The present invention relates generally to fluid management systems used during surgical procedures to provide one or more functions associated with irrigation, distention, fluid warming, fluid deficit monitoring, suction, and the like, and more particularly relates to a method and apparatus for continuously measuring the volume of fluid being returned from the surgical site as it is being delivered to a waste collection system.
A fluid management system (FMS) may be used in connection with a wide variety of medical procedures involving one or more fluid delivery functions including, but not limited to: fluid irrigation; distention of a body cavity; fluid warming; fluid deficit monitoring associated with delivery and return of fluid to/from a surgical site; and suction. The medical procedures may be associated with multiple surgical disciplines including, but not limited to: gynecologic, urologic, orthopedic, colorectal, and general surgical procedures.
During certain medical procedures, patient safety may require that the amount of fluid delivered to the surgical site and the amount of fluid returned from the surgical site be continuously monitored to determine the “fluid deficit.” Accordingly, a FMS may be configured to provide a fluid deficit monitoring function to accurately measure fluid inflow (to the surgical site) and outflow (from the surgical site), and to calculate a fluid deficit in order to monitor a patient's fluid absorption level during a medical procedure as excess fluid absorption can result in serious complications. Typically, fluid returning from the surgical site is collected in one or more fluid collection containers (e.g., canisters). The volume of fluid collected from the surgical site is typically determined by measuring weight. A fluid deficit is then calculated by comparing the volume of fluid delivered to the surgical site with the volume of fluid returned from the surgical site.
Canisters are frequently used as fluid collection containers. When a canister fills with fluid to a maximum capacity during a medical procedure, it becomes necessary to remove the full canister and replace it with a new, empty canister. There are several drawbacks to removing and replacing canisters during a medical procedure. In this regard, such activity can (i) disrupt the medical procedure by necessitating the suspension of suction used to remove fluid from the surgical site, and thereby cause a suspension of fluid deficit monitoring; (ii) cause inconvenience to medical personnel, especially in surgical procedures involving high fluid volumes, as medical personnel have to physically remove full canisters and replace them with new, empty canisters; (iii) potentially introduce errors into fluid deficit monitoring calculations due to disruption of the fluid management system during the canister replacement process (e.g., bumping or moving), which can adversely affect the ability of the fluid management system to accurately weigh the remaining and new canisters; (iv) potentially introduce errors into fluid deficit monitoring calculations due to leaks and spills caused by detaching tubing used to return fluid from the surgical site from full canisters and reattaching such lines to the new, empty canisters, and (v) increase the cost of a surgical procedure by requiring that a number of canisters be used during a surgical procedure which is commensurate with the amount of fluid used.
In view of the foregoing, there is a need for a fluid management system that incorporates a “pass-through” fluid volume measurement system that continuously measures the volume of fluid returning from a surgical site during transit to a waste collection system (e.g., a dedicated fluid collection system or a hospital's waste disposal system) and eliminates the need to replace full canisters with new, empty canisters during a medical procedure.
In accordance with the present invention, there is provided a fluid management system comprising: at least one fluid supply container for storing a fluid to be delivered to a surgical site; a pump for delivering the fluid from the at least one fluid supply container to the surgical site; and a pass-through fluid volume measurement system for determining the volume of fluid returned from the surgical site, said pass-through fluid volume measurement system comprising: a plurality of fluid collection containers, wherein each fluid collection container has (i) a suction input in fluid communication with a suction line for drawing a vacuum in the fluid collection container, (ii) a fluid input in fluid communication with a fluid return line for receiving fluid returning from the surgical site, and (iii) a fluid output in fluid communication with a fluid output line for evacuating the fluid collected in the fluid collection container to a waste collection system; one or more weight sensors for providing signals indicative of the sensed weight of the fluid collection containers; and a plurality of valves moveable between open and closed positions to control the flow of fluid through the suction line, the fluid return line and the fluid output line; a suction source for providing suction in the suction line to draw a vacuum in the fluid collection containers to thereby draw fluid from the surgical site into the fluid collection containers, and for providing suction in the fluid output line to draw fluid collected in the fluid collection containers into the waste collection system; and a control unit for receiving the signals from the one or more weight sensors to monitor a volume of fluid returned from the surgical site to the fluid collection containers, and moving the plurality of valves between the open and the closed positions to alternately fill one of the fluid collection containers while emptying another of the fluid collection containers.
In accordance with another aspect of the present invention, there is provided a fluid management system comprising: at least one fluid supply container for storing a fluid to be delivered to a surgical site; a pump for delivering the fluid from the at least one fluid supply container to the surgical site; and a pass-through fluid volume measurement system for determining the volume of fluid returned from the surgical site, said pass-through fluid volume measurement system comprising: a support member for supporting components of the pass-through fluid volume measurement system; a flow sensing device including: a disposable or single-use fluid measurement tube having an inlet port in fluid communication with a fluid return line for receiving fluid returning from the surgical site, and an outlet port in fluid communication with a fluid output line for receiving the fluid exiting the fluid measurement tube, at least one ultrasonic sensor for providing a signal indicative of the flow rate of fluid passing through the fluid measurement tube, and a clamping mechanism mounted to the support member, said clamping mechanism for temporarily mounting the fluid measurement tube in a proper orientation between the inlet and outlet ultrasonic sensors; a suction source for providing suction in the fluid return line and fluid output line to draw the fluid through the fluid measurement tube and subsequently into a waste collection system; and a control unit for receiving the signals from the inlet and outlet sensors to monitor a volume of fluid returned from the surgical site.
