Abstract: Systems for performing ON-OFF perimetry visual field tests. The systems may include a display apparatus including at least one display, and at least one computing device in electronic communication with the display apparatus. The computing device(s) may be configured to perform the ON-OFF perimetry test on a patient by performing processes including directing the patient to visual focus on an eye fixation region depicted in a visual field. The visual field may be divided into a right side and a left side. The processes performed by the computing device(s) may also include generating a plurality of stimuli in the visual field to be detected by the patient, directing the patient to indicate when the patient detects each stimulus depicted within the visual field, and analyzing the patient's indications to diagnosis a retinal disease, a visual cortex disease, and/or a deficit condition of an eye of the patient.

Abstract: An ophthalmic optical coherence tomography instrument, method, and computer-readable medium. The instrument includes a scanner defining an apparent point source for scanning sample light across a subject position and an objective having a posterior imaging configuration to project the apparent point source onto a pivot point between the objective and the subject position. The objective is settable between the posterior imaging configuration for scanning the sample light across a retina of an eye at the subject position and an anterior imaging configuration for scanning the sample light across a pivot plane. An axial region from which an interferogram is detectable extends across the pivot plane while the objective is in the anterior imaging configuration. A pupil alignment method uses the anterior imaging modality to obtain a structure position of a structure of an eye's anterior segment and then an offset between the structure position and a reference position.

Abstract: Ophthalmic imaging devices and related methods employ self-alignment of a user with an optical axis of the imaging device. An ophthalmic imaging device includes a retinal imaging assembly, a housing assembly, and a viewer assembly. The retinal imaging assembly has an optical axis. The retinal imaging assembly is attached to the housing. The housing assembly is configured to rest on a horizontal surface during operation of the retinal imaging assembly. The optical axis is oriented at an angle from the horizontal surface when the housing assembly rests on the horizontal surface. The viewer assembly is coupled with the housing assembly. The viewer assembly includes an interface surface shaped for engagement with each head of a plurality of different user's and to accommodate repositioning of the head to align a pupil of the user with the optical axis.

Abstract: A blood flow measurement apparatus of an aspect example includes a scanning optical system, a front image acquiring unit, a region-of-interest determining processor, a scan controller, and a blood flow information acquiring unit. The scanning optical system applies OCT scanning to a fundus of a subject's eye. The front image acquiring unit acquires a front image of the fundus. The region-of-interest determining processor determines a region of interest that intersects a blood vessel by analyzing the front image based on a condition set in advance. The scan controller controls the scanning optical system to apply a repetitive OCT scan to the region of interest. The blood flow information acquiring unit acquires blood flow information based on data collected by the repetitive OCT scan.

Abstract: A method to analyze an eye with a mobile device includes capturing an eye image using a mobile device camera coupled to a processor; capturing gyroscope or accelerometer readings as image metadata to aid in orientation normalization and image registration by the processor; extracting features of the eye using the image corrected with image metadata; and applying the extracted features to a deep learning neural network to detect eye focus data or eye gaze data.

Abstract: Systems and methods facilitate the planning and performance of hip and other surgeries. A computer model of a hip may be generated and displayed. A template of a hip component that replaces a native portion of the hip may be superimposed on the model. Changes in leg length, offset, or anterior-posterior (AP) position as well as a virtual distance between a landmark on the model and a location on the template may be determined. During surgery, a physical distance corresponding to the virtual distance may be obtained. The template may be moved relative to the model to match the physical distance, and new change values in leg length, offset, or anterior-posterior (AP) position may be determined. The new change values may be evaluated, and the surgery may proceed, or the process may be repeated using templates corresponding to alternative components.

Abstract: A system for treating tissue of a patient's anatomy at a target site. A localizer generates location data associated with the anatomy. A display unit overlays visual content on the anatomy within a field of view observable by a user. A visualization program on a computing device generates a virtual reference frame, identifies viable and non-viable approaches for fixation elements to engage tissue and secure a stabilizer relative to the target site based on patient-specific imaging data, arranges a virtual viability model within the virtual reference frame based on the location data and comprising viable portions associated with viable approaches and non-viable portions associated with non-viable approaches, and renders the virtual viability model in the visual content displayed by the display unit overlaid onto the anatomy within the field of view to assist the user in visualizing at least one of viable approaches and non-viable approaches.

Abstract: Methods, systems and devices for pre-operatively planned shoulder surgery guides and implants. Pre-operative planning methods for designing a shoulder surgery guide based on considerations of multiple factors affecting the outcome of shoulder surgery. Methods of using surgery guides and implants in patients undergoing shoulder surgery.

