A patient in whom blood diversion due to cerebral venous steal is present, and abolishment of the cerebral venous steal is indicated, is treated by increasing the cerebral venous pressure in the patient. This increase in cerebral venous pressure restores the collapsed cerebral vasculature, thereby increasing cerebral blood flow. The increase in cerebral venous pressure may be achieved using an occluding catheter in the superior vena cava or the internal jugular veins, using external compression of the cervical veins, or any other suitable mechanism. The occlusion may be controlled precisely during treatment, possibly as a function of cerebral blood flow, and after treatment the patient may experience a persistent effect because the cerebral vasculature is no longer collapsed.

Hemostasis systems and related methods are generally described. In some embodiments, a hemostasis system may include an inflatable intrauterine balloon. The balloon may be configured to apply pressure to a patient's uterus to reduce the risk of postpartum hemorrhage. In some embodiments, the balloon may be inserted at least partially into the uterus and inflated. A support, which may be located inside the balloon, may expand from a contracted configuration to an expanded configuration to help maintain the balloon's position relative to the cervix when the balloon is inflated. In some embodiments, the support may contract with and/or due to deflation of the balloon, allowing the balloon to move out of the uterus. The balloon may be covered with a hemostatic covering (e.g., gauze preloaded with a hemostatic agent such as hexatomic acid) to enhance the balloon's hemostasis properties.

A device for dilating an ostium of a paranasal sinus of a human or animal subject may include: a handle; an elongate shaft having a proximal end coupled with the handle and extending to a distal end; a guidewire disposed through at least a portion of the shaft lumen; a dilator having a non-expanded configuration and an expanded configuration; and a slide member coupled with at least one of the guidewire or the dilator through the longitudinal opening of the shaft for advancing the guidewire and/or the dilator relative to the shaft.

An irrigation balloon catheter includes one or more inner balloons inside of an irrigation balloon. The inner balloon(s) can be compliant with a volume that is dynamically adjustable for rapid inflation, rapid deflation, complete deflation, and/or irrigation flow adjustment. An inflator tool can be configured to inflate or deflate the inner balloon to adjust flow from the outer, irrigation balloon to affect temperature at electrodes of the irrigation balloon.

Systems and methods for delivering fluid within a lumen may be provided. For example, a device can include an elongated tubular structure having a central opening through which fluid may flow. The central opening can be defined by an open proximal end and an open distal end. The elongated tubular structure can have an elastic section toward the open distal end. The device can also include a blocking device such as a balloon within the central opening of the elongated tubular structure that can help or be configured to prevent the flow of fluid through the central opening between the open proximal end and the open distal end. The device can further include a balloon disposed on an outer surface of the elongated tubular structure. The balloon can be affixed to the outer surface of the elongated tubular structure at a proximal and/or distal attachment site.

A system for endoscopic surgery within a body lumen of a patient including a flexible catheter having an expandable balloon at a distal portion and an access opening. The expandable balloon is expandable from a collapsed insertion configuration to an expanded configuration to provide an expanded chamber on a first side of the catheter. The access opening provides a window to access target tissue. The catheter includes a lumen dimensioned to receive an endoscopic instrument therethrough such that a distal end of the endoscopic instrument is positionable within the expanded chamber and angled laterally within the expanded chamber to access the target tissue through the window.

Enhanced dual purpose systems enable dilating of at least a lesion within a blood vessel and providing an anti-proliferative medicament in a non-attached form directly into the lumen of the vessel. Likewise provided is the ability to stop blood flow to prevent wash-out of the medicament during dwell time within the body lumen, and the ability to remove the medicament after the dwell time of the device to prevent unwanted exposure of the same within the body.

A handheld resector balloon system includes a balloon catheter with a resecting surface and hub coupled to a handheld pump. The hub includes an inflation port that supplies fluid to a first lumen of the catheter to repeatedly inflate and deflate the balloon in pulsed fashion to resect biological material. The hub may also include a delivery port for delivering an agent, such as drugs, to a second lumen of the catheter for delivery to the distal end of the catheter. The hub may also include an aperture for inserting a device, such as an imaging device, into the second lumen of the catheter. In some embodiments, an imaging module is coupled to a handheld pump, which may include a light source for supplying light, and image circuitry for converting an optical signal from the imaging device to electrical data to be output to a computer.

An endoscopy system including a balloon-equipped endoscope including a balloon which is configured for slidable frictional engagement with an interior wall of a body passageway and axial stretching of the interior wall when inflated to a slidable frictional engagement pressure and displaced axially along the body passageway and a balloon inflation subsystem operative to selectably inflate the balloon to the slidable frictional engagement pressure.

Tissue expansion system includes a pump, a controller, and inflatable bladder, and a pressure sensor. The pump is adapted for substantially continuous operation in response to a pressure within a subcutaneously implanted inflatable bladder. The pump is thus able to deliver inflation medium to the bladder when the pressure within the bladder is below a predetermined lower threshold while stopping delivery of the fluid when the pressure rises above a higher threshold or reaches a predetermined maximum volume.