Abstract: A shaped medical device article prepared from a polymer melt composition comprising a polymer ester, a transesterification catalyst, and a tri- or tetraalkoxy silane, by forming and solidifying said composition, and after solidification, subjecting the composition to reaction conditions to effect hydrolysis at least some alkoxysilyl groups remaining in the composition to form silanol groups and to effect condensation of said silanol groups to form a ceramic network. The polymer ester may be a vinyl ester homopolymer or copolymer, or a polymer having ester groups in the backbone thereof.

Abstract: A method for maintaining clear passageways in an extracorporeal blood flow system. The method comprises intermittently providing one or more anti-clotting agents to a passageway of the extracorporeal blood flow system. Also disclosed is an extracorporeal blood flow system. The system comprises a passageway, and a device operatively connected to provide one or more anti-clotting agents to a least a portion of said passageway.

Abstract: To accomplish isolation and removal of a substance from a vasculature, a catheter is employed to occlude a vessel of the vasculature. The substance is thus isolated in the vasculature and can be removed. In this way, the substance is removed before entering other parts of the circulatory system. This method is applicable to removal of contrast from the coronary sinus shortly after injection of the coronary arteries with the contrast. The method substantially minimizes or avoids renal dysfunction caused by angiographic procedures in which contrast must be injected. Such angiographic procedures are often performed during intervention procedures. This method substantially prevents circulation of the contrast to the kidneys where it could otherwise cause renal dysfunction or failure. The apparatus for implementation of the method is also disclosed.

Abstract: An apparatus for continuously aspirating a fluid from a fluid source. A vacuum source is operatively connected to a first container forming a first chamber and a second container forming a second chamber. A fluid collection tube provides communication between the fluid source and each of the first chamber and the second chamber. A first level sensor is positioned within the first chamber and a second level sensor is positioned within the second chamber. Upon receiving a signal generated by one of the first level sensor and the second level sensor, a relay responsively exposes a vacuum within one of the first chamber and the second chamber to continuously aspirate at least a portion of the fluid from the fluid source. A shut-off valve is preferably positioned within each of the first chamber and the second chamber to prevent communication between the vacuum source and the corresponding chamber with a fluid level within the chamber at a fluid level setpoint.

Abstract: A convenient and preferably wearable system and method for implementing the controlled and sustained delivery of a medical liquid through the tympanic membrane and into the middle ear including port structure that produces a minimal opening in the membrane, a wearable and fixated fluid-conduit structure coupleable to the port structure, a reservoir adapted to contain delivery fluid, and an operationally controllable pump system applied to the fluid conduit structure, and/or an iontophoretic electrode system applied within the fluid conduit structure and to the subject's body, and operable to effect the delivery of reservoir-held fluid or medically active ions through the fluid conduit and port structures to the middle ear.

Abstract: An infusion sleeve of an ultrasonic vibrating needle. The sleeve is collapsible and serrated or scalloped at a distal end. Fluid flows through a passage between the needle and the infusion sleeve in a direction from the proximal end of the sleeve to a distal end of the sleeve. Upon reaching the distal end, the fluid emerges by flowing across valley formations that are between peak formations of the distal end of the infusion sleeve. The peak formations abut the exterior of the incision so that the fluid flow cools tissue at the incision and the needle.

Abstract: Method for draining and decompressing a colon in which a drainage tube is inserted through the anus into the colon to extend through the entire colon. The drainage tube is fixed in position and suction is applied therethrough to cause fecal matter to pass therein through apertures and be withdrawn from the colon. The drainage tube is inserted by inserting a guidewire into the colon through the anus, manipulating and pushing the guidewire to the cecum, passing a filament through the colon wall to engage the guidewire, pulling the guidewire out of the colon and anus to draw the filament through the colon and out of the anus, attaching the drainage tube to the filament and drawing the filament with attached drainage tube through the anus into the colon. The invention also relates to constructions of the guidewire, the drainage tube and methods for inserting drainage tubes using guidewires.

