The present invention relates to the field of medical devices and, more particularly, to methods and apparatus for providing rapid compression therapy treatments to at least one appendage, e.g., an arm or a leg, of a body.
Compression therapy systems are used in several medical applications to apply rapid compressions to one or more appendages (e.g., arms, hands, legs, and feet) of a body. For example, compressions therapy systems are used to treat chronic wounds by applying pressure to an appendage having wounds to improve circulation around the wounds, or to improve blood circulation to treat angina or congestive heart failure (CHF), e.g., as in enhanced external counterpulsation (EECP) devices.
In a conventional compression therapy system, a large compressor compresses air for storage in a storage tank. Moderate amounts of air from the storage tank are then delivered to an inflatable sleeve containing an affected appendage in rapid low pressure bursts to apply compression to the appendage. After each burst of air fills the inflatable sleeve, the inflatable sleeve is opened to release the air and, thus, remove the compression from the appendage. The compressor and storage tanks needed in such systems are loud, bulky, and expensive, making them unsuitable for use in the home. In addition, because of the volume of air required for conventional compression therapies, these systems are generally unable to treat more than one appendage at a time using power from ordinary household outlets (e.g., 1500 watts or less at 120 volts AC).
There is an ever present desire for more convenient and economical medical equipment. Accordingly, rapid compression apparatus and methods are needed that are not subject to the above limitations. The present invention addresses this need among others.
The present invention is embodied in methods and apparatus for providing rapid compression to at least one appendage positioned within an inflatable sleeve. Rapid compression is provided by filling the inflatable sleeve containing the appendage with a gas. A portion of the gas is then repeatedly withdrawn and inserted back into the inflatable sleeve to apply a compression therapy to the at least one appendage.
The invention is best understood from the following detailed description when read in connection with the accompanying drawings, with like elements having the same reference numerals. When a plurality of similar elements are present, a single reference numeral may be assigned to the plurality of similar elements with a small letter designation referring to specific elements. When referring to the elements collectively or to a non-specific one or more of the elements, the small letter designation may be dropped. This emphasizes that according to common practice, the various features of the drawings are not drawn to scale. On the contrary, the dimensions of the various features are arbitrarily expanded or reduced for clarity. Included in the drawings are the following figures:
The present invention is now described in greater detail.
In an exemplary embodiment, the inner layer 200 has a single inflatable section 206 with an opening 208 for coupling to the rapid compression device 102 (
The sleeve 104a may have an optional zipper 210 to minimize application and removal time of the sleeve on the arm. In addition, the sleeve 104a may have one or more optional valves (represented by valve 212) to release excess pressure and to deflate the sleeve 104a for removal from the appendage and for storage. Inflatable leg sleeve 104b is similar to inflatable leg sleeve 104a, except in shape, with similar element being identically numbered, and will not be described in further detail.
Referring back to
A piston driver 112 is coupled to the piston 108 to move the piston 108 back and forth within the cylinder 106 to alter the volume of a pressure cavity 114 within the cylinder 106 defined by the second end 106b of the cylinder 106 and the piston 108. In the illustrated embodiment, the piston driver 112 is coupled to a controller 134 (described below), which controls the piston driver 112 to move/position the piston 108 within the cylinder 106. In an exemplary embodiment, the piston driver 112 is configured to operate using power available from a conventional household outlet, e.g., 1500 watts or less at approximately 120V AC. In an alternative exemplary embodiment, other power sources may be used. A suitable piston driver for use with the present invention will be understood by one of skill in the art from the description herein.
The pressure cavity 114 is coupled directly to the inflatable sleeve 104 such that altering the volume of the pressure cavity 114 alters the pressure of the gas in the volume defined by the inflatable sleeve 104. In an exemplary embodiment, the valve 208 of the inflatable sleeve 104 is coupled to the pressure cavity 114 of the cylinder 106 via a gas transport connector 116 such as a flexible tube or other suitable means for transporting gas between the sleeve 104 and the rapid compression device 102. The gas transport connector 16 may have a diameter that permits the pressure of gas within the cavity 114 of the rapid compression device 102 and the pressure of gas with the inflatable sleeve 104 to equalize rapidly (e.g., within about 50–100 milliseconds). In an exemplary embodiment, the gas transport connector 116 is a flexible tube having a diameter of about at least two inches.
