Abstract: A process of capturing a biopotential signal at a surface of a body includes using a sensor receiver which forms a first signal connection with the body wherein one or more parameters of impedance of the first signal connection are unknown. The biopotential signal is received at an output of a first signal channel having a first transfer function dependent on the one or more unknown first impedance parameters. The biopotential signal is received at an output of a second signal channel having a second transfer function dependent on the one or more unknown first impedance parameters. The process also comprises deriving a set of relations for the biopotential signal based on the transfer function of the first signal channel, the transfer function of the second signal channel, and outputs of the first and second signal channels. The set of relations is solved to determine the captured biopotential signal.

Abstract: In one embodiment the invention provides a process of capturing a biopotential signal at a surface of a body using a sensor receiver which forms a first signal connection the body wherein one or more parameters of impedance of the first signal connection are unknown. The process comprises receiving the biopotential signal at an output of a first signal channel having a first transfer function which is dependent on the one of more unknown first impedance parameters. The process also comprises receiving the biopotential signal at an output of a second signal channel having a second transfer function dependent on the one of more unknown first impedance parameters. The process also comprises deriving a set of relations for the biopotential signal.

Abstract: The present disclosure is drawn to loop-mediated isothermal amplification (LAMP) reaction assemblies including a substantially hygroscopic agent free LAMP reagent mixture in combination with a solid-phase reaction medium. The present disclosure also includes systems for a chromatic LAMP analysis including a substantially non-reactive solid phase reaction medium, and a non-interfering reagent mixture. The present disclosure also includes solid phase LAMP reaction mediums comprising a substrate, an adhesive layer disposed on the substrate, a reaction layer disposed on the adhesive layer, and a spreading layer disposed on the reaction layer. The present disclosure also includes methods of testing for a presence of a target nucleotide sequence including providing a biological sample, and dispensing the sample into a test environment having a solid phase reaction medium in combination with a LAMP reagent mixture and a pH sensitive dye.

Abstract: A liquid biological sample test cartridge is disclosed. The cartridge can include a tray. The cartridge can also include a chemical reaction pad supported by the tray. The cartridge can further include a chemical reaction pad cover disposed over the chemical reaction pad and coupled to the tray. The chemical reaction pad cover can have a sample opening to facilitate depositing a liquid biological sample at a predetermined location on the chemical reaction pad. In addition, the cartridge can include an outer cover operable to at least partially form an enclosure about the chemical reaction pad.

Abstract: A heating device for testing a biological sample is disclosed. The heating device can include a heat source operable to generate heat. In addition, the heating device can include a controller in communication with the heat source and operable to control heat generation by the heat source to heat a biological sample at less than or equal to about 2 degrees C./s. Furthermore, a heating device for testing a biological sample is disclosed that can include a heat source operable to generate heat to heat a biological sample. The biological sample can be at least partially contained within a removable enclosure distinct from the heating device. Additionally, the heating device can include an enclosure interface associated with the heat source. The enclosure interface can be configured to interface with the enclosure such that heat is transferred from the heat source to the enclosure by conduction.

Abstract: In one embodiment the invention provides a process of capturing a biopotential signal at a surface of a body using a sensor receiver which forms a first signal connection the body wherein one or more parameters of impedance of the first signal connection are unknown. The process comprises receiving the biopotential signal at an output of a first signal channel having a first transfer function which is dependent on the one of more unknown first impedance parameters. The process also comprises receiving the biopotential signal at an output of a second signal channel having a second transfer function dependent on the one of more unknown first impedance parameters. The process also comprises deriving a set of relations for the biopotential signal.

Abstract: A central arterial blood pressure waveform is developed from pressure waveforms obtained from proximal and distal blood pressure cuffs on the brachial artery of an arm that are inflated to a supra-systolic pressure. The proximal and distal cuff pressure waveforms associated with at least one cardiac ejection cycle are sensed. The propagation times of a blood pressure pulse from the entry of the artery to the proximal cuff and from the proximal cuff to the distal cuff are calculated, permitting calculation of a reflection coefficient of the pressure pulse at one of the proximal and distal cuffs. Assuming a physical model of wave propagation along the artery between the aorta and the proximal and distal cuffs, an estimated pressure waveform at the opening of the artery can be determined.

