1558results about "Suction drainage containers" patented technology

A system for applying suction to a wound uses a reference airflow for monitoring system operation. A reference airflow (or “controlled leak”) to the suction source is provided when the system is in operation, such that deviation from the reference airflow can be monitored as an indication of a change in operation, such as a leak in the seal of the wound cover, a blockage of airflow from crimping of the suction conduit or overfill of the waste collector, or an inadvertent turn off or disconnect from the suction source.

A wound closure apparatus is disclosed which includes a housing that contains a vacuum pump and a chamber for holding a disposable wound fluid collection canister. The canister resides within the chamber and connects at an outlet with the vacuum pump and at an inlet with a pad. The pad is placed over a wound and adhesively secured thereto. When the vacuum pump activates, it evacuates air from the canister resulting in wound fluids flowing from the wound into the canister. After the canister is filled, it is removed from the chamber and replaced with another canister to continue the removal of wound fluids.

A system for applying suction to a wound uses a reference airflow for monitoring system operation. A reference airflow (or “controlled leak”) to the suction source is provided when the system is in operation, such that deviation from the reference airflow can be monitored as an indication of a change in operation, such as a leak in the seal of the wound cover, a blockage of airflow from crimping of the suction conduit or overfill of the waste collector, or an inadvertent turn off or disconnect from the suction source.

A system to promote the healing of an exuding wound includes a wound dressing, a subatmospheric pressure mechanism, and a collection canister. The wound dressing is dimensioned for positioning relative to a wound bed of a subject. The subatmospheric pressure mechanism includes a control unit disposed within a housing. The control unit includes a vacuum source associated with a vacuum port. The collection canister has an interior wall which defines an internal chamber. The internal chamber is in fluid communication with the vacuum source of the subatmospheric pressure mechanism through the vacuum port and with the wound dressing for collecting exudates removed for the wound bed under influence of the vacuum source. The canister including a baffle mechanism disposed within the internal chamber for dampening the movement of the collected exudates.

An electrosurgical pencil is provided and includes an elongate housing, an electrocautery blade supported within the housing and extending distally from the housing. The electrocautery blade is connected to a source of electrosurgical energy. The pencil also includes an activation button supported on the housing, the activation button being configured and adapted to complete a control loop extending from the source of electrosurgical energy upon actuation thereof. The electrosurgical pencil further includes a manually operated aspirating / irrigating system operatively connected to the housing, wherein the aspirating / irrigating system is configured and adapted to deliver a quantity of fluid to a target surgical site and / or withdraw a quantity of fluid from the target surgical site.

A portable system for subatmospheric pressure therapy in connection with healing a surgical wound, includes a wound dressing dimensioned for positioning relative to a wound bed of a subject, a portable subatmospheric pressure mechanism dimensioned to be carried or worn by the subject and a container for collecting exudates from the wound bed removed under the subatmospheric pressure supplied by the subatmospheric pressure mechanism. The portable subatmospheric pressure mechanism includes a housing, a subatmospheric pressure source disposed within the housing and in fluid communication with the wound dressing to supply subatmospheric pressure to the wound dressing and a power source mounted to or within the housing for supplying power to actuate the subatmospheric pressure source.

A waste collection and disposal system for use in health care facilities is provided. The system includes a mobile waste collection unit for moving between use areas in the health care facility to collect waste material generated during medical procedures including body fluids, body tissues, saline, etc. The waste collection unit includes stacked upper and lower waste containers for receiving the waste material. During use, the upper waste container can be emptied into the lower waste container for temporary storage. In addition, different vacuum levels can be provided in the waste containers during complex procedures. Once a user desires to empty the waste collection unit, the waste collection unit is wheeled to a docking station. At the docking station, the waste material is off-loaded to a waste drain and the waste collection unit is cleaned and rinsed for further use.

The control of fluid introduction into and out of body conduits such as vessels, is of great concern in medicine. As the development of more particular treatments to vessels and organs continues it is apparent that controlled introduction and removal of fluids is necessary. Fluid delivery and removal from such sites, usually referred to as irrigation and aspiration, using fluid exchange devices that control also need to be considerate of potential volume and / or pressure in the vessel or organ are described together with catheter and lumen configurations to achieve the fluid exchange. The devices include several electrically or mechanically controlled embodiments and produce both controlled and localized flow with defined volume exchange ratios for fluid management. The applications in medicine include diagnostic, therapeutic, imaging, and uses for the introduction or removal of concentrations of emboli within body cavities.

