Technologies and implementations for wearable healthcare devices are generally disclosed. An example method performed by a wrist-wearable device includes: detecting, by a sensor, a physiological parameter of a user; determining, by a processor based on the physiological parameter, that the user is experiencing atrial fibrillation (AF); outputting, by a display, a visual signal indicating that the user is experiencing the AF; and transmitting, by a transceiver to a first external computing device, a first wireless signal indicating that the user experienced the AF.

A device for assisting a caregiver in delivering cardiac resuscitation to a patient, the device comprising a user interface configured to deliver prompts to a caregiver to assist the caregiver in delivering cardiac resuscitation to a patient; at least one sensor configured to detect the caregiver's progress in delivering the cardiac resuscitation, wherein the sensor is configured to provide a signal containing information indicative of ventilation; a memory in which a plurality of different prompts are stored, including at least one ventilation progress prompt to guide the rescuer's performance of ventilation; a processor configured to process the output of the sensor to determine a parameter descriptive of ventilation progress and to determine whether the ventilation progress prompt should be selected for delivery. Possible parameters descriptive of ventilation progress include ventilation rate, delivered tidal volume, and flow rate.

A chest compression device for cardiopulmonary resuscitation comprises a support structure 2 for placement about a patient's chest and for holding a chest compressor 6 above a patient's sternum; a chest compressor 6 mounted on the support structure 2; and lateral chest supports 14 attached to the support structure 2 at points laterally either side of the chest when the device is in use, such that the lateral chest supports 14 will apply lateral pressure to the sides of the chest synchronized with a chest compression by the chest compressor 6.

Systems and apparatuses related to the field of cardiac resuscitation, and in particular to devices for assisting rescuers in the administration of cardio-pulmonary resuscitation (CPR) are described herein. The system includes an adhesive pad configured to be adhered to at least a portion of a patient's chest, a sensor configured to be placed on the patient's chest and to measure at least one chest compression parameter during CPR treatment, and a landing pad having a coupling surface at least partially surrounding the sensor and configured for maintaining adherence with an active compression decompression device, the adherence sufficient to transfer decompression force between the active compression decompression device and the patient's chest during the CPR treatment.

A device for assisting a caregiver in delivering cardiac resuscitation to a patient, the device comprising a user interface configured to deliver prompts to a caregiver to assist the caregiver in delivering cardiac resuscitation to a patient; at least one sensor configured to detect the caregiver's progress in delivering the cardiac resuscitation, wherein the sensor is configured to provide a signal containing information indicative of ventilation; a memory in which a plurality of different prompts are stored, including at least one ventilation progress prompt to guide the rescuer's performance of ventilation; a processor configured to process the output of the sensor to determine a parameter descriptive of ventilation progress and to determine whether the ventilation progress prompt should be selected for delivery. Possible parameters descriptive of ventilation progress include ventilation rate, delivered tidal volume, and flow rate.

The apparatus of the invention is used for cardiopulmonary massaging and/or resuscitation of a patient and includes a massaging device (15) which can be reversibly driven in an actuating direction (23) by a drive unit (18) and which has a pressure surface (20) that can be placed in a target contact zone (21) on the rib cage (12) of a patient (11). In order to easily and reliably prevent the pressure surface of the massaging device to deviate from a target pressure point (21), the plunger (19) can be secured to the rib cage (12) of the patient (11) in the target contact zone (21) and is mounted in such a way as to be freely movable in a plane running transversely to the actuating direction (23) at least during an unloaded state between two massaging strokes.

The invention relates to a sensor device for capturing data when carrying out first aid measures for reanimating a person affected by a cardiac arrest. The sensor device is exactly positioned on the chest of the patient by means of a positioning-aid apparatus (5) and affixed by means of a fastening means (2). The thorax compressions, i.e., the pressing-in depth and compression frequency, are detectable by means of a motion sensor. A data-transfer interface allows communication, e.g. wireless communication, with a mobile terminal.

A system includes a guidance device that provides feedback to a user to compress a patient's chest at a rate of between about 90 and 110 compressions per minute and at a depth of between about 4.5 centimeters to about 6 centimeters. The system includes a pressure regulation system having a pressure-responsive valve that is configured to be coupled to a patient's airway. The pressure-responsive valve is configured to remain closed during successive chest compressions in order to permit removal at least about 200 ml from the lungs in order to lower intracranial pressure to improve survival with favorable neurological function. The pressure-responsive valve is configured to remain closed until the negative pressure within the patient's airway reaches about 7 cm H.sub.2O, at which time the pressure-responsive valve is configured to open to provide respiratory gases to flow to the lungs through the pressure-responsive valve.

A respiratory therapy apparatus includes components operable to simultaneously provide a High Frequency Chest Wall Oscillation (HFCWO) therapy and a Mechanical Insufflation/Exsufflation (MIE) therapy to a patient. The respiratory therapy apparatus includes a controller that controls a synchronization of the HFCWO therapy and the MIE therapy to provide respiratory therapy to the patient to effectively clear mucous or induce deep sputum from the lungs of patient.

A device for treating chest wall injuries, including rib fractures, flail chest injuries or surgical incisions is described herein. The device includes a localized airtight compartment external to the chest wall and fully covering the area of injury, and is capable of varying the pressure within the compartment, and providing dynamic real-time counter forces that act reciprocal to the intrathoracic pressure changes that occur during ventilation. In a preferred embodiment, the device has the capability of sensing the patient's chest wall motion created by ventilation, and includes a pressure control component capable of varying the pressure within the airtight compartment such that it opposes pressure changes within the chest. The apparatus would be particularly useful in preventing the paradoxical movement of flail chest injuries. The device would also lessen pain experienced by patients with thoracic injuries such as rib fractures and post operative suffering.