Device for establishing the venous inflow to a blood reservoir of an extracorporeal blood circulation system

Information

  • Patent Grant
  • 11844892
  • Patent Number
    11,844,892
  • Date Filed
    Friday, December 17, 2021
    2 years ago
  • Date Issued
    Tuesday, December 19, 2023
    11 months ago
  • Inventors
  • Original Assignees
    • LivaNova Deutschland GmbH
  • Examiners
    • Anderson; Catharine L
    • Chatrathi; Arjuna P
    Agents
    • Seager, Tufte & Wickhem LLP
Abstract
A device for establishing venous inflow to a blood reservoir of an extracorporeal blood circulation system includes a restricting unit for gradually closing a venous inflow line and a vacuum unit for supplying vacuum to the blood reservoir. The device includes a control unit that supplies a first actuating signal to the restricting unit for restricting venous inflow to the blood reservoir and supplies a second actuating signal to the vacuum unit for establishing a degree of vacuum within the blood reservoir.
Description
TECHNICAL FIELD

The invention relates to a device for establishing venous inflow to a blood reservoir in an extracorporeal blood circulation system.


BACKGROUND

An extracorporeal blood circulation system often includes, in addition to other components, a venous inflow line from a patient to a blood reservoir, for example a venous cardiotomy reservoir for blood and/or priming solution, and an arterial inflow line from the reservoir to the patient. In order to convey blood from the patient into the reservoir, the reservoir is located at a lower level than the patient so that drainage can already occur by means of gravity. Using a blood pump, usually a roller pump, the blood is conveyed out of the reservoir through the arterial inflow line and is delivered to the patient.


So that the venous inflow to the reservoir occurs to a sufficient extent, large tube cross-sections are required in the case of pure gravitational drainage, which is problematic in respect of the strain on the patient which is associated with the drainage line. Furthermore, pure gravitational drainage is unfavorable as regards the ability to influence the venous inflow amount since in order to do so, the difference in height between the reservoir and the patient would have to be altered while maintaining the extracorporeal blood circulation.


As is described, for example, in WO 00/44415 A, it has already been proposed to apply a vacuum to the reservoir in order to reduce the cross-section of the drainage line and to be able to influence the venous inflow. In this regard, WO 00/44415 A discloses a vacuum regulator that simplifies management of the vacuum by the user so as to increase patient safety during an operation. The reason for this is that a reliable regulation of the vacuum first of all enables a simple adjustment of the vacuum by a user and thus a simple adjustment of the venous inflow. A reliable regulation of the vacuum also prevents a vacuum which is too high and which presents a danger to the patient, whereby it must be noted that the withdrawal of the blood from the reservoir using the blood pump which arterially supplies the blood to the patient contributes to the creation and/or increase of the vacuum. In WO 00/44415 A, previously known solutions are referred to as being insufficient and an independent device for regulating the vacuum is described, which reliably regulates the vacuum in the reservoir and optionally also reduces it should this be necessary.


When supplying blood from the reservoir to the patient, care must be taken to ensure that no more blood is removed from the reservoir than is present therein or is supplied thereto. The user must therefore make sure that there is a sufficient minimum amount in the reservoir and additionally coordinate the inflow and outflow such that sufficient amounts are built up in the reservoir but are also supplied to the patient since a physiologically sufficient supply of the patient must always be ensured in an extracorporeal blood circulation system. The user may thereby, for example, increase or reduce the delivery rate of the roller pump or he may reduce the line cross-section of the supply line by means of clamping and/or increase it again. In addition, the user must pay attention to the amount of drained blood and suitably adjust the vacuum in the reservoir—even in the aforementioned vacuum regulator. The user must meet this requirement in an environment which furthermore compels him, in all of his actions, to pay attention to the surgical operation supported by the extracorporeal circulation. Overall, the adjustment of the venous inflow amount to the reservoir of an extracorporeal blood circulation system therefore occurs in a stressful working environment, and thus the previous technical solutions for supporting the user in the adjustment of the venous inflow amount to the reservoir must be regarded as sub-optimal.


Against this background, the technical problem to be solved by the invention is to specify a device for establishing the venous inflow to a blood reservoir of an extracorporeal blood circulation system, which further simplifies the management of the extracorporeal blood circulation system for the user.