The methods and devices disclosed provides for the delivery of agents to an orifice cavity and subsequent aspiration of the agent and orifice contents from the orifice cavity and related areas. In one form, the delivery and aspiration system comprises an agent delivery sub-assembly, an aspiration sub-assembly and a device tip sub-assembly. The subassemblies operate to first deliver an agent contained within the device to an orifice cavity and after an optional time delay, subsequently aspirate the delivered agent and orifice contents from the orifice cavity and related areas. In another form, a removable reservoir is provided whereby the aspirated agent and orifice contents from the orifice are assayed either independent of or within the device itself.

A pump system for applying negative pressure to a wound, including a flow monitor capable of detecting a deviation from a reference airflow rate provided by a controlled leak to determine whether the system is operating normally or abnormally, and a flow status annunciator to indicate a normal operating condition or whether an abnormal condition is a leak or an occluded line in the system. The pump system further includes a pressure controller for regulating operation of a pump to control pressure in the system at a range around a user-selected setpoint. The pump system may also include a waste collector and a level sensor for detecting when the collector is full.

The illustrative embodiments described herein are directed to a system and method for administering reduced pressure at a tissue site. The apparatus includes a reduced pressure source. The reduced pressure source generates a reduced pressure. The apparatus includes a tube having a plurality of lumens. The plurality of lumens includes at least one collection lumen. The reduced pressure source applies the reduced pressure to the tissue site through the plurality of lumens such that the at least one collection lumen receives fluid from the tissue site. The at least one collection lumen stores the fluid received from the tissue site.

The invention relates to a device (100) for treating wounds of the human or animal body using a vacuum and having a gas-tight wound-covering element (4), which, when placed in contact with the body of the patient, forms a wound space (10) between the respective wound and the wound-covering element, at least one connecting site (5.1; 5.2), which is in contact with the wound space (10), an absorption body (2), which is a layer, enclosed in an envelope, of a textile section, interspersed with super-absorbing particles, the envelope being permeable to liquids and having pores, the size of which does not exceed that of the super-absorbing particles. The absorption body (2), which is to be inserted in the wound space (10), has an initial volume, which enlarges in the course of the absorption process, and a final volume, so that, due to the size of the pores of the envelope, the absorbed wound secretions remain within the absorption body (2) and, with that, below the wound-covering element, until the absorption body is removed from the wound space.

A waste collection unit (40) with a primary display (106) on which information about the operation of the unit is presented. In addition to the primary display there is a light assembly (662) adjacent the fitting (614) to which a suction line is attached. The light assembly emits light of selectively colors or in a selected pattern based on an operation state of the waste collection unit.

Irrigation and / or aspiration devices and methods may be configured to aspirate and irrigate alone, sequentially, or concurrently. The devices and methods may provide a base with a removable head, and adapted for partial or complete separation of the irrigation and aspiration functions. The devices and methods can be configured to aspirate and / or irrigate the nasal and sinus cavities. The devices and methods may be manually and / or automatically controlled. The devices and methods may include removable, and / or replaceable, and / or refillable, and easily cleanable reservoirs for aspirant and irrigant. The device head and / or aspirant reservoir may comprise a diagnostic device, i.e., test device and / or container after use of the devices and methods.

An apparatus for drainage of a wound or surgical site of a human or animal fits anatomically, passes from inside the wound or surgical site percutaneously or covering an open wound surface and extends externally for accumulation of fluids. A plurality of fibers each with an internal end, middle and an external end is elongate with a thickness and a length wherein its thickness is substantially less than its length for flexibility. The fibers form a loose bundle with gathered external ends and with internal ends unrestrained for spreading divergently inside the wound or surgical site. A collector is positioned in fluid communication with the gathered external ends for accumulating bodily fluid guided along and amongst the fibers from the internal ends along the middle and to the external ends during drainage. Vacuum connects to draw fluid from the collector. A method has steps of providing fibers with the internal ends unrestrained, the external ends gathered in a collector to accumulate drained fluid. The method guides bodily fluid along and amongst the fibers from the internal ends along the middle and to the gathered together external ends during drainage. The fibers spread divergently for accumulating bodily fluid inside the wound or surgical site. A method of manufacture of the apparatus has the steps of accumulating a plurality of fibers with internal ends, a middle and external ends in a loose bundle but gathering together in a collector at their external ends while leaving the internal ends unrestrained.

A waste collection system for collecting waste during medical / surgical procedures including a mobile container cart with a waste container. A container cart is selectively coupled to a suction cart that includes a vacuum pump. The connection of the carts results in the connection of the vacuum pump to the waste container. The vacuum pump draws a vacuum that results in waste being drawn through a suction line into the waste container. The container cart holds instruments that can be removably attached to the container cart. This facilitates the configuration of the container cart for the specific procedure for which it is necessary to draw a suction.

