Patent Grant
9402941
The present invention is directed to dialysis systems, and more particularly to dialysis systems that may be completely and continuously worn by a patient or dialysis systems that are portable or mobile.
Hemodialysis is a process by which microscopic toxins are removed from the blood using a filtering membrane such as a dialyzer. Typically, hemodialysis is administered to a patient in periodic three to four hour sessions. Each session takes place two or three times per week. There exists a growing body of research that prefers daily dialysis since increased dialysis time improves outcomes, both in terms of quality of life and patient longevity. An additional number of researchers believe that continuous dialysis for twenty-four hours a day, seven days a week would provide the best outcome for a patient in terms of quality of life and longevity. The actual implementation of substantially continuous dialysis has been impossible to date because of technology and cost constraints. Regardless, it is believed that continuous renal replacement therapy (CRRT) would be an enormous improvement over intermittent dialysis because far more toxins can be removed from the blood using a CRRT device seven days a week and for nearly twenty-four hours a day.
Some advantages of providing CRRT include an expected decrease in morbidity and mortality, a decrease in the amount of medications required, a decrease in fluid intake, a decrease of dietary restrictions, and numerous improvements to the quality of life of the end-stage renal disease (ESRD) patients. Present day CRRT machines are stationary, large, heavy machines adapted to provide dialysis, hemofiltration or a combination of both to individual patients. The existing CRRT are cumbersome and require electrical connection to 120-140 volt AC electrical outlets as well as several feet of tubing to connect the machine to the patient. In addition, these machines require a continuous supply of gallons of fresh filtered water to create the dialysate fluid. Furthermore, a patient must remain connected to the existing heavy and cumbersome CRRT machine for many hours each day, which limits his or her ability to perform normal, everyday activities.
An additional problem with existing dialysis machines is that frequent reconnection and disconnection to the machine requires accessing blood flow in a patient by puncturing an artiovenous shunt. These shunts only last for limited periods of time and subject the patient to infection, clotting and other complications which result in numerous hospitalizations and repeated surgical interventions. Another problem with existing dialysis machines is as these machines become smaller and a bit more portable, smaller hemofilters or dialyzer filters must be used that does not clog or clot too quickly so that extended or continuous dialysis can be performed. A common type of dialyzer includes nine hundred or more cylindrical hollow fibers through which blood flow is provided. The hundreds of cylindrical hollow fibers are contained in a shell or container in which dialysate fluid is circulated around and past the exterior walls of the hollow fibers. The exterior walls of the hollow fibers or lumens are semi-porous so that impurities in the blood can be moved from the blood and into the dialysate. One problem that occurs in a dialyzer is the clogging or clotting of blood flow within individual hollow fibers. Such clogging of blood flow through the fibers decreases the effectiveness of the dialyzer's filtration and blood cleaning properties. Furthermore, it is understood that proteins and other compounds or substances in the blood may clog the pores of the semi-porous membrane overtime and decrease the effectiveness of the dialyzer filter. If a dialyzer filter is to be in continuous operation twenty-four hours a day, seven days a week, it is important that such a dialyzer be operational for extended periods of time at or near a continued peak performance without becoming clogged or having its efficiency decreased significantly during usage. Furthermore, it would also be useful if a dialyzer remained efficient and effective when a low-power pump is used to pump blood there through such that a minimum amount of energy is required for the highest possible clearance of impurities from a patient's blood at the lowest amount of required energy.
Dialyzers' membranes have been studied for well over a half of a century. The initial inventors of dialysis or dialactic therapy understand the basics of diffusion and how toxins diffuse across a dialyzer's membrane from blood to a dialysate fluid. There are many factors that influence diffusion in solute transfer across a semi-permeable membrane. Such factors have been explained in various prior articles about the workings of a dialyzer. But, again there has been limited or minimal research on providing a dialysis device wherein the dialyzer operates efficiently over extended periods of time (more than 15 hours) in order to provide a low power completely wearable or portable dialysis device having a dialyzer with increased efficiency over that of previous dialysis machines having a dialyzer with a membrane of the same or similar membrane surface area.
Embodiments of the invention provide a continuous renal replacement therapy (CRRT) device that weighs between 2 and 10 pounds. The CRRT device can be portable, mobile or completely worn on the person of the patient. Blood and dialysate are each pumped in a pulsed or pulsatile manner through a dialyzer such that a significant portion of the peak pulse of the blood flow and pressure coincides with a significant portion of a low pulse flow and pressure portion of the dialysate flow. A differential pressure between a dialysate inlet of the dialyzer and the blood inlet of the dialyzer periodically changes from a high differential pressure of between 70 and 120 mmHg for a first time period and a low differential pressure of between −10 and 10 mmHg for a second time period. The frequency of the high and low differential pressure cycle is between about 0.5 and 4 Hz.
In one aspect thereof an exemplary embodiment of the invention provides a continuous renal replacement therapy (CRRT) device. The CRRT device includes a blood pump channel that establishes a pulsed or pulsatile blood flow. The pulsed blood flow is periodic such that each period of the blood flow comprises a high blood pressure portion having a first duration and a low blood pressure portion having a second duration. The first duration and the second duration have a duration ratio between about 3:4 and 4:3. The duration ratio requires that the time durations of the high blood pressure portion and low blood pressure portions are at least 75 percent (%) of each other. For example, if the high blood pressure portion of the pulse has a duration of one (1) second, then the low blood pressure pulse should have a duration of between about 0.75 and 1.25 seconds. The exemplary embodiment further comprises a dialysate pump channel that provides a pulsed or pulsatile dialysate flow. The pulsed dialysate flow is periodic such that each period comprises a high dialysate pressure portion having said second duration and a low dialysate pressure portion having said first duration. The high blood pressure portion and said low dialysate pressure portion occur, at least in part, during a same first periodic time frame. The exemplary embodiment also comprises a dialyzer or hemofilter. The dialyzer comprises a blood inlet that receives the pulsed blood flow from the blood pump channel. The dialyzer of the exemplary embodiment also comprises a plurality of fibers. Each fiber comprises a semi permeable membrane exterior and a lumen extending the length of the fiber. The lumen provides a passage through the fiber for the pulsed blood flow to flow. The dialyzer further comprises a blood outlet for the pulsed blood flow to exit said dialyzer as well as a dialysate inlet for receiving the pulsed dialysate flow being pumped by the dialysate pump channel. Also the dialyzer has an outer tube that establishes a dialysate container or chamber, about the plurality of fibers. In other words, the fibers are substantially contained in the dialyzer and are within a dialysate chamber or container. The pulsed dialysate flow flows through the dialysate chamber. The semi permeable membranes of the plurality of fibers are the means between each said lumen and said dialysate chamber. The dialyzer includes a dialysate outlet for the pulsed dialysate flow to exit the dialyzer. The combination of the blood pump channel, the dialysate channel and the dialyzer are configured to establish a peak Trans Membrane Pressure (TMP) across the semi permeable membranes of the plurality of fibers and between said pulsed blood flow in the lumens and the pulsed dialysate flow in the dialysate chamber. The peak TMP occurs during the first periodic time frame. The peak TMP is between about 70 mmHg and 120 mmHg.
