Abstract: Systems and methods for coupling a catheter, such as a drainage catheter, to a patient's body and decoupling the catheter from the body are disclosed. Embodiments of the present invention take advantage of the flexibility of a catheter cannula and allow for a self-contained system that secures the catheter cannula within the body while bodily fluid is draining. In one embodiment, the catheter is coupled to the body by compressing a proximal hub member to a distal hub member, causing the cannula to curl and form an anchoring configuration (i.e. a loop, pigtail, j-curve, malecot, etc.). In compressing the portions, one or more fingers within the proximal hub member force a cord into one or more corresponding channels within the distal hub member, thereby shortening the amount of cord in the cannula. The proximal and distal hub members can be locked together in the compressed position for as long as the catheter is to be coupled to the body.

Abstract: A ring oscillator including a voltage-to-current converter for producing at least one control current from at least one control voltage and, a plurality of delay cells coupled to the converter, wherein at least one output of the one of the delay cells is coupled to the input of another of the delay cells, wherein the voltage-to-current converter produces a substantially linear output when the at least one control voltage is varied between zero volts and a rail supply voltage. Since the ring oscillator operates from a low voltage source, it can be used in applications where power supply (e.g., battery size) is small (e.g., pagers, cellular phone applications).

Abstract: A ring oscillator including a voltage-to-current converter for producing at least one control current from at least one control voltage and, a plurality of delay cells coupled to the converter, wherein at least one output of the one of the delay cells is coupled to the input of another of the delay cells, wherein the voltage-to-current converter produces a substantially linear output when the at least one control voltage is varied between zero volts and a rail supply voltage. Since the ring oscillator operates from a low voltage source, it can be used in applications where power supply (e.g., battery size) is small (e.g., pagers, cellular phone applications).

Abstract: A tongue positioning device is disclosed for positioning the tongue within a user's mouth. The device includes a tongue positioning mouthpiece that includes a mouthpiece body with a center hole therein. A flange portion extends around the periphery of the mouthpiece body that forms an acoustic seal with the teeth and lips of a patient during use. A pair of bite blocks protrude from the mouthpiece body on opposing lateral sides of the center hole. A tongue bridge is fixedly secured to the bite blocks via a pair of downwardly extending arms. The tongue bridge includes a platform area where a patient's tongue is placed under when the mouthpiece is used. A cylindrical portion extends from the mouthpiece body in a direction away from the flange. An optional filter is removable from the cylindrical portion and acts as a protective barrier for viruses, bacteria, microbes, and other pathogens. The filter includes a removable filter body containing a filter media.

Abstract: Systems and methods for isolating a pressure gauge from sources of potential contamination so that the pressure gauge may be reused in multiple medical procedures without having to be subjected to a sterilization procedure. The systems of the invention may include a syringe assembly having a pressure gauge removably attached to a syringe. The pressure gauge is isolated from sources of potential contamination in at least two ways. First, a flexible membrane separates a pressure transducer diaphragm of the pressure gauge from the pressurized fluid of the syringe. The flexible membrane prevents the pressure gauge from contacting the fluid and transmits pressure and forces from the fluid to the pressure gauge. Second, a substantially transparent disposable bag or film covers surfaces of the pressure gauge that would be otherwise exposed to human contact or other contaminants. During medical procedures, the pressure gauge maintains its sterile condition.

Abstract: An adaptor for coupling a fluid source to a wound irrigation shield is disclosed. The preferred adaptor, preferably a multi-part adaptor, features spray pattern adjustability, removable coupling to the shield, the capacity for removably coupling to a variety of different fluid sources, and a variety of other features and advantages. In one embodiment, the adaptor has a substantially planar face that is substantially coplanar with the plane defined by the shield, thereby preventing patient puncture.

