Abstract: A catheter is adapted to exchange heat with a body fluid, such as blood, flowing in a body conduit, such as a blood vessel. The catheter includes a shaft with a heat exchange region disposed at its distal end. This region may include hollow fibers which are adapted to receive a remotely cooled heat exchange fluid preferably flowing in a direction counter to that of the body fluid. The hollow fibers enhance the surface area of contact, as well as the mixing of both the heat exchange fluid and the body fluid. The catheter can be positioned to produce hypothermia in a selective area of the body or alternatively positioned to systemically cool the entire body system.

Abstract: A kit for packing and supporting the nasal cavities after surgical procedures performed on the nose comprising two inflatable non-elastomeric balloons (6?, 6?) and inflation means (27) arranged so that, in use, each balloon (6?, 6?) can be located in a nasal cavity and inflated.

Abstract: An improved catheter device for selectively isolating and occluding a portion of the iliac vasculature of a patient includes an elongate hollow catheter shaft which is advanceable though the vascular system of the patient. The catheter shaft has a proximal portion that extends out from the patient and a distal portion adapted to be disposed within the iliac vasculature of the patient. A plurality of expandable members are disposed on the distal portion. One expandable member is dimensioned and configured so that when expanded it rests within the bifurcation of the descending aorta to the common iliac arteries (and/or within the bifurcation of the inferior vena cava that leads to the common iliac veins) so as to fixate the catheter within the iliac vasculature of the patient. At least two other expandable members are spaced apart from the fixation member and configured to selectively isolate and occlude blood flow through different portions of the iliac vasculature.

Abstract: The invention generally relates to internal (e.g., implantable, insertable, etc.) drug delivery devices which contain the following: (a) one or more sources of one or more therapeutic agents; (b) one or more first electrodes, (c) one or more second electrodes and (d) one or more power sources for applying voltages across the first and second electrodes. The power sources may be adapted, for example, to promote electrically assisted therapeutic agent delivery within a subject, including electroporation and/or iontophoresis. In one aspect of the invention, the first and second electrodes are adapted to have tissue of a subject positioned between them upon deployment of the medical device within the subject, such that an electric field may be generated, which is directed into the tissue. Furthermore, the therapeutic agent sources are adapted to introduce the therapeutic agents into the electric field.

Abstract: A combination aspiration/irrigation and illumination device using optical fibers circumferentially disposed around the aspiration conduit for transmitting illuminating light to a cavity to be aspirated. The ends of the optical fibers being formed at an angle relative to the aspiration conduit so as to direct the illuminating light inward to provide intensified illumination ahead of the aspiration conduit.

Abstract: A method of sealing a network of veins which provide drainage to the testes, comprising: (a) inserting a catheter into a main vein of said network; and (b) causing said vein to seal over at least a length, with a single application of vein irritant such that no forward movement of the catheter is required.

Abstract: An endoscope preferably comprising an alternating propulsion system in which an endoscope shaft is advanced by means of an auxiliary means (e.g. a hose preferably including fluid pads or a guiding wire/net) in a canal-shaped cavity by the fact that the endoscope shaft and the auxiliary means are alternately resting with respect to a cavity to be inspected and, at the same time, the element not at rest can be advanced while being guided along the resting element into the cavity, or are simultaneously moved forward, wherein in the latter case the basic stiffness of the auxiliary means is higher than that of the shaft.

Abstract: An enteral feeding unit or system that minimizes the occurrence of gastro-esophogeal-pharynegal reflux during feeding is described. The enteral feeding unit or device includes an automatable feeding pump with a feedback sensor for sensing a relative pressure in a patient's stomach and esophagus, and a regulator system for controlling or monitoring feeding rate to said patient as a function of said relative gastro-esophageal pressure. The system includes a stomach probe that has a fluid-tight closure of the esophagus.