In accordance with still another aspect of the present invention, there is provided a method for continuously measuring a volume of fluid being returned from a surgical site as it is being delivered to a waste collection system, said method comprising: filling the first fluid collection container, by: opening a valve associated with a suction line in fluid communication with a first fluid collection container; opening a valve associated with a fluid return line in fluid communication with the first fluid collection container; closing a valve associated with a fluid output line in fluid communication with the first fluid collection container; closing a valve associated with a suction line in fluid communication with a second fluid collection container; and closing a valve associated with a fluid return line in fluid communication with the second fluid collection container; upon filling the first fluid collection container with fluid to a predetermined volume, emptying the first fluid collection container and filling the second fluid collection container, by closing the valve associated with a suction line in fluid communication with a first fluid collection container; closing the valve associated with a fluid return line in fluid communication with the first fluid collection container; opening the valve associated with a fluid output line in fluid communication with the first fluid collection container; opening the valve associated with a suction line in fluid communication with a second fluid collection container; opening the valve associated with a fluid return line in fluid communication with the second fluid collection container; and closing a valve associated with a fluid output line in fluid communication with the second fluid collection container; and alternately filling and emptying the first and second fluid collection containers until a medical procedure is completed.
In accordance with yet another aspect of the present invention, there is provided a method for continuously measuring a volume of fluid being returned from a surgical site as it is being delivered to a waste collection system, said method comprising the steps of: drawing fluid from the surgical site through a flow sensing device providing signals indicative of a fluid flow rate; monitoring the volume of fluid passing through the flow sensing device using the signals indicative of the fluid flow rate; and passing the fluid from the flow sensing device to the waste collection system until a medical procedure is completed.
An advantage of the present invention is the provision of a fluid management system that continuously measures the volume of fluid returning from a surgical site during transit to a waste collection system.
Another advantage of the present invention is the provision of a fluid management system that eliminates the need to replace full fluid collection containers with new, empty fluid collection containers during a medical procedure.
A still further advantage of the present invention is the provision of a fluid management system having a stand-alone pass-through fluid volume measurement system.
Yet another advantage of the present invention is the provision of a fluid management system capable of fluid delivery, suction, fluid removal/collection, fluid deficit monitoring, and fluid disposal.
These and other advantages will become apparent from the following description of illustrated embodiments taken together with the accompanying drawings and the appended claims
The invention may take physical form in certain parts and arrangement of parts, embodiments of which will be described in detail in the specification and illustrated in the accompanying drawings which form a part hereof, and wherein:
Referring now to the drawings wherein the showings are for the purposes of illustrating embodiments of the invention only and not for the purposes of limiting same,
FMS 10A is generally comprised of a fluid management unit 20A including a main unit 30, a pass-through fluid volume measurement system 60 and an integrated suction source 90. Fluid management unit 20A interfaces with a waste collection system 110, as will be described below. It should be appreciated that suction source 90 may alternatively be arranged as a component of measurement system 60.
As seen in
Main unit 30 includes a control unit comprised of components such as a microprocessor or microcontroller, memory device(s), data storage device(s), output device(s) (e.g., LCD screen, touch screen, conventional display device, audio speaker, printer, and the like), and input device(s) (e.g., touch screen, keypad, keyboard, mouse, mechanical switching devices, and the like). Main unit 30 may also include one or more fluid container supports (such as hangers or hooks) for supporting one or more fluid supply containers (e.g., fluid bags) that store fluid that is to be delivered to a surgical site 200, weight sensors for detecting the weight of fluid in the fluid supply containers, and a pump for pressurizing fluid in the fluid supply containers and delivering the fluid to surgical site 200 via fluid supply line 40. For example, fluid supply line may be connected with a surgical instrument to facilitate a surgical procedure. It should be appreciated that gravity or other means of fluid pressurization may be substituted for the pump. Main unit 30 may also include numerous other components for regulating fluid flow, fluid pressure, fluid temperature (e.g., a fluid heating apparatus), and the like. The control unit controls the supply of fluid delivered to surgical site 200 via fluid supply line 40, monitors the volume of fluid supplied to surgical site 200 (via supply line 40), monitors the volume of fluid returned from surgical site 200 (via return line 43), and determines a fluid deficit. A detailed description of the components and operation of an exemplary fluid management unit, including fluid deficit monitoring, is provided in U.S. Pat. No. 8,444,592, issued May 21, 2013, which is fully incorporated herein by reference.
Pass-through fluid volume measurement system 60 determines the volume of fluid removed from surgical site 200 via fluid return line 43. According to the illustrated embodiment, measurement system 60 includes a first fluid collection container 64, a second fluid collection container 66, and first and second weight sensors 84, 86 respectively associated with fluid collection containers 64, 66. It is contemplated that fluid collection containers 64, 66 may take a variety of forms, including, but not limited to, disposable or re-usable rigid hard-shell canisters, rigid hard-shell canisters with disposable or reusable liners, disposable pouches or bags having a rigid skeleton, fluid containers supportable from mounting brackets or hooks.
The end of return line 43 located at surgical site 200 may include a plurality of input lines that are combined by a manifold. Each of these input lines may be located at different locations at surgical site 200. For example, the input lines may collect fluid from the patient, floor suctioning equipment, a fluid collection drape, and surgical instrument outflow ports.
