74 results about "Anatomic Location" patented technology

A shunt is provided for the flow of aqueous humor from the anterior chamber of the eye to Schlemm's canal and to other anatomical spaces of the eye. The shunt comprises at least one lumen and optionally has at least one anchor extending from a proximal portion of the shunt to assist in placement and anchoring of the device in the correct anatomic position.

A method which coordinates proton beam irradiation with an open magnetic resonance imaging (MRI) unit to achieve near-simultaneous, noninvasive localization and radiotherapy of various cell lines in various anatomic locations. A reference image of the target aids in determining a treatment plan and repositioning the patient within the MRI unit for later treatments. The patient is located within the MRI unit so that the target and the proton beam are coincident. MRI monitors the location of the target. Target irradiation occurs when the target and the proton beam are coincident as indicated by the MRI monitoring. The patient rotates relative to the radiation source. The target again undergoes monitoring and selective irradiation. The rotation and selective irradiation during MRI monitoring repeats according to the treatment plan.

A method of forming an implant having a porous region replicated from scanned bone, the method comprising imaging bone with a high resolution digital scanner to generate a three-dimensional design model of the bone; removing a three-dimensional section from the design model; fabricating a porous region on a digital representation of the implant by replacing a solid portion of the digital implant with the section removed from the digital representation; and using an additive manufacturing technique to create a physical implant including the fabricated porous region.

Modular, miniaturized cardiovascular sensors, systems, methods, and wearable devices for the non-obtrusive evaluation, monitoring, and high-fidelity mapping of cardiac mechanical and electromechanical forces and central arterial blood pressure are presented herein. The sensor manufacturing process is also presented. Using accelerometers, the sensors register body-surface (preferably torso-surface) movements and vibrations generated by cardiac forces. The sensors may contain single-use or reusable components, which may be exchanged to fit different body sizes, shapes, and anatomical locations; they may be incorporated into clothing, bands, straps, and other wearable arrangements. The invention presents a practical, noninvasive solution for electromechanical mapping of the heart, which is useful for a wide range of healthcare applications, including the remote monitoring of heart failure status and the guidance of cardiac resynchronization therapy. Exercise and cardiovascular fitness tracking applications are also presented.

A method of forming an implant having a porous region replicated from scanned bone, the method comprising imaging bone with a high resolution digital scanner to generate a three-dimensional design model of the bone; removing a three-dimensional section from the design model; fabricating a porous region on a digital representation of the implant by replacing a solid portion of the digital implant with the section removed from the digital representation; and using an additive manufacturing technique to create a physical implant including the fabricated porous region.

Methods, apparatus, kits and systems are presented for determining the intraoperative position of at least a first anatomic location of a surgical patient and optionally for measuring the distance between at least first and second anatomic locations of a surgical patient.

The present invention tackles the challenging anatomic characteristics of the coronary artery disease in the bifurcation point and the origin of side-branch. The invention has a specifically designed angioplasty balloon catheter, particularly the balloon shape and profile, to be used in the diseased vessels at these difficult anatomic locations. In stent implanting into a coronary artery, a balloon catheter application is an inseparable requirement. A stent is a passive device that cannot be deployed in a diseased or stenosed artery without a pre-stent, with-stent and / or post-stent balloon dilatation. In majority (more than 95%) of available coronary stents, a stent is deployed by balloon expandable mode, meaning that the stent is delivered and expanded inside a vessel lumen by expanding a delivery balloon. This is done by crimping a stent over a folded balloon for delivery into a coronary artery. When expanded by balloon inflation, a stent is expanded and shaped passively by the inflated balloon shape and profile. The balloon catheter is designed to do angioplasty in the bifurcation and side-branch anatomy of coronary arteries, while minimizing the side effect. This specially designed balloon catheter is not only for balloon angioplasty dilatation of the bifurcation and side-branch anatomy, but is also for delivering and deploying specially designed bifurcation or side-branch stents into these difficult anatomic locations, as a stent delivery system.

Disclosed herein are heretofore undescribed preparations of highly concentrated, solubilized proteins, such as but not limited to, Bone Morphogenetic Proteins. Such protein preparations can be formulated in an aqueous carrier at protein concentrations in excess of 10 mg / ml when using the methods of manufacture taught herein. Such methods yield stable protein preparations in either solubilized or lyophilized form. The protein preparations of the present invention are particularly beneficial when administered either locally or systemically, in part, because low administration volumes can be accomplished. This is especially important for local treatment of certain anatomic locations such as, for example, the synovial fluid of a joint when treating osteoarthritis with BMP-7 or the intradiscal space when treating degenerative disc disease with BMP-7.

