Systems and methods for detecting and characterizing pain
Various systems are disclosed herein for detecting, monitoring, evaluating, and characterizing pain. They systems include a number of connected components, such as a provider device, a body-mapping system, a patient device, a user device, a referred pain device and/or a rectal probe device. Accordingly, the systems allow providers to track location-specific pain intensity for any number of patients over time in order to generate reports and determine treatment recommendations for such patients.
1. A system comprising:
a body-mapping system adapted to determine location information relating to a location on a body of a patient to which a force is applied;
a patient device operated by the patient, the patient device adapted to determine feedback information relating to an intensity of pain experienced by the patient due to the applied force;
the patient device comprising a referred pain device adapted to be used by the patient to indicate referred pain information relating to one or more additional locations on the patient's body where the patient experiences pain due to the applied force;
the body-mapping device further adapted to detect the referred pain information; and
a server in communication with the body-mapping system and the patient device via a network, the server adapted to:
receive the location information from the body-mapping system;
receive the feedback information from the patient device;
receive the referred pain information from the body-mapping device;
store, in a memory, pain information comprising the location information, the feedback information, and the referred pain information; and
generate a report comprising a graphical representation of the pain information.
2. A system according to claim 1 , wherein the location information comprises one or more of the group consisting of: a direction of the applied force, an area over which the force is applied to the location and a depth within the location to which the force is applied.
3. A system according to claim 1 , wherein the body-mapping device comprises:
one or more emitters adapted to project a pattern of spots onto the patient's body;
one or more sensors adapted to capture an image of the projected pattern; and
a processor adapted to:
receive the image; and
determine the location information based on the image.
4. A system according to claim 1 , wherein the body-mapping device comprises one or more sensors adapted to determine the location information, the one or more location sensors selected from the group consisting of: WIFI sensors, cellular network sensors, Bluetooth sensors, and NFC sensors.
5. A system according to claim 1 , wherein:
the body-mapping device is further adapted to determine position information relating to a position of the patient when the force is applied;
the server is further adapted to receive the position information from the body-mapping system; and
the pain information further comprises the position information.
6. A system according to claim 1 , wherein the report comprises a two-dimensional (“2D”) or three-dimensional (“3D”) body map.
7. A system according to claim 1 , wherein the server is further adapted to determine a treatment recommendation for the patient based on the pain information, the treatment recommendation relating to one or more of the group consisting of: a medication, an exercise, a stretch, a diet and sleep.
8. A system according to claim 1 , wherein the patient device comprises an actuator adapted to be actuated by the patient to indicate the intensity of the pain experienced by the patient.
9. A system according to claim 1 , further comprising:
a provider device in communication with the server via the network, the provider device adapted to apply the force to the location and to measure pressure information relating thereto, wherein the server is further adapted to receive the pressure information from the provider device, and wherein the pain information further comprises the pressure information.
10. A system according to claim 9 , wherein the pressure information comprises one or more of a magnitude of the applied force, a start time of the applied force and an end time of the applied force.
11. A system according to claim 9 , wherein the provider device further comprises an output adapted to display an indication relating to the pressure information.
12. A system according to claim 1 , further comprising a user device in communication with the server via the network, wherein:
the user device is adapted to receive patient information relating to the patient, the patient information comprising one or more of: identification information, consent information, billing information, insurance information, medical information and historical pain information; and
the server is further adapted to:
receive the patient information from the user device; and
store the patient information in the memory.
13. A system according to claim 12 , wherein:
the user device is further adapted to receive a pain measurement session plan comprising one or more of: a target pressure, a target location and a target duration; and
the server is further adapted to:
receive the pain measurement session plan; and
store the pain measurement session plan in the memory; and
transmit a notification to the provider device and/or the user device, based on a comparison of the pain information to the pain measurement session plan.
14. A system comprising:
a body-mapping system adapted to determine location information relating to a location on a body of a patient to which a force is applied;
a patient device operated by the patient, the patient device adapted to determine feedback information relating to an intensity of pain experienced by the patient due to the applied force;
a server in communication with the body-mapping system and the patient device via a network;
a rectal probe device in communication with the server via the network, the rectal probe device adapted to be inserted into a rectum of the patient to determine sphincter muscle tone information;
the server adapted to:
receive the location information from the body-mapping system;
receive the feedback information from the patient device;
receive the sphincter muscle tone information;
store, in a memory, pain information comprising the location information, the feedback information, and the sphincter muscle tone information; and
generate a report comprising a graphical representation of the pain information.
15. A system according to claim 14 , wherein the location information comprises one or more of the group consisting of: a direction of the applied force, an area over which the force is applied to the location and a depth within the location to which the force is applied.
16. A system according to claim 14 , wherein the body-mapping device comprises one or more sensors adapted to determine the location information, the one or more location sensors selected from the group consisting of: WIFI sensors, cellular network sensors, Bluetooth sensors, and NFC sensors.
17. A system according to claim 14 , wherein the report comprises a two-dimensional (“2D”) or three-dimensional (“3D”) body map.
18. A system according to claim 14 , wherein the server is further adapted to determine a treatment recommendation for the patient based on the pain information, the treatment recommendation relating to one or more of the group consisting of: a medication, an exercise, a stretch, a diet and sleep.
19. A system according to claim 14 , wherein the patient device comprises a referred pain device adapted to be used by the patient to indicate referred pain information relating to one or more additional locations on the patient's body where the patient experiences pain due to the applied force, wherein:
the body-mapping device is further adapted to detect the referred pain information; the server is further adapted to receive the referred pain information form the body-mapping device; and
the pain information further comprises the referred pain information.
20. A system according to claim 14 , wherein the rectal probe device comprises an inflatable balloon to allow for a diameter of the rectal probe device to be increased and decreased.