In the embodiment shown in
Weight sensors 84, 86 may take the form of load cells that provide signals to main unit 30 indicative of the measured weight of fluid respectively collected in fluid collection containers 64, 66. The control unit of main unit 30 determines the volume of fluid collected in fluid collection containers 64, 66 from the measured weight.
Suction source 90 is fluidly connected with fluid collection containers 64, 66 (via suction line 33) and waste collection system 110 (via suction line 38). Waste collection system 110 is fluidly connected with fluid collection containers 64, 66 (via output line 53). Suction source 90 draws a vacuum in fluid collection containers 64, 66 (via suction line 33) to return fluid from surgical site 200 to fluid collection containers 64, 66 via return line 43. Suction source 90 also provides suction in suction line 38 and output line 53 to subsequently evacuate fluid collected in fluid collection container 64, 66 to waste collection system 110 via fluid output line 53. In the illustrated embodiment, suction source 90 takes the form of a vacuum pump.
Suction line 33 includes a first branch 34 and a second branch 36 for fluid communication with suction inputs (e.g., a suction tube) of fluid collection containers 64, 66, respectively. Branches 34 and 36 may be joined by a y-connector. Valves 34a, 36a respectively control suction along first and second branches 34, 36 of suction line 33. In one embodiment of the present invention, valves 34a, 36a may take the form of pinch valves operable to open and close the fluid pathway through suction line 33. Sections of tubing forming suction branches 34, 36 of suction line 33 are respectively routed through the pinch valves that are controlled by the control unit of main unit 30. Furthermore, a hydrophobic filter may be located within suction line 33 to prevent fluid from being sucked out of fluid collection containers 64, 66 through suction line 33. For example, hydrophobic filters may be located within branches 34 and 36 of suction line 33.
Output line 53 includes a first branch 54 and a second branch 56 for fluid communication with fluid outputs (e.g., a dip tube or bottom suction tube) of fluid collection containers 64, 66, respectively. Branches 54 and 56 may be joined by a y-connector. Valves 54a, 56a respectively control fluid flow along first and second branches 54, 56 of output line 53. In one embodiment of the present invention, valves 54a, 56a may take the form of pinch valves operable to open and close the fluid pathway through output line 53. Sections of tubing forming suction branches 54, 56 of suction line 53 are respectively routed through the pinch valves that are controlled by the control unit of main unit 30.
As indicated above, return line 43, suction line 33, and output line 53 take the form of fluid conduits, such as conventional medical grade flexible plastic tubing. In one embodiment of the present invention, the sections of tubing for branches 44, 46 (return line 43); branches 34, 36 (suction line 33); and branches 54, 56 (output line 53) may each include an integrated strain relief element that “snaps” into, or otherwise attaches to, a support structure (e.g., stand, mounting bracket, frame, etc.) of fluid management unit 20A. For example, the strain relief element may be mounted to a support stand 22, described below with reference to
It is contemplated that waste collection system 110 may take a variety of different forms, including, but not limited to, a mobile fluid collection container or cart, a dedicated stand-alone fluid collection system with integrated suction, or a hospital's waste disposal system which may be accessible in the operating room.
In the illustrated embodiment, a combined tissue/air trap 132 (or individual tissue and air traps) is located within return line 43. A tissue trap (or other similar device) functions to collect tissue carried by fluid returning from surgical site 200 via return line 43 for subsequent analysis and/or to increase the accuracy of fluid deficit calculations. In the absence of a tissue trap, tissue returned from surgical site 200 can increase the weight of fluid collection canisters or interfere with fluid flow sensing measurements. Similarly, an air trap can increase the accuracy of fluid deficit calculations as air bubbles can interfere with fluid flow sensing measurements.
For enhanced safety, it is contemplated that measurement system 60 may also include one or more fluid level sensors for detecting the fluid level within fluid collection containers 64 and 66, and one or more leak sensors for detecting the presence of a leak in fluid collection containers 64, 66 or in a tubing connection associated therewith. A fluid level sensor determines, independently of the control unit of main unit 30, whether a fluid level has reached a predetermined fluid level within fluid collection containers 64, 66 and can close one or more of valves 44a, 46a, 34a, and 36a, if necessary. When a leak sensor detects the presence of a leak, the leak sensor transmits a signal to the control unit of main unit 30. In response to receipt of this signal, the control unit can take appropriate action, such as “closing” one or more of valves 44a, 46a, 34a, 36a and providing a visual and/or audible indicator to alert a user of a potential problem with measurement system 60.
The operation of FMS 10A will now be described in detail with reference to
When a user initiates a procedure using main unit 30 that begins the flow of fluid to surgical site 200 via supply line 40, the control unit “zeroes” any previously stored weight values and begins recording the weight of each fluid collection container 64, 66 as indicated by respective weight sensors 84, 86. Then, valves 34a, 44a associated with the suction input and the fluid input of fluid collection container 64 are “opened” and valve 54a associated with the fluid output of fluid collection container 64 is “closed.” Furthermore, valves 36a and 46a associated with the suction input and fluid input of fluid collection container 66 are “closed.”
