Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
  • A61M1/36—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
  • A61M1/3621—Extra-corporeal blood circuits
  • A61M1/3626—Gas bubble detectors
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M1/00—Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
  • A61M1/36—Other treatment of blood in a by-pass of the natural circulatory system, e.g. temperature adaptation, irradiation ; Extra-corporeal blood circuits
  • A61M1/3621—Extra-corporeal blood circuits
  • A61M1/3627—Degassing devices; Buffer reservoirs; Drip chambers; Blood filters
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01D—SEPARATION
  • B01D19/00—Degasification of liquids
  • B01D19/0042—Degasification of liquids modifying the liquid flow
• • B—PERFORMING OPERATIONS; TRANSPORTING
  • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
  • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
  • B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
  • A61M2206/00—Characteristics of a physical parameter; associated device therefor
  • A61M2206/10—Flow characteristics

Definitions

• the present invention relates to a device for eliminating bubbles of gas from a flow comprising non-Newtonian fluid(s), as well as use. methods, and apparatuses relating to said device. Specifically, the invention relates to air removal in extracorporeal circulation, for instance in dialysis, or infusion therapy with flow infused in venous blood.
• kidney function can be an implication of various diseases, disorders, and trauma situations, and millions of people worldwide rely on renal replacement therapy for their survival.
• Dialysis either through the peritoneal membrane or from the blood (i. e. hemodialysis) is a critical tool in the treatment of patients presenting with acute renal failure, but the technique is equally important for maintenance treatment of patients with chronic kidney diseases of various types and origins. Indications necessitating dialysis include inter alia severe retention of products not wasted by impaired kidneys, for instance urea, creatinine, uric acid, potassium, and phosphate, but also fluid overload, or even acute drug poisoning, to name a few.
• Hemodialysis can be carried out either as an outpatient or as an inpatient therapy, but careful monitoring and surveillance is nevertheless pivotal irrespective of the situation, as numerous side effects and complications, both immediate and long-term, are associated with the procedure. These effects are sometimes dictated by the different types of hemodialysis access methods utilized, but the dialysis procedure per se is also associated with certain inherent risks, normally requiring both staff surveillance and automatic monitoring. Hemodialysis is performed using two separate circuit systems, one circuit carrying the blood from the patient and another carrying dialysis fluid, a solution comprising mineral ions, for removal of waste substances, as well as water, from the blood. The principle behind dialysis is diffusion over a semipermeable membrane, i. e. the dialysis filter, which interconnects the two circuit systems.
• the blood drawn from the patient enters an arterial tube and is subsequently, using a blood pump, flushed into a dialysis filter, where waste products are being removed.
• the cleansed blood is returned to the patient through the venous part of the tubing.
• air is constantly leaking in to the blood flow, either as a result of leakage at the watertight connection sites, or as an implication of air present in the circuit prior to starting the dialysis,
• the apparent insignificance of microbubblcs i. e. bubbles exhibiting sizes around 100 ⁇ m, has been attributed to the collapse and subsequent blood absorption of small bubbles. Additionally, the lungs are considered to function as barriers for bubbles with diameters above 20 ⁇ m, and this paradigm, together with the perceived practical impossibility of preventing microbubble entry, today dictates the industry standards.
• the venous part of the dialysis system is normally arranged with a venous chamber enabling removal of larger amounts of air present within the system, but such a chamber is only effective in separating bubbles of a relatively large size.
• arterial microemboli contribute to the increased prevalence of cerebral atrophy and regression of neurocognitive status, especially in long-term dialysis patients, indicating a significant need for improved devices for separation of microbubbles as well as larger bubbles of air.
• Venous chambers constituting the current art are normally arranged as vertical drip chambers with the inlet at a high point and the outlet at a low point, in order for large bubbles, i. e. bubbles with a buoyancy force overcoming the drag force from the flow, to ascend vertically upwards.