Various embodiments of an exemplary CRRT device require that the low blood pressure portion of the blood flow and the high dialysate pressure portion of the dialysate flow both occur, at least in part, during a second periodic time frame. Furthermore, the blood channel, the dialysate channel and said dialyzer are configured to establish a minimum TMP across the semi permeable membranes of the plurality of fibers during said second periodic time frame. The minimum TMP is between about 10 mmHg and −10 mmHg.
Additionally in various embodiments on an exemplary CRRT device a dual channel ventricle pulsatile pump that comprises the blood pump channel and the dialysate pump channel is incorporated into the device. The same mechanical mechanism may be utilized in the dual channel ventricle pulsatile pump to actuate both the blood pump channel and the dialysate channel.
Furthermore, some embodiments of the invention may be entirely worn on the person of the user, while other embodiments of the CRRT device are light weight (e.g., between 2 and 15 pounds while operating) and mobile such that they may be moved about a medical facility or within a user's home.
Some embodiments of an exemplary CRRT device provide blood pump channel that may provide a pulsed or pulsatile blood flow with a periodic flow rate of between 0.5 and 4 Hz and wherein the dialysate pump channel provides a pulsed or pulsatile dialysate flow with a same or similar periodic flow rate. This periodic flow rate of blood has been found to be the least damaging to the blood cells as they pass through the blood pump channel and also deter clogging or clotting of the blood in the pump channel, the fiber lumens in the dialyzer, as well as in the semi permeable membranes between the fiber lumens and dialysate within the dialysate chamber portion of the dialyzer. The pulsed or pulsatile blood flow described herein appears to provide an unexpected washing or push-pull effect that helps to inhibit clogging for the extended operating time periods of exemplary CRRT devices. It should be noted that exemplary CRRT devices' elements combine in an unexpected manner such that the peak TMP that occurs during the first periodic time frame and the minimum TMP that occurs during the second periodic time frame inhibit clogging of the lumens and the semi permeable membranes.
In another exemplary embodiment a continuous renal replacement therapy (CRRT) device is provided that comprises a blood pump channel for providing a pulsatile blood flow. The pulsatile blood flow is periodic such that each period comprises a high blood pressure portion having a first time duration and a low blood pressure portion having a second time duration. The first time duration and the second time duration have a duration ratio of between about 3:4 and about 4:3, this, of course, includes a duration ratio of 1:1. These exemplary embodiments further include a dialysate pump channel that provides a pulsatile dialysate flow. The pulsatile dialysate flow is a periodic flow such that each period of the flow comprises a high dialysate pressure portion having the second time duration and a low dialysate pressure portion having the first time duration; wherein said high blood pressure portion and said low dialysate pressure portion occur periodically, at least in part, during a same first periodic time frame. The exemplary embodiment further includes a dialyzer. The dialyzer comprises a blood inlet for receiving the pulsatile blood flow. The dialyzer also comprises a plurality of fibers wherein each fiber comprises a lumen extending the length of the fiber and a semi permeable membrane exterior. The lumen is for carrying the pulsatile blood flow through a substantial portion of the dialyzer. The dialyzer further includes a blood outlet for said pulsatile blood flow to exit the dialyzer, a dialysate inlet for receiving the pulsatile dialysate flow, a dialysate compartment area that is around or about the plurality of fibers, for said pulsatile dialysate flow to flow through; and a dialysate outlet for the pulsatile dialysate flow to exit said dialyzer. The combination of the blood pump channel, the dialysate channel and the dialyzer are configured to establish a peak blood inlet-to-dialysate outlet differential pressure that occurs during the first periodic time frame. The peak blood inlet-to-dialysate outlet differential pressure may be in a range of between about 60 mmHg and about 150 mmHg, which provides an unexpected enhanced amount of toxins from a patient's blood to move across the fiber semi permeable membrane into dialysate contained within and pulsing through the dialyzer.
Additional embodiments of an exemplary CRRT device are configured such that the low blood pressure portion and the high dialysate pressure portion both occur, at least in part, during a second periodic time frame. The blood pump channel, the dialysate channel and the dialyzer are configured to establish a minimum blood inlet-to-dialysate outlet differential pressure that occurs during the second periodic time frame and that establishes a differential pressure between about 10 mmHg and about −10 mmHg.
Other embodiments of the invention provide a method of continuous renal replacement therapy (CRRT). An exemplary method of providing CRRT comprises pumping blood, by a pulsatile blood pump, to provide a pulsatile blood flow. The pulsatile blood flow is a periodic flow wherein each period comprises a high blood pressure portion having a first time duration and a low blood pressure portion having a second time duration. The first time duration and the second time duration have a duration ratio that can range between about 3:4 and 4:3. The method of providing CRRT further includes pumping dialysate, by a pulsatile dialysate pump, to provide a pulsatile dialysate flow. The pulsatile dialysate flow, like the pulsatile blood flow, has a period that comprises a high dialysate pressure portion having the second time duration and a low dialysate pressure portion having the first time duration. The high blood pressure portion and the low dialysate portion occur, at least in part, during a first periodic time frame. The exemplary method further establishes a blood inlet-to-dialysate outlet differential pressure between a blood inlet of a dialyzer and a dialysate outlet of the dialyzer, wherein said blood inlet to-dialysate outlet differential pressure oscillates between a maximum differential pressure and a minimum differential pressure at a pump frequency of between 0.5 and 4 Hz. The maximum differential pressure has a range of between about 60 mmHg and about 150 mmHg. The minimum differential pressure has a range of between about 10 mmHg and about −10 mmHg for the pump frequency of between 0.5 and 4 Hz.
All though two separate pulsatile pumps could be used in an exemplary method of CRRT, is various embodiments the pulsatile blood pump and said pulsatile dialysate pump are each a separate pump channel of a dual channel pulsatile pump and are each operated by a same mechanical mechanism. Embodiments of the invention utilize a pulsatile blood pump and a pulsatile dialysate pump that provides an average pulsatile flow rate of between 30 and 90 milliliters/minute (ml/min).
In yet another embodiment of the invention a method of dialysis is provided that comprises receiving blood in a blood circuit of a dialysis device; pumping the blood in a pulsed manner to provide an average pulsatile blood flow rate of between 30 and 90 ml/min; pumping dialysate, in a dialysate circuit of the dialysis device, in a pulsed manner to provide an average pulsatile dialysate flow rate of between 30 and 90 ml/min; receiving the pumped blood at a blood inlet of a dialyzer; receiving the pumped dialysate at a dialysate inlet of said dialyzer, to establish a pressure differential between the blood in said blood inlet and the dialysate in the dialysate inlet that fluctuates at a periodic rate of between 0 mmHg+/−10 mmHg and 120 mmHg+/−20 mmHg; transferring urea molecules from the blood to the dialysate while the blood and the dialysate are passing through the dialyzer; and cleaning said dialysate by a filtration means so that the cleaned dialysate can be reused and recirculated in the dialysate circuit.
