Abstract: Surgical articles, implants and components suitable for female pelvic health procedures are described.

Abstract: Described are devices, implants, insertion tools, combinations, and associated methods, that involve placement of a self-fixating tip at tissue of the pelvic region, wherein an insertion tool includes one or more of an aperture for engaging a guide and an extension guard, the method optionally allowing for initial placement of a self-fixating tip at tissue of the pelvic region and adjustment of the location of the self-fixating tip.

Abstract: A pelvic organ prolapse treatment device includes an implantable support configured to treat a prolapsed area of a patient such as urethrocele prolapse, cystocele prolapse, vault prolapse, uterine prolapse, enterocele prolapse, or rectocele prolapse. The support includes a body portion and an arm connected to the body portion, a knot connecting a suture to an end portion of the arm, and a tubular dilator disposed over and permanently connected to the knot. The tubular dilator has an aspect ratio of greater than 7.

Abstract: A shock-absorbing mechanism includes a shaft having a linear member wound therearound, a base having a relative position fixed to a first end of the linear member and formed with a shock-absorbing space which spreads toward the radial outside from the outer peripheral surface of the shaft, and a passage formed in the base in communication with the shock-absorbing space and the outside of the base and causing a second end of the linear member to extend to the outside of the base.

Abstract: An apparatus is disclosed. In some embodiments, the apparatus comprises an endoscope comprising a first distal end portion, and a tube comprising a second distal end portion, wherein the endoscope and the tube are in a side-by-side relationship and are coupled at distal end portions of the endoscope and the tube using a single coupling device.

Abstract: A method for visualizing the interior of a bodily passageway comprising providing a visualization system comprising a tube, visualization apparatus disposed within the tube, and a deformable helical thread disposed on the exterior surface of the tube, the deformable helical thread being transformable between a first configuration wherein the deformable helical thread comprises a reduced profile and/or a reduced rigidity and a second configuration wherein the deformable helical thread comprises an expanded profile and/or increased rigidity; inserting the visualization system into the bodily passageway at a location remote from the site which is to be visualized, with the deformable helical thread being in its second configuration; rotating the tube so as to induce relative movement between the passageway and the tube, whereby to move the visualization apparatus and the site which is to be visualized closer together; and using the visualization apparatus to visualize the interior of the passageway.

Abstract: An endoscope assembly communicates with a data processing unit by radio waves. The endoscope assembly includes operation switches, which is configured to be operated by an operator, and a control unit. The control unit is configured to enable the operation switches to function as switches for setting wireless communication when connection for wireless communication with the data processing unit is not established. Further, the control unit is configured to enable the operation switches to function as switches for inherent operations including at least an image acquisition operation when connection for wireless communication with the data processing unit is established.

Abstract: A medical device for multiple bends, includes a distal-side traction member which is inserted through the distal-side bending portion and the proximal-side bending portion, which is configured to bend the distal-side bending portion in the bending orientation, and which includes a distal-side fixing portion fixed to the distal end of the distal-side bending portion in the axial direction, and a proximal-side traction member which is inserted through the proximal-side bending portion, which is configured to bend the proximal-side bending portion in the bending orientation, and which includes a proximal-side fixing portion fixed to the distal end of the proximal-side bending portion in the axial direction. The proximal-side fixing portion is disposed at substantially the same position as the distal-side fixing portion in a circumferential direction.

Abstract: An apparatus including an outer articulated tube member, the outer articulated tube member having a first tubular section and a second tubular section. The apparatus further including an inner articulated tube member positioned within the outer articulated tube member, the inner articulated tube member having a first tubular section and a second tubular section. The first tubular section and the second tubular section of at least one of the outer articulated tube member and the inner articulated tube member are movable with respect to one another in a first configuration and fixed with respect to one another in a second configuration.

Abstract: A distal end portion successively provided from an insertion part distal end of an endoscope is provided with an air supply and water supply nozzle, an observation window, and illumination windows, and are formed with mutually parallel first and second flat surfaces. The surface of the observation window is disposed at the same position as the second flat surface. An inclined surface that connects the first flat surface and the second flat surface together is formed at a position that faces the air supply and water supply nozzle. Fluid guide surfaces are formed on both sides of the inclined surface. The fluid guide surfaces incline toward the illumination windows. A fluid jetted from the air supply and water supply nozzle impacts against the inclined surface, spreads to the observation window, and is guided to the fluid guide surfaces, and flows to the illumination windows.