Abstract: An aspiration instrument includes a compliant protective guard for minimizing injury to internal organs and other soft tissue while removing fluids from the body cavity. The compliant protective guard may be constructed from foam, plastic or other like material, including polyethylene and polypropylene. A preferred embodiment of the protective guard takes the shape of a bell. The compliant guard may be connected with the aspiration instrument using adhesives, such as glue or epoxy, or with a snap or friction fit. The compliant guard may define a single opening in fluid communication with the yankauer. The compliant guard may also define a plurality of openings for removing fluids from the body.

Abstract: Electrosurgical methods and apparatus for treating tissue at a target site of a patient. An electrosurgical instrument includes a shaft, having a shaft distal end and a shaft proximal end, and an electrode assembly disposed at the shaft distal end. The electrode assembly includes at least one active electrode disposed on an electrode support. The instrument is adapted for coupling to a high frequency power supply or electrosurgical generator. Each active electrode is adapted for removing tissue from a target site and/or for localized coagulation of the target tissue. In one embodiment, the instrument is adapted for laparoscopic procedures.

Abstract: To provide an irrigation/aspiration apparatus by which a trouble for an operator is reduced and handling is facilitated and which is capable of preventing a sharp decrease of pressure of an anterior chamber with a simple constitution. The apparatus has a chamber storing an irrigation liquid, a vent tube for making the liquid flow into an aspiration tube, a leading vent leading the liquid into the chamber from an irrigation tubes an outflow pipe extended in an up-and-down direction, an opening formed on a wall of the outflow pipe, of which a width is narrow and set such that an opening is closed by the liquid under surface tension when a liquid level of the liquid inside the chamber rises, an outflow vent to which the irrigation tube or a vent tube is connected, and an air chamber which is a space provided above an inflow hole of the outflow pipe.

Abstract: Apparatus and methods for treating an intervertebral disc by ablation of disc tissue. A method of the invention includes positioning at least one active electrode within the intervertebral disc, and applying at least a first high frequency voltage between the active electrode(s) and one or more return electrode(s), wherein the volume of the nucleus pulposus is decreased, pressure exerted by the nucleus pulposus on the annulus fibrosus is reduced, and discogenic pain of a patient is alleviated. In other embodiments, a curved or steerable probe is guided to a specific target site within a disc to be treated, and the disc tissue at the target site is ablated by application of at least a first high frequency voltage between the active electrode(s) and one or more return electrode(s). A method of making an electrosurgical probe is also disclosed.

Abstract: A closed suction catheter includes a valve assembly and a manifold. A catheter tube is attached to the valve assembly and slidably secured within the manifold. The closed suction catheter may include one or more features for promoting an effective, safe, and efficient process for suctioning mucus and other fluids from a patient's lungs, and for cleaning the various components of the catheter system. For example, the closed suction catheter may include a tube wiper having a reinforced leading ridge and/or an internal ledge for efficiently wiping the catheter tube. The valve assembly may include a locking mechanism having a slider unit, a cam arm, and/or ribs that engage openings in the slider unit for maintaining a valve stem in proper alignment and an actuator on the valve assembly in a locked position. The closed suction catheter may include several other features, as well.

Abstract: A suction catheter assembly, particularly adapted for neonatal use includes a distal manifold body including a rotatable connector for connection to an endotracheal tube, a ventilating port member and an ancillary catheter receiving port member. The manifold body is rotatably joined to a catheter tube seal housing. The seal housing includes an irrigation port member. A catheter tube wiper seal and a filter member are disposed in the seal housing which is joined to a suction control valve assembly by an elongated flexible sheath defining an enclosed space through which the catheter tube extends between the valve assembly and the manifold. A resilient closure member actuator and slide lock member are engageable with a closure member of the valve assembly.

Abstract: The invention encompasses a catheter having an outer surface, a distal end, and at least one interior lumen, wherein the outer surface includes multiple aspiration passageways in fluid communication with an interior lumen. A preferred embodiment comprises multiple aspiration passageways formed into a helical pattern.