Abstract: Systems and methods for designing and implementing patient-specific surgical procedures and/or medical devices are disclosed. In some embodiments, a method includes receiving a patient data set of a patient. The patient data set is compared to a plurality of reference patient data sets, wherein each of the plurality of reference patient data sets is associated with a corresponding reference patient. A subset of the plurality of reference patient data sets is selected based, at least partly, on similarity to the patient data set and treatment outcome of the corresponding reference patient. Based on the selected subset, at least one surgical procedure or medical device design for treating the patient is generated.

Abstract: A method, a surgical registration device, a sensor device, a system, a computer program, a computer-readable medium and a data carrier signal are disclosed. The surgical registration device comprises a surface, an optical pattern on the surface, and an interface unit to attach to a tracking system. The method comprises obtaining an image of the surgical registration device, detecting the at least one optical pattern in the image, obtaining surface model data describing the surface, obtaining a location of the optical pattern with respect to the surface, determining, based on the detected optical pattern, the surface model data and the location of the optical pattern, a second pose of the surface, obtaining depth information describing three-dimensional coordinates of the surface and determining, based on the second pose, the surface model data and the depth information, a third pose of the surface of the surgical registration device.

Abstract: Systems and methods for surgical guidance and image registration are provided, in which three-dimensional image data associated with an object or patient is registered to topological image data obtained using a surface topology imaging device. The surface topology imaging device may be rigidly attached to an optical position measurement system that also tracks fiducial markers on a movable instrument. The instrument may be registered to the topological image data, such that the topological image data and the movable instrument are registered to the three-dimensional image data. The three-dimensional image data may be CT or MRI data associated with a patient. The system may also co-register images pertaining to a surgical plan with the three-dimensional image data. In another aspect, the surface topology imaging device may be configured to directly track fiducial markers on a movable instrument. The fiducial markers may be tracked according to surface texture.

Abstract: Systems, devices, and methods for controlling cooperative surgical instruments are provided. Various aspects of the present disclosure provide for coordinated operation of surgical instruments accessing various surgical sites from different or shared surgical approaches to achieve a common or cooperative surgical purpose. For example, various methods, devices, and systems disclosed herein can enable the coordinated treatment of tissue by disparate minimally invasive surgical systems that approach the tissue from varying anatomical spaces and must operate differently, but in concert with, one another to effect a desired surgical treatment.

Abstract: Disclosed herein are ultrasound systems and methods for sustained spatial attention. For example, an ultrasound system can include a console and an ultrasound probe. A display of the console can be configured to display ultrasound images and one or more still or moving images of a procedural field. The ultrasound probe can include a camera integrated into the ultrasound probe for recording the one-or-more still or moving images of the procedural field with a depth of field including a distal end of a probe head and a field of view including a spatial region about the probe head. With the one-or-more still or moving images displayed along with the ultrasound images, a clinician need not switch his or her spatial attention between spatial regions such as the procedural field and the display quite as frequently as with existing ultrasound systems, thereby sustaining spatial attention in one or more spatial regions.

Abstract: The present disclosure is directed to interleaving electrical noise generating operations with impedance measurements in a medical localization system. The systems and methods continuously and simultaneously provide unique frequency drive signals, which are harmonics of a common base frequency, across electrode patches to generate an electrical field. Response signals electrodes in the electric field are measured and synchronously demodulated. A demodulated data stream is then filtered (e.g., decimated) to generate impedance-based values proportional to the location of the electrode for each unique frequency. The demodulated data stream into the filter is paused to allow operation of an electrical noise generating device such a magnetic field-based localization system. More specifically, the data stream is paused for a time period equal to an integer multiple of a base period of the common base frequency. This allows resuming filtering of the demodulated data stream free of any frequency discontinuity.

Abstract: Disclosed is an ultrasound probe including an array of ultrasonic transducers and an orientation system, wherein the orientation system obtains orientation information of the ultrasound probe.

Abstract: Systems and methods are described herein for tracking, localization or controlling an elongate instrument or other medical instrument in an image or patient.

Abstract: Various surgical systems are disclosed. A surgical system comprises a robotic tool, a robot control system, a surgical instrument, and a surgical hub. The robot control system comprises a control console and a control unit in signal communication with the control console and the robotic tool. The surgical hub comprises a display. The surgical hub is in signal communication with the robot control system. The surgical hub is configured to detect the surgical instrument and represent the surgical instrument on the display.