The present invention tackles the challenging anatomic characteristics of the coronary artery disease in the bifurcation point and the origin of side-branch. The invention has a specifically designed angioplasty balloon catheter, particularly the balloon shape and profile, to be used in the diseased vessels at these difficult anatomic locations. In stent implanting into a coronary artery, a balloon catheter application is an inseparable requirement. A stent is a passive device that cannot be deployed in a diseased or stenosed artery without a pre-stent, with-stent and / or post-stent balloon dilatation. In majority (more than 95%) of available coronary stents, a stent is deployed by balloon expandable mode, meaning that the stent is delivered and expanded inside a vessel lumen by expanding a delivery balloon. This is done by crimping a stent over a folded balloon for delivery into a coronary artery. When expanded by balloon inflation, a stent is expanded and shaped passively by the inflated balloon shape and profile. The balloon catheter is designed to do angioplasty in the bifurcation and side-branch anatomy of coronary arteries, while minimizing the side effect. This specially designed balloon catheter is not only for balloon angioplasty dilatation of the bifurcation and side-branch anatomy, but is also for delivering and deploying specially designed bifurcation or side-branch stents into these difficult anatomic locations, as a stent delivery system.

Methods are provided for generating intraluminal prosthetic implants designed to fit onto specific anatomical locations within regions which are stable in terms of their motion in time.

A catheter is used to assist in imaging, e.g., 3D imaging, an anatomical location in a human or veterinary subject. The catheter includes a plurality of horizontal markings which extend in the longitudinal direction between the distal and proximal ends. The horizontal markings can be made throughout the entire length of the catheter, or at one or more locations. At each location, the horizontal markings will appear as successive sets of markings. Each horizontal marking is made of two markings that are the same length. The two markings are arranged such that identically sized gaps between the ends of the markings are positioned on the front and back side of the catheter. In one embodiment, an image where the source and catheter are precisely aligned will show gaps of succeeding larger or smaller sizes. However, when the source is off center the gap lengths will be smaller or not exist. Particular marking locations can be highlighted by using relatively thinner or thicker markings and / or by spacing the markings progressively closer together or further apart.

A plurality of sets of volume data, each of which represent the state of a beating heart in different phases, are obtained. Coronary artery regions are extracted from at least two sets of volume data from among the obtained sets of volume data. A plurality of analysis points are set in each extracted coronary artery region. Correlations are established among analysis points set at the same anatomical positions within the coronary artery regions. Index values that indicate the character of plaque are calculated at each analysis point within all of the coronary artery regions. The character of plaque is evaluated at positions within the coronary artery regions, by integrating the index values calculated at the analysis points corresponding to each of the positions. The evaluation results regarding the character of plaque at each of the positions within the coronary artery regions are output, correlated with information regarding the positions.

A radiopaque marker for more effectively orienting a fluoroscopy image to a patient's body position is disclosed. A method for orienting a radiological image with a patient's anatomical position comprises the step of forming a marker with a first side indicator and a second side indicator formed substantially opposite the first side indicator. A device in accordance with the present invention comprises a radiopaque marker comprising a first side indicator, a second side indicator, and a humanoid shape.

An orthopedic fixation system fuses bone, bones, or bone pieces in a predetermined anatomical position. The orthopedic fixation system includes an implant that transitions between an unconstrained shape and a constrained insertion shape, a drill guide, first and second K-wires, and a cannulated drill bit. The drill guide and the first and second K-wires retain the bone, bones, or bone pieces in an anatomical position corresponding with the predetermined anatomical position. The cannulated drill bit fits over the first and second K-wires and drills, respectively, first and second drilled holes into the bone, bones, or bone pieces. After insertion of the implant into the first and second drilled holes, the implant attempts to transition from its constrained insertion shape to its unconstrained shape such that the implant continuously compresses the bone, bones, or bone pieces thereby holding the bone, bones, or bone pieces in the predetermined anatomical position.