• Modified versions include devices designed so as to promote a circulatory flow in the chamber or devices with various types of geometric appearance, for instance substantially cubic shapes.
• WO 2006/030263 discloses a blood chamber for use in an extracorporeal circuit comprising a blood inlet port, a blood containment chamber, and a first conduit. The chamber is arranged with a relatively large segment for slowing down the blood flow and separate gases from the blood, forming an overlying gaseous zone.
• the venous chambers in the art are constructed to eliminate merely relatively large bubbles, and do not remove microbubbles (i. e. bubbles with sizes under 50-400 ⁇ m) at all.
• many devices provide very blunt tools for gas separation and numerous devices in fact promote air contamination.
• the prior art generally overlook the biological properties of blood, often resulting in coagulation in slow-flowing parts, including filters in connection with stagnant flow or air retention, or corners of the utilized devices, having a negative impact both on the removal of air bubbles but also on the dialysis as such.
• devices of the prior art generally exhibit very complex configurations comprising multiple parts, resulting in manufacturing difficulties and an increased risk of air leakage.
• the object of the present invention to overcome said drawbacks and satisfy existing needs, as well as providing a simple, easily manufactured, and optimized device for efficient separation of gas bubbles, both relatively large bubbles and in particular microbubbles, from an extracorporeal circulation or infusion therapy with flow infused in venous blood. Furthermore, the invention relates to use and methods for removing gas bubbles from a blood flow, as well as apparatuses comprising said device. More specifically, the present invention relates to a device, i.e. a bubble reducer, for eliminating bubbles of gas from a flow comprising non-Newlonian fluid.
• the device is capable of reducing bubbles of various sizes but the fact that it has the capacity to eliminate so called microbubbles from a flow comprising non-Newtonian fluid results in significantly improved properties from a clinical perspective.
• the microbubble reducer may be arranged so that said flow passes not more than one or two other devices prior to entry into a patient, and the microbubble reducer comprises an inlet (10), at a low point, a curved duct means (4).
• said curved duct means comprising a gas outlet (5) at a high point, an outlet (6) at a low point, and a lumen (21) that runs through said inlet (10), said curved duct means (4), said gas outlet (5), and said outlet (6).
• the lumen (21) of the microbubble reducer exhibits an increasing cross-sectional area when running through the inlet (10) towards to curved duct means (4), and, further, the lumen (21) of the inlet (10) is arranged with an angle of between -20° and 75° relative a horizontal plane.
• the microbubble reducer of the present invention also exhibits a complete lack of any sharp angles, corners, or dead spaces (i.e. spaces substantially without flow velocity).
• the fact that the device only exhibits smooth transitions between different parts, as well as the absence of corners, sharp angles, and dead spaces, is conducive for obtaining a laminar flow and for eddy reduction, in order to further enhance the gravity- mediated bubble collection and eliminating areas without flow or with low flow, thereby reducing coagulation.
• the running and/or the passage of the lumen (21) through the inlet (10). through the curved duct means (4), through the gas outlet (5), and through the outlet (6) may be described by at least one continuous function without singularities, i.e. the lumen (21) does not have any sharp angles, corners, or dead spaces where the flow becomes slow, or even substantially motionless and/or stationary.
• the present invention solves the neglected problem of microbubble elimination, and thereby reducing the significant clinical consequences caused by this disregarded but nevertheless decidedly important phenomenon.
• Figure 1 Schematic exemplary illustration of one embodiment of the present invention, displaying an inlet (10) with a continuously increasing cross-sectional area.
• FIG. 1 Schematic exemplary illustration of one embodiment of the present invention, comprising an inlet (10) with three segments (1, 2, 3) ⁇ vith constant but different cross-sectional areas.
• Figure 3 Schematic exemplary illustration of one embodiment of the present invention, with an inlet (10) displaying two initial segments (1, 2) arranged horizontally and a third segment (3) arranged in an inclined fashion.
