A blood-sampling-tube automatic preparation device comprising a blood-sampling-tube containing section having at least two blood-sampling-tube containers, a label printing and pasting unit that prints blood sampling information data and then pastes the printed label on a surface of a blood-sampling-tube, a hand pasting label printer, a blood-sampling-tube collecting section in which one or more blood-sampling-tubes with label pasted and/or one or more printed labels for hand pasting are collected for each patient, a blood-sampling-tube transferring device that receives a blood-sampling-tube from the blood-sampling-tube container and transfers it to the label printing and pasting unit, and a control device that controls each component. All blood-sampling-tube containers of the blood-sampling-tube containing section are arranged in a row on a same horizontal surface and the blood-sampling-tube transferring device, the label printing and pasting unit, and the hand pasting label printer are arranged to be mutually superposed under the blood-sampling-tube containing section.

A method for inversion counting or phlebotomist monitoring can include identifying, by processing circuitry, whether a blood collection tube is present in image data from a camera situated to capture images of a phlebotomist collecting a sample, in response to identifying the blood collection tube is present in the field of view of the camera based on the image data, identifying whether the blood collection tube includes blood therein, after identifying the blood is present in the blood collection tube, counting, based on the image data, a number of inversions performed on the blood collection tube, and in response to determining the number of inversions performed is less than a required number of inversions, issuing an alert indicating that insufficient inversions were performed.

A system for confirmation of fluid delivery to a patient at the clinical point of use is provided. The system includes a wearable electronic device. The wearable electronic device has a housing; at least one imaging sensor associated with the housing; a data transmission interface; a data reporting accessory for providing data to the user; a microprocessor for managing the at least one imaging sensor, the data transmission interface, and the data reporting accessory; and a program for acquiring and processing images from the at least one imaging sensor. The system further includes a fluid delivery apparatus; and one or more identification tags attached to or integrally formed with the fluid delivery apparatus. The program processes an image captured by the at least one imaging sensor to identify the one or more identification tags and acquires fluid delivery apparatus information from the one or more identification tags.

Blood sample optimization systems and methods are described that reduce or eliminate contaminates in collected blood samples, which in turn reduces or eliminates false positive readings in blood cultures or other testing of collected blood samples. A blood sample optimization system can include a blood sequestration device located between a patient needle and a sample needle. The blood sequestration device can include a sequestration chamber for sequestering an initial, potentially contaminated aliquot of blood, and may further include a sampling channel that bypasses the sequestration chamber to convey likely uncontaminated blood between the patient needle and the sample needle after the initial aliquot of blood is sequestered in the sequestration chamber.

A wearable electronic device configured to be worn by a user while performing an invasive procedure for enhancing visualization of desired anatomical structures is provided. The wearable electronic device includes: a housing; at least one imaging sensor associated with the housing; and a visual display integrally formed with or associated with the housing. The device is configured to acquire an image of an invasive access site of a patient with the at least one imaging sensor, process the image to determine a location of a desired anatomical structure, and display a virtual trace of the location to the user via the visual display.

This disclosure relates to a system and method for drawing blood from a user by skin puncture instead of venous puncture and storing it for analysis. The system includes a receptacle configured to engage an area of skin of the user at a blood draw location and store blood drawn from the user; a lancet device disposed within the receptacle configured to puncture the skin of the user at the blood draw location; a vacuum device configured to reduce a pressure within the receptacle such that the skin at the blood draw location is drawn into the receptacle before the lancet device punctures the skin, and to enhance blood flow while blood is drawn from the user; and a housing configured to house the receptacle, the lancet device, and the vacuum device. The receptacle, the lancet device, and the vacuum device may be modular and removably coupled with the housing.

A blood collection tube includes a body, a chamber, a vacuum port, and a cap. The cap includes a first septum, a first conduit having an inlet extending from the first septum and an outlet in fluid communication with the chamber, a second septum, and a second conduit extending radially from the second septum to the first conduit. When a fluid source is fluidically connected to the first septum or the second septum, and a vacuum is applied at the port, the vacuum draws fluid from the fluid source, through the first or second septum, and into the first conduit. A blood collection device includes a vacuum pump and a plurality of reservoirs containing concentrated blood additives. The tube and device form a system for collecting blood samples at low vacuum to tubes previously stored at atmospheric pressure. The system prevents risk of misidentification, mislabeling, or incorrect ordering of tubes.

It is known in the art to use an apparatus to enhance the visual appearance of the veins and arteries in a patient to facilitate insertion of needles into those veins and arteries. This application discloses a number of inventions that add additional data collection and presentation capabilities to a handheld vein enhancement apparatus and a set of processes for the collection of blood and the delivery of IV medicines that use the handheld device to mediate the process.

Blood sample optimization systems and methods are described that reduce or eliminate contaminates in collected blood samples, which in turn reduces or eliminates false positive readings in blood cultures or other testing of collected blood samples. A blood sample optimization system can include a blood sequestration device located between a patient needle and a sample needle. The blood sequestration device can include a sequestration chamber for sequestering an initial, potentially contaminated aliquot of blood, and may further include a sampling channel that bypasses the sequestration chamber to convey likely uncontaminated blood between the patient needle and the sample needle after the initial aliquot of blood is sequestered in the sequestration chamber.

A biological fluid collection device that is adapted to receive a blood sample is disclosed. The biological fluid collection device includes a housing, a puncturing element transitionable between a pre-actuated position wherein the puncturing element is retained within the housing and a puncturing position wherein at least a portion of the puncturing element extends through the housing, and a cartridge removably connectable to a portion of the housing. After collecting a blood sample, the cartridge is removable from the housing and the cartridge is able to transfer the blood sample to a point-of-care testing device. The biological fluid collection device provides a closed system that reduces the exposure of a blood sample and provides fast mixing of a blood sample with a sample stabilizer.