Abstract: A catheter assembly may comprise a guide catheter, a balloon catheter with a steering balloon and a stabilizing balloon and a guide wire. The stabilizing balloon secures the balloon catheter to the guide catheter while the steering balloon secures the catheter assembly to the vessel wall. In another embodiment, the balloon catheter has three balloons engaged to the exterior surface, a steering balloon, a stabilizing balloon and an anchoring balloon.

Abstract: A novel approach to diagnostic and therapeutic interventions in the peritoneal cavity is described. More specifically, a technique for accessing the peritoneal cavity via the wall of the digestive tract is provided so that examination of and/or a surgical procedure in the peritoneal cavity can be conducted via the wall of the digestive tract with the use of a flexible endoscope. As presently proposed, the technique is particularly adapted to transgastric peritoneoscopy. However, access in addition or in the alternative through the intestinal wall is contemplated and described as well. Transgastric and/or transintestinal peritoneoscopy will have an excellent cosmetic result as there are no incisions in the abdominal wall and no potential for visible post-surgical scars or hernias.

Abstract: A gastrostomy tube including a body having a hub portion and a tubular portion. The body defines a primary lumen having a first end in communication with an opening in the hub portion. The primary lumen has a second end in communication with an opening located in the tubular portion. The tube also includes a port supported on the body communicating with a secondary lumen. The port is adapted to engage an end of a luer tip syringe. The tube includes an external balloon located at a proximal end of the body. The tube has an internal balloon located distally from the external balloon. The internal and external balloons are in fluid communication with the port via the secondary lumen such that each is inflatable. The internal and external balloons enable a clinician to indirectly observe the internal balloon by observing the external balloon.

Abstract: A medical device including an element defining a central lumen and a secondary lumen. The device includes a prefilled balloon having an interior surface operatively communicates with the secondary lumen. The device includes a securement balloon having an interior surface communicating with the secondary lumen. The securement balloon, secondary lumen, and prefilled balloon define a closed fluid system. The securement balloon is stronger than the prefilled balloon so fluid in the closed fluid system inflates the prefilled balloon before inflating the securement balloon. The device includes a transfer sleeve movable from a first position spaced from the prefilled balloon to a second position positioned around the prefilled balloon to urge fluid from the prefilled balloon into the securement balloon. When the transfer sleeve is in the first position, the securement balloon is substantially collapsed. When the transfer sleeve is in the second position, the securement balloon is inflated.

Abstract: An assist device (10) for sclerosing treatment of varicose veins, aimed at being partially inserted into a blood vessel (20), including a tubular element (11), which has at least three ways (13, 14, 15), at least two of which (13, 14) are connected each one to at least one related inflatable balloon element (12, 12?, 16) by at least one through hole (30, 31), and at least one remaining way (15) of said three ways (13, 14, 15) has likewise at least one hole (32) for the passage of a sclerosing substance (17), aimed at reaching a wall (18) of said blood vessel (20), in which at least one (16) of said at least two balloon elements (12, 12?, 16) has an elongated shape extending toward at least another balloon element (12, 12?) and a variable volume comprised in the range of 30% to 99% of the space inside said blood vessel, independently from the initial dimensions of the vessel (20), interposed between the external surfaces of the outermost of said at least two balloon elements (12, 12?, 16).

Abstract: A self-expanding medical occlusion device treats a heart defect in a patient and is inserted into the body in minimally invasive fashion using a catheter system, and includes a braiding of thin threads which exhibits a first preliminarily definable shape as the occlusion device is being inserted into the patient's body and a second preliminarily definable shape in the implanted state, whereby the occlusion device is in a collapsed state in the first shape of the braiding and in an expanded state in the second shape of the braiding. The threads of braiding are composed of a shape memory polymer composite such that braiding deforms from a temporary shape to a permanent shape in consequence of an external stimulus, whereby the temporary shape is given in a first profile form of the braiding and the permanent shape is given in a second profile form of the braiding.

