Abstract:
A collection container and a method for collecting a biological sample, particularly whole blood, includes at least one stabilizing agent in an amount effective to stabilize and inhibit protein degradation and/or fragmentation. The stabilizing agent is able to stabilize proteases in the biological sample, particularly at the point of collection, by inhibiting protein degradation and/or fragmentation in the sample when the sample is stored. The stabilizing agent comprises or consists of one or more protease inhibitors.
Abstract:
The invention concerns a test unit for carrying out blood analyses comprising a lancing element that can be pricked into a body part which has a capillary channel for transporting the body fluid that leads from a lancing member to a target site. According to the invention a pretensioned distal sterile cover and a liquid permeable proximal sterile cover are proposed for the lancing element that is advantageously formed as a deep-drawn component.
Abstract:
A method of extracting and analyzing bodily fluids from a patient at the point of care for the patient is provided. The method comprises establishing fluid communication between an analyte detection system and a bodily fluid in the patient. A portion of the bodily fluid is drawn from the patient. A first component of the bodily fluid is separated from the drawn portion, while the analyte detection system remains in fluid communication with the patient. The analyte detection system analyzes the first component to measure a concentration of an analyte in an accurate and timely manner.
Abstract:
A fluid sampling system is disclosed comprising a fluid drawing device and a fluid sampling device. In one embodiment, the fluid drawing device comprises a venous arterial blood management protection apparatus having a housing with a fill chamber in fluid communication with a patient injection site, a piston positionable within the fill chamber to sealingly engage the fill chamber, wherein the piston has a first position and a second position, wherein movement of the piston from the first position to the second position generates a negative pressure in the fill chamber effective to draw fluid from the patient injection site into the fill chamber, biasing means for biasing the piston to the second position relative to the first position, and securing means for selectively securing the piston in the second position. In one embodiment, the fluid sampling device comprises a base portion having a canula, a handle, and a ridge extending around at least a portion of an outer surface; and a top portion having a flange adapted to engage said the ridge to couple the top portion to the base portion.
Abstract:
The invention relates to a blood taking device (1), in particular, for newborn babies and small children or small animals, comprising a blood taking vessel (2), provided on the front end thereof with a cannula (5) with a sharpened tip (4), whereby a porous, gas-permeable limiting element (8) which automatically stops the flow of taken blood, is arranged by pressing in the blood taking vessel (2) in a defined position. The rear end of the blood taking vessel (2) is sealed by a plug (11) which may be temporarily opened for taking blood (11), which dispenses the taken blood by means of a stroke running in a sealed manner in the blood taking vessel (2), which empties under pressure at least a part amount of the blood retained before the limiting element (8).
Abstract:
A medical device having a housing (2) with a bore (3) and a lancet (1) slidably fitting in the bore. The lancet operates as a positive displacement piston. In a retracted position, in which the lancet is rearwardly displaced along the bore to define a fluid-containing space in the bore forwardly on the lancet tip, the fluid-containing space has a cross-section dimension to allow fluid to be retained therein by surface tension. The device has a seal (6) operable substantially to prevent flow of fluid from the fluid-containing space past the seal means on movement of the lancet. Displacement of the lancet between the puncture and retracted positions provides suction for drawing fluid into and along the fluid-containing space from the forward end of the bore, and/or pressure for expelling fluid from the fluid-containing space via the forward end of the bore. Also disclosed are methods for operating the device.
Abstract:
A closed blood sampling system within a pressure monitoring line having a control valve that enables a clearance reservoir to be isolated from the pressure column when no samples are being taken. The valve is a stopcock-like device that includes a rotating valve member and attached control handle with clear visible and tactile indicators for the mode of operation. The rotating valve member has a number of internal and circumferential channels for connecting or disconnecting select ports in the core of the valve. By isolating the clearance reservoir, the quality of the pressure signal is improved such that the sampling line can be lengthened for greater convenience in the intensive care or operating room. The valve may also incorporate a blunt cannula sampling site therewithin.
Abstract:
A withdrawal syringe has a cannula connected to one end of a receiving cylinder having a filter in the other end. A cup shaped piston is in a sliding telescoping relation with the cylinder. The piston has finger grips and a thumb rest is secured from the cylinder in spaced opposition to the finger grips. The syringe is operated by one hand by a squeezing action between the fingers and thumb.
Abstract:
A method for withdrawing a fluid sample from a patient is disclosed comprising the steps of: a) providing a sampling device (10) having a housing (20) and a needle (40) having a sharpened tip for piercing the skin of the patient; b) withdrawing fluid from the patient into the housing; c) retracting the needle so that the sharpened tip of the needle is enclosed within the housing; and d) expelling the fluid from the housing after the needle is retracted.
Abstract:
Kits and methods for closed-system sampling blood in patients are disclosed. The kit includes a four-port stopcock adapted to allow communication at least between two ports. The stopcock has a first port adapted to receive a syringe, a second port for communicating with an infusion solution reservoir, a third port for receiving a flush solution, and a fourth port for communication with a patient. The kit also includes at least one sampling site adapted to fluidically communicate with the fourth port and to be positioned between the four-port stopcock and the patient. At least one of the sampling sites is adapted to allow extraction of a fluid being communicated between the stopcock and the patient.