathologic joint. In order to provide an accurate frame of reference, a specialized marker is placed in the radiographic field. By inspection of the radiographs and by comparison with the marker, the dimensions of the cortical bone and the cancellous bone can be quickly and accurately determined. These dimensions can be used to manufacture a suitable implant and installation tool. Typically, the implant will include a stem from which a post projects. A radially extending collar is located at the intersection between the stem and the post. A mating head is attached to the post. The head closely approximates the size and shape of the natural head being replaced. The stem will be non-round in cross-section to prevent rotation of the stem in the bone.

Abstract: A surgical retractor includes a pair of small grips that are disposed at the ends of arms that can be moved toward or away from each other. The grips engage and separate the sides of an incision that has been made in a patient. A lifting mechanism that can be attached to one of the arms enables one side of the incision to be raised relative to the other side of the incision. The lifting mechanism includes a clamp that can be connected to the retractor and a foot that is connected to the clamp and which is movable relative thereto. The foot is engageable with the patient such that extension of the foot causes a selected grip to be raised. Retraction of the foot permits the selected grip to be lowered. In the preferred embodiment, the foot is disposed at one end of a notched rack; a rotatable pinion is in contact with the notches to extend and contract the rack; and a pivotally movable pawl permits movement of the rack in one direction and prevents movement of the rack in the other direction.

Abstract: A first surgical retractor (302) according to the invention includes a handle (308) that defines an axis (320) and has first and second ends. A retractor blade (306) is secured to the second end of the handle. The blade is of a size and shape to engage the mitral valve of a heart so as to be able to retract the mitral valve and adjacent tissues. A second retractor (304) according to the invention has a relatively narrow, elongate blade (352) that can extend deep into the heart to engage the heart in the region of the atrial appendage so as to be able to retract the atrium and expose the pulmonary veins. The retractors are especially adapted to perform an atrial fibrillation surgical procedure.

Abstract: A surgical drape includes a first, closed container within which a first sheet is disposed. The first sheet has first and second opposed ends, the first end of the first sheet being removable from the container so as to remove a desired portion of the first sheet from the container, the second end of the first sheet remaining within the container. Preferably, the first container is laid across a desired portion of the table prior to placing the patient on the table. After the patient has been positioned properly and prepped, the first sheet can be pulled from underneath the patient and pulled out of the first container so that the sheet covers the table in the area of surgical interest and then covers the entire side or end of the table down to the floor. After the surgical procedure has been completed, the first sheet and the container can be removed and discarded.