Abstract: There is provided a device comprising a funnel connected to a suction tube connectable to a suction device, the funnel comprising a reversibly inflatable portion. The device is preferably a nasopharangeal device suitable for insertion through a mouth of a patient, the funnel being formed so as to be sealably locatable in or around the nasopharangeal opening of the patient. There are further provided methods for protecting an airway of a patient from nasal-derived liquid and/or applying medicament and/or packing to a nasopharynx, oropharynx or nasal cavity of a patient using the inventive device. The device provides a system in which misting of endoscopic lenses is reduced or prevented. Embodiments of the device allow for the strength of applied suction to be controlled.

Abstract: Devices and methods for the effective clearing of artificial tubes, especially in-situ clearing of artificial tubes in a living being are covered in this disclosure. The devices and methods provide an elongated clearing member having a first end that is coupled to a driving mechanism and having a second working end that is subjected to repetitive motion for clearing blockages within the artificial tube. The elongated clearing member includes either a fixed or an adjustable element that selectively defines the portion of the elongated clearing member that is insertable within the artificial tube. The proximal end of the clearing member is releasably secured to the driving mechanism and the driving mechanisms may comprise a wide variety of repetitive motion drivers such as voice coil motors, piezoelectric actuators, pneumatic actuators, DC motors, etc. These devices/methods may comprise a free-standing console for hands-free operation or may comprise hand-held versions.

Abstract: An apparatus for cleansing and applying therapy or prophylaxis to wounds, in which irrigant fluid containing a physiologically active material from a reservoir connected to a conformable wound dressing and wound exudate from the dressing are recirculated 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. The cleansing means (which may be a single-phase, e.g. microfiltration, system or a two-phase, e.g. dialytic system) 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 dressing and a method of treatment using the apparatus.

Abstract: A portable negative pressure wound therapy system includes a dressing assembly for positioning over a wound to apply a negative pressure to the wound and a canister assembly. The canister assembly includes a control unit having a vacuum source and a controller and a collection canister in communication with the dressing assembly operable to receive fluid from the wound. The collection canister has a filter assembly having a filter and a passageway between the filter and a wall of the collection canister. The collection canister also includes a canister interface having a suction port, an inlet port, and a channel. The vacuum source draws air through the suction port from the channel which draws air from the passageway connected to the channel, the air in the passageway is drawn from the collection canister through the filter, and the air in the collection canister is drawn through the inlet port.

Abstract: A method and system for controlling inflammatory response at an internal tissue site of a patient utilizes a reduced-pressure treatment device. Controlling the inflammatory response may be accomplished in a number of ways that involve treating the inflammatory milieu. Treating the inflammatory milieu may include removing or moderating pro-inflammatory stimuli, e.g., fluids, enhancing perfusion of the tissue at or near the internal tissue site, or providing reduced-pressure therapy. The reduced-pressure treatment device is placed at or near the internal tissue site and is fluidly coupled to an external reduced-pressure source. The reduced-pressure treatment device provides reduced pressure proximate the tissue site and treats the inflammatory milieu. The reduced-pressure treatment device for controlling inflammatory response may be a minimally-invasive treatment device.

Abstract: A fluid management system for the treatment of ascites, pleural effusion or pericardial effusion is provided including an implantable device including a pump, control circuitry, battery and transceiver; a charging and communication system configured to periodically charge the battery and communicate with the implantable device to retrieve performance data; and monitoring and control software, suitable for use with conventional personal computers, for configuring and controlling operation of the implantable device and charging and communication system. The implantable device includes a number of features that provide automated movement of fluid to the bladder with reduced risk of clogging, with no patient involvement other than occasional recharging of the battery of the implantable device. The monitoring and control software is available only to the treating physician, such that the physician interacts with the implantable device via the charging and communication system.

Abstract: A fluid management system for the treatment of ascites, pleural effusion or pericardial effusion is provided including an implantable device including a pump, control circuitry, battery and transceiver; a charging and communication system configured to periodically charge the battery and communicate with the implantable device to retrieve performance data; and monitoring and control software, suitable for use with conventional personal computers, for configuring and controlling operation of the implantable device and charging and communication system. The implantable device includes a number of features that provide automated movement of fluid to the bladder with reduced risk of clogging, with no patient involvement other than occasional recharging of the battery of the implantable device. The monitoring and control software is available only to the treating physician, such that the physician interacts with the implantable device via the charging and communication system.