Abstract: A surgical irrigation system is suitable for endoscopic and other surgical procedures. A hand held handpiece has a forward protruding hollow tip for supplying irrigation liquid to a surgical site, a hand actuable control for controlling irrigation liquid flow to the tip, and an irrigation liquid inlet. A self contained pumping unit is locatable adjacent a source of irrigation liquid and remote from the handpiece. The pumping unit comprises a housing containing an outlet for irrigation liquid, a pumping member for pumping irrigation liquid through the outlet, a motor for driving the pumping member, and an electric battery assembly for energizing the motor. An elongate tube connects the pumping outlet to the handpiece irrigation liquid inlet for supplying pumped irrigation liquid to the handpiece.

Abstract: An improved instrument for removing subretinal fluid and performing fluid exchanges in vitreoretinal surgery is disclosed. The instrument includes a cannula with a curved distal portion and a side port on the curved distal portion for aspirating subretinal fluid. The instrument also includes a second port for aspirating a second fluid from the vitreous cavity during a fluid exchange.

Abstract: A system and method to administer a liquid agent into a body cavity of a patient is provided. One exemplary system comprises a lumen disposed into an airway of the patient and a valve assembly coupled to the lumen. The valve assembly comprises a body portion, a first port and a second port. A pump assembly for receiving the liquid agent is coupled to the valve assembly in a fluid tight relationship. The pump assembly provides the liquid to the lumen through the first port of the valve assembly. The liquid along with a portion of secretions generated by the patient are extracted through the lumen and flow out of said valve assembly through the second port for disposal responsive to a natural body function and/or a vacuum from a vacuum source.

Abstract: A powered surgical apparatus can be used with a source of irrigation fluid and a source of suction. The powered surgical apparatus can include a cutting blade assembly and a handle. The handle can include an upper portion defining a distal section connectable to the cutting blade assembly and a lower portion extending downwardly from the upper portion. The handle can be connectable to the source of irrigation fluid and the source of suction. The system can also include a manually actuable input device that provides at least one signal relevant to at least one operation of the system, and a controller that receives the at least one input signal and provides an output signal to perform the at least one operation of the system.

Abstract: An ophthalmic surgical cassette for removably receiving in a cassette receiving mechanism of an ophthalmic surgical system. The system includes first and second plunger valves. The cassette includes a body having a rear surface, an irrigation inlet for receiving irrigation fluid from a source, a first irrigation outlet for providing irrigation fluid to a first ophthalmic microsurgical instrument for use in an anterior segment ophthalmic surgical procedure, a first manifold fluidly coupling the irrigation inlet with the first irrigation outlet, a second irrigation outlet for providing irrigation fluid to a second ophthalmic microsurgical instrument for use in a posterior segment ophthalmic surgical procedure, and a second manifold fluidly coupling the irrigation inlet with the second irrigation outlet.

Abstract: A tool for cementing a liner to the glenoid cavity of a scapula. The tool comprises an elongated, hollow, rigid tube having distal and proximal ends with the distal end of the tube having either an angular portion or a curved portion which has a plurality of openings formed therein. The tube has a length such that the distal end thereof may be positioned in the glenoid vault and so that the proximal end of the tube may be placed in communication with a source of suction. An elongated sleeve member is slidably mounted on the tube and preferably has a sealing gasket at its distal end which may be moved into sealing engagement with the coracoid process around the opening formed therein. A flexible obturator is selectively extended through the tube to clear the tube of debris.

Abstract: Electrosurgical methods and apparatus for the controlled ablation of tissue from a target site of a patient. The instrument includes a shaft having proximal and distal end portion and an active screen electrode on the distal end portion; a return electrode arranged on the shaft spaced from the screen electrode; at least one electrical connector extending through the shaft that connects the active electrode with a high frequency power supply; at least one electrical coupling member (such as a ball wire) adapted to secure the active screen electrode to the shaft and to electrically couple the screen electrode to the at least one electrical connector; and an aspiration lumen within the shaft having a distal opening coupled to the single active electrode wherein the screen electrode inhibits clogging of the aspiration lumen.

Abstract: Male and female mating pieces of a gas-assisted electrosurgical accessory connector are connectable together by radially contacting a sealing surface formed on one mating piece with a resilient radially-compressible sealing member carried on the other mating piece. A gas-tight seal exists along a length of the sealing surface as the two mating pieces connect with relative connection movement. The existence of the gas-tight seal over a range of relative connection movement maintains the seal if the mating pieces should become slightly disconnected. The mating pieces are also restrained against separation from one another. A recess is formed in one of the mating pieces and a retention member carried on the other one of the mating pieces is biased into contact with the recess. Separation of the two connected members requires manual force to extract the retention member from the recess.