Abstract: An endoscopic imaging device for endoscopy in a body vessel is disclosed. The device comprises an annular illumination tube comprising an annular illumination fiber for illuminating a body vessel during endoscopy. The device further includes a first imaging tube comprising a first imaging fiber for gross examination and navigation through the body vessel. The first imaging fiber is disposed within the annular illumination tube. The device further comprises a second imaging tube comprising a second imaging fiber for cellular imaging. The second illumination fiber is disposed adjacent the first imaging tube and within the annular illumination tube.

Abstract: An endoscope includes a rigid portion having an illuminating portion disposed therein and a cover integrally molded to include a transparent first resin member and a colored second resin member. The first resin member configures a first molded portion including an illumination window forming portion which includes an incident surface on which the illumination light is made incident and an emission surface from which the incident illumination light is emitted and an eaves portion projecting from the illumination window forming portion and including a first surface located on the emission surface side and a second surface located on the incident surface side. The second resin member configures a second molded portion forming a cover external shape that covers, the side surface of the illumination window forming portion, the first surface of the eaves portion, and the second surface of the eaves portion.

Abstract: A Glottiscope for assisting with the insertion of an endotracheal tube or an Eschman like stylet into a patient is claimed. The Glottiscope comprises a blade which defines an internal passage for receiving an endotracheal tube or an Eschman like stylet, the blade having a proximal end and a distal end and means for viewing the patient's glottis, wherein the viewing means is disposed at the distal end and in use, below the point of emergence of an endotracheal tube or a stylet/guide (to rail road the endotracheal tube) in the internal passage to provide a view of the patient's glottis, the blade being adapted to direct the viewing means towards the center of the patient's glottis.

Abstract: A surgical access assembly includes a body having first and second body members. Each body member has an opposed side and an outer side. The body members are coupled to one another by a connector and are moveable with respect to one another between an approximated position and a spread position wherein the opposed sides are flexed outwardly and apart from one another to define a passageway therebetween. A flexible membrane is coupled to the first and second body members and extends therefrom such that translating the flexible membrane radially outwardly moves the body members from the approximated position to the spread position.

Abstract: An implantable medical device system and method provide physiological variable monitoring for use in patient management. A target value for a physiological variable and formulations for computing metrics of the physiological variable are stored. Values of the physiological variable are determined from a sensed physiological signal and are used to compute a selected metric. The metric is compared to the stored target value.

Abstract: An implanted device-implemented method of detecting and monitoring congestive heart failure in a patient includes performing ongoing measurements of changes in local impedance of a portion of the patient's body between at least two electrodes on the exterior of the implanted device, the changes representing ventilation of the patient, and including measuring the patient's respiratory rate and respiratory amplitude. A body-implantable device is adapted to detect and monitor congestive heart failure in a patient, and includes a circuit module coupled to plural surface electrodes of the device arranged and adapted, when the device is implanted, for contacting tissue in a portion of the patient's body generally occupied by the lungs, to monitor changes in local impedance of said body portion, and to detect the patient's EKG.

Abstract: An implantable sensing system that includes a sensor for sensing a biological parameter, a processor connected to the sensor for processing the parameter and a drug delivery unit connected to the processor for responding to the processor based on the parameter. The processor is programmed to adjust an output of the sensor by compiling an array of data relating to the sensor, adjusting a sensor parameter a first time based on data in the array, adjusting a curve representing the sensor output based on data in the array and adjusting the sensor parameter a second time based on data in the array.

Abstract: Systems and methods for minimizing or eliminating transient non-glucose related signal noise due to non-glucose rate limiting phenomenon such as interfering species, ischemia, pH changes, temperatures changes, known or unknown sources of mechanical, electrical and/or biochemical noise, and the like. The system monitors a data stream from a glucose sensor and detects signal artifacts that have higher amplitude than electronic or diffusion-related system noise. The system processes some or the entire data stream continually or intermittently based at least in part on whether the signal artifact event has occurred.