When the piston 108 is inserted into the cylinder 106 (i.e., moved toward the second end 106b), the volume of air within the cavity 114 goes down, thereby increasing the pressure in the cavity 114 and in the inflatable sleeve 104 coupled to the cylinder 106 due to a decrease in the combined volume of the cavity 114 and the inflatable sleeve 104. When the piston 108 is extracted from the cylinder 106 (i.e., moved toward the first end 106a), the volume of air within the cylinder 106 goes up, thereby decreasing the pressure in the cavity 114 and in the inflatable sleeve 104 coupled to the cylinder 106 due to the restored combined volume of the cavity 114 and the inflatable sleeve 104.
The illustrated rapid compression device 102 further includes a rear position sensor 118, a front position sensor 120, and a pressure sensor 122. In an exemplary embodiment, the rear position sensor 118 defines the maximum extraction point for the piston 108, the front position sensor 120 defines the maximum insertion point for the piston 108, and the distance between the sensors 118 and 120 defines a maximum stroke length for the piston 108 within the cylinder 106. The pressure sensor 122 senses the pressure in the cavity 114. Suitable position and pressure sensors for use in the present invention will be readily apparent to those of skill in the related arts.
In the illustrated embodiment, manual and automatic valves allow the flow of air in and/or out of the cavity 114. The illustrated embodiment includes a manual release valve 124, an air release solenoid valve 126, an excess pressure relief valve 128, and an air inlet valve 130. The manual release valve 124 opens manually to allow reduction of the pressure within the cavity 114. The air release solenoid valve 126 is a controlled device that opens, e.g., in response to signals from a controller, to allow reduction of the pressure within the cavity 114. The excess pressure relief valve 128 opens when the pressure within the cavity exceeds a predefined value to prevent potentially damaging pressure from developing in the cavity 114. The air inlet valve 130 is a controlled valve that opens to allow air flow into the cavity 114 when the piston 108 is extracted during an initialization phase, described in further detail below. In exemplary embodiments, an optional pump 132 (shown in phantom) initially supplies air to the inflatable sleeve 104 and/or the cavity 114 within the cylinder 106. The pump 132 may be a small pump having characteristics such as those found in aquarium pumps.
The controller 134 monitors and/or controls the sensors, valves (except for the manual release valve 124 and the excess pressure relief valve 128), and piston driver 112 to adjust the pressure/volume within the cavity 114, which, in turn, adjusts the pressure applied to an appendage within the inflatable sleeve 104. The controller 134 is programmed to control the pressure within the cavity 114 by changing the position of the piston 108 within the cylinder 106 via the piston drive 112. In an exemplary embodiment, the controller 134 is programmed with data corresponding to the piston driver 112, the piston 108, and the cylinder 106 that enables the controller 134 to determine the relative position of the piston 108 within the cylinder 106. In certain exemplary embodiments, the controller 134 monitors the rear position sensor 116 and the forward position sensor 118 and does not drive the piston 108 beyond locations corresponding to these sensors to avoid damaging the rapid compression device 102. In certain other exemplary embodiments, the forward and rear sensors are eliminated and the controller 134 is entrusted with this function. Connection lines between the controller 134 and the various sensors and valves are omitted to avoid clutter within
The controller 134 is programmed to vary the pressure/volume within the cavity 114 (and, thus, the inflatable sleeve 104) in accordance with various compression therapies. In an exemplary embodiment, the controller 134 is programmed to vary the pressure/volume in the cavity 114 in accordance with a predetermined program at a certain rate for a certain period of time, e.g., between 0 psi and 2 psi at sixty cycles per minute for twenty minutes. In an alternative exemplary embodiment, the controller 134 is programmed to vary the pressure/volume in the cavity responsive to a cardiac signal generated by the heart of a being associated with the appendage. In accordance with this embodiment, the controller may have an input port 136 for receiving the cardiac signal and may increase pressure (reduce volume) of the cavity 114 substantially concurrent with expansion of the heart and decrease pressure (increase volume) of the cavity 114 substantially concurrent with contraction of the heart.
