Systems and methods for preparing a cytological specimen from a patient sample in a sample container include or employ mechanisms for quickly and accurately adjusting the pressure in a pressure unit during the specimen preparation. The systems include a specimen transfer device configured for being positioned within the sample container, a pressure tank coupled to the specimen transfer device and configured for applying at least one of positive pressure and vacuum pressure through the specimen transfer device, and a temperature adjusting unit coupled to the pressure tank, and configured for incrementally adjusting the pressure in the pressure tank by heating or cooling the tank. The method includes steps of performing a coarse pressure adjustment using a supply valve and/or a bleed valve coupled to the pressure tank, and, after the coarse adjustment, performing a fine pressure adjustment using a temperature adjusting element coupled to the pressure tank.

A solution attachment device includes: an ejection tool having an ejection opening that ejects a solution in a direction of gravitational force; and a solution attachment control portion for controlling attachment of the solution ejected from the ejection opening to at least one attachment subject region of the solution formed on a substrate in a state in which the at least one attachment subject region is disposed below an end surface including the ejection opening of the ejection tool in the direction of gravitational force, and, in the state, a first projection region obtained by projecting the end surface to a surface perpendicular to the direction of gravitational force substantially overlaps a second projection region obtained by projecting the at least one attachment subject region to the surface.

An apparatus is disclosed for separating and preserving biomolecules of a biological fluid sample. The apparatus includes an assembly having sides forming a hollow shape having a first opening at one end and second opening at the opposite end, a sample mixing chamber positioned adjacent the first opening within the assembly, the sample mixing chamber from which a flow of the biological fluid sample is actuated in a direction from the sample mixing chamber to the first matrix layer, the sample mixing chamber being in a direction downstream of the first opening, a first valve positioned between the sample mixing chamber and the first matrix layer, the first valve configured to control the flow to the first matrix layer, a first input in fluid communication with the sample mixing chamber and positioned upstream of the first valve, a second input positioned between the first matrix layer and the second matrix layer, and a second valve positioned between the second matrix layer and the second opening, the second valve configured to control the flow to the second matrix layer.

A digital dispense system and method for preparing samples for analysis. The system includes a fluid droplet ejection system housed in a compact housing unit. The fluid droplet ejection system contains a fluid droplet ejection head and fluid cartridge containing one or more fluids to be dispensed, a cartridge translation mechanism for moving the fluid droplet ejection head and fluid cartridge back and forth over a sample holder in an x direction; and a sample holder translation mechanism for moving a sample back and forth beneath the fluid droplet ejection head and fluid cartridge in a y direction orthogonal to the x direction. A digital display device is attached to the fluid droplet ejection system for displaying fluid volume information to a user. The fluid volume information is selected from relative fluid volume, absolute fluid volume, and a combination of relative and absolute fluid volumes.

A system and method for ejecting one or more fluids from a digital dispense device. The method includes a) inputting to a memory a volume per unit area for each of the one or more fluids to be ejected from the digital dispense device; b) matching the volume per unit area to a device resolution for the digital dispense device; c) formatting fluid ejectors for the digital dispense device for the device resolution; and d) ejecting fluid from the digital dispense device to provide the volume per area for each of the one or more fluids.

Systems and methods for a urinalysis home testing kit are provided. In one implementation, a system may include a container configured to contain a urine sample, a dipstick including a plurality of test reagent pads thereon for measuring differing urinary properties, a blot pad, and a colorized surface containing a dipstick placement region and a plurality of colored reference elements greater than a number of the plurality of test reagent pads. The blot pad may be for removing excess urine from the dipstick after being dipped in urine, to thereby enable non-distorted image capture of the plurality of reagent pads by an image sensor. The colorized surface may be for enabling color normalization of the plurality of test reagent pads using the plurality of colored reference elements.

Systems and methods for tracking healing progress of multiple adjacent wounds are provided. In one embodiment, a system may include a processor configured to receive a first image of a plurality of adjacent wounds near a form of colorized surface having colored reference elements, determine colors of the plurality of wounds, correct for local illumination conditions, receive a second image of the plurality of wounds near the form of colorized surface, to determine second colors of the plurality of wounds in the second image, match each of the plurality of wounds in the second image to a wound of the plurality of wounds in the first image, and determine an indicator of the healing progress for each of the plurality of wounds based on changes between the first image and the second image.

Systems and methods for a color board for use in reagent strip testing are disclosed. One implementation may include a color board surface, a first colored reference element printed on the color board surface, and a second colored reference element printed on the color board surface. The color board may also include a test region on the color board surface configured to receive at least one reagent pad. The color board may also include a unique code, and the code may reflect specific chromatic properties associated with each of the first colored reference element and the second color reference element at a time of printing. The unique code may be machine readable to enable a machine to later normalize a comparison color, for determining chromatic properties of the at least one reagent pad.

Systems and methods automatically populate an electronic medical record of a patient with the results of image analysis. A token is generated for a specific patient in need of a medical test. The token is transmitted to a mobile communications device associated with the specific patient. Once a token-based communications session is initiated between the mobile communications device and a remote server, image-related information is transmitted to the remote server from the mobile communications device to perform an analysis of the image-related data. Upon verification that the transmitted image-related information is associated with the specific patient, an electronic medical record of the specific patient is updated to reflect a test result.

A method of updating an electronic medical record based on patient generated image data includes providing a test kit and a verification code to a patient. The patient performs a procedure associated with the test kit, then captures a medical image. The verification code is used to verify that the image was received from the patient. Upon verification, a notification is sent to a healthcare provider for updating an electronic medical record of the patient with data associated with the new image.