Abstract: A histology tissue embedding apparatus including a reservoir for an embedding medium and an outlet valve connected to the reservoir through which the embedding medium is dispensable, and including trigger means which control the operation of the outlet valve, the trigger means having a rest position in which the outlet valve is closed, wherein the rest position of the trigger means in relation to the outlet valve is adjustable.

Abstract: A tracheal tube assembly includes an outer cannula configured to be positioned in a patient airway and an inner cannula configured to be disposed inside the outer cannula. The tracheal tube assembly further includes a flange member secured about the outer cannula, and a connector coupled to a proximal end of the outer cannula. The connector is configured to provide a view of the inner cannula, and the inner cannula and the connector form a contiguous passageway for exchanging fluid with the patient airway in operation.

Abstract: Various embodiments of tracheostomy tube assemblies including a first subassembly and a flange subassembly are provided. The first subassembly includes a connector and a first spherical bearing element coupled to a first end of the connector. The first spherical bearing element includes at least two protrusions radially offset about a circumference of the first spherical bearing element. The flange subassembly includes an outer spherical bearing element having recesses for receiving the at least two protrusions and being adapted to encapsulate the first spherical bearing element.

Abstract: Various embodiments of tracheostomy tube assemblies including a cannula, a cap, and a flange are provided. The cannula includes a distal end and a proximal end, the distal end being adapted to be inserted into a patient's trachea. The annular cap includes an annular body having a first surface adapted to be received into the proximal end of the cannula to retain a portion of the cap in the annular body. The flange member includes a second surface that engages the proximal end of the cannula such that the proximal end of the cannula is retained between the second surface of the flange member and the first surface of the annular cap. The flange member also includes a third surface adapted to engage an inner surface of the annular body of the annular cap to retain the flange member between the annular cap and the proximal end of the cannula.

Abstract: Systems and methods that utilize tracheal tubes having one or more adjustable flanges are described. The adjustable flanges may be disposed on the tracheal tube at various angles. Further, the adjustable flanges may be repositioned on the tracheal tube, thus allowing a clinician or patient to reconfigure the tracheal tube in situ so as to more comformably fit the tracheal tube to a variety of patient anatomies. Flange extensions are also provided that may extend the overall flange length, and may also be repositioned at various angles. The use of techniques such as adjustable flanges and adjustable flange extensions allow a better fit to a particular patient's anatomy and provide increased patient comfort.

Abstract: Various embodiments of a tracheal tube having a tubular body with an open distal end and a tube wall with a variable thickness are provided. The tube wall may include a thickened section comprising a void. The tracheal tube may also include an offset ventilation lumen disposed in the tubular body and adapted to facilitate airflow to and from a patient. Embodiments of the tracheal tube may also include a suction lumen disposed in the thickened section of the tube wall and terminating in a port opening into the void for removal of secretions from the patient's trachea.

Abstract: A tracheal tube assembly includes a connector body, a cannula extending from the connector body, and an insert that provides rigidity to the connector body and retains the cannula in the connector body. The cannula has a tapered upper end that fits between conforming tapered sections of the connector body inner surface and the insert. The insert may include features to prevent rotation of the cannula as well as rotation of the insert in the connector body. Features of the insert and connector body may also interface to mechanically retain the insert in the connector body. Different sizes of cannula may be accommodated by different inserts, while using the same or different connector bodies.

Abstract: Various embodiments of a tracheal tube having spaced lumens and an associated ported adapter are provided. The lumens of the tracheal tube are spaced around the circumference of the tracheal tube to facilitate evacuation (e.g., suctioning and blowing) and other applications at various locations around the circumference of the tracheal tube. The ported adapter includes lumen extensions that may be inserted into the lumens of the tracheal tube, thereby forming a connection between the ported adapter and the tracheal tube. More specifically, hollow ports extending through the lumen extensions and the body of the ported adapter facilitate connection of the lumens of the tracheal tube with external equipment such as, for example, evacuation equipment for suctioning and blowing into and out of the lumens of the tracheal tube.

Abstract: A histology tissue embedding apparatus including a reservoir for an embedding medium and an outlet valve connected to the reservoir through which the embedding medium is dispensable, and including trigger means which control the operation of the outlet valve, the trigger means having a rest position in which the outlet valve is closed, wherein the rest position of the trigger means in relation to the outlet valve is adjustable.

Abstract: The present disclosure describes a medical which includes a body defining a conduit. The body includes a multilayer wall having at least one edge. The wall including a core layer positioned between an inner layer and an outer layer, wherein at least one of the inner and outer layers encapsulates the core layer along the edge.

Abstract: Methods for identifying defects in blood vessels and treating such defects are provided. The methods comprise administering to a patient a composition comprising a labeled delivery ligand capable of preferentially accumulating at or near blood vessels defects. In some embodiments, the delivery ligand may carry one or more active agents to the defect.

Abstract: A vena-cava filter features an inflatable balloon at or near the distal end of an elongate flexible multiple-lumen core or stem. The balloon is suitably configured in a preferred construction at or near the distal end of an elongate flexible multiple-lumen core. The balloon is suitably configured in a preferred embodiment for femoral-vein insertional installation; and in another embodiment the balloon is suitably configured for jugular-vein insertional installation. In both embodiments, the balloon is deflated prior to insertion; it is inflated to become a filter when properly positioned in the vein, and finally it is deflated for removal purposes. Installation may proceed pursuant to guide-wire techniques commonly used for catheter installation. Each of the indicated two embodiments is described for the case of additionally providing for injection of a tracer or a thrombolytic agent at a location in the vein at proximal (i.e., upstream) offset from the region of filter action.

Abstract: A method for therapeutically or prophylactically treating a diagnosed or potential deep-vein thrombosis involves intermittent application of tourniquet action to the leg at a location preferably close to the ankle, i.e., at the distal-calf region of the leg, in time-coordinated relation to artificially stimulated foot-pump action; the level of tourniquet action is such as to reduce the availability of superficial veins to carry the venous-return flow that is stimulated by foot-pump action, and the level of tourniquet action is also insufficient to materially affect access to deep-veins which are the primary target of therapeutic or prophylactic treatment.In a modification, the sequencing of tourniquet and foot-pump action is changed to enhance the priming of blood in the plantar veins of a foot which must remain elevated above the heart level of a patient confined to bed, whereby circulation can be more effectively stimulated by foot-pump action.