Abstract: The invention pertains to techniques or processes for managing surgical smoke. In one embodiment a suction apparatus evacuates the surgical smoke. For example, the suction apparatus may be arranged adjacent to an electrocautery electrode, which may generate smoke during operation, for evacuating smoke from a surgical site.

Abstract: The invention pertains to techniques or processes for managing surgical smoke. In one embodiment a suction apparatus evacuates the surgical smoke. For example, the suction apparatus may be arranged adjacent to an electrocautery electrode, which may generate smoke during operation, for evacuating smoke from a surgical site.

Abstract: A suction head in fluid communication with a pump head provides a sub-ambient working pressure to a target area, enabling drainage thereof to a waste container. The pump head is coupled non-mechanically to a pump drive. A control system for a suction system is also provided.

Abstract: A multi-layer odor barrier catheter tube for a fecal drainage catheter. The layers of the catheter tube include one or more thermoplastic elastomer layers and one or more odor barrier layers. For example, the catheter tube may comprise an inner thermoplastic elastomer (TPE) layer, an intermediate odor barrier film layer, and an outer TPE layer. Alternately, the multi-layer catheter tube includes an inner TPE layer sandwiched between outer layers of odor barrier film material.

Abstract: A minimally invasive tracheal fluid removal device and corresponding method of use for removing accumulated subglottic secretions in an intubated patient's endotracheal tube. The device may be configured as a dual-track or single-tube suction guidance system. This device presents a significant improvement over the art as it eliminates the need to reintubate the patient each time the suction mechanism is removed to be cleaned.

Abstract: A partially-implantable pneumostoma management device maintains the patency of a pneumostoma while controlling the flow of material through the pneumostoma. A tube of the pneumostoma management device is placed through the chest wall into the lung. The tube comprises a plurality of holes in the distal end to allow the entry of gases and non-gaseous discharge from the lung. A contact surface prevents over-insertion of the tube while releasably securing the device to the chest of the patient. The contact surface has features to reduce irritation of the skin of the chest. The pneumostoma management device may provide a pharmaceutically active substance selected to maintain the patency of the pneumostoma.

Abstract: Provided is a suction catheter including: a catheter main body made of a flexible lengthy body having a lumen inside; a leading-end case portion positioned at a leading-end portion of the catheter main body and including an opening for retrieving an object; and object cutting means partially exposed through the opening and movable in the axial direction within the leading-end case portion. The object cutting means includes a cutting portion exposed through the opening portion, and a power receiving portion driving the cutting portion when receiving power from outside. A leading-end side of the suction catheter is inserted into a blood vessel while a base-end portion of the suction catheter is connected to a suction apparatus. An object sticking to the internal wall of the blood vessel is cut off by operating the object cutting means in the opening of the leading-end case portion while the lumen is vacuumed. The cut-off object is immediately sucked in and retrieved.

Abstract: A co-axial two-piece stiffener for use with an indwelling percutaneous catheter during insertion and removal of the catheter. The stiffener comprises inner and outer stiffener members with the inner member having a large diameter portion with an unconstrained diameter that is the same as or larger than the diameter of the outer stiffener member and a reduced diameter when constrained by the outer stiffener member that is smaller than the diameter of the outer stiffener member.

Abstract: An extra-labia urine voiding apparatus including a container sized and shaped to externally cover a vulval region of a female anatomy. The container has an open side and defines a reservoir that is adapted for receiving urine. The container also includes a surface disposed at a top of the container adapted to face and generally surround a periphery of the vulval region. The voiding apparatus also includes a conduit in fluid communication with the reservoir of the container and adapted for draining urine from the reservoir.

Abstract: This invention relates to achieving or improving uniform distribution of fluid flow in medical devices such as when combined with antibiotics impregnated in a catheter and/or with a drug-eluting catheter to further inhibit the catheter from becoming occluded by debris in the CSF or by bacterial biofilm formation or tissue proliferation in the catheter.

