A computer-implemented system may include a treatment device configured to be manipulated by a user while the user is performing a treatment plan, a patient interface comprising an output device configured to present telemedicine information associated with a telemedicine session, and a first computing device configured to: receive treatment data pertaining to the user while the user uses the treatment device to perform the treatment plan; identify at least one aspect of the at least one measurement pertaining to the user associated with a first treatment device mode of the treatment device; determine whether the at least one aspect of the measurement correlates with a secondary condition of the user; and, in response to a determination that the at least one aspect of the at least one measurement is correlated with the at least one secondary condition of the user, generate secondary condition information indicating at least the secondary condition.

The present disclosure includes various examples for cooling electronics within a medical device while preventing or reducing the risk of an interior of the medical device being contaminated with a pathogen. The present disclosure includes a medical device having an air deflector to deflect potentially contaminated air from infecting a patient or caregiver. The present disclosure also includes medical devices with disinfectant devices installed to disinfect air either before entering the medical device or before exiting the device. Other examples of the present disclosure include medical devices that are sealed from outside air and fluids, and which may include a cooling device on an exterior surface which may be cleaned and/or removed after each use.

A method for maintaining and/or increasing body temperature of a patient may involve delivering heat to a first location on a limb of the patient, delivering heat to a second location on the limb, apart from the first location, and applying intermittent compression to a third location on the limb, located between the first location and the second location. A device for maintaining and/or increasing body temperature of a patient may include a sleeve for positioning over at least part of one of the patient's limbs, first and second heat delivery members coupled with the sleeve, and an intermittent compression member coupled with the sleeve between the first and second heat delivery members.

A system for improving blood circulation, the system comprising a control unit comprising a processor and at least one article of footwear wherein one or more of the at least one articles of footwear together or alone comprise: one or more actuators coupled to and controlled by the control unit; one or more electrically-conductive paths; one or more sensors integrated into the at least one article of footwear and coupled to the processor, for providing measurement signals to the control unit; and the system further comprising an electrical power supply for supplying electrical power to the one or more sensors by means of the one or more electrically-conductive paths.

A vaginal probe with sensing and data transmitting capabilities is shown and described. The probe includes physiological sensors and an optical display including light emitting diodes on a circumferential surface. Data storage and transmission capability is contained in a docking station associated with the probe. Data can be transmitted to a remote location for analysis and/or display.

A compression device for applying pressure to a body part can include a fabric member that can fit over the body part, and one or more actuators coupled to the fabric member, wherein each of the one or more actuators is configured to cause at least a portion of the fabric member to expand or contract along a circumferential direction, thereby decreasing or increasing the pressure applied to the body part adjacent to the actuator. The fabric member can be thin and stretchable, and can contour the body part over which it is worn. The actuators can cause user controlled variable pressure levels to be applied to the body part, including constant pressure levels as well as time varying synchronous or asynchronous pressure patterns.

A percussive therapy device that includes a housing, an electrical source, a motor positioned in the housing, a switch for activating the motor, and a push rod assembly operatively connected to the motor and configured to reciprocate in response to activation of the motor. The percussive therapy device includes at least one of a thermal sensor, a heart rate monitor or a heated massage member.

A device for massaging skin, including, a RF generator adapted to generate a radio frequency AC current to heat the skin tissue, an electrical pulse generator adapted to generate pulses of DC current to provide electrical muscle stimulation for the muscles below the skin tissue, an applicator including one or more heads adapted to be placed in contact with the user's skin; and wherein the heads serve as massage contacts to massage the user's skin by back and forth movement of the massage contacts across the skin tissue and further as electrodes to deliver RF heating and electrical muscle stimulation.

A wearable device measures, tracks, and monitors a wearer's physical physiological conditions during a rehabilitation period. Metrics such as temperature, patellar shifting, limb circumference, and acceleration may be collected. Changes in monitored conditions may be assessed for detecting medical abnormalities which require specialized attention, including for example embolisms or infections. A networked communication system and various user interfaces may be used for medical support personnel and patients alike to stay updated with the patient's rehabilitation progress and to make adjustments in a patient's individual rehabilitation program.

An apparatus may be configured for documenting a code blue scenario when adhered to the chest of a subject undergoing resuscitation by sensing and transmitting information associated with the code blue scenario. Such information may include one or more of vital signs of the subject during resuscitation, information associated with chest movements of the subject during resuscitation, and audio information from an environment of the subject during resuscitation. A computing platform that is separate and distinct from the apparatus may provide code blue documentation conveying information related to the vital signs of the subject and derived from the audio information from the environment of the subject during resuscitation.