MEDICAL PUMP DEVICE FOR CONVEYING A MEDICAL FLUID

Abstract

A pump device for conveying medical fluid includes an elastomeric membrane forming a pump volume. The membrane is elastically expanded in a filling state of the pump volume with medical fluid. The expanded membrane exerts a delivery pressure on the pump volume to deliver medical fluid into a fluid-line system. The pump device also has a throttle device with a channel having an inlet connected to the pump volume and an outlet connectable to the fluid-line system. Delivery of medical fluid through the outlet is finely adjustable to a defined flow rate at the time of manufacture. The throttle device has a first body and a second body. The channel is formed between oppositely arranged surfaces of the bodies. The surfaces are movable relative to each other for fine adjustment of the flow rate at the time of manufacture, so that an effective length of the channel is variable.

Claims

1. A medical pump device for conveying a medical fluid, the medical pump device comprising: an elastomeric membrane, which forms a pump volume for receiving and delivering the medical fluid, wherein the elastomeric membrane is elastically expanded in a filling state of the pump volume at least partially filled with the medical fluid, and wherein, the elastically expanded membrane exerts a delivery pressure on the pump volume in order to deliver the medical fluid into a medical fluid-line system connectable in a fluid-conducting manner to the pump volume, the medical pump device further comprising a throttle device with a channel, wherein the channel has an inlet, which is connected in a fluid-conducting manner to the pump volume, and an outlet, which is connectable in a fluid-conducting manner to the medical fluid-line system, and wherein the channel is designed in such a way that delivery of the medical fluid through the outlet is adjustable to a defined flow rate, wherein the throttle device has at least a first body and a second body, wherein the channel is formed between oppositely arranged surfaces of the first and second bodies, and wherein the surfaces are movable relative to each other for finely adjusting the flow rate in such a way that an effective length of the channel is variable, and wherein the first body has a cylinder bore, and the second body comprises a cylinder, wherein the cylinder is fitted into the cylinder bore, and wherein the channel comprises an at least single-flight helix in a radial direction between the cylinder bore and the cylinder.

2. (canceled)

3. The medical pump device according to claim 1, wherein the channel is designed in the form of an at least double-flight helix with at least a first helical flight and a second helical flight.

4. The medical pump device according to claim 3, wherein the helical flights have mutually opposite winding directions.

5. The medical pump device according to claim 1, wherein the channel is designed by a helical profiling, which is arranged on an inner lateral face of the cylinder bore and/or on an outer lateral face of the cylinder.

6. The medical pump device according to claim 5, wherein the helical profiling is produced by embossing.

7. The medical pump device according to claim 5, wherein the helical profiling has a cross-sectional shape that is chosen from a group of cross-sectional shapes consisting of a rectangle, triangle, circle segment, parabola and trapezoid.

8. The medical pump device according to claim 1, wherein the cylinder and the cylinder bore are joined together with radially elastic pretensioning in such a way that a fluid-tight interference fit is obtained.

9. The medical pump device according to claim 1, wherein the cylinder is made from a dimensionally stable material and the first body has a flexible hose portion that has the cylinder bore.

Description

BRIEF DESCRIPTION OF THE DRAWING FIGURES

[0014] Further advantages and features of the invention will become clear from the following description of preferred exemplary embodiments of the invention, which are explained with reference to the drawings.

[0015] FIG. 1 shows, in a greatly simplified schematic view, an embodiment of a medical pump device according to the invention, which is provided for use in infusion therapy and has a throttle device.

[0016] FIG. 2 shows, in a greatly simplified schematic and partially sectioned detail view, the throttle device of the pump device according to FIG. 1, wherein the throttle device has in particular a second body in the form of a cylinder.

[0017] FIG. 3 shows, in a greatly simplified schematic detail view, a further embodiment of a cylinder for a throttle device according to FIGS. 1 and 2.

[0018] FIG. 4 shows, in a greatly simplified schematic detail view, a further embodiment of a cylinder for a throttle device according to FIGS. 1 and 2.

