Abstract: An extracorporeal blood set may be primed with physiological solution for use in a blood transporting process such as hemodialysis. The set comprises tubing having a patient connector on an end thereof, and a first branch tube in connection with a source of the solution. The branch tube connects with the set between the ends of the set. The branch tube also connects with further branch tubing, having a second connector which is capable of sealing connection with the patient connector. The method comprises the steps of connecting the patient connector and the second connector to form a closed loop of tubing. One then passes the solution from the source in flow through the first branch tube and further branch tubing to fill them and the set tubing with the solution. One then disconnects the patient connector for subsequent connection with the vascular system of a patient.

Abstract: A medical device has an interior for containment of fluids; an opening into the interior, an elastomeric wall comprising a fixedly placed, flexible barrier across the opening; and a retention wall positioned adjacent to a peripheral portion of the elastomeric wall. The retention wall defines a central opening and has a generally rigid retention zone surrounding the central opening, to engage and retain a connector tube which is advanced into the central opening to displace the elastomeric wall and to open a flow aperture through the elastomeric wall, for flow through the wall and connector tube. One of the retention zone and connector tube are made of a material of sufficient hardness that material of the other engaging member is deformed by engagement therewith, which increases the strength of retention between the retention wall and the connector tube.

Abstract: A crimp defines separate parallel bores extending therethrough to receive a wire or cable portion. The crimp has a pair of opposed ends which each define a pair of circumferentially-spaced, outwardly projecting flanges respectively positioned on opposite sides of the crimp. Thus, the flanges may rest against a bone while providing spacing for crimping jaws between a central portion of the crimp and the bone. A design of crimping pliers for use with the crimp is also disclosed.

Abstract: A tubular set portion for circulating blood between a patient and an extracorporeal blood treatment device. The set portion has: an arterial tube for conveying blood from a patient toward the blood treatment device; a venous tube for conveying blood from the blood treatment device back towards the patient; and a pair of spaced, transverse tubes that each connect between the arterial tube and the venous tube, each of the tubes being capable of clamp sealing. The arterial and venous tubes are clamp sealable between the spaced, transverse tubes. Flow reversal on the patient's side of this device is possible by appropriate clamping of two opposed tube sections of the rectangular array which may be formed by the joined tube sections, while flow remains unchanged on the side of the tubular set portion that is connected to the extracorporeal blood treatment device.

Abstract: An implantable, spinal, vertebral replacement device comprises a tubular cage for fitting into a space left by a missing vertebral body and for optionally retaining bone graft material. First and second transverse plates are respectively positioned at opposed ends of the tubular cage for supporting the respective cage ends and for pressing a plate face against an adjacent vertebral body in spinal column-supporting relation. The transverse plates are each joined in transverse relation to a vertebral attachment plate which, in use, extends generally parallel to the spine. The vertebral attachment plate defines screw holes for preferably open helix screw securance to the pair of adjacent vertebral bodies that bracket the space left by the missing vertebral body.

Abstract: Blood lines for hemodialysis and other blood handling procedures may be reused by placing connectors intermediately along the length of the blood lines so that the lines can be disconnected to separate out reusable portions thereof. Specifically, the bulk of the blood lines used may comprise branchless lengths of tubing which are easily reusable, and may be cleaned and stored along with a dialyzer or similar device by connection to a conventional reuse machine. Also, the connectors on the blood lines which are reused may have first and second sealing surfaces. The first sealing surfaces are used in the connections made to form the blood line in its normal form for use. Then, during cleaning and sterilization for reuse, the reusable connectors can connect first and second lengths of blood lines together making use of a second sealing surface, in which the first sealing surfaces are exposed to cleaning/storing solution to cause cleaning and antibacterial action on the first sealing surfaces.

Abstract: A rotary gear device comprises a housing a preferably multiple pairs of rotatable meshing gears in coaxial relation defining spaced teeth which extend helically in the direction of the axis of each gear. First chambers are formed by the meshing gears which move substantially longitudinally while shrinking in size to substantially zero volume as they rotate toward a dead center plane. Second chambers are formed between the spaced teeth rotating away from the dead center plane and increasing in volume. Various improvements are provided to this type of device, which maybe used as an internal combustion engine, a pump or as a chemical reactor.