Embodiments of the invention provide a method to CRRT that can be performed by either a completely wearable or a completely portable dialysis device.
Various embodiments of the invention provide one or more pumping devices that pump the blood and the dialysate such that a peak flow of said blood occurs at alternating times with a peak flow of the dialysate. And, various embodiments of the invention are configured such that the pumping of the blood in a pulsed manner comprises providing, in an alternating manner, a high blood flow rate portion and a low blood flow rate portion, and wherein said pumping dialysate in a pulsed manner comprises providing, in an alternating manner, a high dialysate flow rate portion and a low dialysate flow rate portion. The high blood flow rate portion and the low dialysate flow rate portion each occurring, at least for a majority of their durations, at the same time.
As such, various embodiments of exemplary methods and devices for CRRT have been found to operate to provide enhance clearances in an artificial kidney when a pulsed or pulsatile pump is used in combination with other elements discussed herein to produce an unexpected solution to a problem faced by renal failure patients, but that has never been effectively solved to provide a completely wearable or portable CRRT device that is operable to enhance the quality of life of such patients and to unexpectedly resist clogging or clotting of blood in its dialyzer element.
For a more complete understanding, reference is now made to the following description taken in conjunction with the accompanying Drawings in which:
Referring now to the drawings, wherein like reference numbers are used herein to designate like elements throughout, the various views and embodiments of the exemplary enhanced clearance artificial kidneys incorporating a pulsatile pump are illustrated and described, and other possible embodiments are described. The figures are not necessarily drawn to scale, and in some instances the drawings have been exaggerated and/or simplified in places for illustrative purposes only. One of ordinary skill in the art will appreciate the many possible applications and variations based on the following examples of possible embodiments.
An exemplary embodiment of a wearable CRRT device is depicted in
One or more circuit cards or microcircuits 106 are incorporated within the wearable CRRT device 100. A microcontroller 108 is utilized to control and monitor various-aspects of the wearable CRRT device 100. Microcontroller 108 is preferably a low or very low power microcontroller, but may be substantially any microcontroller adapted to operate in an exemplary CRRT device 100. One of the many functions of the microcontroller 108 is to monitor the battery 110. An exemplary CRRT device 100 will operate continuously for at least five hours to about thirty hours using, on average, less than 10 continuous watts of power. Some embodiments of the wearable CRRT device 100 will use, on average, less than 3 continuous watts of power. Embodiments of the invention will weigh between two and ten pounds when operating.
The battery 110 is removably installed in the wearable CRRT device 100. The battery 110 may be rechargeable and may be recharged either while contained in the wearable CRRT device 100 or while disconnected and removed from the wearable CRRT device 100. The battery 110 can store enough energy to power an exemplary wearable CRRT device 100 for at least five hours and in some embodiments up to thirty or more hours of continuous uninterrupted device operation. The microcontroller 106, by itself, or via additional circuitry, monitors the charge status of the battery 110. If the microcontroller 106 determines that the battery 110 is low on charge or has less than an estimated, predetermined amount of operating time left (e.g., one hour left), the microcontroller 106 may trigger an alarm condition via the alarm circuit 112. Alarm circuit 112 may provide any combination of an audio, visual or physical alarm. The physical alarm signal may include vibrations or small tingle-style shocks to the patient. An alarm condition or warning may be displayed on a display 114, which can be seen by the user. The display 114 may be a liquid crystal display, light-emitting diode display or any other low power display technology. An alarm condition may also shut down all or predetermined parts of the exemplary wearable CRRT device 100. For example, a battery low condition may slow the pump, discussed herein below, to a very low volume of blood movement through the dialyzer in order to save energy and decrease a possibility of blood clotting. The pump may be slowed to one tenth to one half of its normal pumping rate in order to conserve energy until a battery recharge or new battery is provided.
A moisture sensor 116 is in electrical communication with the microcontroller 108. The moisture sensor 116 detects high humidity, condensation, or liquid present inside the packaging or covering over (not specifically shown) the wearable CRRT device 100. In some embodiments a plurality of moisture sensors are positioned at strategic locations within the CRRT device 100. For example, the moisture sensor 116 may be positioned near the pump (to be discussed later) or the filtration and absorption section. In other embodiments, an additional moisture sensor may also be located near the dialyzer input and/or outputs.
The packaging or covering that partially or completely encloses the exemplary CRRT device 100 may be the combination of plastic, cloth, a rubberized material, a poly product, or another suitable material. The covering may cover a portion of the wearable CRRT device 100 and allow access to various parts of the device, such as the display 114 and/or the user or doctor controls 118.
High humidity, condensation or the presence of liquid inside an exemplary wearable CRRT device 100 may be indicative of patient blood leakage, dialysate leakage or other fluid leakage inside the CRRT device 100. Upon sensing moisture, the moisture sensor 116 provides a signal to the microcontroller 108 and an alarm is triggered via the alarm circuit 112. Depending on the location of the moisture sensor within the wearable CRRT device 100, different responses to sensed moisture may occur. For example, if a moisture sensor senses moisture near the blood circuit (to be described below) the CRRT device 100 may turn the pump completely off, providing audible alarm to the patient wearer and utilize the wireless communications circuitry 120 to call an emergency number for help. Conversely, if moisture is sensed near the filtration and pad absorption portion 122 of the wearable CRRT device 100, then in some embodiments the alarm circuit 112 may sound an audible or patient-sensed alarm, slow the pumping rate of the blood and dialysate and make further checks via a gas or pressure sensor for possible air contamination or bubbles within the dialysate loop of the CRRT device 100. It is noted that the wireless communication circuitry 120 may also be able to provide the geographic location of the exemplary wearable CRRT device 100 in via a wireless communication 120 to a third party who may provide help or a service to the patient.
The pump 124 is an electric pulsatile pump. Embodiments of the present invention may have a single channel pulsatile pump or a dual pulsatile pump.
An exemplary wearable CRRT device 100 has two fluid circuits: a blood circuit as indicated by the arrows 132 and a dialysate circuit as indicated by the arrows 134. The dual channel pulsatile pump 124 is used in the exemplary embodiment. The pulsatile pump may have rubberized flexible cartridges 126 and 128 that provide flow in a single direction or in opposing directions. The pulsatile pump 124 shown provides flow across the pump or through the pump in opposing directions. Each cartridge or pump chamber 126 has an input valve at an input side 134 of the chamber and an output valve at the output side 136 of the chamber. The input and output valves are ball values that minimize damage to the blood cells in the blood circuit. Flapper valves may also be used in various embodiments.
In the blood circuit 132 of an exemplary CRRT device 100, blood from a patient enters the blood circuit at the blood input 138 the blood flows through the blood circuit 132 where anticoagulant fluid (e.g., heparin and other reasonable equivalents) may be mixed with the blood via an anticoagulant reservoir 140 and an anticoagulant micropump 142. The anticoagulant micropump may be a piezo or diaphragm MRRO pump or other type of low energy pump for providing small amounts of anticoagulant fluid to the blood flow.
