A method for ventilating a patient during CPR including repeatedly compressing the patient's chest and delivering a positive pressure ventilation to the patient primarily during a decompression phase of the repeated compressions of the patient's chest.

A system for applying external compression to a limb of a user via a system of actuated barrels with compression elements. The system may include a motor, a brake configured to selectively restrict the rotation of different barrels, and a controller configured to operate the brake and motor at different periods of time during use. Sensors may be included, which are coupled to a controller, which, based on sensor data, dictates the timing and degree of compression by controlling the braking system and applied motor current.

Disclosed a system (100) for enacting a positive and a negative pressure on a limb. The system (100) includes an air compressor (102) coupled to a reservoir (104), a piston assembly (106) configured to the reservoir (104), wherein the piston assembly (106) further comprises a piston (108) circumfused inside a tube (107), a pneumatic ring (114) coupled to the system (100) via the piston assembly (106) maintains intermittent pressure and prevents formation of a venous blood clot ischemic injury to a tissue distal to the pneumatic ring (114) compression due to lack of blood flow.

A method of treatment for congestive colon failure (CCF) including evaluating an origin of a lipase and/or an amylase from a biological fluid sample from the subject, optionally analyzing a level of the lipase and/or an amylase from the biological fluid sample from the subject, optionally imaging a colon and a pancreas of the subject and providing laxatives, an anti-fungal composition, fat, a composition selected from a group comprising glucosamine, methylsulfonylmethane (MSM) rhamnan sulfate, Sulodexide, Rosuvastatin, Metformin, Hydrocortisone, Antithrombin, Etanercept, Heparin, Albumin, Fresh frozen plasma (FFP), Poloxamer-188, vitamins, trace elements, a locally acting vasodilator, anaerobic microbial culture, pickled fruits, pickled vegetables, preserved meat, and fermented juices or a combination thereof based upon results of the first three steps.

A treatment system includes a treatment device adapted to contact a vulvar or vaginal tissue of a body and includes a treatment mechanism configured to apply a treatment to the tissue and at least one sensor configured to provide objective sensor data related to the tissue. An external device is configured to receive subjective information provided by a user or a third party and to receive the objective sensor data from the treatment device. The external device includes a processor configured to use the subjective information and the objective sensor data in a decision matrix to issue commands to at least the treatment mechanism that correspond to treatment instructions based on the subjective information and the objective data. The treatment instructions include instructions related to controlling the treatment mechanism and its application of treatment to the tissue and a treatment duration.

A CPR machine (100) is configured to perform compressions on a patient's (182) chest that alternate with releases. The CPR machine includes a compression mechanism (148), and a driver system (141) configured to drive the compression mechanism. A compression force may be sensed, and the driving is adjusted accordingly if there is a surprise. For instance, driving may have been automatic according to a motion-time profile, which is adjusted if the compression force is not as expected (850). An optional chest-lifting device (152) may lift the chest between the compressions, to assist actively the decompression of the chest. A lifting force may be sensed, and the motion-time profile can be adjusted if the compression force or the lifting force is not as expected. An advantage is that a changing condition in the patient or in the retention of the patient within the CPR machine may be detected and responded to.

A medical device can include a housing, an energy storage module within the housing to store an electrical charge, and a defibrillation port to guide via electrodes the stored electrical charge to a person in need of medical assistance. The medical device can also include a processor to perform a patient signal analysis on an electrocardiogram (ECG) signal corresponding to the person and further determine, based on a result of the patient signal analysis, whether post-shock transcutaneous pacing should be performed on the person.

A Cardio-Pulmonary Resuscitation (CPR) device can include a compression mechanism configured to perform successive CPR compressions on a chest of a patient, the compression mechanism including a piston and a contact member attached to the piston, the contact member configured to make and maintain contact with the chest at a first position and a first orientation. The CPR device can also include a controller communicatively coupled with the compression mechanism, the controller configured to: receive at least one input; determine whether the piston should be adjusted based on the at least one input; and responsive to a determination that the piston should be adjusted, cause the piston to move so that the contact member makes and maintains contact with the chest at a second position and a second orientation.

A CPR machine (100) is configured to perform, on a patient's (182) chest, compressions that alternate with releases. The CPR machine includes a compression mechanism (148), and a driver system (141) configured to drive the compression mechanism. A force sensing system (149) may sense a compression force, and the driving can be adjusted accordingly if there is a surprise. For instance, driving may have been automatic according to a motion-time profile, which is adjusted if the compression force is not as expected (850). An optional chest-lifting device (152) may lift the chest between the compressions, to assist actively the decompression of the chest. A lifting force may be sensed, and the motion-time profile can be adjusted if the compression force or the lifting force is not as expected.

Systems, and methods relate to a medical device receiving a treatment parameter operating point within a first operating region defined by a first set of operating points for which automatic incremental adjustment of a parameter in the current operation is permitted. In an illustrative example, incremental adjustment may use artificial intelligence based on patient feedback and sensor measurement of outcomes. Some exemplary devices may receive a request to alter the current treatment parameter operating point to a second treatment parameter operating point outside the first operating region and in a second operating region in a known safe operation zone, bounded by a known unsafe zone unavailable to the user. In the second operating region, some examples may restrict the step size of incremental adjustments requested by the user. Data may be collected for cloud-based analysis, for example, to facilitate discovery of more effective treatment protocols.