Abstract: A medical needle protector sheath comprises a tubular body for surrounding and shielding a needle, with the sheath defining an anchor member integrally attached to the front of the body for manual holding, plus a closure cap for the front end which is integrally attached to the body. Also, a manually removable wing member may be carried about the hub of the needle. A tunnel member typically of the inverted U cross section provides longitudinal securance to the needle and hub while penetrating the skin of the patient while at the same time permitting axial rotation of the needle.

Abstract: A fluorescence spectrometer comprises a laser and at least one beam splitter positioned to receive a light beam from the laser and to divide it into several first light beam portions. Dichroic mirrors are positioned to separately receive the first light beam portions and to reflect the beam portions at an angle to the first light beam portions. Transparent chambers are provided for holding the samples. Objective lens systems are respectively positioned in the path of the reflected beam portions to respectively focus each reflected beam portion to a point within one of the separate transparent chambers. Lenses are positioned to receive fluorescence from a sample for testing within the transparent chambers and to respectively focus the fluorescence at pin holes in opaque partitions. The lenses are positioned to receive the fluorescence, which passes back through the objective lens system and the dichroic mirror.

Abstract: A cable tensioning device comprises tubular shaft having an outer threaded portion, and a handle member surrounding a portion of the shaft, with the shaft and handle member being connected in screw-threaded relation. The shaft moves longitudinally relative to the handle as the handle rotates, driven by the screw threaded connection. A gripping member is carried on the shaft distal to the handle member for holding a replaceable bit, which, in turn, may carry a cable crimp. A cable lock is positioned typically proximal of the handle member to hold the ends of cables extending through the tubular shaft. Rotation of the handle member can cause the shaft to move longitudinally to lengthen the distance between the cable lock and a crimp held by a bit which, in turn, is held by the gripping member, to impose a tension on the cable. A meter is present for measuring the amount of tension applied to the cable.

Abstract: The method of selecting and implanting a permanent venous catheter into a patient for use in chronic, extracorporeal blood treatment procedures. The method comprises determining the Body Surface Area of the patient. One then selects a permanent venous catheter having an actual length which is within 10% of a desired length as indicated in a Table found in this application for the Body Surface Area of the particular patient and a particular vein through which the catheter is to extend. Also, the internal diameter of the tubing is preferably adjusted in a manner correlating with the catheter length. Following catheter selection, the venous catheter is implanted in the venous system of the patient with the distal tip of the catheter being in or adjacent to the upper right atrium of the heart.

Abstract: A medical needle protector sheath comprises a tubular body for surrounding and shielding a needle with the sheath defining an anchor member integrally attached to the front of the body for manual holding, plus a closure cap for the front end which is integrally attached to the body. Also, a manually removable wing member may be carried about the hub of the needle. A tunnel member typically of the inverted U-cross section provides longitudinal securance to the needle and hub while penetrating the skin of the patient while at the same time permitting axial rotation of the needle.

Abstract: Pressure is sensed in blood flow tubing by placing an aqueous, preferably isotonic, substantially cell-free solution into branch connection tubing that connects in branching relation with the blood flow tubing at one end. The branch connection tubing also connects in use with a pressure transducer unit at its other end. An air volume is maintained, occupying a portion of the branch connection tubing which is adjacent to the other end. One flows positively or negatively pressurized blood through the blood flow tubing, with the result that the pressure of the blood is communicated through the aqueous solution and the air volume in the branch connection tubing to the pressure transducer unit, with the blood being spaced from the air volume. Preferably, substantially all of the branch connection tubing containing the aqueous solution and air volume has an inner diameter of substantially no more than 5 mm.

Abstract: A set for conveying blood between a patient and blood treatment apparatus such as a dialyzer. The set comprises a blood flow conduit, a connector for a patient's vascular system, and a connector for the dialyzer. A portion of the conduit comprises an enlarged-diameter, tubular pump segment connected at each pump segment end with a connector. The connectors also are each connected in substantially straight-line relation to other portions of the blood flow conduit. Typically, both connectors also each connect to a branch line in a relation substantially parallel to the connection of the other blood flow conduit portion and the connected tubular pump segment. Thus, the set is more capable of being rolled up and packaged in an automated manner, since it can be free of branching connections which connect at a substantial angle to the overall axis of the set.