Abstract: A thrombectomy catheter system with occluder and method of using same for removal of tissue, such as thrombus and the like, from a vessel in the body. Multiple catheters and an occluder-bearing guidewire tube at a thrombus site provide for expandable deployment of a compliant occluder against the vasculature walls distal to the thrombus. The expanded occluder is maneuvered proximally to urge thrombus into close proximity with a retractable capture cone located distally on a capture catheter where the thrombus is dislodged, entrained, and broken into pieces by the action of a fluid jet emanator and then evacuated through the capture catheter.

Abstract: An aspiration flow resistor 10 includes an inlet 12 and an outlet 14. A housing 16 is connected to the inlet 12 and outlet 14. A series of spaced walls 18 are disposed between the inlet 12 and the outlet 14. The walls 18 and the inlet 12 and the outlet 14 together with the housing 16 define a plurality of aspiration flow chambers 22. As aspirant flows from the inlet 12 to the outlet 14, a pressure decrease in the aspirant flow occurs at each wall 18 to provide resistance to aspirant flow.

Abstract: An improved smoke evacuation system and method for removing gaseous byproducts of surgical procedures and noxious vapors from chemicals is provided. The smoke and vapor evacuation system includes a vacuum head positionable at a surgical site or incorporated into a workstation. The vacuum head includes a plenum, and a plenum support for preventing the plenum from collapsing when a vacuum or low pressure is established therein, and is adapted to facilitate the use of the system in a variety of surgical or commercial procedures at a variety of surgical sites or commercial workstations.

Abstract: Apparatus with a pneumatic or hydraulic or mechanical therapeutic catheter. The therapy energy required to treat internal vessels of the patient is transferred by the same fluid or the same elements from the proximal end section to the distal end section of the catheter that transfer information from the distal end section to the proximal end section of the catheter. The information provides understanding of the estate of the vessel and how the therapy fluid of the therapy element of the catheter acts on the vessel.

Abstract: A suction limiting device with variable control for use in a surgical system includes a main vent body having a fluid carrying bore extending therethrough and a variable vent mechanism having a main vent opening in selective fluid communication with the fluid carrying bore so as to permit introduction of atmospheric air into the fluid carrying bore. The vent mechanism being adjustable so that the degree of airflow into the fluid carrying bore is variable between a fully open position to a fully closed position where atmospheric air is prevented from entering the fluid carrying bore. The suction limiting device also includes a valve disposed within the main vent body and positionable between an open position when negative pressure and a closed position when positive pressure exists in the main vent body.

Abstract: A flexible sheath is attached to an end of a rigid extension tube. The other end of the rigid extension tube is connected with a surgical handpiece. Two flexible sheaths may be used—one as a barrier against contamination of aspiration tubing and the other as a barrier against contamination of irrigation tubing. This is effected by securing two rigid extension tubes between the surgical handpiece and an associated one of the aspiration and irrigation tubings. Each flexible sheath is collapsible and expandable so they may be expanded from a collapsed condition over the associated aspiration or irrigation tubings and secured in the expanded condition. The aspiration and/or irrigation tubings are connected to a cassette of a surgical pack.

Abstract: Methods and apparatus are disclosed for treating body tissue whereby a section of tissue is drawn into contact with the open distal end of the first passageway of the apparatus. A tissue treatment fluid is introduced into the second passageway for treating the desired section of tissue retained within the first passageway. Methods and apparatus are also disclosed for positioning a medical device at a desired location within the heart. A portion of the apparatus is retained at a desired location of the heart and a medical device is extended through a passageway of the apparatus for contacting the heart at the desired location.