The blood flows past a first pressure sensor 144 prior to entering the input valve 134a of the dual channel pulsatile pump. When the pushing member 130 presses against the flexible rubberized tubular cartridge portion 126, the input valve 134a closes and the exit valve 136a opens and allows a pulse of blood to exit the first pulsatile chamber [126]. Additional fluid reservoirs 146 and micropumps 148 may add additional substances to the blood flow, such as anticoagulant fluids or medications. The blood then passes past a second pressure sensor 150 which senses the pressure of the output stroke of the first channel of the pulsatile pump prior to the blood entering the dialyzer 152. An exemplary blood channel pulsatile pump chamber can provide a blood flow rate of between about 15 to 100 ml per minute (pulsatile). An exemplary pulsatile pump 124 may have dimensions of 9.7×7.1×4.6 centimeters with a weight of less than 400 grams when not operating. An exemplary pump uses less than 10 watts of energy to pump two channels of fluids using a single motor, transmission and pushing member that alternately pumps each channel in a pulsatile fashion at or around 180 degrees out of phase. If the pushing means of an exemplary pulsatile pump has difficulty compressing or requires very little energy compressing one of the flexible rubberized tubular chamber portions, the pulsatile pump may provide an alarm to the microcontroller 106 indicating a possible occlusion in the blood or dialysate circuits input or output valves of a pulsatile pump channel. A low power pulsatile pump using from two to about 7 watts, steady state, may also be used successfully in exemplary embodiments of the invention.
The pulsatile pump can be tuned by adjusting the motor transmission or re-orienting the pushing member a small distance from being centered between the tubular portions 126, 128 such that the pulses or cycles of the two pulse chambers are in phase, 180 degrees out of phase, or alternating such that each chamber pumps at a predetermined number of degrees out of phase in order to utilize the pulses of the pump to aid in maximizing the dialysis process occurring in the dialyzer 152. Embodiments of exemplary pulsatile pumps may be slowed such that the blood flow or fluid flow through a chamber of the pump is between 1 and 50 ml per minute during an alarm state in the wearable CRRT device 100.
Other types of pumps can also be successfully used or incorporated into embodiments of the CRRT device 100. For example, two separate pulsatile pumps may be used provided that the pumps can be timed such that the pumps continuously pulse at predetermined alternating output rates. This can be performed with stepper motors and microprocessor control Other pumps that can provide a pulsed output such as a double-sided piston pump that has an intake stroke through one valve and a pump stroke through a second valve may also be used. Such a pump may be magnetic or pneumatically powered.
Still discussing the blood circuit 132, the blood passes by the second pressure sensor 150 and then through the hollow lumens or fibers of the dialyzer 152 (not specifically shown). The dialysis process takes place in the dialyzer wherein impurities in a patient's blood move via a mass transfer through the outer membranes of the porous lumens through which the blood is traveling. The impurities are deposited into the dialysate as they exit the outer surface of a lumen's outer membrane into the dialysate that is flowing through the dialyzer in the dialysate circuit 134.
The blood cleaned exits the dialyzer and travels toward the blood circuit output 154 to go back into the patient. As the blood flows from the dialyzer 152 to the blood circuit output 154, additional medicines, vitamins and other fluids may be added to the blood via reservoirs 156 and micropumps 158.
The pressure of the blood as it exits the dialyzer 152 is sensed at a third pressure sensor or transducer 160.
The microcontroller 108 may display pump status or other pump/flow related information such as pressure, flow rate, or dual channel pump phase difference on the display 114. User controls 118, being buttons, switches, slide controls, knobs, connectors, or touch-sensitive switches (not specifically shown) may be used to enable the patient, a physician, a nurse, technician or computer-based device to adjust various settings and controls on the exemplary CRRT device 100. Furthermore, the communication device 120 may be utilized to send and receive control settings via a paging or other telecom or wireless communication channels or networks for fine tuning or medical adjustment of the exemplary CRRT device. For example, adjustments to the pump 124 rate, flow rate, pump RPM, pulse rate or any of the micropump flow rates may all be monitored or controlled vial the user interface 118 and 114 or the wireless communication circuitry 120. A doctor may be able to monitor the CRRT device from a satellite location and be able to adjust CRRT settings remotely.
The dialyzer 152, is shown as a single dialyzer, but can be a single or multiple dialyzers connected in series or parallel. The dialyzer 152 may take the form of a cartridge that can be “clicked” or quick connected and disconnected into and out of the blood/dialysate circuits by a doctor, nurse or technician. The dialyzer 152 used in an exemplary CRRT device 100 may comprise from 0.2 to about 1 square meters of dialyzing surface area (e.g., semi permeable membrane) on the lumen fibers therein. During dialysis, the blood circuit 132 generally has blood flowing in a direction opposite that of the dialysate circuit flow through the dialyzer 152. Furthermore, it has been determined through experimentation that the pulsing of the pulsatile pumps out of phase aid in maximizing the dialysis process. In particular, embodiments of the invention that incorporate a out of phase pulsatile blood flow and dialysate flow through a dialyzer provide enhanced clearance with respect to the removal of toxins from the blood over similar systems that do not incorporate a pulsed or pulsatile dialysate in blood flow through dialyzer. Such results have been found with exemplary embodiments even when the dialysate and the blood flow through the dialyzer in the same direction.
The combination of the first, second and third pressure sensor/transducers 144, 150 and 160, provide differential measurements that can be analyzed by the microcontroller 108. For example, if the pressure differential across the dialyzer 152 is too high (from blood input to output), it may mean, among other things, that the dialyzer 152 has multiple clots or occlusions in the fiber lumens therein. A high pressure differential may also mean that the dialyzer is being operated at too high a blood flow. As a result, an alarm situation can be initiated by the microcontroller 108 or the blood pump 124 may be automatically adjusted by the microcontroller to operate at a higher or lower torque, pump rate or pulse volume such that the flow rate is decreased in predetermined increments in an attempt to stabilize or decrease the pressure differential so that blood cell damage is minimized. If a pressure at one of the pressure transducers 144, 150, 160, drops below a predetermined low pressure, it may be an indication that a fluid leak has occurred in the blood circuit or that air is being pulled into the blood circuit 132. The microcontroller 108 may shut down or slow predetermined parts of the wearable CRRT device 100 in response to pressure in the blood circuit being measured below a predetermined level. Furthermore, the microcontroller 108 may initiate an alarm condition in conjunction with the alarm circuit 112 and communication circuit 120.
Still referring to
Cleaned, fresh dialysate from the sorbent filters 122 flows through the dialysate circuit 134 past the fourth pressure transducer 162 and is pumped through the dialysate pump rubberized tubular portion 128. The dialysate portion of the dual pulsatile pump can pump dialysate at a flow rate ranging from near 0 to about 200 ml per minute (pulsatile). During normal pumping operations the operational flow rate of the dialysate through the dialysate pump is between about 40 to about 100 ml per minute (pulsatile).