Abstract: A central arterial blood pressure waveform is developed from pressure waveforms obtained from proximal and distal blood pressure cuffs on the brachial artery of an arm that are inflated to a supra-systolic pressure. The proximal and distal cuff pressure waveforms associated with at least one cardiac ejection cycle are sensed. The propagation times of a blood pressure pulse from the entry of the artery to the proximal cuff and from the proximal cuff to the distal cuff are calculated, permitting calculation of a reflection coefficient of the pressure pulse at one of the proximal and distal cuffs. Assuming a physical model of wave propagation along the artery between the aorta and the proximal and distal cuffs, an estimated pressure waveform at the opening of the artery can be determined.

Abstract: A central arterial blood pressure waveform is developed from pressure waveforms obtained from proximal and distal blood pressure cuffs on the brachial artery of an arm that are inflated to a supra-systolic pressure, The proximal and distal cuff pressure waveforms associated with at least one cardiac ejection cycle are sensed, The propagation times of a blood pressure pulse from the entry of the artery to the proximal cuff and from the proximal cuff to the distal cuff are calculated, permitting calculation of a reflection coefficient of the pressure pulse at one of the proximal and distal cuffs. Assuming a physical model of wave propagation along the artery between the aorta and the proximal and distal cuffs, an estimated pressure waveform at the opening of the artery can be determined.

Abstract: A physics-based mathematical model is used to estimate central pressure waveforms from measurements of a brachial pressure waveform measured using a supra-systolic cuff. The method has been tested in numerous subjects undergoing cardiac catheterisation. Central pressure agreement was within 11 mm Hg and as good as the published non-invasive blood pressure agreement between the oscillometric device in use and the so-called “gold standard.” It also exceeds international standards for the performance of non-invasive blood pressure measurement devices. The method has a number of advantages including simplicity of application, fast calculation and accuracy of prediction. Additionally, model parameters have physical meaning and can therefore be tuned to individual subjects. Accurate estimation of central waveforms also allow continuous measurement (with intermittent calibration) using other non-invasive sensing systems including photoplethysmography.

Abstract: A method and apparatus determine certain cardiac medical parameters that are useful is diagnosing cardiovascular disease. The apparatus is designed to carry out the method, which includes the steps of: (a) inflating a blood pressure cuff on the brachial artery to a supra-systolic pressure; (b) sensing a sequence of pressure pulse waveforms associated with the brachial artery that result from a plurality of cardiac ejection cycles; (c) averaging the waveforms to produce an average, representative waveform having an initial, incident wave portion and a reflected wave portion; (d) analyzing the representative waveform to determine a value of one or more cardiac medical parameters including the reflection wave ratio (RWR), the reflected wave transit time (RWTT), the maximum amplitude of the initial pressure wave (PS1), the maximum rise (slope) of the initial pressure wave (dp/dt), and/or the systolic ejection period (SEP); and (e) displaying the value of the medical parameter(s).

Abstract: A reaching device that in one embodiment comprises an elongated member, a jaw, and an actuator for opening and closing the jaw. The jaw includes a pair of holding members, one of which has a tapered lateral side edge. In one embodiment, the reaching device may allow a rural mail carrier to remain seated in the driver's side of a conventional (North American) vehicle, reach through the passenger's window, and perform the following tasks: open a mail box, retrieve mail from the mail box, place mail into the mail box, close the mail box, and raise or lower the indicator flag on the side of the mail box.

Abstract: There is provided a reaching device particularly suitable for rural mail delivery. In one embodiment, the reaching device comprises an elongated member, a jaw, and an actuator for opening and closing the jaw. The jaw includes a pair of holding members, one of which has a tapered lateral side edge. In an illustrated embodiment, a reaching device is provided that allows a rural mail carrier to remain seated in the driver's side of a conventional (North American) vehicle, reach through the passenger's window, and perform the following tasks: open a mail box, retrieve mail from the mail box, place mail into the mail box, close the mail box, and raise or lower the indicator flag on the side of the mail box.

