System and methods for adaptive body positioning during chest compressions
A system for assisting cardio-pulmonary resuscitation (CPR) treatment of a patient includes a defibrillator system including a defibrillator communicatively coupled to a local computing device and configured to receive signals from treatment sensors, a patient support section, and a tilt adjuster coupled to the patient support section. The tilt adjuster is configured to communicatively couple with the defibrillator system, receive a control signal indicative of a target tilt angle from the local computing device, and automatically tilt the patient support section, around a transverse axis, to the target tilt angle in response to the control signal from the local computing device. The system also includes a chest compression device mount disposed on the patient support section and configured to adjustably secure a chest compression device to the patient support section.
1. A system for assisting cardiopulmonary resuscitation (CPR) treatment of a patient, the system comprising:
a defibrillator system comprising a defibrillator communicatively coupled to a local computing device and configured to receive signals from one or more treatment sensors;
at least one physiological sensor configured to detect physiological signals of the patient;
at least one patient support section, and
at least one tilt adjuster coupled to the at least one patient support section,
wherein the local computing device is configured to:
generate a first control signal indicative of a first target tilt angle prior to performing chest compressions for the patient,
during performance of the chest compressions for the patient, receive and process the physiological signals from the at least one physiological sensor,
analyze the received and processed physiological signals to determine a trend of at least one physiological parameter of the patient, and
generate a second control signal indicative of a second target tilt angle based, at least in part, on the determined trend, and
wherein the at least one tilt adjuster is configured to:
communicatively couple with the defibrillator system,
receive the first control signal indicative of the first target tilt angle from the local computing device,
automatically tilt the at least one patient support section, around a transverse axis, to the first target tilt angle in response to the first control signal from the local computing device,
during performance of the chest compressions for the patient, receive the second control signal indicative of the second target tilt angle from the local computing device, and
automatically tilt the at least one patient support section, around the transverse axis, to the second target tilt angle, which is different than the first tilt angle; and
a chest compression (CC) device mount disposed on the at least one patient support section and configured to adjustably secure a CC device to the at least one patient support section.
2. The system of claim 1 , wherein the signals received at the defibrillator system from the one or more treatment sensors are indicative of one or more of trans-thoracic impedance information, chest compression information, and defibrillation shock information.
3. The system of claim 2 , wherein the chest compression information comprises one or more of an elapsed time of CPR treatment, a number of delivered CPR compressions, a number of delivered CPR ventilations, a number of delivered defibrillation shocks, and an interval within a compression cycle.
4. The system of claim 1 , wherein the local computing device comprises at least one of a tablet computer, a watch, a smartphone, an addressable earpiece, or glasses.
5. The system of claim 1 , wherein the local computing device and the defibrillator are communicatively coupled via a bi-directional short range wireless communicative coupling comprising a Bluetooth coupling or a tap-to-connect coupling.
6. The system of claim 1 , comprising an automated position adjuster configured to automatically adjust a position of the CC device relative to the at least one patient support section in response to the first control signal from the local computing device.
7. The system of claim 1 , wherein the one or more treatment sensors comprise one or more of a timer, a motion sensor, a pressure sensor, and electrodes.
8. The system of claim 1 , wherein the at least one tilt adjuster is configured to automatically tilt the at least one patient support section at a rate of angle adjustment based on the first control signal from the local computing device.
9. The system of claim 1 , wherein the at least one patient support section comprises a head support section and a torso support section.
10. The system of claim 9 , wherein the at least one tilt adjuster is configured to automatically tilt the head support section relative to the torso support section in response to the first control signal from the local computing device.
11. The system of claim 10 , wherein the at least one tilt adjuster is configured to automatically tilt the head support section relative to the torso support section such that the head support section is elevated relative to the torso support section.
12. The system of claim 1 , wherein the CC device mount is configured to adjustably secure the CC device to the at least one patient support section such that the CC device remains aligned with a preferred location on a sternum of the patient during tilting of the at least one patient support section by the at least one tilt adjuster.