SUMMARY

A device as according to the invention for establishing the venous inflow to a blood reservoir of an extracorporeal blood circulation system, which includes a venous inflow line from a patient to the reservoir and an arterial inflow line from the reservoir to the patient, further includes, in addition to a restricting unit for gradually closing, in particular clamping, the venous inflow line in order to restrict the venous inflow amount to the reservoir and a vacuum unit for applying a vacuum to the reservoir in order to increase the venous inflow amount to the reservoir, a control means which supplies to the restricting unit a first actuating signal for establishing the degree of closure of the venous inflow line in order to determine the extent of the restriction of the venous inflow amount to the reservoir, and which supplies to the vacuum unit a second actuating signal for establishing the amount of vacuum in the reservoir in order to determine the extent of the increase in the venous inflow amount to the reservoir, and which includes a single operating element for setting of the amount of venous inflow to the reservoir by a user.


By providing a single operating element for setting of the amount of venous inflow to the reservoir by a user, the user is given the opportunity in a simple manner to determine the venous inflow to the reservoir at, above and below a basic value by a single adjustment process. The basic value is set by restricting conveyance in the case of venous inflow amounts below this value and by actively supporting conveyance of the inflow amount, which is otherwise conveyed and defined by gravity, in the case of venous inflow amounts above this value. As a result of the configuration of the control means according to the invention, it is achieved that the device according to the invention appropriately adjusts and regulates the venous inflow. It should be noted that the single operating element described above and in the following is solely for the function of setting the amount of venous inflow to the reservoir by a user. The control means can additionally include further operating elements, such as, for example, an on/off switch, a brightness regulator for optionally provided displays, a selector switch for activating/deactivating an alarm, etc. However, according to some embodiments of the invention, only one single operating element is provided for setting of the amount of venous inflow to the reservoir by a user, said element allowing setting of the venous inflow both at above and below a basic value.


In some embodiments, the control means includes a display device for visual display of a display value corresponding to the amount of venous inflow. By means of this display, an indication of value as regards the venous inflow, the vacuum in the reservoir and/or the amount of blood stored in the reservoir can be displayed to the user.


In some embodiments, the vacuum unit is connected to a vacuum source via a line or alternatively or additionally includes an integrated vacuum source, in particular a pump.


In some embodiments, a vacuum sensor for detecting the vacuum in the reservoir is provided, which is connected to the control means for providing a corresponding measuring signal.


In some embodiments, a level sensor for detecting the level of blood present in the reservoir is provided, which is connected to the control means for providing a corresponding measuring signal.


In some embodiments, an arterial inflow amount sensor for detecting the inflow amount conveyed in the arterial inflow line is provided, which is connected to the control means for providing a corresponding measuring signal.


In some embodiments, the control means generates a third actuating signal which establishes the delivery rate of a blood pump such that the arterial inflow amount can at least be influenced.


In some embodiments, the single operating element is configured for specifying an amount of blood to be stored in a reservoir so that the venous inflow to the reservoir can be set in this manner.


In some embodiments, the vacuum unit includes a safety device which, upon actuation by the control means or if control should fail, interrupts the application of a vacuum to the reservoir and establishes atmospheric pressure in the reservoir.





BRIEF DESCRIPTION OF THE DRAWINGS

The invention will be described in more detail in the following with reference to the drawings, in which:



FIG. 1 shows a view of the basic structure of an extracorporeal blood circulation system having a device according to a first embodiment of the invention;



FIG. 2 shows a view of the basic structure of an extracorporeal blood circulation system having a device according to a second embodiment of the invention;



FIG. 3 shows a view of the basic structure of an extracorporeal blood circulation system having a device according to a third embodiment of the invention; and



FIG. 4 shows a view of the basic structure of an extracorporeal blood circulation system having a device according to a fourth embodiment of the invention.





DETAILED DESCRIPTION

As is shown in FIG. 1 by means of a first embodiment of a device according to the invention, an extracorporeal blood circulation system basically includes, in addition to a reservoir 1, a venous inflow line 2 from a patient P to the reservoir 1 and an arterial inflow line 3 from the reservoir 1 to the patient P. In order to supply blood from the reservoir 1 to the patient P, a pump 9, such as a roller pump or a centrifugal pump, is provided on or in the arterial inflow line 3. As is apparent from FIG. 1, the reservoir 1 is located at a lower level than the patient so that a venous inflow to the reservoir is already possible owing to gravity alone, the extent of which also depends, however, on the cross-section of the tube used in the venous inflow.


In order to restrict the venous inflow to the reservoir 1, the first embodiment of the invention as described herein includes a restricting unit 4, by which the venous inflow line 2 can be gradually closed, for example by clamping or squeezing. For this purpose, the restricting unit 4 includes an electromagnetically, pneumatically or hydraulically-operated clamp which is not shown in detail in FIG. 1. The restricting unit 4 is arranged on the venous inflow line 2 and in some embodiments acts externally on the tube without coming into contact with the blood.