The control unit of main unit 30 monitors the volume of fluid supplied to the surgical site 200 and monitors the volume of fluid returned to fluid collection container 64 via signals received from weight sensor 84. When the fluid volume collected in fluid collection container 64 reaches a predetermined volume, the control unit “closes” valves 34a, 44a respectively associated with the suction input and the fluid input of fluid collection container 64, allows the weight sensor reading to stabilize, records the total weight of fluid collection container 64, and then “opens” valve 54a associated with the fluid output of fluid collection container 64 in order to empty fluid collection container 64 by evacuating the collected fluid to waste collection system 110. Simultaneously, the control unit “opens” valves 36a and 46a respectively associated with the suction input and the fluid input of fluid collection container 66, and “closes” valve 56a associated with the fluid output of fluid collection container 66 to begin filling fluid collection container 66 with the fluid returned from surgical site 200. In this manner, fluid collection from surgical site 200 and fluid deficit monitoring continues uninterrupted. The above-described “alternating” fill/empty process (i.e., alternating the filling and emptying of fluid collection containers 64 and 66), is repeated until the user ends the fluid collection procedure.
In accordance with the present invention, measurement system 60 is adapted to measure any amount of fluid returned from surgical site 200 during a medical procedure, without the burdensome and costly need to change fluid collection containers. Furthermore, the present invention allows fluid management unit 20A to continuously return fluid from surgical site 200, and thus allows uninterrupted determination of the fluid deficit which can be displayed to a user by visual and/or audible indicators (e.g., alarms) that may be appropriate based on the measured or calculated fluid deficit level.
In the embodiment shown in
In the embodiment shown in
In the embodiment shown in
It should be appreciated that the suction sources described herein (i.e., suctions source 90, 95, 100 and 120) may take a variety of forms including, but not limited to, a vacuum pump, a peristaltic pump, rotary vane pump, gerotor pump, piston pump, and the like.
In accordance with an embodiment of the present invention, fluid collection containers 64, 66 and all tubing associated suction line 33, return line 43 and output line 53 are components of a single-use/disposable tubing set. For example,
Tubing sets similar to those illustrated in
Referring now to
It is contemplated that the pass-through fluid volume measurement system of the present invention may take alternative forms. Referring now to
It also contemplated that measurement system 260 may also include one or more temperature sensors 290 for sensing the temperature of the fluid in measurement tube 262. Temperature sensor 290 is properly oriented to measure the temperature of the fluid when measurement tube 262 is received into clamping mechanism 280. Temperature sensor 290 provides fluid temperature information to the control unit of main unit 30, which uses the temperature information to more accurately determine the fluid flow rate through measurement tube 262.
Furthermore, measurement system 260 may also include an accumulator in addition to combined tissue/air trap 132. The accumulator conditions the fluid prior to entering measurement tube 262 by absorbing surges or pulsations in the fluid flow.
Ultrasonic flowmeters use sound waves to determine the velocity of a fluid flowing in a pipe or tube. At “no flow” conditions, the frequencies of an ultrasonic wave transmitted into the tube and its reflections from the fluid are the same. Under flowing conditions, the frequency of the reflected wave is different due to the Doppler effect. When the fluid moves faster, the frequency shift increases linearly. Signals from the transmitted wave and its reflections are processed to determine the flow rate. A “transit time” ultrasonic flowmeter sends and receives ultrasonic waves between transducers in both the upstream and downstream directions in the tube. At “no flow” conditions, it takes the same time to travel upstream and downstream between the two transducers. Under flowing conditions, the upstream wave will travel slower and take more time than the (faster) downstream wave. When the fluid moves faster, the difference between the upstream and downstream times increases. Upstream and downstream times are processed to determine the flow rate.
For the embodiment of measurement system 260 shown in
In
In
It is contemplated in another alternative embodiment that the two ultrasonic sensors 274, 276 may be arranged in positions relative to measurement tube 262 that differ from the positions as depicted in the illustrated figures. For example, ultrasonic sensors 274, 276 may be located at the top and bottom portions of measurement tube 262. Furthermore, it is also contemplated that the measurement system may be configured with only a single ultrasonic sensor (e.g., an ultrasonic transceiver) for determining the volume of fluid flowing through measurement tube 262. For example,
In accordance with an embodiment of the present invention, measurement tube 262, return line 43 and output line 53 are components of a single-use/disposable tubing set. For example,
It should be appreciated that according to an alternative embodiment of the present invention, measurement systems 60 and 260 (including alternative embodiments 260A and 260B) may be configured as stand-alone devices that are physically separated from the fluid management unit. In this alternative embodiment, measurement systems 60, 260 may include their own control unit (independent of the control unit of main unit 30) having a microprocessor/microcontroller, display unit, and input unit. According to this embodiment, the control unit of the measurement system may perform some of the functions (described above) that are carried out by the control unit of main unit 30. Furthermore, measurement systems 60, 260 may also include a wireless or wired communications interface for communicating with main unit 30 of the fluid management unit via a wireless or wired communications medium. As a stand-alone device, measurement systems 60, 260 may be mounted to a portable support structure (e.g., a cart or mobile stand) or fixed support structure (e.g., a wall). Furthermore, the strain relief element discussed above may attach to the support structure that independently supports stand-alone measurement systems 60, 260.
It is contemplated that a variety of modifications and alterations may be made to the illustrated embodiments of the present invention without departing from the spirit and scope of the present invention. For example, the number of fluid collection containers and weight sensors may be greater than the number of fluid collection containers shown in the embodiments described above. In one alternative embodiment, a single weight sensor may be used to sense the weight of multiple fluid collection containers. Moreover, it is contemplated that other suitable means may be substituted for the weight sensors to detect the volume of fluid in the fluid collection containers (e.g., means for counting pump rotations or height of water column as determined through optical sensing). In addition, other types of tube constricting devices may be substituted for the above-described valves, including manually-controllable devices.
