Abstract: Apparatus and associated methods relate to a bi-directional conduit system including a core configured to traverse a container wall and having independent, substantially parallel lumens and a fitting fluidly connected to each lumen on each side of the wall. In an illustrative example, the conduit system may include at least one valve configured to selectively restrict fluid flow in at least one lumen. The core may be flexible. A coupling assembly may be configured to releasably couple the core to the wall. Apparatus and methods further relate to a system including a base module with a control input and a fluid transport system including an impeller powered by the base module to convey fluid via a conduit in response to the control input, wherein in a stowage mode, the base module is configured to store the conduit and to mechanically support, releasably coupled, the impeller to the base module.

Abstract: Systems and related methods for identifying and/or ablating targeted nerves are provided. A probe with stimulating electrodes and/or ablation members are provided. The probe may be inserted into a nasal cavity and current may be introduced through the electrodes to stimulate a targeted area. The response to stimulation may be used to identify the targeted nerve. Once identified, the ablation member may ablate the targeted nerve.

Abstract: Described here are methods and apparatuses for tracking a clot material within a lumen of a suction catheter. For example, an apparatus as described herein may include a flexible elongate body having a suction lumen, a first pair of electrodes within the suction lumen, a second pair of electrodes proximal to the first pair of electrodes, and a controller configured to track a clot material within the suction lumen based on signals from the first pair of electrodes and the second pair of electrodes.

Abstract: Apparatus and associated methods relate to an environmental control system including a fluid driver configured to releasably couple to a buoyant module. In an illustrative example, in a deployment mode, the fluid driver may be brought into register with and releasably coupled to the buoyant module. The fluid driver, for example, be supported by the buoyant module in a body of water. A control unit may, for example, selectively provide energy to the fluid driver such that the fluid driver induces fluid to flow from the body of fluid to a reservoir by a conduit. The control unit may be configured to mechanically support the fluid driver in a stowage mode. Various embodiments may advantageously allow a user to selectively deploy a livewell environment control from a stowed mode into a deployed mode.

Abstract: Described herein are methods and apparatuses for detecting an obstructive material within a lumen of an aspiration catheter using one or more sensors with the lumen of the suction catheter to prevent excess blood loss and improve operation of the apparatus.

Abstract: Described here are methods and apparatuses for tracking a clot material within a lumen of a suction catheter. For example, an apparatus as described herein may include a flexible elongate body having a suction lumen, a first pair of electrodes within the suction lumen, a second pair of electrodes proximal to the first pair of electrodes, and a controller configured to track a clot material within the suction lumen based on signals from the first pair of electrodes and the second pair of electrodes.

Abstract: In an example, a cryotherapy system includes a base station, a cryotherapy applicator, and a cryogen conduit configured to couple the cryotherapy applicator to the base station and supply a cryogen from the base station to the cryotherapy applicator. The base station includes a housing including a canister receptacle that is configured to receive a canister containing the cryogen. The cryotherapy applicator includes a handle, a shaft extending from the distal end of the handle, and an end-effector coupled to the shaft. The end-effector is configured to use the cryogen to ablate a target tissue. An entirety of the cryotherapy applicator is movable relative to an entirety of the base station while the cryogen conduit couples the cryotherapy applicator to the base station.

Abstract: Closure devices that selectively control blood flow between the right atrium and the left atrium of a heart of a patient. The control of blood flow can be based on detected values from a pressure sensor. The closure devices can include a body configured to engage native tissue when the device is deployed across the septal wall. In a first state at least a portion of (an inner surface of) a lumen is closed, preventing blood flow through the closure device. Ina second state, the lumen is open to enable blood flow from the left atrium to the right atrium. A closure element can be selectively adjusted to control the flow of blood through the lumen. A volume of an expandable chamber can be increased or decreased to place the closure device into the first state or the second state.

Abstract: The technology described herein can be embodied in a method that includes obtaining a representation of a first image of a surgical scene using electromagnetic radiation of a first wavelength range outside the visible range of wavelengths, wherein an amount of electromagnetic radiation of the first wavelength range received from a first tissue type is lower than that received for a second tissue type. The method also includes obtaining a representation of a second image using electromagnetic radiation of a second wavelength range outside the visible range of wavelengths, wherein an amount of electromagnetic radiation of the second wavelength range received from the second tissue type is substantially different from that received for the first tissue type. The visual representation of the surgical scene is rendered on the one or more displays using the representation of the first image and the representation of the second image.

Abstract: Devices and methods for treating rhinitis are provided. An integrated therapy and imaging device is provided for single handheld use. The device may have a hollow elongated cannula, a therapeutic element coupled to a distal portion of the cannula, an imaging assembly coupled to the cannula to provide visualization of the therapeutic element, and an articulating region operably coupled to the imaging assembly to articulate the imaging assembly. The imaging assembly may be articulated so as to translate vertically, laterally, axially, and/or rotationally.