Abstract: Materials and Methods for producing localized hypothermia in a patient (e.g., for treatment of acute pancreatitis and pancreatic cancer).

Abstract: Composite fiber reinforced balloons for medical devices prepared by applying a web of fibers to the exterior of a preformed underlying balloon and encasing the web with a matrix material to form a composite balloon. The fiber web is applied to at least the cone portion of the underlying balloon form. Either the cone portion of the underlying balloon form, or the web fibers applied to said cone portion, or both, have a friction-enhancing material coated thereon.

Abstract: A urological medical system for performing a controlled hydrodistention of the urinary bladder for treating a bladder dysfunction problem comprised of a programmed CPU with associated computer equipment for facilitating an automatic control of a treatment procedure to be performed on a patient, a saline solution warmer, a saline solution pump, a four-way catheter wherein a channel is provided for monitoring the pressure within the bladder during the procedure, a syringe for infusing a medicine through the catheter and a strapping device to secure the syringe and to slidingly engage the catheter to a leg of the patient. Desired parameters are monitored during the procedure and a desired pressure is maintained in the bladder for a predetermined time to perform the controlled hydrodistention of the urinary bladder.

Abstract: An improved catheter device for selectively isolating and occluding a portion of the iliac vasculature of a patient includes an elongate hollow catheter shaft which is advanceable though the vascular system of the patient. The catheter shaft has a proximal portion that extends out from the patient and a distal portion adapted to be disposed within the iliac vasculature of the patient. A plurality of expandable members are disposed on the distal portion. One expandable member is dimensioned and configured so that when expanded it rests within the bifurcation of the descending aorta to the common iliac arteries (and/or within the bifurcation of the inferior vena cava that leads to the common iliac veins) so as to fixate the catheter within the iliac vasculature of the patient. At least two other expandable members are spaced apart from the fixation member and configured to selectively isolate and occlude blood flow through different portions of the iliac vasculature.

Abstract: A method for controlling the systemic pressure at the end of a cardiac operation wherein a double-balloon catheter is brought, along a single path, close to the junction of a right atrium with a superior and inferior venacavae. The distance between a first and a second balloon is then adjusted so that they are placed at an adequate position in the superior and inferior venacavae respectively. The balloons are inflated and one checks whether a balance between the outputs of the two sides of the heart has been restored. The balloons are deflated when a new equilibrium is established and the catheter is removed along the same path. A double balloon occlusion device especially designed to perform said operation is also described.

Abstract: A system for examining a colon includes a catheter, such as a rectal catheter, having a proximal end, a distal end, and a central lumen extending from the proximal end to the distal end of the catheter, and a flexible tube coupled with the catheter. The system includes a first balloon located adjacent a distal end of the flexible tube, and a second balloon extending around the catheter and being located between the distal and proximal ends of the catheter, whereby the distance between the first and second balloons is adjustable by sliding the flexible tube through the central lumen of the catheter. The first and second balloons are inflatable for isolating a section of a colon, and a gas or contrast may be introduced into the isolated colon section for conducting the examination.

Abstract: A guiding catheter includes an inner guide movably disposed within an outer guide. Both inner and outer guides include inner and outer balloons, respectively, located at the distal tip of the guides. The inner guide balloon is fluted, thereby allowing blood to flow past the implanted balloon when inflated. The outer balloon is substantially annular in shape and is deployable as an occlusion balloon. Various sensors can be provided at the distal end of the guiding catheter to assist in locating a destination vessel or structure of interest.

Abstract: A kit for performing angioplasty or stenting in a blood vessel, composed of at least two components. One of the components includes a first catheter providing a blood bypass flow path and carrying a blocking balloon and a blood vessel dilation device. Another one of the components includes a second catheter having an imperforate wall enclosing an axial lumen and having an open distal end, a hollow tube surrounding, and movable longitudinally with respect to, the second catheter, and a second blocking balloon carried by the hollow tube.