It is further contemplated that the accuracy of fluid deficit calculations may be improved by using an opacity meter to provide information indicative of the composition of the fluid returned from the surgical site. In this regard, the opacity meter provides a signal to the control unit of main unit 30 that can be used to ascertain or estimate the percentage of blood that comprises the fluid returned from the surgical site. For example, an opacity meter could be used to sense the opacity of the fluid flowing through return line 43, collected in fluid collection containers 64, 66, flowing through measurement tube 262, or flowing through output line 53.
Other modifications and alterations will occur to others upon their reading and understanding of the specification. It is intended that all such modifications and alterations be included insofar as they come within the scope of the invention as claimed or the equivalents thereof.
This application claims the benefit of U.S. Provisional Application No. 61/993,340, filed May 15, 2015, which is hereby fully incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
3475590 | Pins | Oct 1969 | A |
3515137 | Santomieri | Jun 1970 | A |
4180074 | Murry et al. | Dec 1979 | A |
4278078 | Smith | Jul 1981 | A |
4388922 | Telang | Jun 1983 | A |
4464563 | Jewett | Aug 1984 | A |
4574876 | Aid | Mar 1986 | A |
4759749 | Verkaart | Jul 1988 | A |
4844074 | Kurucz | Jul 1989 | A |
4898518 | Hubbard et al. | Feb 1990 | A |
4911691 | Aniuk et al. | Mar 1990 | A |
5013303 | Tamari et al. | May 1991 | A |
5050266 | Schneider | Sep 1991 | A |
5106373 | Augustine et al. | Apr 1992 | A |
5125069 | O'Boyle | Jun 1992 | A |
5137509 | Freitas | Aug 1992 | A |
5178606 | Ognier et al. | Jan 1993 | A |
5195958 | Phillips | Mar 1993 | A |
5224929 | Remiszewski | Jul 1993 | A |
5228646 | Raines | Jul 1993 | A |
5245693 | Ford et al. | Sep 1993 | A |
5250032 | Carter, Jr. et al. | Oct 1993 | A |
5254094 | Starkey et al. | Oct 1993 | A |
5271086 | Kamiyama et al. | Dec 1993 | A |
5303735 | Cerola et al. | Apr 1994 | A |
D350822 | Lanigan | Sep 1994 | S |
5347992 | Pearlman et al. | Sep 1994 | A |
5368569 | Sanese | Nov 1994 | A |
5381510 | Ford et al. | Jan 1995 | A |
5382805 | Fannon et al. | Jan 1995 | A |
5388612 | Cerola et al. | Feb 1995 | A |
5391145 | Dorsey, III | Feb 1995 | A |
D357312 | Riquier et al. | Apr 1995 | S |
5420962 | Bakke | May 1995 | A |
5427144 | Teets et al. | Jun 1995 | A |
5447494 | Dorsey, III | Sep 1995 | A |
5449145 | Wortrich | Sep 1995 | A |
5460490 | Carr et al. | Oct 1995 | A |
5496314 | Eggers | Mar 1996 | A |
5505710 | Dorsey, III | Apr 1996 | A |
5520638 | O'Quinn et al. | May 1996 | A |
5522796 | Dorsey, III | Jun 1996 | A |
5522805 | Vancaillie et al. | Jun 1996 | A |
5551448 | Matula et al. | Sep 1996 | A |
5559924 | Kadotani et al. | Sep 1996 | A |
5562640 | McCabe et al. | Oct 1996 | A |
5573504 | Dorsey, III | Nov 1996 | A |
5586977 | Dorsey, III | Dec 1996 | A |
5607391 | Klinger et al. | Mar 1997 | A |
5626563 | Dodge et al. | May 1997 | A |
5643203 | Beiser et al. | Jul 1997 | A |
5683381 | Carr et al. | Nov 1997 | A |
5690614 | Carr et al. | Nov 1997 | A |
5709670 | Vancaillie | Jan 1998 | A |
5729653 | Magliochetti et al. | Mar 1998 | A |
5733263 | Wheatman | Mar 1998 | A |
D398051 | Lanigan et al. | Sep 1998 | S |
5800383 | Chandler et al. | Sep 1998 | A |
5803510 | Dorsey, III | Sep 1998 | A |
5807313 | Delk et al. | Sep 1998 | A |
5807332 | Augustine et al. | Sep 1998 | A |
5810770 | Chin et al. | Sep 1998 | A |
5814009 | Wheatman | Sep 1998 | A |
5830180 | Chandler et al. | Nov 1998 | A |
5836909 | Cosmescu | Nov 1998 | A |
5875282 | Jordan et al. | Feb 1999 | A |
5882339 | Beiser | Mar 1999 | A |
D409748 | Lanigan et al. | May 1999 | S |
5914047 | Griffiths | Jun 1999 | A |
5956130 | Vancaillie | Sep 1999 | A |
5989423 | Kamen et al. | Nov 1999 | A |
5993410 | Vincent et al. | Nov 1999 | A |
6024720 | Chandler et al. | Feb 2000 | A |
6047108 | Sword et al. | Apr 2000 | A |
6074363 | Beran et al. | Jun 2000 | A |