Embodiments of the wearable CRRT device 100 are designed to operate using less than about 1 liter of dialysate. Other embodiments may function properly and only require between 300 ml and 400 ml of dialysate in the closed dialysate fluid circuit 134. In embodiments designed for young adults or children, the amount of dialysate needed for operation may be between about 100 to 300 ml of dialysate. Minimizing the amount of dialysate decreases the overall weight of an exemplary device and decreases the operating cost by minimizing the amount of medical waste produced by a dialyzer. The combination of dialysate and filters 122 allow the embodiment to circulate dialysate fluid for at least twenty-four hours before a filter requires replacement. In various embodiments filter replacement may be required at intervals between twenty-four and forty-eight hours. Furthermore, because less than a liter of dialysate is all that is needed in the closed dialysate circuit 134, sterile or ultra-pure dialysate can be economically used in exemplary embodiments of the wearable CRRT device 100. It is further understood that in embodiments that provide a portable and/or partially wearable CRRT device, the amount of dialysate in the dialysate circuit 134 may be greater than one liter. In fact, the amount of dialysate or ultra-pure dialysate in a portable or mobile or partially wearable device may range from 300 ml to about 5 or 6 liters of dialysate.
In existing large substantially stationary dialysis machines, it is common to use about 90 liters of dialysate per patient per run. Generally, due to the amount of water required to create the dialysate, filtered water, rather than ultra-pure water, is used in such large dialysis machines. Filtered water is much less-expensive than ultra-pure or sterile water. Filtered water that is used in large present dialysis machines is allowed to have some bacteria in it. Bacteria are larger than the size of the pores in the membranes or fiber lumens used within an exemplary dialyzer 152. Since the bacteria are larger than the pore size in the semi-permeable membranes of the lumens within the dialyzer 152, the bacteria cannot cross the membrane and get into a patient's blood in the blood circuit 132.
Conversely, medical research has provided some results that are uncomfortable with the use of non-sterile dialysate (i.e., dialysate containing filtered water, bacteria, toxins, or microorganisms). Medical research has shown that microorganisms and bacteria within non-sterile dialysate create waste products, toxins or poisons in the dialysate. The waste products from the bacteria can cross the dialyzer porous membrane and get into the patient's blood while the actual bacteria itself cannot. Such toxins are referred to in some cases, as endotoxins. It has been shown that endotoxins that pass from dialysate through the dialyzer membrane to a patient's blood can have a negative impact on a patient's health. The endotoxins may result in making a patient sick.
Since exemplary embodiments of the wearable CRRT device 100 require less than one liter of dialysate, it is economically feasible to use ultra-pure or sterile water as the main ingredient in making the dialysate.
The dialysate exits the pulsatile dialysate pump portion 128 via the exit valve 136b in a pulsed pulsatile fashion and passes a fifth pressure transducer 164, which measures the dialysate pressure on the dialysate input side 222 of dialyzer 152. The dialysate in the dialysate circuit 154 pulses through the dialyzer 152 such that the dialysate moves in a direction opposite to the flow of the blood in the lumen membrane fibers in the dialyzer. Furthermore, fluids being relatively non-compressible, the peaks of the dialysate flow pulses alternate in time with the peaks of the blood flow peaks pulses through the blood circuit 132 in the dialyzer. In other words, the pulsed flow of the dialysate through the dialyzer alternates with the pulsed flow peaks of the blood through the dialyzer. In some embodiments of the invention, the alternating peak flows of the dialysate fluid and the blood through the dialyzer are about 180 degrees out of phase.
While the dialysate is in the dialyzer 152, waste products and toxins in the blood pass through the membranes of the lumens within the dialyzer and into the dialysate due to diffusion and further in embodiments of the present invention due additionally to convection and osmosis forces. The enhanced clearance of toxins from blood that occurs in embodiments of the invention is achieved in part by the trans membrane pressure (TMP) caused by the alternating pulsatile pumping action and pressure differential between the blood within the lumen membranes and the dialysate outside of the lumen fiber membranes.
The dialysate fluid exits the dialyzer 152 and flows through a sixth pressure sensor or transducer 166. The pressure transducer 166 sends a signal to the microcontroller 108 indicating the pressure of the dialysate exiting the dialyzer 152. The sensed pressure may help to indicate a clogged dialyzer, a dialysate leak or other emergency condition.
The dialysate circuit 134 moves the now used dialysate from the output of the dialyzer 152 past the pressure transducer 166 and toward the dialysate filter section 122. The used dialysate in this portion of the dialysate circuit 134 contains toxins, contaminants and other undesirable substances that have been removed from the blood of a patient. The filtration section 122 filters or reacts with the predetermined substances in the used dialysate in order to recycle the dialysate for continued re-circulation and use in the dialysate circuit. Some compounds or substances that are considered toxins or contaminants in the used dialysate are urea, creatinine, and ammonia, along with other various substances that are ordinarily removed by a patient's kidney.
In an exemplary embodiment a first filter 168 in the filtration section 122 contains urease. The urease is used to filter the used dialysate and further functions to break down urea that was removed from the blood in the dialyzer 152. When urease breaks down, urea, at least two unwanted byproducts are created. Generally, the two byproducts of broken-down urea are ammonium (ammonia) and carbon dioxide.
The dialysate with the ammonia and carbon dioxide exit the first filter 168. The urea is substantially removed from the dialysate, but the ammonia and carbon dioxide need to be removed from the dialysate also. The dialysate, ammonia, and carbon dioxide enter the second filter 170. The second filter 170 contains a compound zirconium or zirconium phosphate (i.e., ZrPx). The zirconium in the second filter 170 captures the ammonia. It is understood by those having ordinary skill in the art of dialysis chemistry that various chemicals and derivations thereof can be utilized to achieve the same or similar results.
The zirconium or second filter 170 will eventually become saturated with ammonia. When saturated or near saturation, the zirconium filter 170 will become less efficient at removing ammonia from the dialysate. It is not advantageous to allow ammonia or ammonium to circulate through the dialysate circuit and back to the dialyzer. Thus, in an exemplary wearable or portable CRRT device 100, a sensor 176 is placed in the dialysate circuit after the zirconium filter 170 in order to sense the presence of ammonia in the dialysate. The sensor 176 may be a pH sensor, an ammonia specific sensor, or a conductivity sensor. Various probe and electromagnetic style sensors may be used herein to sense conductivity pH or the amount of ammonia in the dialysate after flowing through the zirconium filter. If an ammonia sensor is used, it will sense whether a predetermined amount of ammonia is present in the dialysate. If a pH sensor is used, it would sense whether the pH of the dialysate has become a predetermined amount more alkaline than an acceptable amount, i.e., the alkalinity of the dialysate is outside of an acceptable range of alkalinity. As more ammonia is present in the dialysate, the dialysate becomes more alkaline. It is noted that depending on the actual chemicals and absorbents used in the filters, the dialysate may become more acidic and as such a sensor would be used to sense the same. If a conductivity sensor is used, it would sense the conductivity changes of the dialysate. If the conductivity of the dialysate is outside of a predetermined range then it could be determined that ammonia is increasing in the dialysate. An electromagnetic sensor may also be used to sense the conductivity across the dialysate in a manner that would sense a changing conductivity (i.e., ammonia) within the dialysate.