Abstract: The invention is directed to a balloon catheter comprising, in addition to one or more balloons and one or more inflating/deflating conduits having a novel design which enables a predetermined sequence of inflation/deflation of a number of balloons via a single lumen. The invention is also directed to an indwelling device for direct organ (renal) perfusion to be harnessed to a standard single lumen pump drive. The invention is also directed to perfusion of a side branch vessel (e.g. renal artery) from a main branch vessel (e.g. aorta) with minimal risk of obstructing the target vessel.

Abstract: One aspect of the invention relates to a device for control of hemorrhage from major blood vessels in acute trauma. The device can be a self sizing expandable/collapsible device placed percutaneously across the site of injury and fitted with intravascular imaging to allow visualization of positioning without the need for x-ray equipment or an operating room. The expandable/collapsible device can be tapered to accommodate a large variance in vessel size and can be textured with treads to prevent movement in high flow vessels. The expandable/collapsible device can be placed at the patient's bedside, provides for vascular control during definitive repair, and can be removed after said repair.

Abstract: A fluid delivery catheter configured to allow optimal fluid distribution through each electrode by varying the diameter of a catheter lumen is disclosed. Uniform or different fluid flow rates through longitudinally spaced apart elution holes may be achieved. Exemplary fluids for use with the catheter include a cooling fluid, a therapeutic fluid, and a medication.

Abstract: A rectal balloon apparatus has a shaft with a fluid passageway extending therethrough. A balloon is affixed over an end of the shaft such that the fluid passageway communicates with an interior of the balloon. The balloon has a laterally flat surface thereon when inflated. The laterally flat surface of the balloon has a longitudinal groove formed thereon. The balloon having a pair of bulges formed thereon when the balloon is inflated. A ring is affixed to the shaft adjacent the balloon. The shaft has a plurality of holes formed thereon opening to an interior of the balloon.

Abstract: The invention relates to an enteral feeding catheter (1) for channelling flowable nutrient into a patient's digestive tract, such as into patients stomach, duodenum or jejunum, said catheter having a first lumen (2), having an opening (3) for connecting it to a supply for of nutrient and channelling said nutrient from the proximal end (P) to the distal end (D), the distal end (D) of the first lumen (2) being provided with several radial outlets (4) for the exit of said nutrient into patient's digestive tract, the catheter (1) further comprising a second lumen (7), for being connected to a source/sink of gas (26) and a gas pressure gauge (24) at its proximal end and being connected to an inflatable and deflatable distal balloon (6) provided on the catheter (1) near the distal end (D). The invention refers also to a computer system and computer program to operate said feeding catheter.

Abstract: An enteral feeding unit or system that minimizes the occurrence of gastro-esophogeal-pharynegal reflux during feeding is described. The enteral feeding unit or device includes an automatable feeding pump with a feedback sensor for sensing a relative pressure in a patient's stomach and esophagus, and a regulator system for controlling or monitoring feeding rate to said patient as a function of said relative gastro-esophageal pressure. The system includes a stomach probe that has a fluid-tight closure of the esophagus.

Abstract: Devices, methods and systems for delivering drugs and therapeutic fluids to the prostate without requiring piercing of the prostate. An infusion catheter includes at least two inflatable balloons including a distal balloon providing a seal between the bladder and the prostatic urethra as well as a proximal balloon for sealing off the prostatic urethra from the penal urethra. The infusion catheter can include a number of lumens such as, for example, a drug delivery lumen, a drainage lumen, and one or more inflation lumens. The infusion catheter can have one or more drug delivery ports located between the distal balloon and the proximal balloon, wherein each drug delivery port is in fluid communication with the drug delivery lumen. In addition, the catheter can include one or more intermediate balloons at selected locations between the proximal balloon and the distal balloon for isolating portions of the prostate from exposure to treatment.