The controller 134 may be programmed to apply the pressure in accordance with one or more pressure waveforms, e.g., a trapezoidal waveform, a triangular waveform, a step waveform, etc. Thus, the pressure may vary continuously or may be held for predetermined periods of time, e.g., at the maximum and/or minimum pressure. In certain exemplary embodiments, the pressure, compression rate, time, and/or pressure waveform are set by an operator using a conventional user interface such as a keypad or through a computer interface.
The controller 134 may apply different pressure levels during the course of the therapy with the time for each pressure level being programmable as well. For example, the controller 134 may be set to vary the pressure between 0 psi and 1 psi at sixty cycles per minute for ten minutes followed by varying the pressure between 0 and 2 psi at eighty cycles per minute (or responsive to a cardiac signal) for fifteen minutes. In addition, the controller 134 may apply pressure at a variable rate.
At block 304, the rapid compression device is initialized. In an exemplary embodiment, the controller 134 (via the piston driver 112) positions the piston 108 at a front initialization position 150 (see
At block 306, the controller 134 identifies a therapy insertion position for the piston within the cylinder. The therapy insertion position is an initial maximum position that the piston may be inserted into the cylinder during a therapy to develop the maximum therapy pressure. In an exemplary embodiment, the therapy insertion position is the front initialization position.
At block 308, the inflatable sleeve 104 is filled with gas. In an exemplary embodiment, the inflatable sleeve is filled with gas using the rapid compression device 102, which will be described in further detail below with reference to blocks 310, 312, and 316. In an alternative exemplary embodiment, the inflatable sleeve is filled with gas using an optional pump 132 instead of, or in addition to, the rapid compression device 102.
At block 310, the controller 134 moves the piston 108 from the first initialization position 150 to a second initialization position 152 within the cylinder 106 (which is at or near the rear position sensor 118) to draw air into the cavity 114. In an exemplary embodiment, the controller 134 opens the air inlet valve 130 (e.g., to expose the cavity to the atmosphere) and withdraws the piston 108 slowly from the inflatable sleeve to ensure that the cavity 114 is filled with gas (e.g., air) external to the rapid compression device 102 and the inflatable sleeve 104, rather than gas from the inflatable sleeve 104.
At block 312, the controller 134 closes the valves and slowly inserts the piston 108 into the cylinder 106 to the first initialization position 150 to fill the inflatable sleeve 104 with gas. In an exemplary embodiment, the controller 134 monitors the pressure within the cavity 114 while the piston 108 is moved forward to ensure that the pressure within the inflatable sleeve 104 does not exceed a predefined maximum therapy pressure level (e.g., 2 psi). If the pressure exceeds the maximum therapy level, the controller may open a valve to release excess pressure as the piston is inserted into the cylinder.
At block 314, the controller 134 determines if a maximum therapy pressure within the cavity with the piston at the therapy insertion position (e.g., first initialization position 150) is met. If the maximum therapy pressure in the cavity is met, processing proceeds at block 316. In an exemplary embodiment, if the desired pressure in the cavity is not met, processing proceeds at block 310 with the steps in blocks 310 and 312 repeated until there is enough air in the cavity 114 and the inflatable sleeve 104 to develop the maximum therapy pressure at the therapy insertion position. For example, if the inflatable sleeve needs 6 liters of air and the rapid compression device 102 can deliver 2 liters of air per stroke, the rapid compression device 102 will cycle at least three times to fill the inflatable sleeve 140.