The present invention, when used by a live actor, allows users to safely simulate hemorrhaging in some of the most challenging blood vessels in the most challenging anatomical locations such as the carotid artery, the axillary artery, and the inguinal artery. The present invention further provides the ability for users to safely perform hemorrhage control procedures, such as compression and ligation. The simulated wound of the present invention may be compressed to control hemorrhage. The simulated wound receptacle of the present invention may be packed with hemostatic or simple gauze to control hemorrhage. The simulated blood vessel of the device may be ligated with hemostats or other ligating instruments or material and bandaged with pressure dressings to control hemorrhage.

Deep fascia anchors provide a convenient way to bring fascia back to its anatomic location, thereby avoiding many of the problems and complications with current approaches. In the preferred embodiment, the anchors are made of a silastic or biodegradable material utilizing a design which mimics the spinous process. The anchors may attach to any suitable form of instrumentation, including rods, plates, and so forth. The anchors are adjustable to suit different mechanical structures. Anchors according to the invention include two opposing flexible arms which wrap around and lock on to the instrumentation, with a center tip portion preferably including attachment points or holes to which the deep fascia may be attached, much like the natural spinous process. Multiple anchors may be used according to the invention as dictated by the length of the instrumentation, and varying sizes and shapes may be provided to mimic anatomic differences in location (i.e., cervical, thoracic, lumbar) and patient (i.e., child, adolescent, adult, male / female).

The invention discloses an experimental animal fixing device, comprising a platform with a supporting leg. A through hole is arranged on the platform. The front of the platform is provided with a detachable rod, while the back of the platform is provided with a fixer. The position of the fixer corresponds to the hole. The experimental animal fixing device of the invention is multifunctional and very helpful for some specialist surgical experiments. Additionally, the experimental animal fixing device can effectively fix a specific anatomic location, and realize the function of an ordinary fixed table on limbs fixation.

There is provided herein a system and a method for guiding insertion of a gastroenteral tube including: an electromagnetic field generator configured to generate an electromagnetic field covering a treatment area; wherein said electromagnetic field generator is external to the patient; a registration sensor configured to mark anatomic locations on the patient's torso; a gastroenteral tube comprising a tip sensor configured to sense its position and / or orientation relative to the electromagnetic field generator; and a processing circuitry configured to: calculate an orientation of the subject relative to the field generator based on the anatomic locations marked by the registration sensor, load a predefined anatomic map representing a torso; aligning the map based on the anatomic locations marked by the registration sensor, and showing on the map a path of the gastroenteral tube insertion; wherein the path is generated according to changes in the strength of the electromagnetic field sensed by the tip sensor's during the insertion of the gastroenteral tube, independent of the subject's movement and independent of deviations in the position and / or orientation of said field generator.

An emergency cardiac and electrocardiogram (ECG) electrode placement device is disclosed herein. The emergency cardiac and electrocardiogram (ECG) electrode placement device incorporates electrical conducting materials and elastic material into a pad that is applied to a chest wall of a patient, which places multiple electrodes in the appropriate anatomic locations on the patient to quickly obtain an ECG in a pre-hospital setting.

Identifying target anatomic locations in a subject's body, and delivering medicinal substances thereto, following transtissual progression (penetrating, cutting through body tissue) and reaching body tissue with medical device distal tip. Involves acquiring mechanical properties of body tissue. Exemplary medicinal substance is, or includes, a drug (anesthetic agent), and exemplary target anatomic location is epidural space in subject's body. Exemplary system includes: cannular member enclosing cannula lumen; pusher-probe having distal end in cannula lumen and positionable from retracted to protruding positions, wherein pusher-probe distal end protrudes out of cannula distal end; and extending mechanism including cam member, a follower shiftable from first to second stations on cam member, and plunger selectively traveling in cannula lumen while forcing relative motion between cam member and follower, wherein pusher-probe distal end repositions between retracted and protruding positions. Optionally, includes data-information analyzing device having triggering mechanism via a winged hub member and associated components.

The present invention provides a medical needle assembly which has a removable at will needle hub for a spinal needle, which can be used to access the epidural or subarachnoid space of the spinal cord. This improvement in spinal needle design allows and facilitates the use of the medical needle for the purposeful creation of a subcutaneous tunnel and the placement of a catheter, or drain, or electrical wire lead which extends to an anatomic location remote from the original surgical incision site.The medical needle assembly has unique features and capabilities: a removable at will needle hub, which not only allows the surgeon to use the epidural / spinal needle initially to access the epidural or subarachnoid space of the spinal cord; but also permits the surgeon to use the same medical needle assembly again as a tunneling instrument. This allows the surgeon to perform the process of subcutaneous tunneling safely and in a manner previously considered to be surgically improbable.