• FIG. 4 Schematic exemplary illustration of one embodiment of the present invention, having an inlet (10) with three inclining segments (1 , 2, 3) with different cross- sectional areas and with different inclination.
• FIG. 5 Schematic exemplary illustration of one embodiment of the present invention, wherein the microbubble reducer is arranged with components commonly utilized in a dialysis setting.
• Figure 7. Comparative graph of microbubbles/min relative various pump flows for device B and a prototype of the present invention.
• Figure 8. Graph showing how the length of the extension channel (30) influences the removal and/or elimination of microbubbles. A longer extension channel (30) further enhances the bubble separation and removal.
• Figure 9 Graph showing the angle of the inlet (10) influences the removal and/or elimination of microbubbles. An angle of approximately 45° relative a horizontal plane optimizes the the bubble separation and removal.
• Figure 10 Graph defining the angular interval utilized for describing the present invention.
• the arrows indicate the direction of the flow.
• Figure 1 Graph showing the how the number of bubbles decreases with increasing length of the lumen (21) of the inlet (10).
• the length designated on the x-axis i.e. the horizontal axis refers to the length from the start of lumen (21) to the point where the flow turns downwards towards a horizontal plane, measured along the lower rim of the lumen (21 ).
• the present invention is concerned with a device, e. g. a venous chamber, for eliminating, removing, and/or significantly reducing bubbles of gas, with sizes down to 2.5 ⁇ m, from a How comprising non-Newtonian fluid, a method for removing gas from a flow comprising non-Newtonian fluid, a dialysis apparatus arranged with the microbubble reducer of the invention, as well as the use of the microbubble reducer in removal of gas bubbles from a flow comprising non-Newtonian fluid, in particular for hemodialysis applications.
• singularity or “singularity point” shall be understood to pertain to a point where an analytical function is not defined and/or a point where a function is not differentiable (that is, essentially a point where a function stops being well-behaved in some particular way).
• non-Newtonian fluid shall be understood to relate to a fluid with a viscosity that changes with changes in the velocity gradient in the fluid (i.e. the shear rate), which in turn depends on the flow velocity.
• Non-Newtonian fluids may for instance be blood, blood plasma, and blood substitute fluids (artifical blood and/or blood surrogates).
• the definition of the angles in accordance with the present invention i.e. the term “from -20° to 75° relative a horizontal plane” shall be understood to relate to the whole interval from -20° to 75°, including 0° ( Figure 10).
• flow passes not more than one or two other devices prior to entry into a patient is clear and unambiguous for the skilled person and shall be understood to describe that not more than one or two other types of medicine technology devices (for instance a security device, and/or a filter) are placed between the micro bubble reducer of the present invention and a patient that is receiving the flow of non-Newtonian fluid from which the bubbles of gas have been removed, eliminated, and/or reduced using the micro bubble reducer.
• medicine technology devices for instance a security device, and/or a filter
• curved duct means relates to a duct displaying a curved shape, preferably a substantially inverted U with curved point placed at the highest point.
• air " ', "gas”, “gas bubbles”, and ''bubbles " ' shall be understood to relate to undesired gaseous components present in the blood flow.
• horizontal plane refers to any plane substantially parallel to the earth plane
• the term “low point” refers to the lower part of device, below the high point and substantially below, before, or after the curved duct means
• the term '"high point refers to the higher part of the device, on top of or laterally arranged in relation to the curved duct means.
• the direction of the flow may be used to define whether an inclination is rising or falling.
• One aspect of the present invention is concerned with a device, i.e. a micro bubble reducer, for eliminating bubbles of gas from a flow comprising non-Newtonian fluid, preferably a blood flow.
• the device is capable of reducing bubbles of various sizes but the fact that it has the capacity to eliminate so called microbubbles from a flow comprising non-Newtonian fluid results in significantly improved properties from a clinical perspective.