6106494 | Saravia et al. | Aug 2000 | A |
6139528 | Kistner et al. | Oct 2000 | A |
6139571 | Fuller et al. | Oct 2000 | A |
6142974 | Kistner et al. | Nov 2000 | A |
6146359 | Carr et al. | Nov 2000 | A |
6149622 | Marie | Nov 2000 | A |
6149674 | Borders | Nov 2000 | A |
6175688 | Cassidy et al. | Jan 2001 | B1 |
6176847 | Humphreys, Jr. et al. | Jan 2001 | B1 |
6213970 | Nelson et al. | Apr 2001 | B1 |
6234205 | D'Amelio et al. | May 2001 | B1 |
6236809 | Cassidy et al. | May 2001 | B1 |
6238366 | Savage et al. | May 2001 | B1 |
6246831 | Seitz et al. | Jun 2001 | B1 |
6257265 | Brunner et al. | Jul 2001 | B1 |
6259074 | Brunner et al. | Jul 2001 | B1 |
6261261 | Gordon | Jul 2001 | B1 |
6336003 | Mitsunaga et al. | Jan 2002 | B1 |
6358224 | Tims et al. | Mar 2002 | B1 |
6406470 | Kierce | Jun 2002 | B1 |
6413233 | Sites et al. | Jul 2002 | B1 |
6464666 | Augustine et al. | Oct 2002 | B1 |
6527743 | Fowler et al. | Mar 2003 | B1 |
6535689 | Augustine et al. | Mar 2003 | B2 |
6572641 | Brugger et al. | Jun 2003 | B2 |
6572689 | Cosby, II et al. | Jun 2003 | B2 |
6585708 | Maaskamp | Jul 2003 | B1 |
6595957 | Griffiths et al. | Jul 2003 | B1 |
6602221 | Saravia et al. | Aug 2003 | B1 |
6620130 | Ginsburg | Sep 2003 | B1 |
6635031 | French et al. | Oct 2003 | B2 |
6635034 | Cosmescu | Oct 2003 | B1 |
6641556 | Shigezawa | Nov 2003 | B1 |
6645232 | Carson | Nov 2003 | B2 |
6648906 | Lasheras et al. | Nov 2003 | B2 |
6652488 | Cover et al. | Nov 2003 | B1 |
6685667 | Delk et al. | Feb 2004 | B1 |
6699184 | Felix et al. | Mar 2004 | B2 |
6699267 | Voorhees et al. | Mar 2004 | B2 |
6722782 | Faries, Jr. et al. | Apr 2004 | B2 |
6743201 | Donig et al. | Jun 2004 | B1 |
6775473 | Augustine et al. | Aug 2004 | B2 |
6788885 | Mitsunaga et al. | Sep 2004 | B2 |
6824528 | Faries, Jr. et al. | Nov 2004 | B1 |
6875198 | Foley | Apr 2005 | B2 |
6882797 | Stewart et al. | Apr 2005 | B2 |
6899697 | Fowler et al. | May 2005 | B2 |
6901216 | Jusiak et al. | May 2005 | B2 |
6918902 | French et al. | Jul 2005 | B2 |
6958058 | Hunter, Sr. et al. | Oct 2005 | B1 |
6997942 | Machold et al. | Feb 2006 | B2 |
7004960 | Daoud | Feb 2006 | B2 |
7010221 | Augustine et al. | Mar 2006 | B2 |
7031602 | Faries, Jr. et al. | Apr 2006 | B2 |
7083601 | Cosmescu | Aug 2006 | B1 |
7094219 | Noice et al. | Aug 2006 | B2 |
7153285 | Lauman et al. | Dec 2006 | B2 |
7158719 | Cassidy | Jan 2007 | B2 |
7164852 | Cazzini et al. | Jan 2007 | B2 |
7207966 | Savare et al. | Apr 2007 | B2 |
7232457 | Schmidt et al. | Jun 2007 | B2 |
7236694 | Chammas | Jun 2007 | B1 |
7238170 | Park | Jul 2007 | B2 |
7258711 | Dunn et al. | Aug 2007 | B2 |
7261557 | Gill et al. | Aug 2007 | B2 |
7273359 | Blight et al. | Sep 2007 | B2 |
7297133 | Nelson et al. | Nov 2007 | B2 |
7316666 | Entenman et al. | Jan 2008 | B1 |
7394976 | Entenman et al. | Jul 2008 | B2 |
7410475 | Krensky et al. | Aug 2008 | B2 |
7458951 | Lauman et al. | Dec 2008 | B2 |
7621898 | Lalomia et al. | Nov 2009 | B2 |
D615191 | McGill et al. | May 2010 | S |
D616539 | McGill | May 2010 | S |
7753880 | Malackowski | Jul 2010 | B2 |
7762989 | Simpson | Jul 2010 | B2 |
D650896 | McGill et al. | Dec 2011 | S |
8123731 | Ryan | Feb 2012 | B2 |
8138925 | Downie et al. | Mar 2012 | B2 |
8388570 | Kumar et al. | Mar 2013 | B2 |
8562577 | Michaels et al. | Oct 2013 | B2 |
8652089 | Kumar et al. | Feb 2014 | B2 |
9492071 | Woolford et al. | Nov 2016 | B2 |
20020032403 | Savagle et al. | Mar 2002 | A1 |
20020096984 | Konishi et al. | Jul 2002 | A1 |
20030004470 | Hickerson et al. | Jan 2003 | A1 |
20030109826 | Fowler et al. | Jun 2003 | A1 |
20030176833 | Libermann | Sep 2003 | A1 |
20030212363 | Shipp | Nov 2003 | A1 |
20030216689 | Bouhuijs et al. | Nov 2003 | A1 |
20040097872 | Delk et al. | May 2004 | A1 |
20040190884 | Stewart et al. | Sep 2004 | A1 |
20040204679 | Visconti et al. | Oct 2004 | A1 |
20050055074 | Tak et al. | Mar 2005 | A1 |
20050095155 | Blight et al. | May 2005 | A1 |
20050142013 | Faries, Jr. et al. | Jun 2005 | A1 |
20050148934 | Martens et al. | Jul 2005 | A1 |