Abstract: A process for treating biological targets in a fluid of a biological organism, including introducing a fluid comprising a biological target to an assembly comprising an inlet connected to receive the fluid and an outlet connected to pass the fluid from the assembly, wherein the assembly comprises a flow chamber for conveying a flow of the fluid, and a capture zone comprising a target-specific binding agent, wherein during flow of the fluid through the flow chamber, the biological target undergoes flux rolling along the target-specific binding agent.

Abstract: 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.

Abstract: A removable manifold for a medical/surgical waste collection system. The manifold is dimensioned to be mounted to a receiver integral with the system. The manifold includes a driver for engaging a complementary valve internal to the receiver. The valve regulates flow between the receiver and the down line components of the waste collection system. The valve is normally closed. When the manifold is fitted to the receiver the driver engages the valve so as move the valve to the open position. This allows fluid flow from the manifold and receiver to the downstream components of the system.

Abstract: Fluid removal systems and methods for removing fluid from a tissue site are presented. The system includes a semi-permeable inbound conduit, which is fluidly coupled to a treatment-fluid delivery unit, for placement proximate to the tissue site, and a semi-permeable outbound conduit, which is fluidly coupled to the inbound conduit and to a treatment-fluid collector, for placement proximate to the tissue site of a patient. The treatment-fluid collector receives a treatment fluid and a recruited fluid from the tissue site. A recruited-fluid determination unit may be coupled to the treatment-fluid collector to determine a volume of fluid recruited from the patient. The treatment fluid is any fluid (including a gas) that pulls fluid from the interstitial and intracellular space. A reduced-pressure treatment subsystem may also be included, among other things, for removing ascites and other fluids from a body cavity.

Abstract: A respiratory access assembly inctudes a distal pJate having one port and cuff and an axially aligned proximal plate including a first port and first cuff and a second port and second cuff. The distal plate is configured to move relative to the proximal plate. The respiratory access assembly includes an actuator, which has a plurality of predetermined positions. When the actuator is positioned in a movement-enabling position, it permits movement of the plates while simultaneously blocking the first port of the proximal plate. When the actuator is positioned in a first or second locked (open) position, it locks the plates together and aligns the port of the distal plate with the respective first or second port of the proximal plate and un-blocks the first port of the proximal plale so that an object, such as a suction catheter, may be positioned through the aligned ports.

Abstract: A wound treatment device comprises a polyurethane or polyether foam pad, adapted for insertion substantially within a wound cavity; a pump for supplying fluid flow to the wound site; and a collection canister for receiving wound fluids drawn from the wound cavity. The foam pad, pump and collection canister are in fluid communication with one another through a single hospital grade hose having a plurality of tiny apertures in the portion that is central to the foam pad. These apertures are adapted to allow fluids from the wound cavity to be drawn into the flow from the pump to the canister according to Bernoulli's theorem.

Abstract: The disclosure relates to the discovery that certain cerebrovascular disorders in humans who exhibit seemingly normal intracranial pressure (ICP) and do not exhibit hydrocephalus can be alleviated or prevented by reducing ICP in the human. Disorders of this type are herein designated normotensive, nonhydrocephalus tenso-responsive cerebrovascular disorder (NNTCDs). The disclosure describes methods of relieving head pain and other symptoms of NNTCDs, for example by withdrawing cerebrospinal fluid (CSF) from the subarachnoid space of a human or by administering a pharmaceutical agent that modulates CSF production, uptake, or both. Methods of assessing whether a human is afflicted with one or more NNTCDs are also described. The disclosure describes numerous pharmaceutical compositions suitable for administration to humans afflicted with NNTCDs to alleviate or prevent such disorders. Such compositions can, for example, include both a CSF-reducing agent and a symptomatic (e.g., head pain) relief agent.

Abstract: A semi-rigid tube connected to an inflatable ring and a vacuum source is provided. The inflatable ring may be inserted into the trachea air passageway of a person, then inflated to form a seal against the inner surface of the air passageway of the person. A central through hole of the ring is in fluid communication with the tube as well as a lower portion of the air passageway of the person below the ring. The vacuum source applies a vacuum to the tube as well as the central through hole of the ring and the lower portion of the air passageway of the person to remove lodged objects stuck in the air passageway of the person. Once the lodged object is removed from the air passageway, the ring may be deflated and the tube/ring removed from the air passageway of the person so that the person can now breathe normally.

