AU2014200720A1

AU2014200720A1 - Improved venous augmentation system

Info

Publication number: AU2014200720A1
Application number: AU2014200720A
Authority: AU
Inventors: Malcolm G. Bock
Original assignee: Covidien LP
Current assignee: KPR US LLC
Priority date: 2010-03-09
Filing date: 2014-02-11
Publication date: 2014-03-06
Anticipated expiration: 2031-03-04
Also published as: AU2014200720B2

Abstract

IMPROVED VENOUS AUGMENTATION SYSTEM Abstract A compression device (10) comprising a sleeve (12) positionable around a limb of a person. The sleeve comprising at least one inflatable bladder; a valve operable to control pressure of air in the at least one inflatable bladder; a pressure sensor disposed to determine the fluid pressure in the inflatable bladder; and a controller (15) in electrical communication with the valve and the pressure sensor. The controller comprising computer-executable instructions and a processor configured to execute the computer-executable instructions, the computer executable instructions comprising instructions for: (a) determining, by sensing pressure in the at least one inflatable bladder, elapsed amounts of time for venous blood flow in the limb to return to a steady state after reducing pressure in the at least one inflatable bladder from respective various different compression pressures to a refill pressure; (b) adjusting the compression pressure based at least in part on a measured relationship between the various different compression pressures and the corresponding elapsed times; and (c) applying compression therapy to the limb with the sleeve including repeatedly pressurizing the inflatable bladder to the adjusted compression pressure and reducing pressure in said at least one pressurizable chamber to allow venous refill.

Description

1 IMPROVED VENOUS AUGMENTATION SYSTEM Field [0001] The present invention generally relates to compression sleeves, and more particularly, compression sleeves for optimizing vascular refill. [0002] The pooling of blood or stasis in a patient's extremities, particularly the legs, occurs when the patient is confined to bed for an extended period of time. Stasis is problematic because it is a significant cause leading to the formation of thrombi. To prevent this occurrence, it is desirable to move fluid out of interstitial spaces in the extremity tissues to enhance circulation. [0003] Intermittent pneumatic compression (PC) devices are used to improve circulation and minimize the formation of thrombi in the limbs of patients. An example of one such IPC device is disclosed in U.S. Patent No. 6,231,53. These devices typically include a compression sleeve or garment having one or more inflatable chambers configured to provide a compressive pulse to the limb. The chamber or chambers are maintained in the inflated state for a predetermined period of time and then deflated. After another predetermined time the chamber or chambers are re-inflated. This vascular refill process increases blood circulation and minimizes the formation of thrombi. During this process the pressure in the chamber or chambers can be monitored to adjust the vascular refill time in response to changing conditions of the patient. [0004] Currently IPC devices are operated using a single predetermined chamber inflation pressure. However, due to the variability in patient's extremities, these devices have inherent shortcomings. Accordingly, there is a need for an IPC device capable of obtaining a more optimum vascular refill for a variety of limb shapes and sizes.

2 Object of Invention [0005] It is an object of the present invention to substantially overcome or at least ameliorate one or more of the disadvantages of the prior art, or to at least provide a useful alternative. Summary of Invention [0006] There is disclosed herein a compression device comprising: a sleeve positionable around a limb of a person, the sleeve comprising at least one inflatable bladder; a valve operable to control pressure of air in the at least one inflatable bladder; a pressure sensor disposed to determine the fluid pressure in the inflatable bladder; and a controller in electrical communication with the valve and the pressure sensor, the controller comprising computer-executable instructions and a processor configured to execute the computer-executable instructions, the computer-executable instructions comprising instructions for: (a) determining, by sensing pressure in the at least one inflatable bladder, elapsed amounts of time for venous blood flow in the limb to return to a steady state after reducing pressure in the at least one inflatable bladder from respective various different compression pressures to a refill pressure; (b) adjusting the compression pressure based at least in part on a measured relationship between the various different compression pressures and the corresponding elapsed times; and (c) applying compression therapy to the limb with the sleeve including repeatedly pressurizing the inflatable bladder to the adjusted compression pressure and reducing pressure in said at least one pressurizable chamber to allow venous refill. [0007] Preferably, the sleeve includes a plurality of inflatable bladders, the controller further includes computer executable instructions to sequentially inflate the plurality of inflatable bladders to apply sequential compression therapy to the limb using the customized pressure. [0008] Preferably, the controller includes computer executable instructions to determine a new customized pressure at a predetermined time.