Abstract: An automated method for detecting a disease state is presented. The method includes identifying a bone surface in one or more image data sets, wherein the one or more data sets correspond to a region of interest in an object of interest. Furthermore, the method includes segmenting a joint capsule region corresponding to the one or more image data sets based on a corresponding identified bone surface. In addition, the method includes analyzing the segmented joint capsule region to identify the disease state. Systems and non-transitory computer readable medium configured to perform the automated method for detecting a disease state are also presented.

Abstract: Embodiments of an ultrasound system for outputting an ultrasound image through an ultrasound examination are disclosed. In one embodiment, an ultrasound system comprises an ultrasound probe, a sensor unit, a processor unit and an input unit. The ultrasound probe transmits and receives an ultrasound beam to and from the examination portion of a target object. The sensor unit is disposed in the ultrasound probe and detects a posture and/or a position of the ultrasound probe to form posture information and/or position information of the ultrasound probe. The processor unit moves an image indicator corresponding to the posture information and/or the position information. The image indicator includes an ultrasound beam direction marker that is indicative of a transmission direction of the ultrasound beam transmitted from the ultrasound probe to the target object. The input unit is configured to control the processor unit.

Abstract: An ultrasound diagnostic system is provided that includes an ultrasound imaging device having an ultrasound probe that is configured to provide an ultrasound image of the heart during an ultrasound imaging session. The diagnostic system also includes a user interface including an operator display that is configured to concurrently display a reference image frame and the ultrasound image of the ultrasound imaging session. The user interface is configured to receive operator inputs to adjust a view of the heart in the ultrasound image and acquire a set of image frames of the heart. The diagnostic system also includes a cardiac analyzer that is configured to automatically identify a measurement frame from the set of image frames. The measurement frame includes the heart at a designated orientation and at a designated cardiac condition.

Abstract: An ablation catheter comprises: an elongated catheter body extending along a longitudinal axis; at least one ablation element disposed in a distal portion which is adjacent the distal end of the catheter body to ablate a targeted tissue region outside the catheter body; a single pulse-echo ultrasonic transducer disposed in the distal portion and arranged to emit and receive an acoustic beam along a centroid in a beam direction, at a transducer angle of about 30-60 degrees relative to a distal direction of the longitudinal axis at a location of intersection between the longitudinal axis and the beam direction of the centroid of the acoustic beam; and a mechanism to manipulate the distal portion in movement including rotation of at least the distal portion around the longitudinal axis. The single ultrasonic transducer emits and receives acoustic pulses to provide lesion information in the targeted tissue region being ablated.

Abstract: Various methods and devices for minimally invasive treatment and prevention of conditions of the fascia are provided. In one aspect, a method includes providing an acoustic wave source effective to deliver a focused acoustic wave to a target site within a patient's body, and focusing an acoustic wave through a patient's skin such that at least one location in the patient's fascia is fenestrated in a desired pattern.

Abstract: A method of processing an ultrasound image includes generating a plurality of two-dimensional (2D) ultrasound images from three-dimensional (3D) ultrasound volume data of an object to be diagnosed, generating a plurality of tissue edge images of an edge of at least one tissue component in the object to be diagnosed based on values of a plurality of pixels forming each of the 2D ultrasound images generated from the 3D ultrasound volume data, and generating a 2D ultrasound image from which a noise component has been removed by discriminating the edge of the at least one tissue component from a position of the noise component based on a difference between a similarity of the edge of the at least one tissue component in the tissue edge images and a similarity of the noise component in the tissue edge images.

Abstract: A method for evaluation of renal perfusion with power Doppler ultrasonography is disclosed in the present invention. Serial renal vascular images at different vascular areas including the whole vascular tree, interlobar, arcuate, and interlobular vessels were captured. Imaging processing software was designed to analyze the changes of power Doppler intensity of colored pixels within regions of interest (ROI). Power Doppler Vascularity index (PDVI) has been defined as the percentage of vascular perfusion within a region of interest (ROI). The renal vascular perfusion index (RVPI) is defined as the maximal power Doppler vascular index divided by minimal power Doppler vascular index (PDVImax/PDVImin) among the serial images. The mean of weighted power Doppler vascular index (WPDVImean) is defined as the average of the intensity of color pixels among the ROI within the serial images.