Abstract: The present invention provides devices for closing septal defects, such as a patent foramen ovale (PFO). The closure devices include a proximal anchor member, a distal anchor member, and at least one flexible center joint connecting the two anchor members. According to some embodiments, the proximal and/or distal anchor members may include a generally cylindrical member split along the central portion of its length to form an elongate oval. The proximal and/or distal anchor members may further include a tissue scaffold. At least some of the closure devices according to the present invention are repositionable and retrievable.

Abstract: The present invention provides a method and system for treating an ostium of a side-branch vessel. The system includes a catheter, a first inflatable member, a stent disposed on the first inflatable member, and a second inflatable member. The first inflatable member is disposed on a distal portion of the catheter, while the second inflatable member is disposed on a proximal portion of the catheter. The first inflatable member is inflated a first time to expand the stent within the side branch. The first inflatable member is then deflated, advanced, and inflated a second time to anchor the system while the second inflatable member is inflated to conform a portion of the stent to the ostium of the side-branch vessel.

Abstract: Methods and devices for treating vulnerable plaque deposits within a blood vessel, having an inner surface and one or more plaque deposits containing a core material are disclosed. A device in accordance with an exemplary embodiment of the present invention includes an elongate shaft having a proximal end and a distal end, a balloon disposed about the elongate shaft for engaging one or more plaque deposits and extracting the core material therefrom, a first venturi section disposed proximally of the balloon, and a second venturi section disposed distally of the balloon.

Abstract: An apparatus and method for measuring the compliance of the lower esophageal sphincter (LES), the apparatus including a catheter having a plurality of extendable members for both measuring the compliance of the LES and stimulating the esophagus which relaxes the LES to obtain a more clinically relevant measurement of LES compliance. In one embodiment, the plurality of extendable members include a first balloon which is located and inflated within the esophagus to trigger esophageal motility, a second, non-elastic balloon that is positioned within the LES, and a third balloon which is inflated within the stomach to help align the second balloon with LES. Incrementally increasing volumes of air are introduced into the second balloon, with the resulting pressures exerted by the LES calculated and compared to normative values to assess the condition of the LES.

Abstract: A central venous catheter includes coolant supply and return lumens which communicate coolant to and from first and second heat exchange membranes arranged along the distal segment of the catheter. The coolant in the heat exchange membranes removes heat from the patient. Additional lumens are provided for conventional central venous catheter uses.

Abstract: Apparatus for hemostasis of an artery having a puncture after arterial catheterization, the apparatus includes a catheter introducer having a forward end and a hemostasis device including an elongate flexible hollow shaft having an inflatable anchor balloon at a forward end thereof and an inflatable peripheral balloon adjacent the forward end of the flexible hollow shaft, the hemostasis device being arranged to be insertable into an artery via the catheter introducer.

Abstract: A medical device system and method allows an arterial bypass graft to be proximally anastomosed to an aorta during a beating heart procedure without substantial loss of blood by use of an endolumenal aorta isolation assembly provided along the distal end portion of an elongate catheter body. The aorta isolation assembly includes proximal and distal portions that are separated by an isolation region and that are adjustable to first and second extended positions, respectively, which are adapted to circumferentially engage the aortic wall and isolate upstream and downstream aspects of an exterior space between the elongate body and the aortic wall. The intermediate region is adapted to be positioned along the proximal anastomosis site such that the distal and proximal portions when adjusted to the first and second extended positions circumferentially engage the aortic wall on upstream and downstream sides of the proximal anastomosis site.

Abstract: A vascular catheter assembly includes an over-the-wire stent deployment catheter and a flow-by-channel assembly. The stent deployment catheter is positioned just below the occluded artery in accordance with standard procedures. The flow-by-channel then shunts blood, and thus all friable plaque, from the high pressure carotid occlusion to the negative pressure extremity to effectively reverse the flow of blood through the occluded artery. The stent is then advanced into the narrowed artery and deployed. Thus, the vascular catheter assembly takes advantage of the collateral blood flow to solve the problem of stroke during endovascular procedures.