Abstract: The present invention relates to an ocular implant, particularly a glaucoma stent. It is the object of the present invention to devise an ocular implant which allows the ocular eye pressure to be regulated, i.e., to be maintained at a desired level, while preventing the flow resistance from increasing over time, for example due to fibrosis. In order to achieve this object, the ocular implant according to the invention comprises a small tube (5), the wall surface (3) of which encloses a hollow duct that is open on both sides in the longitudinal direction of the hollow duct, wherein a first opening (1) allowing ocular humor to flow in and a second opening (2) allowing the ocular humor to be discharged is provided, and wherein the wall surface (3) is formed by a liquid-tight material, and wherein at least one pressure-controlled valve (4) is disposed in the area of the wall surface (3).

Abstract: Equipment for use in changing a catheter, preferably of the type used for drainage of the urinary tract. The urinary catheter is used as an aid in emptying the urinary bladder in conditions where this cannot be done in the normal manner. The equipment of the present invention includes a sleeve mounting unit which is mounted to an indwelling catheter, and which has a branch member formed in one piece therewith and extending at an acute angle therefrom, for reception of an elongated sleeve having a longitudinal slit. The sleeve is positioned on the branch member and then progressively advanced onto the catheter, causing the slit to become enlarged as the sleeve surrounds the upstream portion of the catheter in a yielding manner. The catheter may then be quickly removed through the sleeve and a new catheter inserted in its place.

Abstract: Provision of a blood purification system comprising a blood purification tubing and a blood purification apparatus particularly suitable for use in continuous hemofiltration in which in the treatment of a patient with renal disease, multiple organ failure, and the like, the amount of water removed from the patient and the amount of supply to the patient can be more accurately controlled, and in which preparation operation is easy. A blood purification system comprising a blood purification tubing and a blood purification apparatus wherein the soft tubes of flow paths connecting a first planar panel and a second planar panel, and the location of the soft tubes are selected to satisfy a formula of a predetermined condition.

Abstract: A modular, reduced-pressure, wound-closure system for providing a closing force on a surface would includes a flexible strap operable to be formed into a closed loop inbound and around the surface wound and a plurality of modular closing members coupled to the flexible strap. A reduced-pressure source is fluidly coupled to the plurality of modular closing members. The modular closing members are operable to generate a closing force on the surface wound. A portion of the modular closing members are releasably attached to the patient's epidermis proximate the surface wound and another portion are attached to the flexible strap. A reduced pressure from the reduced-pressure source is delivered to each modular closing member to generate the closing force on the surface wound. Methods and other systems are presented.

Abstract: A method for removing an object from a body lumen includes dispensing fluid into the body lumen, and causing the dispensed fluid to propel the object along the body lumen. A device for removing an object from a body lumen includes a fluid dispenser for dispensing fluid into the body lumen, and a pump in fluid communication with the dispenser.

Abstract: An open-cavity, reduced-pressure treatment device and system for treating a cavity in a patient's body, such as an abdominal cavity, is presented. In one instance, an open-cavity, reduced-pressure treatment device includes a plurality of encapsulated leg members, each having an interior portion with a leg manifold member and formed with fenestrations operable to allow fluid flow into the interior portion, and a central connection member fluidly coupled to the plurality of encapsulated leg members. The central connection member has a connection manifold member. The open-cavity, reduced-pressure treatment devices, systems, and methods allow for, among other things, removal of fluids.

Abstract: A control device for controlling drainage of waste from a surgical stoma of a human body. The control device comprises a first cylindrical hollow body member, a drain tube extending from the first cylindrical hollow body member, a second cylindrical hollow body member rotatably coupled to the first cylindrical hollow body member and a knob configured on the second cylindrical hollow body member. The first cylindrical hollow body member comprises a skirt portion extending radially outward for being removably attached to a surface surrounding the surgical stoma of the human body. The second cylindrical hollow body member comprises an aperture configured on the second sidewall. A rotation of the knob is capable of aligning the aperture of the second cylindrical hollow body member with the drain tube of the first cylindrical hollow body member thereby forming a passage for draining the waste.

Abstract: The invention relates, generally, to medical appliances. More particularly, it relates to tubular shaped devices used as drains for draining fluids (liquids and/or gases) from antrums or other parts of the human or animal body. According to the present invention a drain is provided, which is suitable for draining a human or animal antrum, which drain comprises a synthetic biodegradable material, preferably a biodegradable polymer.