3 [0009] Preferably, the controller further includes computer executable instructions to adjust the compression pressure to between 20 mm Hg to 70 mm Hg. [0010] Preferably, the controller further includes computer executable instructions to record multiple elapsed times for each compression pressure and average the recorded multiple elapsed times at each compression pressure. [0011] Preferably, the controller further includes computer executable instructions to adjust the compression pressure based at least in part on a measured relationship between the various different compression pressures and the corresponding averaged elapsed times. [0012] Preferably, the controller further includes computer executable instructions to plot the elapsed times for the corresponding compression pressures. [0013] Preferably, the controller further includes computer executable instructions to fit a best fit line to the relationship between the elapsed times and the corresponding compression pressures. [0014] Preferably, the controller further includes computer executable instructions to adjust the compression pressure to correspond to the maximum of the best fit line. [0015] Preferably, the controller further includes computer executable instructions to record the elapsed times during compression therapy, average the recorded elapsed times, and adjust the time between consecutive pressurizations of the at least one inflatable bladder based on the averaged elapsed times. Brief Description of Drawings [0016] A preferred embodiment of the invention will now be described, by way of example only, with reference to the accompanying drawings, wherein: [0017] Fig. 1 is a pneumatic circuit implemented with a single-chambered sleeve of the present invention; 4 [0018] Fig. 2 is a graph illustrating a prior art pressure profile during a procedure to determine venous refill time; [0019] Fig. 3 is a graph illustrating a prior art compression cycle after determining venous refill time; [0020] Figs. 4A-4E are graphs illustrating a pressure profile during a procedure to determine venous refill time according to the present invention; [0021] Fig. 5 is a graph illustrating a customized venous refill determination based on the pressure profiles in Figs. 4A-4E; and [0022] Fig. 6 is a perspective of a controller and compression sleeve of the present invention. [0023] Corresponding reference characters indicate corresponding parts throughout the drawings. Description of Embodiments [0024] With reference to the figures, Fig. 1 in particular illustrates a pneumatic circuit in association with an intermittent pneumatic compression (IPC) device 10 to determine venous refill time according to the present invention. In the IPC device 10, a compression sleeve 12 having a single chamber 13 is connected, for example, via tubing 14, to a controller 15 having a processor 17 operatively connected to an air supply 16 (e.g., a compressor) which provides compressed air to the chamber of the sleeve. A two-way normally open valve 18 and a three way normally closed valve 19 are provided between the sleeve 12 and the air supply 16. A pressure transducer 20 downstream of the valve 18 monitors the pressure in the chamber. The sleeve 12 can have two or more chambers without departing from the scope of the invention. For example, the sleeve 12 shown in Fig. 6 has three chambers 13. [0025] The sleeve 12 is configured to be wrapped around a patient's extremity (e.g., leg) (Fig. 6). To provide a compressive pulse to the leg, the valve 19 is opened and the air supply 16 is activated to provide compressed air to the chamber 13 until the pressure in the chamber reaches a suitable value for operation in a compression cycle, as is known in the art. Upon completion of the pressurization, the air supply 16 is deactivated and the chamber 13 is allowed to depressurize 5 by, for example, venting back through the tubing to the controller. Air may be vented to the atmosphere through the three-way valve 19. [0026] In prior art designs, when it is desired to determine the venous refill time for the patient, the chamber is permitted to depressurize until the pressure in that chamber reaches a lower value, typically 10 mm Hg (after approximately 2.5 seconds of depressurization). Alternatively, the chamber could be permitted to depressurize for a predetermined period of time. The two way valve 18 is then closed to prevent further depressurization of the chamber. Alternatively, the chamber could be allowed to depressurize fully and could then be repressurized only until the pressure reaches the predetermined value, for example, 10 mm Hg. The pressure in the chamber is then sensed by the pressure transducer 20 for a time sufficient to allow the venous system in the leg to refill. The pressure rises