[0019] FIG. 5 shows different cross-sectional shapes of a channel of the throttle device according to FIGS. 1 and 2, in each case in a greatly simplified and cut-away schematic cross-sectional view.

[0020] FIG. 6 shows, in a view according to FIG. 2, a further embodiment of a throttle device for the pump device according to FIG. 1.

DETAILED DESCRIPTION

[0021] According to FIG. 1, a medical pump device 1 is provided for delivering a medical fluid 4 in the context of outpatient and/or inpatient infusion therapy. The medical pump device 1 can also be designated as an elastomeric infusion pump or a medical elastomeric pump.

[0022] The medical pump device 1 has an elastomeric membrane 2 which forms a pump volume 3 for receiving and delivering the medical fluid 4. In the present case, the medical fluid is a liquid medicament not defined in any more detail. With reference to FIG. 1, the medical pump device 1 is shown in a filling state. In this filling state, the elastomeric membrane 2 is flexibly expanded like a balloon on account of a mechanical action of the medical fluid 4. In FIG. 1, the elastomeric membrane 2 is illustrated with an exaggerated wall thickness for graphic reasons. By contrast, in a state when not filled with the medical fluid 4, the membrane 2 is slack or at any rate less elastically expanded. For filling the pump volume 3 or the membrane 2 with medical fluid 4, a reclosable filling nozzle 5 is provided, which is attached to the membrane 2 in a fluid-tight manner known in principle.

[0023] The elastically expanded elastomeric membrane 2 subjects the pump volume 3 to a delivery pressure p. By means of the delivery pressure p produced in this way, the medical fluid 4 can be delivered through a passage nozzle 6, connected in a way known in principle and in a fluid-conducting manner to the elastomeric membrane 2, from the pump volume 3 into a medical fluid-line system 7 that is connected in a fluid-conducting manner to the pump device 1. In FIG. 1, the medical fluid-line system 7 is only shown in a greatly simplified schematic and partially cut-away dashed-line view. In the present case, the medical fluid-line system is a patient line 7 of a well known central venous catheter, through which the medical fluid 4 can be administered to a patient (not shown in any detail in the drawing). In the present case, starting from the passage nozzle 6, the pump device 1 is connectable in a fluid-conducting manner to the patient line 7 by means of a hose line 8. For this purpose, the hose line 8, at its end directed toward the pump volume 3, is connected non-releasably in the present case to the passage nozzle 6. At its opposite end, the hose line 8 has a fluid connector 9. In the present case, the fluid connector is designed in the form of a well known Luer attachment 9. The Luer attachment 9 is provided for connection to a complementary Luer attachment of the patient line 7. In an embodiment not shown in the drawing, the fluid connector 9 can be designed in the form of an attachment marketed under the federally registered trademark NIRFit®.

[0024] In the present case, the medical pump device 1 is dimensioned in such a way that it can be readily worn on the body by a patient and can be used without an external energy supply, particularly in the context of outpatient therapy. The medical pump device 1 is accordingly light and dimensionally compact, wherein in the present case the pump volume 3 has a nominal size of 400 ml. It goes without saying that the pump volume 3 may also differ from this, for example dimensioned with a nominal size of between 50 ml and 750 ml.

[0025] In particular to rule out overdosing of the medical fluid 4, a suitable throttling of the delivery pressure p is necessary. For this purpose, the medical pump device 1 moreover has a throttle device 10. The throttle device 10 is in the present case arranged outside the pump volume 3 in the region of the hose line 8, but this does not necessarily have to be the case. In an embodiment not shown in detail in the drawing, the throttle device 10 can be integrated for example in the pump volume 3 or the passage nozzle 6. The throttle device 10 has a channel 11, which is shown in a greatly simplified schematic view in FIG. 1. The channel has an inlet 12 and an outlet 13. The inlet 12 is in the present case connected in a fluid-conducting manner to the pump volume 3 via the hose line 8 and the passage nozzle 6. The outlet 13 is in the present case connected in a fluid-conducting manner to the patient line 7 via the hose line 8 and the fluid connector 9.