Abstract: Compositions, methods, kits, and apparatus are provided for delivering a macromolecular assembly such as a plasmid, virus vector, or other gene vector, to an extravascular tissue such as muscle tissue. The composition comprises the macromolecular assembly and a vascular permeability-enhancing agent. In another embodiment, the composition further comprises a vasodilating agent. The method of the invention comprises proving a vascular permeability-enhancing agent to a blood vessel and providing a macromolecular assembly to the vessel. An oxygenator useful for providing oxygen to a fluid extracorporeally prior to providing the fluid to a blood vessel of a mammal is included in the invention. Kits, apparatus, and methods for using the catheters described herein for isolating cardiac circulation, diverting caval blood flow from the right atrium, and for other purposes, are also described.

Abstract: A system and methods are described for performing catheter based procedures on high risk patients that mitigate the risk to the patient and extend the acceptable time window for response when emergencies or complications arise. The system is useful for stopped heart catheter procedures or as a safety backup in beating heart catheter procedures and is compatible with concurrent or sequential surgical interventions. The system combines a therapeutic or diagnostic catheter subsystem with a selective aortic perfusion and cardiopulmonary bypass subsystem. The catheter subsystem may include catheters for angioplasty, stent delivery, atherectomy, valvuloplasty or other diagnostic or therapeutic procedures.

Abstract: A system for controlling patient temperature uses a central venous line catheter having axially spaced distal and proximal heat exchange balloons. The central venous line catheter is provided with one or more lumens for providing access to the central blood supply of the patient, and with additional lumens for communicating heat exchange fluid to the balloons. Heat exchange fluid temperature is controlled through a feed back loop in which patient temperature is sensed and used to control a temperature control unit comprising a heating device and/or a cooling device in heat exchange relationship with the heat exchange fluid. A tubing set transports the heat exchange fluid between the central venous line and the temperature control unit, with a pump serving to circulate the fluid in a closed fluid circuit in the system.

Abstract: A system for controlling patient temperature uses a central venous line catheter having axially spaced distal and proximal heat exchange balloons. The central venous line catheter is provided with one or more lumens for providing access to the central blood supply of the patient, and with additional lumens for communicating heat exchange fluid to the balloons. Heat exchange fluid temperature is controlled through a feed back loop in which patient temperature is sensed and used to control a temperature control unit comprising a heating device and/or a cooling device in heat exchange relationship with the heat exchange fluid. A tubing set transports the heat exchange fluid between the central venous line and the temperature control unit, with a pump serving to circulate the fluid in a closed fluid circuit in the system.

Abstract: A fluid operated retractor for use in surgery. The retractor has a portion that is expandable upon the introduction of fluid under pressure. The expandable portion, is made of a material strong enough, and is inflated to enough pressure, to spread adjoining tissues within the body. The retractor is especially useful in fiber optic surgery because it can be inserted percutaneously through a small opening then expanded to a much larger dimension when in the desired location, to retract tissue from within. The retractor may be used to spread a joint such as a knee joint or a shoulder joint, or may be used to separate tissue planes generally, to improve visualization and create a working space for the surgeon.

Abstract: The balloon catheter comprises a catheter tube surrounded distally by an elongated inflatable balloon. Throughout the catheter tube is a longitudinal lumen for positioning a radioactive radiation emitter within the balloon. The catheter comprises a second lumen for directing inflation fluid into the balloon. Belt means creating a waist are mounted on the balloon to squeeze it down to nearly the diameter of the catheter thereby leaving a small passage for the inflation fluid. The belt means divide the balloon into sections to assure a close center fit of the catheter within the balloon.