Abstract: The present disclosure provides a precise performance three-dimensional ultrasound scanner that is lightweight for an easy hold by suggesting a novel constitution of a swing mechanism wherein an arrangement of the drive motor perpendicular to the swing axis requires a smaller capacity motor and eliminating a backlash. The swing mechanism includes: an arm holder connected to a rotational axis of the motor; an arm connected to the arm holder so that the arm swings within a certain angular range; a link, attached to the arm, for moving in unison with the arm; a shaft, connected to the link, for transmitting a rotary power of the arm to the transducer unit. The swing mechanism can be operated using the smaller capacity motor and eliminates the need for a pulley, gear or belt eliminating backlashes to promote implementation of lightweight precision three-dimensional ultrasound scanners.

Abstract: Improved apparatus and methods for non-invasively assessing one or more hemodynamic parameters associated with the circulatory system of a living organism. In one aspect, the invention comprises an apparatus adapted to automatically and accurately place and maintain a sensor (e.g., tonometric pressure sensor) with respect to the anatomy of the subject. The apparatus comprised of a sensor device removably coupled to an actuator which is used to position the sensor during measurements. Methods for positioning the alignment apparatus and sensor, and operating the apparatus, are also disclosed.

Abstract: Methods, systems, and apparatus for powering and/or recharging medical devices implanted within the body are described. An illustrative power generation module disposable within the interior space of an implantable medical device includes a module body that defines an interior cavity as well as a flexible diaphragm that spans the interior cavity. The flexible diaphragm includes a first electrical conductor, a piezoelectric layer disposed adjacent to the first electrical conductor, and a second electrical conductor disposed adjacent to the piezoelectric layer. The piezoelectric layer is configured to displace within the interior cavity and generate a voltage differential between the first electrical conductor and the second electrical conductor.

Abstract: A cuff for a blood pressure monitor includes a bag-shaped cover body containing an air bag and a curled elastic member as a curved elastic plate. The bag-shaped cover body is formed by stacking an inner cover member located on a living body side when applied and an outer cover member located on a side opposite to the living body side when applied, one on the other, and sewing their rims. The curled elastic member contained in the bag-shaped cover body includes a large curvature region and a small curvature region in a winding direction thereof to fit a measurement site. In a state where the air bag is not inflated, the inner cover member at a portion corresponding to the large curvature region of the curled elastic member is stretched in a width direction thereof. With this configuration, a cuff for a blood pressure monitor which is less likely to have wrinkles in a bag-shaped cover body can be provided.

Abstract: A blood pressure information measurement device includes a servo control unit for performing a servo control of a pressure adjustment unit so that a value of an arterial volume signal matches a control target value and a fluctuation detection unit for detecting rapid fluctuation of the arterial volume signal at an initial stage during a period of the servo control. The fluctuation detection unit determines that the rapid fluctuation occurred when a control deviation representing a level of the arterial volume signal having the control target value as a reference becomes greater than or equal to a predetermined magnification of a reference deviation. The blood pressure information measurement device further includes an adjustment processing unit for adjusting a control amount of the pressure adjustment unit by the servo control unit so that an excessive response is not made when the rapid fluctuation is detected by the fluctuation detection unit.

Abstract: A pulse rate counting device includes: a short-term average value calculation unit for calculating an average interval of predetermined previous pulses; a fluctuation amount calculation device for calculating the amount of fluctuation on the basis of the difference between the average interval and an actual pulse wave interval; a search range determination unit for calculating the width of the search range, calculating an amount of displacement on the basis of a time change of the average interval, and determining as a search range a range including an appearance prediction value of the next detection point calculated from the average interval and indicated by the width of the search range from a starting point determined on the basis of the amount of displacement; and a pulse wave interval detection unit for detecting the detection point in the determined search range, and outputting a pulse wave interval.

Abstract: In accordance with an embodiment of the present technique, there is provided methods and systems for detecting the location of a sensor and determining calibration algorithms and/or coefficients for calculation of physiological parameters based on the detected location. An exemplary embodiment includes receiving a signal corresponding to absorption of at least one wavelength of light by a patient's tissue, generating a plethysmographic waveform from the signal, determining an identifying characteristic of the plethysmographic waveform, and determining a location of the sensor based on a comparison of the identifying characteristic with at least one defined criterion.