Abstract: A device and method for suctioning mucus and secretions from a patient's tracheostomy tube is described. The device utilizes a reusable squeezable bulb with check valves to regulate air flow in and out of the squeezable bulb and a disposable mucus trap and suction catheter to suction a tracheostomy tube effectively and discretely without using an electrically powered suction machine.

Abstract: A medical apparatus having a nasogastric tube with hypopharyngeal suctioning capability. In one embodiment, the medical apparatus has a flexible nasogastric tube for insertion through a patient's nose. The nasogastric tube has a first end defining a first opening, a distal, second end that defines a second opening, and a length sufficient to allow the second opening to be positioned in a patient's stomach. The medical apparatus also has a flexible oropharyngeal tube for insertion through a patient's mouth. The oropharyngeal tube has a first end defining a first opening and a distal, second end that defines a suction intake. The oropharyngeal tube has a length that is less than the length of the nasogastric tube and which allows the suction intake to be positioned in a patient's hypopharynx region.

Abstract: Methods and devices for treatment of damaged tissue are disclosed, including treatment of wounds by employing non-electrically powered, reduced pressure therapy devices. Maintenance and control of the sub atmospheric pressure exerted may be provided by such devices while minimizing discomfort to the user. The devices may be configured to be worn inconspicuously underneath clothing.

Abstract: A flexible filament controlled locking medical catheter having a flexible tube with at least one drainage or feeding hole, a restraining portion at its distal end and a housing at its proximal end, and a filament having a proximal control portion for controlling the restraining portion of the tube. The flexible filament passes through an open port in the sidewall of the housing and an elastomeric cover as well as through the interface between the cover and a seal sleeve over the cover. A locking mechanism to lock the filament in position is provided and may comprise corresponding teeth with means for moving the teeth into tight engagement to clamp the flexible filament therebetween.

Abstract: A cleansing device for cleaning a body cavity is provided to a user. The cleansing device comprises an inner membrane fabricated from an elastomeric material and an outer membrane fabricated from a hypoallergenic material. The inner surface of the inner membrane defines a cavity that conforms to and accommodates the user's finger. The inner membrane is in contact with and enveloped by the outer membrane to form the cleansing device. The user inserts the finger into the cavity of the cleansing device, where the inner surface of the inner membrane contacts the inserted finger, and the outer surface of the outer membrane is exposed for cleaning the body cavity. The user introduces the enclosed finger into the body cavity for cleaning. A string attached between the outer surface of the inner membrane and the inner surface of the outer membrane enables removal of the cleansing device from the user's finger.

Abstract: A reduced pressure treatment system includes a liquid-collection canister for collecting liquid from a tissue site to which reduced pressure treatment is applied. The canister includes a first space configured to collect the liquid from the tissue site and a filter having a frame and a non-planar filter element. The filter defines a second space within the canister separated from the first space by the filter element. The filter element substantially prevents liquid from passing from the first space into the second space. The filter element substantially allows gaseous communication between the first space and the second space when the second space is exposed to a reduced pressure.

Abstract: An ostomy drainage system comprising an ostomy bag or pouch connected by tubes to a container which is connected via tubes to a vacuum device whereby the contents of the ostomy bag can be suctioned into the container to prevent frequent changing of the ostomy bag thereby improving sanitation and convenience for ostomy patients.

Abstract: A novel collection device for collection, storage and disposal of biological products, in conjunction with an improved cleansing method. Disclosed is an apparatus which includes a locking closing member handle to allow for safe transport and disposal of medical waste. Closing member allows for secure containment of medical waste and subsequent apparatus cleaning. Closing member design includes a gap between closing member and housing which facilitates device cleaning after waste disposal.

Abstract: A collection device for retrieving a medical capsule discharges from the anus of a patient is disclosed. Medical capsules have been widely used for monitoring and diagnostic purposes. The capsule has to be retrieved to obtain the on-board data or for reuse of the capsule. Accordingly, cost effective, easy-to-deploy, and comfortable-to-use collection devices are disclosed for retrieving the capsule. The capsule collection device for retrieving a capsule discharged from anus of a patient into a bowl comprises a capture device to capture the capsule and to pass feces discharged from the anus, and a wand to pick up the capsule. A collapsible capture device is also disclosure which comprises a flange to adapt to a rim of the bowl, a sifting piece to separate the capsule from the feces, and a collapsible side walls to couple the sifting piece to the capture opening of the flange. Furthermore, a wand having ejection capability for ejecting a picked capsule is disclosed.