Abstract: One example method for detecting phases of a surgical procedure via video processing includes accessing a video of the surgical procedure and dividing the video into one or more blocks, each of the blocks containing one or more video frames. For each of the blocks, the method includes applying a prediction model on the video frames of the respective block to obtain a phase prediction for each of the video frames. The prediction model is configured to predict, for an input video frame, one of the plurality of phases of the surgical procedure. The method further includes generating an aggregated phase prediction for the respective block by aggregating the phase predictions of the video frames, and modifying the video of the surgical procedure to include an indication of a predicted phase of the respective block based on the aggregated phase prediction.

Abstract: A system, device, and method for therapeutic deep tissue massage is disclosed. The therapeutic deep tissue massage device includes an apparatus for use in therapeutic massage applications in which forces are provided to an outer surface of a user's body, whether human or animal, and subcutaneously within the user's tissues.

Abstract: An interface structure for detachably interfacing a surgical robot arm to a surgical instrument, the interface structure comprising: a base portion comprising a first surface for facing the surgical instrument and a second surface for facing the surgical robot arm; and a plurality of first fasteners supported by the base portion and protruding from the first surface, the plurality of first fasteners configured to engage the surgical instrument so as to retain the interface structure to the surgical instrument. The interface structure engages the surgical robot arm so as to retain the interface structure to the surgical robot arm, wherein the plurality of first fasteners and the remainder of the interface structure are shaped such that when the surgical instrument is detached from the surgical robot arm the interface structure is retained to the surgical robot arm.

Abstract: An instrument drive connector includes a housing assembly, an elongated shaft extending distally from the housing assembly, and a first drive assembly at least partially disposed within the housing assembly and the elongated shaft. The first drive assembly includes a first drive screw, a first input drive coupler non-rotatably coupled to a proximal end of the first drive screw, a first drive nut threadedly engaged with a threaded body portion of the first drive screw and longitudinally movable relative thereto in response to rotation of the first drive screw, and a locking link. The locking link includes an elongated body having a proximal end portion coupled to the first drive nut and longitudinally movable relative thereto between a proximal non-locking position and a distal locking position, and a distal end portion including a switch actuation assembly including a switch actuating arm biased towards the distal locking position.

Abstract: Systems and methods may be used for performing a robotic revision knee arthroplasty. For example, a robotic surgical device may be used to perform a cut. The cut may be planned to remove an existing implant based on information about the existing implant (e.g., reference points on the existing implant, an implant type, a maker of the implant, degradation information about the implant, a failure reason for the implant, or the like). In an example, a new plan may be developed for a new implant to replace the existing implant.

Abstract: A system for performing a treatment procedure, comprising a robotic movement controller coupled to a treatment device, the robotic movement controller configured to control movement of the treatment device in three dimensions. A manual override system configured to interrupt the robotic movement controller to allow a user to manually control movement of the treatment device. The robotic movement controller is configured to resume operations when the user has completed manual movement of the treatment device.

Abstract: A robotic surgical system and method of selectively binding articulation limits to a surgical instrument includes detecting a proximal or a distal linear movement of the surgical instrument, calculating a distance between a tool center point of the surgical instrument after the proximal or the distal linear movement and a remote center of motion, assigning and binding an articulation limit to the surgical instrument based on the calculated distance when the detected linear movement is distal linear movement, and assigning a non-binding articulation limit to the surgical instrument based on the calculated distance when the detected linear movement is proximal a linear movement.

Abstract: This application relates to methods and systems for laparoscopic surgery with assist robot and controlling methods for laparoscopic surgery system with assist robot. In one aspect, the method includes arranging a control assist robot on one region of a bed and a motion assist robot on another region of the bed to be spaced a certain distance apart from the control assist robot. The motion assist robot includes a surgical instrument that moves according to a control of the control assist robot. The method also includes performing laparoscopic surgery in a state in which an operator is positioned next to the control assist robot and grips a manual type instrument with one hand and the control assist robot with the other hand.

Abstract: A surgical tool includes a driven portion, a cord-shaped element, and a rotor. To the driven portion, a driving force is transmitted from an external portion. The cord-shaped element transmits a movement of the driven portion. The rotor has a circumferential surface around which the cord-shaped element extending from the driven portion is wound. The circumferential surface includes two or more grooves arranged side by side in a direction of a central axis of the rotor so that the cord-shaped element is windable therearound, and at least one cut-out portion connecting adjacent grooves among the two or more grooves so that the cord-shaped element is placeable through the adjacent grooves.