Abstract: The present technology relates to intracardiac sensors and associated systems and methods. In some embodiments, the present technology includes a device for monitoring pressure within a patient's heart. The device can include an implantable capacitor having a capacitance value that is variable based on the pressure within the patient's heart and a sensing circuit configured to measure the capacitance value. The device can also include an implantable inductor and a power circuit configured to wirelessly receive power from an external source via the inductor. When the device is in a first configuration, the capacitor can be electrically coupled to the sensing circuit and the inductor can be electrically coupled to the power circuit. When the device is in a second configuration, the capacitor can be electrically coupled to the inductor to form a resonant circuit.

Abstract: The present technology relates to interatrial shunting systems and methods. In some embodiments, the present technology includes interatrial shunting systems that include a shunting element having a lumen extending therethrough that is configured to fluidly couple the left atrium and the right atrium when the shunting element is implanted in a patient. The system can also include an energy receiving component for receiving energy from an energy source positioned external to the body, an energy storage component for storing the received energy, and/or a flow control mechanism for adjusting a geometry of the lumen.

Abstract: The present technology relates to adjustable interatrial shunts that are configured to shunt blood between the left atrium and the right atrium. In particular, the adjustable interatrial shunts can include a flow control element moveable through a plurality of discrete position, with each discrete position being associated with a particular shunt geometry, and with each particular shunt geometry being associated with a different fluid resistance and/or relative drainage resistance through the shunt for a given pressure differential between the left atrium and the right atrium. The flow control element can be selectively moveable between the plurality of discrete positions by operation of an actuation assembly. In some embodiments, the adjustable interatrial shunts include a ratchet mechanism that controls the movement of flow control element through the plurality of discrete positions, and can hold or lock the shunt in a desired position or configuration.

Abstract: The technology described herein can be embodied in a method that includes obtaining a representation of a first image of a surgical scene using electromagnetic radiation of a first wavelength range outside the visible range of wavelengths, wherein an amount of electromagnetic radiation of the first wavelength range received from a first tissue type is lower than that received for a second tissue type. The method also includes obtaining a representation of a second image using electromagnetic radiation of a second wavelength range outside the visible range of wavelengths, wherein an amount of electromagnetic radiation of the second wavelength range received from the second tissue type is substantially different from that received for the first tissue type. The visual representation of the surgical scene is rendered on the one or more displays using the representation of the first image and the representation of the second image.

Abstract: The present technology relates to intracardiac sensors and associated systems and methods. In some embodiments, the present technology includes a device for monitoring pressure within a patient's heart. The device can include an implantable capacitor having a capacitance value that is variable based on the pressure within the patients heart and a sensing circuit configured to measure the capacitance value. The device can also include an implantable inductor and a power circuit configured to wirelessly receive power from an external source via the inductor. When the device is in a first configuration, the capacitor can be electrically coupled to the sensing circuit and the inductor can be electrically coupled to the power circuit. When the device is in a second configuration, the capacitor can be electrically coupled to the inductor to form a resonant circuit.

Abstract: The present technology includes systems and methods for invasively adjusting implantable devices for selectively controlling fluid flow between a first body region and a second body region of a patient. For example, in many of the embodiments described herein, a catheter can be used to mechanically and/or electrically engage an implanted medical device. Once the catheter engages the medical device, the catheter can (i) increase a dimension associated with the medical device, such as through mechanical expansion forces, and/or (ii) decrease a dimension associated with the medical device, such as by heating a shape memory component of the medical device above a phase transition temperature.

Abstract: The present technology relates to intracardiac pressure monitoring devices, and associated systems and methods. In some embodiments, the present technology includes a device for monitoring pressure within a patient's heart. The device can include a pressure sensor configured to reside within a first chamber of a heart of a patient, and a pressure transmission element configured to extend from the first chamber through a septal wall to a second chamber of the heart of the patient. When the device is implanted in the patient's heart, the pressure transmission element is configured to transmit pressure from the second chamber to the pressure sensor residing within the first chamber.

Abstract: The present technology relates to intracardiac sensors and associated systems and methods. In some embodiments, the present technology includes a device for monitoring pressure within a patient's heart. The device can include an implantable capacitor having a capacitance value that is variable based on the pressure within the patients heart and a sensing circuit configured to measure the capacitance value. The device can also include an implantable inductor and a power circuit configured to wirelessly receive power from an external source via the inductor. When the device is in a first configuration, the capacitor can be electrically coupled to the sensing circuit and the inductor can be electrically coupled to the power circuit. When the device is in a second configuration, the capacitor can be electrically coupled to the inductor to form a resonant circuit.

Abstract: The present technology relates to interatrial shunting systems and methods. In some embodiments, the present technology includes interatrial shunting systems that include a shunting element having a lumen extending therethrough that is configured to fluidly couple the left atrium and the right atrium when the shunting element is implanted in a patient. The system can also include an energy receiving component for receiving energy from an energy source positioned external to the body, an energy storage component for storing the received energy, and/or a flow control mechanism for adjusting a geometry of the lumen.