166results about "Surgery" patented technology

A stent delivery system and method for intraluminal delivery and deployment of a self-expanding prosthesis at a site within a body canal is provided. The delivery system comprises a housing removably attached to a delivery tool. The housing stores the self-expanding prosthesis in an expanded state. The delivery tool has a catheter assembly with a capture zone. The capture zone receives and contains the self-expanding prosthesis in a compressed state. A securing mechanism couples the catheter assembly to the self-expanding prosthesis, wherein the securing mechanism transfers the self-expanding prosthesis from the housing to the capture zone immediately prior to the delivery and deployment procedure.

An intraluminal device is provided with a porous structure. The porous structure may be loaded with a bioactive substance to treat surrounding tissues after the intraluminal device has been implanted. The porous structure may be made by depositing a metal film on a foam structure using chemical vapor deposition. Porous structures may also be made by sintering or applying a ceramic layer to the intraluminal device. An intraluminal device is also provided with a ceramic material applied to generally straight portions of the device structure but not to portions adapted to bend. One advantage is that the ceramic material is less likely to fracture since it is applied to regions that experience less strain.

A gastrostomy device includes a tubular portion and an internal bolster having a radial wing secured to the tubular portion. The internal bolster is flexible and permits elastic deformation between a first orientation with the wing wrapped into a generally cylindrical configuration and a second orientation with the wing unfuried. A constraining member encases the internal bolster to retain the internal bolster in the first orientation and to cover at least a major portion of the wrapped wing. Removal of the casing permits the internal bolster to move from the first orientation to the second orientation. The internal bolster may be deployed by a ripcord, freeing the internal bolster into the patient' stomach and deploying the internal bolster to the second orientation. Alternatively, the internal bolster may be deployed by the constraining member being dissolved by the patient's bodily fluids located inside the patient's stomach.

An intra-oral cavity device for preventing contact between upper and lower teeth of an anesthetized patient. The device includes an elongate pillow that when gripped between the teeth of a patient, prevents contact between the teeth and/or gums and thereby prevents damage to the teeth and/or gums. The pillow may be made of a fibrous, porous and/or absorbent material. The device is adapted for single use and thus disposal after use by a patient. A method of the use of performing surgery using such a device is also provided.

Retrievable intravascular filters for insertion within a blood vessel are disclosed. A retrievable intravascular filter in accordance with an illustrative embodiment of the present invention includes an apical head operatively coupled to a number of elongated filter legs that can be used to collect blood clots contained within a blood vessel. A bendable anchoring member coupled to or formed integrally with one or more of the elongated filter legs can be used to temporarily or permanently secure the intravascular filter to the wall of the blood vessel.

The invention is a dilation catheter which comprises an elongated catheter shaft, a guide wire tube, and an angioplasty balloon. The distal end of the balloon is attached to the distal portion of the guide wire tube, and the proximal portion of the balloon is attached to the distal portion of the catheter shaft. A stiffening wire is attached to the inner wall of the catheter shaft at a plurality of points along its length. The distal extremity of the guide wire tube is decreased in size relative to the proximal portion of the guide wire tube. A fluid is contained within the guide wire lumen.

A correcting portion of an endoscope subjects a reference image to a magnification correction process so that the distance between a first mark and a second mark within the reference image is substantially equal to the distance between a first mark and a second mark within a comparative image. Next, the corrected reference image is subjected to a rotation correction process so that the orientation of the second mark with respect to the first mark within the reference image is substantially equal to the orientation of the second mark with respect to the first mark image within the comparison image. Further, the corrected reference image is subjected to a brightness distribution correction process so that the brightness distribution thereof becomes equal to that of the comparison image. The display state of the reference image and comparison image are made substantially equal, comparative diagnosis is facilitated, and diagnostic efficiency is improved.

The present invention relates to systems and methods for photometric endoscope imaging. The methods can further include chromoendoscopy and computer aided detection procedures for the imaging of body lumens and cavities.

A retractor may be used during spinal surgery. The retractor may include a frame and one or more retractor blades. Each retractor blade may include a coupling arm, a retainer, and a retraction component. The coupling arms may be coupled to the frame such that the coupling arms are able to move inward or outwards relative to the frame. The retainer may secure the retraction component to the coupling arm. In some embodiments, the retraction blades may be made of a radiolucent material that allows radiological images to be taken during a surgical procedure with the retractor in place. A position of retraction components relative to the frame may be changed during a surgical procedure. One or more of the retraction components may be replaced during a surgical procedure without removing the retractor from the patient.

