Abstract:
A surgical stereoscopic visualization system having a microscope head, dual cameras mounted on or proximate the microscope head for real time video capture of a subject in an operative field, a video processing and display system to receive separate video streams from the cameras and to combine the separate video streams into a time-aligned stereoscopic image. The processed image is displayed on a matrix display screen in at least one movable head-mounted stereoscopic display. Movement of the head mounted display is accomplished with a support structure on a headband that accurately positions the display screen in front of the user's eyes, yet allows the user to precisely move the display screen either manually or by motorized means into and out of the user's line of sight, thereby facilitating uninterrupted use of the hands while working in the surgical suite.
Abstract:
A surgical stereoscopic visualization system having a microscope head, dual cameras mounted on or proximate the microscope head for real time video capture of a subject in an operative field, a video processing and display system to receive separate video streams from the cameras and to combine the separate video streams into a time-aligned stereoscopic image. The processed image is displayed on a matrix display screen in at least one movable head-mounted stereoscopic display. Movement of the head mounted display is accomplished with a support structure on a headband that accurately positions the display screen in front of the user's eyes, yet allows the user to precisely move the display screen either manually or by motorized means into and out of the user's line of sight, thereby facilitating uninterrupted use of the hands while working in the surgical suite.
Abstract:
A method of performing cryotherapy on a patient can include positioning an outer surface of a distal portion of a cryotherapy catheter in contact with body tissue to be treated; performing a treatment phase, including regulating a temperature of the outer surface at a treatment value for a first period of time; performing a recovery phase comprising allowing the temperature of the outer surface to warm up to a recovery value that is higher than treatment value but substantially lower than a normal body temperature of the patient; and performing one or more additional treatment phases for a second period of time. Each of the first and second periods of time can be selected to allow a cold front having a cold front temperature to propagate from the outer surface and through a therapeutic portion of a thickness of the body tissue, but not substantially beyond the thickness.
Abstract:
An asset management system (100) is disclosed, and is adapted for use to rate the condition of a physical asset component, such as a roof (102), estimate the service life of the asset, and provide a basis for decisions regarding the selection of repair alternatives and/or replacement options associated with the asset. Rating and evaluation of the asset is initiated by an operator (104) performing a “survey” of the asset to determine problem defects. Data representative of such defects is entered into the memory of an instrument (106) and transmitted to a central processing system (108). The central processing system (108) is adapted to allow the user to selectively review and evaluate the impact and financial feasibility of alternative repair and replacement options relating to the problems or defects associated with the asset.
Abstract:
A securement assembly for releasably securing an expandable stent or stent-graft relative to a delivery tube. The securement assembly comprises a belt base configured for securement relative to the delivery tube. The belt base defines a release member passage and a receiving portion. A first end of a belt is fixed relative to the belt base. The opposite end of the belt includes a retainment portion configured to releasably engage the receiving portion of the belt base. A release member is removably positioned through the release member passage and aligned with the belt retainment portion such that the retainment portion is maintained engaged with the receiving portion until the release member is moved to a non-aligned position. A method of releasably securing a portion of an expandable stent or stent-graft relative to a delivery tube is also provided.
Abstract:
A branch graft stent system includes a tubular primary graft having a branch graft opening which when deployed is located in alignment with a side branch vessel emanating from the primary vessel in which a branch graft is deployed. A connector (flange) member forms a perimeter of the branch graft opening and is constructed so that the connector member is substantially flush with the wall of the tubular primary graft. The tubular branch graft has a first expandable ring and a second expandable ring spaced apart from each other as part of a connection section located at a proximal end of the tubular branch graft. The first expandable ring, the second expandable ring, and graft or other material spaced between the first expandable ring and the second expandable ring when engaged with the perimeter of the branch graft opening of the primary graft, the assembly forms a flexible sealed connection between the primary graft and branch graft lumens to continue to exclude the aneurysm while providing a conduit for blood flow to the branch vessel. A distal end of the branch graft can be anchored by a balloon expandable or a self-expanding stent to the wall of the branch vessel beyond the aneurysm.
Abstract:
A branch graft stent system includes a tubular primary graft having a branch graft opening which when deployed is located in alignment with a side branch vessel emanating from the primary vessel in which a branch graft is deployed. A connector (flange) member forms a perimeter of the branch graft opening and is constructed so that the connector member is substantially flush with the wall of the tubular primary graft. The tubular branch graft has a first expandable ring and a second expandable ring spaced apart from each other as part of a connection section located at a proximal end of the tubular branch graft. The first expandable ring, the second expandable ring, and graft or other material spaced between the first expandable ring and the second expandable ring when engaged with the perimeter of the branch graft opening of the primary graft, the assembly forms a flexible sealed connection between the primary graft and branch graft lumens to continue to exclude the aneurysm while providing a conduit for blood flow to the branch vessel. A distal end of the branch graft can be anchored by a balloon expandable or a self-expanding stent to the wall of the branch vessel beyond the aneurysm.