A system and method which performs translumbosacral neuromodulation therapy in a subject by outputting pulses of magnetic energy onto the lumbar and sacral nerves of the subject is described. The system includes a control unit, an anorectal probe, at least one skin electrode, a first magnetic coil, a second magnetic coil, and a neurophysiological recorder. The control unit manages the system components. The anorectal probe and the skin electrode detect muscle activity when a nerve from the back of the subject is stimulated. The first magnetic coil outputs singular pulses of magnetic energy to localize a plurality of optimal stimulation sites. The second magnetic coil outputs repetitive pulses of magnetic energy to each of the plurality of optimal stimulation sites in order to treat medical problems. The neurophysiological recorder displays motor-evoked potential (MEP) data that is detected by the anorectal probe and the skin electrode through electromyographic sensors.

An electrical stimulation therapeutic device includes a pair of application electrodes which are disposed at the back of a sacral bone of a person to be treated and supplies an electrical stimulation signal from the back of the sacral bone, a detection electrode which is disposed on a surface of a toe of the person to be treated and detects a myoelectric signal of the toe, a display portion which determines whether the myoelectric signal of the toe is generated in response to the stimulation signal, and a myoelectric signal processing portion which processes the myoelectric signal detected by the detection electrode to display it visually on the display portion, in which the myoelectric signal processing portion does not detect the myoelectric signal of the toe during a predetermined detection stop period of time from output of the stimulation signal, and the detection stop period of time is set on the basis of a quotient (x/v) obtained when a distance (x) from a sacral bone of a human body to a surface of a toe is divided by a transmission velocity (v) of a nerve which passes through the sacral bone of the human body or the vicinity of the sacral bone.

Provided are devices and methods for preventing an episode of incontinence in an individual in need thereof. The devices comprise a sensor and a stimulator electrode that can be implanted into the body of the individual. Once the device is implanted in the individual, the sensor of the device senses a parameter that is associated with a response from the individual that is intended to prevent an episode of incontinence. Then, the device provides an electrical stimulation using the electrode that, together with the response, helps to prevent the episode of incontinence.

The disclosure provides for a systems and methods for monitoring uterine contractions of a uterus of a mammal by reconstructing three-dimensional images of uterine surface electrical activity based on a noninvasively obtained body-uterus geometry and a plurality of body surface electrical potential maps.

In part, the disclosure relates to a safety monitor and related methods to evaluate and manage intrapartum uterine contractions induced or augmented by Pitocin or other contraction inducing agents. The systems and methods include measuring a contraction parameter that may include one or more of frequency, strength, and duration of uterine contractions through a measurement device connected to a monitor. The systems and methods are programmed to stop the pump-based administration of a contraction inducing agent. Various lock out protocols and control over the ability to re-start a given pump are also described herein.

A sensor network for pregnancy monitoring of a subject includes a plurality of sensor systems time-synchronized to each other, each sensor system placed on a respective region of the subject and having a sensor member configured to detect data associated with at least one of physiological parameters of the subject, and a Bluetooth low energy system-on-a-chip configured to process and transmit the detected data; and a controller adapted in wireless communication with the plurality of sensor systems and configured to receive, from the plurality of sensor systems, to process, and to display the physiological parameters.

A sensor network for pregnancy monitoring of a subject includes a plurality of sensor systems time-synchronized to each other, each sensor system placed on a respective region of the subject and having a sensor member configured to detect data associated with at least one of physiological parameters of the subject, and a Bluetooth low energy system-on-a-chip configured to process and transmit the detected data; and a controller adapted in wireless communication with the plurality of sensor systems and configured to receive, from the plurality of sensor systems, to process, and to display the physiological parameters.

A pessary system for providing pelvic floor support for USL and other ligaments. The pessary has an elongated probe with independently inflatable balloons each located substantially the same distance from the insertion end of the probe and which inflate into separate radial sectors. The probe can be inserted into a vaginal cavity and the balloons inflated provide mechanical support to the USLs. Independent inflation of each balloon allows the mechanical USL support provided to be varied on left and right sides to compensate for differences in the degree of degradation and positioning of the USL ligaments on either side.

An example method includes delivering one or more electrical stimulation signals to a patient, sensing a composite stimulation-evoked signal comprising a composite of signals generated by one or more signal sources in response to the one or more electrical stimulation signals, and controlling delivery of electrical stimulation therapy to the patient based on the composite stimulation-evoked signal.

A pessary system for providing pelvic floor support for USL and other ligaments. The pessary has an elongated probe with independently inflatable balloons each located substantially the same distance from the insertion end of the probe and which inflate into separate radial sectors. The probe can be inserted into a vaginal cavity and the balloons inflated provide mechanical support to the USLs. Independent inflation of each balloon allows the mechanical USL support provided to be varied on left and right sides to compensate for differences in the degree of degradation and positioning of the USL ligaments on either side.