as the leg gets larger, filling with blood. The pressure plateaus when the leg has refilled and returned to a steady state, indicated by the solid curve 1 in Fig. 2. The time between the start of depressurizing the pressurizable chamber and when this plateau occurs is determined to be the venous refill time and is taken by the controller 15 as the basis for the depressurization time for subsequent cycles. Based on this venous refill procedure, a compression cycle is performed at about 45 mm Hg with a depressurization time of about 20 seconds (Fig. 3). [0027] Referring to Figs. 4A-4E, in the present invention, the processor 17 is configured to execute computer-executable instruction to pressurize the chamber 13 to determine a customized venous refill time for the chamber. The computer-executable instructions for determining the venous refill time comprise pressurizing the chamber 13 to a first compression pressure (e.g., 20 mm Hg) to move the blood in the leg from a region (e.g., calf) underlying the chamber. After pressurizing the chamber 13 to the first compression pressure, the pressure in the chamber is reduced to a refill pressure (e.g., 10 mm Hg) to allow the blood to re-enter the region of the limb underlying the chamber. The pressure in the chamber 13 is then sensed by the pressure transducer 20 until it is determined that blood flow has been completely restored to the region of the limb underlying the chamber. The time elapsed to restore blood flow is characterized as a first venous refill time tl and is stored by the controller 15. The chamber 13 is then pressurized to a second compression pressure (e.g., 30 mm Hg) and the same process is performed as was performed for the first compression pressure, resulting in a second venous refill time t2. The chamber 13 can then be pressurized to even more compression pressures (e.g., 45, 60 and 75 mm Hg) and the process performed for the first and second compression pressures can be 6 repeated for each pressure level to produce venous refill times t3, t4, t5, tn for each additional pressure level. It is understood that pressure amounts other than those described above and shown in Figs. 4A-4E can be used in the venous refill process without departing from the scope of the invention. Additionally, the venous refill process at each pressure level can be performed multiple times to produce multiple venous refill times for each pressure level. [0028] Using the determined venous refill times tl-tn, the processor 17 determines a customized compression pressure by plotting the venous refill times for each selected pressure level on a graph as shown in Fig. 5 and fitting a best fit line to the plot using standard linear regression analysis. The apex A of the best fit line corresponds to a customized compression pressure Pc for producing a maximum venous refill time Tmax. The determined compression level Pc and refill time Tmax are then incorporated into the compression therapy of the limb wherein the chamber 13 in the sleeve 12 is repeatedly pressurized to the customized compression pressure Pc, maintained at the customized compression pressure for a period of time and subsequently reduced to the refill pressure for the determined maximum refill time Tmax to facilitate blood circulation in the limb. In the instance where multiple venous refill times are recorded for each selected compression pressure level, the refill times are averaged by the processor 17 to produce an average value for the given pressure level. These average values are then plotted and a best fit line is fit to the plot of the average values and the customized compression pressure and maximum venous refill time are extrapolated from the plot in the same manner as described above. If the sleeve 13 includes multiple chambers (e.g., ankle, calf and thigh bladders as shown in Fig. 6), the controller 15 can be configured to operate the IPC device 10 to apply sequential compression therapy to the limb using the customized pressure and maximum refill time. [0029] After applying compression therapy to the limb for a period of time the process for determining the customized compression pressure and maximum venous refill time can be repeated to determine new values. Additionally or alternatively, memory in the controller 15 can record the venous refill times sensed by the pressure transducer 20 during the compression therapy and average the recorded values to adjust the time between consecutive pressurizations of the chamber 13 based on the averaged refill times. These two processes ensure that the compression therapy being delivered to the limb adapts to the changing characteristics of the limb so that a customized compression therapy is delivered to the limb through the duration of the compression therapy.

