Abstract:
A naso/orogastric device having backflow blocking means and comprises a naso/orogastric tube sized and shaped for being disposed within the esophagus so that at least a distal end thereof being placed in the stomach lumen of a patient, at least one elastic esophageal body, positioned along the naso/orogastric tube, having a pressure dependent volume, at least one esophageal sensor that detects fluid around at least one segment of the naso/orogastric tube, and a pressure regulator that regulates a pressure within the elastic esophageal body according to the detection.
Abstract:
Apparatus is provided for repairing a valve of a patient, the valve including an annulus and at least first and second leaflets. The apparatus includes at least a first discrete segment and a second discrete segment of an annuloplasty structure, each segment being shaped to provide a respective lateral wall, each lateral wall being shaped to define at least one lumen of the respective segment. The apparatus further includes at least a first and a second control wire, each control wire configured for sliding advancement through both the first and second segments. The first control wire is configured to control a relative disposition of a first end of the first segment and a first end of the second segment. The second control wire is configured to control a relative disposition of a second end of the first segment and a second end of the second segment. Other embodiments are also described.
Abstract:
Apparatus is provided for use with a subject's body, vagina, vaginal fornix, uterus, and uterine artery. A fornix-engaging structure is inserted into the vagina and engages the vaginal fornix. A rod is inserted into the subject's body via the fornix-engaging structure, such that a distal end of the rod passes through vaginal tissue at a first vaginal site until the distal end of the rod is at a first extrauterine site outside of the uterine artery, but in a vicinity of a portion of the uterine artery that supplies a uterine fibroid. A rod-guide is coupled to the fornix-engaging structure, and guides the distal end of the rod to the first extrauterine site. A uterine artery compression device is disposed on the distal end of the rod. Other embodiments are also described.
Abstract:
A method is provided, including distally advancing an implant through a urethra of a patient until the implant emerges in a bladder of the patient, and facilitating expanding of a pre-operative perimeter of a portion of the urethra to a post-operative perimeter of the portion of the urethra that is larger than the pre-operative perimeter by proximally retracting the implant and implanting the implant in prostate tissue surrounding the urethra. Other embodiments are also described.
Abstract:
An assisted anastomosis apparatus and a method thereby for reconnecting the urethral stump to the neck of the bladder after removal of the prostate during a prostatectomy, comprising two suture units, namely a urethral stump suturing unit (1a) and a bladder suturing unit (1b), at least a section of said urethral stump suturing unit (1a) has suitable dimensions to be introduced into a bladder neck and at least a section of said bladder suturing unit (1b) has suitable dimensions to be introduced into a urethral stump; such that each needle pulls the suture leading from its equivalent position on the urethral stump through the wall of the bladder neck.
Abstract:
Apparatus is provided, including a tube (421) shaped to define a tube lumen at least one implant (100) reversibly coupled to the tube (421), and configured for implantation within a body of a patient. The apparatus also comprises two or more longitudinal guide members (470) disposed at least in part along a distal portion of the tube (421), the longitudinal guide members (470) having distal portions thereof configured to be reversibly coupled to the implant (100), and arranged such that application of a force to a first one of the longitudinal guide members (470) steers the distal portion of the tube (421) toward a first location along the implant (100), and application of a force to a second one of the longitudinal guide members (470) steers the distal portion of the tube (421) toward a second location along the implant (100). Other embodiments are also described.
Abstract:
Apparatus is provided for use with a subject's body, vagina, vaginal fornix, uterus, and uterine artery. A fornix-engaging structure is inserted into the vagina and engages the vaginal fornix. A rod is inserted into the subject's body via the fornix-engaging structure, such that a distal end of the rod passes through vaginal tissue at a first vaginal site until the distal end of the rod is at a first extrauterine site outside of the uterine artery, but in a vicinity of a portion of the uterine artery that supplies a uterine fibroid. A rod-guide is coupled to the fornix-engaging structure, and guides the distal end of the rod to the first extrauterine site. A uterine artery compression device is disposed on the distal end of the rod. Other embodiments are also described.
Abstract:
An articulating medical instrument comprising of: a substantially straight proximal segment; a substantially straight distal segment; an articulation mechanism having a straight configuration in which the proximal and distal segments form a substantially straight line and at least one articulated configuration in which the proximal and distal segments form an articulation angle of less than 180 degrees between the segments, the articulation mechanism being configured for increasing or decreasing the articulation angle; and one or more drive mechanisms configured for transferring force from the proximal segment to the distal segment, wherein the drive mechanism does not follow substantially straight lines between the proximal and distal segments passing through the apex of the articulation angle.