Disclosed embodiments relate to apparatuses and methods for wound treatment. In some embodiments, a wound dressing apparatus can comprise a wound contact layer, a spacer layer, an absorbent layer positioned on the spacer layer, an electronics unit comprising a negative pressure source and/or electronic components, wherein the absorbent layer comprises a recess configured to receive the electronics unit and the absorbent layer is configured to be in fluid communication with the electronics unit, and a cover layer configured to cover and form a seal over the wound contact layer, the spacer layer, the absorbent layer, and the electronics unit.

According to certain embodiments, an apparatus for applying negative pressure to a wound can include a negative pressure source, a sensor, and a controller. The negative pressure source can be configured to couple via a fluid flow path to a wound dressing and provide negative pressure to the wound dressing. The sensor can be configured to monitor a magnitude or frequency of pressure in the fluid flow path generated by the negative pressure source. The controller can be configured to determine an activity classification, such as breathing, changing positions while lying, sitting, walking, standing, jumping, traversing stairs, leg extending, leg bending, and performing chair squats, based on a change in the magnitude of pressure over time while the negative pressure source maintains the magnitude of pressure in the fluid flow path below a negative pressure threshold. The controller can output an indication of the activity classification.

Disclosed herein are embodiments of a wound treatment apparatus with electronic components integrated within a wound dressing. In some embodiments, a wound dressing apparatus can comprise a wound dressing. The wound dressing can comprise an absorbent material, an electronics unit comprising a negative pressure source, the electronics unit integrated within the wound dressing and at least partially encapsulated by a flexible film. The flexible film can comprise a window or aperture configured to permit fluid communication between the absorbent material and the negative pressure source.

An implantable pump includes a rigid housing with an oblate spheroid shape and having an inner chamber divided by a movable elastomeric membrane into a gas sub-chamber which is connectible through a drive line to an external pneumatic source, and a blood sub-chamber which is connectible through a graft assembly to an anatomical heart. The housing includes a blood port opening oriented at an angle and at the upper apex of the housing and connected to the blood sub-chamber, and a gas port opening to the gas sub-chamber that is situated at a lower apex of the housing. The pump is provided with a drive line that includes a gas conduit and a heart sensor, the drive line connectible to a drive system that is capable of delivering gas flow through the drive line gas conduit in response to signals driven by the heart sensor.

A fluid management system for an ophthalmic surgical system includes an irrigation system and an aspiration system. The irrigation system carries fluid toward a handpiece and includes an irrigation pump or a plurality of pumps. The aspiration system carries fluid away from the handpiece and includes an aspiration pump or the plurality of pumps. The pumps include at least one magnetic pump configured to move the fluid. The magnetic pump includes a plug system and a magnetic field system. The plug system includes one or more plugs disposed within a housing, where each plug comprises a magnetic material. The magnetic field system generates a magnetic field to move one or more of the plugs in order to move the fluid in a pumping direction.

Methods and devices for positioning of subdural drain within an evacuated hematoma cavity. Embodiments include a tethered subdural drain with a puck attached to a leading end of a tether and a subdural drain attached to the terminal end of the tether. The puck is placed in vivo through a first hole in a cranium. A ex vivo guide manipulates the puck and tether through an evacuated hematoma cavity to be retrieved through a second hole in the cranium. Pulling the tether through the second hole advances the subdural drain attached thereto through the first hole and into the hematoma cavity.

A method for synchronizing operation of a heart assist pump device to a patient's cardiac cycle includes obtaining a signal from a motor of a heart assist pump device and filtering the signal to remove noise. The method also includes determining a speed synchronization start point at which time the motor of the heart assist pump device will begin a change in speed of operation based on the filtered signal. The method further includes modulating a speed of the motor of the heart assist pump device to a target speed at the speed synchronization start point, thereby synchronizing the change in speed of operation with a patient's cardiac cycle.

A method for synchronizing operation of a heart assist pump device to a patient's cardiac cycle includes obtaining a signal from a motor of a heart assist pump device and filtering the signal to remove noise. The method also includes determining a speed synchronization start point at which time the motor of the heart assist pump device will begin a change in speed of operation based on the filtered signal. The method further includes modulating a speed of the motor of the heart assist pump device to a target speed at the speed synchronization start point, thereby synchronizing the change in speed of operation with a patient's cardiac cycle.

A method and apparatus that reduces the time and trauma associated with tissue removal procedures such as Ultrasound Assisted Liposuction, which emulsifies and then extracts unwanted adipose from a patient's target zone. Emulsification and suction are optimized and performed in a synchronous manner by a single apparatus to improve the outcome and minimize, if not eliminate, the limitations, risks and complications caused by current state of the art techniques.

Disclosed herein are systems and methods for safe operation of a wound treatment apparatus with electronic components integrated on or within a wound dressing. In some embodiments, the electronic components include a power source, an isolation circuit, a controller, a capacitor, and a negative pressure source. The isolation circuit provides multiple activation states with at least one state preventing application of power to the other electronic components capable of storing electrical energy, thereby providing a safe operation of the apparatus. For example, sterilization of the apparatus can be performed safely.