Abstract: A patient console for a robotic surgical system can include a base, a vertical lift attached to a top of the base and configured to provide up and down motion in a vertical axis, a yaw rotation device attached to the top of the vertical lift and configured to provide a yaw rotation about the vertical axis, a pitch rotation device attached to the top of the yaw rotation device and configured to provide a pitch rotation about a pitch axis orthogonal to the vertical axis, a translation device attached to the top of the pitch rotation device and configured to provide sliding translation along a translation axis, and a roll rotation device attached to the translation device to roll relative to the translation device about a roll axis to provide a roll to an instrument controller assembly. An angle of the translation axis and the roll axis relative to horizontal can be a function of the pitch rotation provided by the pitch rotation device.

Abstract: An apparatus for guiding a flexible instrument includes a first plurality of linkages forming a first side of a channel of a support assembly and a second plurality of linkages forming a second side opposite the first side. In an elongated configuration, each linkage of the first plurality of linkages is interlocked between two adjacent linkages of the second plurality of linkages. Each linkage of the first plurality of linkages is hingedly coupled to an adjacent linkage of the first plurality by a bridging element that maintains a spacing between each linkage of the first plurality of linkages and each respective adjacent linkage. The support assembly transitions from the elongated configuration to a separated configuration as the support assembly is advanced along a longitudinal axis defined by the channel. In the separated configuration, each linkage of the first plurality of linkages is unlocked from between the two adjacent linkages.

Abstract: Certain aspects relate to medical instruments including wrists with hybrid redirect surfaces. Such medical instruments can include, for example, a shaft with a wrist positioned at a distal end. The wrist can include a proximal clevis connected to the shaft and a distal clevis pivotally connected to the proximal clevis. The wrist can also include a static redirect surface, such as a face of a clevis, and a dynamic redirect surface, such as a pulley. The instrument can include an end effector connected to the distal clevis. A plurality of pull wires can extend through the shaft and the wrist and engage with and actuate the wrist and the end effector. A first pull wire segment of the plurality of pull wires can engage the static redirect surface, and a second pull wire segment of the plurality of pull wires can engage the dynamic redirect surface.

Abstract: A method for engaging and disengaging a surgical instrument of a surgical robotic system including receiving a sequence of user inputs from one or more user interface devices of the surgical robotic system; determining, by one or more processors communicatively coupled to the user interface devices and the surgical instrument, whether the sequence of user inputs indicates an intentional engagement or disengagement of a teleoperation mode in which the surgical instrument is controlled by user inputs received from the user interface devices; in response to determining of engagement, transition the surgical robotic system into the teleoperation mode; and in response to determining of disengagement, transition the surgical robotic system out of the teleoperation mode such that the user interface devices are prevented from controlling the surgical instrument.

Abstract: An aspect of the present invention provides a drape unit that is disposed between a medical robot holding a surgical instrument and the surgical instrument to isolate the surgical instrument and the medical robot from each other. The drape unit transmits power in a forward/backward direction from a power transmission part of the medical robot to a movable part provided in the surgical instrument. The drape unit comprises: a movable intervening part that receives the power from the power transmission part; and a fixed intervening part that is detachably attached to the medical robot. The fixed intervening part has a through-hole through which a part of the movable intervening part is inserted. The fixed intervening part has a housing portion that covers a part of the movable intervening part as viewed in a penetrating direction of the through-hole when the movable intervening part moves to an end portion in the forward/backward direction.

Abstract: A sterile adapter retaining device for mounting a surgical drape to a surgical drape installation aid comprises a body having a central portion and plurality of legs extending radially from the central portion. Each leg of the plurality of legs is configured to receive mounted thereon a respective instrument sterile adapter of a plurality of instrument sterile adapters attached to a surgical drape. The body is configured to fit within an interior volume of a surgical drape installation aid in a state of the plurality of instrument sterile adapters mounted on the plurality of legs.

Abstract: The invention refers to a system for delivering a machine-learning based behavioral intervention for the care of withdraw symptoms such as Neonatal Abstinence Syndrome in neonates. The system obtains biosensor or behavioral information about a patient from a wearable device on the patient and makes a determinative recommendation or takes appropriate action based on its evaluation. The biosensor and behavioral information is collected by way of a wearable device over progressive periods of time. When the data is indicative of a need for treatment because the patient is exhibiting symptoms or indicating relapse traits, this information is sent to the system for evaluation. When the data is indicative of a need for treatment, action is taken in the form of a recommendation or when the device is configured to support direct treatment, direct action can be taken to modify alleviate the patient.