• the microbubblc reducer may be arranged so that said flow passes not more than one or two other devices prior to entry into a patient, and the microbubble reducer comprises an inlet ( 10), at a low point, a curved duct means (4), said curved duct means comprising a gas outlet (5) at a high point, an outlet (6) at a low point, and a lumen (21 ) that runs through said inlet ( 10).
• the lumen (21) of the microbubble reducer exhibits an increasing cross-sectional area when running through the inlet (10) towards to curved duct means (4), and, further, the lumen (21 ) of the inlet (10) is arranged with an angle of between -20° and 75° relative a horizontal plane.
• the increasing cross-sectional area along the inlet (10) towards the curve duct means (4) results in a decreased velocity of the blood flow, mediating ascent and thereby separation of gas bubbles present in the flow.
• the separated gas is removed from the device through a gas outlet (5), before the non-Newtonian fluid is conveyed through the outlet (6) further in the venous direction.
• the non-Newtonian fluid is introduced into the system through an inlet (10).
• the inlet (10) is arranged with an angle -20° to 75° relative a horizontal plane (i.e. including 0°), with the purpose of distributing any gas bubbles present in the non-Newtonian fluid to the upper part of the flow. For bubbles displaying small diameters, this is most easily achieved at a high shear rate when the viscosity of the blood is lower.
• the lumen (21) of the inlet ( 10) of the present invention has an increasing cross-sectional area in the venous direction, i. e. along the flow, with implications such as decreased flow velocity, fluid decompression, and. upon oversaturation, further upward distribution of the gases and/or gas bubbles present.
• the length of the inlet (10), and thereby of the lumen (21), can be modified in order to influence the separation of the gas bubbles, e.g. a longer inlet facilitating ascent of gas bubbles.
• the non- Newtonian flow reaches the curved duct means (4), where gas bubbles are removed through the gas outlet (5), substantially arranged at the high point of the curved duct means (4).
• the upper part of the device, i.e. the curved duct means (4), enables bubble fusion, creating larger bubbles for facilitated removal through the gas outlet (5).
• the gas outlet (5) can be constructed in numerous ways, according to the preferred embodiments of the skilled person.
• the non-Newtonian fluid returns to the patient through the outlet (6).
• the physical characteristics of the device mediate separation of both relatively large bubbles and microbubblcs, reducing the risk of adverse events occurring in patients undergoing renal replacement therapies, plasmapheresis and apheresis, hemoperfusion, plasma filtration, or similar techniques (i. e. extracorporeal blood processing with venous infusion), including infusion therapies.
• the inclination and the expanding cross-sectional area of the lumen (21) of the inlet (10) results in facilitated bubble ascent, and the absence of corners and angles results in a laminar flow without disturbances.
• the resultant force between the blood flow and the buoyant force of the gas bubbles constantly directs the bubbles to the upper surface of the tube, except after the curved duct means (4), resulting in a distinct advantage relative devices currently employed within the art.
• the device is completely devoid of any sharp angles, corners and/or dead space imply significant advantages in terms of reduced disturbance and reduced eddy formation, as well as absence of dead spaces and reduction of slow-flowing fluid, in particular blood, improving separation of bubbles of all sizes, including microbubbles, as well as inhibiting coagulation processes, which are commonly encountered problems associated with numerous other devices for gas separation. Furthermore, the combination of the above features results in a laminar flow for optimized elimination of gas in the non-Newtonian flow.
• the running and/or the passage of the lumen (21) through the inlet (10), through the curved duct means (4), through the gas outlet (5), and through the outlet (6) may be described by at least one continuous function without singularities, i.e. the lumen (21) does not have any sharp angles, corners, or dead spaces where the flow becomes slow, or even substantially motionless and/or stationary.
• the curved duct means (4) is in the form of a substantially inverted U.
• the U chamber is arranged with exclusively smooth transitions in order to further promote a laminar flow without any disturbances.
• the tubing component i.e. the lumen (21 ) and/or (41 ) as per below, of the present invention preferably has a substantially circular cross-sectional area, but other geometrical shapes devoid of sharp angles or corners, for instance ovals, are also within the spirit of the invention.