Abstract: This invention includes improved IP sensors that both have improved sensitivity, performance, and other properties and are multifunctional. The improved IP sensors have IP sensor conductors with waveforms having legs that are substantially parallel throughout the operating range of stretch. The multifunctional IP sensors include, in addition to IP sensors, accessory conductors, additional sensors, and other compatible modules. This inventions also includes embodiments of apparel incorporating the improved IP sensors. This apparel can range from band-like to shirt-like, and so forth, and include one or more IP sensors sensitive to expansions and contractions of underlying regions of a monitored subject.

Abstract: The systems, methods and associated devices performing diagnostic hearing tests which use a computer network to allow interaction between a test administration site and one or a plurality of remote patient sites. The test can be administered by an audiologist or clinician at a site remote from the patient, in a manner, which can allow interaction between the user and the clinician during at least a portion of the administration of the test. The diagnostic hearing tests can be performed such that they meet standardized guidelines such as ANSI requirements or certification standards and can include distortion product emission level measurements or middle ear compliance measurements.

Abstract: Catheter devices for diagnosing and treating discogenic pain are provided. The catheter devices comprise a tubular body configured for insertion into an intervertebral disc and a pressure measuring device disposed along the length of the tubular body, the pressure measuring device configured to measure the pressure within the intervertebral disc. The catheter devices are capable of measuring the pressure within an intervertebral disc of a subject while the subject is moving.

Abstract: A medical device for reducing the force necessary to penetrate living being tissue using a variety of reciprocating motion actuators, including piezoelectric, voice coil, solenoids, pneumatics or fluidics. The reciprocating actuator drives a penetrating member, such as a needle, through the tissue at a reduced force while the device detects the passage of the penetrating member through the tissue. Upon passage of the penetrating member through the tissue, electrical power to the reciprocating actuator is automatically terminated. One exemplary method for detecting this passage is via a fluid-containing syringe that is coupled to a channel within the penetrating member. Once the penetrating member tip has passed through the living tissue, the fluid within the syringe no longer experiences any pressure and a plunger within the syringe displaces indicating passage of the penetrating member tip.

Abstract: A diagnostic system has a diagnostic module with an integrated lancet system and a magazine module separate from the diagnostic module. The diagnostic device also has a connecting device that is used for tensioning the lancet system.

Abstract: The present invention generally relates to a medical surgical device and specifically a wire guide for percutaneous placement within a body cavity. In one embodiment, the wire guide includes an elongated core member having a proximal stop and a distal stop and a rib positioned between the proximal stop and the distal stop. A first coil is positioned over the elongated core member and extends between the proximal stop and the rib. A second coil is positioned over the elongated core member and extends between the rib and the distal stop.

Abstract: The present disclosure is directed to the detection of coughs and coughing episodes using acoustic signals. In various examples, an implantable medical device processes an acoustic signal obtained from an acoustic sensor to determine whether a patient has coughed. In some examples, the implantable medical device also performs a cough severity assessment. In some examples, the cough severity assessment may include a determination of the depth of the cough, the duration of the coughing episode, or whether the cough was wet or dry.

Abstract: Disclosed herein is a method of defining a mating surface in a first side of an arthroplasty jig. The mating surface is configured to matingly receive and contact a corresponding patient surface including at least one of a bone surface and a cartilage surface. The first side is oriented towards the patient surface when the mating surface matingly receives and contacts the patient surface. The method may include: a) identifying a contour line associated with the patient surface as represented in a medical image; b) evaluating via an algorithm the adequacy of the contour line for defining a portion of the mating surface associated with the contour line; c) modifying the contour line if the contour line is deemed inadequate; and d) employing the modified contour line to define the portion of the mating surface associated with the contour line.

Abstract: Devices and methods for determining fallopian tube occlusion. The methods may include determining fallopian tube occlusions through a pressurization or volumetric determination.

Abstract: A spine measurement system includes at least one spinal instrument and a remote system. The spinal instrument comprises a handle, a shaft, an accelerometer, a sensored head, and an electronic assembly. The sensored head includes one or more sensors that are operatively coupled to the electronic assembly. The sensored head can be inserted between vertebra and report vertebral conditions such as force, pressure, orientation and edge loading. A GUI of remote system can report position via the accelerometer to show spinal instrument relative to vertebral bodies as the instrument is placed in the inter-vertebral space. The system can report optimal prosthetic size and placement in view of the sensed load and location parameters including optional orientation, rotation and insertion angle along a determined insert trajectory.