The sensor 176 is in electrical communication with the microcontroller 108. If the signal provided by the sensor 176 to the microcontroller 108 indicates that ammonia within the dialysate exceeds a predetermined amount (i.e., the pH or conductivity are outside a predetermined range), then the microcontroller may conclude that the zirconium filter 170 is not absorbing a majority of or a predetermined percentage of the ammonia in the dialysate flow there through. As a result, an alarm condition may be triggered by the microcontroller 108. The alarm condition may instruct the user that one or more of the filter cartridges for filter sections in the filtration section 122 require replacement. The alarm condition may also decrease the pumping rate or flow rate of one or both channels of the pulsatile pump 124. Slowing the pump rate of the dual channel pulsatile pump 124 may increase, the amount of ammonia absorbed by the zirconium filter 170 due to a decreased flow rate of the dialysate there through. Furthermore, the alarm condition may decrease the dialysate flow rate and increase or decrease the blood flow rate through an exemplary wearable or portable CRRT device 100 by adjusting the position or motion of the pressing means 130.
The sensor 176 that is used to sense the presence of ammonia in the dialysate should be placed after the second filter 170 containing the zirconium phosphate. In other embodiments, the sensor 176 may be placed after the third filter 174, which contains hydrous zirconium oxide or after the fourth filter 178, which contains carbon. In other embodiments of the invention, a single filter may be used containing layers or a mixture of the contents of the four filters discussed above. Furthermore, a parallel filter 172 may be placed in parallel with another filter, for example filter 168, in order to decrease the pressure drop across one or more filters in the filtration section 122. Both filters that are in parallel (i.e., 172 and 176) may each be layered filters with various filtration and adsorbent substances therein. Furthermore, the layers may be mixed, for example, carbon particles may be mixed throughout the entire filter among the layers of urease and zirconium or zirconium phosphate. Furthermore, the zirconium and zirconium phosphate may be mixed together within one or more filters. All in all, the filtration section 122 of an exemplary embodiment may comprise one or more filter cartridges or filters that react with or adsorb substances found in the used dialysate such that the dialysate will be renewed for continued circulation and usage in the dialysate circuit 134.
The third exemplary filter 174 comprises hydrous zirconium oxide, which may further remove contaminants and ammonia from the dialysate. A bubbler, degasser, valve device, or hydrophilic membrane (“degasser”) 180 may be part of each of the filters or filtered portions or be a separate element there from. A degasser 180 is used in an exemplary embodiment to remove air, carbon dioxide and other gas bubbles that may form or be found in the dialysate circuit 134. It is important that a very limited amount of gas bubbles go through the dialyzer 152. As such, a degasser 180 should be positioned prior to the dialysate pump portion of the pulsatile pump 124 and after one or more of the filtration filters in the filtration section 122 with respect to the dialysate flow direction in the dialysate circuit 134.
A fourth exemplary filter 178 contains carbon and is used to further clean the dialysate of impurities via adsorption. The first, second, third and fourth filter sections 168, 170, 174, 178, may be designed as combinational or separate filter sections. Each cartridge can be inserted and removed from an exemplary wearable portable CRRT device 100 by the patient, doctor, technician, or nurse. Each filter cartridge may contain layers or combinations of chemicals or adsorbents. In fact, an exemplary embodiment may have a single cartridge filter containing layers of required substances to clean and refresh the dialysate after passing through the dialyzer 152. The cartridges may be installed in a series, a parallel or a combination of a series and parallel formation. Furthermore, the filter cartridge or cartridges may incorporate a degasser 180 thereon or such a degasser may be separate element downstream from one or more of the dialysate filters or the dialysate filter section 122.
The filter section or individual filter cartridges require replacement at intervals ranging from about twelve hours to forty-eight hours. Through experimentation, if the total volume of all of the combinations of all the sorbent materials needed, in necessary quantities, combined, will be between 400 cm3 and 2,500 cm3 and will not require changing or replacement for 24 to 48 hours while the embodiment is pumping dialysate at a flow rate of about 20 to 70 ml/min.
An additive reservoir 182 and micropump 184 may be connected to the dialysate circuit 134 after the filtration section 122, but before the dialysate input side 133b. Although not specifically shown in
In various exemplary wearable or portable CRRT devices 100, ultrafiltrate or other fluids may be removed from the patient's blood in addition the dialysis process. If a patient's kidneys are not functioning properly, it may be important to remove excess fluids from the patient's blood as well as blood contaminants such as urea and creatinine. In the dialysate circuit between where the dialysate exits the dialyzer 152 and enters the filtration section 122 of various exemplary embodiments, ultrafiltrate/dialysate, along with other contaminants and fluids obtained via the dialyzer 152, can be tapped off or removed from the dialysate circuit 134. The ultrafiltrate 188 may be deposited in a bladder or reservoir 190. The bladder or reservoir 190 may be contained within or hang below an exemplary wearable or portable CRRT device 100 and be able to store from about 0.1 to perhaps 2 liters of ultrafiltrate fluid. A fullness sensor associated with the fluid bladder 190 is in electrical communication with the microcontroller 108 to enable an alarm condition or fluid fullness reading in the ultrafiltrate bladder 190 when the bladder fullness reaches a certain level or volume. The fluid bladder 190 may also be incorporated into the wearable or portable CRRT device 100 as an empty cartridge that is filled via a micropump and valve combination (not specifically shown). A fullness sensor 200 may aid the microcontroller to determine the fullness of the cartridge bladder 190 and may turn off the ultrafiltrate supplying pump and provide a signal to the user that the cartridge needs emptying. In various embodiments, the fluid bladder or cartridge 190 may contain an absorbent material (also not specifically shown) for absorbing fluid present in the bladder and to prevent sloshing. The absorbent material may be cotton, polymer, sponge, a compressed material, powder, a gel, or other material that absorbs fluid and/or limits the sloshing in the bladder or cartridge. The bladder may be designed to expand as it fills. The bladder may press against the micro switch (not specifically shown) when it is full or expanded thereby providing a fullness signal to the microprocessor 108.
In some embodiments, the ultrafiltrate cartridge or bladder 190 may incorporate a means for emptying the fluid bladder 202 thereon in the form of a cap, stopper, valve, removable inner bladder tubing or otherwise.
Exemplary embodiments of a wearable or portable CRRT device 100 can provide therapy to a patient that incorporates basic dialysis, a complex dialysis regime, ultrafiltration and various medicinal therapies to and for patient. As discussed, there continues to be a growing body of literature indicating that increasing dialysis time, which incorporates both longer and more frequent dialysis treatments, may be associated with improved outcomes and treatment of End Stage Renal Disease (ESRD) patients, both in terms of life expectancy as well as expected morbidity and mortality.