In order to increase the venous inflow to the reservoir 1, the first embodiment of a device according to the invention includes a vacuum unit 5 for applying a vacuum to the reservoir 1. For this purpose, the vacuum unit 5 is connected via a vacuum line 10 to the reservoir 1 which is accordingly designed so as to be pressure-tight. If the vacuum unit 5 is itself not configured for generating the vacuum, for example by integration of a suitable pump, the vacuum unit 5, as is the case in the first embodiment shown in FIG. 1, is connected to a vacuum source via a vacuum source line 11. Suitable vacuum sources are generally available in the form of stationary installations in hospitals where the device according to the invention is primarily used.


According to the invention, the setting of the venous inflow by the user occurs in a simple and comfortable yet also safe manner via a control means 6 which is shown in FIG. 1. The control means 6 supplies to the restricting unit 4, via a first actuation line 4a, a first actuating signal for establishing the degree of closure of the venous supply line 2 in order to carry out restriction of the venous inflow amount to the reservoir. The control means 6 furthermore supplies to the vacuum unit 5, via a second actuation line Sa, a second actuating signal for establishing the amount of vacuum in the reservoir 1 in order to carry out an increase in the venous inflow amount to the reservoir.


According to the invention, the control means 6 includes a single operating element 7 for setting of the amount of venous inflow to the reservoir by a user of the device. Solely by actuating this single operating element 7, the user can set the venous inflow amount to the reservoir 1 and thereby undertake both an increase to beyond the amount which is essentially determined by the gravitational drainage and the cross-section of the tube used on the venous side, as well as a reduction to below this value. The control means 6 according to the invention converts the setting carried out by the user by means of the single operating element 7 into a corresponding actuation of the restricting unit 4 or the vacuum unit 5 so as to thereby cause a reduction of the venous inflow amount by closing (clamping) the venous inflow tube line 2 or an increase in the venous inflow amount by creating a vacuum in the reservoir 1.


As is shown by FIG. 1, the first embodiment includes a pressure sensor 12, which is arranged on or in the reservoir 1 so as to detect the vacuum in the reservoir 1 and provide a corresponding first measuring signal. The measuring signal of the vacuum sensor 12 is supplied via a first measuring signal line 12a to the control means 6, which can carry out regulation of the vacuum taking into account this measuring value.


The control means 6 according to the first embodiment furthermore includes a display 8 which indicates to the user the set venous inflow amount and/or the set vacuum.



FIG. 2 shows a second embodiment of a device according to the invention, which includes all of the aspects of the first embodiment, and thus reference can be made to the description of the first embodiment in connection with FIG. 1 as regards these points. The second embodiment additionally includes a level sensor 13 that detects the level of blood actually present in the reservoir 1 and thus detects the amount of stored blood. The level sensor 13 generates a second measuring signal which is supplied to the control means 6 via a second measuring signal line 13a. With the aid of the second measuring signal, the control means 6 is able to take the amount of blood actually present in the reservoir 1 into account during vacuum regulation so as to increase the vacuum in the reservoir 1 and thus increase the venous inflow to the reservoir 1 if the level of blood in the reservoir 1 sinks below a predetermined limit. The control means 6 according to the second embodiment can furthermore monitor the reaching of a predetermined upper fill level of the reservoir 1 so as to restrict the venous inflow.



FIG. 3 shows a third embodiment of a device according to the invention, which includes all of the aspects of the first embodiment, and thus reference can be made to the description of the first embodiment in connection with FIG. 1 as regards these points. The third embodiment additionally includes an inflow amount sensor 14 that detects the arterial inflow amount and hence the amount of blood which is supplied to the patient P via the arterial inflow line 3 and is thus removed from the reservoir 1. The amount sensor 14 is arranged on the arterial inflow line 3 either downstream, as shown in FIG. 3, or upstream of the pump 9. The amount sensor 14 outputs a third measuring signal that is supplied to the control means 6 via a third measuring signal line 14a. Owing hereto, the control means 6 is able to take the amount of blood removed from the reservoir 1 into consideration during vacuum regulation and configure the venous inflow accordingly. So as to have an influence on the arterial inflow, the control means 6 in the third embodiment can output a third actuating signal to the pump 9 via a third actuation line 9a, by means of which the delivery rate of the pump is adjusted or at least influenced.