Abstract: A system includes one or more sensors to detect activities of a mobile object; and a processor coupled to the sensor and the wireless transceiver to classify sequences of motions into groups of similar postures each represented by a model and to apply the models to identify an activity of the object.

Abstract: A system includes: an aortic pressure sensor configured to measure aortic blood pressure of an individual; a distal sensor configured to measure a parameter in a blood vessel; a receiver configured to receive both (i) a signal representing the measured aortic blood pressure value, and (ii) a signal representing the parameter, the receiver comprising a display configured to display data that is based on at least the measured aortic blood pressure value and the measured parameter; and a communication interface configured to (i) receive a signal representing the measured aortic blood pressure value from the aortic pressure sensor via a wired connection, (ii) provide a signal representing the measured aortic blood pressure value to a monitoring device via a wired connection, and (iii) send a signal representing the measured aortic blood pressure value to the receiver via a wireless connection.

Abstract: A physiological data acquisition system includes an array electrode sensor (220) having plural electrodes and configured to acquire physiological data; a single electrode sensor having a single electrode and configured to acquire additional physiological data; and a hub that is configured to receive the physiological data from the array electrode sensor and the additional physiological data from the single electrode sensor only along body communication channels. At least one of the array electrode sensor and the single electrode sensor is configured to send an energy request signal to the hub, along the body communication channels. The hub, in response to the received energy request signal, emits radio frequency signals, which are used by the at least one of the array electrode sensor and the single electrode sensor to harvest energy.

Abstract: Provided herein are image registration methods comprising providing a wide view image of a target area by a first imager; providing a narrow view image of the target area by a second imager; aligning the narrow view image on the wide view image of the target area; capturing an optical image by an optical imager, wherein the optical imager is configured to locate the optical image in the narrow view image; and displaying the position of the optical image on the narrow view image and the wide view image of the target area; and the systems thereof.

Abstract: A system for performing a minimally invasive procedure includes a flexible catheter, an elongate instrument, an optical coherence tomographic sensor, and a control system. The flexible catheter has a lumen extending therethrough. The elongate instrument is sized for passage through the lumen. The optical coherence tomographic sensor is coupled to the elongate instrument. The control system includes one or more processors and is configured to receive sensor data from the optical coherence tomographic sensor, profile a tissue based on the received sensor data, and determine a distance between the elongate instrument and the profiled tissue.

Abstract: A processing device may receive a plurality of intraoral scans of the patient that were generated by an intraoral scanner, determine a three-dimensional surface of at least a portion of one or more dental arch of the patient using the plurality of intraoral scans, automatically determine whether a restorative dental object is represented in at least one of the three-dimensional surface or one or more intraoral scans of the plurality of intraoral scans, and automatically generate a prescription for treating the one or more teeth based at least in part on at least one of a) a presence or absence of a restorative dental object in at least one of the three-dimensional surface or the one or more intraoral scans or b) a location of the restorative dental object in the one or more dental arch of the patient.

Abstract: Methods, devices and systems for confocal microscopy of human tissues or other samples are described that can be manufactured at a low cost, and are small and portable. One apertureless confocal microscope includes a dispersion element that produces output beams having different spectral components for illumination of a target, such as a tissue. The confocal microscope also includes one or more lenses that receive reflected beams from the target and focus the reflected beams onto a linear variable filter. The linear variable filter is positioned to receive the focused light to allow a particular range of spectral components of light to pass through the linear variable filter that is a function of a spatial location of the focused light incident on the linear variable filter. The described confocal microscopes, among other features and benefits, can greatly facilitate disease diagnosis in medical applications.

Abstract: A medical system may utilize a modular and extensible sensing device to derive a two-dimensional (2D) or three-dimensional (3D) human model for a patient in real-time based on images of the patient captured by a sensor such as a digital camera. The 2D or 3D human model may be visually presented on one or more devices of the medical system and used to facilitate a healthcare service provided to the patient. In examples, the 2D or 3D human model may be used to improve the speed, accuracy and consistency of patient positioning for a medical procedure. In examples, the 2D or 3D human model may be used to enable unified analysis of the patient's medical conditions by linking different scan images of the patient through the 2D or 3D human model. In examples, the 2D or 3D human model may be used to facilitate surgical navigation, patient monitoring, process automation, and/or the like.