During experimentation with embodiments of the present invention, there were concerns related to continuous and consistent solute transport across the membranes of the hollow fibers within the dialyzer 152 for the extended 24 hour periods of time. Furthermore, additional concerns related to potential clotting or clogging of the individual fiber membranes in the dialyzer 152 that would limit the lifespan and usefulness of the dialyzer 152 for less than twenty-four to forty-eight hours. Different types of pumps including roller pumps, centrifuge pumps and pulsatile pumps were used as a pumping mechanism for the blood circuits and dialysate circuits of various embodiments. The different types of pumps all operated and produced a working portable or wearable CRRT device, but the embodiments that incorporated a dual channel pulsatile pump wherein the dialysate circuit 134 and the blood circuit 132 were being alternatively pumped in a pulsatile fashion at or about 180 degrees out of phase provided some unexpected, positive results. It was found that the clearance levels of blood toxins across the hollow fiber membrane dialyzer is higher when an alternating, out of phase dual channel pulsatile pump was used with respect to in phase pulsatile pumps or pumps, such as roller pumps and centrifuge pumps were used and which, did not provide as large a pressure differential across the dialyzer's membranes between the dialysate circuit and the blood circuit. Furthermore, unexpectedly the use of the pulsatile pump decreased clogging of the hollow fiber dialyzer membranes due to protein buildup or up, clotting or other fluid-flow inhibitors in experimental devices over experimental configurations that did not incorporate the pulsed pumping provided by a pulsatile pump in both the blood and dialysate circuits.
The mechanisms of solute transport across the membrane of a hollow fiber dialyzer have been studied for more than half a century. Historically, it appears that pioneers of dialytic therapy were well aware of the diffusion phenomena when they designed dialyzers based on counter-current mass exchangers. It was soon realized that convection also played a role as a mechanism in ultrafiltration and “the solvent drag” phenomena. The factors influencing solute transport across semi-permeable membranes have been summarized in various papers including Ronco et al., “Evolution of Synthetic Membranes for Blood Purification,” Nephrol Dial Transplant (2003) 18 [Suppl 7]: vii 10-vii 20. In short, blood flow rates greatly affect the clearance of small solutes such as urea, but larger solutes are affected mainly by ultrafiltration rates.
In the past a push-pull hemodiafiltration (HDF) device provided a rapid forward and backward filtration through a dialyzer. This HDF mechanism led to alternating the flow of body fluid and dialysate across a high flux hollow fiber membrane. Although this technique worked, it had various drawbacks. One of the main drawbacks of conventional push-pull HDF devices are the necessity of a disposable blood reservoir bag that was required to prevent flow variation, as well as the difficulty of maintaining a trans-membrane pressure (TMP) across the hollow fiber membranes that would not lead to a collapse of the hollow fibers during back-filtration. One remedy to these push-pull HDF device problems has been to use volume controllers for ultrafiltrate removal and rigid synthetic hollow fibers made out of polyacrylonitrile, polysulfone, and polyamide.
An exemplary wearable or portable artificial kidney or CRRT device 100, as shown in
The basic elements of an exemplary wearable or portable CRRT device, as shown in
It is well known that conventional hemodialysis devices use quasi-steady counter flows of blood and dialysate in a dialyzer. It was believed that such a steady counter-flow of liquids across the hollow fiber membrane in a dialyzer may contribute or be responsible for greater or increased performance in various dialyzers. Using embodiments of the present invention, a study was performed to compare the impact of a pulsatile flow in the transport of solutes in a high flux dialyzer compared with steady or quasi-steady counter flows in a substantially identical high flux dialyzer. Comparative experimental studies and numerical investigations were deployed to clarify and verify the roll of parameters influencing the transport phenomena across a dialyzer's membrane when counter-phased pulsatile flow is used in both blood and dialysate circuits of an exemplary portable or wearable CRRT device as compared to using the same CRRT device with a standard power hungry roller pump commercially used in dialysis equipment. It should be noted that the flow generated by a commercial roller pump somewhat resembles pulsation of either blood or dialysate provided by a pulsatile pump but with a significantly-lower amplitude. The following equations have been adopted to assess the clearance and standard weekly urea Kt/V as measures for evaluating the solute removal efficiency of a high flux dialyzer in the comparative investigations.
Equation 1a can be applied to both the blood side and dialysate compartments of an exemplary dialyzer. Equation 1b accounts for the effects of solute distribution volume in blood, in interstitial space and recirculation.
The comparison study was performed to provide data that explains the enhanced clearances provided by a dual channel pulsatile pump in an exemplary wearable or portable CRRT device. The experiments and comparison study provided support for the hypothesis that the enhanced clearances of exemplary pulsatile pumped devices are due to counter-phased pulsatile blood and dialysate flows generated by the pulsatile pump(s) along with pulse created washing out effects established by the time-dependent flow inside the hollow fibers of the dialyzer. Such washing-out effects prohibit near-wall accumulation of large molecules. The large molecules may include proteins and other large substances that may be found in a patient's bloodstream but do not readily pass through the fiber membranes into the dialysate.
Referring now to
Referring to both
Referring to
The dialyzer 152 may comprise fibers having from 0.2 to about 1 m2 in membrane surface area about the hollow membrane lumens.
Referring now to
The dialyzer 152 contained approximately 4,500 lumen membranes each having a length L 210 of about 15 cm.
For the standard or roller pump configurations, pumping rates were made similar to the pulsatile pump rates provided in the dual pulsatile pump embodiment such that the blood and dialysate flow rates in the configuration of
Comparisons of the input and output pressures of the dialyzer's dialysate inputs and outputs as well as the blood inputs and outputs were compared in both experimental configurations. Furthermore, the clearance of toxins and solutes were carefully studied based on samples of dialysate going in and coming out of the dialyzer as well as samples of blood going in and out of the dialyzer.
Unexpected clearance results occurred and were measured in the comparative dialysis configurations using different pumps. In particular, the clearance of the pulsatile pump configuration of
The results of testing configurations using exemplary dual channel pulsatile pump 124 in comparison with two standard roller pumps one for blood 306 and one for the dialysate circuit 308. Flow rates and pressures were sensed at the dialyzer blood input 218 and dialyzer blood output 220. Pressure and flow readings were also sensed at the dialysate input 222 and dialysate output 224. Flow rates were measured using high resolution Doppler ultrasonography and pressures were sensed using micropressure sensors. Results of the testing were divided into two categories; a first category was the ultrafiltration results and the second category was the clearance results. It was determined that the ultrafiltration output of the dialyzer was found to be mathematically proportional to the pressure difference between the blood within the dialyzer lumens and the pressure of the dialysate in the dialysate compartment 216. The measurements were taken during a steady-state operation of an exemplary embodiment; thus, there was a preload pressure in the inlet to an afterload pressure in the outlet from the pumps. The preload was induced by the pump head pressure and the afterload was created by the resistance of the dialysate filtration and absorption section 122 of an exemplary embodiment.
