Described herein are systems and apparatuses for enhanced comfort through contact pressure reduction. In particular, the systems and apparatuses disclosed herein prevent or otherwise mitigate pressure by actively orienting a patient over an anatomy-specific pressure-mitigating contact surface on which the patient rests. A pressure-mitigating contact portion of the contact surface includes a plurality of independently pressurized chambers configured in a specific geometric pattern that is designed to mitigate contact pressure between a support surface (e.g., bed or chair) and a specific anatomic region of a patient's body when the specific anatomic region of the patient's body is oriented over an epicenter of the geometric pattern. Additionally, a plurality of elevated side support portions and a wedge interconnected on the base material are configured to actively orient the specific anatomic region of the patient's body over the epicenter of the geometric pattern.

Disclosed herein is a pressure-relief mattress comprising: a plurality of inflatable bladders; a pressure sensor pad arranged to detect pressure exerted on a subject, the pressure sensor pad comprising a plurality of pressure sensor cells being arranged in a matrix with at least one row and at least one column; a pressure-sensing electronic unit electrically connected with the plurality of pressure sensor cells; and a pressure-control electronic unit communicatively connected with the pressure-sensing electronic unit; wherein the pressure-sensing electronic unit is configured for generating a measurement result indicative of a pressure exerted upon the subject at one or more of the pressure sensor cells, the pressure control electronic unit is configured for controlling operation of one or more of the inflatable bladders according to the pressure measurement result.

A patient support apparatus, such as a hospital bed, communicates with an electronic medical record (EMR) system in healthcare facility. The hospital bed includes a patient support structure to support a patient, a graphical user interface coupled to the patient support structure, and control circuitry coupled to the graphical user interface. The graphical user interface displays at least one input that may be used by a caregiver to chart data into an electronic medical record (EMR) of a patient supported by the patient support structure.

The present invention relates to a mat for use in lateral positioning. The invention provides an inflatable mat for use in lateral positioning in angled lateral decubitus, the mat comprising: a mat foil with a longitudinal direction, the mat foil having an upper side and a first side extending in the longitudinal direction, and a second side extending in the longitudinal direction, a first longitudinal section, comprising one or more inflatable air chambers, being arranged on the upper side of the mat foil along the first side of the mat foil, and a second longitudinal section, comprising one or more inflatable air chambers, being arranged on the upper side of the mat foil along the second side of the mat foil, the mat foil having a centre in the longitudinal direction, one or more first transverse sections, each comprising one or more inflatable air chambers, being arranged successively in a row in the longitudinal direction, the first transverse sections extending from the centre out towards the first side, so that the one or more transverse sections are arranged lying above the first longitudinal section away from the mat foil, one or more second transverse sections, each comprising one or more inflatable air chambers, being arranged successively in a row in the longitudinal direction, the transverse sections extending from the middle out towards the second side, the transverse sections being arranged lying above the second longitudinal section away from the mat foil, wherein the first longitudinal section, the second longitudinal section and the one or more first transverse sections and the one or more second transverse sections are connected to one or more air ducts arranged in each of the inflatable air chambers of said longitudinal and transverse sections, wherein the longitudinal and transverse sections can be individually inflated, the first side of the mat having a total first lateral height, which is the sum of a height of the first longitudinal section in the inflated state and a height of the first transverse section in the inflated state, the second side of the mat having a total second lateral height, the second lateral height being the height of the second longitudinal section in the inflated state, or the second side of the mat having a total second lateral height, which is the sum of a height of the second longitudinal section in the inflated state and a height of the second transverse section in the inflated state, and the first side of the mat having a total first lateral height, the first lateral height being the height of the first longitudinal section in the inflated state.

A fluid source comprises a connector assembly for connecting a fluid supply device to either a first therapy device or to a second therapy device. A controller automatically provides a first configuration of a user interface associated with a first therapy when a supply connector is operatively coupled to the first therapy device and provides a second configuration of the user interface associated with a second therapy, different than the first configuration, when the supply connector is operatively coupled to the second therapy device. A hanger assembly is provided to hang the fluid source on different support structures. The fluid source also comprises a housing with a watershed region to shed liquid away from the user interface.

A pressure injuries therapeutic support surface is illustrated. The surface comprises an integrated system designed for a concurrent physical and psychoneuroimmunological approach over a user, wherein the system comprises one or a plurality of independent fluid-filled main chambers, made of waterproof, flexible, extendable, and elastic material and at least two accessory chambers connected to each main chamber with at least with two free-flow conduits. The system is managed through a powered mechatronic array with its own hardware and software based on microcontrollers for the simultaneous operation of specific multidisciplinary devices.

A multi-position airflow control assembly includes a valve housing, a valve body received by the valve housing, a plurality of connectors coupled to the valve body, each connector configured to fluidly connect to an inflation zone of a cellular cushion, and a control assembly partially received by the valve body. The control assembly includes a seal member, and an actuation assembly operably connected to the seal member and configured to rotate the seal member relative to the valve body. The seal member is configured to rotate between a first position and a second position.

An air valve assembly includes a housing defining an internal channel, a plunger member positioned in the internal channel and configured to slide relative to the housing, a biasing member positioned in the internal channel and configured to apply a biasing force onto the plunger member, a sealing member defining a first inflation aperture, the plunger member slidably received by the first inflation aperture, a second deflation aperture defined by the housing and in fluid communication with the internal channel, and a deflation control member slidably connected to the housing, the deflation control member configured to selectively seal the second deflation aperture.

A system for monitoring medical conditions including pressure ulcers, pressure-induced ischemia and related medical conditions comprises at least one sensor adapted to detect one or more patient characteristic including at least position, orientation, temperature, acceleration, moisture, resistance, stress, heart rate, respiration rate, and blood oxygenation, a host for processing the data received from the sensors together with historical patient data to develop an assessment of patient condition and suggested course of treatment, including either suspending or adjusting turn schedule based on various types of patient movement. Compliance with Head-of-Bed protocols can also be performed based on actual patient position instead of being inferred from bed elevation angle. The sensor can include bi-axial or tri-axial accelerometers, as well as resistive, inductive, capacitive, magnetic and other sensing devices, depending on whether the sensor is located on the patient or the support surface, and for what purpose.

A support surface assembly includes a covering defining an interior. Bladders are disposed within the interior. The bladders are operable between a deployed state and a non-deployed state. A manifold assembly is disposed within the interior of the covering. The manifold assembly includes a manifold core defining an inlet and multiple outlets. An engagement surface of the manifold core defines an inlet-connecting aperture in fluid communication with the inlet and multiple outlet-connecting apertures each in fluid communication with one of the multiple outlets. A connector includes an inner side that abuts the engagement surface of the manifold core. The inner side defines a recessed region. The connector is configured to be rotated by a motor to fluidly couple the inlet-connecting aperture with at least one of the outlet-connecting apertures to adjust the respective bladders between the deployed state and the non-deployed state.