[0026] In particular, the elastomeric membrane 2 is subject to dimensional tolerances arising from its manufacture. The properties of the material of the elastomeric membrane 2 may also be subject to certain tolerances. These tolerances produce a tolerance-affected delivery pressure p and thus a tolerance-affected delivery of the medical fluid 4. This is undesirable from the medical point of view, since a flow rate F of the medical fluid 4 that can be administered with the medical pump device 1 has to be achieved as exactly as possible. To ensure that this is the case, the channel 11 is designed in such a way that the delivery of the medical fluid 4 through the outlet 13 can be finely adjusted to a defined flow rate F at the time of manufacture. Accordingly, by way of the fine adjustment by means of the channel 11 at the time of manufacture, in particular dimensional or material tolerances of the elastomeric membrane 2 can be compensated. Further structural and functional features of the throttle device 10 can be seen in particular from FIG. 2.

[0027] The throttle device 10 has a first body 14 and a second body 15. The channel 11 is formed between oppositely arranged surfaces 16, 17 of the two bodies 14, 15. A first surface 16 is assigned to the first body 14. A second surface 17 is assigned to the second body 15. To finely adjust the flow rate F and thus effect the above-described tolerance compensation, the two surfaces 16, 17 are movable relative to each other in such a way that an effective length of the channel 11 is variable. The effective length (not defined in any more detail) of the channel 11 runs between the inlet 12 and the outlet 13. The smaller the effective length of the channel 11, the lesser a flow resistance and thus a throttling action on the delivery of the medical fluid 4. The greater the effective length of the channel 11, the greater the flow resistance and thus a throttling action on the delivery of the medical fluid 4. Accordingly, a reduction in the effective length can produce an increase in the flow rate F and, conversely, an increase in the effective length can produce a reduction in the flow rate F for the purpose of the fine adjustment. For the fine adjustment of the flow rate F, the second body 15 is in the present case moved in an axial direction A relative to the first body 14. As can be seen from FIG. 2, this changes the effective length of the channel 11, formed between the surfaces 16, 17, and thus changes the flow resistance of the channel 11. If, starting from the configuration that can be seen in FIG. 2, the second body 15 is moved farther downward in the axial direction A, with respect to the drawing plane of FIG. 2, this produces an increase in the effective length of the channel 11. If the second body 15 is moved upward in the opposite direction for this purpose, this produces a reduction in the effective length of the channel 11. In the present case, provision is made that the above-described adaptation of the effective length, i.e. the fine adjustment, takes place at the time of manufacture and thus in a separate production and/or assembly step. By contrast, an adaptation of the effective length of the channel 11 in a state when the pump device 1 is ready for use is not provided for in the present case.

[0028] In the present case, the first body 14 has a cylinder bore 18, and the second body is designed in the form of a cylinder 15 and fitted into the cylinder bore 18. The channel is designed in the form of an at least single-flight helix 11 in a radial direction R between the cylinder bore 18 and the cylinder 15. The helix 11 can also be designated as a screw or cylindrical spiral. By virtue of this design of the channel 11, a long effective length of the channel 11 can be achieved with a comparatively compact structural volume. Compared to a channel extending for example in a straight line in axial direction A between the inlet 12 and the outlet 13, a comparatively greater effective cross section can be achieved with the same flow resistance and thus with the same throttling action. In this way, it is possible to counteract interface phenomena that may be associated with a very small effective diameter. In particular, by virtue of the design of the channel in the form of the helix 11, it is possible to avoid a delayed onset of the delivery and/or a premature blockage of the delivery on account of said interface phenomena.

[0029] The cylinder bore 18 is designed as a circular cylinder in the present case. Accordingly, the cylinder 15 is a circular cylinder. The helix 11 extends coiling in the circumferential direction with a pitch (not defined in any more detail) relative to the axial direction A over the entire length of the cylinder 15. The helix 11 has a constant pitch in the present case.