• an oval lumen/tubing i. e. a lumen/tubing having two different radii
• a vertical radius exceeding its horizontal radius would induce a higher shear rate, a desirable feature at certain blood concentrations.
• the lumen/tubing can display different cross- sectional shapes along for instance the inlet, e. g. an initial oval shape followed by a substantially spherical shape, or vice versa.
• both different segments displaying different cross-sectional shapes and different shapes together with continuous transitions lie within the scope of the present invention.
• the lumen (21 ) of the inlet (10) may have a length of at least 2 cm, of at least 3 centimeter, of at least 4 cm, of at least 5 cm, of at least 10 cm. of at least 15 cm, of at least 20 cm, of at least 25 cm, of at least 30 cm. of at least 35 cm, of at least 40 cm, of at least 45 cm, of at least 50 cm, of at least 55 cm, of at least 60 cm. or of at least 1 m.
• Hgure 11 shows hos the bubble removal increased with increasing length of the lumen (21) of the inlet (10), i.e. the longer the lumen (21) the more efficient is the bubble removal/elimination.
• the microbubble reducer may further comprise an extension channel (30) comprising a lumen (41), wherein said lumen (41) of said extension channel (30) is arranged to empty into and/or transit into the lumen (21) of the inlet (10) (Figure 4).
• the extension channel (30) may have a length of at least 2 cm, of at least 3 centimeter, of at least 4 cm, of at least 5 cm, of at least 10 cm, of at least 15 cm, of at least 20 cm, of at least 25 cm, of at least 30 cm, of at least 35 cm, of at least 40 cm, of at least 45 cm, of at least 50 cm, of at least 55 cm, of at least 60 cm, or of at least 1 m.
• Figure 8 clearly illustrates how the length of the extension channel (30) contributes to enhanced removal and/or elimination of bubbles of different sizes.
• the extension channel (30) may be arranged with an angle of between -20° and 75° relative a horizontal plane, that is including 0° (the extension channel (30) may thus be horizontally arranged), in order to distribute the gas bubbles along the upper part of the flow.
• the distance from the start of the inlet (10) to the highest point of the lumen (21 ) of the curved duct means (4) may be at least 3 centimeter, of at least 4 cm, of at least 5 cm, of at least 10 cm, of at least 15 cm, of at least 20 cm, of at least 25 cm, of at least 30 cm, of at least 35 cm, of at least 40 cm, of at least 45 cm, of at least 50 cm, of at least 55 cm, of at least 60 cm, or of at least 1 m.
• the distance from the start of the inlet (10) to the highest point of the lumen (21 ) of the curved duct means (4) shall be understood to relate to the distance from a central point in a cross-section of the lumen (21) at the start of the inlet (10) to the highest point of the lumen (21) of the curved duct means (4).
• the inlet may have an angle of between 0° to 75° relative a horizontal plane, preferably between 35° and 55°, and most preferably approximately 45° relative a horizontal plane, in order to avoid bubble adherence and instead facilitate upward bubble migration in the microbubble reducer (i. e.
• the inlet (10) may display increasing cross- sectional area towards the curved duct means, either arranged so as to increase in a segment-by-segment (1, 2, and 3 in Figures 2-5) fashion or through continuous expansion ( Figure 1).
• the lumen (21) of the inlet (10) is arranged with at least two segments, wherein each one of said segments has an angle of between -20° and 75° relative horizontal plane, preferably between 0° and 75°, more preferably between 35° to 55°, and most preferably approximately 45° relative a horizontal plane, in order to optimize bubble separation.
• a horizontal arrangement i.e. 0°, also falls within the scope of the present invention.
• Figure 1 represents an embodiment of the present invention with continuously increasing cross- sectional area of the lumen (21) of the inlet (10), where the blood flow enters the microbubble reducer through segment (1) and continues upwards through segment (2) and (3). I he increasing area and the inclination of the inlet relative the horizontal plane facilitate the separation of gas bubbles of all sizes.
• the blood is further conveyed to the curved duct means (4), where gas bubbles are removed through the gas outlet (5), before it is returned to the patient through the outlet (6).
• the segments in figure 1 are naturally primarily for illustrative purposes and shall not be considered as limiting the device, i.e. the microbubble reducer, in any way.
• the lumen (21) of the inlet (10) is not linear but wherein its shape can be described for instance by an exponential function or a logarithm function, or additional shapes mutatis mutandis.