FIG. 4 shows a fourth embodiment of a device according to the invention, which includes all of the aspects of the first three embodiments, and thus reference can be made to the description of the first three embodiments in connection with FIGS. 1, 2 and 3 as regards these points. By combining all of the aspects of the embodiments described above, a device for establishing the venous inflow to the reservoir 1 is created, which allows an almost fully automatic control/regulation of the amount of blood stored in the reservoir 1. The reason for this is that via the gradual closure of the venous inflow line and the regulation of the vacuum in the reservoir 1, the control means 6 can set the amount of blood supplied to the reservoir 1, the current amount of which is respectively detected by the level sensor 13. The control means 6 can at the same time detect the arterial inflow amount via the amount sensor 14 and set or influence it by control of the pump 9. Accordingly, the operating element 7 of the control means 6 can also be configured in the fourth embodiment such that the amount of blood stored in the reservoir 1 is set by the user. This design is taken into consideration in FIG. 4 insofar as the actual fill level of the reservoir 1 is also shown on the display 8. On the basis of the specification of the amount of blood by the user and taking into consideration the physiological marginal conditions that ensure supply of the patient, the control means 6 then effects in a fully automatic manner the adjustment of the venous inflow to the reservoir 1 and the arterial outflow from the reservoir 1 of the extracorporeal blood circulation system.


As is shown in FIGS. 1 to 4, the vacuum unit 5 can be equipped in all of the embodiments with a safety device 15 which, upon corresponding actuation by the control means 6 or if control should fail, interrupts the application of a vacuum to the reservoir 1 and establishes atmospheric pressure in the reservoir 1.

Claims
  • 1. A device for establishing venous inflow to a blood reservoir of an extracorporeal blood circulation system including a venous inflow line from a patient to the blood reservoir and an arterial inflow line extending from the blood reservoir to the patient, the device comprising: a restricting unit configured for gradually restricting the venous inflow line in order to restrict a venous inflow amount to the blood reservoir;a vacuum unit configured for applying a vacuum to the blood reservoir in order to increase the venous inflow amount to the blood reservoir;and a control device that includes only one single operating element for setting the venous inflow amount to the blood reservoir, the single operating element having a plurality of operating positions and configured to be manipulated in a single manipulation by a user to establish both a degree of restriction of the venous inflow line and an amount of vacuum in the blood reservoir for venous inflow to the blood reservoir at, above or below a basic value established by gravitational conveyance.
  • 2. The device of claim 1, wherein the control device is configured to control the venous inflow to the blood reservoir and the amount of vacuum in the blood reservoir without the use of a blood level sensor and blood level signals.
  • 3. The device of claim 1, further comprising a level sensor configured to detect a level of blood in the blood reservoir.
  • 4. The device of claim 1, further comprising an inflow amount sensor configured to detect an amount of arterial inflow supplied to the patient.
  • 5. The device of claim 1, wherein the control device further comprises a display device for visual display of a display value corresponding to the venous inflow amount.
  • 6. The device of claim 1, wherein the vacuum unit is connected to a vacuum source via a line.
  • 7. The device of claim 1, wherein the vacuum unit comprises an integrated vacuum source.
  • 8. The device of claim 1, further comprising a vacuum sensor for detecting the vacuum in the blood reservoir, the vacuum sensor connected to the control device for providing a first measuring signal.
  • 9. The device of claim 1, further comprising a blood pump disposed along the arterial inflow line, to which an actuating signal corresponding to a delivery rate of the blood pump established by the user is supplied by the control device to the blood pump, wherein the delivery rate controls a rate at which blood is pumped from the blood reservoir to the patient.
  • 10. The device of claim 1, wherein at each operating position of the plurality of operating positions, the control device is configured to supply a different combination of a restricting unit setting that corresponds to the operating position to the restricting unit for establishing the degree of restriction of the venous inflow line to define an extent of a restriction of the venous inflow amount to the blood reservoir based on a manipulation of the single operating element in the single manipulation, and a vacuum unit setting that corresponds to the operating position to the vacuum unit for establishing the amount of vacuum in the blood reservoir to define an extent of the increase in the venous inflow amount to the blood reservoir based on the manipulation of the single operating element in the single manipulation.