7 [0030] Referring to Fig. 6, the controller 15 is located in a housing 22. A control or front panel 24 on the housing 22 includes controls and indicators for operation. An output connector 26 is disposed on the housing 22 and is adapted to receive the tubing 14 for connecting the controller 15 and air supply 16 to the sleeve 13. Figure 6 shows an embodiment of the IPC device 10 wherein the sleeve 12 includes three chambers 13. [0031] Having described the invention in detail, it will be apparent that modifications and variations are possible without departing from the scope of the invention defined herein. [0032] When introducing elements of the present invention or the preferred embodiments(s) thereof, the articles "a", "an", "the" and "said" are intended to mean that there are one or more of the elements. The terms "comprising", "including" and "having" are intended to be inclusive and mean that there may be additional elements other than the listed elements. [0033] In view of the above, it will be seen that the several objects of the invention are achieved and other advantageous results attained. [0034] As various changes could be made in the above constructions and methods without departing from the scope of the invention, it is intended that all matter contained in the above description and shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense.

Claims

1. A compression device comprising: a sleeve positionable around a limb of a person, the sleeve comprising at least one inflatable bladder; a valve operable to control pressure of air in the at least one inflatable bladder; a pressure sensor disposed to determine the fluid pressure in the inflatable bladder; and a controller in electrical communication with the valve and the pressure sensor, the controller comprising computer-executable instructions and a processor configured to execute the computer-executable instructions, the computer-executable instructions comprising instructions for: (a) determining, by sensing pressure in the at least one inflatable bladder, elapsed amounts of time for venous blood flow in the limb to return to a steady state after reducing pressure in the at least one inflatable bladder from respective various different compression pressures to a refill pressure; (b) adjusting the compression pressure based at least in part on a measured relationship between the various different compression pressures and the corresponding elapsed times; and (c) applying compression therapy to the limb with the sleeve including repeatedly pressurizing the inflatable bladder to the adjusted compression pressure and reducing pressure in said at least one pressurizable chamber to allow venous refill.

2. The compression device of claim 1, wherein the sleeve includes a plurality of inflatable bladders, the controller further includes computer executable instructions to sequentially inflate the plurality of inflatable bladders to apply sequential compression therapy to the limb using the customized pressure.

3. The compression device of claim 1, wherein the controller includes computer executable instructions to determine a new customized pressure at a predetermined time.

4. The compression device of claim 1, wherein the controller further includes computer executable instructions to adjust the compression pressure to between 20 mm Hg to 70 mm Hg. 9

5. The compression device of claim 1, wherein the controller further includes computer executable instructions to record multiple elapsed times for each compression pressure and average the recorded multiple elapsed times at each compression pressure.

6. The compression device of claim 5, wherein the controller further includes computer executable instructions to adjust the compression pressure based at least in part on a measured relationship between the various different compression pressures and the corresponding averaged elapsed times.

7. The compression device of claim 1, wherein the controller further includes computer executable instructions to plot the elapsed times for the corresponding compression pressures.

8. The compression device of claim 1, wherein the controller further includes computer executable instructions to fit a best fit line to the relationship between the elapsed times and the corresponding compression pressures.

9. The compression device of claim 8, wherein the controller further includes computer executable instructions to adjust the compression pressure to correspond to the maximum of the best fit line.

10. The compression device of claim 1, wherein the controller further includes computer executable instructions to record the elapsed times during compression therapy, average the recorded elapsed times, and adjust the time between consecutive pressurizations of the at least one inflatable bladder based on the averaged elapsed times. Covidien LP Patent Attorneys for the Applicant/Nominated Person SPRUSON & FERGUSON