Abstract: The present invention relates to a system for irrigating a wound with wound irrigation fluid and for preventing substantial splashback of the wound irrigation fluid. The system comprises: (i) fluid delivery device for delivering wound irrigation fluid; and (ii) a flexible wound irrigation shield configured such that the shield prevents substantial splashback of the irrigation fluid upon irrigation of a wound. The shield is configured to be disposed, preferably removably, on the fluid delivery device. The flexible shield is substantially conformable to a desired wound area, enabling the practitioner to irrigate awkward, uneven, and hard to reach areas. The shield can be folded into a compact position, then opened into a larger shield. The fluid delivery device comprises (i) a fluid source for providing wound irrigation fluid; and (ii) an adaptor for transmitting fluid from the fluid source to the wound.

Abstract: A blood containment device for use with a vascular entry needle provides visual and tactile confirmation that a blood vessel has been properly entered. The device includes a blood visualization chamber defined by a compliant member which provides a visual indication that a needle connected to the device has accessed a selected blood vessel. The blood visualization chamber is vented to allow air to escape therefrom as it is displaced by blood entering the visualization chamber, while a gas permeable membrane in communication with the vent to prevent significant blood from escaping from the blood containment device. A sealing member formed on an outer surface at one end of the compliant member works in conjunction with the gas permeable membrane to prevent significant leakage of blood from the device. The compliant member pulsates with changes in blood pressure, thereby providing continuous tactile confirmation that the needle tip is properly positioned within the selected blood vessel.

Abstract: A hemostasis valve which includes a tubular body having a lumen therethrough and an elongated housing attached to the tubular body. The body has a recess formed in one end. The housing has a longitudinal bore at one end and a compression chamber formed at another end which communicates with the bore. A resilient seal which comprises a cone-shaped membrane portion disposed in the recess for substantially blocking and controlling the loss of body fluids from the lumen. A compressible second seal for selectively opening and closing the bore in response to a compressive force is disposed in the compression chamber. The compressible seal has a longitudinal first passageway that communicates with the bore and a raised annular portion which serves as a selective opening to the bore. The compressible seal responds to compressive forces so as to reduce or increase the size of the opening provided by the raised annular portion to selectively seal or unseal the bore.

Abstract: A novel catheter apparatus for use in delivering an anesthetic agent or other fluid medicament to the portion of subcutaneous tissue through which a catheter device has been inserted into a patient, thereby allowing the catheter device to be retracted without causing pain or discomfort to the patient. The catheter device has an indwelling cannula adapted for insertion through subcutaneous tissue into a patient's body. A sheath is selectively disposed about the cannula so as to be positioned within the subcutaneous tissue once the cannula has been inserted into the body. The sheath may include a plurality of longitudinal bores which act as a lumen to provide fluid medicament to delivery holes on the outside of the sheath. The delivery holes permit the anesthetic agent or fluid medicament to be delivered to the subcutaneous tissue. A light permeable hub means may be used to maintain a fluid tight connection between the sheath means and a storage container for anesthetic agent or fluid medicament.

Abstract: A pulse oximeter sensor apparatus which is sealed against liquid penetration during its formation by overmolding, and methods for overmolding. The pulse oximeter sensor apparatus disclosed comprises a preform first section, oximeter sensor components, and an overmolded second section bonded to the preform first section during the overmolding process to form a liquid resistant seal comprising a mechanical bond of overlapping elements.

Abstract: A novel catheter apparatus for use in delivering an anesthetic agent or other fluid medicament to the portion of subcutaneous tissue through which a catheter device has been inserted into a patient, thereby allowing the catheter device to be retracted without causing pain or discomfort to the patient. The catheter device has an indwelling cannula adapted for insertion through subcutaneous tissue into a patient's body. A helical sheath is formed from an elongate band that is wrapped around the cannula in a helical fashion so as to be capable of being positioned within the subcutaneous tissue once the cannula has been inserted into the body. The helical sheath has formed therein a lumen into which the anesthetic agent or other fluid medicament can be delivered via a hub that is connected to the proximal end of the helical sheath. The helical sheath has formed therein a plurality of delivery holes that form a fluid communication path with the lumen.

