Abstract: Transvaginal and/or transcervical fetal oximetry probes may be configured to take measurements in the endocervical canal of a pregnant mammal that may be used to determine a fetal hemoglobin oxygen saturation level using, for example, oximetry, pulse oximetry, and/or tissue oxygen saturation calculations. Transurethral fetal oximetry probes may be configured to be inserted into a urethra of a pregnant mammal and be positioned proximate to a wall of a bladder of the pregnant mammal proximate to the fetus. Once in position, the Transurethral fetal oximetry probe may take measurements that may be used to determine a fetal hemoglobin oxygen saturation level using, for example, oximetry, pulse oximetry, and/or tissue oxygen saturation calculations.

Abstract: Systems, devices, and methods for performing trans-abdominal fetal oximetry and/or trans-abdominal fetal pulse oximetry using physiological characteristics and/or a calibration factor may receive a physiological characteristic of a pregnant mammal and determine one or more potential impact(s) of the physiological characteristic on a behavior of an optical signal projected into the abdomen of the pregnant mammal Then a calibration factor for the optical signal responsively to the impact. The calibration factor may then be used to calibrate a fetal detected electronic signal so that a level of fetal hemoglobin oxygen saturation may be determined.

Abstract: A method of ablating a uterine fibroid using a particular trocar is disclosed. The trocar comprises a plurality of ablation stylets. The trocar is adjustable to assume a plurality of configurations, each of the configurations having the stylets extended to a different extent from the trocar. A region to he ablated is imaged, The size of the region to be ablated is noted. The size of the region to be ablated is compared to a matrix of known ablation regions, each of the known ablation regions being associated with one of the configurations of the particular trocar. The region to be ablated is associated with a most nearly matching known ablation region by comparison of the region to be ablated to the known ablation regions. A trocar is inserted into the uterine fibroid at a position, which more closely matches the position of the particular trocar with respect to the known ablation region. The stylets are deployed from the trocar to an extent corresponding to the configuration.

Abstract: A method of ablating a uterine fibroid using a particular trocar is disclosed. The trocar comprises a plurality of ablation stylets. The trocar is adjustable to assume a plurality of configurations, each of the configurations having the stylets extended to a different extent from the trocar. A region to he ablated is imaged. The size of the region to be ablated is noted. The size of the region to be ablated is compared to a matrix of known ablation regions, each of the known ablation regions being associated with one of the configurations of the particular trocar. The region to be ablated is associated with a most nearly matching known ablation region by comparison of the region to be ablated to the known ablation regions. A trocar is inserted into the uterine fibroid at a position, which more closely matches the position of the particular trocar with respect to the known ablation region. The stylets are deployed from the trocar to an extent corresponding to the configuration.

Abstract: A method of ablating a uterine fibroid using a particular trocar is disclosed. The trocar comprises a plurality of ablation stylets mounted for movement from within the trocar to positions extending from the trocar. The trocar is adjustable to assume a plurality of configurations, each of the configurations having the stylets extended to a different extent from the trocar. A region to be ablated is imaged. The region may correspond to all or a portion of a uterine fibroid. The size of the region to be ablated is noted. The size of the region to be ablated is compared to a matrix of known ablation regions, each of the known ablation regions being associated with one of the configurations of the particular trocar, and each of the known ablation regions being associated with a position of the trocar relative to the known ablation region. The region to be ablated is associated with a most nearly matching known ablation region by comparison of the region to be ablated to the known ablation regions.

Abstract: A method of ablating a uterine fibroid using a particular trocar is disclosed. The trocar comprises a plurality of ablation stylets mounted for movement from within the trocar to positions extending from the trocar. The trocar is adjustable to assume a plurality of configurations, each of the configurations having the stylets extended to a different extent from the trocar. A region to be ablated is imaged. The region may correspond to all or a portion of a uterine fibroid. The size of the region to be ablated is noted. The size of the region to be ablated is compared to a matrix of known ablation regions, each of the known ablation regions being associated with one of the configurations of the particular trocar, and each of the known ablation regions being associated with a position of the trocar relative to the known ablation region. The region to be ablated is associated with a most nearly matching known ablation region by comparison of the region to be ablated to the known ablation regions.

Abstract: A cryosurgical system using a low-pressure liquid nitrogen supply, which requires only 0.5 to 15 bar of pressure to provide adequate cooling power for treatment of typical breast lesions. The pressure may be provided by supplying lightly pressurized air into the dewar, by heating a small portion of the nitrogen in the dewar, or with a small low pressure pump.

Abstract: A medical device, such as a cryogenic biopsy device, includes a disposable unit and a reusable unit. The disposable unit, such as a treatment needle or probe, is at least partially insertable into the body of a medical subject and includes an encodable device for storing information. The reusable unit is connectable to the disposable unit and includes a controller. The disposable unit transfers the information to the controller in the reusable unit. The controller then directs activities of the medical device in response to the information stored in the disposable unit.