13. The system of claim 1 , wherein the CC device comprises a piston-based CC device that includes a suction cup with compression pad.
14. The system of claim 1 , wherein the CC device mount is configured to couple to a complementary mounting structure of the CC device.
15. The system of claim 1 , wherein the CC device mount is configured to secure the CC device without coupling to a complementary mounting structure on the CC device.
16. The system of claim 1 comprising one or more indicators of a position of an anatomical reference point of the patient relative to the at least one patient support section,
wherein the one or more indicators comprise one or more of a bump, a protrusion, a marking, a divot, and a lighted indication.
17. The system of claim 1 , comprising one or more tilt angle indicators coupled to an alarm configured to emit an alarm signal if a current tilt angle differs from the target tilt angle.
18. The system of claim 1 , wherein the at least one patient support section comprises two or more patient support sections, and comprising a spacer pivotally coupled to the two or more patient support sections and configured to elevate one of the two or more patient support sections relative to another of the two or more patient support sections.
19. The system of claim 1 , wherein the signals received at the defibrillator system from the one or more treatment sensors are indicative of CPR data associated with one or more of a CPR performance of a care provider and a response of the patient to CPR.
20. The system of claim 19 , wherein the defibrillator system is configured to provide the CPR data for review of and feedback on the CPR performance of the care provider.
21. The system of claim 1 , wherein the at least one tilt adjuster is configured to automatically tilt the at least one patient support section to the first target tilt angle during a predetermined first time interval, and, after the first time interval, automatically tilt the at least one patient support section to the second target tilt angle during a predetermined second time interval.
22. The system of claim 1 , wherein the local computing device is configured to generate the second control signal based, at least in part, on the signals from the one or more treatment sensors.
23. The system of claim 1 , wherein the first target tilt angle and the second target tilt angle are inclined relative to a horizontal axis.
24. The system of claim 1 , wherein the first target tilt angle is inclined 10 degrees to 20 degrees relative to a horizontal axis, and the second target tilt angle is inclined 20 degrees to 30 degrees relative to the horizontal axis.
25. The system of claim 1 , wherein the physiological signals comprise at least one of the following signals: electrocardiogram (ECG), invasive blood pressure, non-invasive blood pressure, pulse oximetry, capnography, impedance cardiography, impedance pneumography, heart sounds, or lung sounds.
26. The system of claim 1 , wherein the determined trend comprises a decrease of cerebral oxygenation, cardiac output, and/or blood flow over a predetermined period of time comprising multiple compression cycles.
27. The system of claim 26 , wherein the second target tilt angle increases an elevation of the patient's head relative to the patient's heart compared to the first target tilt angle.
28. The system of claim 26 , wherein a difference between the first target tilt angle and the second target tilt angle is proportional to the decrease of cerebral oxygenation, cardiac output, and/or blood flow.
29. The system of claim 1 , wherein the physiological signals comprise an electrocardiogram (ECG) signals, and the trend comprises frequency of detected or estimated medical premonitory events.
30. The system of claim 1 , further comprising a user interface comprising a tilt selection button, and wherein the at least one tilt adjuster is configured to tilt the at least one patient support section to a preset third tilt angle, which is above a horizontal axis and different from the first target tilt angle and the second target tilt angle, in response to at least one indication of a button press of the tilt selection button received by the user interface.
31. The system of claim 1 , wherein the local computing device controller is configured to generate the second control signal indicative of the second target tilt angle when the determined trend indicates that a change in a physiological phase of the patient has occurred.
32. The system of claim 31 , wherein the change in physiological phase of the patient comprises occurrence of a return of spontaneous circulation (ROSC), an identified cardiac event, an identified respiratory event, or a change from one of an electrical phase, a metabolic phase, or a circulatory phase of the patient to another of the electrical phase, the metabolic phase, or the circulatory phase of the patient.
33. The system of claim 1 , wherein the local computing device controller is configured to generate the second control signal indicative of the second target tilt angle when the determined trend indicates that the patient has achieved a return of spontaneous circulation (ROSC).