Abstract: A physical card game or electronically simulated card game is provided in which each of one or more players received cards which define two or more card hands, with at least one card in common. In one embodiment, the initial cards are arranged in a rectangular array with rows, columns and/or diagonals of the array defining the hands. Each hand can be played and/or evaluated using certain aspects of blackjack, poker or other traditional card game play or evaluation. At least some prizes or top winning outcomes for a round of play must include winning outcomes from at least two, and preferably from all, of the hands played by a given player. The relatively low odds of achieving highest-winning combinations on all hands makes it feasible to provide the game with relatively large prizes associated with such low-probability outcomes. In one embodiment, certain subcombinations of a player's cards, such as all initially-dealt cards, are evaluated for instant win combinations.

Abstract: An implantable, spinal, vertebral replacement device comprises a tubular cage for fitting into a space left by a missing vertebral body and for optionally retaining bone graft material. First and second transverse plates are respectively positioned at opposed ends of the tubular cage for supporting the respective cage ends and for pressing a plate face against an adjacent vertebral body in spinal column-supporting relation. The transverse plates are each joined in transverse relation to at least one vertebral attachment plate which, in use, extends generally parallel to the spine. The vertebral attachment plate defines screw holes for screw securance to at least one vertebral body adjacent to the space. Preferably, one or more vertebral attachment plates are connected to the pair of adjacent vertebral bodies that bracket the space left by the missing vertebral body.

Abstract: A flow-through blood treatment device such as a hemodialyzer comprises a housing, a blood inlet, a blood outlet, and at least one membrane in the housing defining a blood flow path between the blood inlet and outlet on one side of the membrane, plus a second flow path defined on the other side of the membrane. At least one of the blood inlet and outlet is connected to blood flow tubing, which blood flow tubing carries a connector spaced from the housing for access to the vascular system of a patient. The blood flow tubing also defines at least one connection site along its length permitting repeated, temporary connection and subsequent disconnection with branch conduits, for connection with sources of additive solutions or measuring devices. Typically, the blood flow tubing is free of permanently attached, flexible branch tubings a method of use in disclose.

Abstract: An extracorporeal blood set may be primed with physiological solution for use in a blood transporting process such as hemodialysis. The set comprises tubing having a patient connector on an end thereof, and a first branch tube in connection with a source of the solution. The branch tube connects with the set between the ends of the set. The branch tube also connects with further branch tubing, having a second connector which is capable of sealing connection with the patient connector. The method comprises the steps of connecting the patient connector and the second connector to form a closed loop of tubing. One then passes the solution from the source in flow through the first branch tube and further branch tubing to fill them and the set tubing with the solution. One then disconnects the patient connector for subsequent connection with the vascular system of a patient.

Abstract: The quantitative determination of various materials in highly scattering media such as living tissue may be determined in an external, photometric manner by the use of a plurality of light sources positioned at differing distances from a sensor. The light from said sources is amplitude modulated, and, in accordance with conventional frequency domain fluorometry or phosphorimetry techniques, the gain of the sensor is modulated at a frequency different from the frequency of the light modulation. Data may be acquired from each of the light sources at differing distances at a frequency which is the difference between the two frequencies described above. From these sets of data from each individual light source, curves may be constructed, and the slopes used to quantitatively determine the amount of certain materials present, for example glucose, oxyhemoglobin and deoxyhemoglobin in living tissue.

Abstract: A tubular set is provided for the extracorporeal treatment of blood, for example hemodialysis. The set comprises a patient arterial line and a patient venous line, each line having a patient connector at one end thereof. Each patient line connects at its other end to a reversing flow valve. The valve also connects to respective first ends of a blood processing unit arterial line and a blood processing unit venous line. Each of the unit lines carry a connector at ends opposed to the first ends for connection respectively to arterial and venous ports of a blood processing device, typically a dialyzer. The reversing flow valve has a first position that respectively connects the patient and unit arterial lines with the patient and unit venous lines. The reversing flow valve has a second position that connects the patient arterial line with the unit venous line, and the unit arterial line with the patient venous line.