The ultrafiltration characteristics are depicted with additional experimental results in
Looking at
In
Looking at
Referring back to
The experimental results of the clearance levels provided similarly unexpected results via the experimentation. In the experimental setup of the exemplary embodiment using a dual channel pulsatile pump, the dual channel pulsatile pump was operating at a pulsatile rate of about 2 hertz. It is understood that a larger pulse chamber tubular pump chamber or smaller pump chamber would enable a pulsatile pump to operate an oscillation frequency of between about half a hertz to about 4 hertz. Pulsatile pumping at a rate higher than 4 hertz might be damaging to the blood cells in the blood flow, but would probably be acceptable for the dialysate circuit. It is believed that the best pulsed flow rate for the blood and dialysate should be between 1 and 3 hertz such that the liquids flow at rates between about 20 and 100 ml/min.
In the dialysate compartment, the dual channel pulsatile pump establishes a relatively large pulsed negative pressure leading to a large transmembrane pressure (TMP) having a peak of about 140 mmHg, but generally ranging between around 70 and 120 mmHg. A TMP caused by the pulsatile or shuttle pump is more of a general approximation due to the imperfect out of phase or counter-phased pulses of fluids (i.e., blood and dialysate) flowing through the dialyzer and opposing directions. Furthermore, pressure measurements were only made at the inputs and outputs of the dialyzer because the actual TMP across a membrane inside the dialyzer could only be computer modeled.
The ultrafiltration rate in the pulsatile pump embodiment is unexpectedly large relative to the blood flow rate (30-50%). It was determined that in a pulsatile pump configuration, the convection urea transfer is about 31% of the total urea transfer while in the roller pump configuration, the convection urea transfer was only about 17%. It is believed that the larger convection contribution to the urea transfer in the pulsatile configuration is a significant part of the reason why the exemplary pulsatile configuration is a superior configuration for a wearable or portable CRRT or artificial kidney design.
Referring to
Based on detailed studies and numerical investigations, it is determined that the flow of solutes across a dialyzer membrane varies depending upon the pumping mechanism used to move the dialysate and blood through the dialyzer. In particular, it has been determined that the use of a dual channel pulsatile pump configuration, wherein one pumping channel is for dialysate and a second pumping channel is for blood and where the channels are pumped alternately, counter-phased, or 180+/−90 degrees out of phase, provides a superior ultrafiltration function and clearance of solutes from blood with respect to previously used roller pump and centrifuged pump configurations. By use of experimental and numerical processes, the parameters influencing the transport phenomena across the dialyzer membrane, when counter-phased pulsatile flows are used in both the blood and dialysate compartments of the dialyzer, exemplary embodiments provided unexpected superior ultrafiltration and clearance of toxic solutes from the blood over more expensive, heavy and power-inefficient roller and centrifugal pumps configurations. The results of the exemplary dual channel pump configuration have been compared with a configuration using standard roller pumps or centrifuge pumps that are used in conventional dialysis equipment. Even though the flow of dialysate and blood generated by a roller pump flow resembles a pulsatile flow, a lower amplitude flow and pressure is provided by a roller pump and its flow pulse is much longer than its non-flow or zero pressure pulse on the roller pump. Conversely, the pulsatile pump provides a substantially equally divided flow/high pressure pulse and no-flow/low pressure pulse.
The use of an exemplary dual channel pulsatile pump utilizes important, newly uncovered discoveries with respect to flow and pressure behavior of certain fluids, such as blood and dialysate as they pass through a dialyzer. Furthermore, improved clearance is established for urea creatine and potassium thereby allowing the exemplary pump system to operate at a slower rate for longer periods of time and use a mere 3 to 5 watts of energy to operate the pumping. Furthermore, when using an exemplary pulsatile pump configuration with the filtration and absorption section of an exemplary wearable or portable CRRT device substantially twice the TMP (100-140 mmHg) was established across the membrane when compared with the TMP established with a roller pump or centrifocal pump configuration. The reason for the improved TMP in exemplary embodiments is due to the counter-phased pulsatile flow of the blood and dialysate through the dialyzer establishing the difference in pressures between the blood within the fiber lumens and the dialysate chamber of the dialyzer.
Additional advantages of the exemplary dual channel pulsatile configuration for a wearable or portable CRRT device are that the relationship between the amount of ultrafiltration and the TMP is not linear, as previously understood a roller and centrifuge pump configurations. Instead the relationship between ultrafiltration and TMP builds to a nonlinear second order differential equation.
It is important to note that one of the important aspects of the dual channel pulsatile pump configuration is its high efficiency in removing urea, creatine and other solutes from the blood.
A numerical simulation performed in addition to actual experimentation revealed that the enhanced transmembrane transport of an exemplary dual channel pulsatile pump configuration is primarily governed by diffusion across the fiber membranes, but the transmembrane transport is significantly increased over other pumping configurations due to the added convection created by the large, pulsed TMP across the membrane, which was produced by the counter-phased pulsatile pumping of the dialysate and blood circuits. Furthermore, it is believed that the enhanced clearances achieved by exemplary embodiments may be attributed to a washout or push-pull-like effect associated with the pulsatile flows through and along the fiber membrane boundaries. Referring back to
It will be appreciated by those skilled in the art having the benefit of this disclosure that this enhanced clearance in an artificial kidney incorporating a pulsatile pump provides an energy efficient device for performing dialysis. Such an exemplary device can be worn in-total on a patient as a completely wearable dialysis device or it may be incorporated into a portable device that may be carried or pushed (on a cart) by the patient or medical personnel. It should be understood that the drawings and detailed description herein are to be regarded in an illustrative rather than a restrictive manner, and are not intended to be limiting to the particular forms and examples disclosed. On the contrary, included are any further modifications, changes, rearrangements, substitutions, alternatives, design choices, and embodiments apparent to those of ordinary skill in the art, without departing from the spirit and scope hereof, as defined by the following claims. Thus, it is intended that the following claims be interpreted to embrace all such further modifications, changes, rearrangements, substitutions, alternatives, design choices, and embodiments.
This is a divisional of U.S. application Ser. No. 12/977,931, filed Dec. 23, 2010, which issued as U.S. Pat. No. 8,641,655 on Feb. 4, 2014, which is a divisional of U.S. application Ser. No. 11/942,626, filed Nov. 19, 2007, which issued as U.S. Pat. No. 7,871,390 on Jan. 18, 2011, which is a continuation-in-part of U.S. application Ser. No. 10/940,862, filed Sep. 14, 2004, entitled WEARABLE CONTINUOUS RENAL REPLACEMENT THERAPY DEVICE, which issued as U.S. Pat. No. 7,309,323 on Dec. 18, 2007, which is a continuation-in-part of U.S. application Ser. No. 10/085,349, filed Nov. 16, 2001, entitled WEARABLE CONTINUOUS RENAL REPLACEMENT THERAPY DEVICE, which issued as U.S. Pat. No. 6,960,179 on Nov. 1, 2005, all of which are hereby incorporated by reference. Said U.S. application Ser. No. 11/942,626, filed Nov. 19, 2007, also claims priority from U.S. Provisional Application No. 60/866,357, filed Nov. 17, 2006, entitled ENHANCED CLEARANCE IN AN ARTIFICIAL KIDNEY INCORPORATING A PULSATILE PUMP, which is also incorporated herein by reference.
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