Abstract: Disclosed herein are in vivo non-invasive methods and devices for the measurement of the hemodynamic parameters, such as such as blood pressure, stroke volume, cardiac output, performance of the aortic and mistral heart valves, arterial blood velocity profile, blood viscosity and the blood flow induced arterial wall shear stress, hypertensive/hypotensive and vasodilation/vasocontraction state and aging status of a subject, and the mechanical anelastic in vivo properties of the arterial blood vessels.

Abstract: A method and apparatus of automatically locating in an image of a blood vessel the lumen boundary at a position in the vessel and from that measuring the diameter of the vessel. From the diameter of the vessel and estimated blood flow rate, a number of clinically significant physiological parameters are then determined and various user displays of interest generated. One use of these images and parameters is to aid the clinician in the placement of a stent. The system, in one embodiment, uses these measurements to allow the clinician to simulate the placement of a stent and to determine the effect of the placement. In addition, from these patient parameters various patient treatments are then performed.

Abstract: An apparatus, method and computer program is described comprising: applying an electrical signal to a first electrical circuit formed between a first device electrode and a first eyelid electrode, an eyeball electrical path between the first eyelid electrode and a second eyelid electrode, the second eyelid electrode and a second device electrode, and the second device electrode and the first device electrode; and determining current and/or voltage measurements of the first electrical circuit, wherein a current and/or voltage is generated in the first electrical circuit in response to the applied electrical signal, and wherein the first device electrode is configured to form a first capacitor with the first eyelid electrode and the second device electrode is configured to form a second capacitor with the second eyelid electrode.

Abstract: Featured are intravaginal devices and methods of using the devices to observe the state of an individual's pelvic floor muscles in order to diagnose, treat, or prevent pelvic floor disorders (e.g., pelvic organ prolapse and incontinence) and their accompanying symptoms and methods of using the devices to treat or prevent vaginal disorders (e.g., skin laxity) in a subject using an energy transmitter (e.g., a radiofrequency transmitter). Also featured are algorithms to detect pelvic floor movements and physiological indicia from sensor data.

Abstract: An apparatus and method for detecting a bio-signal feature are provided. The apparatus according to one aspect may include: a bio-signal acquirer configured to acquire a bio-signal; and a processor configured to generate an envelope signal of the bio-signal, and detect at least one feature of the bio-signal based on a difference between the envelope signal and the bio-signal.

Abstract: A biometric data measurement system and method, including a transmitting device including a measurement unit configured to measure a first biometric data, a setting unit configured to set a first reference time corresponding to an occurrence time of a first feature value of the first biometric data, and a transmission unit configured to transmit a signal at a time when a predetermined first time period has elapsed since the first reference time, and a receiving device including a measurement unit configured to measure a second biometric data, a setting unit configured to set a second reference time corresponding to an occurrence time of a second feature value of the second biometric data, and a reception unit configured to maintain an awaiting state for the signal during a third time period from a time when a second time period has elapsed since the second reference time.

Abstract: An embodiment optical blood pressure monitor includes a laser Doppler blood flowmeter, which measures the blood flow velocity in a peripheral blood vessel, a photoplethysmography monitor, which measures the pulse waveform in a peripheral blood vessel, a heart rate monitor, which measures data relating to the pulsation of a heart, a characteristic point extraction portion, which extracts a characteristic point relating to the pulsation from the data relating to the pulsation of the heart, a first calculation portion, which determines the pulse wave velocity from the pulse waveform, and a second calculation portion, which determines the blood pressure based on the pulse wave velocity and the blood flow velocity.

Abstract: A blood pressure measurement device includes: a case including an outer case, a base housed in the outer case, and a back cover that covers an opening of the outer case; a movable portion arranged in a gap between the outer case, the base and the back cover, and including a bag-shaped cuff that inflates when a fluid is supplied to an internal space; and a seal member that is formed of a gel body having a lower elastic modulus than that of the cuff, and that is provided in the gap to seal the gap.

Abstract: According to an aspect there is provided an inflation apparatus (10) for use in an inflation-based non-invasive blood pressure, NIBP, measurement apparatus, the inflation apparatus comprising: an outlet (110) configured to be coupled to a cuff of the inflation-based NIBP measurement apparatus; a plurality of pumps (120) each configured to output a flow of gas to the outlet; and a control unit (130) configured to enable at least one of the plurality of pumps to output a flow of gas to the outlet based on a required flow rate to inflate the cuff and/or to control a flow rate of at least one of the plurality of pumps to output a flow of gas to the outlet based on a required flow rate to inflate the cuff.