Disclosed is a manufacturing method of a skull guiding formwork for calvarium reconstruction surgery. The manufacturing method includes building a three-dimensional outline model of a skull of a patient; predicting a surgical objective model; determining a cutting path of craniotomy and the quantity and the shapes of bone flaps required to be cut and cutting and obtaining the bone flaps according to the cutting path; building a three-dimensional cutting guiding formwork model; designing splicing structures among the bone flaps and building a three-dimensional splicing guiding formwork model; and manufacturing a cutting guiding formwork and a splicing guiding formwork according to the cutting guiding formwork model and the splicing guiding formwork model. The skull guiding formwork for calvarium reconstruction surgery comprises the cutting guiding formwork and the splicing guiding formwork, and an outline of an edge of a cutting guiding formwork body shows the cutting path during surgery; and a mortise connecting structure which is spliced with the adjacent splicing guiding formwork or a skull base is arranged at the outer edge of a splicing guiding formwork body. The manufacturing method has the advantages that important anatomy position can be protected during surgery, excessive cutting to the bone flaps is avoided, and the manufacturing method is favorable for postoperation recovery and healing.

A method and system of and for securing a lumen or catheter, after placement in a patient, to prevent unwanted removal or dislodgement of the lumen or catheter caused by patient movement and / or further medical interventions such as cardiopulmonary chest compressions, electrical defibrillation, surgical procedures, and the like. The method and system comprising simple and sterile materials that preclude the use of excessive suturing and ineffective ad-hoc methods with tape and gauze. The catheter is secured by a rubber on plastic frictional force and will resist external forces while preventing the tube structure from bending and subsequent occlusion. The device can be comfortably attached to the patient in all of the anatomical locations typically targeted for large catheter installment. The method of securement is rapid and requires only a single personnel to handle the device and the catheter tube simultaneously.

An interchangeable orthopedic blade that includes an internal portion and an external portion. The internal portion threads onto either a pre-installed K-wire or a pre-installed screw so as to more accurately place the interchangeable orthopedic blade in, without excessive damage to, the bone when repairing a fracture in the bone, and ultimately providing absolute stable fixation by the interchangeable orthopedic blade holding the fracture in its anatomic position and resisting applied forces while healing, to thereby provide a stable anatomic restoration and eliminate a need for revision surgery due to failure of fixation or malunion. The internal portion is received in the external portion, and rotates relative to the external portion, but has the external portion move non-rotatably axially with the internal portion into the bone as the internal portion threads onto either the pre-installed K-wire or the pre-installed screw.

Modular, miniaturized cardiovascular sensors, systems, methods, and wearable devices for the non-obtrusive evaluation, monitoring, and high-fidelity mapping of cardiac mechanical and electromechanical forces and central arterial blood pressure are presented herein. The sensor manufacturing process is also presented. Using accelerometers, the sensors register body-surface (preferably torso-surface) movements and vibrations generated by cardiac forces. The sensors may contain single-use or reusable components, which may be exchanged to fit different body sizes, shapes, and anatomical locations; they may be incorporated into clothing, bands, straps, and other wearable arrangements. The invention presents a practical, noninvasive solution for electromechanical mapping of the heart, which is useful for a wide range of healthcare applications, including the remote monitoring of heart failure status and the guidance of cardiac resynchronization therapy. Exercise and cardiovascular fitness tracking applications are also presented.

The present invention provides a medical needle assembly which has a removable at will needle hub for a spinal needle, which can be used to access the epidural or subarachnoid space of the spinal cord. This improvement in spinal needle design allows and facilitates the use of the medical needle for the purposeful creation of a subcutaneous tunnel and the placement of a catheter, or drain, or electrical wire lead which extends to an anatomic location remote from the original surgical incision site.The medical needle assembly has unique features and capabilities: a removable at will needle hub, which not only allows the surgeon to use the epidural / spinal needle initially to access the epidural or subarachnoid space of the spinal cord; but also permits the surgeon to use the same medical needle assembly again as a tunneling instrument. This allows the surgeon to perform the process of subcutaneous tunneling safely and in a manner previously considered to be surgically improbable.