  • 11. A device for establishing venous inflow to a blood reservoir of an extracorporeal blood circulation system including a venous inflow line from a patient to the blood reservoir and an arterial inflow line extending from the blood reservoir to the patient, the device comprising: a restricting unit configured for gradually restricting the venous inflow line in order to restrict a venous inflow amount to the blood reservoir;a vacuum unit configured for applying a vacuum to the blood reservoir in order to increase the venous inflow amount to the blood reservoir;a control device that includes only one single operating element for setting the venous inflow amount to the blood reservoir, the single operating element having a plurality of operating positions and configured to be manipulated in a single manipulation by a user to establish both a degree of restriction of the venous inflow line and an amount of vacuum in the blood reservoir for venous inflow to the blood reservoir at, above or below a basic value established by gravitational conveyance; anda blood pump disposed along the arterial inflow line, to which an actuating signal corresponding to a delivery rate of the blood pump established by the user is supplied by the control device to the blood pump, wherein the delivery rate controls a rate at which blood is pumped from the blood reservoir to the patient.
  • 12. The device of claim 11, further comprising an inflow amount sensor configured to detect an amount of arterial inflow supplied to the patient.
  • 13. The device of claim 11, wherein the control device further comprises a display device for visual display of a display value corresponding to the venous inflow amount.
  • 14. The device of claim 11, wherein the vacuum unit is connected to a vacuum source via a line.
  • 15. The device of claim 14, wherein the vacuum unit comprises an integrated vacuum source.
  • 16. The device of claim 11, further comprising a vacuum sensor for detecting the vacuum in the blood reservoir, the vacuum sensor connected to the control device for providing a first measuring signal.
  • 17. The device of claim 11, wherein the control device is configured to control the venous inflow to the blood reservoir and the amount of vacuum in the blood reservoir without the use of a blood level sensor and blood level signals.
  • 18. The device of claim 11, further comprising a level sensor configured to detect a level of blood in the blood reservoir.
  • 19. The device of claim 11, wherein the vacuum unit further comprises a safety device configured such that, upon actuation by the control device or upon failure of the control device, an application of the vacuum to the blood reservoir is interrupted which establishes atmospheric pressure in the blood reservoir.
  • 20. A device for establishing venous inflow to a blood reservoir of an extracorporeal blood circulation system including a venous inflow line from a patient to the blood reservoir and an arterial inflow line extending from the blood reservoir to the patient, the device comprising: a restricting unit configured for gradually restricting the venous inflow line in order to restrict a venous inflow amount to the blood reservoir;a vacuum unit configured for applying a vacuum to the blood reservoir in order to increase the venous inflow amount to the blood reservoir;a control device that includes only one single operating element for setting the venous inflow amount to the blood reservoir, the single operating element having a plurality of operating positions and configured to be manipulated in a single manipulation by a user to establish both a degree of restriction of the venous inflow line and an amount of vacuum in the blood reservoir for venous inflow to the blood reservoir at, above or below a basic value established by gravitational conveyance; anda safety device configured such that, upon actuation by the control device or upon failure of the control device, an application of the vacuum to the blood reservoir is interrupted which establishes atmospheric pressure in the blood reservoir.
Priority Claims (1)
Number Date Country Kind
102009026592.9 May 2009 DE national
CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No. 16/180,870, filed Nov. 5, 2018, which is a division of U.S. application Ser. No. 13/322,844, filed Feb. 7, 2012, which is a National Phase Application of PCT/EP2010/055522, filed pursuant to 35 U.S.C. § 371, which claims priority to DE 102009026592.9, filed May 29, 2009, the entirety of which are incorporated herein by reference.