Abstract: In a scanning microscope, slides are fed automatically from a magazine to the imaging system. Each slide is labeled in some fashion with information for selecting the appropriate modality of operation of the scanner for that slide and the modality is implemented automatically. The information is preferably tied to and defined by a laboratory information system (LIS). For example, the instructions may regard the type of microscopy (i.e., trans- or epi-illumination), multi-spectral imaging with particular spectral bands combined with a particular set of z-positions, alternative filters, settings for the numerical aperture of the condenser, alternative detector operation for different resolutions, and alternative post-scan analyses of the data, as deemed optimal for the scan. The label may also contain the slide's identity, a pathologist's name, desired post-scan handling protocol, etc. The preferred array microscope to carry out the invention is also described.

Abstract: A method for estimating an intra-arterial blood pressure waveform, from pressure waveforms obtained from a blood pressure cuff, comprises the steps of: a. inflating a blood pressure cuff on a brachial artery of an arm to a pressure at least as great as the diastolic pressure; b. holding the molar amount of fluid in the blood pressure cuff constant; c. sensing a sequence of cuff pressure waveforms associated with the brachial artery that result from at least one cardiac ejection cycle; and cc.

Abstract: A method and apparatus are disclosed for determining certain cardiac medical parameters that are useful is diagnosing and treating cardiovascular disease.

Abstract: A physics-based mathematical model is used to estimate central pressure waveforms from measurements of a brachial pressure waveform measured using a supra-systolic cuff. The method has been tested in numerous subjects undergoing cardiac catheterisation. Central pressure agreement was within 11 mm Hg and as good as the published non-invasive blood pressure agreement between the oscillometric device in use and the so-called “gold standard.” It also exceeds international standards for the performance of non-invasive blood pressure measurement devices. The method has a number of advantages including simplicity of application, fast calculation and accuracy of prediction. Additionally, model parameters have physical meaning and can therefore be tuned to individual subjects. Accurate estimation of central waveforms also allow continuous measurement (with intermittent calibration) using other non-invasive sensing systems including photoplethysmography.

Abstract: A method and apparatus are disclosed for the non-invasive measurement, processing and utility of blood pressure cuff oscillation signals from a blood pressure cuff applied to a body part when the blood pressure cuff pressure is at supra-systolic pressures. Oscillometric cardiac pulse waveforms associated with the peripheral artery are monitored during a plurality of cardiac ejection cycles while at supra-systolic pressure, and are measured pneumatically and transduced by an oscillometric pressure sensor. The analog signal is amplified, processed and digitized to provide a recordable waveform that can be analyzed to obtain information relating to the patient's cardiovascular status.

Abstract: A blood pressure cuff includes: (a) a flexible, hollow bladder adapted to surround the arm of the patient, which has an inside surface adapted to apply pressure to a surface of the arm above an artery, an outside surface opposite this inside surface, and an inlet line for receiving a fluid to cause the bladder to expand; (b) at least one first sensor element arranged on a inside and/or outside surface of the bladder in a location adjacent the artery when the bladder is in its operative position surrounding the patient's arm; and possibly also (c) at least one second sensor element arranged on a surface of the bladder that is opposite to the surface on which the first sensor element is disposed, and in a location adjacent the artery when the bladder is in its operative position surrounding the patient's arm.

Abstract: In a scanning microscope, slides are fed automatically from a magazine to the imaging system. Each slide is labeled in some fashion with information for selecting the appropriate modality of operation of the scanner for that slide and the modality is implemented automatically. The information is preferably tied to and defined by a laboratory information system (LIS). For example, the instructions may regard the type of microscopy (i.e., trans- or epi-illumination), multi-spectral imaging with particular spectral bands combined with a particular set of z-positions, alternative filters, settings for the numerical aperture of the condenser, alternative detector operation for different resolutions, and alternative post-scan analyses of the data, as deemed optimal for the scan. The label may also contain the slide's identity, a pathologist's name, desired post-scan handling protocol, etc. The preferred array microscope to carry out the invention is also described.