20060122576 | Raja et al. | Jun 2006 | A1 |
20060148279 | German et al. | Jul 2006 | A1 |
20060210255 | Cassidy | Sep 2006 | A1 |
20060222350 | Cassidy | Oct 2006 | A1 |
20060253075 | Faries, Jr. et al. | Nov 2006 | A1 |
20070045272 | French et al. | Mar 2007 | A1 |
20070129707 | Blott et al. | Jun 2007 | A1 |
20070142773 | Rosiello et al. | Jun 2007 | A1 |
20070142775 | Visconti et al. | Jun 2007 | A1 |
20070159337 | Tethrake et al. | Jul 2007 | A1 |
20070161978 | Fedenia et al. | Jul 2007 | A1 |
20070217948 | Ghelli et al. | Sep 2007 | A1 |
20070233003 | Radgowski et al. | Oct 2007 | A1 |
20070242934 | Entenman et al. | Oct 2007 | A1 |
20070265689 | Frey | Nov 2007 | A1 |
20080031773 | Eccleston | Feb 2008 | A1 |
20080039815 | Ogawa | Feb 2008 | A1 |
20080077087 | Martens | Mar 2008 | A1 |
20080093276 | Roger et al. | Apr 2008 | A1 |
20080145249 | Smisson et al. | Jun 2008 | A1 |
20080154095 | Stubkjaer et al. | Jun 2008 | A1 |
20090008306 | Cicchello | Jan 2009 | A1 |
20090009290 | Kneip et al. | Jan 2009 | A1 |
20100151785 | Steeger et al. | Jun 2010 | A1 |
20100152656 | Music | Jun 2010 | A1 |
20100228222 | Williams et al. | Sep 2010 | A1 |
20100228224 | Pyles | Sep 2010 | A1 |
20110144812 | Davis et al. | Jun 2011 | A1 |
20110162333 | Cook et al. | Jul 2011 | A1 |
20110288524 | Gelfand | Nov 2011 | A1 |
20120022441 | Kelly | Jan 2012 | A1 |
20120271110 | Kumar | Oct 2012 | A1 |
20130079702 | Klein et al. | Mar 2013 | A1 |
20130345621 | Cicchello | Dec 2013 | A1 |
20140217029 | Meyer | Aug 2014 | A1 |
20150119795 | Germain | Apr 2015 | A1 |
20160151557 | Woolford et al. | Jun 2016 | A1 |
Number | Date | Country |
---|---|---|
0 776 670 | Jun 1997 | EP |
0 575 512 | May 1998 | EP |
2 242 367 | Oct 1991 | GB |
WO 8700759 | Feb 1987 | WO |
WO 9217040 | Oct 1992 | WO |
WO 9613216 | May 1996 | WO |
WO 0047283 | Aug 2000 | WO |
WO 2010104878 | Sep 2010 | WO |
Entry |
---|
International Search Report and Written Opinion for International Application No. PCT/US2010/026698, dated Jun. 29, 2010. |
The Surgical Company, Fluido® Product Information obtained from website www.fluido.nl, Jan. 18, 2008. |
Smiths-Medical.com, Blood & Fluid Warming Systems (Level 1®) H-1200 Fast Flow Fluid Warmer with Integrated Air Detector/Clamp, 2008. |
Ranger Blood/Fluid Warming, Ranger® Blood and Fluid Warming Systems Product Specifications, 2008. |
Paladin Biomedical Corporation, In-Line Microwave Fluid Warming Technology1,2, T900™ system, 2004. |
Smiths-Medical.com, Blood & Fluid Warming Systems (Level 1®), NormoFlo® Irrigating System, Level 1, 2008. |
Ranger Irrigation Fluid Warming, Ranger® Blood and Fluid Warming Systems, Ranger Irrigation Fluid Warming System, 2008. |
Socomed, Endoflow® by Socomed, slide presentation, prior to Sep. 2008. |
Stryker® UK, Strykflow 2 Suction & Irrigation System, 2008. |
Stryker, Stryket AHTO™ Irrigation System, Dec. 2004. |
Olympus, Surgiflow, Irrigation Pump, Feb. 2006. |
Olympus, Surgipump, Suction/Irrigation Pump, Feb. 2006. |
Olympus, Eco-Pump, Irrigation Pump, Feb. 2006. |
CardinalHealth, Hydroline® and PulseWave® Laparoscopic Suction/Irrigation Systems, 2003. |
Gaymar®, Medi-Temp III™, Blood/Fluid Warming, prior to Sep. 2008. |
Belmont Instrument Corporation, FMS 2000 Rapid Infuser, 2003. |
Belmont Instrument Corporation, buddy™, Fluid Warmer, 2003. |
Astotherm®, Astotherm® plus 220, Blood and Infusion Wanner, prior to Sep. 2008. |
Futuremed®, Animec™ AM-25, Fluid Warmer, 2000-2007. |
Vital Signs Inc., Medical Products, enFlow®, IV Fluid/Blood Warming System, prior to Sep. 2008. |
Smiths-Medical.com, Blood & Fluid Warming Systems (Level 1®) Hotline® Blood and Fluid Warmer, 2008. |
Stryker®, Pulsed Lavage, Interpulse—Pulsed Lavage, Wound Care, 2008. |
Simpulse* VariCare* System, Wound Management, 2007. |
Zimmer, Pulsavac®, Wound Debridement System, 1998. |
Zimmer, Pulsavac Plus System, Wound Debridement System, Nov. 2, 2005. |
Zimmer, Pulsavae Plus AC, Wound Debridement System, Jun. 8, 2008. |
Richard Wolf Medical Instruments Corporation, The Richard Wolf Fluid Manager, Hysteroscopic Fluid Monitoring, prior to Sep. 2008. |