US Referenced Citations (178)
Number Name Date Kind
3551072 Zimmerly Dec 1970 A
3588589 Vonk et al. Jun 1971 A
3588859 Petree Jun 1971 A
3851181 Heule Nov 1974 A
3927980 Eonard Dec 1975 A
4006745 Sorenson et al. Feb 1977 A
4170765 Austin et al. Oct 1979 A
4177649 Venema Dec 1979 A
4193004 Anderson et al. Mar 1980 A
4275726 Schael Jun 1981 A
4309871 Venema Jan 1982 A
4374088 Stenberg et al. Feb 1983 A
4464164 Troutner Aug 1984 A
4466804 Hino Aug 1984 A
4490331 Steg, Jr. Dec 1984 A
4518318 Jensen et al. May 1985 A
4530696 Bisera et al. Jul 1985 A
4599093 Steg, Jr. Jul 1986 A
4602344 Ferretti et al. Jul 1986 A
4642089 Zupkas et al. Feb 1987 A
4664682 Monzen May 1987 A
4678404 Lorett et al. Jul 1987 A
4701101 Sapoff Oct 1987 A
4705497 Shitaokoshi et al. Nov 1987 A
4782451 Mazzarella et al. Nov 1988 A
4828543 Weiss et al. May 1989 A
4846800 Ouriel et al. Jul 1989 A
4876066 Bringham et al. Oct 1989 A
4955874 Farrar et al. Sep 1990 A
4984462 Hass et al. Jan 1991 A
4991433 Warnaka et al. Feb 1991 A
5039430 Corey, Jr. Aug 1991 A
5039482 Panzani et al. Aug 1991 A
5043707 Heinze Aug 1991 A
5049146 Bringham et al. Sep 1991 A
5055198 Shettigar Oct 1991 A
5060512 Kanashige et al. Oct 1991 A
5061236 Sutherland et al. Oct 1991 A
5078677 Gentelia et al. Jan 1992 A
5110549 Gordon May 1992 A
5112480 Hukasawa May 1992 A
5120303 Hombrouckx Jun 1992 A
5135485 Cohen et al. Aug 1992 A
5147187 Ito et al. Sep 1992 A
5149318 Lindsay Sep 1992 A
5158533 Strauss et al. Oct 1992 A
5178603 Prince Jan 1993 A
5186431 Tamari Feb 1993 A
5215519 Shettigar Jun 1993 A
5226265 Kelly et al. Jul 1993 A
5240380 Mabe Aug 1993 A
5266265 Raible Nov 1993 A
5270005 Raible Dec 1993 A
5282783 Lindsay Feb 1994 A
5303585 Lichte Apr 1994 A
5304164 Lindsay Apr 1994 A
5318510 Cathcart Jun 1994 A
5399074 Nose et al. Mar 1995 A
5403273 Lindsay Apr 1995 A
5411705 Thor et al. May 1995 A
5458566 Derrig et al. Oct 1995 A
5458567 Cathcart Oct 1995 A
5458579 Chodorow et al. Oct 1995 A
5563490 Kawaguchi et al. Oct 1996 A
5563584 Rader et al. Oct 1996 A
5586085 Lichte Dec 1996 A
5591399 Goldman et al. Jan 1997 A
5604315 Briefer et al. Feb 1997 A
5619993 Lee Apr 1997 A
5645540 Henniges Jul 1997 A
5667485 Lindsay Sep 1997 A
5725357 Nakazeki et al. Mar 1998 A
5756940 Van et al. May 1998 A
5770073 Bach et al. Jun 1998 A
5775879 Durando Jul 1998 A
5800721 McBride Sep 1998 A
5823045 Van et al. Oct 1998 A
5826576 West Oct 1998 A
5849186 Raneri et al. Dec 1998 A
5928180 Krivitski et al. Jul 1999 A
5955672 Van et al. Sep 1999 A
6017493 Cambron Jan 2000 A
6048363 Nagyszalanczy et al. Apr 2000 A
6123519 Kato et al. Sep 2000 A
6146411 Noda et al. Nov 2000 A
6164325 Braun Dec 2000 A
6287270 Fini Sep 2001 B1
6337049 Tamari Jan 2002 B1
6345214 Dulphy-Vigor et al. Feb 2002 B1
6475176 Fini Nov 2002 B2
6542848 Neeser et al. Apr 2003 B1
6562012 Brown et al. May 2003 B1
6564627 Sabini et al. May 2003 B1
6592340 Horo et al. Jul 2003 B1
6631639 Dam et al. Oct 2003 B1
6652495 Walker Nov 2003 B1
6694570 Chen Feb 2004 B2
6770048 Fini Aug 2004 B2
6931926 Van Ee Aug 2005 B1
7072769 Fletcher-Haynes et al. Jul 2006 B2
7147614 Fini Dec 2006 B2
7591812 Tamari Sep 2009 B1
7694570 Dam et al. Apr 2010 B1
7982612 Braun Jul 2011 B2
8105265 Demers et al. Jan 2012 B2
8394321 Franzoni et al. Mar 2013 B2
8409124 Steffens et al. Apr 2013 B2
8500673 Zanotti et al. Aug 2013 B2
8506513 Rossi et al. Aug 2013 B2
8734376 Simpson et al. May 2014 B2
9011769 Silvestri et al. Apr 2015 B2
10213541 Silvestri et al. Feb 2019 B2
10458833 Rossi Oct 2019 B2
11229729 Knott Jan 2022 B2
20010013822 Nazarian et al. Aug 2001 A1