At block 316, the controller 134 identifies a therapy extraction position for the piston 108 within the cylinder 106. In an exemplary embodiment, the controller 134 monitors the pressure within the cavity 114 while the piston 108 is extracted from the cylinder 106 until a minimum therapy pressure is met (e.g., 0 psi). The controller 134 then identifies the position of the piston 108 when the minimum therapy pressure is met as the therapy extraction position. In an exemplary embodiment, the controller identifies the position of the therapy extraction position relative to the therapy insertion position.
At block 318, the rapid compression device 102 withdraws a portion of the gas from the inflatable sleeve into a cavity (e.g., the gas transport connector 116 and/or the cavity 114). In an exemplary embodiment, the controller 134 moves the piston 108 from the therapy insertion position to the therapy extraction position to increase the volume of the cavity 114, thereby drawing a portion of the gas from the inflatable sleeve into the cavity to reduce the pressure in the inflatable sleeve.
At block 320, the rapid compression device 102 inserts the withdrawn portion of the gas from the cavity (e.g., the gas transport connector 116 and/or the cavity 114) back into the inflatable sleeve. In an exemplary embodiment, the controller 134 moves the piston 108 from the therapy extraction position to the therapy insertion position to decrease the volume of the cavity 114, thereby inserting the withdrawn portion of the gas back into the inflatable sleeve to increase the pressure in the inflatable sleeve.
At block 322, the controller 134 determines if the therapy is complete. If the therapy is complete, processing ends at block 324. If the therapy is not complete, processing proceeds at block 318 with blocks 318 and 320 rapidly repeated until the therapy is complete. In an exemplary embodiment, the controller 134 performs the steps of blocks 318 and 320 to apply the therapy to the appendage such that the piston is cycled rapidly between the first and second therapy positions at a predetermined rate, e.g., between 30 and 120 cycles per minute. In an alternative exemplary embodiment, the piston is cycled responsive to an external signal, e.g., a cardiac signal produced by the heart of a being whose appendage is being treated. In accordance with this embodiment, the controller 134 may control the piston driver 112 such that the piston 108 is inserted into the cylinder 106 to increase the applied pressure substantially concurrent with (or in anticipation of) expansion of the heart and the piston 108 is withdrawn from the cylinder 106 to decrease the applied pressure substantially concurrent with (or in anticipation of) contraction of the heart.
In an exemplary embodiments, the controller 134 monitors the pressure in the cavity 114 and increases or decreases the stroke length (e.g., by shifting the therapy insertion position and/or the therapy extraction position) responsive to the monitored pressure such that the desired minimum and maximum pressures are maintained throughout the therapy. For example, if the pressure produced when the piston is positioned at the therapy insertion position is below the maximum therapy pressure (e.g., due to leaks within the system), the controller may reposition the therapy insertion position 150 closer to the maximum insertion position to decrease the volume of the cavity 114 and increase the pressure when piston is at the new therapy insertion position 150a (see
After the maximum therapy pressure is developed within the pressure cavity 114 with the piston 108 at the therapy insertion position 150 within the cylinder 106, the rapid compression device 102 can alter the pressure applied to an appendage within the inflatable sleeve 104 simply by moving the piston within the cylinder between the therapy insertion and extraction positions. Thus, the rapid compression device is able to deliver rapid compressions to an appendage in a more efficient manner by reusing the air rather than releasing the air and then completely replenishing the air in the inflatable sleeve as in conventional systems.
Additional details regarding the rapid compression device are now provided. Assuming an inflatable sleeve (hereinafter sleeve) with a 15 liter volume, only 1/15th of the volume of the sleeve needs to be displaced by the piston 108 within the cylinder 106 to develop 1 psi of pressure. Typical pressure therapies are performed with a maximum of 1 to 2 psi of pressure. Based on this information, the desired displacement will typically be no more than 2 liters for a 15 liter sleeve to be pressurized at 2 psi. A 5″ diameter piston will have to move only 3.25″ inches to develop 1 psi in a 15-liter sleeve. This distance traveled over a period of 300 milliseconds translates into a system that moves at a speed of approximately 10 inches per second.
