CPR compression device and method including a fluid filled bladder
Improved automatic chest compression systems which use constricting belts, repeatedly inflating bladders, or reciprocating pistons to compress the chest. A bladder is placed between the chest and the particular mechanism used to compress the chest during CPR. The bladder maximizes the effectiveness of chest compressions.
1. A system for performing CPR on a patient, said system comprising:
a chest compression means comprising a belt adapted to be disposed at least partially about the chest of the patient and a means for repetitively tightening the belt at a resuscitative rate, said means operably connected to the belt;
a bladder disposed between the chest compression means and the chest of the patient, and at least two dividers disposed within the bladder, such that the bladder is divided to form a left lateral section in fluid communication with a central section and a right lateral section in fluid communication with said central section, and wherein each section contains a pressure-transmitting medium, and the bladder is disposed relative to the belt during use between the belt and the chest of the patient and the central section is disposed over the sternum of the patient.
2. The system of claim 1 wherein the bladder is filled with an open-celled foam.
3. The system of claim 2 further comprising a defibrillator operably connected to the patient.
4. The system of claim 2 further comprising a means for measuring biological parameters operably connected to the patient.
5. The system of claim 2 wherein the bladder further comprises an aperture communicating from the interior of the bladder to the exterior of the bladder, and a valve controlling the aperture, wherein the valve is open when atmospheric pressure is about equal to the pressure inside the bladder and wherein the valve closes during a compression.
6. The system of claim 2 further comprising:
a defibrillator operably connected to the patient;
a means for measuring biological parameters operably connected to the patient;
an aperture in the bladder, and a valve controlling flow through the aperture, wherein the valve is open when atmospheric pressure is about equal to the pressure inside the bladder and wherein the valve closes during a compression.
7. The bladder of claim 1 wherein the bottom surface of the central section is made of an elastic material.
8. The bladder of claim 5 wherein the bottom surface of the central section is made of an elastic material.
9. The bladder of claim 6 wherein the bottom surface of the central section is made of an elastic material.
10. The bladder of claim 1 wherein the bottom surface of the central section is pleated.
11. The bladder of claim 10 wherein the bottom surface of the central section is comprised of an elastic material.
12. The device of claim 1 , wherein the bladder further comprises a first fluid pathway connecting the left lateral section and the central section and a second fluid pathway connecting the right lateral section and the central section.
13. A device for compressing the chest of a patient comprising:
a base adapted for placement over the central region of a patient's chest;
an actuator connected to a belt configured to wrap around the patient's chest;
a force converter mounted on the base and coupled to the actuator and the belt, said force converter operable to convert forces applied downwardly on the actuator into tangential forces applied to the belt; and
a fluid-filled bladder disposed between the base and the patient's chest, and at least two dividers disposed within the bladder, such that the bladder is divided to form a left lateral section in fluid communication with a central section and a right lateral section in fluid communication with said central section.
14. The device of claim 13 wherein the bladder comprises:
a right lateral section adapted to be disposed over the right side of the patient's chest, a center section adapted to be disposed over the center of the patient's chest, and a left lateral section adapted to be disposed over the left side of the patients chest, and the bladder having a first relaxed configuration which it assumes when the belt is loosened about the chest and a second pressurized configuration which it assumes when the belt is constricted about the chest of the patient;
wherein in said relaxed configuration the right lateral section, center section and left lateral section are each filled with fluid and in said pressurized configuration the right lateral section and left lateral section are substantially compressed and the fluid therein is forced into the center section.
15. The device of claim 13 , wherein the bladder further comprises:
a resilient foam substantially filling the bladder.
16. The device of claim 14 , wherein the bladder further comprises:
a resilient foam substantially filling the bladder.
17. The device of claim 13 , wherein the bladder spans substantially the entire breadth of the patient's chest.
18. The device of claim 13 , wherein the bladder spans substantially the entire breadth and height of the patient's chest.
19. The device of claim 13 , wherein the bladder is about 16 inches wide and 8 inches high, relative to the patient.
20. The device of claim 14 , wherein the bladder spans substantially the entire breadth of the patient's chest.
21. The device of claim 14 , wherein the bladder spans substantially the entire breadth and height of the patient's chest.
22. The device of claim 14 , wherein the bladder is about 16 inches wide and 8 inches high, relative to the patient.
23. A system for performing CPR on a patient, said system comprising:
a chest compression means comprising a belt adapted to be disposed at least partially about the chest of the patient and a means for repetitively tightening the belt at a resuscitative rate, said means operably connected to the belt;
a bladder disposed between the chest compression means and the chest of the patient, and at least two dividers disposed within the bladder, such that the bladder is divided to form a left lateral section in fluid communication with a central section and a right lateral section in fluid communication with said central section, and wherein each section contains a pressure-transmitting medium, and the bladder is disposed relative to the belt during use between the belt and the chest of the patient and the central section is disposed over the sternum of the patient;
wherein the pressure-transmitting medium comprises an open-celled foam;
wherein the bladder further comprises an aperture communicating from the interior of the bladder to the exterior of the bladder, and a valve controlling the aperture, wherein the valve is open when atmospheric pressure is about equal to the pressure inside the bladder and wherein the valve closes during a compression.
24. The system of claim 23 further comprising:
a defibrillator operably connected to the patient;
a means for measuring biological parameters operably connected to the patient.
25. The bladder of claim 23 wherein the bottom surface of the central section is made of an elastic material.
26. The bladder of claim 24 wherein the bottom surface of the central section is made of an elastic material.
27. The system of claim 23 wherein the bladder is filled with an open-celled foam.