SUB-ATMOSPHERIC PRESSURE CHAMBER FOR MECHANICAL ASSISTANCE OF BLOOD FLOW

• US 20090312675A1
• Filed: 07/19/2007
• Published: 12/17/2009
• Est. Priority Date: 07/19/2006
• Status: Abandoned Application

• Current Assignee: Brigham and Women's Hospital Incorporated
• Original Assignee: Brigham and Women's Hospital Incorporated
• Inventors: Chedid, Loutfallah Georges, Ysasi, Adam, Serra, Lorenzo, Scully, Christopher, Zomar, Dennis, Sampson, Christian E.
• Application Number:
  US12/374,442
• Publication Number:
  US 20090312675A1
• Time in Patent Office: Days
• US Class Current: 601/10
• CPC Class Codes: A61H 2201/5007 computer controlled
• CPC Class Codes: A61H 2205/06 Arms
• CPC Class Codes: A61H 2230/06 Heartbeat rate
• CPC Class Codes: A61H 9/005 Pneumatic massage
• CPC Class Codes: A61H 9/0057 Suction suction kneading A61H7/008

Abstract

A sub-atmospheric pressure treatment device may include a chamber, a vacuum source, a pulse sensor, and a controller.

Claims

1. A subatmospheric pressure treatment device comprising:

a chamber sized to receive an extremity of a subject, the chamber comprising;

a housing having an interior space and being so formed from one or more materials and so sized and shaped as to hold up to a subatmospheric pressure in the interior space of the chamber of at least 25 mmHg below an ambient pressure outside the chamber, the interior space being so sized and shaped as to receive the extremity of the subject;

an inlet communicating with the interior space of the chamber, the inlet so sized and shaped as to pass the extremity of the subject;

a flange attached to the chamber housing and defining the inlet, the flange comprising;

at least two supporting rings affixed to one another by at least one strut; and

a sleeve of material having two ends, each end mounted to a respective one of the supporting rings, the sleeve being;

so pliable as to;

 

form an air-tight seal around the extremity of the subject when the interior space of the chamber is at the subatmospheric pressure; and

 

exert essentially no pressure on the extremity of the patient when the interior space of the chamber is at the ambient pressure outside the chamber; and

so rigid as to resist involution into the interior space of the chamber when the interior space of the chamber is at the subatmospheric pressure;

a vacuum source communicating with the chamber, the vacuum source having sufficient capacity to produce the subatmospheric pressure in the interior space of the chamber;

a pulse sensor configured to produce a signal indicative of a pulse waveform representative of the subject'"'"'s pulse; and

a controller coupled to the vacuum source and to the pulse sensor and so configured as to command the vacuum source, in response to the signal indicative of the pulse waveform, to achieve the subatmospheric pressure in the interior space of the chamber.

2. The device of claim 1, further comprising a pressure gauge in communication with the interior space of the chamber to measure pressure in the interior space.

3. The device of claim 1, further comprising a data acquisition system so coupled to the pulse sensor as to receive one or more signals indicative of at least one of the subject'"'"'s pulse rate, pulse occurrences, and an oxygenation state of the subject'"'"'s blood.

4. The device of claim 1, wherein the sleeve material comprises neoprene.

5. The device of claim 1, wherein the vacuum source has sufficient capacity to lower the interior space pressure from the ambient pressure to the subatmospheric pressure in at most 0.1 seconds.

6. The device of claim 1, wherein the controller is so configured as to command the vacuum source to achieve the subatmospheric pressure in the interior space of the chamber in synchrony with a systolic portion of the subject'"'"'s pulse as sensed by the pulse sensor.

7. The device of claim 6, wherein the controller is so configured as to command the vacuum source to achieve the subatmospheric pressure in the interior space of the chamber with each pulse.

8. The device of claim 6, wherein the controller is so configured as to command the vacuum source to achieve the subatmospheric pressure in the interior space of the chamber with every other pulse.

9. The device of claim 6, wherein the controller is so configured as to command the vacuum source to restore the interior space of the chamber to ambient pressure in between each command to achieve the subatmospheric pressure.

10. The device of claim 9, wherein the controller is so configured as to command the vacuum source to restore the interior space of the chamber to ambient pressure at about the start of a diastolic portion of the subject'"'"'s pulse as sensed by the pulse sensor.

11. The device of claim 6, wherein the controller is so configured as to command the vacuum source to achieve the subatmospheric pressure in the interior space of the chamber over the course of two or more pulses and then to restore the interior space of the chamber to ambient pressure for two or more pulses.

12. The device of claim 6, wherein the controller is so configured as to command the vacuum source to achieve the subatmospheric pressure in the interior space of the chamber at about the start of the systolic portion of the subject'"'"'s pulse as sensed by the pulse sensor.

13. The device of claim 1, wherein the subatmospheric pressure is at least 75 mm Hg below the ambient pressure.

14. The device of claim 1, wherein the subatmospheric pressure is at least 100 mm Hg below the ambient pressure.

15. The device of claim 1, wherein the pulse sensor comprises a pulse oximeter.

17. A method of increasing blood flow in a subject'"'"'s extremity using the device of claim 1, the method comprising:

affixing a pulse sensor to the extremity;

passing the subject'"'"'s extremity through the inlet and into the interior space of the chamber;

sensing the subject'"'"'s pulse; and

causing the controller to command the vacuum source to alternately achieve the ambient pressure and the subatmospheric pressure in the interior space of the chamber in response to the sensed pulse.

18. The method of claim 17, wherein the subject'"'"'s pulse is detected when the extremity is in a low-perfusion state.

19. The method of claim 17, wherein the subatmospheric pressure is at least 100 mm Hg below the ambient pressure.

16. A subatmospheric pressure treatment device comprising:

a chamber sized to receive an extremity of a subject, the chamber comprising;

a housing having an interior space and being so formed from one or more materials and so sized and shaped as to hold up to a subatmospheric pressure in the interior space of the chamber of at least 25 mmHg below an ambient pressure outside the chamber, the interior space being so sized and shaped as to receive the extremity of the subject;

an inlet communicating with the interior space of the chamber, the inlet so sized and shaped as to pass the extremity of the subject and to seal around the subject when the interior space of the chamber is at the subatmospheric pressure;

a vacuum source communicating with the chamber, the vacuum source having sufficient capacity to produce a pressure in the interior space of the chamber that is at least 25 mmHg below the ambient pressure outside the chamber;

a pulse sensor configured to produce a signal indicative of a pulse waveform representative of the subject'"'"'s pulse; and

a microcontroller coupled to the vacuum source and to the pulse sensor and so programmed as to command the vacuum source, in response to the signal indicative of the pulse waveform, to achieve a pressure in the interior space of the chamber that is at least 25 mmHg below the ambient pressure outside the chamber.

20. (canceled)