Exemplary volume calculations follow to illustrate that moving a 5 inch diameter piston 3 and ½ inches will displace 1 liter of air and moving the piston 7 inches will displace 2 liters of air.
Thus, to displace 1 liter, an approximately 3.5″ translation of a 5″ diameter piston is necessary and to displace 2 liters twice as much translation is necessary, e.g., 7″. The development of suitable piston driver 112 to provide the necessary translation will be readily apparent to those of skill in the art.
Exemplary pressure calculations follow to illustrate that displacing one liter of air in a 15 liter inflatable sleeve develops approximately 1 psi and displacing two liters of air in a 15 liter inflatable sleeve develops approximately 2 psi. Pressure, volume and temperature of a given gas are related as shown in equation 1.
p1*v1/t1=p2*v2/t2, (1)
where p1, v1 and t1 are pressure, volume and temperature before the compression, respectively, and p2, v2 and t2 are the pressure, volume and temperature after compression, respectively.
Assuming t1=t2 (which is a valid assumption for low pressure differentials, e.g., 1–2 psi), and atmospheric pressure=15 psi, when we develop 1 psi above atmospheric pressure, we develop actually 16 psi absolute pressure in the inflatable sleeve where it used to be 15 psi.
Thus, if we start with 16 liters (15 liters in the inflatable sleeve plus 1 liter in the cylinder) and compress that extra 1 liter into the inflatable sleeve and solve for p2 we get:
p1*v1=p2*v2
15*16=p2*15
p2=16 (or 1 psi above atmospheric pressure)
Thus, adding 1 liter of air to a 15 liter inflatable sleeve raises the pressure by 1 psi and adding 2 liters of air (v1=17) raises the pressure by 2 psi. It will be readily apparent to those of skill in the art that pressure may be represented in units other than psi, e.g., millimeters of mercury (1 psi=50 mm of Hg) or inches of water (1 psi=27.7″ of water).
Based on the information provided above, a compression therapy can be applied to a single arm or leg in a 15 liter inflatable sleeve (which is a relatively large inflatable sleeve compared to a typical inflatable sleeve having a volume of 5 liters or less) using approximately 300 watts of power. Thus, four appendage (e.g., two arm and two legs) can be treated concurrently using only 1200 watts of power or less, which is well within the power (1500 watts at 120V AC) available in a typical residential home. In addition, the rapid compression device is smaller, cheaper, and quieter than conventional compression devices, which makes them better suited for use in residential homes and in medical facilities.
Although the invention is described herein primarily with reference to a single rapid compression device 102 controlling the pressure of an inflatable sleeve 104 having a single inflatable section 206, the present invention may be applied to inflatable sleeves having multiple inflatable sections. In an exemplary embodiment, as depicted in
In an alternative exemplary embodiment, as depicted in
In an exemplary embodiment, the same pressure may be applied to multiple appendages and/or sections simultaneously. In alternative exemplary embodiments, different pressures are applied concurrently to different appendages and/or sections. For example, the rapid compression device 102 may apply 75 mm of Hg to a patient's legs and 50 mm of Hg to the patient's arms. In an exemplary embodiment, a controlled valve (such as valve 500a) is positioned between the rapid compression device 102 and each inflatable sleeve 104 (or individual sections 206 of sleeves) that receives an appendage to enable the application of different pressures.
Although the invention is illustrated and described herein with reference to specific embodiments, the invention is not intended to be limited to the details shown. For example, pressure may be sensed in the inflatable sleeve rather than in the cavity within the cylinder of the rapid compression device. Various other modifications may be made in the details within the scope and range of equivalents of the claims and without departing from the invention.
This application claims the benefit of the filing date of provisional application No. 60/479,315 entitled “RAPID COMPRESSION APPARATUS AND METHOD” filed Jun. 18, 2003, the contents of which are incorporated herein by reference.
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