Endoscopic arrangement comprising a first distal end, an imaging device arranged at the first distal end, a first proximal end for connection to a supply unit, a data transmission element embodied as a light guide and having a second distal end and a second proximal end, and comprising an electro-optical converter, wherein the electro-optical converter is configured to convert digital data generated by the imaging device into an optical signal, wherein the data transmission element at its second distal end is optically coupled to the electro-optical converter for coupling the optical signal into the data transmission element, wherein the imaging device comprises at least two data outputs each having a digital output signal, and wherein a first signal converter is provided between the imaging device and the electro-optical converter for combining the digital output signals into a digital combined output signal.

The multi-section deployable and articulating endoscope is designed with tubing and flat cables that are small enough that the endoscope becomes a thin stick that is minimally invasive and usable with other devices in a common port. The endoscope includes very thin flat cables that are used for electrical connectivity and threaded above and below an articulation and deployment hinge for opening the endoscope passively using an adjustable tension spring, or by pulling on a first cable and closing the endoscope by pulling on a second cable, When in a tubular configuration the endoscope may be inserted into the port and an insufflation membrane inside the port forms an air seal with the endoscope, which aids in insufflation and desufflation.

The endoscope includes one or more tubes for creating an air jet stream above the camera to act as a shield for keeping the camera clean.

The present invention relates to management of information relating to medical fluids, containers therefor, and medical fluid administration devices for administering such medical fluids to patients. Data tags (e.g., RFID tags) are generally associated with containers of the invention and may be electromagnetically read from and/or written to using an electromagnetic device, for example, that may be associated with a medical fluid administration device of the invention.

Methods of controlling the degradation profile of a biodegradable stent scaffolding are disclosed. Disclosed methods include controlling features of the degradation profile including the time to loss of radial strength and the degradation time of the stent.

A light source locating and visualization apparatus comprises one or more than one LEDs capable to radiate a red light source with a wavelength of 600˜650 nm to locate superficial veins or specific structures; and a method of locating superficial veins with a LED light source comprises to proceed a skin-tightly radiating by using the source locating and visualization apparatus to emitting a red LED light source with wavelength of 600˜656 nm; to produce a lateral scattering and illumination effect by way of emitting red LED light source penetrating through a fat structure to cause reflection and scattering; and to locate superficial veins by naked eyes due to said superficial veins capable of absorbing red light spectrum easily and appearing as a located blood vessel shadow under the lateral scattering and illumination effect; therefore, physicians and nurse are capable by naked eyes to see the size, curve, and bifurcation of subcutaneous blood vessels visually and then select an appropriate injection position along the blood vessel for intravenous puncture easily.

A magnetically guidable medical device for use within the large intestine of a human body. A magnetically guidable guide wire is introduced into the rectum of a body of a patient and maneuvered through the colon under the influence of a controlled magnetic field to a desired location within the body of the patient. An external magnetic field applying means applies an external magnetic field effective to guide the magnetically guidable member within the body of the patient. A colonoscope is advanced over the guide wire so that the advancement and placement of the colonoscope is aided by the magnetically guided guide wire. Either or both the magnetically guidable guide wire and the colonoscope can be viewed using a fluoroscope to assist in positioning it within the body of the patient.

An intelligent tissue mimicking ultrasonic phantom, which is a temperature-sensitive polymer gel having the following acoustic properties and other physical characteristics: acoustic velocity: 1500-1550 m/s; acoustic impedance: (1.50−1.60)×10⁶ Pa·s/m; density: 1.01-1.06 g/cm³; and a denaturation temperature, namely, a Lower Critical Solution Temperature (LCST) or a Volume Phase Transition Temperature at which the volume of the phantom changes, adjustable by changing the ratio of raw materials, around which there is a reversible phase transformation between the opaque phase and the transparent phase. Said gel can be a polymer of isopropylacrylamide (NIPA). Said ultrasonic phantom has a transparent appearance, and an adjustable thermal denaturation temperature; the thermal denaturation region of the ultrasonic phantom is distinct and has a well-defined boundary; the material of the phantom is stable and deterioration-resistant, and can ensure the consistency of the quality; the phantom is thermal denaturable with the appearance thereof turning white, while the phantom recovers when the heat is removed, such that it can be used repeatedly.