Abstract: Apparatuses are disclosed that is adapted and configured to cause and control joint motion of a patient. Apparatuses comprise, for example, a first motion member configured to engage a patient proximal to a target joint; a second motion member configured to engage a patient distal to a target joint; and a coupling member configured to connect the first motion member to the second motion member and further adapted to allow rotation of the first and second motion member around an axis, wherein the apparatus is engageable with a medical diagnostic device and further configured to capture patient specific data.

Abstract: The apparatus for immobilizing and treating a subject includes a suitable apparatus for performing mechanical CPR secured to an immobilization casing. The airtight flexible casing is secured to the apparatus for performing CPR, the casing having variable rigidity which varies as a function of the amount of air within the casing. Two or more slots through the casing permit passage of one or more elements of the CPR apparatus to pass through the casing. One or more incompressible windows may be included in the casing to optimize the performance of mechanical CPR by permitting one or more elements of the subject's skeleton to contact the CPR apparatus. A device for evacuating the air from within the flexible casing to control the rigidity of the casing is included within the CPR apparatus.

Abstract: An airway clearance combines a force multiplying percussor and a self-applicator assembly. The percussor has an anvil, a hammer, a coil, and a pulse generator. The anvil has a force receiving surface and a force delivering surface. The hammer also has a force-receiving surface and a force-delivering surface, and is attached to the anvil such that the hammer's force delivering surface and the anvil's force receiving surface are mechanically free to come together or move apart. When energized with an electrical current, the coil forces the hammer's force delivering surface and the anvil's force receiving surface to separate. The pulse generator supplies pulses of electrical current to the coil.

Abstract: A handheld massage device includes an actuator mechanism and a massage unit received in an outer housing. The actuator includes a motor, a bearing and a tilting piece having a first shaft coupled with the motor and a second shaft fitted into the bearing. The crank-shaped first and second shafts do not lie on a straight line. The massage unit has a base plate and massage elements mounted on the base plate. The massage elements protrude from one end of the outer housing. The bearing is fitted in the base plate. Because the first and second shafts form an angle therebetween, the base plate is tilted and swings like a conical pendulum. Therefore, the massage elements on the base plate move back and forth along a direction of an axle of the motor, thereby providing kneading and percussion massages on the user's body.

Abstract: The present invention is to provide an air traction belt structure, which includes an inner inflatable traction belt having an air valve thereon for communicating with an inflatable space therein and, and an outer solid support belt having a smaller width than the inner inflatable traction belt and movably surrounding outside of the inner inflatable traction belt. Since a first end of the outer solid support belt can pass through a through hole formed on the inner inflatable traction belt and extend to an inner side of the inner inflatable traction belt, a second end of the outer solid support belt can easily pass through a fixing ring provided on the first end of the outer solid support belt and be pulled by a user, for firmly tightening both the inflated inner inflatable traction belt and the outer solid support belt onto the user's waist at the same time.

Abstract: A surgical cast venting material comprises a waterproof, flexible substrate made of a plastics material and having first and second sides. The first side has a plurality of shallow, concave recesses distributed over the substrate and spaced-apart from one another while the second side has a plurality of protrusions distributed across the substrate. The substrate is perforated with a plurality of small holes distributed across its length and width. Also, a surgical cast venting device is disclosed for venting a bent region of a patient's limb. It has a flexible, central portion that can cover a major part of the bent region of the limb including opposite side surfaces and a front or rear surface. The device also has flexible connecting straps extending from two corners of the central portion.

Abstract: Devices and processes used to treat ankle equinus for users with specific conditions such as young age, diabetes, or clubfoot. More specifically, the present disclosure relates to a brace and the corresponding method of use to treat equinus by stretching the Gastrocnemius muscle.

Abstract: An apparatus for supporting a patient's hand, wrist, and at least a portion of the forearm in order to expose the radial artery to receive an arterial line. The apparatus including a substantially flexible, unitary body adapted to underlie the posterior of the patient's hand, wrist and forearm. The unitary body including a forward portion having an upturned cutout portion for receiving finger portions of a patient's hand. The forward portion configured for mating engagement with the posterior surface of the hand. The unitary body further including a rear portion sloping downward from the forward portion and having an upturned cutout portion for receiving a forearm portion of a patient.