Abstract: A surgical/medical irrigator with a handpiece in which there is a pump from which irrigating fluid is discharged. The irrigating fluid is discharged from a discharge tube attached to the handpiece. Irrigating fluid is removed from the site to which it is applied through a suction tube also attached to the handpiece. A splash shield is removably attached to the ends of the discharge and suction tubes to limit fluid discharge. The splash shield is formed with a discharge chamber into which the fluid from the discharge chamber is discharged. The splash shield has a bore that leads from the discharge chamber to the suction tube through which fluid is drawn away from the discharge chamber. Seals between the discharge and suction tubes and the splash shield prevent fluid flow between the tubes and the splash shield.

Abstract: A medical/surgical irrigating handpiece with both a discharge line through which fluid is applied to the site and a suction line through which the discharge fluid is drawn away. The handpiece has a variable speed pulse pump. A single, variable-speed motor actuates the pump to regulate the pumping rate. Power to actuate the motor comes from a battery pack that remote to the handpiece. A control mechanism attached to the handpiece regulates the energization signal applied to the motor so as to regulate motor speed.

Abstract: An electrosurgical instrument for spinal procedures comprises a generally scoop-shaped cup whose periphery is electrically active and is capable of applying RF electrosurgical currents to spinal tissue. The active electrode may comprise an exposed bare wire at the leading edge of the cup. A conduit in a handle section can convey suction to the cup. A tissue clearing member is pivotably mounted on or inside the cup and can be manipulated via a lever on the handle to help dislodge tissue. The tissue clearing member may be a radially-extending vane for rotation in the plane of the cup edge. The tissue clearing member may also be made electrically active thus selectively providing unipolar or bipolar operation.

Abstract: The invention provides a variety of surgical instruments for forming a liquid jet, which are useful for performing a wide variety of surgical procedures. In some embodiments, the invention provides surgical liquid jet instruments having a pressure lumen and an evacuation lumen, where the pressure lumen includes at least one nozzle for forming a liquid jet and where the evacuation lumen includes a jet-receiving opening for receiving the liquid jet when the instrument is in operation. In some embodiments, the pressure lumen and the evacuation lumen of the surgical liquid jet instruments are constructed and positionable relative to each other so that the liquid comprising the liquid jet, and any tissue or material entrained by the liquid jet can be evacuated through the evacuation lumen without the need for an external source of suction.

Abstract: An electro-cauterizing cannula assembly for use in a power-assisted liposuction instrument having a hand-holdable housing and a mechanism for reciprocating the cannula assembly. The electro-cauterizing cannula assembly includes an inner and an outer cannula, each having a distal and proximal end and at least one aspiration aperture about the distal end. The inner cannula is disposed within the outer cannula and the inner and outer aspiration apertures are in at least partial registration to form an effective aspiration aperture. During aspiration of tissue, high-voltage RF power signals are supplied to the inner and outer cannulas to effect hemostasis about the reciprocating aspiration aperture. Such hemostasis is achieved by causing protein molecules within aspirated tissue to coagulate in response to the high-voltage RF signals being supplied across the reciprocating cannulas. The cannula assembly is releasably detachable from the hand-holdable housing to facilitate cleaning and sterilization of the same.

Abstract: The present invention provides systems and methods for selectively applying electrical energy to a target location within a patient's body, particularly including tissue in the spine. The present invention applies high frequency (RF) electrical energy to one or more electrode terminals in the presence of electrically conductive fluid to contract collagen fibers within the tissue structures. In one aspect of the invention, a system and method is provided for removing a vertebral disc in preparation for implanting a prosthetic disc or removing a portion of the vertebral disc such as the nucleus pulposus in preparation for placing a prosthetic nucleus within the annulus of the disc. The present invention also teaches shrinking residual tissue in preparation for placing the implants.

Abstract: A surge-flow regulator (36) for use with an ophthalmic surgical instrument (12) having an infusion line (20) adapted to irrigate a surgical site with fluid and an aspiration line (24) adapted to carry the fluid and particles of lenticular debris away from the surgical site. The surge-flow regulator (36) includes a flow limiting device (40) that is placed in fluid communication with the aspiration line (24) to control surge-flow of the aspirated fluid and lenticular debris through the aspiration line (24). The lenticular debris carried in the aspiration line (24) is processed into smaller particles before the fluid and debris are introduced to the flow limiting device (40).