• a lumen (21) of an inlet (10) displaying continuously increasing cross-sectional area has inherent advantages associated with aspects such as ease of manufacture and facilitated post-production modifications.
• Figure 2 represents another embodiment of the invention, where the lumen (21) of the inlet (10) is comprised of three segments with different but constant intra-segment cross-sectional areas, i. e. with the cross-sectional area of segment (1) being smaller than the cross-sectional area of segment (2), which in turn has a smaller cross-sectional area than segment (3).
• the non-Newtonian flow enters the device through segment (1), continues to segment (2) and segment (3) with concomitant reduction in flow velocity for optimized bubble separation, before it enters the curved duct means (4), where gas is removed through the gas outlet (5).
• the blood is returned to the patient through the outlet (6).
• the lumen of segment (1) and segment (2) of the inlet (10) are horizontally arranged, i. c. with an angle of 0° relative a horizontal plane, exhibiting essentially constant intra-segmcnt cross-sectional areas, with segment (2) having a larger cross-sectional area than segment ( 1 ), in order to mediate efficient gas bubble separation.
• the flow rises approximately 45° through segment (3), and subsequently enters the curved duct means (4).
• the curved duct means (4) exhibits a shape closely resembling an inverted U, with the gas outlet (5) placed on the high point of said U shape.
• the blood leaves the device through the outlet (6). which is essentially perpendicularly arranged relative a horizontal plane, and continues in the venous direction.
• the lumen of segment (1 ) of the inlet (10) has a lower angle relative a horizontal plane than the remaining segments of the inlet (10), as well as a smaller cross-sectional area, in order to optimize the gas separation and removal.
• segment (1) has a substantially constant cross-sectional area throughout its length
• segment (2) which has a steeper inclination than segment (1), exhibits an increasing intra-segment cross- sectional area, leading the non-Newtonian flow, notably blood, into segment (3), and subsequently into the curved duct means (4).
• the gas is removed through the gas outlet (5), before the blood flow leaves the device through the outlet (6).
• the microbubble reducer represented by Figure 3 is arranged together with components commonly employed in a dialysis setting.
• the device is arranged together with the holding means (8) of the dialysis apparatus, a venous clamp (9), and a priming detector and/or a bubble detector (6). Further, the device is equipped with additional holding means (11) and (12), in order to increase the safety of the arrangement.
• segmented inlets (10) of certain embodiments of the present invention can optionally be manufactured individually, so as to enable individual modification and even substitution of a specific segment.
• a segmented inlet of the device can be fabricated in one piece, for facilitated manufacture.
• the lumen (21) of the inlet (10), the curved duct means (4), the gas outlet (5), and the outlet (6) may have a cross- sectional area of between 1 mm 2 and 800 mm 2 .
• a first segment of the lumen (21 ) of the inlet (10) may have a cross-sectional area of between 1 mm 2 and 30 mm 2 , preferably approximately 16 mm .
• a second segment of the lumen (21 ) of the inlet (10) may display a cross-sectional area of between 1 mm 2 and 210 mm , preferably approximately 150 mm .
• a third segment of the lumen (21 ) of the inlet (10) has a cross-sectional area of between 1 mm 2 and 275 mm , preferably approximately 200 mm 2 .
• the purpose of the various segments relates to the shear stress the lumen/tubing exerts on the blood flow; accordingly, optimization of the cross-sectional area is critical.
• the lumen (21 ) of the outlet (6) may preferably have a perpendicular arrangement relative a horizontal plane, preferably with a deviation from said perpendicular arrangement with less than 80° in any direction, more preferably with less than 45° in any direction, and most preferably with less than 20° in any direction.
• the preferred arrangement of the outlet (6) pertains inter alia to the usage of the device, and the connections to various types of dialysis machines.
• the microbubble reducer i.e. the lumen (21) and when relevant the lumen (41), may be substantially completely filled with non-Newtonian liquid, notably blood, during the course of operation, in order to optimize the air removal from the blood flow.
• non-Newtonian liquid notably blood
• said device does not require a gaseous zone, resulting in facilitated handling and improved gas removal.