Abstract: A novel catheter apparatus for use in delivering an anesthetic agent or other fluid medicament to the portion of subcutaneous tissue through which a catheter device has been inserted into a patient, thereby allowing the catheter device to be retracted without causing pain or discomfort to the patient. The catheter device has an indwelling cannula adapted for insertion through subcutaneous tissue into a patient's body. A helical sheath is formed from an elongate band that is wrapped around the cannula in a helical fashion so as to be capable of being positioned within the subcutaneous tissue once the cannula has been inserted into the body. The helical sheath has formed therein a lumen into which the anesthetic agent or other fluid medicament can be delivered via a hub that is connected to the proximal end of the helical sheath. The helical sheath has formed therein a plurality of delivery holes that form a fluid communication path with the lumen.

Abstract: A novel catheter apparatus for use in delivering an anesthetic agent or other fluid medicament to the portion of subcutaneous tissue through which a catheter device has been inserted into a patient, thereby allowing the catheter device to be further manipulated or retracted without causing pain or discomfort to the patient. The catheter device has an indwelling cannula adapted for insertion through subcutaneous tissue into a patient's body. A cylindrical sleeve around the cannula can be positioned within the subcutaneous tissue once the cannula has been inserted into the body. The cylindrical sleeve has formed therein one or more lumens into which the anesthetic agent or other fluid medicament can be delivered via a hub that is connected to the proximal end of the cylindrical sleeve. The cylindrical sleeve has formed therein a plurality of delivery holes that form a fluid communication path with the one or more lumens.

Abstract: A pulse oximeter sensor apparatus which is sealed against liquid penetration during its formation by overmolding, and methods for overmolding. The pulse oximeter sensor apparatus disclosed comprises a preform first section, oximeter sensor components, and an overmolded second section bonded to the preform first section during the overmolding process to form a liquid resistant seal comprising a mechanical bond of overlapping elements.

Abstract: A novel catheter apparatus for use in delivering an anesthetic agent or other fluid medicament to the portion of subcutaneous tissue through which a catheter device has been inserted into a patient, thereby allowing the catheter device to be retracted without causing pain or discomfort to the patient. The catheter device has an indwelling cannula adapted for insertion through subcutaneous tissue into a patient's body. A cylindrical sheath is placed on the cannula so as to be positioned within the subcutaneous tissue once the cannula has been inserted into the body. The cylindrical sheath has formed therein a lumen into which the anesthetic agent or other fluid medicament can be delivered via a hub that is disposed on the catheter apparatus. The cylindrical sheath has formed therein a plurality of one-way slit valves. The one-way slit valves permit the anesthetic agent or fluid medicament to be delivered to the surrounding subcutaneous tissue, and also prevent any bodily fluids from entering the lumen.

Abstract: A tape burnishing device presents aligned stretches of burnishing tape at each side of a rotating disk. Air nozzles at each side of the disk urge an elliptical pattern of the respective stretches of tape into contact with the disk. During burnishing the tape is stationary while the device is advanced to burnish the desired surface of the disk. The tape stretches, that are portions of a single tape, are positioned at an angle with respect to the radius of the disk and the device is advanced in a radial direction to optimize the burnishing action relative to the rotating disk surface. The tape is advanced between burnishing operations twice the dimension of use during a burnishing operation with the two operating locations out of phase to enable the single tape to advance past both burnishing locations while presenting an unused surface at each location and using the entire surface of the tape.

Abstract: An oximeter apparatus especially adapted to reflectance oximetry includes a sensor having a red LED, an infrared LED and a photosensor resiliently mounted in a carrier to provide constant linear pressure characteristics. The LED's and photodetector are fixed to a flexible circuit board. The d.c. components of the reflectance signals are fed back to control the brightness of the LED's A.c. component signals from the photodetector are rejected in the determination of oxygen saturation when the red and infrared a.c. components differ by more than a determined amount. The difference between the maximum and minimum values of each pulse is employed in the determination of oxygen saturation, with two measurements being taken for each pulse.