Abstract: An improved irrigation system for removing arthritis causing fragments from a joint in the body includes a handpiece and a tip that is connectible to the handpiece. The tip includes a shaft that forms an irrigation lumen, and a debrider disposed along at least a part of the shaft. The debrider defines a substantially planar debriding surface for debriding the interior surfaces of the joint. The debrider may include a plurality of bristles extending from the shaft to the debriding surface.

Abstract: The present invention provides a coupling device for attaching a sleeve (40) to a surgical aspirator tip (10) that allows airflow between the external environment and the interior of the sleeve (40). The coupling device includes a male member (26) attached to the tip (10) and a female member (42) formed in the proximal end of the sleeve (40). The male member (26) includes at least one longitudinal groove (100). When the male member (26) is received into the female member (42), at least one venting channel (80) is defined between at least one longitudinal groove of the male member (26) and the inner surface of the female member (42). Venting channel (80) permits airflow between the external environment and the interior of the sleeve (40).

Abstract: A transdermal transport device includes a reservoir for holding a formulation of an active principle, and one or more needles. Each needle has a bore through which the formulation is transported between the reservoir and a biological body, and has an end portion that is substantially aligned in a plane parallel to a surface of the biological body when the device is placed on the surface. The device also includes a vacuum generator which creates a suction to draw a portion of the surface beyond the plane of the end portions to enable the end portions to penetrate the portion of the surface as the needles are translated along an axis that is substantially parallel to the plane.

Abstract: The liposuction apparatus (1) comprises in combination a tubular canula (3) having at its distal extremity (18) one or more suction orifices (24) and connected at its proximate extremity (19) to a suction source (14) in communication with these orifices, and a hand piece (2) delivering a spray of working liquid (4) under pressure. The hand piece delivers the spray of liquid under pressure using a conduit opening into an ejection orifice which, when the canula is attached to the hand piece, is located opposite an ejection orifice in the canula located at its distal extremity. A liposuction method using the apparatus is also taught. This invention is of interest to manufacturers and users of surgical equipment.

Abstract: A decompressing and feeding device for safely feeding in the gastrointestinal tract of a recovering patient continuously aspirates and feeds at a rate commensurate with the ability of the intestines to absorb fluids including nutrient. Air is also aspirated in the process so that neither air nor excess fluids cause distension in the gastrointestinal tract. Digestive juices and nutrients that are aspirated are continuously refed together with unused feeding material into the gastrointestinal tract at a location that more efficiently moves and digests the food. The device may include two aspirate reservoirs to which and from which aspirate is alternatingly and continuously transferred. To provide the continuous and alternating flow, a solenoid valve and timer switch device is provided. Alternatively, a device is provided with a single aspirate reservoir to which and from which aspirate is continuously transferred.

Abstract: A system for removing cells from an interior portion of an eye, including a continuous passageway adapted to pass a fluid therethrough. A first cutting device is coupled to an exterior portion of the continuous passageway for dislodging cells from the interior portion of the eye. The first cutting device moves relative to the exterior portion of the continuous passageway due to the passing of the fluid through the continuous passageway.

Abstract: The present invention is directed to a proximal catheter assembly that is configured to facilitate natural or suction-assisted aspiration through a catheter lumen. The proximal catheter assembly comprises a relief valve configured to regulate the level of suction-assisted aspiration provided through the working lumen of the catheter. When the level of suction-assisted aspiration exceeds a predetermined threshold, the relief valve opens to allow fluid to be drawn from tubing coupled to the proximal catheter assembly, thereby mitigating the relatively high levels of aspiration imposed upon the working lumen and the patient's vessel.

Abstract: A medical fluid suctioning device for selectively applying varied levels of suction pressure at a device-tissue interface includes a direct “trumpet”-type control mechanism in conjunction with a “venturi”-type control. A valve manifold is adapted to couple a vent pathway and a suction pathway simultaneously to the vacuum conduit adapted for connection to a vacuum source. The amount of resistance to flow due to vacuum pressure is adjusted simultaneously in both the vent pathway and the suction pathway in order to achieve controlled, selected levels of suction. Similarly shaped valve apertures are provided in inverse and reciprocal orientation along an axis of motion of a valve manifold. The apertures translate across ports to the suction and venting pathways simultaneously to vary applied suction to those pathways inversely.