20010050256 Krivitski Dec 2001 A1
20020032399 Fini Mar 2002 A1
20020033181 Groth et al. Mar 2002 A1
20020038392 De La Huerga Mar 2002 A1
20020085952 Ellingboe et al. Jul 2002 A1
20020094300 Yokoyama et al. Jul 2002 A1
20020128582 Farrell et al. Sep 2002 A1
20020133066 Miller et al. Sep 2002 A1
20030033871 Carroll et al. Feb 2003 A1
20030035730 Schob Feb 2003 A1
20030045772 Reich et al. Mar 2003 A1
20030139643 Smith et al. Jul 2003 A1
20030144646 Se et al. Jul 2003 A1
20030163078 Fallen et al. Aug 2003 A1
20030175151 Ghelli et al. Sep 2003 A1
20040047737 Nose et al. Mar 2004 A1
20040064292 Beck et al. Apr 2004 A1
20040152944 Medvedev et al. Aug 2004 A1
20050025630 Ayre et al. Feb 2005 A1
20050119600 Ucke et al. Jun 2005 A1
20050230313 O'Mahony et al. Oct 2005 A1
20060015056 Ellingboe et al. Jan 2006 A1
20060089695 Bolea et al. Apr 2006 A1
20060092360 Hong May 2006 A1
20060122558 Sherman et al. Jun 2006 A1
20060150596 Takahashi et al. Jul 2006 A1
20060167400 Ellingboe et al. Jul 2006 A1
20060226087 Robinson et al. Oct 2006 A1
20060260392 Hedrick Nov 2006 A1
20060277269 Dent et al. Dec 2006 A1
20070017518 Farrugia et al. Jan 2007 A1
20070110612 Ito May 2007 A1
20070142923 Ayre et al. Jun 2007 A1
20070194981 Hagg et al. Aug 2007 A1
20070209662 Bowen et al. Sep 2007 A1
20080027368 Kollar et al. Jan 2008 A1
20080078382 LeMahieu et al. Apr 2008 A1
20080171960 Brieske et al. Jul 2008 A1
20080245530 Kuzmichev Oct 2008 A1
20080275377 Paolini et al. Nov 2008 A1
20090012443 Ghelli et al. Jan 2009 A1
20090099498 Demers et al. Apr 2009 A1
20090149950 Wampler Jun 2009 A1
20100042038 Urdahl et al. Feb 2010 A1
20100140182 Chapman et al. Jun 2010 A1
20100275953 Orue et al. Nov 2010 A1
20100280430 Caleffi et al. Nov 2010 A1
20110098625 Masala et al. Apr 2011 A1
20110257576 Simpson et al. Oct 2011 A1
20110257578 Zanotti et al. Oct 2011 A1
20110257579 Rossi et al. Oct 2011 A1
20120067133 Waldrop et al. Mar 2012 A1
20120130299 Knott et al. May 2012 A1
20120226446 Nelson et al. Sep 2012 A1
20130017119 Silvestri et al. Jan 2013 A1
20130303965 Rossi et al. Nov 2013 A1
20130331758 Meibaum et al. Dec 2013 A1
20140278156 Thompson et al. Sep 2014 A1
20150100253 Austerlitz et al. Apr 2015 A1
20150196703 Silvestri et al. Jul 2015 A1
20150367120 Kusters et al. Dec 2015 A1
20170089746 Rossi Mar 2017 A1
20190167886 Silvestri et al. Jun 2019 A1
Foreign Referenced Citations (79)
Number Date Country
86103696 Jan 1987 CN
1147964 Apr 1997 CN
1197677 Nov 1998 CN
1458851 Nov 2003 CN
2455229 May 1976 DE
2754894 Jun 1979 DE
3935502 May 1991 DE
19840399 Mar 1999 DE
102004040441 Jun 2006 DE
102005001779 Sep 2006 DE
102005029682 Dec 2006 DE
102007026010 Nov 2010 DE
0371173 Jun 1990 EP
0587251 Mar 1994 EP
0472480 Aug 1995 EP
0820775 Jan 1998 EP
0952433 Oct 1999 EP
1053760 Nov 2000 EP
1070509 Jan 2001 EP
0690730 May 2002 EP
1210956 Jun 2002 EP
1003575 Oct 2004 EP
0766974 Sep 2006 EP
2754458 Jul 2014 EP
2435106 Nov 2014 EP
2842584 Mar 2015 EP
2811752 Jan 2002 FR
2009862 Jun 1979 GB
2109934 Jun 1983 GB
S5623960 Mar 1981 JP
S57500411 Mar 1982 JP
S62258671 Nov 1987 JP
H0391352 Sep 1991 JP
H0819602 Jan 1996 JP
H08506982 Jul 1996 JP
H11506701 Jun 1999 JP
2944749 Sep 1999 JP
2000000299 Jan 2000 JP
2001503665 Mar 2001 JP
2001204815 Jul 2001 JP
2001514939 Sep 2001 JP
2001523339 Sep 2001 JP
2002165878 Jun 2002 JP
2002336348 Nov 2002 JP
2003052717 Feb 2003 JP
200312646 May 2003 JP
2005066013 Mar 2005 JP
2006025531 Jan 2006 JP
2006325750 Dec 2006 JP
2007130290 May 2007 JP
2008000597 Jan 2008 JP
2008194386 Aug 2008 JP
2008270595 Nov 2008 JP
2009240428 Oct 2009 JP