Multi-functional urine collection devices, embodiments of which can include a self-expanding container having a receptacle for receiving urine from the tubing, a pump for moving urine through the tubing and into a receptacle, extendable tubing that may be shortened and / or lengthened, and / or one or more meters for monitoring, measuring, transmitting or storing a characteristic from the urine.

A reduced pressure treatment system is provided that includes a canister that is fluidly connected to a tissue site and is configured to receive fluid drawn from the tissue site under the influence of a reduced pressure. A reduced pressure source provides the reduced pressure and is fluidly connected to the tissue site by a fluid communication path, which may include a source conduit, the canister, and a target conduit. A sensing device communicates with the source conduit and is configured to sense a pressure in the source conduit. A valve communicates with the source conduit and is configured to vent the reduced pressure. A processing unit communicates with the sensing device and the valve and is configured to open the valve for a selected amount of time, determine a decay of reduced pressure, and determine a fill status of the canister based on the decay of reduced pressure.

A portable system for subatmospheric pressure therapy in connection with healing a surgical wound includes a wound dressing dimensioned for positioning relative to a wound bed of a subject and a portable subatmospheric pressure mechanism dimensioned to be carried or worn by the subject. The subatmospheric pressure mechanism includes a housing having a control unit, a collection canister, and means for releasably connecting the housing and the canister. The collection canister collects exudates from the wound bed which has been removed under subatmospheric pressure supplied by the control unit. The connection means between the housing and the canister permits the removal of the canister for emptying thereof or replacement with a new collection canister.

A device for making an incision in the tympanic membrane, withdrawing fluid from the tympanic cavity and administering a medicament to the space behind the tympanic membrane is provided. The device has a barrel-shaped casing (1) having a rotatable end turret (38). A first trigger (2) allows a shaft (18) to pierce the tympanic membrane and a tubular vacuum cartridge (32). The cartridge allows aspiration of fluid. A second trigger (4) causes medicament (34) to be released into the space behind the tympanic membrane.

A wound exudate removal and isolation system includes a porous dressing, a canister in fluid communication with the dressing, and a first valve positioned between the dressing and the canister. The first valve is positionable between an open position and a closed position. A disposal line is fluidly connected to the canister and includes a second valve that is positionable between an open position and a closed position. A pump is fluidly connected to the canister and is configured to draw wound exudate from the dressing into the canister when the first valve is open and the second valve is closed. The pump is configured to force wound exudate from the canister into the disposal line when the first valve is closed and the second valve is open.

Methods and apparatuses for detecting full waste canister and / or fluid flow path blockage conditions are disclosed. Also disclosed are methods and apparatuses for controlling a pump. In some embodiments, flow of fluid can be restricted in a portion of the fluid flow path. A controller can be configured to compare a difference in pressure values upstream and downstream of a fluid flow restrictor to a pressure difference threshold, and determine based on the comparison whether to activate an alarm indicating the full waste canister condition or the fluid flow path blockage condition. The controller can be additionally or alternatively configured to determine a fluid flow using a flow meter, open a selectable valve in response to a comparison of the fluid flow with a fluid flow threshold, determine fluid flow after opening the valve, and determine based on the fluid flow after opening the valve whether to activate the alarm.

An aspiration collection cassette 10 includes a housing 12 for receiving aspiration fluids from a surgical site. An aspiration port 14 is attached to the housing 12 for connection to an aspiration tube 50 and for providing a passage way to an interior 22 of the housing 12. A vacuum port 16 is disposed in the housing 12 and communicates with the housing interior 22 for cooperation with a vacuum pump. A length of tubing 20 is connected to the housing 12 on each end, such that the tubing 20 will be placed between a peristaltic pump head and a backing plate.

A wound closure apparatus to promote tissue healing at a wound is provided and includes a porous pad positioned at the wound and a suction pump in fluid communication with the porous pad to provide a negative pressure to the porous pad. The suction pump is disposed within a housing. A canister is fluidly connected between the porous pad and the suction pump to collect fluids drawn from the wound by the suction pump, and the canister is removably received by a recess in the housing. A wound cover is positioned over the porous pad to secure the porous pad at the wound, and a switch provides a signal indicating that the canister properly resides within the recess when the switch is pressed.

A reduced pressure treatment system includes a porous pad positioned at a tissue site and a canister having a collection chamber, an inlet, and an outlet. The inlet is fluidly connected to the porous pad. A reduced pressure source is fluidly connected to the outlet of the canister to such that fluid from the tissue site may be drawn into the collection chamber. A hydrophobic filter is positioned adjacent the outlet to prevent liquid from exiting the collection chamber through the outlet. A baffle is positioned within the canister to create a tortuous path between the inlet and the outlet to prevent premature blocking of the hydrophobic filter.