Abstract: A subcutaneous drain, preferably for implantation into the skull of a patient comprises a basically hollow cap and a stem with an inside, central passageway passing from top of the cap through the stem. A lumen is provided through at least a portion of the inside, central passageway with the lumen preferably exiting the cap through a side slit in the cap and stem. The lumen is provided with a supporting ledge to reduce kinkage and promote an unimpeded fluid path. The side slit is resilient to allow for the selective removal of the lumen. The cap and stem are, as mentioned, substantially hollow and defines a chamber in communication with the subdural space, so that with the device in place, a physician can use a hypodermic needle to gain access to fluid in the subdural space by piercing the needle tip of the hypodermic syringe or needle through the thin wall of the cap of the device. A circumferential flange is provided to facilitate location of the device. Also, the stem is slightly inwardly tapered.

Abstract: A wound bed preparation device for delivering a fluid jet to tissue includes a handpiece having a deck height in the range of ?0.0254 mm to 0.2032 mm, a channel width in the range of 0.8636 mm to 1.1684 mm, and a nozzle diameter in the range of 0.10668 mm to 0.12192 mm. The handpiece has a constant channel width over a majority of a tissue impacting section of the handpiece.

Abstract: An apparatus includes a pressure housing configured to be coupled to a vacuum source and a diaphragm sealingly coupled to the pressure housing. The diaphragm is configured to move in response to the vacuum source. A magnet is coupled to the diaphragm. A magnetic switch is disposed opposite the magnet and is configured to be actuated by the magnet when the magnet is a predetermined distance from the magnetic switch. The magnetic switch is configured to selectively actuate the vacuum source.

Abstract: A reduced-pressure, wound closure system is presented that generates a closing force on a surface wound and optionally provides reduced pressure to a body cavity or tissue site. The sealed contracting member, when placed under reduced pressure, generates the closing force. One illustrative system includes a first attachment member and a second attachment member, a sealed contracting member coupled to the first attachment member and the second attachment member, and wherein the closing force is generated between the first attachment member and the second attachment member when reduced pressure is supplied to the sealed contracting member. Other systems and methods are presented.

Abstract: A catheter device and methods useable to extract material from a body conduit, e.g., a blood vessel, are provided. The catheter comprises a flexible catheter advanceable into the body conduit, an opening in a wall of the catheter in fluid communication with a material collection chamber, and a controllably arcuate segment near the distal tip of the catheter and the opening. The catheter may include a sliding member, located within a lumen of the catheter, used to move the material entering the catheter through the arcuate segment opening, into the material collection chamber and away from said opening. The catheter may include a single mechanism utilized to both generate a vacuum to cause material to enter the catheter at the arcuate segment opening and also cause the sliding member to travel, inside the catheter, moving material away from the opening and into the material collection chamber.

Abstract: Methods and devices are provided for performing surgical procedures using tissue retractors. In general, the methods and devices allow a surgeon to use a retractor to capture a large or small amount of tissue in the retractor and to move the retractor to relocate tissue to one or more convenient locations during a surgical procedure. The retractor can be configured from a pliable state to a substantially rigid state to hold the retractor and the tissue in a substantially fixed position during the procedure.

Abstract: An apparatus for cleansing and applying therapy or prophylaxis to wounds, in which irrigant fluid containing a physiologically active material from a reservoir connected to a conformable wound dressing and wound exudate from the dressing are recirculated 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. A biodegradable scaffold underlies the dressing on the wound bed to promote tissue growth. The cleansing means (which may be a single-phase, e.g. micro-filtration, system or a two-phase, e.g. dialytic system) 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 dressing, an assembly comprising the dressing and scaffold, and a method of treatment using the apparatus.

Abstract: Devices that are adapted to insert a sinus dilator into a stenotic opening of a paranasal sinus in a subject patient using minimally invasive insertion procedures are provided. The devices and methods can be used to treat sinusitis and other nasal and/or sinus disorders.