Olympus, Fluid Management Products, Dolphin® II and Disten-U-Flo Fluid Management Systems for Hysteroscopy, 2008. |
Olympus, HysteroFlow/HysteroBalance, Fluid Management, prior to Sep. 2008. |
Stryker, Stryker Fluid Management, FluidSafe Fluid Management System, prior to Sep. 2008. |
Young, RN. et al., Perioperative Fluid Management, AORN Journal, vol. 89, No. 1, Jan. 2009, pp. 167-183. |
Smith et al., Principles of Fluid and Blood Warming in Trauma, International TraumaCare (ITACCS), vol. 18, No. 1, 2008, pp. 71-79. |
Bard, Medical Division, Company Information obtained from website www.bardmedical.com, Jan. 29, 2008. |
C Change Surgical, Press Release obtained from website www.cchangesurgical.com, Jul. 24, 2007. |
C Change Surgical, IntraTemp™, Product Information obtained from website www.cchangesurgical.com, Jan. 18, 2008. |
C Change Surgical, Press Releases, Jul. 2004-Feb. 2008. |
CardinalHealth, Medi-Vac® Suction and Wound and Drainage Product Information obtained from website www.cardinal.com, Jan. 18, 2008. |
Davol Inc., Laparoscopy Surgical Product Information obtained from website www.davol.com, Jan. 18, 2008. |
Ethicon, Inc., Product Catalog obtained from website ecatalog.ethicon.com, Jan. 18, 2008. |
Johnson & Johnson Gateway®, Product Information, Fluid Management System, obtained from website www.jnjgateway.com, Jan. 18, 2008. |
Gyrus ACMI, Gyrus Medical, Niagara TRS® Thermal Retention System Product Information obtained from website www.acmicorp.com, Jan. 18, 2008. |
Innercool Therapies, Inc., Celsius Control System™, Product Information obtained from website www.innercool.com, Jan. 28, 2008. |
Medical Solutions, Inc., Fluid Warming System, Product Information obtained from website www.warmiv.com, Jan. 25, 2008. |
Nellcor Press Release, Nellcor Expands Warmflo Fluid and Blood Warming Solutions with New Warming Cassette, obtained from website www.cyperus.com, Jan. 18, 2008. |
Nellcor, Products Listing obtained from website www.nellcor.com, Jan. 18, 2008. |
Nellcor, Warmflo® Pressure Infusor Product Information obtained from website www.nellcor.com, Oct. 2, 2007. |
Nellcor, Warmflo® Fluid Warming System Brochure, 2002. |
Olympus, High Definition Video Laparoscopes, HD Endoeye™, Product Information obtained from website www.olympussurgical.com, Jan. 24, 2008. |
Olympus, UHI-3 High Flow Insufflation Unit Product Information obtained from website www.olympusmedical.co.kr, Jan. 18, 2008. |
Olympus, UHI-3 High Flow Insufflation Unit Product Information obtained from website www.olympusaustralia.com.au, Jan. 18, 2008. |
Paladin Biomedical Corporation, ThermoStat™ 900 Blood and Fluid Warmer Product Information obtained from paladinbiomedical.com, Jan. 22, 2008. |
Radiant Medical, Inc. Company Profile obtained from Silicon Valley/San Jose Business Journal website www.bizjournals.com, Jan. 25, 2008. |
Radiant Medical, Inc. Press Release, Oct. 12, 2005. |
Sanese Medical Corp., Thermo-Flo System 3, Product Information, search results for “new products” search of website speechtherapist.com, pp. 4-5, Jan. 18, 2008. |
Karl Storz, Suction and Irrigation Systems Product Information obtained from website www.websurg.com, Jan. 28, 2009. |
Stryker, Endoscopy, Stryket AHTO™ Irrigation System Product Catalog, Dec. 2004. |
Stryker® Instruments, Orthopedics, InterPulse Battery Powered Irrigation Product Catalog, prior to Sep. 2008. |
Stryker, Stryker StrykeFlow 2 Product Information obtained from website www.stryker.com, Jan. 18, 2008. |
Stryker, Stryker AHTO Irrigation System Product Information obtained from website www.stryker.com, Jan. 18, 2008. |
TSCI Company Profile obtained from website www.fluido.nl, Jan. 18, 2008. |
TSCI Press Release obtained from website www.fluido.nl, Jan. 18, 2008. |
CystoMedix, Company/Product Information obtained from website www.cystomedix.com, Jan. 28, 2010. |
Number | Date | Country | |
---|---|---|---|
20150328379 A1 | Nov 2015 | US |
Number | Date | Country | |
---|---|---|---|
61993340 | May 2014 | US |