Abstract: The present invention provides an aortic catheter having an upstream occlusion member positioned in the ascending aorta between the coronary arteries and the brachiocephalic artery and a downstream anchoring member positioned in the descending aorta, downstream of the aortic arch. The upstream occlusion member is in the form of a narrow, disk-shaped inflatable balloon. The downstream anchoring member may be a larger inflatable balloon or other anchoring structure that provides sufficient friction to prevent migration of the balloon catheter in the upstream or downstream direction. In addition, an arch perfusion lumen, a corporeal perfusion lumen and a cardioplegia lumen are provided for performing selective perfusion and cardioplegic arrest.

Abstract: A medical device assembly is adapted to isolate the heart from systemic circulation while perfusing oxygenated blood to the systemic arterial circulation during a minimally invasive bypasss procedure. An arterial catheter with an external shunt valve forms a funnel which shunts antegrade aortic blood flow from the aortic root, into a distal flow port and through an internal flow lumen in the catheter, out an intermediate flow port along the catheter proximally of the anchor, and into the systemic arterial circulation. A distal internal valve selectively occludes the shunted antegrade aortic blood flow between the distal flow port and the intermediate flow port and isolates the left heart chambers from the systemic arterial circulation. Oxygenated blood may then flow from a cardiopulmonary bypass pump, distally through the internal flow lumen, out the intermediate port.

Abstract: Methods and devices for treating vulnerable plaque deposits within a blood vessel, having an inner surface and one or more plaque deposits containing a core material are disclosed. A device in accordance with an exemplary embodiment of the present invention includes an elongate shaft having a proximal end and a distal end, a balloon disposed about the elongate shaft for engaging one or more plaque deposits and extracting the core material therefrom, a first venturi section disposed proximally of the balloon, and a second venturi section disposed distally of the balloon.

Abstract: A method for treating loosely formed, friable or fragile lesions in a patient's blood vessel. A catheter having a pair of sealing mechanisms is advanced such that the sealing mechanisms are positioned distal to and proximal to the lesion. The sealing mechanisms are activated to seal the vessel on either side of the lesion. A medication is then delivered through the catheter to the sealed area of the vessel. The medication interacts with the lesion in order to partially or completely solidify it. Once the lesion is solidified, the catheter is removed and the lesion can be treated with a conventional intravascular device.

Abstract: A catheter and a method of using the catheter are disclosed that serve to create an efficient and rapid controlled manner of regulating a patient's body temperature. The catheter is a heat exchange catheter insertable into a blood vessel of a patient, circulating a heat exchange fluid therein, and including a spiral-shaped inflatable balloon that mixes laminar layers of the heat exchange fluid flowing inside the balloon.

Abstract: A balloon catheter having a first balloon member and a second distal expandable member. The increased distal profile of the catheter with inflation of the second distal expandable member can deflect the distal-most end away from stent walls and edges. Another catheter has a distal region including longitudinal slits and a pre-stressed body configured to expand upon exposure to warm body fluids. Another catheter has a distal region including a first, inner tube disposed about a second, innermost tube. The inner and innermost tubes are secured at the distal-most end. The distal region includes longitudinal slits through the inner tube, thereby defining flaps between the slits. The innermost tube can be retracted relative to the inner tube disposed about the innermost tube, thereby causing the longitudinal flaps to expand outward, thereby increasing the maximum radial extent of the distal region. In yet another embodiment, a balloon catheter having a first guide wire tube is provided.

Abstract: The emboli protection system provides one or more inflatable blocking balloons for isolation of a section of a blood vessel to prevent migration of emboli from the section during an interventional procedure, and fluid infusion and evacuation ports for flushing emboli from the isolated section. One embodiment provides for a distal blocking balloon catheter, over which an interventional device can be introduced, and a proximal blocking balloon catheter to be introduced over the interventional device for isolating a portion of a blood vessel to be treated. The blocking balloons can be perforated to provide the infusion ports, and thrombolytic inflation fluid may be used to break down and dissolve thrombus and plaque in the isolated portion of the blood vessel.