Abstract: Liposuction devices and methods and surrounding aspiration systems and methods that reduce the chances of burning and necrosis. The devices include an evacuation tube surrounding an ultrasonic probe, including the distal end thereof to define a liquefaction and/or rupture chamber. The evacuation tube has one or more openings in the distal end through which tissue such as fatty tissue may enter for rupture/liquefaction therein. Containing the ultrasonic probe within the evacuation tube avoids any possible contact with surrounding tissue other than tissue that gets drawn into the liquefaction and/or rupture chamber. The size of the liquefaction and/or rupture chamber may be variable by adjustment of the axial position of the evacuation tube relative to the ultrasonic probe, or by selection of evacuation tubes of the desired length. Various embodiments are disclosed.

Abstract: A method and apparatus provided for controlling fluid control to and from an eye or a phacoemulsification handpiece. The handpiece includes an ultrasonically driven, hollow, sleeved needle and the method includes inserting the needle and sleeve into an eye for phacoemulsification of eye tissue and introducing fluid into the eye through an annulus established between the sleeve and the needle. Aspiration of fragmented tissue and fluid from the eye is conducted through the hollow needle. An initial irrigation fluid pressure is determined and the irrigation fluid flow and aspiration fluid flow are adjusted based upon the initial determination. Thereafter continued determination of irrigation fluid pressure is utilized to continuously adjust irrigation fluid flow and/or aspiration fluid flow.

Abstract: A method and apparatus provided for controlling fluid control to and from an eye or a phacoemulsification handpiece. The handpiece includes an ultrasonically driven, hollow, sleeved needle and the method includes inserting the needle and sleeve into an eye for phacoemulsification of eye tissue and introducing fluid into the eye through an annulus established between the sleeve and the needle. Aspiration of fragmented tissue and fluid from the eye is conducted through the hollow needle. An initial irrigation fluid pressure is determined and the irrigation fluid flow and aspiration fluid flow are adjusted based upon the initial determination. Thereafter continued determination of irrigation fluid pressure is utilized to continuously adjust irrigation fluid flow and/or aspiration fluid flow.

Abstract: The present invention provides improved methods, systems, devices and kits for performing lung volume reduction in patients suffering from chronic obstructive pulmonary disease or other conditions where isolation of a lung segment or reduction of lung volume is desired. The methods are minimally invasive with instruments being introduced through the mouth (endotracheally) and rely on isolating the target lung tissue segment from other regions of the lung. Isolation is achieved by deploying an obstructive device in a lung passageway leading to the target lung tissue segment. Once the obstructive device is anchored in place, the segment can be aspirated through the device. This may be achieved by a number of methods, including coupling an aspiration catheter to an inlet port on the obstruction device and aspirating through the port.

Abstract: The present invention is directed to a proximal catheter assembly that is configured to facilitate aspiration through a catheter lumen. The proximal catheter assembly enables natural aspiration to be achieved within the catheter lumen, for example, using an arterial-venous shunt, and further enables suction-assisted aspiration or infusion to be applied through the catheter lumen. This allows a physician to provide a substantially continuous level of retrograde flow within a vessel during a medical procedure without damaging the vessel wall, while providing the option of suction-assisted aspiration, when necessary, to further influence the level of aspiration within the vessel.

Abstract: Apparatus and methods for treating an intervertebral disc by ablation of disc tissue. A method of the invention includes positioning at least one active electrode within the intervertebral disc, and applying at least a first high frequency voltage between the active electrode(s) and one or more return electrode(s), wherein the volume of the nucleus pulposus is decreased, pressure exerted by the nucleus pulposus on the annulus fibrosus is reduced, and discogenic pain of a patient is alleviated. In other embodiments, a curved or steerable probe is guided to a specific target site within a disc to be treated, and the disc tissue at the target site is ablated by application of at least a first high frequency voltage between the active electrode(s) and one or more return electrode(s). A method of making an electrosurgical probe is also disclosed.