Abstract: A cryosurgical system using a low-pressure liquid nitrogen supply, which requires only 0.5 to 1 bar of pressure to provide adequate cooling power for treatment of typical breast lesions. The pressure may be provided by supplying lightly pressurized air into the dewar, by heating a small portion of the nitrogen in the dewar, or with a small low pressure pump.

Abstract: A cryoprobe having an exhaust heater placed in fluid communication with exhausting cryogen to heat the cryogen prior to being vented to the atmosphere.

Abstract: A cryoprobe for use in cryosurgery and other applications comprising a rigid outer tube, an inner coolant inlet tube a short rigid penetrating segment extending distally from the distal end of the outer tube and a helical-shaped baffle having a heating element disposed about the outer surface of the inlet tube. The baffle is adapted to produce turbulent fluid flow improving heat transfer and is able to warm target tissue during rapid freezing and thawing cycles.

Abstract: A biopsy device comprising a housing and a releasable coring module having an internal needle adapted for securing a suspect mass to the internal needle and an external cutting cannula adapted to slide over the internal needle to cut the suspect mass from any surrounding tissue.

Abstract: Embodiments of the present invention relate to a sensor for facilitating detection of a physiological characteristic of a patient. Specifically, one embodiment includes a detector configured to obtain signals from the patient, the signals being indicative of the physiological characteristic and to send the signals to a monitor, and a sensor memory coupled with the sensor and separate from the monitor, the sensor memory storing patient physiological data derived by the monitor from the signals, the patient physiological data being indicative of the physiological characteristic.

Abstract: A device for biopsy of body tissue. The device is driven by liquid CO2, and is provided with a control system to control various components to effectuate rotating core biopsies.

Abstract: An improved electromagnetic shield for a photodetector which uses a wire mesh screen laminated to an insulating layer. A portion of the wire mesh screen and laminated layer sandwich can then be cut out to provide an individual electromagnetic shield. The sandwich combination is flexible, and can be easily wrapped around the photodetector. Preferably, an adhesive is on one side of the insulating layer, to allow the wrapped combination to adhere to the photodetector.

Abstract: A conformable sensor which uses a flexible substrate, preferably a polyester strip is disclosed. The emitter and detector are mounted on one portion of the strip with conductive traces connecting to them. The second portion of the strip is folded over to cover the emitter and detector and traces, with openings for the emitter and detector. A conductive coating is applied to the strip to provide shielding from electromagnetic interference. Preferably, a second portion of the strip, which folds over the first portion, also has a Faraday shield covering the opening over the detector. The detector and emitter semiconductor chip die (rather than use encapsulated chips) may be mounted directly on the polyester strip so that it is in contact with one of the conductive traces.

Abstract: A conformable sensor which uses a flexible substrate, preferably a polyester strip is disclosed. The emitter and detector are mounted on one portion of the strip with conductive traces connecting to them. The second portion of the strip is folded over to cover the emitter and detector and traces, with openings for the emitter and detector. A conductive coating is applied to the strip to provide shielding from electromagnetic interference. Preferably, a second portion of the strip, which folds over the first portion, also has a Faraday shield covering the opening over the detector. The detector and emitter semiconductor chip die (rather than use encapsulated chips) may be mounted directly on the polyester strip so that it is in contact with one of the conductive traces.

Abstract: A conformable sensor which uses a flexible substrate, preferably a polyester strip is disclosed. The emitter and detector are mounted on one portion of the strip with conductive traces connecting to them. The second portion of the strip is folded over to cover the emitter and detector and traces, with openings for the emitter and detector. A conductive coating is applied to the strip to provide shielding from electromagnetic interference. Preferably, a second portion of the strip, which folds over the first portion, also has a Faraday shield covering the opening over the detector.

Abstract: A pulse oximeter sensor that is designed to surround an appendage of the patient, such as a finger, toe or foot is disclosed. The sensor has a reusable member which preferably includes a photodetector. A disposable, flexible member preferably contains the photoemitter and can be wrapped around the patient's appendage to secure it to the appendage and the reusable member. When secured, the photoemitter and photodetector end up on opposite sides of the appendage. The disposable member connects to the reusable member to establish electrical contact. The reusable member is connected to a cable which can be plugged into a sensor monitoring system.

Abstract: A pulse oximeter sensor that is designed to surround an appendage of the patient, such as a finger, toe or foot is disclosed. The sensor has a reusable member which preferably includes a photodetector. A disposable, flexible member preferably contains the photoemitter and can be wrapped around the patient's appendage to secure it to the appendage and the reusable member. When secured, the photoemitter and photodetector end up on opposite sides of the appendage. The disposable member connects to the reusable member to establish electrical contact. The reusable member is connected to a cable which can be plugged into a sensor monitoring system.