• the operator is intended to use the device filled to the top, with the fluid monitored manually or by the detector at the top, in order to optimize the bubble reduction and to minimize the blood gas/air contact to prevent clotting.
• the microbubble reducer may be arranged with at least one filter.
• Said filter could be arranged anywhere within the device, but preferably in, or close to. the outlet (6), in order to remove potential blood clots.
• the device may be arranged with at least one level detector, selected from the group comprising inter alia an optical detector, an ultrasound detector, and a conductance detector, or a bubble detector on the outlet line after the device.
• the curved duct means (4) or the gas outlet (5) of the device is arranged with means to enable manual fluid level detection or fluid level monitoring with the aid of a monitoring device. Said means facilitate optimized fluid level detection, further improving the handling and safety of the invention.
• the non-Newtonian fluid may be selected from the group comprising blood, blood plasma, blood substitute liquids, plasma proteins, plasma substitutes, blood substitutes, solutions of albumin and/or other plasma proteins, gelatine compositions and haemoglobin crosfumaril, as well as relatively high-viscous liquids such as dextran solutions and hydroxy ethyl starch, etc.
• an additional wall is arranged in the lumen (21 , 41) of the device, in order to increase the shear rate at certain flows and during certain conditions, when this is desirable. Furthermore, including an additional wall may reduce the viscosity of the blood, an interesting feature for instance at low flow rates.
• One aspect of the present invention relates to a method for removing gas from flow comprising non-Newtonian fluid, for instance blood.
• the method comprises the steps of contacting the microbubble reducer with a source of fluid/liquid, transporting the fluid through the lumen (21) of the microbubble reducer, separating any gas present in the non-Newtonian fluid, removing the gas through the gas outlet (5), and, finally, removing the blood through the outlet (6), in order to transfer it back to the patient.
• the gas outlet (5) may be utilized to maintain the flow level as high as possible in the upper part of the curved duct means (4).
• an apparatus comprising the device for eliminating bubbles is connected to a dialysis machine.
• another aspect of the present invention concerns the use of the device for dialysis or substantially similar treatments, obvious to a person skilled in the art. and more specifically, in one embodiment, for hemodialysis.
• a prototype developed based on the present invention was compared to products currently on market, device A and device B.
• a standardized bubble generator was employed to generate bubbles of varying size, including microbubbles, in a solution commonly used as a blood substitute within the dialysis field.
• the utilized solution contains dextran and albumin and has the same viscosity as normal blood.
• the solution was re-circulated from the solution-containing vessel, wherein bubbles had been produced by the bubble generator, into a dialysis tubing system of either device A or device B, or the prototype of the present invention, alternately. Bubbles present downstream of the venous chamber were detected and measured using a IIatteland Instrument (Royken, Norway), as previously described elsewhere. The measurements were performed alternately between the systems for each blood flow measured in order to reduce the risk of uneven bubble distribution and potential bubble variation.

Landscapes

• Health & Medical Sciences (AREA)
• Vascular Medicine (AREA)
• Heart & Thoracic Surgery (AREA)
• Chemical & Material Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Anesthesiology (AREA)
• Biomedical Technology (AREA)
• Hematology (AREA)
• Engineering & Computer Science (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Cardiology (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Organic Chemistry (AREA)
• External Artificial Organs (AREA)

Priority Applications (3)

Applications Claiming Priority (4)

Publications (1)

Family

ID=43411292

Family Applications (1)

Country Status (5)

Cited By (2)

Families Citing this family (8)

Citations (7)

Family Cites Families (2)

• 2010
  • 2010-07-02 WO PCT/SE2010/050764 patent/WO2011002410A1/en not_active Ceased
  • 2010-07-02 EP EP10794463.9A patent/EP2448615B1/en active Active
  • 2010-07-02 IN IN782DEN2012 patent/IN2012DN00782A/en unknown
  • 2010-07-02 US US13/381,569 patent/US8894749B2/en active Active
  • 2010-07-02 SE SE1050729A patent/SE536054C2/sv unknown

Patent Citations (7)

Also Published As

Similar Documents

Legal Events