[0030] The channel 11 is designed here by means of a helical profiling P, which in the present case is arranged on an outer lateral face M of the cylinder 15. The profiling P has a rectangular cross-sectional shape (FIG. 5a) and is produced by means of embossing. For this purpose, the cylinder 15 is produced from a dimensionally stable material W which can be embossed by means of a method that is well known in the field of production engineering.

[0031] Departing from the cross-sectional shape in the form of a rectangle 19 as can be seen in FIG. 5a), further cross-sectional shapes are alternatively possible and are shown in the further figures FIGS. 5b) to 5e). Thus, the profiling P can alternatively have a cross-sectional shape in the form of a triangle 20, a circle segment 21, a parabola 22 or a trapezoid 23.

[0032] The first body 14 has a flexible hose portion S through which the cylinder bore 18 extends. The cylinder bore 18 is designed to be flexibly resilient at least in the radial direction R. The cylinder 15 is pressed into the cylinder bore 18 under radially elastic pretensioning of the latter, such that a fluid-tight interference fit between the cylinder 15 and the cylinder bore 18 is obtained. This ensures that the medical fluid 4 is delivered in a functionally correct manner along the channel 11 and is not for example forced past the outer circumference of the cylinder 15.

[0033] FIG. 3 shows a further embodiment of a cylinder 15a which can be fitted instead of the cylinder 15 into the cylinder bore 18. The cylinder 15a substantially corresponds to the cylinder 15 in terms of its design features and functional features. To avoid repetition, reference is made to the disclosure in connection with the cylinder 15, which disclosure correspondingly applies for the cylinder 15a. Only the differences between the cylinder 15a and the cylinder 15 are discussed below. In contrast to the cylinder 15, a channel 11a is provided. The channel is designed in the form of a double-flight helix 11a and has a first helical flight 24a and a second helical flight 25a. The first helical flight 24a has a first winding direction (not described in more detail). The second helical flight 25a has a second winding direction (not described in more detail). The two winding directions correspond. In addition, the helical flights 24a, 25a have an identical pitch. By means of the double-flight configuration of the helix 11a, it is possible in particular to counteract an undesired blockage of the channel 11a. For example, if the helical flight 24a is clogged by a foreign body, the medical fluid can still be delivered along the further helical flight 25a, and vice versa.

[0034] FIG. 4 shows a further embodiment of a cylinder 15b. To avoid repetition, reference is again made to the disclosure in connection with the cylinder 15 and the cylinder 15a, each of which disclosures applies correspondingly for the cylinder 15b. Only the differences between the cylinder 15b and the cylinder 15a are discussed below. The cylinder 15b has in turn a channel in the form of a double-flight helix 11b which is designed with a first helical flight 24b and a second helical flight 25b. The helical flights 24b, 25ba have winding directions opposite to each other (not described in more detail). In this way, the helical flights 24b, 25b form points of intersection 26b. The helical flights 24b are thus connected to each other in a fluid-conducting manner.

[0035] FIG. 6 shows a throttle device 10c in a greatly simplified schematic view. The throttle device 10c can be used instead of the throttle device 10 for the medical pump device 1 according to FIG. 1. In terms of its design and function, the throttle device 10c largely corresponds to the throttle device 10. To avoid repetition, reference is therefore made to the disclosure in connection with the throttle device 10, which disclosure applies correspondingly to the throttle device 10c. The throttle device 10c has a channel 11c. The channel is in turn designed in the form of a single-flight helix 11c between a cylinder bore 18c and a cylinder 15c. The cylinder 15c is shown shortened in the axial direction for graphic reasons, in order to better reveal the helix 11c. In contrast to the channel 11, the channel 11c is formed by means of a profiling Pc which is arranged on an inner lateral face I of the cylinder bore 18c. Accordingly, the profiling Pc is embossed into the inner lateral face I. The profiling Pc in the present case has a cross-sectional shape in the form of a circle segment 21 according to FIG. 5c), but this does not necessarily have to be the case. Instead of the circle segment 21, the further cross-sectional shapes according to FIG. 5 or other kinds of cross-sectional shapes can also be provided.