2009287593 Dec 2009 JP
2011076394 Apr 2011 JP
9421311 Sep 1994 WO
9624397 Aug 1996 WO
9733672 Sep 1997 WO
9820957 May 1998 WO
9848868 Nov 1998 WO
9908734 Feb 1999 WO
9965413 Dec 1999 WO
0015154 Mar 2000 WO
0044415 Aug 2000 WO
0147442 Jul 2001 WO
0176656 Oct 2001 WO
0239931 May 2002 WO
0239933 May 2002 WO
02095675 Nov 2002 WO
03026724 Apr 2003 WO
2006021295 Mar 2006 WO
20060576650 Jun 2006 WO
2006122282 Nov 2006 WO
2007018513 Feb 2007 WO
2008119993 Oct 2008 WO
2009144522 Dec 2009 WO
2010041604 Apr 2010 WO
2014041604 Mar 2014 WO
Non-Patent Literature Citations (20)
Entry
Catalog of Products, 2009 Terumo Europe Cardiovascular Systems, 142 pages.
Definition of “Cylinder”, downloaded from http:// dictionary reference.com/browse/cylinder, 3 pages, download on Apr. 28, 2014.
European Search Report and Search Opinion Received for EP Application No. 14164506.9, 10 pages, dated Sep. 19, 2014.
European Search Report issued in EP Application No. 1173655, 9 pages, completed Nov. 30, 2011.
Extended European Search Report issued in 14188440.3, 7 pages, dated Jan. 30, 2015.
Fischer, “Betriebsmesstechnik, unveranderte Auflage, VEB Verlag Tecknik,” 3 pages (machine translations: Business measuring technique, unchanged edition), 1986.
Henriksen et al; “Envisioning Patient Safety in the year 2025: Eight Perspectives”, Advances in Patient Safety: New Directions and Alternative Approaches, Agency for Healthcare Research and Quality, vol. 1, Aug. 2008.
International Preliminary Report on Patentability issued in PCT/IB2014/061491 12 pages, dated Dec. 1, 2016.
International Preliminary Report on Patentability received for PCT Patent Application No. PCT/IB2011/051639, 10 pages, dated Nov. 1, 2012.
International Preliminary Report on Patentability received for PCT Patent Application No. PCT/IB2012/053497, 10 pages, dated Jan. 23, 2014.
International Preliminary Report on Patentability, Chapter II, issued in PCT/EP2010/055522, (with translation) 13 pages, dated May 31, 2011.
International Search Report and Written Opinion issued in PCT/EP2010/055522, (with translation) 10 pages, dated Aug. 6, 2010.
International Preliminary Report on Patentability issued in PCT/IB2011/051639, 15 pages, dated Nov. 18, 2011.
International Search Report and Written Opinion issued in PCT/IB2014/061491, 16 pages, dated Mar. 6, 2015.
International Search Report and Written Opinion received for PCT Patent Application No. PCT/IB2012/053497, 12 pages, dated Nov. 15, 2012.
Klonoff, “Designing an Artificial Pancreas to be Compatible with Other Medical Devices”, Journal of Diabetes Science and Technology, vol. 2, No. 5, pp. 741-745, Sep. 2008.
Terumo Europe Cardiovascular Systems, Innovative Products for the Treatment of Cardiovascular Disease, Terumo Europe, 105 pages. 2006.
Van Der Togt, et al; “Electromagnetic Interference From Radio Frequency Identification Inducing Potentially Hazardous Incidents in Critical Care Medical Equipment”, JAMA, vol. 299, No. 24, 7 pages, Jun. 25, 2008.
Weber, “Talking Barcodes that Change our Lives”, BBC News 3 pages, published Apr. 2004.
Wikipedia. “Fullstandmessung” [online]. Retrieved from https://de.wikipedia.org/w/index.php?title=F%C3%BC11standmessung&oldid=69998631, last modified Jan. 30, 2010. English translation retreived from https://en.wikipedia.org/wiki/Level_sensor, Oct. 18, 2016.
Related Publications (1)
Number Date Country
20220105253 A1 Apr 2022 US
Divisions (1)
Number Date Country
Parent 13322844 US
Child 16180870 US
Continuations (1)
Number Date Country
Parent 16180870 Nov 2018 US
Child 17554393 US