The present disclosure suggests methods of selecting a stimulation site for stimulating a patient's brain or methods of effectuating a neural-function of a patient associated with an impaired body function. In one exemplary implementation, such a neural function may be effectuated by selecting a stimulation site, positioning at least a first electrode at the stimulation site, and applying an electrical potential to pass a current through the first electrode. If one aspect, this stimulation site may be selected by a) identifying a second body function that is a corollary to the impaired body function, and b) determining a corollary location of the patient's brain that is associated with the second body function and is ipsilateral to the impaired body function.

The present invention relates to a method for reducing adhesions associated with post-operative surgery. The present method comprises administering or affixing a polymeric composition preferably comprising chain extended, coupled or crosslinked polyester/poly(oxyalkylene) ABA triblocks or AB diblocks having favorable EO/LA ratios to a site in the body which has been subjected to trauma, e.g. by surgery, excision or inflammatory disease. In the present invention, the polymeric material provides a barrier to prevent or reduce the extent of adhesions forming.

A coaxial stabilizing and sealing catheter provides increased support to a guide catheter that is seated in an ostium of a branch artery by extending through and out of a distal end of the guide catheter and anchoring in position within the vessel that is being treated. The stabilizing and sealing catheter includes, as part of a relatively flexible distal section, a balloon that locks the distal end of the stabilizing and sealing catheter in place to provide support to the therapeutic devices that are introduced and further seals the artery to prevent blood from entering the artery. A sealing cuff at a proximal end of the stabilizing and sealing catheter provides a seal between the exterior of the stabilizing and sealing catheter and the interior of the guide catheter. In addition, a fixing mechanism it utilized to lock the guide catheter in place to exchange therapeutic devices.

In various embodiments, a phacoemulsification cutting tip with a straight shaft and an angled portion off of the straight shaft may include a hook on the angled portion to move an axis of rotation of the cutting tip closer to alignment with an extended centerline of the shaft. The cutting tip may be configured to torsionally rotate back and forth on an axis perpendicular to a centerline of the shaft (e.g., rotation around a y-axis). In some embodiments, lateral vibrations (e.g., side to side along an x-axis or z-axis perpendicular to the y-axis) that result from torsional rotation around the y-axis in a cutting tip without the hook may be reduced through use of the hook to balance the otherwise eccentrically weighted hook.

A method and apparatus for projecting an image of a patient to intersect a display screen which is nonperpendicular to an adjacent portion of an optical path and adjacent a sterile operative field. A video projector system and accompanying optics impart at least one of a tilted focal plane or depth of focus to the projected image. The optical path of the projected image is located adjacent the surgical field. An initially sterile display screen is located in the optical path adjacent the sterile field so that a normal to the screen is noncoincident with the optical path and the projected image on the screen is of constant focus across the screen. The initially sterile display screen may be degradable upon cleaning and resterilization so that a new screen must be used with each procedure, thus insuring the optical quality and sterility of the screen. The display screen may be supported adjacent the surgical field by an articulated rod assembly. The rod assembly may have an upper rod shaped like a "dog leg" for providing easy access by the surgical team for rotating and moving the system up and down. A lower rod of the rod assembly may be connected to the upper rod with a universal joint for adjusting screen location and quickly moving the display screen out of the surgical field.

The exemplary embodiments illustrated provide the discovery of systems, methods, and apparatuses of endoscope stabilization devices for use with, for example, slim scopes, so as to provide, for example, a flexible outer structure capable of bending and holding a fixed position so as to provide, for example, support to make cannulation with a slim scope and target anatomy easier and more efficient.

The invention is applicable to the technical field of medical image processing and application, and provides a marker point registration method and device and a surgical navigation system. The method comprises that a space positioning error of each physical space marker point is calculated according to physical coordinate values of physical space marker points obtained many times and the average value of the physical coordinate values; a weight matrix of the physical space marker point is calculated according to the space positioning error; according to the average value of the physical coordinate values of the physical space marker points, and the average value of image coordinate values of the image space marker points, by combining the weight matrix, under the premise that the minimum marker point registration error FRE is ensured, a translation vector t and a rotation matrix R are solved by an iterative method. According to the utility model, the anisotropic nature of the space positioning error of the optical positioning system can be fully considered, so that the navigation accuracy of the entire surgical navigation is improved finally.