Patent classifications
A61M3/0216
A levelling device for positioning of a medical device
A levelling device for positioning of a medical device in relation to a patient is disclosed. The levelling device comprises a tube having fluid communication between a first end and a second end, wherein the first end is configured for connection to the medical device and the second end is configured for connection to the patient. The levelling device comprises a control unit connected to a sensor, wherein the sensor is configured to transmit sensor data to the control unit which is indicative of a pressure difference between the first and second end of the tube, and an actuator connected to the control unit, wherein the actuator is configured to connect to the medical device and to arrange a position of the medical device in relation to the patient in dependence on said pressure difference.
Wound cleansing apparatus in-situ
An apparatus for cleansing wounds, in which wound exudate is removed from a wound bed and selectively cleansed and returned to the wound. The cleansing means removes materials deleterious to wound healing, and the cleansed fluid, still containing materials that are beneficial in promoting wound healing, is returned to the wound bed. The associated wound dressing and cleansing means are conformable to the wound, and may have irrigant fluid circulated from a reservoir by a device for moving fluid through a flow path which passes through the dressing and a means for fluid cleansing and back to the dressing.
Control apparatus for delivery of therapy to wounds and related methods of use
In various aspects, the wound therapy apparatus disclosed herein includes a wound interface that defines an enclosed space over a wound bed that is fluid tight when secured to a skin surface around the wound bed. The wound therapy apparatus includes a control group that cooperates with the wound interface to regulate input of input fluid comprising a gas having an O.sub.2 concentration greater than atmospheric air into the enclosed space and to regulate the withdrawal of output fluid from the enclosed space in order to vary an actual pressure p.sub.a within the enclosed space generally between a minimum pressure p.sub.min and a maximum pressure p.sub.max. Related methods of use of the wound therapy apparatus are disclosed herein.
IRRIGATION DEVICE AND SYSTEM FOR DELIVERING PRESSURIZED FLUID TO SAME FOR WOUND LAVAGE AND BIOFILM CONTROL
A medical device is provided for irrigation of a patient wound site. The device contains a tube having a proximal portion adapted to receive an irrigation solution, a distal portion having a nozzle and an intermediate portion for transporting the solution. The tube has a barrel portion that may be manipulated by a user to position the device relative to the wound site. A distinctive nozzle has a body formed with a distally leading channel presenting a semispherical first spatial conformation and a proximally leading opening formed in the body presenting a second spatial conformation intersecting the semispherical terminus. This geometry, derived from principles of flow mechanics discussed herein, defines what will be described as an effective diameter of the nozzle. An assembly and system utilizing the device are also disclosed. The invention utilizes a fluid-isolating durable peristaltic pump for a continuous flow of irrigation solution, along with a single use tube set that embodies the device.
REDUCING UNCOMFORTABLE SIDE EFFECTS OF ABDOMINAL DISTENSION IN PATIENTS TREATED IN HYDROCOLONIC PREPARATION UNITS
Systems and methods are provided to limit abdominal distension and alleviate uncomfortable side effects related to itin patients treated in hydrocolonic preparation units. Systems may comprise a water delivery unit comprising a controllable water supply, configured to introduce water controllably into the patient's large intestine, a drainage configured to drain, by gravity, the introduced water with contents of the patient's large intestine and a controller. The drainage comprises a drainage pipe and sensor(s) such as camera(s) configured to continuously measure the amount of drained water drained by the drainage pipe. The controller is configured to control the water introduction with respect to the measured amount of drained water, keeping an amount of water retained in the patient below a specified water retention threshold to reduce uncomfortable side effects of abdominal distension.
Medical systems and methods
A fluid management system for use in a tissue resection procedure includes a controller. An inflow pump is operated by the controller and configured to provide fluid inflow through a flow path to a site in patient's body. An outflow pump is operated by the controller and configured to provide fluid outflow through a flow path from the site in patient's body. A motor driven resecting device may be provided for resecting tissue at the site. The controller is configured to actuate an inflow pump and an outflow pump in response to various signals and various algorithms are provided to provide malfunction warnings and assure safe operation.
OCCLUSION-ACTIVATED HEAT SUPRESSION INFUSION SLEEVE
Described is a phacoemulsification device for eye surgery that generally comprises an ultrasonically vibrating aspiration needle that withdraws ocular material from inside of the eye. The ocular material withdrawn from the eye is equally replaced with irrigation fluid provided through irrigation ports in an irrigation sleeve surrounding the aspiration needle. In the event the aspiration needle stops withdrawing ocular material, such as if it becomes occluded with a chunk of ocular material, irrigation fluid is directed to the outside of the eye via at least one irrigation aperture to keep the eye cool where the needle is ultrasonically vibrating.
SYSTEM AND METHOD FOR MONITORING AND CONTROLLING INTRAUTERINE PRESSURE USING A PRESSURE CUFF
A method of determining a pressure of a body cavity with a controller of a fluid management system includes determining a pressure and a volume of a cuff disposed about a collapsible bag, determining a volume of the collapsible bag based on the pressure and the volume of the cuff, and determining a pressure of the collapsible bag based on the volume of the collapsible bag. The method also includes calculating a fluid flow from the collapsible bag into a body cavity from the collapsible bag and determining a pressure of the body cavity based on the fluid flow
Fluid Exchange Sensing Catheter
A catheter for use in a fluid exchange system, including: an external catheter wall extending between a proximal end and a distal end of the catheter; a fluid column chamber at a distal region of the catheter, with the fluid column chamber including a plurality of fluid exchange apertures disposed in the external catheter wall; a first lumen in fluid communication with the fluid column chamber and adapted for aspirating fluid from the fluid column chamber; a second lumen in fluid communication with the fluid column chamber and adapted for irrigating fluid into the fluid column chamber; and a first sensor positioned to measure a fluid pressure within a fluid column of the fluid column chamber, with the first sensor disposed at a distal end of a lead, and the lead extending through a first dedicated lumen formed within the catheter or on an exterior of the catheter.
IRRIGATION ASSEMBLY
An assembly structured for concurrent irrigation and aspiration of a nasal cavity including a housing having a supply container disposed therein for the removable retention of irrigating fluid. A nasal applicator comprises first and second passages respectfully structured to deliver irrigating fluid to the nasal cavity and concurrently remove waste fluid therefrom. An activating assembly includes a plunger biased into a continuous pressure applying, dispensing relation to the irrigating fluid and a valve assembly is selectively disposable into an open position facilitating fluid communication between the supply container and the applicator for the delivery of the irrigating fluid therethrough into the nasal cavity. The activating assembly is further structured to create a negative pressure within the chamber which communicates with the second passage of the applicator to facilitate delivery of the waste fluid therefrom along a path of travel to an interior of the chamber.